Microbiologia/Virologia
Os inibidores de microbiologia e virologia são compostos que têm como alvo microrganismos, incluindo bactérias, vírus e fungos, interrompendo seu crescimento, replicação ou sobrevivência. Esses inibidores são essenciais para estudar a patogênese microbiana, entender os mecanismos de resistência e desenvolver novas terapias antimicrobianas e antivirais. Os inibidores nessa categoria são usados para combater doenças infecciosas, explorar a ecologia microbiana e investigar as interações hospedeiro-patógeno. Na CymitQuimica, oferecemos uma ampla seleção de inibidores de alta qualidade para microbiologia e virologia para apoiar sua pesquisa em doenças infecciosas, microbiologia e virologia.
Subcategorias de "Microbiologia/Virologia"
- Antibacteriano(2.949 produtos)
- Antibiótico(918 produtos)
- Antifecção(23 produtos)
- DHFR(32 produtos)
- Síntese de DNA/RNA(706 produtos)
- HBV(176 produtos)
- HIV Protease(447 produtos)
- HSV(91 produtos)
- Integrase(2 produtos)
- Ribossomo(13 produtos)
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Foram encontrados 5832 produtos de "Microbiologia/Virologia"
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(-)-Rabdosiin
CAS:<p>(-)-Rabdosiin, identified as a novel phenolic marker in Symphytum officinale L., exhibits antioxidant, neuroprotective, and anti-HIV activities [1].</p>Fórmula:C36H30O16Cor e Forma:SolidPeso molecular:718.61Chevalone C
CAS:<p>Chevalone C: antituberculosis (MIC 6.3μg/ml), anti-breast cancer (IC50 8.7μg/ml), fights multidrug-resistant bacteria, kills colorectal cancer cells.</p>Fórmula:C28H40O5Cor e Forma:SolidPeso molecular:456.61Nafcillin sodium
CAS:<p>Nafcillin sodium: an antibiotic, β-lactamase inhibitor, treats staph infections.</p>Fórmula:C21H21N2NaO5SCor e Forma:SolidPeso molecular:436.46Antituberculosis agent-13
<p>Antituberculosis agent-13 (Compound 11) demonstrates antituberculosis activity, effectively inhibiting both wild-type and mutant strains of Mycobacterium tuberculosis, with an IC50 range of 4-62.5 nM. Additionally, Antituberculosis agent-13 exhibits anti-leukemia properties, inhibiting MOLM-13 with an IC50 of 3.8 μM.</p>Fórmula:C15H14N2O5Cor e Forma:SolidPeso molecular:302.282Elvucitabine
CAS:<p>Elvucitabine, a reverse transcriptase inhibitor, is used potentially for the treatment of HBV infection and HIV infection.</p>Fórmula:C9H10FN3O3Cor e Forma:SolidPeso molecular:227.19Peniterphenyl A
CAS:<p>Peniterphenyl A from deep-sea Penicillium blocks HSV-1/2 entry by targeting glycoprotein D, hindering adsorption and fusion.</p>Fórmula:C19H14O6Cor e Forma:SolidPeso molecular:338.31Antibiotic LB 10517
CAS:<p>Antibiotic LB 10517 is a catechol-substituted cephalosporin with a broad spectrum of antibacterial.</p>Fórmula:C27H25N9NaO9S2Pureza:98%Cor e Forma:SolidPeso molecular:706.66Pomolic acid 3-acetate
CAS:<p>Pomolic Acid 3-Acetate, an antitubercular compound, exhibits a minimum inhibitory concentration (MIC) of 32 μM against Mycobacterium tuberculosis H37Rv [1].</p>Fórmula:C32H50O5Cor e Forma:SolidPeso molecular:514.74Furaltadone L-tartrate
CAS:<p>Furaltadone L-tartrate, a nitrofuran, may help study Salmonella enteritidis in chickens; it's an antibacterial agent against staphylococci.</p>Fórmula:C17H22N4O12Cor e Forma:SolidPeso molecular:474.38Lankacyclinone C
<p>Lankacyclinone C, a congener of lankacidin C devoid of the δ-lactone moiety, exhibits antitumor activity.</p>Fórmula:C24H33NO5Cor e Forma:SolidPeso molecular:415.52Obtusalin
CAS:<p>Obtusalin, a triterpenoid initially identified in R. dauricum, exhibits UV absorption at 210 nm and possesses antibacterial properties.</p>Fórmula:C30H50O2Cor e Forma:SolidPeso molecular:442.726-Deoxy-8-O-methylrabelomycin
CAS:<p>6-Deoxy-8-O-methylrabelomycin is a useful organic compound for research related to life sciences.</p>Fórmula:C20H16O5Cor e Forma:SolidPeso molecular:336.343Anti-MERS-D12 mAb
<p>Anti-MERS-D12 mAb is a human IgG1 that neutralizes MERS-CoV by blocking its Spike RBD's interaction with DPP4.</p>Cor e Forma:Odour LiquidGuignardone K
CAS:<p>Guignardone K, a meroterpene compound extracted from solid cultures of the endophytic fungus Guignardia sp., exhibits antifungal activity [1].</p>Fórmula:C17H24O6Cor e Forma:SolidPeso molecular:324.37Neuraminidase-IN-16
<p>Neuraminidase-IN-16 (43b) inhibits H5N1, H5N8, H1N1, H3N2, H5N1-H274Y, H1N1-H274Y neuraminidases; IC50: 0.031-10.08 μM.</p>Fórmula:C26H35FN2O4Cor e Forma:SolidPeso molecular:458.57Antiviral agent 66
<p>Antiviralagent 66 (Compound 60) serves as an inhibitor of filoviruses (Filovirus), effectively suppressing pseudoviruses of Ebola, Marburg, Zaire, Sudan, Bundibugyo, Reston, and Tai Forest, with EC50 values of 0.16, 2.24, 0.16, 0.89, 0.21, 0.21, and 0.11 μM, respectively.</p>Fórmula:C27H29F3N4O3Cor e Forma:SolidPeso molecular:514.539Isatropolone A
CAS:<p>Isatropolone A from Streptomyces Gö66 has a 1,5-diketone; it's potent against Leishmania with IC50 of 0.5μM.</p>Fórmula:C24H24O9Cor e Forma:SolidPeso molecular:456.44(-)-Cleistenolide
CAS:<p>(-)-Cleistenolide, an α,β-unsaturated δ-lactone derived from Cleistochlamys kirkii Oliver, exhibits antibacterial and antitumor activity [1].</p>Fórmula:C18H18O8Cor e Forma:SolidPeso molecular:362.33(R)-Mucronulatol
CAS:<p>(R)-Mucronulatol is a natural product that can be used as a reference standard. The CAS number of (R)-Mucronulatol is 57128-11-7.</p>Fórmula:C17H18O5Cor e Forma:SolidPeso molecular:302.3Flambalactone
CAS:<p>Flambalactone is a degradation product formed by methanolysis of the antibiotic flambamycin.</p>Fórmula:C21H26Cl2O10Cor e Forma:SolidPeso molecular:509.338-NH2-ATP
CAS:<p>8-NH2-ATP is an inactive derivative of adenosine triphosphate (ATP), synthesized from 8-NH2-Ado.</p>Fórmula:C10H17N6O13P3Cor e Forma:SolidPeso molecular:522.207-TFA-ap-7-Deaza-ddA
CAS:<p>Compound 19c is a nucleotide derivative for DNA sequencing dye terminators.</p>Fórmula:C16H16F3N5O3Cor e Forma:SolidPeso molecular:383.331Trypanothione synthetase-IN-2
<p>Trypanothione synthetase-IN-2: competitive inhibitor for Leishmania TryS, IC50 5.4 μM with spermidine.</p>Fórmula:C41H69N7O11Cor e Forma:SolidPeso molecular:836.03Antitubercular agent-35
<p>Antitubercular agent-35 (42l) inhibits Mtb H37Rv (MIC 90=1.25 μg/mL) and M. Marinum (MIC 90=2 μg/mL), resists liver degradation, for TB research.</p>Fórmula:C19H13ClN4O2SCor e Forma:SolidPeso molecular:396.85NS5A-IN-1
<p>NS5A-IN-1 is a proagent of the HCV NS5A inhibitor Pibrentasvir (ABT-530).</p>Fórmula:C72H86F5N10O14PCor e Forma:SolidPeso molecular:1441.48Dalbavancin hydrochloride
CAS:<p>Dalbavancin HCl (MDL-63397 HCl), a semi-synthetic antibiotic, targets Gram-positive bacteria with low MICs for S. aureus and B. anthracis.</p>Fórmula:C88H101Cl3N10O28Cor e Forma:SolidPeso molecular:1853.15Anti gram-positive/negative bacteria agent 1
<p>Anti gram-positive/negative bacteria agent 1 is an antibiotic linked with a synthetic MECAM-based siderophore, serving as a conjugate aimed at combating gram-</p>Fórmula:C67H68N10O21SCor e Forma:SolidPeso molecular:1381.38Antibacterial agent 40
CAS:<p>Antibacterial agent 40 is an antibacterial agent.</p>Fórmula:C12H17N5O6SCor e Forma:SolidPeso molecular:359.36Antibacterial agent 272
<p>Antibacterialagent 272 (Compound Z22) is a potential antibacterial agent that targets the DNA and DNA-topoisomerase II (DNA-Topo II) complex. It exhibits strong antibacterial activity, with a minimum inhibitory concentration (MIC) of 1 μg/mL against Staphylococcus aureus 25923 and 29213, 2 μg/mL against Staphylococcus epidermidis 12228, 2-4 μg/mL against Enterococcus faecalis, and 4 μg/mL against Pseudomonas aeruginosa 9027 and 27853. Antibacterialagent 272 binds by intercalating between DNA base pairs, disrupting the normal function of bacterial DNA, and is suitable for research into bacterial infectious diseases.</p>Cor e Forma:Odour SolidXinjiachalcone A
CAS:<p>Xinjiachalcone A, from Glycyrrhiza inflata, kills H. pylori effectively (MIC: 12.5-50 μM, 17 strains).</p>Fórmula:C21H22O4Pureza:98%Cor e Forma:SolidPeso molecular:338.44-Deoxy-4α-phorbol
CAS:<p>4-Deoxy-4α-phorbol, a tetracyclic diterpene identified in E.</p>Fórmula:C20H28O5Cor e Forma:SolidPeso molecular:348.43Curvulamine A
CAS:<p>Curvulamine A, an antibacterial alkaloid, shows potent antibacterial activity [1] .</p>Fórmula:C20H24N2O2Cor e Forma:SolidPeso molecular:324.42Antibacterial agent 61
CAS:<p>Antibacterial agent 61 (example 27) is a antibacterial agent.</p>Fórmula:C9H11N5NaO7SCor e Forma:SolidPeso molecular:356.26Zegruvirimat
CAS:<p>Zegruvirimat is an antiviral agent. Zegruvirimat has antiviral activity [1] .</p>Fórmula:C49H70N4O5SCor e Forma:SolidPeso molecular:827.17Erythromycin A enol ether
CAS:<p>Erythromycin A enol ether is a degradation product of Erythromycin A which is a macrolide antibiotic.</p>Fórmula:C37H65NO12Pureza:99.94%Cor e Forma:SolidPeso molecular:715.91DprE1-IN-13
<p>DprE1-IN-13 (Compound 42) is an inhibitor of decaprenyl-phosphoryl-β-d-ribose oxidase (DprE1) with an IC50 value of 12.72 μM. It effectively inhibits Mycobacterium tuberculosis H37Ra, with a MIC50 of 1.071 μM.</p>Fórmula:C14H11N5O4Cor e Forma:SolidPeso molecular:313.27Rivabazumab
CAS:<p>Rivabazumab is a recombinant antibody against Pseudomonas aeruginosa pcrV [1] .</p>Cor e Forma:LiquidHatomamicin
CAS:<p>Hatomamicin is a biochemical.</p>Fórmula:C22H31NO5Cor e Forma:SolidPeso molecular:389.492HCV-IN-41
CAS:<p>HCV-IN-41: potent HCV inhibitor; EC50 - 0.006762 nM (1b), 5.183 nM (2a), 1.365 nM (3a), 142.2 nM (4a); hinders RNA replication.</p>Fórmula:C48H56N6O8Cor e Forma:SolidPeso molecular:844.99Abbeymycin
CAS:<p>Abbeymycin is an antibiotic</p>Fórmula:C13H16N2O3Cor e Forma:SolidPeso molecular:248.28Amdoxovir
CAS:<p>Amdoxovir is a reverse transcriptase inhibitor.</p>Fórmula:C9H12N6O3Cor e Forma:SolidPeso molecular:252.23SDZ 283-910
CAS:<p>SDZ 283-910 is used as a statine-derived inhibitor.</p>Fórmula:C46H59N5O9Pureza:98%Cor e Forma:SolidPeso molecular:826.004Aurachin SS
CAS:<p>Aurachin SS, a natural product isolated from Streptomyces sp. NA04227, is an antibiotic compound with demonstrated antibacterial activity [1].</p>Fórmula:C21H27NO2Cor e Forma:SolidPeso molecular:325.44Malacidin B
CAS:<p>Malacidin B, a macrocyclic lipopeptide antibiotic, demonstrates calcium-dependent antibacterial activity [1] [2].</p>Fórmula:C57H90N12O20Cor e Forma:SolidPeso molecular:1263.39Ogalvibart
CAS:<p>Ogalvibart is a humanized IgG1 monoclonal antibody targeting SARS-CoV-2 spike RBD, effective in COVID-19 prevention in rhesus monkeys.</p>Cor e Forma:LiquidCeratotoxin B
CAS:<p>Ceratotoxins B, an antibacterial peptide, is produced by sexually mature females of Ceratitis capitata (medfly).</p>Fórmula:C135H235N35O32Pureza:98%Cor e Forma:SolidPeso molecular:2860.53Antifungal agent 41
<p>Compound B01, an antifungal, inhibits Candida albicans in vitro/vivo for invasive fungal infection research.</p>Fórmula:C22H18Cl4N4Se2Cor e Forma:SolidPeso molecular:638.14Penicillin G benzathine tetrahydrate
CAS:<p>Penicillin G Benzathine Tetrahydrate (Benzathine Benzylpenicillin Tetrahydrate) serves as an antibiotic effective against numerous bacterial infections [1].</p>Fórmula:C48H64N6O12S2Cor e Forma:SolidPeso molecular:981.18SARS-CoV-2-IN-26
<p>SARS-CoV-2-IN-23: Antiviral diphosphate ester, disrupts membranes; IC50: 8.2 & 2.6 μM; EC50: 4.4 μM.</p>Fórmula:C52H52O8P2Cor e Forma:SolidPeso molecular:866.91HIV-1 integrase inhibitor 10
<p>HIV-1 integrase inhibitor 10: oral ALLINI, blocks NLRepRluc virus in MT-2 cells, EC50 of 3-5 nM, used in HIV-1 research.</p>Fórmula:C40H45N7O4Cor e Forma:SolidPeso molecular:687.83Antifungal agent 15
CAS:<p>Antifungal agent 15 exhibits remarkable potency, with EC50 values of 0.52 and 0.50 μg/mL against S. sclerotiorum and B. cinerea, respectively.</p>Fórmula:C19H11F8N3O2Cor e Forma:SolidPeso molecular:465.30Antibacterial agent 109
CAS:<p>Compound C-2, a non-mutagenic antibacterial against gram-positive/negative bacteria, inhibits protein synthesis.</p>Fórmula:C50H75N7O8Cor e Forma:SolidPeso molecular:902.17Tinophyllol
CAS:<p>Tinophyllol, a furanoditerpenoid derived from Arcangelisia flava MERR., exhibits effective activity against Botrytis cinerea [1] [2].</p>Fórmula:C21H26O6Cor e Forma:SolidPeso molecular:374.43HAA-09
CAS:<p>HAA-09: oral anti-influenza with EC50 of 0.03μM; inhibits PB2, IC50 0.06μM; non-toxic, blocks virus replication.</p>Fórmula:C17H18F2N6O2Cor e Forma:SolidPeso molecular:376.36CEF19, Epstein-Barr Virus latent NA-3A (458-466)
CAS:<p>CEF19 is the EBV NA-3A (458-466) epitope YPLHEQHGM from the B95.8 strain.</p>Fórmula:C49H70N14O14SPureza:98%Cor e Forma:SolidPeso molecular:1111.23RNA splicing modulator 3
CAS:<p>RNA Splicing Modulator 3 (Compound 236) is an effective RNA splicing modulator, exhibiting an AC50 value of less than 100 nM [1].</p>Fórmula:C19H20N6OSCor e Forma:SolidPeso molecular:380.477-Oxoganoderic acid Z
CAS:<p>7-Oxoganoderic acid Z is a useful organic compound for research related to life sciences. The catalog number is T123920 and the CAS number is 929248-72-6.</p>Fórmula:C30H46O4Cor e Forma:SolidPeso molecular:470.694Antimicrobial agent-36
<p>Antimicrobial agent-36 (Compound 8b) is an antimicrobial compound that significantly inhibits DNA gyrase with an IC50 value of 4.56 µM. It is also utilized in the preparation of nanoparticle drug formulations and can be employed in the research and development of new antibiotics.</p>Fórmula:C31H20N4O2SCor e Forma:SolidPeso molecular:512.581(8′α,9′β-Dihydroxy)-3-farnesylindole
<p>(8'α,9'β-Dihydroxy)-3-farnesylindole exhibits significant inhibitory effectiveness (EC 50 9.8 μM) against B. subtilis.</p>Fórmula:C23H31NO2Cor e Forma:SolidPeso molecular:353.5JM 1397
CAS:<p>JM 1397 is a bioactive chemical.</p>Fórmula:C16H18O2OsCor e Forma:SolidPeso molecular:432.54Potassium clavulanate mixture with silicon dioxide (1:1)
<p>Potassium Clavulanate Mixture with Silicon Dioxide (1:1) is a compound consisting of an equal parts ratio, specifically one part Potassium Clavulanate to one</p>Fórmula:C8H8KNO7SiCor e Forma:SolidPeso molecular:297.34Succinate dehydrogenase-IN-7
<p>Succinate dehydrogenase-IN-7 (Compound 2f) is a succinate dehydrogenase inhibitor with an IC50 value of 2.51 μM and exhibits bactericidal properties.</p>Fórmula:C11H5Cl2F3N2O2SCor e Forma:SolidPeso molecular:357.14Antimalarial agent 17
CAS:<p>Antimalarial agent 17 doubles as a herbicide, inhibiting photosystem II with effectiveness akin to market herbicides.</p>Fórmula:C19H21ClN2O3SCor e Forma:SolidPeso molecular:392.9A 201A
CAS:<p>A 201A is a nucleoside antibiotic, it is isolated from Streptomyces capreolus.</p>Fórmula:C37H50N6O14Cor e Forma:SolidPeso molecular:802.835Antimalarial agent 23
<p>Antimalarial 23: a benzimidazole with IC50s 0.08 μM (PfNF54), 0.10 μM (PfK1), inhibits β-hematin but not hemozoin formation.</p>Fórmula:C24H23ClF3N5OCor e Forma:SolidPeso molecular:489.92Monascorubrin
CAS:<p>Monascorubrin, from Monascus purpureus mycelium, is an antibiotic against Bacillus subtilis and Candida pseudotropicalis.</p>Fórmula:C23H26O5Cor e Forma:SolidPeso molecular:382.452'-OMe-Ac-C Phosphoramidite
CAS:<p>2'-OMe-Ac-C Phosphoramidite, a modified phosphoramidite, is utilized in the synthesis of oligonucleotides.</p>Fórmula:C42H52N5O9PCor e Forma:SolidPeso molecular:801.86CSN5-IN-2
<p>CSN5-IN-2 (Compound 31) is a CSN5 inhibitor with an IC50 of 0.36 μM. It increases Cullin 1 neddylation levels in cancer cells and downregulates the expression of RAD51 and PD-L1. CSN5-IN-2 exhibits antitumor activity, which is enhanced when used in combination with Talazoparib.</p>Cor e Forma:Odour SolidFlurithromycin
CAS:<p>Flurithromycin is an orally active, broad-spectrum antibiotic for bacterial infection research.</p>Fórmula:C37H66FNO13Cor e Forma:SolidPeso molecular:751.92A 83016F
CAS:<p>A 83016F, an antibiotic from an actinomycete designated A83016, exhibits weak antimicrobial activity.</p>Fórmula:C37H55NO10Cor e Forma:SolidPeso molecular:673.83Mildiomycin
CAS:<p>Mildiomycin, an antibiotic from Streptoverticillium, targets barley mildew, some Mycobacterium, Rhodotorula, but not most fungi/bacteria.</p>Fórmula:C19H30N8O9Cor e Forma:SolidPeso molecular:514.49Ganorbiformin B
CAS:<p>Ganorbiformin B, a lanostane triterpenoid, is C-3 epimer of ganoderic acid T, active against Mycobacterium tuberculosis.</p>Fórmula:C34H50O7Cor e Forma:SolidPeso molecular:570.76Ceftizoxime Sodium
CAS:<p>Ceftizoxime, a 3rd-gen cephalosporin, targets PBPs in Gram-positive/negative bacteria, like cefotaxime, but not metabolized.</p>Fórmula:C13H12N5NaO5S2Cor e Forma:White To Light Yellow Crystalline PowderPeso molecular:405.38M+B 5124
CAS:<p>M+B 5124 is a bioactive chemical.</p>Fórmula:C22H29NO4Cor e Forma:SolidPeso molecular:371.47Antibacterial agent 108
CAS:<p>Compound 1h (Antibacterial agent 108) is a potent antibacterial agent, demonstrating a minimum inhibitory concentration (MIC) of 3 μM against both MRSA and</p>Fórmula:C22H20O3Cor e Forma:SolidPeso molecular:332.39(2S,5S)-Censavudine
<p>(2S,5S)-Censavudine, a potent HIV inhibitor and nucleoside reverse transcriptase blocker.</p>Fórmula:C12H12N2O4Cor e Forma:SolidPeso molecular:248.23Peritassine A
CAS:<p>Peritassine A, an alkaloid derived from Tripterygium wilfordii Hook. f., exhibits anti-HIV properties.</p>Fórmula:C38H47NO18Cor e Forma:SolidPeso molecular:805.783Dihydroaeruginoic Acid
CAS:<p>Dihydroaeruginoic acid, an antibiotic sourced originally from P. fluorescens, exhibits antimicrobial efficacy in disc assays against diverse pathogens, including R. solani, P. ultimum, B. cinerea, S. rolfsii, C. gloeosporioides, F. oxysporum, and S. tritici fungi, along with B. subtilis, E. herbicola, and S. albus bacteria, at a concentration of 200 μg/disc.</p>Fórmula:C10H9NO3SCor e Forma:SolidPeso molecular:223.2523-Oxa-OSW-1
CAS:<p>23-Oxa-OSW-1 (SBF-1), a derivative of OSW-1, serves as a potent inhibitor of the osterol-binding protein (OSBP) with demonstrated antitumor activity [1] [2].</p>Fórmula:C54H82O16Cor e Forma:SolidPeso molecular:987.22Maximin 31
<p>Maximin 31, an antimicrobial peptide originating from toad brain, exhibits activity against Staphylococcus aureus and Escherichia coli, exhibiting Minimum</p>Fórmula:C107H181N31O29Cor e Forma:SolidPeso molecular:2365.77Antifungal agent 75
<p>Antifungal agent 75 (compound 6r) effectively combats Candida albicans by substantially inhibiting biofilm formation, enhancing cell membrane permeability,</p>Cor e Forma:Odour SolidSaquayamycin D
CAS:<p>Saquayamycin D is a glycoside of aquayamycin.</p>Fórmula:C43H50O16Cor e Forma:SolidPeso molecular:822.8572,3-Diphosphoglyceric acid
CAS:<p>2,3-Diphosphoglyceric acid (2,3-DPG), an intermediate of the glycolytic pathway, allosterically binds to deoxygenated hemoglobin, stabilizing it and</p>Fórmula:C3H8O10P2Cor e Forma:SolidPeso molecular:266.04MCF
CAS:<p>MCF, an antimicrobial peptide originating from bee venom, exhibits activity against E.</p>Fórmula:C84H144N28O19Cor e Forma:SolidPeso molecular:1850.22SDH-IN-4
<p>SDH-IN-4 (compound B6) is a selective succinate dehydrogenase (SDH) inhibitor with an IC50 of 0.28 µg/mL, exhibiting potent and wide-ranging antifungal effects</p>Fórmula:C11H9Cl2F3N4O2SCor e Forma:SolidPeso molecular:389.18DprE1-IN-6
<p>DprE1-IN-6 (Compound 56) is a DprE1 inhibitor with demonstrated anti-TB activity, exhibiting a minimum inhibitory concentration (MIC) of 1 μM against the Mtb</p>Fórmula:C22H24N6OCor e Forma:SolidPeso molecular:388.47Antifungal agent 57
CAS:<p>Compound A19 is a potent antifungal, effective against Fluconazole-resistant Candida with MIC 0.5-2 μg/mL; outperforms Miconazole.</p>Fórmula:C18H15ClF2N2SeCor e Forma:SolidPeso molecular:411.73Bombinin H3
<p>Bombinin H3, an antimicrobial peptide sourced from the Bombina variegata (moth) skin, exhibits lethal concentrations of 3.7 μM and 2.4 μM against Escherichia</p>Fórmula:C90H163N23O21SCor e Forma:SolidPeso molecular:1935.46Maximin 32
<p>Maximin 32, an antimicrobial peptide originating from toad brain, exhibits activity against Staphylococcus aureus and Escherichia coli, with minimum inhibitory</p>Fórmula:C121H208N34O33Cor e Forma:SolidPeso molecular:2667.15Antibacterial agent 138
<p>Antibacterial agent 138 effectively targets multi-drug resistant bacteria by inhibiting protein synthesis.</p>Fórmula:C34H52INO4SCor e Forma:SolidPeso molecular:697.75XT-1
CAS:<p>XT-1, an antimicrobial peptide sourced from Xenopus tropicalis skin secretions, exhibits potent activity against S.</p>Fórmula:C134H227N37O31Cor e Forma:SolidPeso molecular:2852.47Parvodicin C2
CAS:<p>Parvodicin C2, a glycopeptide antibiotic derived from A. parvosata and part of the parvodicin complex, serves as a component of the A40926 antibiotic complex utilized as a precursor for synthesizing dalbavancin. It exhibits activity against methicillin-sensitive and methicillin-resistant strains of S. aureus, S. epidermidis, S. saprophyticus, S. hemolyticus, and E. faecalis.</p>Fórmula:C83H88Cl2N8O29Cor e Forma:SolidPeso molecular:1732.53Phosphomannose isomerase
CAS:<p>Phosphomannose isomerase, the initial enzyme in GDP-Man biosynthesis, catalytically facilitates the interconversion of fructose-6-phosphate (Fru6P) and mannose-</p>Cor e Forma:SolidAverufin
CAS:<p>Averufin is a natural product that can be used as a reference standard. The CAS number of Averufin is 14016-29-6.</p>Fórmula:C20H16O7Cor e Forma:SolidPeso molecular:368.341Enzyme-IN-2
<p>Enzyme-IN-2 (compound 15) serves as a potent urease inhibitor, exhibiting anti-ureolytic activity with a K i of 2.36 µM and an IC 50 of 0.75 µM [1].</p>Fórmula:C9H11O7PCor e Forma:SolidPeso molecular:262.15Nikkomycin N
CAS:<p>Nikkomycin N is a bioactive chemical.</p>Fórmula:C15H20N4O10Cor e Forma:SolidPeso molecular:416.343Antibacterial agent 56
CAS:<p>Antibacterial agent 56 (example 22) is a antibacterial agent.</p>Fórmula:C11H13N4NaO8SCor e Forma:SolidPeso molecular:384.30Kadsuralignan A
CAS:<p>Kadsuralignan A (compound 1), a dibenzocyclooctadiene lignan extracted from the leaves and stems of Schisandra lancifolia, exhibits anti-HIV activity, with an</p>Fórmula:C22H26O7Cor e Forma:SolidPeso molecular:402.44Antifungal agent 60
<p>Antifungal agent 60 (compound 16), a broad-spectrum ergosterol biosynthesis inhibitor, demonstrates potent activity against seven human pathogenic fungal</p>Fórmula:C22H18F2N4O2Cor e Forma:SolidPeso molecular:408.4Burnettramic Acid A
CAS:<p>Burnettramic acid A: Fungus-derived, fights B. subtilis, S. aureus, C. albicans, S. cerevisiae. Toxic to NS-1 cells, not to fibroblasts.</p>Fórmula:C41H71NO12Cor e Forma:SolidPeso molecular:770.00Antibacterial agent 165
<p>Antibacterial agent 165 (compound 3), a hydroxyquinoline derivative, effectively inhibits methicillin-resistant Staphylococcus aureus (MRSA) [1], demonstrating</p>Cor e Forma:Odour SolidIboxamycin
CAS:<p>Iboxamycin: potent, orally active antibiotic effective against Gram-positive and Gram-negative bacteria in mice.</p>Fórmula:C22H39ClN2O6SCor e Forma:SolidPeso molecular:495.07Dihydroobionin B
<p>Dihydroobionin B exhibits potent (please insert the rest of the sentence for revision).</p>Fórmula:C21H26O5Cor e Forma:SolidPeso molecular:358.43TWH106
<p>TWH106 is an inhibitor of the cyclophilin (Cyp) enzyme, exhibiting strong affinity for CypA and CypB with dissociation constants (KD) of 53 nM and 139 nM, respectively. It effectively inhibits the replication of HIV and HCV, demonstrating antiviral activity.</p>Cor e Forma:Odour SolidST166 free acid
CAS:<p>ST166 free acid is an inhibitor of the PhoP-DNA complex formation, with IC50 values of 18 μM and 24 μM, effectively hindering the binding of PhoP and MtrAC to DNA. Additionally, ST166 free acid exhibits antibacterial activity against Mycobacterium marinum.</p>Fórmula:C6H12O6S6Cor e Forma:SolidPeso molecular:372.55Lactoferricin B (4-14), bovine TFA
<p>Lactoferricin B (4-14), bovine (TFA), a 4-14 residue peptide from lactoferrin, has broad-spectrum antimicrobial properties.</p>Cor e Forma:LiquidAmp1EP9
<p>Amp1EP9: antimicrobial peptide, non-toxic, combats multidrug-resistant bacteria.</p>Fórmula:C90H173N21O16Cor e Forma:SolidPeso molecular:1805.47Cyclopetide 1
CAS:<p>Cyclopeptide 1 (Compound 1) is an antimicrobial peptide exhibiting moderate efficacy in inhibiting B.</p>Fórmula:C20H28N4O8Cor e Forma:SolidPeso molecular:452.46BING
CAS:<p>BING is an antimicrobial peptide isolated from Japanese medaka fish. It exhibits broad-spectrum toxicity against pathogenic bacteria, including resistant strains. BING disrupts the periplasmic peptidyl-prolyl isomerase in Gram-negative bacteria and reduces RNA levels of cpxR, which plays a crucial role in the development of antibiotic resistance.</p>Fórmula:C67H125N21O15Cor e Forma:SolidPeso molecular:1464.84Pseudin-2
CAS:<p>Pseudin-2, an AMP from Pseudis paradoxa, inhibits Gram-negative bacterial growth.</p>Fórmula:C122H202N36O32Cor e Forma:SolidPeso molecular:2685.13Maximin 77
<p>Maximin 77 is an antimicrobial peptide with antibacterial activity against S.</p>Fórmula:C104H183N31O29Cor e Forma:SolidPeso molecular:2331.76Human Immunoglobulin G
<p>Human Immunoglobulin G (HumanIgG) is an immunoglobulin that plays a protective role in humoral immunity by generating antibody responses against specific pathogens, such as Bacteroides forsythus and Prevotella intermedia. It serves as an antibody standard for quantification in enzyme-linked immunosorbent assays (ELISA). Additionally, Human Immunoglobulin G antibody levels are utilized in research on rheumatoid arthritis (RA) and periodontal disease.</p>Cor e Forma:Odour SolidMaximin Hv
<p>Maximin Hv, an antimicrobial peptide sourced from the Bombina maxima toad [1], exhibits potent activity against a variety of microorganisms.</p>Cor e Forma:Odour SolidAureonuclemycin
CAS:<p>Aureonuclemycin, isolated from Staphylococcus aureus to obtain its biosynthetic gene cluster, exists in two forms: Type A and Type B. Aureonuclemycin A is a nucleoside antibiotic structurally similar to herbicides and contains adenine, while Aureonuclemycin B contains 5′-deoxyadenosine and exhibits antibacterial activity. Aureonuclemycin can be used in research on bacterial leaf blight in rice, citrus canker, and bacterial leaf spot in rice. [1] [2]</p>Fórmula:C16H19N5O9Cor e Forma:SolidPeso molecular:425.35Pyrrhocoricin
CAS:<p>Pyrrhocoricin is a bioactive peptide exhibiting antimicrobial activity against Gram-negative bacteria.</p>Fórmula:C119H190N34O38Cor e Forma:SolidPeso molecular:2704.99Hepatitis b virus pre-s region (120-145)
CAS:<p>Hepatitis B Virus Pre-S Region (120-145) is a preS2 peptide that effectively blocks the attachment of single-chain Fv fragment (scFv) or IgG to recombinant</p>Fórmula:C135H199N39O38SCor e Forma:SolidPeso molecular:3008.33Bombinin-like peptide 7
CAS:<p>Bombinin-like peptide 7, an antimicrobial peptide sourced from the Oriental fire-bellied toad (Bombina orientalis) [1], demonstrates bioactive properties.</p>Fórmula:C114H192N34O32Cor e Forma:SolidPeso molecular:2550.95Defensin HNP-1 human TFA
<p>Defensin HNP-1 human TFA: a compound with anti-microbial actions and a role in atherosclerosis.</p>Fórmula:C152H229F3N44O40S6Cor e Forma:SolidPeso molecular:3556.05Decanoyl-RVKR-CMK TFA
CAS:<p>Decanoyl-RVKR-CMK (DecRVKRcmk) TFA effectively hinders the processing of over-expressed gp160 and suppresses HIV-1 replication.</p>Fórmula:C36H67ClF3N11O7Cor e Forma:SolidPeso molecular:858.45Im5
<p>Im5, an antimicrobial peptide, exhibits antibacterial activity, with minimum inhibitory concentrations (MIC) of 10 μM for E.</p>Fórmula:C134H222N34O31Cor e Forma:SolidPeso molecular:2805.41InhA-IN-9
<p>InhA-IN-9 (compound 7h) is an inhibitor of the Mycobacterium tuberculosis enzyme InhA (an enoyl ACP reductase). It has the ability to bind with InhA and demonstrates anti-tuberculosis activity with a MIC value of 2 μg/mL.</p>Fórmula:C17H19BrN2OCor e Forma:SolidPeso molecular:347.25Temporin C
CAS:<p>Temporin C is an antimicrobial peptide effective against Legionella pneumophila [1].</p>Fórmula:C65H116N16O15Cor e Forma:SolidPeso molecular:1361.71PAA-38
<p>PAA-38 is an effective and selective inhibitor targeting bacterial prolyl-tRNA synthetase (ProRS). It inhibits Pseudomonas aeruginosa ProRS (PaProRS) with a Kd of 0.399 nM and an IC50 of 4.97 nM. The IC50 for human cytoplasmic ProRS (HsProRS) is 35.5 nM. In vitro, PAA-38 exhibits a minimum inhibitory concentration (MIC) of 4-8 μg/mL.</p>Cor e Forma:Odour SolidThe K4 peptide
CAS:<p>K4 peptide exhibits potent antimicrobial properties, effectively targeting both Gram-positive and Gram-negative bacteria, particularly pathogenic strains like</p>Fórmula:C87H132N18O15Cor e Forma:SolidPeso molecular:1670.09PROTAC Vif degrader-1
<p>PROTACVif degrader-1 (Compound L15) is a Vif-targeted PROTAC degrader exhibiting anti-HIV-1 virucidal activity, with an EC50 of 33.35 μM against HIV-1IIIB.</p>Cor e Forma:Odour SolidNaphthomycin B
CAS:<p>Naphthomycin B is an antibiotic that was originally isolated from Streptomyces sp. It exhibits antibacterial activity against gram-positive bacteria and various fungi.</p>Fórmula:C39H44ClNO9Cor e Forma:SolidPeso molecular:706.22PBP10 TFA
<p>PBP10 selectively inhibits FPR2 over FPR1, is cell-permeable, and has N-terminal rhodamine, bactericidal against gram-positive/negative bacteria.</p>Fórmula:C86H128F3N24O17Cor e Forma:SolidPeso molecular:1827.08Pardaxin P 4
CAS:<p>Pardaxin P 4 is an antimicrobial peptide found in the secretions of the Red Sea Moses sole (Red Sea Moses sole). It functions as a biolfilm perforating agent, interacting with phospholipid bilayers of varying compositions to induce cytotoxicity and pore formation. Pardaxin P 4 is used in the research of antimicrobial.</p>Fórmula:C154H248N36O45Cor e Forma:SolidPeso molecular:3323.83JB-95 acetate
<p>JB-95 acetate, a β-hairpin macrocyclic peptide, demonstrates potent antimicrobial properties, selectively compromising the outer membrane of Escherichia coli</p>Fórmula:C92H151N35O14·xC2H4O2Cor e Forma:SolidPeso molecular:1971.41 (free base)Brain Derived Basic Fibroblast Growth Factor (1-24)
CAS:<p>FGF basic 1-24: synthetic peptide with anti-bacterial and anti-HBV properties, used in infectious and immune disease research.</p>Fórmula:C118H173N31O33Cor e Forma:SolidPeso molecular:2553.82Polistes mastoparan
CAS:<p>Polistes mastoparan, an antimicrobial peptide, enhances K+ efflux in S. aureus cells and reduces cell viability, exhibiting an EC50 of 5 μM [1].</p>Fórmula:C77H127N21O18Cor e Forma:SolidPeso molecular:1634.96N-Ethylbenzimidazole
CAS:<p>N-Ethylbenzimidazole exhibits antibacterial activity against Staphylococcus aureus, Escherichia coli, and Aspergillus niger and can be used in related research in the field of life sciences.</p>Fórmula:C9H10N2Pureza:99.68%Cor e Forma:SolidPeso molecular:146.19Succinate dehydrogenase-IN-9
<p>Succinate dehydrogenase-IN-9 (Compound Iik) is an inhibitor of succinate dehydrogenase with an IC50 of 3.6 μM. It demonstrates strong inhibitory activity against various fungi, such as S. sclerotiorum, with an EC50 of 1.14 μg/mL. Additionally, Succinate dehydrogenase-IN-9 enhances nitrate reductase activity, promoting plant growth.</p>Fórmula:C24H29F2N3O5Cor e Forma:SolidPeso molecular:477.20753Ashimycin B
CAS:<p>Ashimycin B is a streptomycin analogue that exhibits broad-spectrum antibacterial activity.</p>Fórmula:C23H41N7O14Cor e Forma:SolidPeso molecular:639.61PfSUB1-IN-1
<p>PfSUB1-IN-1 (compound 4c) is an inhibitor of Plasmodium falciparum subtilisin-like serine protease 1 (PfSUB1), exhibiting potent activity with an IC50 value of 15 nM. PfSUB1 is a key target in antimalarial research. PfSUB1-IN-1 demonstrates a 13-fold greater inhibitory effect on the growth of transgenic Plasmodium falciparum strains (expressing lower levels of PfSUB1 compared to the wild-type) than on wild-type parasite strains.</p>Cor e Forma:Odour SolidBRP
<p>BRP, a peptide related to BRINP2, exhibits anti-obesity activity through the activation of FOS. It triggers FOS activation in the central nervous system, and its effect is independent of leptin, GLP-1 receptor, and melanocortin 4 receptor.</p>Cor e Forma:Odour SolidGallinamide A TFA
CAS:<p>Gallinamide A TFA is a peptide that exhibits linear deposition and serves as a potent inhibitor of cathepsin L (CatL) with an IC50 of 17.6 pM. It inhibits SARS-CoV-2 infection by targeting CatL (EC50: 28 nM) and also inhibits Plasmodium falciparum with an IC50 of 50 nM [1] [2].</p>Fórmula:C33H53F3N4O9Cor e Forma:SolidPeso molecular:706.79Farobin A
CAS:<p>Farobin A, a natural compound, exhibits antibacterial, antioxidant, and anti-inflammatory properties. It is effective against Streptococcus mutans ATCC 25175 and Streptococcus sobrinus ATCC 33478. Additionally, Farobin A demonstrates anti-inflammatory activity by targeting cytokine IL-6 and TNF-α [1].</p>Fórmula:C27H30O14Cor e Forma:SolidPeso molecular:578.52Pyrrocidine A
CAS:<p>Pyrrocidine A, an antibiotic known for its antibacterial properties, can be isolated from LL-Cyan426.</p>Fórmula:C31H37NO4Cor e Forma:SolidPeso molecular:487.63CJ-21,058
CAS:<p>CJ-21,058 is an effective SecA inhibitor with an IC50 of 15 µg/mL. It inhibits the ATP-dependent translocation of precursor proteins across bacterial cell membranes. Additionally, CJ-21,058 exhibits antibacterial activity against Gram-positive bacteria.</p>Fórmula:C23H33NO4Cor e Forma:SolidPeso molecular:387.51Macropin
CAS:<p>Macropin (MAC-1 peptide) is an antimicrobial peptide found in the venom of the solitary bee Macropis fulvipes. It exhibits antibacterial properties against both Gram-positive and Gram-negative bacteria, demonstrates inhibitory effects on fungi, and possesses moderate hemolytic activity on human red blood cells. Macropin is utilized in research for anti-infective therapies.</p>Fórmula:C68H121N17O13SCor e Forma:SolidPeso molecular:1416.86LMW peptide
CAS:<p>LMW peptide, an antimicrobial peptide, exhibits activity against both Gram-positive and Gram-negative bacteria, including B.</p>Fórmula:C75H121N21O20S2Cor e Forma:SolidPeso molecular:1701.02SPR741 acetate
<p>SPR741 acetate, a polymyxin B derivative, enhances antibiotics against gram-negative bacteria by disrupting their outer membrane.</p>Fórmula:C46H77N13O15Pureza:98.57%Cor e Forma:SolidPeso molecular:1052.18Anhydrotetracycline hydrochloride
CAS:<p>Anhydrotetracycline (hydrochloride) is a potent competitive inhibitor of broad-spectrum tetracycline destructase enzymes.</p>Fórmula:C22H23ClN2O7Pureza:98.90%Cor e Forma:SolidPeso molecular:462.88Clindamycin palmitate hydrochloride
CAS:<p>Clindamycin palmitate hydrochloride (Clindamycin palmitate HCl) is the hydrochloride salt of clindamycin and palmitate, a lincosamide antibiotic.</p>Fórmula:C34H63ClN2O6S·HClPureza:98%Cor e Forma:SolidPeso molecular:699.85SARS-CoV-2-IN-81
<p>SARS-CoV-2-IN-81 (compound 12e) is an effective AAK1 inhibitor with an IC50 value of 9.38 nM. It demonstrates antiviral activity against SARS-CoV-2 by reducing AAK1-induced phosphorylation of threonine 156 on AP2M1 and disrupting the direct interaction between AP2M1 and ACE2, ultimately inhibiting SARS-CoV-2 infection.</p>Fórmula:C25H20N4O2Peso molecular:408.1586328-O-Imidazolyl-azepano-betulin
<p>SARS-CoV-2-IN-70 (compound 6) is an effective inhibitor of SARS-CoV-2, with an IC50 value of 3.2 μM.</p>Fórmula:C34H53N3O2Peso molecular:535.41378Mpro ligand 1
<p>Mpro ligand 1 is the target protein ligand for PROTACSARS-CoV-2 Mpro degrader-3. It is the active form of Mpro ligand 2.</p>Fórmula:C22H32N3NaO9SPeso molecular:537.1757OP-145
CAS:<p>OP-145 is a derivative of the antimicrobial peptide LL-37, known for its antibacterial properties against multiple MRSA strains. This compound is applicable in studies on chronic suppurative otitis media.</p>Fórmula:C142H246N46O31Peso molecular:3093.76SARS-CoV-2 Mpro-IN-13
<p>SARS-CoV-2 Mpro-IN-13 (compound 20j) is a covalent inhibitor of the SARS-CoV-2 main protease (MPro) with an IC50 value of 19.0 nM and exhibits antiviral activity with an EC50 value of 138.1 nM.</p>Fórmula:C29H41F2N5O6SPeso molecular:625.27456Globomycin derivative G2A
<p>Globomycin derivative G2A (Compound G2A) is an inhibitor of lipoprotein signal peptidase II (LspA), with an IC50 of 604 nM. It exhibits inhibitory activity against E. coli, P. aeruginosa, and A. baumannii, displaying minimum inhibitory concentrations (MIC) ranging from 12.5 to 32 μg/mL.</p>Fórmula:C34H62N6O8Peso molecular:682.46291Antibacterial agent 185
<p>Antibacterialagent 185 (compound IP-01) is a potent antibacterial agent. It inhibits the polymerization and bundling of filamentous temperature-sensitive mutant Z (FtsZ) by enhancing GTP hydrolysis. Antibacterialagent 185 is effective against Streptococcus pneumoniae and displays a narrow spectrum of activity.</p>Fórmula:C18H17BrN2O3SPeso molecular:420.01433Herbimycin C
CAS:<p>Herbimycin C (AntibioticTAN 420D) is a bacterial metabolite originally isolated from S. hygroscopicus. It is cytotoxic to HeLa and Ehrlich cells, with IC50 values of 7.3 and 1.2 μg/mL, respectively.</p>Fórmula:C29H40N2O9Peso molecular:560.27338KN-17
<p>KN-17, a modified derivative based on the cecropin B structure, effectively disrupts bacterial growth and induces the migration of human bone marrow stromal cells (hBMSCs). This compound significantly stimulates angiogenesis both in vitro and in vivo.</p>Fórmula:C46H48N4O10Peso molecular:816.33704Dechlorogriseofulvin
CAS:<p>Dechlorogriseofulvin is a useful organic compound for research related to life sciences. The catalog number is T124937 and the CAS number is 3680-32-8.</p>Fórmula:C17H18O6Cor e Forma:SolidPeso molecular:318.325AB023a
CAS:<p>AB023a is an antibiotic with antifungal properties.</p>Fórmula:C31H50O8Pureza:98%Cor e Forma:SolidPeso molecular:550.72Kasugamycin sulfate
CAS:<p>Kasugamycin sulfate is a bioactive chemical.</p>Fórmula:C14H25N3O9H2O4SCor e Forma:SolidPeso molecular:428.4Rifamexil
CAS:<p>Rifamexil is a rifamycin (antibiotic produced naturally by the bacterium Amycolatopsis rifamycinica) derivative.</p>Fórmula:C42H55N3O11SPureza:98%Cor e Forma:SolidPeso molecular:809.97Trimethacarb
CAS:<p>Trimetharba is a kind of insecticide.</p>Fórmula:C11H15NO2Pureza:98%Cor e Forma:SolidPeso molecular:193.24Antibiotic SF 2132
CAS:<p>Antibiotic SF 2132 is a bioactive chemical.</p>Fórmula:C30H52N12O10Pureza:98%Cor e Forma:SolidPeso molecular:740.82Leucinostatin K
CAS:<p>Leucinostatin K is a new peptide antibiotic from Paecilomyces lilacinus.</p>Fórmula:C62H111N11O14Pureza:98%Cor e Forma:SolidPeso molecular:1234.633DK06
<p>DK06 (compound DK06) inhibits the growth of Listeria, disrupts biofilm formation, and reduces the levels of extracellular polymeric substances.</p>Cor e Forma:Odour Solid7-Deazaxanthine
CAS:<p>7-Deazaxanthine (7DX) is an inhibitor of thymidine phosphorylase (TPase) and reduces TPase activity in a concentration-dependent manner, with an IC50 value of 40 μM. Additionally, 7-Deazaxanthine exhibits significant anti-angiogenic properties.</p>Fórmula:C6H5N3O2Cor e Forma:SolidPeso molecular:151.12NSC65847
CAS:<p>NSC65847 is a novel dual inhibitor of viral and Streptococcus pneumoniae neuraminidase.</p>Fórmula:C34H26N6Na4O13S4Cor e Forma:SolidPeso molecular:946.81apo-Enterobactin
CAS:<p>apo-Enterobactin is a derivative of Enterobactin, which is a bacterial iron carrier that facilitates iron absorption.</p>Fórmula:C30H29N3O16Cor e Forma:SolidPeso molecular:687.56Alahopcin
CAS:<p>Alahopcin is a new dipeptide antibiotic generated by Streptomyces albulus subsp. ochragerus subsp. nov.</p>Fórmula:C9H15N3O6Cor e Forma:SolidPeso molecular:261.234Laccase-IN-4
<p>Laccase-IN-4 (compound 5g) exhibited significant laccase inhibitory activity.</p>Cor e Forma:Odour SolidDA 1131
CAS:<p>DA 1131 is a new carbapenem antibiotic. It undergoes renal metabolism by renal dehydropeptidase I.</p>Fórmula:C18H27N3O6S2Cor e Forma:SolidPeso molecular:445.55Solanidine
CAS:<p>Solanidine is a cholestane alkaloid isolated from potato species with antitumor effects. Solanidine inhibits proliferation.</p>Fórmula:C27H43NOPureza:96.83%Cor e Forma:SolidPeso molecular:397.64Prumycin dihydrochloride
CAS:<p>Prumycin dihydrochloride is an agent of antifungal antibiotic.</p>Fórmula:C8H18ClN3O4Pureza:98%Cor e Forma:SolidPeso molecular:255.701-Methoxy-3-methylbenzene
CAS:<p>1-Methoxy-3-methylbenzene is a potential acetylcholinesterase inhibitor identified through QSAR (quantitative structure-activity relationship) analysis</p>Fórmula:C8H10OPureza:99.66%Cor e Forma:Clear To Slightly Yellow LiquidPeso molecular:122.16Suricapavir
CAS:<p>Suricapavir is an effective viral replication inhibitor with antiviral activity.</p>Fórmula:C41H29ClF9N9O4SCor e Forma:SolidPeso molecular:950.23Hexylene glycol
CAS:<p>Hexylene glycol (Diolane), colorless liquid, is a chiral diol. It is an industrial compound produced from diacetone alcohol by hydrogenation.</p>Fórmula:C6H14O2Pureza:99.82%Cor e Forma:Liquid LiquidPeso molecular:118.17Hemsloside Ma 1
CAS:<p>Hemsloside Ma 1 is a useful organic compound for research related to life sciences. The catalog number is T123850 and the CAS number is 95851-41-5.</p>Fórmula:C47H74O18Cor e Forma:SolidPeso molecular:927.091Atropine Oxide
CAS:<p>Atropine Oxide is derived from Atropine, a drug that blocks muscarinic receptors and treats nerve agent poisoning and bradycardia.</p>Fórmula:C17H23NO4Cor e Forma:SolidPeso molecular:305.37RU 44790
CAS:<p>RU 44790 is a synthetic monocyclic beta-lactam antibiotics.</p>Fórmula:C15H16FN9O5SCor e Forma:SolidPeso molecular:453.414-Nitrosodiphenylamine
CAS:<p>4-Nitrosodiphenylamine exhibits significant antibacterial activity, with an EC50 value of 5.715 mg/L against [Erwinia amylovora].</p>Fórmula:C12H10N2OCor e Forma:SolidPeso molecular:198.22Piericidin B
CAS:<p>Piericidin B, from S. mobaraensis, is insecticidal, antimicrobial, and inhibits mitochondrial respiration.</p>Fórmula:C26H39NO4Cor e Forma:SolidPeso molecular:429.601Metiram
CAS:<p>Metiram is a polymeric dithiocarbamic fungicide used in agriculture. Metiram is now a mixture and is not assigned an ISO name. Metiram is used frequently in the protection of tomatoes, potatoes, apples, grapevines, and other crops.</p>Fórmula:C4H6N2S4ZnPureza:98%Cor e Forma:SolidPeso molecular:275.73Lysine hydroxamate
CAS:<p>Lysine hydroxamate is a bioactive chemical.</p>Fórmula:C6H15N3O2Cor e Forma:SolidPeso molecular:161.2TXY541
CAS:<p>TXY541 is an orally active antibacterial agent that is converted into PC190723 under physiological conditions. It demonstrates strong antibacterial activity against Staphylococcus aureus and exhibits low cytotoxicity towards mammalian cells.</p>Fórmula:C21H19ClF2N4O3SCor e Forma:SolidPeso molecular:480.92Ropidoxuridine
CAS:<p>Ropidoxuridine (IPdR), a novel oral prodrug, is a halogenated thymidine analogue that may sensitize human tumors.</p>Fórmula:C9H11IN2O4Pureza:97.07%Cor e Forma:SolidPeso molecular:338.1Evoxine
CAS:<p>Evoxine blocks CO2's dampening effect on IL-6 and CCL2 in THP-1 macrophages.</p>Fórmula:C18H21NO6Pureza:98%Cor e Forma:SolidPeso molecular:347.36MRSA Antibiotic 2
CAS:<p>MRSA antibiotic 2 is an antibiotic compound effective against various Gram-positive bacteria, including B. subtilis, S. aureus, and methicillin-resistant S. aureus (MRSA).</p>Fórmula:C15H10BrCl2NO4Cor e Forma:SolidPeso molecular:419.05Bivittoside B
CAS:<p>Bivittoside B is a non-sulfated hexoside analog obtained from Bovine sea cucumber with antifungal activity and potential antitumor activity.</p>Fórmula:C54H88O22Pureza:98%Cor e Forma:SolidPeso molecular:1089.276BO 1165
CAS:<p>BO 1165 is an monobactam antibiotic.</p>Fórmula:C13H14FN5O8S2Cor e Forma:SolidPeso molecular:451.4Antibacterial agent 255
CAS:<p>Antibacterialagent 255 (compound (±)-1) is a potent antibacterial agent, acting as an effective and selective inhibitor of 4-diphosphocytidyl-2-C-methyl-D-erythritol (IspE). It exhibits IC50 values of 13.0, 8.0, and 20 µM against EclspE, KplspE, and AblspE, respectively.</p>Fórmula:C14H18N4O3S2Cor e Forma:SolidPeso molecular:354.45Josamycin propionate
CAS:<p>Josamycin propionate is a macrolide antibiotic.</p>Fórmula:C45H73NO16Pureza:98%Cor e Forma:SolidPeso molecular:884.07Ivermectin B1a aglycone
CAS:<p>Ivermectin B1a aglycone, from ivermectin's disaccharide hydrolysis, inhibits nematode larvae growth without paralysis.</p>Fórmula:C34H50O8Cor e Forma:SolidPeso molecular:586.766DB722
CAS:<p>DB722 is a furamidine analogues with DNA binding activity. DB722 shows antiproliferative activity.</p>Fórmula:C20H16N4OPureza:99.91%Cor e Forma:SoildPeso molecular:328.37Pivampicillin Hydrochloride
CAS:<p>Piampicillin Hydrochloride is a Hydrochloride form of an oral active ampicillin new spray with antimicrobial activity.</p>Fórmula:C22H30ClN3O6SCor e Forma:SolidPeso molecular:500.01FliC, Serotype a (427-441), S.paratyphi A
CAS:<p>Amino acids 427-441 of FliC epitope from S. serotype a recognized by CD4+ T cells in C57BL/6 mice; common to various Salmonella, in FliC's C-terminus.</p>Fórmula:C69H113N23O24Pureza:98%Cor e Forma:SolidPeso molecular:1648.78Luteoskyrin
CAS:<p>Luteoskyrin is a hepatotoxic and hepatocarcinogenic bisdihydroanthraquinone produced by Penicillium islandicum Sopp.</p>Fórmula:C30H22O12Cor e Forma:Yellow Rectangular Crystals SolidPeso molecular:574.49Pimodivir HCl
CAS:<p>Pimodivir (VX-787) prevents flu virus replication, inhibiting PB2, with an EC50 of 1.6 nM against various strains.</p>Fórmula:C20H19F2N5O2ClHH2OPureza:98%Cor e Forma:SolidPeso molecular:444.86Gilvocarcin M
CAS:<p>Gilvocarcin M, an antibiotic, is effective against S. aureus, inhibits KB cell growth, and is DNA intercalating but toxic to rats.</p>Fórmula:C26H26O9Cor e Forma:SolidPeso molecular:482.485Adicillin
CAS:<p>Adicillin is a penicillin antibiotic that works against vancomycin-resistant enterococci.</p>Fórmula:C14H21N3O6SCor e Forma:SolidPeso molecular:359.4VPC-18005
CAS:<p>VPC-18005: a luciferase inhibitor that blocks ERG-induced transcription by binding ERG-ETS, hindering DNA attachment.</p>Fórmula:C15H17N3O3SPureza:99.95%Cor e Forma:SoildPeso molecular:319.38cTEV6-2
<p>cTEV6-2 covalently inhibits the Tobacco Etch Virus protease (TEV protease) by binding to its cysteine residue (C151), with an IC50 of 81.7 nM.</p>Fórmula:C63H93N17O22S3Cor e Forma:SolidPeso molecular:1536.71Agrocin 84
CAS:<p>Agrocin 84 is a microbial metabolite that inhibits DNA and protein synthesis, as well as amino acid transport, in the susceptible and virulent Agrobacterium strain H-38-9.</p>Fórmula:C22H36N6O16P2Cor e Forma:SolidPeso molecular:702.499SARS-CoV-2-IN-110
<p>SARS-CoV-2-IN-110 (compound Bb1) is an inhibitor of SARS-CoV-2, demonstrating antiviral efficacy with an EC50 of 1.10 μM, and significantly reduced toxicity compared to Lapatinib. The compound exhibits a CC50 of greater than 100 μM against SARS-CoV-2, with a selectivity index (SI) exceeding 91.</p>Fórmula:C28H20ClFN4O2Cor e Forma:SolidPeso molecular:498.94
