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(2,968 products)
- Antibiotic(922 products)
- Antifection(23 products)
- DHFR(33 products)
- DNA/RNA Synthesis(711 products)
- HBV(177 products)
- HIV Protease(451 products)
- HSV(91 products)
- Integrase(2 products)
- Ribosome(13 products)
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Found 5863 products of "Microbiology/Virology"
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R 87366
CAS:R 87366 is used as a water-soluble HIV protease inhibitor.Formula:C32H39N7O6Purity:98%Color and Shape:SolidMolecular weight:617.73-Cyanovinylcarbazole phosphoramidite
CAS:<p>3-Cyanovinylcarbazole phosphoramidite: an antiviral, hinders viral DNA synthesis, modifies ribonucleotides.</p>Formula:C50H53N4O6PColor and Shape:SolidMolecular weight:836.95Gusperimus trihydrochloride
CAS:Gusperimus trihydrochloride is a derivative of the antitumor antibiotic spergualin with immunosuppressant activity.Formula:C17H40Cl3N7O3Purity:98%Color and Shape:SolidMolecular weight:496.9Antileishmanial agent-23
CAS:<p>Antileishmanial agent-23 (compound G1/9), a potent and selective trypanothione reductase (TR) inhibitor, exhibits an IC50 of 2.24 ± 0.52 μM.</p>Formula:C20H17N3O4S2Purity:98%Color and Shape:SolidMolecular weight:427.5Emtricitabine triphosphate tetrasodium salt
CAS:<p>Emtricitabine triphosphate tetrasodium salt is the tetrasodium salt form of the phosphorylated anabolite (-)-Emtricitabine triphosphate, an active nucleoside</p>Formula:C8H9FN3Na4O12P3SPurity:98%Color and Shape:SolidMolecular weight:575.11Ganfeborole HCl
CAS:<p>Ganfeborole HCl (GSK3036656 HCl) is a compound with anti-tuberculosis activity and is an inhibitor of Mycobacterium tuberculosis (Mtb) leucyl-tRNA synthetase.</p>Formula:C10H14BCl2NO4Purity:99.88%Color and Shape:SolidMolecular weight:293.94Fervenulin
CAS:<p>Fervenulin, from Streptomyces sp. CMU-MH021, halts egg hatch (MIC: 30 μg/mL) and kills J2 larvae (MIC: 120 μg/mL) of M. incognita.</p>Formula:C7H7N5O2Purity:99.75%Color and Shape:SolidMolecular weight:193.16RNA polymerase II-IN-1
CAS:<p>RNA polymerase II-IN-1 (19iv), an amatoxin, inhibits Pol II at 36.66 nM IC50, is more toxic to cancer cells, less to normal cells than α-Amanitin.</p>Formula:C38H53N11O12SPurity:98%Color and Shape:SolidMolecular weight:887.964-Hydroxy-2-methylbenzenesulfonic acid ammonium
CAS:<p>4-Hydroxy-2-methylbenzene ammonium: Policresulen impurity, inhibits NS2B/NS3 protease (IC50: 0.48 μg/mL), hinders DENV2 in BHK-21 cells (IC50: 4.99 μg/mL).</p>Formula:C7H11NO4SPurity:98%Color and Shape:SolidMolecular weight:205.23ZIKV-IN-1
CAS:<p>ZIKV-IN-1 blocks Zika virus effectively (EC50: 2.8 μM, EC90: 6.8 μM), targets the RdRp domain, and is low-toxic.</p>Formula:C21H18BrF2N3O3Color and Shape:SolidMolecular weight:478.29NVS-SM2
CAS:<p>NVS-SM2 boosts SMN2 splicing, enhances exon 7 inclusion, and raises SMN protein levels orally.</p>Formula:C23H30N6OColor and Shape:SolidMolecular weight:406.52ZINC475239213
CAS:<p>ZINC475239213 acts as an inhibitor targeting the SARS-CoV-2 Nsp14 N7-Methyltransferase with an IC50 value of 20 μM [1].</p>Formula:C21H15N5O2Purity:98%Color and Shape:SolidMolecular weight:369.38SARS-CoV-2-IN-66
CAS:<p>SARS-CoV-2-IN-66 (1), a derivative of vitamin K, functions as an inhibitor of SARS-CoV-2, exhibiting an effective concentration (EC50) of 70.8 μM in VeroE6/</p>Formula:C28H30O2Purity:98%Color and Shape:SolidMolecular weight:398.54MurA-IN-4
CAS:<p>MurA-IN-4 exhibits antibacterial properties as a MurA inhibitor, impeding the synthesis of bacterial cell walls [1].</p>Formula:C8H12ClNO3Color and Shape:SolidMolecular weight:205.64OM173-αA
CAS:<p>OM173-αA is a quinone bacterial metabolite that inhibits the growth of the bacteria M.</p>Formula:C17H16O6Color and Shape:SolidMolecular weight:316.31MoTPS1-IN-1
CAS:MoTPS1-IN-1 is a potent MoTPS1 inhibitor with antifungal anti-inflammatory activity that acts through interaction with Glu396 study ulcerative colitis.Formula:C23H27F3N2O4Purity:99.76%Color and Shape:SoildMolecular weight:452.47Influenza virus-IN-6
CAS:<p>Influenza virus-IN-6 (Compound 35) serves as a potent inhibitor targeting the N-terminal domain of the polymerase acidic protein (PA N ) endonuclease subunit of</p>Formula:C27H26ClNO7Purity:98%Color and Shape:SolidMolecular weight:511.95MsbA-IN-6
CAS:<p>MsbA-IN-6: potent antibiotic, hinders MsbA in gram-negative bacteria, kills E. coli, effective on drug-resistant strains.</p>Formula:C24H20Cl2N4OPurity:98%Color and Shape:SolidMolecular weight:451.35HIV-IN-8
CAS:<p>HIV-IN-8 (Compound 9) acts as an HIV inhibitor, suppressing HIV replication with an effective concentration (EC50) of 13 μg/mL [1].</p>Formula:C36H30O16Color and Shape:SolidMolecular weight:718.61MPI8
CAS:<p>MPI8 is a SARS-CoV-2 Protease inhibitor (IC50 = 105 nM).</p>Formula:C32H48N4O7Color and Shape:SolidMolecular weight:600.75Antifungal agent 24
CAS:<p>Antifungal agent 24 (Compound 6) is an antifungal agent that inhibits Candida albicans (MIC: 0.03 μg/ml).</p>Formula:C24H18F2N4OColor and Shape:SolidMolecular weight:416.42L 687908
CAS:<p>L 687908 is a potent inhibitor of hydroxyethylene-containing HIV protease.</p>Formula:C40H51N5O5Purity:98%Color and Shape:SolidMolecular weight:681.86WRN inhibitor 5
CAS:<p>WRN Inhibitor 5 (Example 157), a cyclic vinyl sulfone-based compound, serves as an inhibitor of Werner Syndrome ATP-dependent helicase enzyme (WRN).</p>Formula:C23H20N2O6SColor and Shape:SolidMolecular weight:452.48Cefteram
CAS:<p>Cefteram (T-2525), an orally active ester of the cephalosporin class, is the free acid form of Cefteram pivoxil.</p>Formula:C16H17N9O5S2Color and Shape:SolidMolecular weight:479.49KY386
CAS:<p>KY386 is a potent and selective DHX33 helicase inhibitor with an IC50 value of 19 nM.</p>Formula:C21H19N5O2SColor and Shape:SolidMolecular weight:405.478-NH2-ATP tetrasodium
CAS:<p>8-NH2-ATP tetrasodium, an inactive ATP variant, originates from 8-NH2-Ado tetrasodium, which triggers the apoptosis-associated cleavage of poly (ADP-ribose) polymerase [1] [2].</p>Formula:C10H13N6Na4O13P3Color and Shape:SolidMolecular weight:610.12Inz-5
CAS:Inz-5 is a fungal-selective inhibitor of mitochondrial cytochrome bc1. Inz-5 impairs fungal virulence. It also prevents the evolution of drug resistance.Formula:C18H14F4N6Color and Shape:SolidMolecular weight:390.34β-Gal-NONOate
CAS:<p>Beta-gal-nonoate, a β-galactosidase dependent nitric oxide (NO) donor, releases NO upon activation by β-galactosidase. It exhibits bactericidal activity, thus serving as an effective bactericide [1].</p>Formula:C10H19N3O7Color and Shape:SolidMolecular weight:293.27Emzadirib
CAS:<p>Emzadirib (RAD51-IN-2) is a potent RAD51 inhibitor with potential anticancer activity for the study of DNA damage repair.</p>Formula:C27H40N4O6S2Purity:99.79% - 99.9%Color and Shape:SolidMolecular weight:580.76Tobevibart
CAS:<p>Tobevibart, an IgG1-lambda humanized monoclonal antibody targeting the hepatitis B virus (HBV) surface envelope protein, exhibits antiviral activity [1].</p>Purity:98%Color and Shape:LiquidSARS-CoV-2-IN-62
CAS:<p>SARS-CoV-2-IN-62 (Compound R3b) effectively inhibits SARS-CoV-2 replication in Vero E6 and Calu-3 cells, demonstrating low cytotoxicity and EC50 values of 2.97</p>Formula:C17H21N3O3SePurity:98%Color and Shape:SolidMolecular weight:394.33Roseoflavin
CAS:<p>Roseoflavin, a chemical analog of FMN and riboflavin that has antimicrobial activity, can directly bind to FMN riboswitch aptamers and downregulate the</p>Formula:C18H23N5O6Purity:99.81% - 99.89%Color and Shape:SolidMolecular weight:405.41YH-53
CAS:<p>YH-53: potent inhibitor for SARS-CoV-1 (Ki=6.3 nM) & SARS-CoV-2 3CLpro (Ki=34.7 nM); hinders SARS-CoV-2 replication; aids COVID-19 research.</p>Formula:C30H33N5O5SColor and Shape:SolidMolecular weight:575.68NNRTIs-IN-1
CAS:<p>NNRTIs-IN-1 is a potent non-nucleoside reverse transcriptase inhibitor (NNRTI) with notable anti-resistance efficacy, effectively inhibiting both the wild-type</p>Formula:C28H22N6O3Color and Shape:SolidMolecular weight:490.51CDD-1819
CAS:<p>CDD-1819, a non-covalent and non-peptide compound, serves as a potent SARS-CoV-2 Mpro inhibitor, exhibiting a K i value of 5 nM.</p>Formula:C35H31N5O2Purity:98%Color and Shape:SolidMolecular weight:553.65Galidesivir hydrochloride
CAS:Galidesivir hydrochloride is an inhibitor of viral RNA-dependent RNA polymerase (RdRp). It inhibits SARS-CoV-2 by tightly binding to its RdRp.Formula:C11H16ClN5O3Purity:98%Color and Shape:SolidMolecular weight:301.73MK-3281
CAS:<p>MK-3281: Oral, potent HCV NS5B inhibitor with promising properties and efficacy in replication trials, suitable for clinical use.</p>Formula:C29H37N3O3Color and Shape:SolidMolecular weight:475.62D1N8
CAS:<p>D1N8 is a potent inhibitor of the SARS-CoV-2 3CL protease, displaying an IC50 value of 0.44 μM and a CC50 value of greater than 20 μM.</p>Formula:C19H14ClN5O3Purity:98%Color and Shape:SolidMolecular weight:395.8Tuberculosis inhibitor 8
CAS:<p>Tuberculosis inhibitor 8 (compound 3b), a 3-methoxy-2-phenylimidazo[1,2-b]pyridazine derivative, exhibits potent activity against both Mycobacterium</p>Formula:C21H19FN4OColor and Shape:SolidMolecular weight:362.44'-Acetyl-chrysomycin B
CAS:<p>4'-Acetyl-chrysomycin B, a 4'-acetylated analog of chrysomycin B, exhibits anti-Gram-positive bacterial and antimicrobial activities [1].</p>Formula:C29H30O10Color and Shape:SolidMolecular weight:538.54Methyl 3,4-dimethoxycinnamate
CAS:<p>Methyl 3,4-dimethoxycinnamate impedes uredospore germination and concurrently inhibits global DNA methylation in Hep3B cells [1] [2].</p>Formula:C12H14O4Color and Shape:SolidMolecular weight:222.24Dup-721
CAS:<p>DuP-721: broad-spectrum, oral antibiotic targeting various bacteria, including M. tuberculosis.</p>Formula:C14H16N2O4Purity:99.84%Color and Shape:SolidMolecular weight:276.29Antibacterial agent 135
CAS:<p>Antibacterial Agent 135 (example 7) effectively inhibits various bacteria, including P.</p>Formula:C11H15N5O6SColor and Shape:SolidMolecular weight:345.33Valnemulin
CAS:<p>Valnemulin, a broad-spectrum pleuromutilin antibiotic, targets peptidyl transferase within the 50S ribosomal subunit, effectively used in veterinary medicine to address swine diseases such as B. hyodysenteriae and M. hyopneumoniae.</p>Formula:C31H52N2O5SColor and Shape:SolidMolecular weight:564.83Antibacterial compound 1
CAS:<p>Antibacterial compound 1 is an antibacterial compound.</p>Formula:C14H16FN3O4Purity:98%Color and Shape:SolidMolecular weight:309.29UNC2170 maleate
CAS:<p>53BP1-binding protein 1 (53BP1) engages with dimethylated lysine 20 on histone 4 (H4K20me2) through its tandem tudor domains within a homodimer configuration, crucial for the DNA damage response. UNC2170, a micromolar 53BP1 ligand, selectively interacts with this site, demonstrating at least 17-fold preference for 53BP1 over similar proteins. This interaction occurs in a pocket formed by the 53BP1's tudor domains. Moreover, UNC2170 acts as an antagonist to 53BP1 in cellular lysates, effectively inhibiting class switch recombination, a process dependent on the functional 53BP1 tudor domain, thus confirming its cellular activity.</p>Formula:C14H21BrN2OC4H4O4Color and Shape:SolidMolecular weight:429.31Bio-AMS
CAS:<p>Bio-AMS is a potent inhibitor of bacterial biotin protein ligase, exhibiting selective activity against Mycobacterium tuberculosis (Mtb) and disrupting fatty</p>Formula:C20H29N9O7S2Color and Shape:SolidMolecular weight:571.63Antitrypanosomal agent 14
CAS:Antitrypanosomal agent 14 (Compound 1), a potent T.Formula:C14H23N3OSPurity:98%Color and Shape:SolidMolecular weight:281.42NCI-B16
CAS:<p>NCI-B16 is a small-molecule RNA binder that inhibits HCV (hepatitis C virus) replication [1].</p>Formula:C27H26N8O4Color and Shape:SolidMolecular weight:526.55Daldinone A
CAS:<p>Daldinone A (Compound 4), isolated from Nigrospora oryzae, exhibits antibacterial properties, specifically demonstrating antimicrobial potential against P. aeruginosa [1].</p>Formula:C20H16O5Color and Shape:SolidMolecular weight:336.34
