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(2,959 products)
- Antibiotic(921 products)
- Antifection(23 products)
- DHFR(33 products)
- DNA/RNA Synthesis(708 products)
- HBV(176 products)
- HIV Protease(449 products)
- HSV(91 products)
- Integrase(2 products)
- Ribosome(13 products)
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Found 5843 products of "Microbiology/Virology"
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(R)-Gyramide A hydrochloride
CAS:<p>(R)-Gyramide A HCl inhibits DNA gyrase in bacteria (IC50: 875 μM), with MIC 10-80 μM against P. aeruginosa & E. coli, sparing topoisomerase IV.</p>Formula:C21H28ClFN2O3SColor and Shape:SolidMolecular weight:442.97Cefmenoxime
CAS:<p>Cefmenoxime: IV/IM cephalosporin antibiotic, resists beta-lactamase, targets Enterobacteriaceae, gram-positive/negative bacteria.</p>Formula:C16H17N9O5S3Purity:98%Color and Shape:Almost White Or Almost Yellow Crystalline PowderMolecular weight:511.558Anticancer agent 34
CAS:<p>Anticancer agent 34, a sulfonylurea, inhibits Mycobacterium, E. coli, C. albicans (MIC 0.039-0.156 mg/ml), and A549, PC3 cancers (IC50 8.4, 7.8 μg/ml).</p>Formula:C17H14BrN3O3S2Color and Shape:SolidMolecular weight:452.35EGFR/HER2/TS-IN-2
CAS:<p>EGFR/HER2/TS-IN-2: Strong EGFR, HER2 & TS inhibitor; EGFR IC50=0.173μM, HER2 IC50=0.125μM, TS IC50=1.12μM; kills MDA-MB-231 cells (IC50=1.69μM).</p>Formula:C26H21N7OS2Color and Shape:SolidMolecular weight:511.62NIT
CAS:<p>NIT is an HIV-1 protease inhibitor.</p>Formula:C15H7N3O4S2Purity:98%Color and Shape:SolidMolecular weight:357.36Cap-dependent endonuclease-IN-16
CAS:<p>Cap-dependent endonuclease-IN-16, a pyridone derivative, inhibits CEN, showing promise for flu research.</p>Formula:C28H25F2N3O7SColor and Shape:SolidMolecular weight:585.58MtInhA-IN-1
<p>MtInhA-IN-1: an oral selective MtInhA inhibitor, IC50 0.23 μM, effective against M. tuberculosis with MIC 0.4 μM.</p>Formula:C21H22BrN3Color and Shape:SolidMolecular weight:396.32Antileishmanial agent-9
CAS:<p>Compound 16c: potent anti-Leishmania agent, IC50=4.01 μM, low toxicity in L-6 cells, IC50=40.1 μM.</p>Formula:C23H26O4Color and Shape:SolidMolecular weight:366.45B1912
CAS:<p>B1912 has antibacterial activity.</p>Formula:C30H27ClN4Purity:98%Color and Shape:SolidMolecular weight:479.02Lufotrelvir
CAS:<p>Lufotrelvir (PF-07304814), a prodrug of PF-00835231, is a potent SARS-CoV-2 3CL protease inhibitor with antiviral properties, Ki 174nM.</p>Formula:C24H33N4O9PPurity:99.43% - >99.99%Color and Shape:SolidMolecular weight:552.51Antimalarial agent 18
<p>Potent antimalarial, lipophilic, inhibits P. falciparum (IC50=50nM) & A. baumanii (IC50=390nM), blocks non-mevalonate pathway.</p>Formula:C23H44NO9PColor and Shape:SolidMolecular weight:509.57HIV-1 inhibitor-36
CAS:<p>HIV-1 inhibitor-36 (Compound 2) is a potent HIV-1 inhibitor with significant potential as a novel latency reversing agent [1].</p>Formula:C14H14Cl2N2O2SColor and Shape:SolidMolecular weight:345.24Antibacterial agent 73
CAS:<p>Compound 7a: antitubercular (MIC 0.65 μg/mL Mtb), antibacterial, antifungal; cytotoxic (IC50 8.20 μM MCF-7).</p>Formula:C15H17FN2OColor and Shape:SolidMolecular weight:260.31Antitrypanosomal agent 8
CAS:<p>Antitrypanosomal agent 8 (compound 3b) showed a strong antitrypanosomal effect against Trypanosoma brucei (IC50: 0.79 μM). The IC50 value was 80.95 μM.</p>Formula:C23H19N5O2SColor and Shape:SolidMolecular weight:429.49TMC310911
CAS:<p>TMC310911 is an oral HIV-1 protease inhibitor with an EC50 of 2.2-14.2 nM, effective against various HIV-1 strains.</p>Formula:C38H53N5O7S2Purity:98%Color and Shape:SolidMolecular weight:755.99Liroldine
CAS:<p>Liroldine is a new synthetic agent with antiamoebic activity.</p>Formula:C20H20F2N4Color and Shape:SolidMolecular weight:354.4Antileishmanial agent-11
CAS:<p>Antileishmanial agent-11: Potent against L. brazilensis (28.3 μM), L. infantum (24.8 μM), T. cruzi (13.0 μM) with strong antiprotozoal efficacy.</p>Formula:C27H24ClN3O4Color and Shape:SolidMolecular weight:489.95Antifungal agent 73
CAS:<p>Antifungal agent 73 (compound A32) effectively combats azole-resistant candidiasis by disrupting the fungal cell wall and membrane.</p>Formula:C21H16Cl2N2O3Color and Shape:SolidMolecular weight:415.27VP-4556
CAS:<p>VP-4556 is a potent anti-MRSA compound with >95% inhibition at 8 μg/mL MIC.</p>Formula:C12H12N2O4SColor and Shape:SolidMolecular weight:280.3Fenpropimorph
CAS:<p>Fenpropimorph is used as a small molecule fungicide.</p>Formula:C20H33NOColor and Shape:SolidMolecular weight:303.48Sulfamethomidine
CAS:<p>Sulfamethomidine has antibacterial activity [1].</p>Formula:C12H14N4O3SColor and Shape:SolidMolecular weight:294.33Antitubercular agent-20
CAS:<p>Antitubercular agent-20 is an orally active antitubercular agent. agent-20 showed low cytotoxicity and good tolerability in BALB/c mice.</p>Formula:C25H22F6N4O3SColor and Shape:SolidMolecular weight:572.52AV-1101
CAS:<p>AV-1101, a cytokine production inhibitor, is used potentially for the treatment of HIV infection.</p>Formula:C19H20N2O4Purity:98%Color and Shape:SolidMolecular weight:340.37Antibacterial agent 111
CAS:<p>Compound 3: potent against B. cereus & K. pneumonia; MICs: 3.90 & 0.49 μg/mL; targets tyrosyl-tRNA synthetase.</p>Formula:C18H12N6SColor and Shape:SolidMolecular weight:344.39Antitrypanosomal agent 4
CAS:<p>Compound 19: potent, blood-brain penetrant antitrypanosomal; IC50: T. cruzi 1.2 μM, T.b. brucei 70 nM.</p>Formula:C18H14ClN3O5SColor and Shape:SolidMolecular weight:419.84Ofurace
CAS:<p>Ofurace is a fungicide.</p>Formula:C14H16ClNO3Purity:98%Color and Shape:SolidMolecular weight:281.73Halofuginone hydrobromide
CAS:<p>Halofuginone specifically inhibits collagen type I and MMP-2 gene expression, which may result in the suppression of angiogenesis and tumor cell growth.</p>Formula:C16H17BrClN3O3·HBrPurity:97.01% - 99.73%Color and Shape:SolidMolecular weight:495.59Bulaquine
CAS:<p>Bulaquine, a 8-aminoquinoline derivative, targets liver stage of P. falciparum and dormant P. vivax/ovale.</p>Formula:C21H27N3O3Color and Shape:SolidMolecular weight:369.46Beaucage reagent
CAS:<p>Beaucage reagent, which is found to be effective in causing DNA cleavage.</p>Formula:C7H4O3S2Purity:98.50%Color and Shape:White To Off-White PowderMolecular weight:200.23PNU-101603
CAS:<p>PNU-101603, a Sutezolid metabolite, effective against TB including drug-resistant strains, works solo or with SQ109.</p>Formula:C16H20FN3O4SColor and Shape:SolidMolecular weight:369.41Antibacterial agent 117
CAS:<p>Triazole-derived Antibacterial 117 inhibits R. prowazekii MetAP1 with a 15 μM IC50 and rickettsial growth.</p>Formula:C9H9ClN4SColor and Shape:SolidMolecular weight:240.71Nifuroxime
CAS:<p>Nifuroxime, an anti-infective agent, is utilized in researching fungal infections.</p>Formula:C5H4N2O4Color and Shape:SolidMolecular weight:156.1VP-4509
CAS:<p>VP-4509: Anti-MRSA, MIC 49.3 μM; combats Pseudomonas aeruginosa.</p>Formula:C14H16N2O5SColor and Shape:SolidMolecular weight:324.35DPC-681
CAS:<p>DPC-681 is a potent and selective HIV protease inhibitor (IC90s: 4 to 40 nM for wild-type HIV-1).</p>Formula:C35H48FN5O5SColor and Shape:SolidMolecular weight:669.85Vapendavir
CAS:<p>Vapendavir binds enterovirus capsids; effective against EV71 with EC50 of 0.5-1.4 μM.</p>Formula:C21H26N4O3Purity:98%Color and Shape:SolidMolecular weight:382.46DMA-135 hydrochloride
CAS:<p>DMA-135 hydrochloride (DMA-135 HCl) is an antiviral active compound that targets RNA and inhibits enterovirus 71 IRES-dependent translation and replication.</p>Formula:C16H18ClN7OPurity:98.04%Color and Shape:SolidMolecular weight:359.81Chitin synthase inhibitor 13
CAS:<p>Chitin Synthase Inhibitor 13 (compound 12g), a non-competitive antagonist of chitin synthase, demonstrates broad-spectrum antifungal activity and has an</p>Formula:C21H19N5O5SColor and Shape:SolidMolecular weight:453.47HIV-1 inhibitor-19
CAS:<p>HIV-1 inhibitor-19 is a potent NNRTI targeting L100I, K103N, V106A/F227L mutants; EC50s: 7.3, 9.2, 21.0 nM respectively.</p>Formula:C24H22BClN2O5SColor and Shape:SolidMolecular weight:496.77RYL-552S
CAS:<p>RYL-552S is a drug-resistant strain of Plasmodium falciparum that effectively kills the asexual blood stage of the parasite in vitro.</p>Formula:C24H17F4NOSColor and Shape:SolidMolecular weight:443.46HIV-1 inhibitor-15
CAS:<p>HIV-1 inhibitor-15 (compound 9d): Potent, broad-spectrum, EC50=1.7-9 nM for various strains, good solubility/safety, oral use.</p>Formula:C24H20N6Color and Shape:SolidMolecular weight:392.46HBV-IN-19
CAS:<p>HBV-IN19 suppresses HBV, cutting HBsAg output, useful for chronic HBV study.</p>Formula:C24H30N2O6Color and Shape:SolidMolecular weight:442.5Antiparasitic agent-9
CAS:<p>Antiparasitic agent-9 (compound 47) - orally active with high efficacy against human parasites.</p>Formula:C18H20N6O2SColor and Shape:SolidMolecular weight:384.46Anti-Trypanosoma cruzi agent-4
CAS:<p>Anti-Trypanosoma cruzi Agent-4 is a Trypanosoma cruzi inhibitor utilized for the investigation of infections caused by this parasite.</p>Formula:C17H16N2O3Color and Shape:SolidMolecular weight:296.32Taribavirin hydrochloride
CAS:<p>Taribavirin HCl: oral drug targeting HCV in liver, spares red blood cells, aims to reduce anemia risk.</p>Formula:C8H14ClN5O4Purity:98%Color and Shape:SolidMolecular weight:279.68D-Xylofuranose, 1,2,3,5-tetraacetate
CAS:<p>1,2,3,5-Tetra-O-acetyl-D-xylofuranose is a starting material for the synthesis of nucleosides.</p>Formula:C13H18O9Color and Shape:SolidMolecular weight:318.28Methenamine mandelate
CAS:<p>Methenamine mandelate-loaded nanoparticles can induce DNA damage and apoptosis of cancer cells.</p>Formula:C14H20N4O3Color and Shape:SolidMolecular weight:292.3310-Formyl-5,8-dideazafolic acid
CAS:<p>10-Formyl-5,8-dideazafolic acid is a thymidylate synthase inhibitor.</p>Formula:C22H21N5O7Purity:96.04%Color and Shape:SolidMolecular weight:467.43Ro 14-9578
CAS:<p>Ro 14-9578 is anantibacterial agent in the class of tricyclic quinolone.</p>Formula:C16H13NO5Purity:98%Color and Shape:SolidMolecular weight:299.28Flaviviruses-Inhibitor-I
CAS:<p>Flaviviruses-Inhibitor-I is several viruses belonging to the family of Flaviviridae inhibitor.</p>Formula:C17H17N3O3SPurity:98%Color and Shape:SolidMolecular weight:343.4Trovirdine hydrochloride
CAS:<p>Trovirdine hydrochloride is a reverse transcriptase inhibitor.</p>Formula:C13H14BrClN4SPurity:98%Color and Shape:SolidMolecular weight:373.7Exeporfinium chloride
CAS:<p>Exeporfinium chloride(XF-73) is an antimicrobial agent that can weaken bacterial cell walls.</p>Formula:C44H50Cl2N6O2Color and Shape:SolidMolecular weight:765.81Saquayamycin B
CAS:<p>Saquayamycin B, a glycoside, targets Gram-positive bacteria and both adriamycin-sensitive and -resistant P388 leukemia cells.</p>Formula:C43H48O16Color and Shape:SolidMolecular weight:820.83Antiviral agent 18
CAS:<p>Compound 5, an antiviral agent, effectively targets murine norovirus, with potential in infectious disease and oncology research.</p>Formula:C11H13ClN4O4Color and Shape:SolidMolecular weight:300.7FPI-1602
CAS:<p>FPI-1602 is a β-lactamase inhibitor with strong antimicrobial activity against Pseudomonas aeruginosa, Escherichia coli, and Enterobacter species [1].</p>Formula:C11H17N5O7SColor and Shape:SolidMolecular weight:363.35Quinfamide
CAS:<p>Quinfamide is a compound with the potential to treat tropical parasitic infections such as Amoebiasis and Helminthiasis.</p>Formula:C16H13Cl2NO4Purity:99.92%Color and Shape:SolidMolecular weight:354.18TachypleginA
CAS:<p>TachypleginA is a parasite motility and invasion inhibitor.</p>Formula:C22H21F2NOPurity:98%Color and Shape:SolidMolecular weight:353.4Grazoprevir sodium salt
CAS:<p>Grazoprevir sodium salt is a selective Hepatitis C virus NS3/4a protease inhibitor with broad activity across genotypes and resistant variants.</p>Formula:C38H50N6NaO9SPurity:98%Color and Shape:SolidMolecular weight:789.9Antifungal agent 67
CAS:<p>Compound 9 (Antifungal agent 67), an imidazole class antifungal, exhibits efficacy against Candida and possesses a CC50 value of 33.6 μM in neonatal rat</p>Formula:C23H25ClN2O3Color and Shape:SolidMolecular weight:412.91UNC10201652
CAS:<p>UNC10201652 inhibits intestinal L1-specific β-glucuronidases; effective against E. coli (IC50: 0.117 μM).</p>Formula:C20H25N7OSColor and Shape:SolidMolecular weight:411.523-Fucosyllactose
CAS:<p>3-Fucosyllactose, a key fucosylated oligosaccharide in human milk, offers prebiotic and immune benefits.</p>Formula:C18H32O15Color and Shape:SolidMolecular weight:488.44Glucocorticoid receptor modulator 1
CAS:<p>Glucocorticoid receptor modulator 1 is a orally NF-κB and AP-1 inhibitor, inflammatory factors IL-6, IL-1β, TNF-α, and MMP-13, alleviating skin inflammation.</p>Formula:C24H23ClN2O4SPurity:99.79%Color and Shape:SolidMolecular weight:470.97Antibacterial agent 141
CAS:<p>Compound B14 (Antibacterial agent 141) exhibits antibacterial activity against the plant pathogens Xoo, Xac, Psa, and Cmm, with an EC50 value of 1.28 μM.</p>Formula:C23H27ClN2O3Color and Shape:SolidMolecular weight:414.93Antifungal agent 31
CAS:<p>Orally active triazole, antifungal 31 with pyrrolizinone structure, combats Candida, reduces mortality and renal infection in mice.</p>Formula:C25H22F2N6O3Color and Shape:SolidMolecular weight:492.48β-Lactamase-IN-1
CAS:β-Lactamase-IN-1 (4-(1,3-dihydroxypropan-2-yl)-6-methoxypyrido[2,3-b]pyrazin-3-one) is a β-Lactamase inhibitor and targets the infection of NeisseriaFormula:C11H13N3O4Purity:99.89%Color and Shape:SolidMolecular weight:251.24S 2720
CAS:<p>S 2720 is a human immunodeficiency virus type 1 (HIV-1)-specific reverse transcriptase (RT) inhibitor quinoxaline.</p>Formula:C14H15ClN2O2SColor and Shape:SolidMolecular weight:310.8Antibacterial agent 96
CAS:<p>Compound 4k is potent against drug-susceptible and resistant M. tuberculosis but toxic to HepG2 and Vero cells.</p>Formula:C18H15Cl2NO2Color and Shape:SolidMolecular weight:348.22Rufloxacin hydrochloride
CAS:<p>Rufloxacin HCl (MF-934 HCl): a fluoroquinolone that inhibits topoisomerase and B-cell differentiation.</p>Formula:C17H19ClFN3O3SPurity:99.80%Color and Shape:SolidMolecular weight:399.867Levovirin valinate HCl
CAS:<p>Levovirin valinate HCl is a valine ester prodrug of levovirin as a new investigational drug for the therapy of the hepatitis C virus.</p>Formula:C13H22ClN5O6Purity:98%Color and Shape:SolidMolecular weight:379.8GAK inhibitor 2
CAS:<p>GAK inhibitor 2, IC50: 0.024μM, strongly blocks GAK; potent against dengue virus, EC50: 1.049μM.</p>Formula:C20H23N3O3SColor and Shape:SolidMolecular weight:385.48Netzahualcoyonol
CAS:<p>Netzahualcoyonol has antibacterial/cytotoxic effects; isolated with tingenone as active compounds.</p>Formula:C30H38O5Purity:98%Color and Shape:SolidMolecular weight:478.62Antimicrobial agent-4
CAS:<p>Antimicrobial agent-4 (6a) has potent activity against pathogens; binds target enzyme with 10.0 kcal/mol affinity.</p>Formula:C22H16ClN5O2SColor and Shape:SolidMolecular weight:449.91Chlorfenson
CAS:<p>Chlorfenson is used to treat onychomycosis as the primary indication.</p>Formula:C12H8Cl2O3SColor and Shape:SolidMolecular weight:303.16Inz-4
CAS:<p>Inz-4 is a fungal-selective inhibitor of mitochondrial cytochrome bc1.</p>Formula:C18H14F4N2O2Color and Shape:SolidMolecular weight:366.312,3-Dehydro-2-Deoxy-N-Acetylneuraminic Acid
CAS:<p>2,3-Dehydro-2-Deoxy-N-Acetylneuraminic Acid is a pan-sialidase (neuraminidase, NEU) inhibitor with inhibitory activity and against various influenza viruses.</p>Formula:C11H17NO8Color and Shape:SolidMolecular weight:291.26Neuraminidase-IN-10
CAS:<p>Neuraminidase-IN-10 inhibits flu virus strains H1N1, H5N1, and H5N8 with IC50 values of 2.6, 5.1, and 1.65 nM respectively.</p>Formula:C26H34N2O5SColor and Shape:SolidMolecular weight:486.62Epsiprantel
CAS:<p>Epsiprantel is an orally active antiparasitic drug that inhibits various tapeworms, including Echinococcus granulosus (granular echinococcus), in dogs.</p>Formula:C20H26N2O2Purity:98.09%Color and Shape:SolidMolecular weight:326.43MDRTB-IN-1
CAS:<p>MDRTB-IN-1 (5aα) is an antibiotic which is against Mycobacterium tuberculosis H37Rv(MIC90 :10.5 μM).</p>Formula:C15H18N2O3Purity:98%Color and Shape:SolidMolecular weight:274.32FWM-3
CAS:<p>FWM-3 is a potent SARS-CoV-2 NSP13 helicase inhibitor [1].</p>Formula:C16H16N6O2SColor and Shape:SolidMolecular weight:356.4Antitubercular agent-24
CAS:<p>Compound 1: Antitubercular, fights M. tuberculosis H37Rv, IC50 - extracellular 0.83 μM, intracellular 0.17 μM.</p>Formula:C18H19N3O2S2Color and Shape:SolidMolecular weight:373.49BM 21.1298
CAS:<p>BM 21.1298 is a inhibition of HIV-1 reverse transcriptase.</p>Formula:C16H13NOSPurity:98%Color and Shape:SolidMolecular weight:267.35HSV-1/HSV-2-IN-2
CAS:<p>HSV-1/HSV-2-IN-2 is a compound that acts as an inhibitor of HSV-1, HSV-2, and VV, demonstrating antiviral activity with EC50 values of 6.8, 8.9, and 8.9 μM,</p>Formula:C17H14ClFN4OSColor and Shape:SolidMolecular weight:376.84MK-4965
CAS:<p>MK-4965 is a new type of non-nucleoside reverse transcriptase inhibitor with antiviral activity.</p>Formula:C20H13Cl2N5O2Color and Shape:SolidMolecular weight:426.26Adenallene
CAS:<p>Adenallene inhibits replication and cytopathic effects of HIV in vitro.</p>Formula:C9H9N5OPurity:98%Color and Shape:SolidMolecular weight:203.2Penflufen
CAS:<p>Penflufen, a broad-spectrum succinate dehydrogenase inhibitor (SDHI), serves effectively as a fungicide.</p>Formula:C18H24FN3OColor and Shape:SolidMolecular weight:317.4β-Lactamase-IN-7
CAS:<p>β-Lactamase-IN-7 (compound 14) effectively inhibit Klebsiella pneumoniae that is a potent inhibitor of VIM-Type metallo-β-lactamase with Ki values of 1.26 μM</p>Formula:C16H15N3S2Color and Shape:SolidMolecular weight:313.44Stemphyperylenol
CAS:<p>Stemphyperylenol: antifungal, targets Alternaria solani, MIC at 1.57 μM.</p>Formula:C20H16O6Color and Shape:SolidMolecular weight:352.34UGM-IN-3
CAS:<p>UGM-IN-3 inhibits UGM (Kd=66 μM) and M. tuberculosis growth (MIC=6.2 μg/mL).</p>Formula:C18H16INO2Color and Shape:SolidMolecular weight:405.23Viral 2C protein inhibitor 1
CAS:<p>Potent 2C protein inhibitor 6aw targets various enteroviruses with low toxicity, EC50: 0.1-3.6μM.</p>Formula:C19H18FN3OColor and Shape:SolidMolecular weight:323.36Haloprogin
CAS:<p>Haloprogin is an antifungal agent used as a topical cream for the treatment of beriberi and other fungal infections.</p>Formula:C9H4Cl3IOColor and Shape:SolidMolecular weight:361.39TachypleginA-2
CAS:TachypleginA-2 is a parasite motility and invasion inhibitor.Formula:C22H23NOPurity:98%Color and Shape:SolidMolecular weight:317.42Neuraminidase-IN-6
CAS:<p>Neuraminidase-IN-6, a 1,3,4-triazole derivative, is a strong NA inhibitor (IC50 = 0.11 μM) used in anti-influenza drug development.</p>Formula:C16H16N4O2SColor and Shape:SolidMolecular weight:328.39MLAF50
CAS:<p>MLAF50 is an inhibitor of the REV1 UBM2-Ubiquitin interaction.</p>Formula:C15H12I2O4Color and Shape:SolidMolecular weight:510.062-Keto-D-galactose
CAS:<p>2-Keto-D-galactose inhibits DNA synthesis and inhibits the proliferation of in vitro grown Ehrlich ascites tumor cells.</p>Formula:C6H10O6Purity:98%Color and Shape:SolidMolecular weight:178.14CGP 53353
CAS:<p>CGP 53353 (DAPH-7) is a PKC inhibitor with inhibitory effects on PKCβII and PKCβI and can be used to study atherosclerosis.</p>Formula:C20H13F2N3O2Purity:98.11%Color and Shape:SolidMolecular weight:365.33Pirlindole free base
CAS:<p>Pirlindole is a reversible inhibitor of monoamine oxidase A (RIMA). It is structurally and pharmacologically related to metralindole.</p>Formula:C15H18N2Color and Shape:SolidMolecular weight:226.32DA-7867
CAS:<p>DA-7867, an oxazolidinone, has lower MIC(≤0.25 μg/ml) against aerobic gram-positive bacteria than linezolid, with MIC(90) at 0.125 μg/ml.</p>Formula:C19H18FN7O3Color and Shape:SolidMolecular weight:411.39NS2B/NS3-IN-6
CAS:<p>Compound 1a: DENV/ZIKV NS2B/NS3 protease inhibitor; IC50: ZIKV 2.23 μM, DENV 25.2 μM.</p>Formula:C19H19N3O5S2Color and Shape:SolidMolecular weight:433.5Tunicamine
CAS:<p>Tunicamine is a reversible polyprenol-phosphate inhibitor.</p>Formula:C11H21NO9Purity:98%Color and Shape:SolidMolecular weight:311.29INSCoV-614(1B)
CAS:<p>INSCoV-614(1B), a potent Mpro inhibitor, may help fight SARS-CoV-2, per patent WO2021219089A1.</p>Formula:C23H21ClF3N5O3Color and Shape:SolidMolecular weight:507.89Cgp 53820
CAS:<p>CGP 53820 is a pseudosymmetric inhibitor of HIV-1 Protease.</p>Formula:C31H51N5O5Color and Shape:SolidMolecular weight:573.77
