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(2.957 produtos)
- Antibiótico(920 produtos)
- Antifecção(23 produtos)
- DHFR(33 produtos)
- Síntese de DNA/RNA(708 produtos)
- HBV(176 produtos)
- HIV Protease(449 produtos)
- HSV(91 produtos)
- Integrase(2 produtos)
- Ribossomo(13 produtos)
Exibir 2 mais subcategorias
Foram encontrados 5842 produtos de "Microbiologia/Virologia"
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Enoxacin hydrate
CAS:<p>Enoxacin hydrate (AT-2266 hydrate) is a broad-spectrum 6-fluoronaphthyridinone antibacterial agent.</p>Fórmula:C15H17FN4O3H2OPureza:99.50%Cor e Forma:SolidPeso molecular:347.34Nosiheptide
CAS:<p>Nosiheptide, a thiopeptide antibiotic from Streptomyces actuosus, boosts animal growth; it blocks protein synthesis in bacteria.</p>Fórmula:C51H43N13O12S6Pureza:95.37%Cor e Forma:SolidPeso molecular:1222.36Benzalkonium chloride
CAS:<p>Benzalkonium chloride: a cationic surfactant, biocide, and phase transfer agent with varied alkyl chains.</p>Fórmula:C6H5CH2N(CH3)2RCl(RC8H17toC18H37)Pureza:98% - >99.99%Cor e Forma:SolidPeso molecular:N/ABenfotiamine
CAS:<p>Benfotiamine (S-Benzoylthiamine O-monophosphate) is a synthetic S-acyl derivative of thiamine (vitamin B1), used as an antioxidant dietary supplement.</p>Fórmula:C19H23N4O6PSPureza:99.2% - 99.91%Cor e Forma:Shinning Black PowderPeso molecular:466.45Clavulanate lithium
CAS:<p>Clavulanate lithium (Clavulanic acid lithium) is an inhibitor of β-lactamase.</p>Fórmula:C8H8LiNO5Pureza:99.79%Cor e Forma:SolidPeso molecular:205.09Dimetridazole
CAS:<p>Dimetridazole (1, 2-Dimethyl-5-nitroimidazole) is a agent that combats protozoan infections. Dimetridazole is a nitroimidazole class drug.</p>Fórmula:C5H7N3O2Pureza:99.88%Cor e Forma:SolidPeso molecular:141.13Adenine
CAS:<p>Adenine: a purine nucleobase vital for ATP, NAD, FAD production, and DNA/RNA synthesis.</p>Fórmula:C5H5N5Pureza:99.39% - 99.95%Cor e Forma:SolidPeso molecular:135.13Enibarcimab
CAS:<p>Enibarcimab is a humanized monoclonal antibody targeting Adrenomedullin (ADM), used in cardiovascular disease research.</p>Pureza:>95%Cor e Forma:LiquidClimbazole
CAS:<p>Climbazole (BAY-e 6975) is a broad-spectrum imidazole antifungal agent with anti-dandruff benefits.</p>Fórmula:C15H17ClN2O2Pureza:98.23%Cor e Forma:White Solid CrystallinePeso molecular:292.76Procaine hydrochloride
CAS:<p>Procaine HCl is a benzoic acid derivative used as a local anesthetic, blocking nerve impulses and sensation.</p>Fórmula:C13H20N2O2·HClPureza:99.1% - 99.22%Cor e Forma:White Crystalline PowderPeso molecular:272.774-Methylherniarin
CAS:<p>4-Methylherniarin (7-Methoxy-4-methylcoumarin) is a coumarin derivative and fluorescent label, it displays good activity against B. subtilis.</p>Fórmula:C11H10O3Pureza:98.05%Cor e Forma:Off-White SolidPeso molecular:190.2N-(Ketocaproyl)-DL-homoserine lactone
CAS:<p>N-(Ketocaproyl)-DL-homoserine lactone is a quorum sensing (QS) autoinducer. N-(Ketocaproyl)-DL-homoserine lactone also is a natural and active ligand of LuxR.</p>Fórmula:C10H15NO4Pureza:99.91%Cor e Forma:SolidPeso molecular:213.23Clotrimazole
CAS:<p>Clotrimazole (FB 5097), an imidazole derivative with a broad spectrum of antimycotic activity, inhibits biosynthesis of the sterol ergostol.</p>Fórmula:C22H17ClN2Pureza:99.89%Cor e Forma:Crystals SolidPeso molecular:344.84JSF-4898
<p>JSF-4898 is an orally bioactive inhibitor of Mycobacterium tuberculosis MenG enzyme. It exhibits a minimum inhibitory concentration (MIC) of 0.78 μM against Mycobacterium tuberculosis H37Rv. Additionally, JSF-4898 enhances the efficacy of rifampicin in a subacute infection model of Mycobacterium tuberculosis in mice.</p>Cor e Forma:Odour SolidPP102
<p>PP102, an antimicrobial peptide, exhibits activity against gram-positive bacteria, including B.</p>Fórmula:C173H285N53O58S3Cor e Forma:SolidPeso molecular:4131.63Altromycin C
CAS:<p>Altromycin C is a new pluramycin-like antibiotic.</p>Fórmula:C46H57NO17Pureza:98%Cor e Forma:SolidPeso molecular:895.94N36Mut(e,g)
<p>N36Mut(e,g) is an HIV fusion peptide inhibitor targeting gp41. It functions by disrupting the formation of the homotrimeric coiled coil of the N-terminal helix in the pre-hairpin intermediate, leading to the creation of a heterotrimer.</p>Fórmula:C189H317N55O56Cor e Forma:SolidPeso molecular:4255.87Trinactin
CAS:<p>Trinactin is a nonactin homolog that has Immunosuppressive effects.</p>Fórmula:C43H70O12Cor e Forma:SolidPeso molecular:779.01Mezlocillin
CAS:<p>Meloxicillin: a liver-excreted penicillin effective against Gram-negative and some Gram-positive bacteria; treats biliary infections.</p>Fórmula:C21H25N5O8S2Cor e Forma:SolidPeso molecular:539.58Bombinin H1
<p>Bombinin H1, an antimicrobial peptide originating from the skin of the Bombina variegata moth, exhibits lethal concentrations of 3.8 μM against Escherichia coli</p>Fórmula:C90H163N23O21SCor e Forma:SolidPeso molecular:1935.46cis-β-Terpineol
CAS:<p>Cis-β-Terpineol, a monoterpene derived from the aerial parts of Anthemis turcomanica, exhibits antibacterial activity as evidenced by studies on the stems,</p>Fórmula:C10H18OCor e Forma:SolidPeso molecular:154.25Histone H4 (2-21)
CAS:<p>Histone H4 (2-21) is a pivotal core histone involved in the process of chromatinization specific to the genomes of herpes simplex virus 1 (HSV-1).</p>Fórmula:C82H150N36O22Pureza:98%Cor e Forma:SolidPeso molecular:1992.33Protorubradirin
CAS:<p>Protorubradirin is an antibiotic that can be isolated from the non-pigmented Streptomyces achromogenes var. rubradiris alongside Rubradirin. It exhibits inhibitory activity against HIV reverse transcriptase. In vitro studies show that Protorubradirin also inhibits strains of Staphylococcus aureus and Streptococcus. In infected mice, subcutaneous administration of Protorubradirin demonstrates in vivo efficacy against antibiotic-resistant Staphylococcus aureus strains. However, oral administration may significantly reduce its activity compared to Rubradirin, possibly due to its C-nitroso sugar decomposing more rapidly in acidic gastric conditions.</p>Fórmula:C48H46N4O19Peso molecular:982.89UX4O
<p>UX4O is an allosteric inhibitor of UDP-glucose dehydrogenase (UGDH). The human UGDH (hUGDH) is a hexamer that catalyzes the oxidation of UDP-glucose to UDP-glucuronic acid. It exists in an active (E) state and an inactive (EΩ) state, which requires binding with the allosteric inhibitor UDP-xylose (UDP-Xyl) to stabilize the inactive form. UX4O may also serve as a physiologically relevant inhibitor of bacterial allosteric UGDH that does not produce UDP-Xyl.</p>Fórmula:C14H22N2O17P2Cor e Forma:SolidPeso molecular:552.28ML-60218
CAS:<p>ML-60218 inhibits RNA pol III in yeast/humans with IC50s of 32/27 μM; disrupts and prevents viroplasms.</p>Fórmula:C19H15Cl2N3O2S2Pureza:98.1%Cor e Forma:SolidPeso molecular:452.38Histatin-3
CAS:<p>Histatin-3, a 32-amino-acid peptide, exhibits potent antimicrobial activities and serves as a substrate for proprotein convertase 1 (PC1), where it is primarily</p>Fórmula:C178H258N64O48Cor e Forma:SolidPeso molecular:4062.35Antimicrobial agent-24
<p>Compound E8 (Antimicrobial agent-24) is a hydrazide with broad-spectrum fungicidal properties, disrupting the plasma membrane's functionality and inducing</p>Fórmula:C19H17F2N3O3Cor e Forma:SolidPeso molecular:373.35Deoxyfusapyrone
CAS:<p>Deoxyfusapyrone, an antifungal α-pyrone, combats C. neoformans and Aspergillus species; ineffective against yeast and B. megaterium.</p>Fórmula:C34H54O8Cor e Forma:SolidPeso molecular:590.79TPS1-IN-1
<p>TPS1-IN-1 (Compound O1) is a potent and broad-spectrum inhibitor of TPS1. It exhibits IC50 values of 14.73 μM for MoTPS1 (Magnaporthe oryzae TPS1) and 59.99 μM for BcTPS1 (Botrytis cinerea TPS1). TPS1-IN-1 exerts its broad-spectrum fungicidal effects by disrupting spore germination, appressorium formation, and turgor pressure accumulation in fungi. With good safety profiles, TPS1-IN-1 has potential as a candidate for novel fungicide development.</p>Fórmula:C19H26F3N5O4SCor e Forma:SolidPeso molecular:477.50Aurachin 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:325.443'Ome-m7GpppAmpG
CAS:<p>3'Ome-m7GpppAmpG is a trinucleotide cap with LNA, boosting translation; useful in mRNA vaccines and gene therapy.</p>Fórmula:C33H45N15O24P4Cor e Forma:SolidPeso molecular:1159.696-Prenylindole
CAS:<p>6-Prenylindole, from Streptomyces, is antifungal/antimalarial, active against A. brassicicola, F. oxysporum, and resistant P. falciparum.</p>Fórmula:C13H15NCor e Forma:SolidPeso molecular:185.26Crexavibart
CAS:<p>Crexavibart (BMS-986413; C-144-LS), an IgG1 λ2 antibody, specifically targets the receptor-binding domain of the SARS-CoV-2 spike (S) glycoprotein [1].</p>Pureza:98%Cor e Forma:LiquidAurein 3.2
CAS:<p>Aurein 3.2 is an antimicrobial peptide with antibiotic properties and exhibits anticancer activity [1].</p>Fórmula:C82H138N22O21Pureza:98%Cor e Forma:SolidPeso molecular:1768.11Enopeptin A
CAS:<p>Enopeptin A: depsipeptide antibiotic with unique amino acids, combats Gram-positive/negative bacteria, not antifungal.</p>Fórmula:C47H57N7O11Cor e Forma:SolidPeso molecular:896.011SARS-CoV-2-IN-56
<p>SARS-CoV-2-IN-56 (Compound 63) is a SARS-CoV-2 inhibitor with antiviral activity, demonstrating inhibition of the virus in Vero E6 cells with an IC50 of 0.7 μM</p>Fórmula:C70H72N12O19S3Pureza:98%Cor e Forma:SolidPeso molecular:1481.58Dermcidin-1L (human)
CAS:<p>Dermcidin-1L (human), an antibiotic peptide secreted by sweat glands, exhibits antimicrobial activity and is utilized in the research of inflammatory skin</p>Fórmula:C210H359N57O71Pureza:98%Cor e Forma:SolidPeso molecular:4818.44H-Arg-OtBu dihydrochloride
CAS:<p>H-Arg-OtBu (dihydrochloride) is a membrane-targeting antimicrobial that engages the negatively charged bacterial membrane through electrostatic and hydrophobic</p>Fórmula:C10H24Cl2N4O2Pureza:98%Cor e Forma:SolidPeso molecular:303.23Aurein 2.6
CAS:<p>Aurein 2.6, an antibiotic antimicrobial peptide, exhibits activity against various Gram-positive bacteria with minimum inhibitory concentrations (MIC) of 25, 25</p>Fórmula:C77H133N19O19Pureza:98%Cor e Forma:SolidPeso molecular:1629Antifungal agent 53
CAS:<p>Antifungal 53 inhibits Candida CYP51, blocks biofilms, and is safe.</p>Fórmula:C18H15Cl3N2SeCor e Forma:SolidPeso molecular:444.64Aurein 5.2
CAS:<p>Aurein 5.2 is an antibiotic antimicrobial peptide [1].</p>Fórmula:C110H194N28O32SPureza:98%Cor e Forma:SolidPeso molecular:2452.95SARS-CoV-2 3CLpro-IN-21
<p>SARS-CoV-2 3CLpro-IN-21 (Compound D6) is an irreversible, covalent inhibitor of SARS-CoV-2 3CL pro, demonstrating potent inhibition with an IC50 of 0.03 μM.</p>Fórmula:C14H10BrN3O2SPureza:98%Cor e Forma:SolidPeso molecular:364.22BO-1
<p>BO-1, a benzoate ester, exhibits antibacterial properties, effectively inhibiting multidrug-resistant Staphylococcus aureus.</p>Fórmula:C21H19ClO6Cor e Forma:SolidPeso molecular:402.82RSV-IN-2
CAS:<p>RSV-IN-2, a dual inhibitor for wild-type/mutant RSV fusion proteins, has EC50 of 0.27 nM (wild-type) and 0.70 nM (D486N mutant).</p>Fórmula:C27H31ClN6O4Cor e Forma:SolidPeso molecular:539.03Dabcyl-KTSAVLQSGFRKME-Edans TFA
<p>Fluorogenic peptide Dabcyl-KTSAVLQSGFRKME-Edans TFA measures protease activity, may aid in COVID-19 research.</p>Fórmula:C97H142F3N25O26S2Cor e Forma:SolidPeso molecular:2195.44Surgumycin
CAS:<p>Surgumycin is a carbonyl-conjugated pentaenic antibiotic.</p>Fórmula:C36H60O11Cor e Forma:SolidPeso molecular:668.865Hp1404
CAS:<p>Hp1404 is a novel cationic antimicrobial peptide with specific inhibitory activity against Gram-positive bacteria, including Laburnetin-resistant Staphylococcus aureus (MRSA). Its antibacterial properties, low toxicity, and low likelihood of inducing resistance make it a useful candidate for antimicrobial agent research.</p>Fórmula:C75H119N17O18Cor e Forma:SolidPeso molecular:1546.85EV-A71-IN-3
<p>EV-A71-IN-3 (Compound IRE-03-3) is an inhibitor of the enterovirus A71 (EV-A71). It targets the internal ribosome entry site (IRES) of EV-A71, blocking IRES-mediated translation and thereby preventing viral proliferation, with an EC50 of 11.96 μM.</p>Fórmula:C21H17F3N4O3Cor e Forma:SolidPeso molecular:430.38KC12
<p>KC12 acts as an inhibitor of the FOXM1 transcription factor. In cancer cells of the MDA-MB-231 line, KC12 exhibits cytotoxicity with an IC50 of 6.13 µM.</p>Fórmula:C23H17F3N2O3SCor e Forma:SolidPeso molecular:458.453Destomycin A
CAS:<p>Destomycin A, an aminoglycoside antibiotic, exhibits activity against bacterial (Gram-positive and Gram-negative), antifungal, and anthelmintic agents. It inhibits peptide synthesis in Escherichia coli cells and stimulates adenylate cyclase in animal tissues.</p>Fórmula:C20H37N3O13Cor e Forma:SolidPeso molecular:527.52Ap4dT
CAS:<p>Ap4dT serves as an inhibitor of human adenylate kinase isozyme 1 (hAK1), effectively suppressing the synthesis of ATP and ADP, with IC50 values of 42 μM and 38 μM, respectively.</p>Fórmula:C20H41N11O20P4Cor e Forma:SolidPeso molecular:879.511-Keto fusidic acid
CAS:<p>11-Keto fusidic acid exhibits potent antibacterial efficacy against Staphylococcus aureus, demonstrating a minimum inhibitory concentration (MIC) of 0.078 μg/mL</p>Fórmula:C31H46O6Cor e Forma:SolidPeso molecular:514.697-O-Demethyl rapamycin
CAS:<p>Novolimus is a macrocyclic lactone with anti-proliferative properties. It has similar efficacy to currently available agents but requires a lower dose.</p>Fórmula:C50H77NO13Cor e Forma:SolidPeso molecular:900.16CRAMP-18 (mouse)
CAS:<p>CRAMP-18 (mouse) is an antibiotic peptide with demonstrated efficacy against Gram-negative bacteria, including S.</p>Fórmula:C101H171N27O24Pureza:98%Cor e Forma:SolidPeso molecular:2147.6GRL-1720 TFA
<p>GRL-1720 TFA is a potent SARS-CoV-2 Mpro inhibitor, demonstrating anti-SARS-CoV-2 activity with an EC50 of 15 μM [1].</p>Pureza:98%Cor e Forma:Odour SolidTerephthalonitrile
CAS:<p>Terephthalonitrile exhibits antibacterial activity against Staphylococcus aureus and Pseudomonas aeruginosa and can be used in related research in the field of life sciences.</p>Fórmula:C8H4N2Pureza:99.04%Cor e Forma:SolidPeso molecular:128.13WYFA-15
<p>WYFA-15 is an inhibitor of sphingomyelin synthase 1 (SMS1) that has been shown to protect mice from lethal SFTSV infection and reduce the replication and pathogenicity of SARS-CoV-2. WYFA-15 is applicable for antiviral research.</p>Fórmula:C22H16Cl2N2OCor e Forma:SolidPeso molecular:395.281HAT-IN-8
<p>HAT-IN-8 (Compound 38), a blood-brain barrier-permeable inhibitor of Trypanosoma brucei with an EC50 of 0.18 μM, is utilized in the study of Human African</p>Fórmula:C14H15F2N3O2SPureza:98%Cor e Forma:SolidPeso molecular:327.35Iturin A
CAS:<p>Iturin A: antifungal compound targeting cell membranes, forms ion pores in yeast/fungi.</p>Cor e Forma:Solid(R)-Ofloxacin
CAS:<p>(R)-Ofloxacin is a R-isomer of Ofloxacin, an antibiotic used to treat a number of bacterial infections.</p>Fórmula:C18H20FN3O4Pureza:98%Cor e Forma:SolidPeso molecular:361.37Lipofermata
CAS:<p>Lipofermata is a fatty acid transport protein (FATP) inhibitor that prevents lipid transport to melanoma cells and reduces melanoma growth and invasion.</p>Fórmula:C15H10BrN3OSPureza:99.22% - 99.57%Cor e Forma:SolidPeso molecular:360.23Polycarpine hydrochloride
CAS:<p>Polycarpine hydrochloride (1a), a broad-spectrum Mpro inhibitor (IC 50 = 30 nM), is sourced from Polycarpa aurata and functions as an anti-coronaviral agent. This compound exhibits both antiviral and antifungal properties, with IC 50 values of 30.0 nM against SARS-CoV-2 Mpro and 0.12 μM against PEDV Mpro [1].</p>Fórmula:C22H26Cl2N6O2S2Cor e Forma:SolidPeso molecular:541.52Malacidin B
CAS:<p>Malacidin B, a macrocyclic lipopeptide antibiotic, demonstrates calcium-dependent antibacterial activity [1] [2].</p>Fórmula:C57H90N12O20Cor e Forma:SolidPeso molecular:1263.39Polymyxin E2 sulfate
CAS:<p>Polymyxin E2, a key component of the cationic lipopeptide antibiotic colistin, was originally derived from B.</p>Fórmula:C52H98N16O13·XH2SO4Cor e Forma:SolidPeso molecular:1155.40LF 11 acetate
<p>LF 11 acetate exhibits antibacterial activities and can be used for the development of endotoxin-neutralizing and antibacterial agents.</p>Fórmula:C71H116N26O16Pureza:98.85%Cor e Forma:SolidPeso molecular:1589.85Antimalarial agent 46
CAS:<p>Antimalarial agent 46 (Compound 42a) is a compound with antimalarial activity, effective in inhibiting P. falciparum lines.</p>Fórmula:C21H17Cl3N4OCor e Forma:SolidPeso molecular:447.75Ac-rC Phosphoramidite
CAS:<p>Ac-rC Phosphoramidite can modify phosphodisulfide oligonucleotides.</p>Fórmula:C47H64N5O9PSiPureza:98.29%Cor e Forma:SolidPeso molecular:902.1Mpro 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:537.1757Furaltadone 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:474.38Spergualin trihydrochloride
CAS:<p>Spergualin trihydrochloride is a natural product that first identified as an antibiotic from culture filtrates of Bacillus laterosporus BMG162-aF2[1].</p>Fórmula:C17H38ClN7O4Cor e Forma:SolidPeso molecular:439.99HAA-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:376.36Lankacyclinone 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:415.52PLpro-IN-8
<p>PLpro-IN-8 (compound 1) serves as an inhibitor of the SARS-CoV papain-like protease (PLpro), exhibiting IC50 values of 5.9 μM for SARS-CoV-2 PLpro and 0.46 μM for SARS-CoV-1 PLpro. Additionally, it hinders the Wuhan SARS-CoV-2 strain WK-521 with an EC50 of 2.7 μM.</p>Fórmula:C23H22N2O4Cor e Forma:SolidPeso molecular:390.43Lincosamine
CAS:<p>Lincosamine is a lincosamide antibiotic produced by Streptomyces lincolnensis.</p>Fórmula:C8H17NO6Cor e Forma:SolidPeso molecular:223.22Plonmarlimab
CAS:<p>Plonmarlimab(TJ003234) is an anti-GM-CSF monoclonal antibody with potential antiviral activity for the study of immune disorders and novel coronavirus infection</p>Pureza:96.2% (SDS-PAGE); 95.4% (SEC-HPLC) - 96.2% (SDS-PAGE); 95.4% (SEC-HPLC)Cor e Forma:LiquidCefuzonam sodium
CAS:<p>Cefuzonam sodium: second-gen cephalosporin, effective against Staph aureus where third-gen fails.</p>Fórmula:C16H15N7NaO5S4Cor e Forma:SolidPeso molecular:536.57Anti-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 LiquidAmcipatricin L-aspartate
CAS:<p>Amcipatricin diaspartate (SPA-S-753), a semi-synthetic polyene antibiotic, exhibits potent broad-spectrum antifungal activity [1].</p>Fórmula:C75H117N7O27Cor e Forma:SolidPeso molecular:1548.76Guignardone 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:324.37DS-8587
CAS:<p>DS-8587 is a DNA topoisomerase inhibitor, effective against drug-resistant A. baumannii and F. necrophorum in mice; efflux pump inhibitors don't alter its MIC.</p>Fórmula:C21H27ClF3N3O5Cor e Forma:SolidPeso molecular:493.90Antiviral 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:514.539LU9
<p>LU9 is an effective 3CLpro inhibitor with an IC50 of 0.34 µM and potential application in SARS-CoV-2 research.</p>Fórmula:C22H29Cl2N9O4Cor e Forma:SolidPeso molecular:554.43Methylclonazepam
CAS:<p>Methylclonazepam is a benzodiazepine with anxiolytic properties. It inhibits the uptake of 5-hydroxytryptamine by Schistosoma mansoni, and its derivatives exhibit anti-Schistosoma mansoni activity.</p>Fórmula:C16H12ClN3O3Cor e Forma:SolidPeso molecular:329.74WRN inhibitor 18
CAS:<p>WRN inhibitor 18 (compound 306) is an orally active inhibitor of WRN with demonstrated anticancer activity in vivo.</p>Fórmula:C35H35F6N5O5SCor e Forma:SolidPeso molecular:751.74Antimalarial agent 47
<p>Antimalarial agent 47 (compound F14) is a chemical compound effective against Plasmodium falciparum, specifically targeting the W2 strain with an IC50 value of 235 nM.</p>Fórmula:C16H14ClF2NOCor e Forma:SolidPeso molecular:309.74Extracellular Death Factor TFA
<p>Extracellular death factor TFA (EDF TFA) is a linear pentapeptide that communicating cells produce and release, which activates the cell death pathway.</p>Pureza:98.77%Cor e Forma:Odour SolidSe2h
<p>Se2h is a cruzain inhibitor exhibiting potent activity against intracellular amastigotes of Trypanosoma cruzi (EC50< 1 μM, SI> 10), with an inhibitory effect on cruzain of IC50< 100 nM (SI> 5.55). Compared to Benznidazole and cruzain inhibitor K777, Se2h shows superior selectivity and inhibition while its selenazole structure reduces selenium-related toxicity. Se2h demonstrates antiparasitic activity and holds promise for Chagas disease research.</p>Fórmula:C12H13ClN4O2SeCor e Forma:SolidPeso molecular:359.67Quorum sensing-IN-7
<p>Quorum sensing-IN-7 (compound HSL 4) is an effective quorum sensing (QS) inhibitor. It interacts with the binding sites Leu 72 and Gln 95 of CviR. As an antimicrobial agent, Quorum sensing-IN-7 effectively inhibits the production of homoserine lactones (HSLs) and biofilms in C. violaceum at concentrations ranging from 0.25-1 mg/mL.</p>Cor e Forma:Odour SolidBRD-9327
<p>BRD-9327 is an EfpA inhibitor that binds to the external vestibule, yet it does not entirely block the substrate's path to the outside, suggesting it may inhibit the movement necessary for the transporter's alternative pathway. BRD-9327 is applicable in tuberculosis research.</p>Cor e Forma:Odour SolidButylboronicacid
CAS:<p>Butylboronicacid is a competitive inhibitor of urease and acts as a monosaccharide complexing reagent.</p>Fórmula:C4H11BO2Pureza:99.96%Cor e Forma:SolidPeso molecular:101.94Lenacapavir sodium
CAS:Lenacapavir, also known as GS-6207, is an HIV-1 capsid inhibitor. It demonstrates an average EC50 of 50 pM (ranging from 20-160 pM) against 23 clinical isolates of HIV-1 from diverse subtypes, with tests performed in peripheral blood mononuclear cells (PBMCs). In vitro, Lenacapavir exhibits picomolar potency and shows no cross-resistance with existing antiretroviral compounds. Furthermore, Lenacapavir displays significant antiviral activity in individuals with HIV-1, regardless of prior treatment history, with no pre-existing resistance detected.Fórmula:C39H31ClF10N7NaO5S2Peso molecular:990.26ent-Heronamide C
<p>Ent-Heronamide C possesses antifungal properties and is utilized as a probe for analyzing the mode of action of heronamide C [1].</p>Fórmula:C29H41NO3Cor e Forma:SolidPeso molecular:451.64Nocardicin A
CAS:<p>Nocardicin A, a moderate antibiotic agent, shows inhibitory for a wild spectrum of gram-negative bacteria.</p>Fórmula:C23H24N4O9Pureza:98%Cor e Forma:SolidPeso molecular:500.46Rabbit neutrophil peptide 3b
<p>Rabbit Neutrophil Peptide 3b is an antimicrobial peptide isolated from rabbit peritoneal neutrophils [1].</p>Cor e Forma:Odour SolidTrypanothione synthetase-IN-3
CAS:<p>Trypanothione synthetase-IN-3: noncompetitive TryS inhibitor, Ki: 0.8 μM, useful in parasite research.</p>Fórmula:C68H54O43Cor e Forma:SolidPeso molecular:1559.13Penetratin-Arg
CAS:<p>Penetratin-Arg is an antimicrobial and is used for drug delivery vehicle [1] .</p>Fórmula:C104H168N42O20SCor e Forma:SolidPeso molecular:2358.78Amoxicillin, L-
CAS:<p>Amoxicillin, L- is an antibiotic. It is also useful for the treatment of a number of bacterial infections.</p>Fórmula:C16H19N3O5SCor e Forma:SolidPeso molecular:365.40Orotidine 5′-monophosphate trisodium
CAS:<p>Orotidine 5'-monophosphate trisodium, a pyrimidine nucleotide, is synthesized through the de novo DNA synthesis pathway by various microorganisms, including M.</p>Fórmula:C10H10N2Na3O11PCor e Forma:SolidPeso molecular:434.14Gilvocarcin 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:482.485
