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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Cap-dependent endonuclease-IN-21
CAS:<p>Cap-dependent endonuclease-IN-21 inhibits CEN and flu virus replication, potential against influenza A. (From patent WO2021233302A1, compound 8B/8A)</p>Formula:C26H23F2N3O7Color and Shape:SolidMolecular weight:527.47DMA-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:359.81A 80987
CAS:<p>A 80987 is an inhibitor of HIV-1 protease.</p>Formula:C37H43N5O6Color and Shape:SolidMolecular weight:653.77GW-695634
CAS:<p>GW-695634, a non-nucleoside reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.</p>Formula:C26H21Cl2N3O6SColor and Shape:SolidMolecular weight:574.43HIV-1 inhibitor-31
CAS:<p>HIV-1 inhibitor-31 (compound 4) is a potent inhibitor of HIV-1. HIV-1 inhibitor-31 can be used in the study of AIDS.</p>Formula:C21H13Cl2N3O2Color and Shape:SolidMolecular weight:410.25NB-598 hydrochloride
CAS:<p>NB-598 hydrochloride is a competitive squalene epoxidase (SE) inhibitor.</p>Formula:C27H32ClNOS2Purity:98%Color and Shape:SolidMolecular weight:486.13D77
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:596.45Neuraminidase-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:533.46S-(N-PhenethylthiocarbaMoyl)-L-cysteine
CAS:<p>PEITC-Cys: anticarcinogenic, antileukemic, inhibits DNA synthesis in HL60, P450 inhibitor.</p>Formula:C12H16N2O2S2Color and Shape:SolidMolecular weight:284.4S-1360
CAS:<p>S-1360 is an inhibitor of HIV-1 integrase.</p>Formula:C16H12FN3O3Purity:98%Color and Shape:SolidMolecular weight:313.28Antitumor agent-85
<p>Antitumor agent-85 stabilizes G4-DNA with potent anti-tumor effects.</p>Formula:C24H33N7Color and Shape:SolidMolecular weight:419.57DC07090 Dihydrochloride
CAS:<p>DC07090 Dihydrochloride is a potent inhibitor of human enterovirus 71 3C protease.</p>Formula:C18H16Cl2N4OColor and Shape:SolidMolecular weight:375.25Benzylurea
CAS:<p>Benzylurea (AI3-61350) competitively inhibits dehydrogenase/cytokinin oxidase.</p>Formula:C8H10N2OPurity:98%Color and Shape:SolidMolecular weight:150.18FabG1-IN-1
CAS:<p>FabG1-IN-1 (Compound 29) is a potent inhibitor of MabA (FabG1) (IC50: 38 μM).</p>Formula:C14H8Cl2INO3Color and Shape:SolidMolecular weight:436.03VIM-2-IN-1
CAS:<p>VIM-2-IN-1 (compound 1dj) is a β-lactamase inhibitor with antibacterial activity. IC50: 48 μM) and New Delhi Metal (NDM-1) (IC50: 231 μM).</p>Formula:C12H13IN4O4SColor and Shape:SolidMolecular weight:436.23Antimalarial 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:322.42Antiviral agent 23
CAS:<p>Antiviral agent 23 targets EV71 with 94 nM EC50 and suppresses METTL3/14, useful in infection research.</p>Formula:C18H21N5O4Color and Shape:SolidMolecular weight:371.39Tolindate
CAS:<p>Tolindate, a potent PXR agonist, demonstrates antifungal activity and possesses an EC50 value of 8.3 µM.</p>Formula:C18H19NOSColor and Shape:SolidMolecular weight:297.41V-06-018
CAS:<p>V-06-018 is a quorum-sensing modulator. It also acts as a LasR antagonist.</p>Formula:C18H27NO2Purity:98%Color and Shape:SolidMolecular weight:289.41PF-46396
CAS:<p>PF-46396 is a HIV maturation inhibitor and can be used against HIV-1 clade B and C.</p>Formula:C27H29F3N2OColor and Shape:SolidMolecular weight:454.53WAY 150138
CAS:<p>WAY 150138 inhibits the herpes simplex virus.</p>Formula:C22H18Cl2FN3O3SColor and Shape:SolidMolecular weight:494.37RmlA-IN-1
CAS:<p>RmlA-IN-1 inhibits RmlA enzyme with 0.073 μM IC50, affecting l-Rhamnose synthesis and bacterial wall permeability.</p>Formula:C18H18N4O4SColor and Shape:SolidMolecular weight:386.42NC00075159
CAS:<p>NC00075159 is an opener of human KCNQ4 (Kv7.4) potassium channel.</p>Formula:C15H16N2O3S2Purity:98%Color and Shape:SolidMolecular weight:336.43PXYC2
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:226.21Antifungal agent 32
CAS:<p>Antifungal 32 (1a) strongly inhibits Candida albicans growth, filamentation, biofilm, and adhesion.</p>Formula:C25H28N2OColor and Shape:SolidMolecular weight:372.5HCV-IN-33
CAS:<p>HCV-IN-33 (Compound (S)-3i) is an inhibitor of HCV entry.</p>Formula:C31H36ClN5Color and Shape:SolidMolecular weight:514.1Alalevonadifloxacin HCl
CAS:<p>Alalevonadifloxacin HCl is a novel l-alanine ester prodrug of levonadifloxacin.</p>Formula:C22H27ClFN3O5Purity:98%Color and Shape:SolidMolecular weight:467.92Sulfoxone 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:350.26Anti-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:386.42TCMDC-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:399.83Finafloxacin hydrochloride
CAS:<p>"Finafloxacin is a fluoroquinolone antimicrobial agent optimized for maximum effectiveness in mildly acidic conditions."</p>Formula:C20H20ClFN4O4Color and Shape:SolidMolecular weight:434.858-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:490.197HIV-1 inhibitor-39
CAS:<p>HIV-1 inhibitor-39: blocks HIV-1, anti-RT (IC50=15.75 μM), toxic to MT-4 cells (CC50=112.9 μM).</p>Formula:C20H17ClN4O4S4Color and Shape:SolidMolecular weight:541.09MTH1-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:469.55hRSV-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:447.17SCH-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:247.68Fuberidazole
CAS:<p>Fuberidazole is an antifungal agent.</p>Formula:C11H8N2OPurity:98.95%Molecular weight:184.19SPC-839
CAS:<p>SPC-839 is an IKK-2 Inhibitor with oral activity.</p>Formula:C18H14N4O3SColor and Shape:SolidMolecular weight:366.39Norstictic acid
CAS:<p>Norstictic acid: a potent, selective transcription regulator with anticancer, antioxidant, and antimicrobial properties.</p>Formula:C18H12O9Color and Shape:SolidMolecular weight:372.28BM635
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:392.51Antimicrobial agent-6
<p>Antimicrobial agent-6: MIC 4-8 μg/mL for gram+ & gram- bacteria, anti-inflammatory.</p>Formula:C40H64N16Color and Shape:SolidMolecular weight:769.0415(S)-HpETE
CAS:<p>15(S)-HpETE is a product of arachidonic acid formed in the 15-lipoxygenase pathway and inhibits angiogenesis.</p>Formula:C20H32O4Color and Shape:SolidMolecular weight:336.47HIV-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:695.04HIV-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:262.3Antimicrobial agent-1
CAS:<p>Antimicrobial Agent-1 (compound 6C) shows strong activity (MIC = 2 μg/mL) against TolC mutant E.</p>Formula:C22H21N3O2SColor and Shape:SolidMolecular weight:391.49As-358 hydrochloride
CAS:<p>As-358 (hydrochloride) shows well in vivo safety as well as inhibits Ebola virus and Marburg virus with IC 50 values of 9.1 μM and 18.1 μM [1].</p>Formula:C18H32ClNO2Color and Shape:SolidMolecular weight:329.91Antiviral agent 9
<p>Antiviral agent 9: EC50 0.006 nM vs HIV-1, 300x more selective than TAF.</p>Formula:C38H50N7O8PColor and Shape:SolidMolecular weight:763.82ERCC1-XPF-IN-1
CAS:<p>ERCC1-XPF-IN-1: potent ERCC1-XPF inhibitor (IC50: 0.49 μM), hampers CPD removal, boosts UV toxicity, hinders DNA repair.</p>Formula:C28H32ClN5O2Color and Shape:SolidMolecular weight:506.04Antibacterial 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:473.458(-)-Pinocembrin
CAS:<p>(-)-Pinocembrin: Anti-tuberculosis (IC50: 1.11 mg/mL dormant, 1.21 mg/mL active), antiproliferative (IC50: 1.88-11 mg/mL on various cell lines).</p>Formula:C15H12O4Color and Shape:SolidMolecular weight:256.25Inarigivir
CAS:<p>Inarigivir (ORI-9020) is a dinucleotide that can significantly reduce liver HBV DNA.</p>Formula:C20H26N7O10PSPurity:98%Color and Shape:SolidMolecular weight:587.5RO5464466
CAS:<p>RO5464466 is an inhibitor of influenza A virus (H1N1) fusion.</p>Formula:C16H26N2O3SColor and Shape:SolidMolecular weight:326.45Antitubercular agent-31
CAS:<p>Antitubercular agent-31 is an antitubercular agent that inhibits M. tuberculosisH37Rv (MIC: 0.03 μM) and also inhibits DprE1 (IC50: 1.1 μM).</p>Formula:C20H24F2N4O5S2Color and Shape:SolidMolecular weight:502.56HIV-1 inhibitor-16
CAS:<p>HIV-1 inhibitor-16: potent with EC50 1.3 nM for wild-type; inhibits K103N, E138K, Y181C, L100I strains; good solubility; stable; low CYP impact; non-toxic.</p>Formula:C23H16F2N6Color and Shape:SolidMolecular weight:414.4116,17-Dihydroheronamide C
CAS:<p>16,17-Dihydroheronamide C is a probe used for the analysis of the mode of action of heronamide C, which has antifungal properties.</p>Formula:C29H41NO3Color and Shape:SolidMolecular weight:451.64Quinoprazine
CAS:<p>Quinoprazine: inhibits Vaccinia virus (IC50=10μM), antimalarial vs Plasmodium berghei, reduces PrPSc, antiprion.</p>Formula:C25H26N4Color and Shape:SolidMolecular weight:382.5LabMol-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:388.37(Rac)-ACT-451840
CAS:<p>(Rac)-ACT-451840 is an isomer of ACT-451840 exhibiting antimalarial activity against Plasmodium falciparum NF54.</p>Formula:C47H54N6O3Purity:99.25%Color and Shape:SolidMolecular weight:750.97HIV-1 inhibitor-29
CAS:<p>HIV-1 inhibitor-29: Blocks HIV-1 IIIB (EC50: 2.18μM), resists F227L/V106A (EC50: 0.974μM), low toxicity (CC50: 211μM), for AIDS research.</p>Formula:C30H36N6O5Color and Shape:SolidMolecular weight:560.64(-)-5′-Noraristeromycin
CAS:<p>(-)-5′-Noraristeromycin is an antiviral agent.</p>Formula:C10H13N5O3Color and Shape:SolidMolecular weight:251.24Antistaphylococcal agent 1
CAS:<p>Antistaphylococcal agent 1 is an antistaphylococcal therapeutic agent.</p>Formula:C22H16N6O2Color and Shape:SolidMolecular weight:396.4LHVS
CAS:<p>LHVS effectively blocks T.</p>Formula:C28H37N3O5SPurity:98%Color and Shape:SolidMolecular weight:527.68SARS-CoV-IN-3
CAS:<p>SARS-CoV-IN-3 is an effective SARS-CoV replication inhibitor.</p>Formula:C25H28ClFeN3OPurity:98%Color and Shape:SolidMolecular weight:477.81Mesoxalic acid
CAS:<p>Mesoxalic acid is a dicarboxylic acid and a ketonic acid which blocks RT translocation.</p>Formula:C3H2O5Purity:98%Color and Shape:SolidMolecular weight:118.04Enisamium iodide
CAS:<p>Enisamium iodide is used as an antiviral agent.</p>Formula:C14H15IN2OColor and Shape:SolidMolecular weight:354.19Antiviral agent 19
CAS:<p>Antiviral agent 19 (Compound 3) is a selective inhibitor of Zika virus (EC50: 1.3 μM) with low cytotoxicity.</p>Formula:C29H35NO5Color and Shape:SolidMolecular weight:477.59Antibacterial agent 64
CAS:<p>Potent antibacterial, YycG inhibitor with 6.1 µM IC50. Synergistic with ampicillin against biofilm bacteria.</p>Formula:C29H20ClN3O6S2Color and Shape:SolidMolecular weight:606.07Vebufloxacin
CAS:<p>Vebufloxacin (OPC-7251) shows potent antibacterial activity against gram-positive and -negative bacteria, including Staphylococcus aureus and Pseudomonas</p>Formula:C19H22FN3O3Purity:98%Color and Shape:SolidMolecular weight:359.39Hydroxyethylamine
CAS:<p>Hydroxyethylamine (VII) is a SARS-CoV-2 inhibitor with an IC50 of ~10 μM, showing notable antiviral activity.</p>Formula:C25H41N3O3Color and Shape:SolidMolecular weight:431.61Amcinafal
CAS:<p>Amcinafal is an active diol,and used against virus replication and interferon production.</p>Formula:C26H35FO6Purity:98%Color and Shape:SolidMolecular weight:462.55SAMT-247
CAS:<p>SAMT-247 is an HIV inhibitor that acts by modifying the nucleocapsid NCp7 region of Gag in infected cells and blocking Gag processing and reducing infectivity.</p>Formula:C12H14N2O3SColor and Shape:SolidMolecular weight:266.32Influenza virus-IN-4
CAS:<p>Influenza virus-IN-4 (compound 11e) is a potent inhibitor of influenza virus neuraminidase, acting on H5N1 (IC50: 3.4 μM), H5N2 (IC50: 0.094 μM), H5N6 (IC50: 0.</p>Formula:C23H31FN2O4Color and Shape:SolidMolecular weight:418.5LY 186826
CAS:<p>LY 186826 is an antibacterial agent with bicyclic pyrazolidinone properties.</p>Formula:C15H16N6O6SPurity:98%Color and Shape:SolidMolecular weight:408.39P163-0892
CAS:<p>P163-0892: potent, specific antifungal for Cryptococcus; moderate blood-brain barrier penetration.</p>Formula:C19H20N2O3SColor and Shape:SolidMolecular weight:356.44Mycobacterial Zmp1-IN-1
<p>Zmp1-IN-1: An inhibitor of mycobacterial Zmp1 with dose-dependent anti-tuberculosis effects.</p>Formula:C26H27N3O7SColor and Shape:SolidMolecular weight:525.57Antitubercular agent-21
CAS:<p>Antitubercular agent-21 (Compound 15) has low toxicity, MIC of 0.4 μg/mL against M. tuberculosis, but is less effective on other microbes.</p>Formula:C15H22N6OSColor and Shape:SolidMolecular weight:334.44DprE1-IN-4
CAS:<p>DprE1-IN-4: Potent DprE1 inhibitor (IC50: 0.90 μg/mL), good pharmacokinetics, kills TB bacteria in mice.</p>Formula:C20H21N3O5SColor and Shape:SolidMolecular weight:415.46PNR-7-02
CAS:<p>PNR-7-02 is an inhibitor of human DNA polymerase eta (Polη).</p>Formula:C24H16ClN3O2SColor and Shape:SolidMolecular weight:445.92SARS-CoV-2 nsp13-IN-5
CAS:<p>SARS-CoV-2 nsp13-IN-5 inhibits nsp13, affects ssDNA+/-ATPase (IC50: 50/55 μM), useful for COVID-19 research.</p>Formula:C28H30N4O4SColor and Shape:SolidMolecular weight:518.63OYYF-175
CAS:<p>OYYF-175: potent antimicrobial antifolate; targets multi-drug resistant Gram-Negative bacteria; DHFR inhibitor with 2.36 nM IC50 against E. coli.</p>Formula:C17H14FN5Color and Shape:SolidMolecular weight:307.33Levomecol
CAS:<p>Levomecol: Streptomyces-made antibiotic with Chloramphenicol & Methyluracil, halts bacterial growth by blocking protein synthesis.</p>Formula:C16H18Cl2N4O7Purity:98%Color and Shape:SolidMolecular weight:449.24360A iodide
CAS:<p>360A iodide is a selective stabilizer of G-quadruplex and inhibits telomerase activity (IC50: 300 nM in TRAP-G4 assay).</p>Formula:C27H23I2N5O2Purity:98%Color and Shape:SolidMolecular weight:703.31BDM91514
CAS:<p>BDM91514 enhances antibiotic efficacy by inhibiting AcrB, effectively curbing the proliferation of E.</p>Formula:C13H19Cl3N6OColor and Shape:SolidMolecular weight:381.69Soporidine
CAS:<p>Soporidine, a strigolactone antagonist, blocks AtHTL, hindering SL signaling and seed germination.</p>Formula:C27H30F3NO3Purity:98%Color and Shape:SolidMolecular weight:473.53Antitubercular agent-25
CAS:<p>Compound 28: Antitubercular with extracellular IC50 0.42 μM, intracellular 0.20 μM against M. tuberculosis, metabolically stable.</p>Formula:C18H16N4O3S2Color and Shape:SolidMolecular weight:400.47ORM-3819
CAS:<p>ORM-3819 is a potent and selective PDE III inhibitor. ORM-3819 promotes cardiac contractility through Ca(2+) sensitization.</p>Formula:C19H19N5O5Purity:98%Color and Shape:SolidMolecular weight:397.38KAR425
CAS:<p>KAR425 is a bipyrrole tambjamines. KAR425 has antimalarial activity against multidrug-resistant P. yoelii in mice.</p>Formula:C19H27N3Color and Shape:SolidMolecular weight:297.44Sakyomicin A
CAS:<p>Sakyomicin A is an inhibitor of reverse transcriptase.</p>Formula:C25H26O10Color and Shape:SolidMolecular weight:486.47Elsamitrucin
CAS:<p>Elsamitrucin, a heterocyclic antibiotic, disrupts DNA replication by intercalating into G-C sequences and inhibiting topoisomerases.</p>Formula:C33H35NO13Color and Shape:SolidMolecular weight:653.63Polyketide synthase 13-IN-2
CAS:<p>Comp 42 is a potent PKS13 inhibitor in M. tuberculosis with MIC of 0.25 μg/mL.</p>Formula:C22H21NO5Color and Shape:SolidMolecular weight:379.41MMV008138
CAS:<p>MMV008138 inhibits the growth of P. falciparum Dd2 strain (IC50 of 250 nM).</p>Formula:C18H14Cl2N2O2Color and Shape:SolidMolecular weight:361.2241F5
CAS:<p>41F5: Anti-fungal with MIC50 0.4-0.8 μM and IC50 0.87 μM against Histoplasma; 62x more selective for yeast vs host cells.</p>Formula:C21H22N2OSColor and Shape:SolidMolecular weight:350.48RSV/IAV-IN-3
CAS:<p>RSV/IAV-IN-3 is a dual inhibitor of RSV (EC50: 2.92μM) and IAV (EC50:1.90μM), blocking virus replication post-entry.</p>Formula:C19H19BrN2O3SColor and Shape:SolidMolecular weight:435.33Afabicin disodium
CAS:<p>Afabicin (Debio 1450), a Debio1452 precursor, targets Staphylococcus by inhibiting lipid synthesis.</p>Formula:C23H22N3Na2O7PColor and Shape:SolidMolecular weight:529.396Antibacterial 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:270.71EP39
<p>EP39 is a potent HIV-1 inhibitor, stabilizing the SP1 domain's helix and blocking virus maturation.</p>Formula:C38H62N2O5Color and Shape:SolidMolecular weight:626.91Posaconazole hydrate
CAS:<p>Posaconazole: broad-spectrum antifungal, second-gen triazole, strong C14α demethylase inhibitor (IC50: 0.25 nM).</p>Formula:C37H44F2N8O5Purity:98%Color and Shape:SolidMolecular weight:718.792,6-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:238.11Antitumor agent-84
<p>Antitumor agent-84 stabilizes G-quadruplex DNA, exhibits potent anti-tumor effects.</p>Formula:C24H31N7Color and Shape:SolidMolecular weight:417.55Lipoxamycin
CAS:<p>Lipoxamycin is an inhibitor of serine palmitoyl-transferase.</p>Formula:C19H36N2O5Purity:98%Color and Shape:SolidMolecular weight:372.5Cefroxadine
CAS:<p>Cefroxadine: an oral cephalosporin antibiotic, broad-spectrum, bactericidal, effective for acute uncomplicated cystitis.</p>Formula:C16H19N3O5SPurity:98%Color and Shape:SolidMolecular weight:365.4Aztreonam lysine
CAS:<p>Aztreonam lysine is an inhaled anti-pseudomonal treatment for people who have pulmonary Pseudomonas aeruginosa infection with cystic fibrosis (CF).</p>Formula:C19H31N7O10S2Purity:98%Color and Shape:SolidMolecular weight:581.62Antiviral agent 10
CAS:<p>Antiviral agent 10 effectively inhibits the respiratory syncytial virus (RSV) [1], serving as a potent anti-viral compound.</p>Formula:C22H24N2O5Color and Shape:SolidMolecular weight:396.44Ingavirin
CAS:<p>Ingavirin, a novel inhibitor of the influenza virus reproduction, inhubits the formation of the virus specific hemagglutinin.</p>Formula:C10H15N3O3Purity:98%Color and Shape:SolidMolecular weight:225.243-Chlorogentisyl alcohol
CAS:<p>3-Chlorogentisyl alcohol: E. coli β-glucuronidase inhibitor (IC50=0.74µM, Ki=0.58µM), antiproliferative, for anti-cancer/inflammatory research.</p>Formula:C7H7ClO3Color and Shape:SolidMolecular weight:174.58Influenza A virus-IN-4
CAS:<p>Influenza A virus-IN-4 (23b), a potent neuraminidase inhibitor derived from Oseltamivir, effectively targets influenza viruses.</p>Formula:C19H28N4O4Color and Shape:SolidMolecular weight:376.45Antifungal agent 2
CAS:<p>Antifungal agent 2 suppresses growth of Cryptococcus, Candida, Aspergillus at ≥0.5 μg/mL.</p>Formula:C19H11Br2F3N4O2Purity:98%Color and Shape:SolidMolecular weight:544.12Phen-DC3
CAS:<p>Phen-DC3 is a G-quadruplex (G4) specific ligand which can inhibit FANCJ and DinG helicases (IC50s of 65±6 and 50±10 nM, respectively).</p>Formula:C34H26N6O2Purity:98%Color and Shape:SolidMolecular weight:550.61Silthiofam
CAS:<p>Silthiofam effectively combats Ggt, a wheat take-all fungus, now widely used for control in China.</p>Formula:C13H21NOSSiPurity:98%Color and Shape:SolidMolecular weight:267.46FtsZ-IN-2
CAS:<p>FtsZ-IN-2, a bacterial FtsZ inhibitor, hampers GTPase; has anti-MRSA/MSSA effects with 2 μg/ml MIC.</p>Formula:C30H35N5SColor and Shape:SolidMolecular weight:497.74,4'-Dicyanostilbene
CAS:<p>4,4'-Dicyanostilbene: potent anti-Dd2 malaria, EC50=27nM; effective vs. MRSA.</p>Formula:C16H10N2Color and Shape:SolidMolecular weight:230.26Antibacterial agent 101
CAS:<p>Antibacterial agent 101 exhibited antibacterial and antifungal effects (MIC=4-32 μg/mL).</p>Formula:C28H29BrN2OColor and Shape:SolidMolecular weight:489.45Reverse transcriptase-IN-3
<p>Reverse transcriptase-IN-3, a pyrimidine carboxamide, inhibits HIV-1 including mutant strains.</p>Formula:C28H31N7O4SColor and Shape:SolidMolecular weight:561.66WC-9
CAS:<p>WC-9 is a squalene synthase inhibitor. It acts by binding to TcSQS and HsSQS.</p>Formula:C15H13NO2SPurity:98%Color and Shape:SolidMolecular weight:271.33RSV/IAV-IN-2
CAS:<p>RSV/IAV-IN-2 (compound 14c) is a potent dual RSV/IAV inhibitor with lower toxicity than Ribavirin, promising for research.</p>Formula:C19H20N2O3SColor and Shape:SolidMolecular weight:356.442-Fluoroadenine
CAS:<p>2-Fluoroadenine (NSC-27364) has toxicity in nonproliferating and proliferating tumor cells. 2-Fluoroadenine can be used for anticancer studies.</p>Formula:C5H4FN5Purity:98.84% - 99.62%Color and Shape:White To Light Yellow Crystal PowderMolecular weight:153.12Phenosulfazole
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:256.3SQ109
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:382.35OX11
CAS:<p>OX11 is a selective inhibitor of S. pneumoniae, P. aeruginosa and E. coli bacteria.</p>Formula:C17H10Cl2N4O3S2Color and Shape:SolidMolecular weight:453.32Hexamide
CAS:<p>Hexamide is a protein inhibitor.</p>Formula:C13H17NOColor and Shape:SolidMolecular weight:203.28HCV-IN-3
CAS:<p>HCV-IN-3 is a hepatitis C virus (HCV) NS3/4a protein inhibitor (IC50: 20 μM; Kd: 29 μM).</p>Formula:C13H11F2NOPurity:98%Color and Shape:SolidMolecular weight:235.23LasR-IN-4
CAS:<p>LasR-IN-4 is a potent inhibitor of LasR which inhibits Pseudomonas aeruginosa and its biofilm formation, pyocyanin production, and rhamnolipids production [1].</p>Formula:C18H20N4Color and Shape:SolidMolecular weight:292.38Ribocil B
CAS:<p>Ribocil-B is the active S-isomer of ribocil which can inhibit flavin mononucleotide (FMN,KD of 6.6 nM).</p>Formula:C19H22N6OSPurity:98%Color and Shape:SolidMolecular weight:382.48Antiparasitic agent-10
CAS:<p>Antiparasitic agent-10 (Compound 94) targets Schistosoma mansoni, shows promise for treating Schistosomiasis.</p>Formula:C13H17N3O4S3Color and Shape:SolidMolecular weight:375.49DQBS
CAS:<p>DQBS is an HIV-1 Nef function antagonist.</p>Formula:C22H17ClN4O4SPurity:98%Color and Shape:SolidMolecular weight:468.91DHFR-IN-1
CAS:<p>DHFR-IN-1: selective DHFR blocker, IC50 40.71 nM, antifungal, strong against Gram-positive/negative bacteria, synergizes with Levofloxacin (FIC=0.249).</p>Formula:C22H22N6O4S2Color and Shape:SolidMolecular weight:498.58HIV-1 integrase inhibitor 7
CAS:<p>HIV-1 integrase inhibitor 7 is a potent HIV-1 integrase inhibitor (IC50: 33.3 nM).</p>Formula:C30H26O16Purity:98%Color and Shape:SolidMolecular weight:642.52Methisazone
CAS:<p>Methisazone is an effective antiviral agent against poxviruses.</p>Formula:C10H10N4OSPurity:98%Color and Shape:SolidMolecular weight:234.28β-L-D4A
CAS:<p>beta-L-D4A inhibits HIV-1 reverse transcriptase, stopping DNA synthesis.</p>Formula:C10H11N5O2Purity:99.45%Color and Shape:SolidMolecular weight:233.23Gln-AMS
CAS:<p>Gln-AMS is an inhibitor of aminoacyl-tRNA synthetases (AARS). It specifically binds to the A-domain located within the NRPS enzymes.</p>Formula:C15H22N8O8SPurity:98%Color and Shape:SolidMolecular weight:474.45Syncytial Virus Inhibitor-1
CAS:<p>Syncytial Virus Inhibitor-1: Potent, oral RSV fusion blocker (EC50: 0.002-0.004 μM for Long, A2, B strains).</p>Formula:C23H26N4O3SPurity:98%Color and Shape:SolidMolecular weight:438.54BPH-1086
CAS:<p>BPH-1086 inhibits IspH, which with RPS1 binds mRNA or integrates into bacterial ribosomes.</p>Formula:C4H8O7P2Color and Shape:SolidMolecular weight:230.05LmCPB-IN-1
CAS:<p>LmCPB-IN-1, compound 35, is a reversible inhibitor of LmCPB with strong binding (pKi 9.7).</p>Formula:C18H30N6O2Color and Shape:SolidMolecular weight:362.47Globosuxanthone A
CAS:<p>Globosuxanthone A: a dihydroxanthenone with anticancer and antifungal properties (MIC: F. graminearum 4, F. solani 8, B. cinerea 16 μg/mL).</p>Formula:C15H12O7Color and Shape:SolidMolecular weight:304.25BRD-8000.3
CAS:<p>BRD-8000.3 is a narrow-spectrum antimycobacterial targeting EfpA, inhibiting lipid transport in drug-tolerant Mtb and useful in structural and functional.</p>Formula:C19H21BrN4OPurity:99.78% - 99.78%Color and Shape:SolidMolecular weight:401.3HIV-1 protease-IN-2
CAS:<p>HIV-1 protease-IN-2: strong HIV-1 protease blocker, IC50 2.53 nM, fights DRV-sensitive/resistant HIV-1.</p>Formula:C27H34N4O7SColor and Shape:SolidMolecular weight:558.65Antifungal agent 59
CAS:<p>Antifungal agent 59 exhibits potent activity, reflected by MIC values ranging from 0.01 to 1 μg/mL, and inhibits the formation of fungal biofilms, while</p>Formula:C18H15BrF2N2SeColor and Shape:SolidMolecular weight:456.19pUL89 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:395.36HIV-1 inhibitor-57
CAS:<p>HIV-1 Inhibitor-57 (Compound 12g) is an antiviral agent that potently inhibits both wild-type and five common NNRTI-resistant strains of HIV-1, exhibiting EC50</p>Formula:C25H24FN5O3SColor and Shape:SolidMolecular weight:493.55Flomoxef sodium
CAS:<p>Flomoxef sodium, an antibiotic belonging to the oxacephem group, exhibits excellent activity against a broad spectrum of Gram-positive bacteria.</p>Formula:C15H17F2N6NaO7S2Purity:97.88%Color and Shape:SolidMolecular weight:518.44gp120-IN-1
CAS:<p>gp120-IN-1 (4e) is a potent HIV-1 inhibitor, IC50 2.2 μM, CC50 100.90 μM, and blocks HIV entry.</p>Formula:C15H18N2O4SColor and Shape:SolidMolecular weight:322.38Abimtrelvir
CAS:<p>Abimtrelvir exhibited antiviral activity.</p>Formula:C24H17ClF3N7O2Color and Shape:SolidMolecular weight:527.89Antimicrobial agent-5
<p>Antimicrobial agent-5: potent, selective for Gram-negative/positive bacteria, blocks LPS-CD14/TLR4, anti-inflammatory.</p>Formula:C32H48N16Color and Shape:SolidMolecular weight:656.83HIV-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:448.97BPH-1358 free base
CAS:<p>BPH-1358 inhibits UPPS (IC50: 110 nM) and FPPS (IC50: 1.8 µM), effective against S. aureus (MIC ~250 ng/mL).</p>Formula:C32H28N6O2Purity:98%Color and Shape:SolidMolecular weight:528.6SARS-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:697.7HIV-1 inhibitor-25
CAS:<p>Compound R-12a is a potent HIV-1 reverse transcriptase inhibitor (IC50: 0.1061 nM), with low cytotoxicity and effective against multiple mutants.</p>Formula:C26H19N5O2Color and Shape:SolidMolecular weight:433.46Alamifovir
CAS:<p>Alamifovir: HBV-specific antiviral, purine analog prodrug; active against wild-type/lamivudine-resistant HBV; inhibits DNA initiation/packaging.</p>Formula:C19H20F6N5O5PSColor and Shape:SolidMolecular weight:575.42Anticancer 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:452.35NIT
CAS:<p>NIT is an HIV-1 protease inhibitor.</p>Formula:C15H7N3O4S2Purity:98%Color and Shape:SolidMolecular weight:357.36RSV/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:360.86Antileishmanial 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:366.45EGFR/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:511.62HIV-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:345.24Cap-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:396.32Antitrypanosomal 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:755.99Metallo-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:274.3VP-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:280.3Antimicrobial 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:269.32Antitubercular 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:340.37Anti-infective agent 2
CAS:<p>Compound 3k is antiprotozoal/antimycobacterial, with IC50s: P. falciparum 0.07 μM, T. brucei 2.20 μM; MIC: M. smegmatis 32 μg/mL.</p>Formula:C15H8ClNO2Color and Shape:SolidMolecular weight:269.68Antitrypanosomal 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:281.73HBV-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:357.4Cap-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:527.47MmpL3-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:382.54Antibacterial 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:382.46Chitin 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:496.77HIV-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:442.5Anti-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:296.32DuP 105
CAS:<p>DuP 105 is an oral oxazolidinone, a novel synthetic antimicrobial compound effective against gram-positive bacteria.</p>Formula:C13H16N2O4SPurity:99.82%Color and Shape:SolidMolecular weight:296.34Bulaquine
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:200.23Methenamine 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:820.83Etisazole
CAS:<p>Etisazole is an animal antifungal agent with skin sensitizing properties to humans.</p>Formula:C9H10N2SColor and Shape:SolidMolecular weight:178.25Grazoprevir 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:411.52SARS-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:302.32Antitubercular 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:430.54
