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(2,957 products)
- Antibiotic(920 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 5842 products of "Microbiology/Virology"
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Xenalamine
CAS:<p>Xenalamine is a synthetic compound of antiviral.</p>Formula:C23H21NO4Purity:98%Color and Shape:SolidMolecular weight:375.42HIV-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:345.24SJ-3366
CAS:<p>SJ3366 is a unique and highly potent nonnucleoside reverse transcriptase human immunodeficiency virus type 1 and HIV-2 inhibitor.</p>Formula:C21H24N2O3Color and Shape:SolidMolecular weight:352.43SP187
CAS:<p>SP187 (MON-DNJ) is a host-targeted iminosugar. It has anti-filovirus infection activity.SP187 is used for therapeutic use against influenza and dengue viruses.</p>Formula:C16H33NO5Purity:99.18%Color and Shape:SolidMolecular weight:319.44BPH-1358
CAS:<p>BPH-1358 (NSC-50460) inhibits FPPS and UPPS (IC50: 1.8 μM, 110 nM), active against S. aureus (MIC ~250 ng/mL).</p>Formula:C32H30Cl2N6O2Purity:99.74%Color and Shape:SolidMolecular weight:601.53Phenosulfazole
CAS:<p>Phenosulfazole is a potent antiviral agent which has the potential for the research of poliomyelitis virus [1].</p>Formula:C9H8N2O3S2Color and Shape:SolidMolecular weight:256.3Antitrypanosomal 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:755.99Antitubercular agent-19
CAS:<p>Antitubercular agent-19: effective against MTB H37Rv/MDR strains (MIC <0.016μg/ml), low cytotoxicity, high acute toxicity in BALB/c mice.</p>Formula:C24H20F6N4O3SColor and Shape:SolidMolecular weight:558.5Finafloxacin hydrochloride
CAS:<p>"Finafloxacin is a fluoroquinolone antimicrobial agent optimized for maximum effectiveness in mildly acidic conditions."</p>Formula:C20H20ClFN4O4Color and Shape:SolidMolecular weight:434.85VP-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:280.3Antitubercular 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:340.37F8-S40
CAS:<p>F8-S40 is a SARS-CoV-2 main protease inhibitor (IC 50 = 10.88 μM) [1].</p>Formula:C13H11N3O3SColor and Shape:SolidMolecular weight:289.31Antitrypanosomal 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:281.73SQ109
CAS:<p>SQ109 (NSC-722041) is an effective inhibitor of the trypomastigote form of the parasite (IC50 = 50 nM). SQ109 is an antitubercular agent and targets MmpL3.</p>Formula:C22H38N2Purity:99.70% - 99.91%Color and Shape:SolidMolecular weight:330.55Pralurbactam
CAS:<p>Pralurbactam is a β-Lactamase inhibitor utilized in the research of bacterial infections.</p>Formula:C10H18N6O8SColor and Shape:SolidMolecular weight:382.35SCH-43478
CAS:<p>SCH-43478 is a non-nucleoside agent of antiviral. It has an effective and selective activity against herpes simplex virus type 2 (HSV-2).</p>Formula:C12H10ClN3OPurity:98%Color and Shape:SolidMolecular weight:247.68Cylindrospermopsin
CAS:<p>Cylindrospermopsin: a toxic cyanobacterial uracil derivative, disrupts protein/glutathione synthesis in hepatocytes, and is genotoxic.</p>Formula:C15H21N5O7SColor and Shape:SolidMolecular weight:415.42SARS-CoV-2-IN-36
<p>SARS-CoV-2-IN-36: strong Mpro inhibitor, IC50=2.37μM, Kd=1.19μM, fights UC-1074/RG2674/NVDBB-2220 variants.</p>Formula:C17H21N5O3Color and Shape:SolidMolecular weight:343.38Lufotrelvir
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:552.51MMT5-14
CAS:<p>MMT5-14: potent SARS-CoV-2 inhibitor, improves antiviral activity (2-7x), boosts prodrug in plasma/lungs (200-300x), raises NTP in lungs (5x).</p>Formula:C39H55N6O8PColor and Shape:SolidMolecular weight:766.86HCV-IN-34
CAS:<p>HCV-IN-35, an oral HCV blocker, has an EC50 of 0.010 μM and a CC50 of 7.5 μM, indicating strong antiviral effects.</p>Formula:C31H36ClN5Color and Shape:SolidMolecular weight:514.1Antibacterial 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:156.1DPC-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:382.46Dapabutan
CAS:<p>Dapabutan is an antimicrobial agent active against Gram-positive bacteria.</p>Formula:C19H40N2O2Color and Shape:SolidMolecular weight:328.53Dabequin
CAS:<p>Dabequin is a derivative of aminoquinoline. It is said to have pharmacological activity against Plasmodium fukiparum.</p>Formula:C19H29N3O8P2Color and Shape:SolidMolecular weight:489.4Chitin 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:496.77MMV024101
CAS:<p>MMV024101: PI4K inhibitor, P. falciparum NF54 IC50 543 nM, poor solubility (<5 μM), fast mouse liver clearance.</p>Formula:C16H12N6O2SColor and Shape:SolidMolecular weight:352.37HIV-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:442.5Acibenzolar-S-methyl
CAS:<p>Acibenzolar-S-methyl, a fungicide, boosts plant defenses by upregulating W-box genes like CAD1, NPR1, PR2.</p>Formula:C8H6N2OS2Purity:99.64% - 99.86%Color and Shape:Beige Fine PowderMolecular weight:210.28Anti-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:296.32SARS-CoV-2 Mpro-IN-4
<p>SARS-CoV-2 Mpro-IN-4 inhibits Mpro (IC50: 900 nM) & CatL (IC50: 60 nM), blocks virus replication (IC50: 8.2 nM).</p>Formula:C30H38N4O5Color and Shape:SolidMolecular weight:534.65pUL89 Endonuclease-IN-2
CAS:<p>pUL89 Endonuclease-IN-2 inhibits HCMV with a 3.0 μM IC50, showing potent antiviral effects.</p>Formula:C17H12F3N3O3SColor and Shape:SolidMolecular weight:395.36Methenamine mandelate
CAS:<p>Methenamine mandelate-loaded nanoparticles can induce DNA damage and apoptosis of cancer cells.</p>Formula:C14H20N4O3Color and Shape:SolidMolecular weight:292.33Ro 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:299.28Saquayamycin 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:820.83CWHM-1008
CAS:<p>CWHM-1008: Oral antimalarial, EC50 - 46 nM (3D7 strain), 21 nM (Dd2 resistant).</p>Formula:C22H26F3N3OColor and Shape:SolidMolecular weight:405.46Grazoprevir 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:411.52Antibacterial 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:414.93INSCoV-601I(1)
CAS:<p>INSCoV-601I(1) is a strong 3CLpro inhibitor, key in SARS-CoV-2 replication; potential for research use - WO2021219089A1.</p>Formula:C23H22ClF2N5O2SColor and Shape:SolidMolecular weight:505.97Laburnetin
CAS:<p>Laburnetin: an isoflavone antibacterial, combats fungi/S. vesicarium, boosts MRSA methicillin susceptibility, used in pest control.</p>Formula:C20H18O6Color and Shape:SolidMolecular weight:354.35S 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:310.8HIV-1 inhibitor-46
CAS:<p>HIV-1 inhibitor-46, compound 13d, is a potent non-nucleoside reverse transcriptase inhibitor with an EC50 of 1.425 μM, useful in AIDS research.</p>Formula:C24H21ClN4OSColor and Shape:SolidMolecular weight:448.97Anti-Influenza agent 4
CAS:<p>Anti-Influenza agent 4 selectively inhibits A/Parma (EC50: 62 nM) and A/Roma (EC50: 150 nM) influenza strains.</p>Formula:C19H18N2O5SPurity:98.94% - 98.95%Color and Shape:SolidMolecular weight:386.42SARS-CoV-2-IN-12
CAS:<p>SARS-CoV-2-IN-12: strong 3C-like protease inhibitor; prevents viral replication; Ki=32.1 pM; useful in COVID-19 research.</p>Formula:C32H42F3N5O9Color and Shape:SolidMolecular weight:697.7RSV/IAV-IN-1
CAS:<p>RSV/IAV-IN-1, a dual inhibitor of RSV/IAV, is less toxic than Ribavirin and holds research potential for RSV/IAV infections.</p>Formula:C18H17ClN2O2SColor and Shape:SolidMolecular weight:360.86Chlorfenson
CAS:<p>Chlorfenson is used to treat onychomycosis as the primary indication.</p>Formula:C12H8Cl2O3SColor and Shape:SolidMolecular weight:303.16LabMol-319
CAS:<p>LabMol-319 is a potent Zika virus (ZIKV) NS5 RdRp inhibitor with antiviral activity for the study of ZIKV virus.</p>Formula:C22H16N2O5Purity:99.92%Color and Shape:SolidMolecular weight:388.37Inz-4
CAS:<p>Inz-4 is a fungal-selective inhibitor of mitochondrial cytochrome bc1.</p>Formula:C18H14F4N2O2Color and Shape:SolidMolecular weight:366.31Fosravuconazole
CAS:<p>Fosravuconazole is a ravuconazole prodrug. It has antifungal activity.</p>Formula:C23H20F2N5O5PSPurity:98%Color and Shape:SolidMolecular weight:547.47VU0420373
CAS:<p>VU0420373 activates HssRS at EC50 10.7 μM, induces heme synthesis, toxic to S. aureus.</p>Formula:C15H11FN2OColor and Shape:SolidMolecular weight:254.26CAY10704
CAS:<p>CAY10704: Potent HCV inhibitor, EC50=17 nM, low cytotoxicity, good in mice, liver-targeted, not hepatotoxic, weak against dengue.</p>Formula:C18H20Cl2N2Color and Shape:SolidMolecular weight:335.27Neuraminidase-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:486.62Anti-infective agent 4
CAS:<p>Oral Trypanosoma cruzi inhibitor (IC50: 0.016 μM), Anti-infective agent 4 reduces in vivo parasite load.</p>Formula:C19H12F3N5O4Color and Shape:SolidMolecular weight:431.32FWM-3
CAS:<p>FWM-3 is a potent SARS-CoV-2 NSP13 helicase inhibitor [1].</p>Formula:C16H16N6O2SColor and Shape:SolidMolecular weight:356.4MtInhA-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:396.32Laromustine
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:307.78MK-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:426.26DDD100097
CAS:<p>DDD100097 is a N-myristoyltransferase inhibitor with potential inhibitory effects on Trypanosoma brucei, which can be used to study neurological disorders.</p>Formula:C22H30Cl2F2N4O2SPurity:98.89%Color and Shape:SolidMolecular weight:523.47Penflufen
CAS:<p>Penflufen, a broad-spectrum succinate dehydrogenase inhibitor (SDHI), serves effectively as a fungicide.</p>Formula:C18H24FN3OColor and Shape:SolidMolecular weight:317.4Metallo-β-lactamase-IN-7
CAS:<p>Metallo-β-lactamase-IN-7 is a potent inhibitor of VIM -Type metallo-β-lactamase with IC 50 s of 0.019 μM, 13.64 μM, 0.38 μM for VIM-2, VIM-1 and VIM-5,</p>Formula:C12H10N4O2SColor and Shape:SolidMolecular weight:274.3UGM-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:405.23Antimicrobial agent-3
CAS:<p>Antimicrobial agent-3 (Compound U10) is an antimicrobial agent that is used against bacterial, fungal, and tubercular infections [1].</p>Formula:C14H11N3OSColor and Shape:SolidMolecular weight:269.32Antimalarial 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:509.57Viral 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:323.36HBV-IN-25
CAS:<p>HBV-IN-25: oral HBV cccDNA reducer, anti-HBeAg, anti-HBV (IC50: 0.58/1.15 μM), soluble (>452 μg/mL), non-toxic.</p>Formula:C18H14ClNO4Color and Shape:SolidMolecular weight:343.76MmpL3-IN-1
CAS:<p>MmpL3-IN-1 (compound 32) inhibits MmpL3 with <0.016 μg/mL MIC against M. tuberculosis, aiding drug-resistant TB research.</p>Formula:C20H21F2N3OColor and Shape:SolidMolecular weight:357.4CGP 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:365.33Cap-dependent endonuclease-IN-23
CAS:<p>Cap-dependent endonuclease-IN-23 hinders influenza virus replication by inhibiting CEN, with potential for flu research.</p>Formula:C26H23F2N3O7Color and Shape:SolidMolecular weight:527.47CRK12-IN-1
CAS:<p>CRK12-IN-1: strong inhibitor of CRK12, kills T.b. brucei & T. congolense (EC50s: 1.3 & 18 nM).</p>Formula:C20H26F2N4O3S2Purity:99.72%Color and Shape:SolidMolecular weight:472.57NS2B/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:433.5BA-53038B
CAS:<p>BA-53038B is an HBV core protein allosteric modulator (CpAM), binding to the HAP pocket and modulating HBV capsid assembly in a distinct manner (EC50: 3.32 μM).</p>Formula:C14H16ClNOColor and Shape:SolidMolecular weight:249.74MmpL3-IN-2
CAS:<p>MmpL3-IN-2, an inhibitor targeting MmpL3, exhibits low cytotoxicity and moderate metabolic stability, making it suitable for tuberculosis research [1].</p>Formula:C27H30N2Color and Shape:SolidMolecular weight:382.54IDD388
CAS:<p>IDD388 is a selective and potent aldose reductase (ALR2) inhibitor with antitumor activity that inhibits the ALR1 receptor.</p>Formula:C16H12BrClFNO4Purity:99.56%Color and Shape:SolidMolecular weight:416.63Lagociclovir
CAS:<p>Lagociclovir (MIV-210), a nucleoside analogue antiviral, treats HBV by inhibiting its replication in liver cancer cells.</p>Formula:C10H12FN5O3Purity:99.18% - 99.33%Color and Shape:SolidMolecular weight:269.23Tuberculosis inhibitor 3
CAS:<p>Tuberculosis inhibitor 3 is a highly potent and oral anti-tuberculosis drug against both drug-sensitive and drug-resistant Mycobacterium , H37RV & MDR-TB.</p>Formula:C21H22F6N4O3SPurity:98.8%Color and Shape:SolidMolecular weight:524.48LEDGIN6
CAS:<p>HIV-1 integrase inhibitor 2 is used for the treatment of human immunodeficiency virus (HIV) infection.</p>Formula:C21H20ClNO2Color and Shape:SolidMolecular weight:353.84Furalazine
CAS:<p>Furalazine: antimicrobial, treats cholera, more effective than chloramphenicol in shortening stool culture positivity.</p>Formula:C9H7N5O3Purity:98%Color and Shape:SolidMolecular weight:233.18Bulaquine
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:200.23trans-ccc_R08
CAS:<p>trans-ccc_R08: potent cccDNA inhibitor, IC50 0.08 µM, may help research HBV.</p>Formula:C22H19ClO6Color and Shape:SolidMolecular weight:414.84SARS-CoV-2 nsp13-IN-2
CAS:<p>SARS-CoV-2 nsp13-IN-2 (Compound C2) is a small molecule inhibitor of SARS-CoV-2 non-structural protein 13 (nsp13) that acts on nsp13 ssDNA+ATPase (IC50: 42 μM).</p>Formula:C20H18N6OS2Color and Shape:SolidMolecular weight:422.53Antibacterial agent 125
CAS:<p>Antibacterial agent 125 shows strong activity against Gram-positive pathogens; MICs: 0.25-8 μM; used in antimicrobial resistance research.</p>Formula:C15H11ClN2OPurity:98.45%Color and Shape:SoildMolecular weight:270.71RSV-IN-3
CAS:<p>RSV-IN-3 is a dual RSV/IAV inhibitor with an EC50 of 32.70 μM against RSV.</p>Formula:C16H12Cl2N2OSColor and Shape:SolidMolecular weight:351.25MAC-0547630
CAS:<p>MAC-0547630 potent and selective inhibitor of UppS.</p>Formula:C19H21FN4Purity:98%Color and Shape:SolidMolecular weight:324.4Mycobactin-IN-1
CAS:<p>Mycobactin-IN-1, a pyrazoline analogue, inhibits MbtA, key in mycobactin synthesis, targeting mycobacteria.</p>Formula:C15H13ClN2OColor and Shape:SolidMolecular weight:272.73Chitin synthase inhibitor 3
CAS:<p>Compound 2d is a potent chitin synthase inhibitor (IC50: 0.16 mM, MIC: 1 μg/mL vs. Candida albicans) with antifungal properties.</p>Formula:C20H19N3O4Color and Shape:SolidMolecular weight:365.38Fosclevudine alafenamide
CAS:<p>Fosclevudine alafenamide (Compound EIDD-02173) is an antiviral agent that acts against HBV (EC50: 1.71 μM).</p>Formula:C22H29FN3O9PColor and Shape:SolidMolecular weight:529.45PNU-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:369.41TbPTR1 inhibitor 1
CAS:<p>TbPTR1 inhibitor 1 effectively targets kinetochore PTR1 with IC50 <0.1 nM, EC50 0.66 μM against Trypanosoma brucei.</p>Formula:C22H21N7OColor and Shape:SolidMolecular weight:399.45Lascufloxacin
CAS:<p>Lascufloxacin: potent, oral fluoroquinolone antibiotic for respiratory infections, effective against quinolone-resistant strains.</p>Formula:C21H24F3N3O4Purity:98%Color and Shape:SolidMolecular weight:439.43Oxaquin
CAS:<p>Oxaquin, a water-soluble injectable prodrug, converts to active MCB3681 post-IV to fight Gram-positive bacteria.</p>Formula:C31H33F2N4O11PPurity:98%Color and Shape:SolidMolecular weight:706.58HBV-IN-7
CAS:<p>HBV-IN-6 is a potent inhibitor of HBV (EC50: 5 nM).</p>Formula:C18H17ClFN3O5S2Color and Shape:SolidMolecular weight:473.93Kumbicin C
CAS:<p>Kumbicin C inhibits the growth of NS-1 mouse myeloma cells (IC50 = 0.74 μg/ml) and the growth of the Gram-positive bacteria B. subtilis (MIC = 1.6 μg/ml).</p>Formula:C28H24N2O3Color and Shape:SolidMolecular weight:436.5Cyclophilin inhibitor 3
CAS:<p>Cyclophilin inhibitor 3 (compound 7c), a potent inhibitor of cyclophilin A (CypA), exhibited potent anti-HCV effects with an EC50 value of 4.2 μM.</p>Formula:C34H38N4O6Color and Shape:SolidMolecular weight:598.69SS148
CAS:<p>SS148 inhibits nsp14/nsp16 MTase, selective vs human MTases; promising for potent, selective coronavirus MTase inhibitors.</p>Formula:C16H20N6O5SColor and Shape:SolidMolecular weight:408.43Texaline
CAS:<p>Texaline is an agent of the antitubercular.</p>Formula:C15H10N2O3Purity:98%Color and Shape:SolidMolecular weight:266.25SARS-CoV-2 Mpro-IN-1
CAS:<p>SARS-CoV-2 Mpro-IN-1 (compound 16b-3) is a potent, selective and irreversible SARS-CoV-2 main protease (Mpro) inhibitor (IC 50 = 116 nM) [1].</p>Formula:C15H11FN2O2SColor and Shape:SolidMolecular weight:302.32BMS-986094
CAS:<p>INX 08189 is an RNA-directed RNA polymerase (NS5B) inhibitor.</p>Formula:C30H39N6O9PColor and Shape:SolidMolecular weight:658.64Antitubercular agent-39
CAS:<p>Antitubercular agent-39 (Compound P1) is a potent agent effective against both drug-resistant strains and drug-susceptible clinical isolates of tuberculosis,</p>Formula:C26H30N4O2Color and Shape:SolidMolecular weight:430.54Leu-AMS
CAS:<p>Leu-AMS, a leucine analogue with 22.34 nM IC50, inhibits LRS and bacterial growth without affecting mTORC1.</p>Formula:C16H25N7O7SPurity:98%Color and Shape:SolidMolecular weight:459.48GlyRS-IN-1
CAS:<p>GlyRS-IN-1 is an inhibitor of glycyl-tRNA synthase (GlyRS). It can inhibit the growth of bacteria.</p>Formula:C12H17N7O7SColor and Shape:SolidMolecular weight:403.37DSHS00884
CAS:<p>DSHS00884 is a potent inhibitor of human papillomavirus E6 (IC50: 10 μM).</p>Formula:C12H12N4O2S2Color and Shape:SolidMolecular weight:308.38RYL-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:443.46Acetarsone
CAS:<p>Acetarsone is an antiinfective agent. Acetarsone also inhibits protozoa growth.</p>Formula:C8H10AsNO5Color and Shape:SolidMolecular weight:275.09DENV-IN-4
CAS:<p>DENV-IN-4: Effective DENV inhibitor (EC50=4.79 μM), low toxicity (CC50>100 μM), and strong selectivity (SI>20.9); suppresses DENV2 and RdRp.</p>Formula:C28H32N4O4SiColor and Shape:SolidMolecular weight:516.66HIV-1 inhibitor-24
CAS:<p>HIV-1 inhibitor-24 (S-12a) blocks HIV reverse transcription effectively (IC50: 9.5 nM), low toxicity, well-tolerated in mice, good heart safety.</p>Formula:C26H19N5O2Color and Shape:SolidMolecular weight:433.46HBV-IN-9
CAS:<p>HBV-IN-9 inhibits HBsAg (IC50: 10 nM) and HBV DNA replication (IC50: 0.15 nM) per WO2018001952A1.</p>Formula:C22H24FN7OColor and Shape:SolidMolecular weight:421.47TXA6101
CAS:<p>TXA6101: FtsZ inhibitor, blocks bacterial division, MIC 1 μg/mL against MRSA, effective on TXA707-resistant mutants. Potential anti-Gram-negative agent.</p>Formula:C18H10BrF5N2O3Color and Shape:SolidMolecular weight:477.18Antiviral 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:300.7L-573655
CAS:<p>L-573655, an antibacterial agents, targets lipid A biosynthesis in gram-negative bacteria.</p>Formula:C10H10N2O3Purity:98%Color and Shape:SolidMolecular weight:206.2Kayahope
CAS:<p>Kayahope is a novel antifungals.</p>Formula:C15H14ClNO3SPurity:98%Color and Shape:SolidMolecular weight:323.79Crisnatol
CAS:<p>Crisnatol (BWA770U) is an oral anticancer DNA intercalator, toxic to breast cancer cells, not skin fibroblasts.</p>Formula:C23H23NO2Color and Shape:SolidMolecular weight:345.43Antileishmanial agent-10
CAS:<p>Antileishmanial agent-10 (Compound 7h) is an antiprotozoal agent.</p>Formula:C25H41NO2SColor and Shape:SolidMolecular weight:419.66Endochin
CAS:<p>Endochin is an experimental antimalarial. Endochin and analogues thereof are causal prophylactic and potent erythrocytic stage agents in avian models.</p>Formula:C18H25NO2Purity:98%Color and Shape:SolidMolecular weight:287.4Antiparasitic agent-5
CAS:<p>Compound 8h: Antiparasitic, selective against L. infantum (IC50: 2.50 μM); cytotoxic to HepG2 cells (CC50: 6.78 μM).</p>Formula:C20H16ClN3O3Color and Shape:SolidMolecular weight:381.81Antifungal 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:492.48Antibacterial 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:348.22Nucleoside-Analog-1
CAS:<p>Nucleoside-Analog-1 is a 4′-Azidocytidine analogue, used to against Hepatitis C virus replication.</p>Formula:C9H9N5O5Purity:98%Color and Shape:SolidMolecular weight:267.2Acoziborole
CAS:<p>Acoziborole (SCYX-7158), a benzoxaborole derivative, is a novel, safe HAT agent with a MIC of 0.6 µg/mL against T. b. brucei S427.</p>Formula:C17H14BF4NO3Color and Shape:SolidMolecular weight:367.1MtTMPK-IN-4
CAS:<p>MtTMPK-IN-4, a para-piperidine, blocks MtTMPK in tuberculosis with 6.1 μM IC50 and also inhibits tyrosinase.</p>Formula:C23H25N3O3Color and Shape:SolidMolecular weight:391.46Antimycobacterial agent-2
CAS:<p>Antimycobacterial agent-2 has MIC99 0.8 μM vs M.tb H37Rv; cytotoxic with IC50 48.1 μM on CHO cells.</p>Formula:C31H50O5Color and Shape:SolidMolecular weight:502.73GAK 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:385.48TDRL-X80
CAS:<p>TDRL-X80 inhibits XPA DNA binding; effective on single, double, and cisplatin-damaged DNA; IC50: 18-29 μM (FP), 21-39 μM (ELISA).</p>Formula:C23H15ClN2O6Color and Shape:SolidMolecular weight:450.83Antimicrobial 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:449.91(Z)-Fluoxastrobin
CAS:<p>(Z)-Fluoxastrobin is a fungicide that exhibits effective control of important seed and soil-borne pathogens.</p>Formula:C21H16ClFN4O5Color and Shape:SolidMolecular weight:458.83Riodoxol
CAS:<p>Riodoxol is an antiviral agent that effectively affects the reproduction and maturation of viruses.</p>Formula:C6H3I3O2Color and Shape:SolidMolecular weight:487.8Antibacterial agent 131
<p>Antibacterial agent 131 is a compound with antibacterial properties.</p>Formula:C24H17ClN4OSPurity:99.06%Color and Shape:SolidMolecular weight:444.94HI-236
CAS:<p>HI-236 is used as a non-nucleoside HIV-1 reverse-transcriptase inhibitor.</p>Formula:C16H18BrN3O2SPurity:98%Color and Shape:SolidMolecular weight:396.3JNJ-2408068
CAS:<p>JNJ-2408068 inhibits RSV with EC50 of 2.1 nM; blocks fusion (EC50=0.9 nM) by targeting F protein.</p>Formula:C22H30N6OPurity:98%Color and Shape:SolidMolecular weight:394.51Anti-MRSA agent 1
CAS:<p>Anti-MRSA agent 1 is an MRSA inhibitor with an MIC value of 0.5 μg/mL and is effective in alleviating the effects of MRSA resistance.</p>Formula:C26H29N7O4SColor and Shape:SolidMolecular weight:535.62Sisapronil
CAS:<p>Sisapronil is a member of the phenylpyrazole class of antiparasitics.</p>Formula:C15H6Cl2F8N4Color and Shape:SolidMolecular weight:465.13CBL 0100 free base
CAS:<p>CBL0100 is an inhibitor of viral transcriptional elongation, blocking both HIV-1 replication and reactivation.</p>Formula:C24H26N2O2Purity:98.18% - 98.86%Color and Shape:SolidMolecular weight:374.48As-358
CAS:<p>As-358 has inhibitory effects against Ebola virus (IC50 = 47.5 μM) and Marburg virus (IC50 = 3.7 μM) [1].</p>Formula:C18H31NO2Color and Shape:SolidMolecular weight:293.4413(S)-HpOTrE
CAS:<p>13(S)-HpOTrE, a fatty acid from soy LO-2 action on α-linolenic acid, forms in soybeans (9:1 ratio). It generates plant defense signals against pests.</p>Formula:C18H30O4Color and Shape:SolidMolecular weight:310.43G0507
CAS:<p>G0507, a potent pyrrolopyrimidinedione, blocks E. coli growth by activating σE stress and targeting LolCDE ABC Transporter.</p>Formula:C18H15N3O3SColor and Shape:SolidMolecular weight:353.39AN11251
CAS:<p>AN11251: oral anti-Wolbachia, treats onchocerciasis & lymphatic filariasis, EC50=1.5nM (LDW1), 15nM (C6/36).</p>Formula:C29H38BFO7Purity:98%Color and Shape:SolidMolecular weight:528.422,6-Dichlorodiphenylamine
CAS:<p>2,6-Dichlorodiphenylamine shows activity against Candida albicans infections. 2,6-Dichlorodiphenylamine elevated the MIC by 4-fold of diclofenac sodium (DFNa).</p>Formula:C12H9Cl2NPurity:99.81%Color and Shape:Off White To Cream Coloured Crystalline SolidMolecular weight:238.11Urease-IN-4
<p>Urease-IN-4 inhibits urease (IC50: 1.64 µM), targets P. vulgaris (IC50: 15.27 µg/mL), and is low in cytotoxicity.</p>Formula:C16H20N2O3SColor and Shape:SolidMolecular weight:320.41SPR39
<p>SPR39 inhibits SARS-CoV-2 protease (Ki: 0.252µM), with lesser effect on hCatL/B, and has antiviral, cytotoxic properties.</p>Formula:C24H31N3O5Color and Shape:SolidMolecular weight:441.52DPC-961
CAS:<p>DPC-961, a reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.</p>Formula:C14H10ClF3N2OColor and Shape:SolidMolecular weight:314.694-((4-((4-Aminophenyl)sulfonyl)phenyl)amino)-4-oxobutanoic acid
CAS:<p>4-((4-((4-Aminophenyl)sulfonyl)phenyl)amino)-4-oxobutanoic acid is a sulfonamide compound that can be used as an anti infective agent [1].</p>Formula:C16H16N2O5SColor and Shape:SolidMolecular weight:348.37BO3482
CAS:<p>BO3482 is an antimicrobial compound and can inhibit the growth of methicillin-resistant Staphylococci (MIC90: 6.25 mg/mL).</p>Formula:C14H20N2NaO5S2Purity:98%Color and Shape:SolidMolecular weight:383.43β-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:352.34Haloprogin
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:361.39Neuraminidase-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:328.39Nitracrine
CAS:<p>Nitracrine: a 1-nitroacridine, hypoxia-selective, anti-tumor agent; inhibits RNA synthesis, binds DNA reversibly and forms covalent adducts.</p>Formula:C18H20N4O2Purity:98%Color and Shape:SolidMolecular weight:324.38B07 hydrochloride
CAS:<p>B07 hydrochloride is a CCR5 antagonist-based inhibitor of HIV-1 entry.</p>Formula:C29H38ClFN4O2Purity:98%Color and Shape:SolidMolecular weight:529.09SC-58272
CAS:<p>SC-58272 is an inhibitor of N-myristoyltransferase (Nmt), a target for anti-fungal and anti-viral therapy.</p>Formula:C33H52N6O4Purity:98%Color and Shape:SolidMolecular weight:596.8Neuraminidase-IN-5
CAS:<p>Neuraminidase-IN-5: potent NA inhibitor, IC50=0.02μM, potential anti-influenza, dihydrofurocoumarin derivative.</p>Formula:C19H11NO7Color and Shape:SolidMolecular weight:365.29MLAF50
CAS:<p>MLAF50 is an inhibitor of the REV1 UBM2-Ubiquitin interaction.</p>Formula:C15H12I2O4Color and Shape:SolidMolecular weight:510.06YM-53601
CAS:<p>YM-53601 is an SQS inhibitor that inhibits adipogenic biosynthesis and lipid secretion in rodents.YM-53601 is a cholesterol-lowering agent that inhibits FDFT1.</p>Formula:C21H22ClFN2OPurity:99.65%Color and Shape:SolidMolecular weight:372.86JFN05510
CAS:<p>Compound: 3'-O-tert-BDMS-5'-O-DMT-N2-IBG 2'-CE phosphoramidite; has anticancer properties and activates enzymes.</p>Formula:C50H68N7O9PSiColor and Shape:SolidMolecular weight:970.18Dihydropteroate synthase-IN-1
CAS:<p>"Dihydropteroate synthase-IN-1 (5g) inhibits DHPS and cytochrome P450, useful as radiographic diagnostic material."</p>Formula:C19H23N5O4S2Color and Shape:SolidMolecular weight:449.55Pirlindole 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:226.32INSCoV-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:507.89Antibacterial agent 26
CAS:<p>Antibacterial agent 26 is an antimicrobial compound that is a potent DHFR inhibitor (S. aureus DHFR Ki of 0.020 nM).</p>Formula:C19H17N5O2Purity:98.86%Color and Shape:SolidMolecular weight:347.37FR-198248
CAS:<p>FR-198248, a new anti-influenza agent, shows antiinfluenza virus activity in Madin-Darby canine kidney (MDCK) cells in vitro.</p>Formula:C9H10O5Color and Shape:SolidMolecular weight:198.17Antitubercular agent-37
CAS:<p>Antitubercular Agent-37 exhibits antimycobacterial properties and functions as an antibacterial agent with an MIC (minimum inhibitory concentration) value of 0.</p>Formula:C22H22N8O2Color and Shape:SolidMolecular weight:430.46IMB-26
CAS:<p>IMB-26 is an HCV inhibitor (EC50: 2.1 μM) and has shown potent anti-HCV effects.</p>Formula:C20H23BrN2O6Color and Shape:SolidMolecular weight:467.31GCA-186
CAS:<p>GCA-186 is an effective non-nucleoside HIV-1 reverse transcriptase inhibitor.</p>Formula:C19H26N2O3Purity:98%Color and Shape:SolidMolecular weight:330.42Antitubercular agent-36
CAS:<p>Antitubercular agent-36 inhibits Mycobacterium tuberculosis with MIC90 of 1.25 μg/mL, used in TB research.</p>Formula:C18H17N3O3Color and Shape:SolidMolecular weight:323.35HIV-1 inhibitor-43
CAS:<p>HIV-1 Inhibitor-43 suppresses HIV-1, with EC50: 21.3 nM (Y188L), 6.2 nM (K103N-Y181C), <0.7 nM (K103N/Y181C), and lowers HIV RNA/p24 protein.</p>Formula:C24H21ClN2O4SColor and Shape:SolidMolecular weight:468.95L 739594
CAS:<p>L 739594 is an inhibitor of HIV-1 protease.</p>Formula:C31H47N3O6Purity:98%Color and Shape:SolidMolecular weight:557.72SARS-CoV MPro-IN-1
CAS:<p>MProinhibitor 11b blocks SARS-CoV-2 main protease (IC50=0.04 μM), cuts viral yield and RNA in Vero E6 cells (EC50=0.72 μM).</p>Formula:C25H25FN4O4Color and Shape:SolidMolecular weight:464.49Antileishmanial agent-7
CAS:<p>Compound 23: Strong against Leishmania, IC50: 6.89 μM (L. donovani), 259 μM (L-6).</p>Formula:C20H18O8Color and Shape:SolidMolecular weight:386.35BiPNQ
CAS:<p>BiPNQ is a Trypanosoma cruzi inhibitor. Trypanosoma cruzi is the etiological agent of Chagas disease (American trypanosomiasis).</p>Formula:C16H12N6OColor and Shape:SolidMolecular weight:304.31GSK3494245
CAS:<p>GSK3494245: potent, selective oral proteasome inhibitor targeting WTL.donovani with an IC50 of 0.16 μM; safe, affects human proteasome too.</p>Formula:C21H23FN6O2Color and Shape:SolidMolecular weight:410.44Mpro/PLpro-IN-1
CAS:<p>Compound 29 inhibits SARS-CoV-2 Mpro (IC50:1.72μM) & PLpro (IC50:0.67μM) proteases effectively.</p>Formula:C25H27ClN4O3Color and Shape:SolidMolecular weight:466.96PD 113270
CAS:<p>PD 113,270 is an analog of the fermentation products fostriecin with antitumor activity in vitro and in vivo.</p>Formula:C19H27O8PColor and Shape:SolidMolecular weight:414.39Zidebactam sodium salt
CAS:<p>Zidebactam sodium salt is a potent inhibitor of β-lactamase, and also is an inhibitor of penicillin-binding protein2 (PBP2)(IC50 of 0.26 μg/mL).</p>Formula:C13H21N5NaO7SPurity:98%Color and Shape:SolidMolecular weight:414.39INSCoV-600K(1)
CAS:<p>INSCoV-600K(1) is a potent inhibitor of Mpro (3CLpro), key in viral replication, with potential against SARS-CoV-2 (Patent WO2021219089A1).</p>Formula:C23H22ClF2N5O2SColor and Shape:SolidMolecular weight:505.97Synucleozid
CAS:<p>Synucleozid is a potent the SNCA mRNA inhibitor that encodes α-synuclein protein (IC50=1.5 μM), has the potential for the investigation of Parkinson’s disease.</p>Formula:C22H20N6Purity:98%Color and Shape:SolidMolecular weight:368.43Anti-parasitic agent 3
CAS:<p>Anti-parasitic agent 3 is an anti-parasitic agent active against drug-resistant parasites.</p>Formula:C21H22FN5O3Purity:98%Color and Shape:SolidMolecular weight:411.43Buclosamide
CAS:<p>Buclosamide is a topical antimycotic agent that can be used in dermatomycoses [1].</p>Formula:C11H14ClNO2Color and Shape:SolidMolecular weight:227.693'-Deoxyuridine-5'-triphosphate
CAS:<p>3'-dUTP, a nucleotide analogue, competitively inhibits RNA polymerases I & II, with a Ki of 2.0 µM.</p>Formula:C9H15N2O14P3Color and Shape:SolidMolecular weight:468.14BMS-433771 free base
CAS:<p>BMS-433771, a novel inhibitor of respiratory syncytial virus (RSV), binds the RSV F glycoprotein and inhibits membrane fusion.</p>Formula:C21H23N5O2Color and Shape:SolidMolecular weight:377.44Amorolfine
CAS:<p>Amorolfine is available in the nail lacquer and can be used to treat fungal nail infections.</p>Formula:C21H35NOColor and Shape:White To Off-White Crystalline PowderMolecular weight:317.517Braco-19 trihydrochloride
CAS:<p>BRACO19 3HCl inhibits telomerase, blocking its capping function, and prevents HAdV viral replication.</p>Formula:C35H46Cl3N7O2Purity:98.74%Color and Shape:SolidMolecular weight:703.14Bofumustine
CAS:<p>Bofumustine is a chloroethyl nitrosourea with anti tumor properties.</p>Formula:C18H21ClN4O9Color and Shape:SolidMolecular weight:472.83MMV666693
CAS:<p>MMV666693 is a selective allosteric Plasmodium Kinesin-5 inhibitor.</p>Formula:C18H15NO4Color and Shape:SolidMolecular weight:309.32HIV-1 inhibitor-33
CAS:<p>HIV-1 inhibitor-33, potent against HIV-1 (EC50: 8.6 nM), low toxicity to MT-4 cells (CC50: 18 μM), useful for AIDS research.</p>Formula:C25H28N6OColor and Shape:SolidMolecular weight:428.53Antileishmanial agent-12
CAS:<p>Compound 5a: potent anti-leishmanial, IC50 - L. brazilensis 14.9μM, L. infantum 21.3μM; antiprotozoal against T. cruzi 9.3μM.</p>Formula:C25H21N3O4Color and Shape:SolidMolecular weight:427.45Datelliptium chloride
CAS:<p>Datelliptium chloride is a DNA-intercalating agent derived from ellipticine. Datelliptium chloride shows anti-tumor activities.</p>Formula:C23H28ClN3OPurity:98%Color and Shape:SolidMolecular weight:397.94HIV-1 inhibitor-20
CAS:<p>HIV-1 inhibitor-20 is a potent HIV-1 inhibitor.</p>Formula:C19H11ClF3N3O2Color and Shape:SolidMolecular weight:405.76SARS-CoV MPro-IN-2
CAS:<p>SARS-CoV MPro-IN-2, a potent SARS-CoV-2 main protease inhibitor (IC50: 72.07 nM), may aid COVID-19 research.</p>Formula:C13H10O4Color and Shape:SolidMolecular weight:230.22DENV-IN-9
CAS:<p>DENV-IN-9 is a DENV2 inhibitor with an EC 50 of 0.88 μM .</p>Formula:C15H9BrO5Color and Shape:SolidMolecular weight:349.135-Dehydroepisterol
CAS:<p>5-Dehydroepisterol, an anti-fungal episterol form, made by C-5 sterol desaturase, turns into 24-methylenecholesterol.</p>Formula:C28H44OPurity:98%Color and Shape:SolidMolecular weight:396.65Chaetoglobosin C
CAS:<p>Chaetoglobosin C (Compound 4), an anthraquinone-chromone derivative of Chaetomium globosum KMITL-N0802, exhibits anti-tuberculosis activity [1].</p>Formula:C32H36N2O5Color and Shape:SolidMolecular weight:528.64HBV-IN-22
CAS:<p>HBV-IN-22 (Compound LC5f) is an HBV DNA replication inhibitor that acts on both wild-type HBV (IC50: 0.71 μM) and drug-resistant HBV (IC50: 0.84 μM).</p>Formula:C26H29N3O2S2Color and Shape:SolidMolecular weight:479.66Thiambutosine
CAS:<p>Thiambutosine exhibits inhibitory activity against Mycobacterium leprae and mushroom tyrosinase, making it suitable for infection studies.</p>Formula:C19H25N3OSPurity:99.95%Color and Shape:SolidMolecular weight:343.49
