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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SARS-CoV-2 3CLpro-IN-1
CAS:<p>SARS-CoV-2 3CLpro-IN-1 is a potent inhibitor of the key enzyme 3CL pro in coronaviruses, promising for antiviral drug R&D.</p>Formula:C27H30ClN3O3SColor and Shape:SolidMolecular weight:512.06YKAs3003
CAS:<p>YKAs3003 inhibits KAS III with MICs 128-256 μg/mL against multiple bacteria.</p>Formula:C13H17NO2Purity:98%Color and Shape:SolidMolecular weight:219.28Bunamidine hydrochloride
CAS:<p>Bunamidine hydrochloride is a veterinary anthelmintic that acts against Echinococcus granulosus and Tapeworm.</p>Formula:C25H39ClN2OColor and Shape:SolidMolecular weight:419.05SARS-CoV-2 3CLpro-IN-3
CAS:SARS-CoV-2 3CLpro-IN-3 is a SARS CoV-2 3CLpro inhibitor that exhibits antiviral, antibacterial, and antifungal effects.Formula:C23H21BrN6O2SColor and Shape:SolidMolecular weight:525.42CBR-6672
CAS:<p>CBR-6672, a potent anti-tuberculosis agent; type II NADH dehydrogenase inhibitor; MIC: 0.14 μM.</p>Formula:C17H20FN3O2SColor and Shape:SolidMolecular weight:349.42(3R,4R)-A2-32-01
CAS:<p>(3R,4R)-A2-32-01 is the (R,R)-enantiomer of A2-32-01 and has potential antibacterial activity.</p>Formula:C19H27NO2Purity:98.19%Color and Shape:SolidMolecular weight:301.42ACH-806
CAS:<p>ACH-806 is an NS4A antagonist. It can inhibit Hepatitis C Virus (HCV) replication with an EC50 of 14 nM.</p>Formula:C19H20F3N3O2SPurity:98%Color and Shape:SolidMolecular weight:411.44ZTB23(R)
CAS:<p>ZTB23(R) is the first potent and selective inhibitor of Mycobacterium tuberculosis Zmp1.</p>Formula:C20H15NO5S2Purity:98%Color and Shape:SolidMolecular weight:413.47Sulfaethoxypyridazine
CAS:<p>Sulfaethoxypyridazine is a antibacterial agent that can induce cataracts in rats and dogs.</p>Formula:C12H14N4O3SPurity:99.91%Color and Shape:SolidMolecular weight:294.33DVR-01
CAS:<p>DVR-01 is an HBV capsid inhibitor and can be used in studies about the treatment of Hepatitis B virus (HBV) infection and related conditions.</p>Formula:C20H23ClN2O3SPurity:99.95%Color and Shape:SolidMolecular weight:406.93MurA-IN-2
CAS:<p>MurA-IN-2: potent MurA inhibitor, IC50 of 39μM, chloroacetamide with aliphatic amine; has antibacterial properties.</p>Formula:C12H20ClNOColor and Shape:SolidMolecular weight:229.75SABA1
CAS:<p>SABA1 has antibacterial activity, inhibiting Pseudomonas aeruginosa and Escherichia coli, and also inhibits biotin carboxylase.</p>Formula:C22H19ClN2O5SPurity:98.36%Color and Shape:SolidMolecular weight:458.92HadAB-IN-1
CAS:<p>HadAB-IN-1: potent TB research chemical; IC50 = 0.03μM; inhibits HadAB, affecting Mtb mycolic acid synthesis.</p>Formula:C19H17BrClN3O3SColor and Shape:SolidMolecular weight:482.78Thiarabine
CAS:<p>Thiarabine displays effective anti-tumor activity. It also inhibition of DNA synthesis.</p>Formula:C9H13N3O4SPurity:98%Color and Shape:SolidMolecular weight:259.28ThrRS-IN-1
CAS:<p>ThrRS-IN-1 inhibits Salmonella ThrRS with IC50 1.4μM, Kd 1.36μM, targets tRNA/L-threonine sites, has strong antibacterial effects.</p>Formula:C16H18Cl2N4O3Color and Shape:SolidMolecular weight:385.25Adafosbuvir PM
CAS:<p>Adafosbuvir PM (AL-335 PM) is a small molecule NS5B inhibitor that can be used to study chronic hepatitis C.</p>Formula:C10H13FN2O6Purity:97.08%Color and Shape:SolidMolecular weight:276.22Lexithromycin
CAS:<p>Lexithromycin is an erythromycin A derivative. It has antibacterial activity.</p>Formula:C38H70N2O13Purity:98%Color and Shape:SolidMolecular weight:762.97Antibacterial agent 67
CAS:<p>Antibacterial agent 67 blocks succinate dehydrogenase more effectively than haloperidol, with IC50 of 0.03 μM vs 4.40 μM.</p>Formula:C24H15F6N5OColor and Shape:SolidMolecular weight:503.4Pyribencarb
CAS:<p>Pyribencarb, a benzylcarbamate-type fungicide, exhibits broad-spectrum activity against various plant pathogenic fungi.</p>Formula:C18H20ClN3O3Purity:99.75%Color and Shape:SolidMolecular weight:361.82HIV-1 protease-IN-1
CAS:<p>HIV-1 protease-IN-1, potent HIV inhibitor; IC50=90pM, fights B/C-HIV strains with EC50=89-13.59/8.23nM.</p>Formula:C25H35N3O6SColor and Shape:SolidMolecular weight:505.63Chelator 1a
CAS:<p>Chelator 1a has antifungal activity, inhibiting Aspergillus and Candida, and can be used to study fungal infections and cancer.</p>Formula:C16H12BrN3OSColor and Shape:SolidMolecular weight:374.26BTZ-N3
CAS:<p>BTZ-N3 is an effective and selective anti-tuberculosis drug candidate.</p>Formula:C17H16F3N5O3SColor and Shape:SolidMolecular weight:427.42-Hydroxydocosanoic acid
CAS:<p>2-Hydroxydocosanoic acid exhibits antioxidant, cholinesterase inhibitory, and antimicrobial properties [1].</p>Formula:C22H44O3Color and Shape:SolidMolecular weight:356.58RSV604 racemate
CAS:<p>RSV604 (A-60444) racemate, a racemic mixture, exhibits lower potency against strains of respiratory syncytial virus (RSV) compared to its S-isomer.</p>Formula:C22H17FN4O2Color and Shape:SolidMolecular weight:388.39Antitubercular agent-17
CAS:<p>Compound 8a: Antitubercular with MIC of 2 μg/ml for H37Rv, Spec 192, 210; 128 μg/ml for Spec 800. Selective effects.</p>Formula:C14H12BrN5OColor and Shape:SolidMolecular weight:346.18SARS-CoV-2-IN-16
CAS:<p>SARS-CoV-2-IN-16 strongly inhibits NPro, with EC50 of 3.69 μM and Kd of 7.82 μM, suggesting effective binding and antiviral properties.</p>Formula:C17H20N2O2Color and Shape:SolidMolecular weight:284.35FtsZ-IN-1
CAS:<p>FtsZ-IN-1: potent quinoline-based FtsZ inhibitor; targets Gram-positive bacteria, minimal hemolysis, resists drug resistance.</p>Formula:C26H32IN3Color and Shape:SolidMolecular weight:513.467HIV-1 inhibitor-38
CAS:<p>HIV-1 inhibitor-38, or Compound 91, shows promise as a strong latency reversing agent against HIV-1.</p>Formula:C15H13Cl3N6Color and Shape:SolidMolecular weight:383.66Rustmicin
CAS:<p>Rustmicin is a 14-membered macrolide identified as an inhibitor of plant pathogenic fungi.</p>Formula:C21H32O6Color and Shape:SolidMolecular weight:380.48Cefepime chloride
CAS:<p>Cefepime chloride, a broad-spectrum cephalosporin, combats Gram-positive/negative bacteria and can induce neurotoxicity.</p>Formula:C19H25ClN6O5S2Color and Shape:SolidMolecular weight:517.02Antileishmanial agent-8
CAS:<p>Compound 18: Antileishmanial, IC50=5.64 μM for L. donovani, low toxicity in L-6 cells, IC50=73.9 μM.</p>Formula:C18H16O4Color and Shape:SolidMolecular weight:296.32Laromustine
CAS:<p>Laromustine (VNP40101M) is a sulfonyl hydrolysis alkylation prodrug for cancer treatment with significant anticancer activity, inhibiting thioredoxin reductase.</p>Formula:C6H14ClN3O5S2Purity:≥98%Color and Shape:SolidMolecular weight:307.78Ribocil-C Racemate
CAS:<p>Ribocil-C Racemate is a racemic mix and selective inhibitor of E. coli riboflavin riboswitches affecting vitamin B2 synthesis.</p>Formula:C21H21N7OSPurity:98%Color and Shape:SolidMolecular weight:419.5Naftoxate
CAS:<p>Naftoxate is an antimicotic. It is effective against both gram-positive and gram-negative bacteria as well as yeasts and other fungi in plant cell culture.</p>Formula:C19H14N2OS2Purity:98%Color and Shape:SolidMolecular weight:350.46Antibacterial agent 97
CAS:<p>Antibacterial agent 97 is potent; MIC: 16 μg/mL for E. coli and S. aureus.</p>Formula:C19H23N5SColor and Shape:SolidMolecular weight:353.48Antiviral agent 30
CAS:<p>Antiviral Agent 30 (Example 118) is an active compound against HCV and RSV with an inhibitory concentration (IC 50) of greater than 25μM [1].</p>Formula:C21H32N2O3SColor and Shape:SolidMolecular weight:392.56Mtb-cyt-bd oxidase-IN-1
<p>Mtb-cyt-bd oxidase-IN-1, a Mycobacterium tuberculosis inhibitor, IC50: 0.13 μM, useful for TB research.</p>Formula:C26H35NO2Color and Shape:SolidMolecular weight:393.56Ametoctradin
CAS:<p>Ametoctradin is a Qo-site inhibitor of mitochondrial respiratory complex III and is used in the study of oomycete diseases.</p>Formula:C15H25N5Purity:99.65%Color and Shape:SolidMolecular weight:275.39HIV-1 inhibitor-30
CAS:<p>HIV-1 inhibitor-30 (10i) targets RT enzyme, EC50=40nM, IC50=80nM. Effective against seven NNRTI-resistant HIV-1 strains.</p>Formula:C19H20ClN3O2Color and Shape:SolidMolecular weight:357.83R 82150
CAS:<p>R 82150 is an antiviral and a member of the tetrahydroimidazo[4,5,1-jk]-[1,4]-benzodiazepin-2(1H)-thione family.</p>Formula:C16H21N3SPurity:98%Color and Shape:SolidMolecular weight:287.42Direct Black 38 free acid
CAS:<p>Ferristatin II (Direct Black 38 free acid) is a polysulphonated dye and promotes the degradation of transferrin receptor-1 in vitro and in vivo.</p>Formula:C34H27N9O7S2Purity:98%Color and Shape:SolidMolecular weight:737.77Antitubercular agent-14
CAS:<p>Antitubercular agent-14 (Compound 1) shows antitubercular activity. The MIC value of Antitubercular agent-14 against M. tuberculosis is 0.3 μg/mL [1].</p>Formula:C20H27ClN2Color and Shape:SolidMolecular weight:330.89Anticandidal agent-1
CAS:<p>Compound C2 is a broad-spectrum anticandidal, blocking biofilm and filament growth with MIC50 of 13.51μg/mL (C. glabrata) and 8.65μg/mL (C. albicans).</p>Formula:C19H22O5Color and Shape:SolidMolecular weight:330.38RD3-0028
CAS:<p>RD3-0028 is a potent and selective RSV replication inhibitor(EC50 of 4.5 μM).</p>Formula:C8H8S2Purity:98%Color and Shape:SolidMolecular weight:168.28CID 5951923
CAS:<p>CID 5951923 is an inhibitor of KLF5 transcription factor with an IC50 of 603 nM.</p>Formula:C16H18N2O7SPurity:99.95%Color and Shape:SolidMolecular weight:382.39LabMol-301
CAS:<p>LabMol-301 blocks NS5 RdRp/NS2B-NS3pro (IC50: 0.8/7.4µM), protects cells from ZIKV death.</p>Formula:C18H16N6Color and Shape:SolidMolecular weight:316.36Cap-dependent endonuclease-IN-3
CAS:<p>Cap-dependent endonuclease-IN-3 inhibits CEN, promising for studying influenza A/B. (Patent WO2019141179A1, compound III-2)</p>Formula:C29H25F2N3O7SColor and Shape:SolidMolecular weight:597.59CRK12-IN-2
CAS:<p>CRK12-IN-2, a potent CRK12 inhibitor, has EC50 of 3.2 nM for T. congolense and 0.08 nM for T. vivax; treats trypanosomiasis in animals.</p>Formula:C23H33F2N5O3S2Purity:99.26% - 99.70%Color and Shape:SolidMolecular weight:529.67RyRs activator 1
CAS:<p>RyRs activator 1 triggers ranibulin receptors; 100% larvicidal at 0.5 mg/L, 90% at 0.01 mg/L.</p>Formula:C21H14ClF3N6O4Color and Shape:SolidMolecular weight:506.82Urease-IN-5
<p>Urease-IN-5: urease inhibitor, IC50 1.473 µM, low cytotoxicity, IC50 17.78 µg/mL on P. vulgaris.</p>Formula:C16H20N2O3SColor and Shape:SolidMolecular weight:320.41HBV-IN-16
CAS:<p>HBV-IN-16, a quinoline derivative, inhibits HBV cccDNA, key for viral replication (from patent WO2019121357A1).</p>Formula:C22H20ClNO4Color and Shape:SolidMolecular weight:397.85D77
CAS:<p>D77 is anti-HIV-1 inhibitor. D77 inhibits HIV-1(IIIB) replication by EC50 value of 23.8 μg/ml in MT-4 cell (5.03 μg/ml for C8166 cells).</p>Formula:C28H22BrNO7SPurity:98%Color and Shape:SolidMolecular weight:596.45Crisnatol mesylate
CAS:<p>Crisnatol, a potent and selective DNA intercalator, has potential anticancer activity.</p>Formula:C24H27NO5SColor and Shape:SolidMolecular weight:441.54Isobellidifolin
CAS:<p>Isobellidifolin, a xanthone compound, serves as a free radical scavenger and antioxidant. It exhibits a potent antifungal effect.</p>Formula:C14H10O6Color and Shape:SolidMolecular weight:274.23DMJ-I-228
CAS:<p>DMJ-I-228 is a specific inhibitor of HIV-1 entry through interaction with the Env spike by virtue of the incorporation of a guandinium group.</p>Formula:C19H19ClFN5O4Color and Shape:SolidMolecular weight:435.84S-(N-PhenethylthiocarbaMoyl)-L-cysteine
CAS:<p>PEITC-Cys: anticarcinogenic, antileukemic, inhibits DNA synthesis in HL60, P450 inhibitor.</p>Formula:C12H16N2O2S2Color and Shape:SolidMolecular weight:284.4Marasmic acid
CAS:<p>Marasmic acid is a bioactive antifungal.</p>Formula:C15H18O4Color and Shape:SolidMolecular weight:262.3EV-A71-IN-1
CAS:<p>EV-A71-IN-1: potent EV-A71 capsid inhibitor, EC50 0.27 μM, disrupts VP1/hSCARB2 interaction, broad-spectrum antiviral, non-toxic to human cells.</p>Formula:C21H15N5SColor and Shape:SolidMolecular weight:369.44Werner syndrome RecQ helicase-IN-3
CAS:<p>Potent WRN inhibitor, Werner syndrome RecQ helicase-IN-3, is orally active with 0.06 µM IC50; exhibits antiproliferative and anticancer effects.</p>Formula:C31H30ClF3N8O5Color and Shape:SolidMolecular weight:687.07Benzylurea
CAS:<p>Benzylurea (AI3-61350) competitively inhibits dehydrogenase/cytokinin oxidase.</p>Formula:C8H10N2OPurity:98%Color and Shape:SolidMolecular weight:150.18Antimalarial agent 12
CAS:<p>Antimalarial 12 inhibits P. falciparum, EC50: 136-155 nM, not E. coli (MIC >250,000 nM), affects HEK-293/hPHep, CC50: 10,000-50,000 nM.</p>Formula:C26H18BrClN2O2Color and Shape:SolidMolecular weight:505.79Pirlindole mesylate
CAS:<p>monoamine oxidase type A inhibitor</p>Formula:C16H22N2O3SPurity:98%Color and Shape:SolidMolecular weight:322.42Antibacterial agent 122
CAS:<p>Thiourea derivative 122 is a low-toxicity antibacterial used in tuberculosis research with anti-mycobacterial properties.</p>Formula:C15H14N2O3SColor and Shape:SolidMolecular weight:302.35Cadrofloxacin
CAS:<p>Cadrofloxacin (Caderofloxacin, CS-940) is a novel fluoroquinolone antimicrobial agent.</p>Formula:C19H20F3N3O4Color and Shape:SolidMolecular weight:411.38V-06-018
CAS:V-06-018 is a quorum-sensing modulator. It also acts as a LasR antagonist.Formula:C18H27NO2Purity:98%Color and Shape:SolidMolecular weight:289.41BMY-27709
CAS:<p>BMY-27709 inhibits influenza growth (IC50: 3-8 μM, A/WSN/33), targets H1/H2 subtypes via hemagglutinin, ineffective against H3/B Lee/40.</p>Formula:C17H24ClN3O2Purity:98.37% - 98.55%Color and Shape:SolidMolecular weight:337.84WAY 150138
CAS:<p>WAY 150138 inhibits the herpes simplex virus.</p>Formula:C22H18Cl2FN3O3SColor and Shape:SolidMolecular weight:494.37NC00075159
CAS:<p>NC00075159 is an opener of human KCNQ4 (Kv7.4) potassium channel.</p>Formula:C15H16N2O3S2Purity:98%Color and Shape:SolidMolecular weight:336.43Sitamaquine tosylate
CAS:<p>Sitamaquine: antileishmanial, targets L. donovani species, EC50 = 9.5-19.8 μM, inhibits mitochondrial complex II, induces apoptosis in promastigotes.</p>Formula:C28H41N3O4SColor and Shape:SolidMolecular weight:515.71PXYC2
CAS:<p>PXYC2 is an RpsA-CTD antagonist; Kd: 6.35 μM for RpsA-CTD, 5.11 μM for RpsA-CTD Δ438A; vital in trans-translation.</p>Formula:C7H6N4O3SColor and Shape:SolidMolecular weight:226.21Antimalarial agent 11
CAS:<p>Antimalarial compound 1: Spirocyclic chromane, EC50 - D6: 1.48 μM, ARC08-022: 1.81 μM.</p>Formula:C25H25F2NO3Color and Shape:SolidMolecular weight:425.47SARS-CoV-2 3CLpro-IN-7
CAS:<p>SARS-CoV-2 3CLpro-IN-7 is a reversible covalent inhibitor of the SARS-CoV-2 3CL protease, exhibiting an inhibitory concentration (IC50) value of 1.4 µM.</p>Formula:C24H17ClN2O6Color and Shape:SolidMolecular weight:464.85Alalevonadifloxacin HCl
CAS:<p>Alalevonadifloxacin HCl is a novel l-alanine ester prodrug of levonadifloxacin.</p>Formula:C22H27ClFN3O5Purity:98%Color and Shape:SolidMolecular weight:467.92DHQZ 36
CAS:<p>DHQZ 36: retrograde trafficking inhibitor, anti-parasite, stops Leishmania amazonensis (EC50: 13.63 μM).</p>Formula:C21H18F2N2OSPurity:98%Color and Shape:SolidMolecular weight:384.44gp120-IN-2
CAS:<p>gp120-IN-2 is a potent HIV-1 inhibitor (IC50 = 7.5 μM) with low cytotoxicity (CC50 = 112.93 μM).</p>Formula:C15H18N2O5Color and Shape:SolidMolecular weight:306.31Mt KARI-IN-2
CAS:<p>Mt KARI-IN-2, an inhibitor for Mtb KARI (Ki: 2.02 μM) and Mtb H37Rv (MIC: 0.78 μM), has low cytotoxicity (HEK IC50: >86 μg/mL).</p>Formula:C14H11N5O4S2Color and Shape:SolidMolecular weight:377.4Sulfoxone sodium
CAS:<p>Sulfoxone sodium ( Adesulfone Sodium) is an anti-leprosy drug.</p>Formula:C14H16N2NaO6S3Color and Shape:SolidMolecular weight:427.46Antifungal agent 65
CAS:<p>Compound 5d (Antifungal Agent 65) exhibits potent fungicidal activity against Fusarium oxysporum f.sp.</p>Formula:C29H29N3O2S2Color and Shape:SolidMolecular weight:515.69Antifungal agent 36
CAS:<p>Antifungal agent 36 is a potent anti-fungal agent that shows anti-fungal activity for Basidiomycetes [1].</p>Formula:C14H21NO2Color and Shape:SolidMolecular weight:235.32HIV-1 inhibitor-34
CAS:<p>HIV-1 inhibitor-34 (5q): potent, selective; EC50: 6.4 nM; MT-4 CC50: 16 μM; useful in AIDS research.</p>Formula:C26H27N7OColor and Shape:SolidMolecular weight:453.54Dextrorotation nimorazole phosphate ester
CAS:<p>Dextrorotation nimorazole phosphate ester: new, efficient, well-tolerated antibacterial and antiparasitic fourth-gen nitroimidazole.</p>Formula:C11H19N4O7PColor and Shape:SolidMolecular weight:350.26TCMDC-125457
CAS:<p>TCMDC-125457 aids calcium redistribution and treats artemisinin-resistant parasites with artesunate, not affecting heme crystallization.</p>Formula:C19H18ClN5O3Color and Shape:SolidMolecular weight:399.838-Azido-ADP disodium
CAS:<p>8-Azido-ADP (disodium) is a covalent inhibitor of ADP/ATP exchange in mitochondria, causing irreversible inhibition in light.</p>Formula:C10H13N8NaO10P2Color and Shape:SolidMolecular weight:490.197MTH1-IN-2
CAS:<p>MTH1-IN-2 is an inhibitor of MutT homolog 1 (MTH1), with anti-tumor activity.</p>Formula:C24H27N3O5SPurity:98%Color and Shape:SolidMolecular weight:469.55A 80987
CAS:<p>A 80987 is an inhibitor of HIV-1 protease.</p>Formula:C37H43N5O6Color and Shape:SolidMolecular weight:653.77hRSV-IN-1
CAS:<p>hRSV-IN-1 is an inhibitor of respiratory syncytial virus (hRSV) .</p>Formula:C24H25N5O3SColor and Shape:SolidMolecular weight:463.55Tenofovir diphosphate
CAS:<p>TFV-DP inhibits DNA polymerases, mimics dATP, and is used by HIV-1's reverse transcriptase.</p>Formula:C9H16N5O10P3Color and Shape:SolidMolecular weight:447.17Fuberidazole
CAS:<p>Fuberidazole is an antifungal agent.</p>Formula:C11H8N2OPurity:98.95%Molecular weight:184.19Chitin synthase inhibitor 4
CAS:<p>Chitin synthase inhibitor 4: a CHS inhibitor with antimicrobial properties, potential fungicide.</p>Formula:C20H15FN4OPurity:99.74%Color and Shape:SolidMolecular weight:346.36SPC-839
CAS:<p>SPC-839 is an IKK-2 Inhibitor with oral activity.</p>Formula:C18H14N4O3SColor and Shape:SolidMolecular weight:366.39Antibacterial agent 105
CAS:<p>Compound 17, a phenanthrolinic quinolone, fights M. tuberculosis (MIC 90: 2.64 μM) and various bacteria (MIC 90: 0.70-44.70 μM).</p>Formula:C14H9N3O5Color and Shape:SolidMolecular weight:299.24PqsR/LasR-IN-3
CAS:<p>PqsR/LasR-IN-3 (Compound 7a) inhibits hERG with the IC 50 of 109.01 μM which is also a PqsR and LasR systems inhibitor in P. aeruginosa [1].</p>Formula:C14H17NO5SColor and Shape:SolidMolecular weight:311.35BM635
CAS:<p>BM635 is an MmpL3 inhibitor with outstanding anti-mycobacterial activity (MIC50: 0.12 μM against M. tuberculosis H37Rv).</p>Formula:C25H29FN2OColor and Shape:SolidMolecular weight:392.51HIV-1 integrase inhibitor 4
CAS:<p>HIV-1 integrase inhibitor 4 is an HIV-1 integrase strand transfer (INST) inhibitor (IC50: 3.7 nM).</p>Formula:C24H20F2N4O5SPurity:98%Color and Shape:SolidMolecular weight:514.5Silicon Phthalocyanine 4
CAS:<p>Silicon Phthalocyanine 4 is a drug with anti-cutaneous neoplasms activity.</p>Formula:C39H35N9O2Si2Color and Shape:SolidMolecular weight:717.93CAY10711
CAS:<p>CAY10711: potent bactericide for Gram-positive/negative bacteria including MRSA, inhibits biofilms, synergizes with kanamycin, low mammalian toxicity.</p>Formula:C41H54N6S2Color and Shape:SolidMolecular weight:695.04Antitrypanosomal agent 11
<p>Antitrypanosomal Agent 11 is a chemical compound effective against Trypanosoma cruzi, exhibiting an inhibition concentration (IC 50) of 0.23 μM.</p>Formula:C16H10F6N6OColor and Shape:SolidMolecular weight:416.28HIV-IN-4
CAS:<p>HIV-IN-4 (Compound 12) is a potent HIV inhibitor that exhibits promising anti-HIV activities [1].</p>Formula:C14H18N2O3Color and Shape:SolidMolecular weight:262.3Antibacterial agent 100
CAS:<p>Compound 7c: Antibacterial/fungal, effective on S. aureus, C. albicans (MIC 4 μg/mL), C. neoformans (MIC 8 μg/mL).</p>Formula:C28H29BrN2Color and Shape:SolidMolecular weight:473.458Neuraminidase-IN-9
CAS:<p>Neuraminidase-IN-9 inhibits flu virus neuraminidase H5N1 (IC50: 0.12 μM), H5N2 (IC50: 0.049 μM), H5N6 (IC50: 0.16 μM).</p>Formula:C24H33BrN6O3Color and Shape:SolidMolecular weight:533.46
