
Microbiology/Virology
Microbiology and virology inhibitors are compounds that target microorganisms, including bacteria, viruses, and fungi, disrupting their growth, replication, or survival. These inhibitors are essential for studying microbial pathogenesis, understanding resistance mechanisms, and developing new antimicrobial and antiviral therapies. Inhibitors in this category are used to combat infectious diseases, explore microbial ecology, and investigate host-pathogen interactions. At CymitQuimica, we provide a broad selection of high-quality microbiology and virology inhibitors to support your research in infectious diseases, microbiology, and virology.
Subcategories of "Microbiology/Virology"
- Antibacterial(3,387 products)
- Antibiotic(940 products)
- Antifection(27 products)
- DHFR(30 products)
- DNA/RNA Synthesis(803 products)
- HBV(185 products)
- HIV Protease(506 products)
- HSV(99 products)
- Integrase(2 products)
- Ribosome(6 products)
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Found 6396 products of "Microbiology/Virology"
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Arizonin A1
CAS:Arizonin A1 is a biochemical.Formula:C17H14O7Color and Shape:SolidMolecular weight:330.29Methylclonazepam
CAS: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.Formula:C16H12ClN3O3Color and Shape:SolidMolecular weight:329.74Galbinic Acid
CAS:Galbinic acid, a lichen-derived depsidone from U. undulata, inhibits B. cereus, B. subtilis, S. aureus, and E. coli, with varying MICs.Formula:C20H14O11Color and Shape:SolidMolecular weight:430.32Antifungal agent 58
CAS:Compound A21 is a potent anti-Candida drug effective against Fluconazole-resistant strains, surpassing Miconazole, with MIC 0.06-8 μg/mL.Formula:C18H15F3N2SeColor and Shape:SolidMolecular weight:395.28Laidlomycin
CAS:Laidlomycin, a polyether, polycyclic, monocarboxylic acid, possesses inhibitory activity against various Mycoplasma species, especially Acholeplasma laidlawii.Formula:C37H62O12Purity:98%Color and Shape:SolidMolecular weight:698.88Y 12896
CAS:Y 12896 has a wide range of applications in life science related research.Formula:C17H25Cl2N3O7Color and Shape:SolidMolecular weight:454.33,3'-((2-Chlorophenyl)methylene)bis(4-hydroxy-2H-chromen-2-one)
CAS:3,3'-((2-Cl-phenyl)methylene)bis(4-OH-2H-chromen-2-one): ENPP1 inhibitor, Ki=50μM; urease inhibitor, IC50=84.53μM.Formula:C25H15ClO6Color and Shape:SolidMolecular weight:446.843,4-Dihydroxyallylbenzene 3,4-di-O-glucoside
CAS:3,4-Dihydroxyallylbenzene 3,4-di-O-glucoside (1,2-Di-O-β-D-glucopyranosyl-4-allylbenzene) is a natural product found in the tuber of Ophiopogon japonicus Ker-Formula:C21H30O12Purity:98%Color and Shape:SolidMolecular weight:474.46Propargylcholine
CAS:Propargylcholine, an alkyne-modified choline, blocks Dgc-catalyzed demethylation in P. aeruginosa.Formula:C7H14BrNOPurity:99.70%Color and Shape:SolidMolecular weight:208.1RNA MTase-IN-1
RNA MTase-IN-1 (Compound 47) is an inhibitor of RNA methyltransferase (RNA MTase), exhibiting an IC50 of 68 μM against 16S rRNA (m1A1408) methyltransferase (NpmA). It demonstrates significant inhibitory activity against aminoglycoside resistance linked to pathogens and is applicable in research on antibiotic-resistant bacterial infections.Color and Shape:Odour SolidNUDT5/14 antagonist 1
NUDT5/14 antagonist 1 (Compound 9) is a dual selective antagonist for nucleotide diphosphate kinases NUDT5 and NUDT14, exhibiting IC50 values of 0.27 and 0.16 μM, respectively. Additionally, NUDT5/14 antagonist 1 binds to Bruton's tyrosine kinase (BTK) with an IC50 of 0.377 μM.Formula:C23H24N6OMolecular weight:400.201161-O-Methylemodin
CAS:1-O-Methylemodin, a natural product isolated from Zopfiella longicaudata, exhibits antifungal activity [1].Formula:C16H12O5Color and Shape:SolidMolecular weight:284.26ledoxantrone
CAS:Ledoxantrone, a benzopyranoindazole, stabilizes DNA-topoisomerase II complexes and blocks helicases; shows preclinical promise.Formula:C21H27N5OSColor and Shape:SolidMolecular weight:397.54Propioxatin B
CAS:Propioxatin B is an enkephalinase B inhibitor isolated from actinomycete.Formula:C18H31N3O6Purity:98%Color and Shape:SolidMolecular weight:385.461DENV-IN-10
DENV-IN-10 is a potent tetravalent inhibitor of the dengue virus, exhibiting half-maximal effective concentrations (EC50s) of 1.36, 0.87, 0.94, and 0.95 μMFormula:C26H25N3O4SColor and Shape:SolidMolecular weight:475.56Bis-Br-ANT-ATP tetrasodium
Bis-Br-ANT-ATP(tetrasodium) is a fluorescent derivative of adenosine-5'-triphosphate (ATP). It selectively inhibits the adenylyl cyclase toxin CyaA of Bordetella pertussis with a Ki of 12.6 nM. This compound is utilized in research related to whooping cough.Color and Shape:Odour SolidAntiparasitic agent-14
Antiparasitic agent-14: potent, cytotoxic, inhibits trypomastigote and amastigote growth.Formula:C19H20N4OSColor and Shape:SolidMolecular weight:352.45Fusion glycoprotein (92-106)
CAS:Fusionglycoprotein92-106 is a peptide derived from the respiratory syncytial virus (RSV) fusion protein. It functions as an MHC class I-restricted cytotoxic T lymphocyte (CTL) epitope, with all 15 amino acids effectively recognized by CTLs.Formula:C73H124N22O25SMolecular weight:1741.96Abacavir Carboxylate
CAS:Abacavir carboxylate, an inactive abacavir metabolite, forms via aldehyde intermediates bonding to valine in proteins.Formula:C14H16N6O2Color and Shape:SolidMolecular weight:300.322Aureonitol
CAS:Aureonitol, a fungal metabolite with antiviral properties, hinders influenza A (H3N2 and H1N1) replication and hemagglutination.Formula:C13H18O2Color and Shape:SolidMolecular weight:206.28Influenza A NP(366-374) Strain A/PR/8/35
CAS:This peptide is an H2-Db-restricted epitope from the Influenza A/PR/8/34 nucleoprotein.Formula:C38H63N11O18S2Purity:98%Color and Shape:SolidMolecular weight:1026.1Antibacterial agent 143
CAS:Compound 5a: MICs of 25, 25, 50, 50 μg/mL vs. B. subtilis, S. aureus, P. aeruginosa, E. coli.Formula:C17H13BrN2OSColor and Shape:SolidMolecular weight:373.27Bombinin H3
Bombinin H3, an antimicrobial peptide sourced from the Bombina variegata (moth) skin, exhibits lethal concentrations of 3.7 μM and 2.4 μM against EscherichiaFormula:C90H163N23O21SColor and Shape:SolidMolecular weight:1935.46Adustin
CAS:Adustin is an antifungal antibiotic characterized as a polypeptide that inhibits translation. It effectively suppresses translation in a cell-free rabbit reticulocyte lysate system, exhibiting an IC50 of 0.34 μM.Formula:C11H8O3Color and Shape:SolidMolecular weight:188.1798-NH2-ATP
CAS:8-NH2-ATP is an inactive derivative of adenosine triphosphate (ATP), synthesized from 8-NH2-Ado.Formula:C10H17N6O13P3Color and Shape:SolidMolecular weight:522.20Omiganan-FITC
Omiganan-FITC: a peptide conjugated with fluorescein (FITC) for catheter infection prevention.Color and Shape:Odour SolidWYFA-15
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.Formula:C22H16Cl2N2OColor and Shape:SolidMolecular weight:395.2817-TFA-ap-7-Deaza-ddA
CAS:Compound 19c is a nucleotide derivative for DNA sequencing dye terminators.Formula:C16H16F3N5O3Color and Shape:SolidMolecular weight:383.331Psoracorylifol C
Psoracorylifol C is a useful organic compound for research related to life sciences and the catalog number is T124015.Formula:C18H24O3Color and Shape:SolidMolecular weight:288.387D-Hexamannuronic acid
CAS:D-Hexamannuronic acid: alginate from brown algae & some bacteria, used in pain and dementia research.Formula:C36H50O37Color and Shape:SolidMolecular weight:1074.759Antibacterial agent 162 trifluoromethanesulfonate
Antibacterial agent 162 trifluoromethanesulfonate (compound 7), a dual-function molecule, demonstrates potent inhibitory effects on Staphylococcus aureus,Color and Shape:Odour Solid16-epi Latrunculin B
CAS:16-epiLatrunculin B, a stereoisomer of the actin polymerization inhibitor latrunculin B, was initially isolated from the Red Sea sponge N. magnifica. At concentrations of 5-10 µg/ml, it disrupts microfilament activity in actin disruption assays and exhibits cytotoxic effects on mouse KA31T and NIH3T3 tumor cells, with GI50 values of 1 and 4 µg/ml, respectively. Furthermore, it shows antiviral activity against herpes simplex type 1 virus, with an ED50 of 1 µg/ml.Formula:C20H29NO5SColor and Shape:SolidMolecular weight:395.5ω-azido-C6 Ceramide
CAS:ω-azido-C6 Ceramide reduces membrane potential and exhibits antibacterial activity against Neisseria, with a minimum inhibitory concentration (MIC) of 2 µg/mL for N. meningitidis MC58 and N. gonorrhoeae FA1090.Formula:C24H46N4O3Color and Shape:SolidMolecular weight:438.65Deltamycin A1
CAS:Deltamycin A1 is a novel macrolide antibiotic.Formula:C39H61NO16Purity:98%Color and Shape:SolidMolecular weight:799.90Feglymycin
CAS:Feglymycin, a 13-amino acid peptide, counters Gram-positive bacteria and HIV, blocks E. coli enzymes MurA & MurC.Formula:C95H97N13O30Molecular weight:1900.86Cefazolin-13C2,15N
CAS:Cefazolin-13C2,15N, a standard for GC/LC-MS cefazolin quantification, is effective against many bacteria with MICs of 0.1-25 μg/ml.Formula:C14H14N8O4S3Color and Shape:SolidMolecular weight:457.49Pyrazine-2-carbaldehyde
CAS:Pyrazine-2-carbaldehyde inhibits nicotinamidase in Mycobacterium tuberculosis and can be used for tuberculosis researchFormula:C5H4N2OPurity:99.67%Color and Shape:SolidMolecular weight:108.1Farinomalein A
CAS:Farinomalein A, a maleimide derivative, is isolated from the entomopathogenic fungus Paecilomyces farinosus. It exhibits effective inhibitory activity against soybean pathogen Phytophtora sojae.Formula:C10H13NO4Color and Shape:SolidMolecular weight:211.21Fosetyl-aluminum
CAS:Fosetyl-aluminum is a systemic fungicide that controls downy mildews and Phytophthora diseases, used on a variety of crops including fruits and vegetables。Formula:C6H18AlO9P3Purity:99.52%Color and Shape:SolidMolecular weight:354.1Antimalarial agent 46
CAS:Antimalarial agent 46 (Compound 42a) is a compound with antimalarial activity, effective in inhibiting P. falciparum lines.Formula:C21H17Cl3N4OColor and Shape:SolidMolecular weight:447.755-Hydroxytoluene-2,4-disulphonic acid diammonium
5-Hydroxytoluene-2,4-disulphonic acid diammonium is a Policresulen impurity that inhibits the NS2B/NS3 protease and DENV2 virus replication.Color and Shape:SolidAtropine Oxide
CAS:Atropine Oxide is derived from Atropine, a drug that blocks muscarinic receptors and treats nerve agent poisoning and bradycardia.Formula:C17H23NO4Color and Shape:SolidMolecular weight:305.37SpeB cysteine protease
CAS:SpeB cysteine protease is a potent modifier capable of degrading proteins that are crucial for both host and bacterial immunology. It can break down streptolysin O (SLO) contained within extracellular vesicles.Color and Shape:SolidAntibacterial agent 40
CAS:Antibacterial agent 40 is an antibacterial agent.Formula:C12H17N5O6SColor and Shape:SolidMolecular weight:359.36Amphotericin B methyl ester hydrochloride
CAS:Amphotericin B methyl ester hydrochloride, an antifungal and anti-HIV cholesterol binder, is a methyl ester of Amphotericin B.Formula:C48H76ClNO17Color and Shape:SolidMolecular weight:974.57SARS-CoV-2 Mpro-IN-37
SARS-CoV-2 Mpro-IN-37 (compound 8r) is an inhibitor of the SARS-CoV-2 main protease (Mpro), with an IC50 value of 0.0199 μM. It exhibits IC50 values of 0.00945 μM against SARS-CoV-1 Mpro and 0.111 μM against MERS-CoV Mpro. SARS-CoV-2 Mpro-IN-37 demonstrates potent antiviral activity in the nanomolar range without showing cytotoxicity.Formula:C25H30N2O3SColor and Shape:SolidMolecular weight:438.582Antibacterial agent 33
CAS:Antibacterial Agent 33 boosts Ceftazidime's efficacy by lowering its MIC.Formula:C12H17N5O6SColor and Shape:SolidMolecular weight:359.36(S)-Dinotefuran
CAS:(S)-Dinotefuran, a neonicotinoid, more toxic to bees than its R-isomer, targets α8 nAChR.Formula:C7H14N4O3Color and Shape:SolidMolecular weight:202.21Anti-MRSA agent 25
Anti-MRSA agent 25 (Compound 10c) is an antibacterial compound with a minimum inhibitory concentration (MIC) of 0.25 μg/mL against methicillin-resistant Staphylococcus aureus (MRSA). Its antimicrobial activity is achieved by inhibiting biofilm formation, disrupting the cell wall (interacting with peptidoglycan and lipoteichoic acid), acting on the cell membrane (causing depolarization, increasing permeability, and compromising integrity), reducing metabolic activity, interfering with cellular redox homeostasis, and binding to DNA. Anti-MRSA agent 25 holds potential for research in the field of anti-infective therapeutics.Color and Shape:Odour Solid5-Methylcytidine 5′-triphosphate trisodium
5-Methylcytidine 5′-triphosphate trisodium (5-Methyl-CTP trisodium), a modified nucleoside triphosphate, enhances translational properties and stability, while
Formula:C10H15N3Na3O14P3Color and Shape:SolidMolecular weight:563.13Bombinin-like peptide 7
CAS:Bombinin-like peptide 7, an antimicrobial peptide sourced from the Oriental fire-bellied toad (Bombina orientalis) [1], demonstrates bioactive properties.Formula:C114H192N34O32Color and Shape:SolidMolecular weight:2550.95TAT-NSF700scr
TAT-NSF700scr, a control peptide, contains a TAT domain, glycine linker, and scrambled NSF amino acids, not inhibiting SNARE exocytosis.Formula:C186H315N61O44Molecular weight:4109.87NDM-1 inhibitor-8
NDM-1 inhibitor-8 (Compound 18b) is a covalent inhibitor of New Delhi metallo-β-lactamase-1 (NDM-1), with an IC50 of 7.03 μM. It effectively inhibits resistant bacterial strains and demonstrates synergistic antibacterial effects when used in combination with Meropenem. In mouse models, NDM-1 inhibitor-8 exhibits anti-infective activity.Formula:C28H23Cl2N3O4SSeColor and Shape:SolidMolecular weight:647.43Carbazomycin D
CAS:Carbazomycin D, from Streptomyces, fights fungi T. asteroides and T. mentagrophytes, M. tuberculosis, and is cytotoxic to various cells.Formula:C17H19NO3Color and Shape:SolidMolecular weight:285.34ent-Heronamide C
Ent-Heronamide C possesses antifungal properties and is utilized as a probe for analyzing the mode of action of heronamide C [1].Formula:C29H41NO3Color and Shape:SolidMolecular weight:451.64Influenza A virus-IN-1
CAS:Influenza A virus-IN-1, a dihydropyrrolidone, blocks IAV subtypes (IC50: 3.11-7.13 μM), boosts IFN-β and MxA antivirals.Formula:C27H20F6N2O3Color and Shape:SolidMolecular weight:534.458Trypanothione synthetase-IN-3
CAS:Trypanothione synthetase-IN-3: noncompetitive TryS inhibitor, Ki: 0.8 μM, useful in parasite research.Formula:C68H54O43Color and Shape:SolidMolecular weight:1559.13Antibacterial agent 34
CAS:Antibacterial agent 35 is a compound that effectively reduces the minimum inhibitory concentration (MIC) of Ceftazidime, enhancing its antibacterial activity.Formula:C13H19N5O6SColor and Shape:SolidMolecular weight:373.38meso-2,6-Diaminopimelic acid
CAS:Meso-2,6-diaminopimelic acid is an essential precursor in the biosynthesis of the amino acid L-lysine and a critical component of peptidoglycan in the cell walls of various bacteria.Formula:C7H14N2O4Color and Shape:SolidMolecular weight:190.2Antibacterial agent 71
Improved compound potency against E. coli, A. baumannii, and B. cenocepacia; up to >128-fold increase in effectiveness.Formula:C26H27F3N4OColor and Shape:SolidMolecular weight:468.51SARS-CoV-2-IN-28 disodium
SARS-CoV-2-IN-28 disodium: antiviral diphosphate ester, tweezers structure, IC50 of 0.4μM (virus) & 1.0μM (spike), disrupts membranes, EC50 of 4.4μM.Formula:C56H58Na2O8P2Color and Shape:SolidMolecular weight:966.98Amycolatopsin C
Amycolatopsin C, from Amycolatopsis, targets M. bovis/tuberculosis and fights colorectal/lung cancer. Not effective on common bacteria.Color and Shape:SolidGuaiacylglycerol-β-guaiacyl Ether
CAS:Guaiacylglycerol-beta-guaiacyl Ether is degraded by microorganisms and is commonly used as a substrate to mimic microbial degradation of cell walls of lignin-living plants.Formula:C17H20O6Purity:99.08%Color and Shape:SolidMolecular weight:320.34Isoprothiolane
CAS:Isoprothiolane is a foliar spray fungicide with eradicant and protectant activities against fungal diseases of rice plant caused by Pyvioutavia oryzae Cav.
Formula:C12H18O4S2Purity:99.50%Color and Shape:SolidMolecular weight:290.40FR179642
CAS:FR179642 is a key intermediate for making Micafungin, a drug from the echinocandin class.Formula:C35H52N8O20SColor and Shape:SolidMolecular weight:936.9ART899
CAS:ART899, a derivative of ART558, is a potent and specific conformational inhibitor of DNA polymerase θ (Polθ). It specifically inhibits the MMEJ activity of Polθ with an IC50 of 180 nM. Additionally, ART899 selectively enhances the radiosensitivity of tumor cells and possesses a strong independent antitumor effect on cancer cells.Formula:C19H16ClF4N3O4Color and Shape:SolidMolecular weight:464.8111-Keto fusidic acid
CAS:11-Keto fusidic acid exhibits potent antibacterial efficacy against Staphylococcus aureus, demonstrating a minimum inhibitory concentration (MIC) of 0.078 μg/mLFormula:C31H46O6Color and Shape:SolidMolecular weight:514.69Antibacterial agent 127
Antibacterial agent 127 (Compound 23) is a potent antibacterial agent [1] .Formula:C28H37N3O5SColor and Shape:SolidMolecular weight:527.68Carumonam
CAS:Carumonam, an antibiotic, could enhance the reactivity of Escherichia coli with mono- and polyclonal antisera to rough Escherichia coli J5.Formula:C12H14N6O10S2Purity:98%Color and Shape:SolidMolecular weight:466.40Cefamandole
CAS:Cefamandole is a broad-spectrum cephalosporin antibiotic with antibacterial activity against Bacillus subtilis and Escherichia coli.Formula:C18H18N6O5S2Purity:99.38%Color and Shape:SolidMolecular weight:462.5SARS-CoV-2-IN-53
ARS-CoV-2-IN-53 (Compd 5d) exhibits an inhibitory effect on SARS-CoV-2 replication, with an effective concentration (EC50) value of 14.3 μM, and demonstratesFormula:C23H18F2N2O4SPurity:98%Color and Shape:SolidMolecular weight:456.46Anticancer agent 140
Compound 140 (Compd 3) exhibits potential anticancer and antiparasitic activities [1].Formula:C20H26N2OPurity:98%Color and Shape:SolidMolecular weight:310.43MptpB-IN-2
MptpB-IN-2 (compound 20), a selective inhibitor for mycobacterium tuberculosis protein tyrosine phosphatase B (MptpB), exhibits half maximal inhibitoryFormula:C23H20F3NO3S2Purity:98%Color and Shape:SolidMolecular weight:479.54Isoreserpiline
CAS:Isoreserpiline, an indole alkaloid discovered in R. tetraphylla, exhibits a range of biological activities. This compound enhances the antibacterial efficacy of nalidixic acid against both nalidixic acid-sensitive and -resistant E. coli strains through a synergistic effect. Additionally, at a dosage of 25 mg/kg, it mitigates amphetamine-induced hyperactivity in mice.Formula:C23H28N2O5Color and Shape:SolidMolecular weight:412.486HBV-IN-36
HBV-IN-36 (also known as compound 42) is a hepatitis B virus (HBV) inhibitor with an IC50 of 2 μM, exhibiting anti-HBV activity characterized by an EC50 of 0.58Formula:C21H18ClFN4O2Purity:98%Color and Shape:SolidMolecular weight:412.84MPI60
MPI60 is a potent inhibitor of SARS-CoV-2 main protease (M^pro) exhibiting high antiviral efficacy, low cellular cytotoxicity, and considerable in vitroFormula:C24H31N3O5Purity:98%Color and Shape:SolidMolecular weight:441.52E07 aptamer
SARS-CoV-2 nsp14-IN-4 (Compound 12q) is a selective inhibitor of the SARS-CoV-2 nsp14 methyltransferase with an IC50 of 19 ± 2.5 nM.Purity:98%Color and Shape:Odour SolidNPD-2975
NPD-2975 (compound 30) is an orally active antitrypanosomal agent effective against Human African Trypanosomiasis (HAT), demonstrating acceptable metabolicFormula:C14H13FN4OPurity:98%Color and Shape:SolidMolecular weight:272.28AAK1-IN-6
AAK1-IN-6 is an inhibitor of AP-2 associated protein kinase 1 (AAK1, IC50 = 12 nM) and exhibits antiviral activity against Dengue virus (DNEV2, EC50 = 0.24 μM) and Venezuelan equine encephalitis virus (VEEV, EC50 = 0.30 μM). AAK1-IN-6 is applicable in antiviral research.Formula:C24H19N3O3Molecular weight:397.43D-4-77
D-4-77 is a potent inhibitor of SARS-CoV-2 Mpro, exhibiting an IC 50 of 0.95 μM, and possesses antiviral activity with an EC 50 of 0.49 μM.Formula:C23H34BrN3O5Purity:98%Color and Shape:SolidMolecular weight:512.44Cangorinine E-1
CAS:Cangorinine E-1 (compound 11), a dihydroagarofuran sesquiterpenoid derivative, exhibits weak inhibitory effects on herpes simplex virus type II (HSV) [1].Formula:C43H49NO18Purity:98%Color and Shape:SolidMolecular weight:867.85Angolamycin
CAS:Angolamycin is a macrolide antibiotic (antibiotic) effective against Gram-positive bacteria.Formula:C46H77NO17Color and Shape:SolidMolecular weight:916.1Acryl42-10
Acryl42-10 serves as a covalent inhibitor for the SARS-CoV-2 Nsp14 N7-Methyltransferase, exhibiting an inhibition concentration (IC50) of 7 μM [1].Formula:C20H24ClN3O4Purity:98%Color and Shape:SolidMolecular weight:405.8823-O-Demycinosyltylosin
CAS:23-O-Demycinosyltylosin (23-DMT), an acyl derivative of tylosin, exhibits antibacterial activity [1].Formula:C38H63NO13Color and Shape:SolidMolecular weight:741.91GT-1
CAS:GT-1 (LCB10-0200), a siderophore cephalosporin, fights P. aeruginosa, K. oxytoca, Proteus, S. marcescens, E. aerogenes.Formula:C29H30ClN11O11S2Color and Shape:SolidMolecular weight:808.2Streptothricin E
CAS:Streptothricin E is a biochemical.
Formula:C25H46N10O9Color and Shape:SolidMolecular weight:630.69Nornidulin
CAS:Nornidulin, a depsidone from A. nidulans, fights various bacteria, fungi, MRSA (MIC=2 μg/ml), and has larvicidal (LC50=1.7 μg/ml) and cytotoxic properties.Formula:C19H15Cl3O5Color and Shape:SolidMolecular weight:429.67Cajaninstilbene acid
CAS:Cajaninstilbene acid is a useful organic compound for research related to life sciences. The catalog number is T124035 and the CAS number is 87402-84-4.Formula:C21H22O4Color and Shape:SolidMolecular weight:338.403Azidocillin
CAS:Azidocillin, a semi-synthetic oral β-lactam antibiotic, treats various bacterial infections including osteitis and septicemia.Formula:C16H17N5O4SColor and Shape:SolidMolecular weight:375.40Pap12-6
Pap12-6 is a 12-peptide derived from the antimicrobial peptide Papiliocin, which originates from the larvae of the yellow-patterned butterfly. It exhibits potent antibacterial activity by penetrating and disrupting bacterial membranes. Additionally, Pap12-6 exerts anti-inflammatory effects through the TLR4-mediated NF-κB signaling pathway.Formula:C83H133N23O12Molecular weight:1644.050412-Bromoaldisine
CAS:2-Bromoaldisine, a pyrrole alkaloid isolated from Stylissa carter, is known to inhibit HIV-1 infection and suppress the Raf/MEK/MAPK pathway.Formula:C8H7BrN2O2Color and Shape:SolidMolecular weight:243.06PLpro-IN-8
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.Formula:C23H22N2O4Color and Shape:SolidMolecular weight:390.43(3R,6R)-Vaborbactam
(3R,6R)-Vaborbactam ((3R,6R)-Vaborbactam (Iso-1360457-46-0)) is a cyclic boronic acid pharmacophore β-lactamase inhibitor.Formula:C12H16BNO5SPurity:98.86%Color and Shape:SoildMolecular weight:297.14Dechlorogriseofulvin
CAS: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.Formula:C17H18O6Color and Shape:SolidMolecular weight:318.325Landomycin A
CAS:Landomycin A is a prominent angucycline hexasaccharide antibiotic from Streptomyces sp.Formula:C55H74O22Purity:98%Color and Shape:SolidMolecular weight:1087.175BMS-955176 TFA
CAS:GSK3532795: Oral HIV-1 maturation inhibitor, broad virus coverage, EC50: 15 nM, good preclinical pharmacokinetics.Formula:C44H64N2O8SPurity:98%Color and Shape:SolidMolecular weight:781.06Antibiotic WB
CAS:Antibiotic WB is a useful organic compound for research related to life sciences. The catalog number is T125208 and the CAS number is 247919-66-0.Formula:C19H27ClO6Color and Shape:SolidMolecular weight:386.87Neuraminidase-IN-12
CAS:NDV-IN-1 is an antiviral inhibiting neuraminidase and the Newcastle disease virus, preventing virion release from Vero cells.Formula:C11H13F3N4O7Color and Shape:SolidMolecular weight:370.24Protein kinase G inhibitor-1
CAS:Protein kinase G inhibitor-1 is a potent Protein kinase G inhibitor, IC50= 0.9 uM.Formula:C14H18N2O2SPurity:98.64%Color and Shape:SoildMolecular weight:278.37Ref: TM-T67755
1mg71.00€1mL*10mM (DMSO)161.00€5mg170.00€10mg250.00€25mg371.00€50mg525.00€100mg705.00€200mg954.00€Oxadixyl
CAS:Oxadixyl is used as a fungicide.Formula:C14H18N2O4Purity:98%Color and Shape:SolidMolecular weight:278.30

