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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Berkeleylactone E
CAS:<p>Berkeleylactone E, a macrolide antibiotic [1], exhibits antimicrobial properties.</p>Formula:C20H32O7Color and Shape:SolidMolecular weight:384.469CDD-1819
CAS:<p>CDD-1819, a non-covalent and non-peptide compound, serves as a potent SARS-CoV-2 Mpro inhibitor, exhibiting a K i value of 5 nM.</p>Formula:C35H31N5O2Purity:98%Color and Shape:SolidMolecular weight:553.65D1N8
CAS:<p>D1N8 is a potent inhibitor of the SARS-CoV-2 3CL protease, displaying an IC50 value of 0.44 μM and a CC50 value of greater than 20 μM.</p>Formula:C19H14ClN5O3Purity:98%Color and Shape:SolidMolecular weight:395.8DprE1-IN-9
CAS:<p>DprE1-IN-9 (compound B18) is an efficient reversible inhibitor of DprE1, interacting with the enzyme's receptor cavity.</p>Formula:C22H25F3N4O2Color and Shape:SolidMolecular weight:434.456-Chloro-7-deazapurine-β-D-riboside
CAS:<p>6-Chloro-7-deazapurine-β-D-riboside shows antifungal activity.</p>Formula:C11H12ClN3O4Purity:98.26%Color and Shape:SolidMolecular weight:285.68AB131
CAS:<p>AB131, an inhibitor of MSMEG 6649 and Rv2172c (KD values of 0.16 and 0.02 μM, respectively), enhances the antimycobacterial efficacy of the antitubercular agent</p>Formula:C21H19NO6SColor and Shape:SolidMolecular weight:413.44Antitrypanosomal agent 14
CAS:Antitrypanosomal agent 14 (Compound 1), a potent T.Formula:C14H23N3OSPurity:98%Color and Shape:SolidMolecular weight:281.42OfChi-h-IN-2
CAS:<p>OfChi-h-IN-2 (compound TQ19) is a potent inhibitor of OfChi-h, exhibiting a K i of 0.33 μM, and significantly impairs the growth and development of Ostrinia</p>Formula:C25H28ClN5O3Purity:98%Color and Shape:SolidMolecular weight:481.98SIMR3030
CAS:<p>SIMR3030, a potent inhibitor of SARS-CoV-2 PLpro, possesses an IC50 of 0.0399 µg/mL and demonstrates antiviral activity by diminishing the expression of SARS-</p>Formula:C27H29N3O2Purity:98%Color and Shape:SolidMolecular weight:427.54COH1
CAS:<p>COH1 is a ribonucleotide reductase (RR) inhibitor utilized in research pertaining to cancer, mitochondrial diseases, and neurodegenerative disorders [1].</p>Formula:C11H10N2O3SPurity:98%Color and Shape:SolidMolecular weight:250.27Rosoxacin
CAS:<p>Rosoxacin (Acrosoxacin) shows antibacterial activities against a broad spectrum of Gram-negative bacteria including Neisseria gonorrhoeae (MIC90 = 0.03mg/ml).</p>Formula:C17H14N2O3Purity:99.1%Color and Shape:SolidMolecular weight:294.33,4'-Dihydroxyflavone
CAS:<p>3,4'-Dihydroxyflavone (3,4'-DHF) is an oral active flavonoid. 3,4'-Dihydroxyflavone (3,4'-DHF) shows antiviral activity against Influenza A virus.</p>Formula:C15H10O4Purity:98.33%Color and Shape:SolidMolecular weight:254.24Eugenitin
CAS:<p>Eugenitin, a polyketide from Mycoleptodiscus indicus, exhibits inhibitory activity against Leishmania major with an LD50 of 39.9 μM and demonstrates low</p>Formula:C12H12O4Purity:98%Color and Shape:SolidMolecular weight:220.22Loflucarban
CAS:<p>Loflucarban (Fluonilid) is an antimycotic compoud.</p>Formula:C13H9Cl2FN2SPurity:98.08% - 98.15%Color and Shape:SolidMolecular weight:315.19SARS-CoV-2-IN-59
CAS:<p>SARS-CoV-2-IN-59 (compound E07), an imidazoline derivative, is a non-peptide small molecule that inhibits SARS-CoV-2 by targeting its main protease (Mpro).</p>Formula:C10H9N3Purity:98%Color and Shape:SolidMolecular weight:171.2H3B-968
CAS:<p>H3B-968 is a potent inhibitor of Werner syndrome protein (WRN) with an IC50 of approximately 10 nM, effectively targeting its helicase, ATPase, and exonuclease</p>Formula:C22H18F6N4O4SPurity:98%Color and Shape:SolidMolecular weight:548.46SHR5133
CAS:<p>SHR5133 is a potent, orally active regulator of HBV capsid assembly that reduces HBV DNA (EC50: 26.6 nM).</p>Formula:C19H18F4N6O2Color and Shape:SolidMolecular weight:438.38HBV-IN-41
CAS:<p>HBV-IN-41 (compound 45) is a potent, orally active inhibitor of Hepatitis B Virus (HBV), exhibiting an EC50 value of 0.027μM [1].</p>Formula:C18H19ClFN5O3Purity:98%Color and Shape:SolidMolecular weight:407.83NSC 288387
CAS:<p>NSC 288387, a pan-flavivirus MTase inhibitor, binds to the SAM-binding pocket and effectively inhibits Zika virus (ZIKV) with an IC50 of 0.2 μM, also preventing</p>Formula:C19H16N4O3Purity:98%Color and Shape:SolidMolecular weight:348.36Antimalarial agent 15
CAS:<p>Antimalarial agent 15 halts Plasmodium falciparum growth with a 20 nM IC50.</p>Formula:C29H30N2O6Color and Shape:SolidMolecular weight:502.56RSV L-protein-IN-2
CAS:<p>RSV L-protein-IN-2 (Compound A), a noncompetitive inhibitor of the RSV polymerase (IC50: 4.5 μM), exhibits antiviral activity against long RSV strains (EC50: 1.</p>Formula:C32H36N4O5Purity:98%Color and Shape:SolidMolecular weight:556.65AB-836
CAS:<p>AB-836, an orally active hepatitis B virus (HBV) capsid inhibitor, hampers viral replication by engaging with the HBV core protein.</p>Formula:C20H15F3N4O2Color and Shape:SolidMolecular weight:400.35Antiproliferative agent-18
CAS:<p>Compound 5k (Antiproliferative Agent-18) is an antiproliferative agent that exhibits moderate antibacterial and antifungal activities [1].</p>Formula:C26H27FN2OSColor and Shape:SolidMolecular weight:434.57RNA polymerase II-IN-1
CAS:<p>RNA polymerase II-IN-1 (19iv), an amatoxin, inhibits Pol II at 36.66 nM IC50, is more toxic to cancer cells, less to normal cells than α-Amanitin.</p>Formula:C38H53N11O12SPurity:98%Color and Shape:SolidMolecular weight:887.964-Hydroxy-2-methylbenzenesulfonic acid ammonium
CAS:<p>4-Hydroxy-2-methylbenzene ammonium: Policresulen impurity, inhibits NS2B/NS3 protease (IC50: 0.48 μg/mL), hinders DENV2 in BHK-21 cells (IC50: 4.99 μg/mL).</p>Formula:C7H11NO4SPurity:98%Color and Shape:SolidMolecular weight:205.23Antileishmanial agent-17
CAS:<p>Antileishmanial agent-17, a coumarin hybrid, exhibits potent antileishmanial activity (IC50 <0.78 μM) while proving non-toxic to normal VERO cells.</p>Formula:C27H37N5O5Purity:98%Color and Shape:SolidMolecular weight:511.61Votoplam
CAS:<p>Votoplam functions as a gene splicing modulator, employed in the inhibition of Huntington's disease [1].</p>Formula:C21H25N9OPurity:98%Color and Shape:SolidMolecular weight:419.48Cap-dependent endonuclease-IN-13
CAS:<p>Cap-dependent endonuclease-IN-13 is a potent inhibitor of cap-dependent endonuclease (CEN) and shows research potential against influenza virus infection (</p>Formula:C25H20F2N4O4SColor and Shape:SolidMolecular weight:510.51Mansonone F
CAS:<p>Mansonone F is a topoisomerase II inhibitor with cytotoxic and topo inhibitory potencies.</p>Formula:C15H12O3Color and Shape:SolidMolecular weight:240.25Koshidacin B
CAS:<p>Koshidacin B, a cyclic tetrapeptide, inhibits malaria strains FCR3/K1 (IC50: 0.89/0.83 μM), showing promise for antiplasmodial research.</p>Formula:C28H40N4O7Color and Shape:SolidMolecular weight:544.64Anti-MRSA agent 8
CAS:<p>Anti-MRSA Agent 8 (Compound 7g), a derivative of DAPG, exhibits potent antibacterial properties by interacting with bacterial cell membranes and is useful for</p>Formula:C20H30O5Color and Shape:SolidMolecular weight:350.45Besifovir Dipivoxil maleate
CAS:<p>Besifovir Dipivoxil maleate, an oral HBV prodrug (LB80380), suppresses HBV DNA in naive and lamivudine-resistant CHB cases.</p>Formula:C22H34N5O8PPurity:98%Color and Shape:SolidMolecular weight:527.51Flurofamide
CAS:<p>Flurofamide is an effective bacterial urease inhibitor and has potential in the treatment of infected urinary calculi.</p>Formula:C7H9FN3O2PPurity:96.01% - 98%Color and Shape:SolidMolecular weight:217.14Ganfeborole HCl
CAS:<p>Ganfeborole HCl (GSK3036656 HCl) is a compound with anti-tuberculosis activity and is an inhibitor of Mycobacterium tuberculosis (Mtb) leucyl-tRNA synthetase.</p>Formula:C10H14BCl2NO4Purity:99.88%Color and Shape:SolidMolecular weight:293.94APX2039
CAS:<p>APX2039 is an orally active fungal Gwt1 enzyme inhibitor and a prodrug of the novel Gwt2096 inhibitor APX1.APX2039 exhibits potent anti-Kryptococcal activity</p>Formula:C20H15FN4O2Purity:98.72% - 99.07%Color and Shape:SolidMolecular weight:362.36SARS-CoV-2/MERS Mpro-IN-2
<p>SARS-CoV-2/MERS Mpro-IN-2 is a potent inhibitor of the main proteases of SARS-CoV-2 and MERS, demonstrating IC50 values of 0.21 and 0.07 µM, respectively.</p>Formula:C28H30Cl2N4O6Color and Shape:SolidMolecular weight:589.47AVG-233
CAS:<p>AVG-233 is an RNA-dependent RNA polymerase (RdRp) inhibitor with antiviral activity for the study of respiratory syncytial virus infections.</p>Formula:C26H22ClN5O3Purity:99%Color and Shape:SolidMolecular weight:487.94Chitin synthase inhibitor 14
CAS:<p>Chitin Synthase Inhibitor 14 (compound 4n), a potent chitin synthase (CHS) inhibitor, exhibits antifungal activity and is effective against drug-resistant</p>Formula:C25H26ClN5O5Color and Shape:SolidMolecular weight:511.96L 680833
CAS:<p>L 680833 is an orally active monocyclic beta-lactam human polymorphonuclear leukocyte elastase inhibitor.</p>Formula:C27H34N2O5Color and Shape:SolidMolecular weight:466.57DHX9-IN-4
CAS:<p>DHX9-IN-4 is an ATP-dependent RNA helicase DHX9 inhibitor used in cancer research.</p>Formula:C21H22ClN5O4S2Purity:98.12%Color and Shape:SolidMolecular weight:508.01Zevotrelvir
CAS:<p>Zevotrelvir (Compound 52) serves as an inhibitor of coronavirus, demonstrating IC50 values below 0.1 μM for 229E hCoV protease and below 0.1 mM for SARS-CoV-3C-</p>Formula:C28H26F3N5O3Purity:98%Color and Shape:SolidMolecular weight:537.53Antibacterial agent 159
CAS:<p>Compound 6d (Antibacterial agent 159) is an antibiotic effective against impetigo and Clostridium difficile infection (CDI), with no observed recurrence for CDI</p>Formula:C51H50N16O10S6Purity:98%Color and Shape:SolidMolecular weight:1239.435-DACTHF
CAS:<p>5,11-methenyltetrahydrohomofolate blocks GAR & AIR transformylase; used as an anti-purine drug.</p>Formula:C19H24N6O6Purity:98%Color and Shape:SolidMolecular weight:432.43A 74704
CAS:<p>A 74704 is a pseudo C2-symmetric inhibitor of HIV-1 protease and its diester analog.</p>Formula:C43H52N4O7Purity:98%Color and Shape:SolidMolecular weight:736.9Deacylketoconazole
CAS:<p>Deacylketoconazole (Deacyl ketoconazole) is a Ketoconazole derivative and is also an antifungal agent.</p>Formula:C24H26Cl2N4O3Purity:98.35%Color and Shape:SolidMolecular weight:489.39L-697661
CAS:<p>L-697661, a reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.</p>Formula:C16H15Cl2N3O2Color and Shape:SolidMolecular weight:352.22Emzadirib
CAS:<p>Emzadirib (RAD51-IN-2) is a potent RAD51 inhibitor with potential anticancer activity for the study of DNA damage repair.</p>Formula:C27H40N4O6S2Purity:99.79% - 99.9%Color and Shape:SolidMolecular weight:580.76Azaconazole
CAS:<p>Azaconazole, an agricultural fungicide, is used for controlling powdery mildew on crops and bean rust.</p>Formula:C12H11Cl2N3O2Color and Shape:SolidMolecular weight:300.14Pexiganan acetate
CAS:<p>Pexiganan acetate (MSI 78), a 22-residue peptide analogue of magainin 2, disrupts bacterial membranes or walls, leading to antibacterial activity.</p>Formula:C122H210N32O22·xC2H4O2Purity:99.88%Color and Shape:SolidMolecular weight:2477.22 (free base)DAM-IN-1
CAS:<p>DMA-IN-1 is a DNA adenine methyltransferase (DAM) inhibitor with an IC50 value of 48 μM.</p>Formula:C16H17NO4Purity:98%Color and Shape:SolidMolecular weight:287.31SDH-IN-3
CAS:<p>SDH-IN-3 is a succinate dehydrogenase (SDH) inhibitor, demonstrating potent antifungal activity with an inhibition concentration (IC50) of 7.2 μg/mL and an</p>Formula:C15H11F2N3OSPurity:98%Color and Shape:SolidMolecular weight:319.33XSJ2-46
CAS:<p>XSJ2-46, a 5'-amino NI analog, is an antiviral agent possessing anti-Zika virus properties and demonstrates reasonable inhibition of RNA-dependent RNA</p>Formula:C25H24ClF3N6O3Purity:98%Color and Shape:SolidMolecular weight:548.95RSV L-protein-IN-3
CAS:<p>RSV L-protein-IN-3 is an inhibitor of the wild-type RSV polymerase, exhibiting an IC50 of 10.4 μM and an EC50 of 2.1 μM (against RSV), and possesses lower</p>Formula:C31H34N4O4Purity:98%Color and Shape:SolidMolecular weight:526.63DGKα-IN-8
CAS:<p>DGKα-IN-8 (Example 51) is a potent diacylglycerol kinase alpha (DGKα) inhibitor, exhibiting an IC50 of 22.491 nM and an EC50 of 0.256 nM.</p>Formula:C23H19ClF3N5OColor and Shape:SolidMolecular weight:473.884-Aminosalicylic acid hemicalcium
CAS:<p>4-Aminosalicylic acid hemicalcium, an orally active antibiotic, shows potential in tuberculosis research [1].</p>Formula:C7H7NO3CaColor and Shape:SolidMolecular weight:172.17AG 85
CAS:<p>AG 85 is a major secretion protein of Mycobacterium tuberculosis.</p>Formula:C27H22N4O3SColor and Shape:SolidMolecular weight:482.559-Deazaguanine
CAS:<p>9-Deazaguanine is a nucleoside analogue exhibiting inhibitory activity against bovine purine nucleoside phosphorylase (PNP).</p>Formula:C6H6N4OPurity:98%Color and Shape:SolidMolecular weight:150.14Antituberculosis agent-8
CAS:<p>Antituberculosis agent-8: MIC 3.53 μM vs M. tuberculosis, antifungal MIC 62.50 μM vs A. niger.</p>Formula:C25H19F3N2O3Color and Shape:SolidMolecular weight:452.43ALS-8112
CAS:<p>ALS-8112 is a inhibitor of respiratory syncytial virus (RSV) polymerase. The 5'-triphosphate form of ALS-8112 inhibits RSV polymerase (IC50: 0.02 μM).</p>Formula:C10H13ClFN3O4Purity:98.90%Color and Shape:SolidMolecular weight:293.68HIV-1 inhibitor-10
CAS:<p>HIV-1 inhibitor-10 is a nanomolar HIV-1 maturation inhibitor.</p>Formula:C39H54O6Color and Shape:SolidMolecular weight:618.84Roseoflavin
CAS:<p>Roseoflavin, a chemical analog of FMN and riboflavin that has antimicrobial activity, can directly bind to FMN riboswitch aptamers and downregulate the</p>Formula:C18H23N5O6Purity:99.81% - 99.89%Color and Shape:SolidMolecular weight:405.41SARS-CoV-2-IN-63
CAS:<p>SARS-CoV-2-IN-63 (Compound R3e) serves as an inhibitor of SARS-CoV-2 replication, demonstrating low cytotoxicity.</p>Formula:C20H21N3O3SePurity:98%Color and Shape:SolidMolecular weight:430.36Zika virus-IN-2
CAS:<p>Zika virus-IN-2 (Compd 3) is a Zika virus inhibitor (EC 50= 7.4 μM).</p>Formula:C24H23N3O3Color and Shape:SolidMolecular weight:401.46Antileishmanial agent-16
CAS:<p>Antileishmanial agent-16 (compound 14c), an anti-Leishmania agent, exhibits potent activity against Leishmania major promastigotes (IC50 = 0.59 µM) and</p>Formula:C27H37N5O4Purity:98%Color and Shape:SolidMolecular weight:495.61Propamidine
CAS:<p>Propamidine acts as a covalent inhibitor of TMPRSS2 and exhibits antibacterial properties. [1]</p>Formula:C17H20N4O2Purity:98%Color and Shape:SolidMolecular weight:312.37HCoV-OC43-IN-1
CAS:<p>HCoV-OC43-IN-1 (Compound IV-16) serves as an inhibitor of the coronavirus HCoV-OC43, exhibiting antiviral efficacy with an EC50 of 90 nM.</p>Formula:C23H22F6N4O2Purity:98%Color and Shape:SolidMolecular weight:500.44SARS-CoV-2 3CLpro-IN-15
CAS:<p>SARS-CoV-2 3CLpro-IN-15 (compound a), a beta-nitrostyrene derivative, acts as an inhibitor of the SARS-CoV-2 3CL protease (3CLpro), effectively inhibiting viral</p>Formula:C8H6N2O4Purity:98%Color and Shape:SolidMolecular weight:194.14NK007
CAS:<p>NK007 is a novel anti-SARS-CoV-2 agent with an EC 50 value of 30 nM.</p>Formula:C28H33NO9Color and Shape:SolidMolecular weight:527.56RyRs activator 2
CAS:<p>RyRs activator 2: potent ranibulin receptor stimulant, 30% larvicidal activity, equals chlorfenvinphos, outperforms cyanobenzamide.</p>Formula:C23H18Cl2F3N5O2Color and Shape:SolidMolecular weight:524.32Targeting the bacterial sliding clamp peptide 46
CAS:<p>Peptide 46 is a short peptide that inhibits SC-dependent DNA synthesis by targeting the bacterial sliding clamp (SC).</p>Formula:C47H64N8O11Color and Shape:SolidMolecular weight:917.06Laxifloran
CAS:<p>Laxifloran possesses antibacterial and antifungal properties.</p>Formula:C17H18O5Color and Shape:SolidMolecular weight:302.32SARS-CoV-2-IN-43
CAS:<p>Compound 8h, also known as SARS-CoV-2-IN-43, is a powerful inhibitor effective in obstructing the replication of SARS-CoV-2, exhibiting significant antiviral</p>Formula:C16H12O3Purity:98%Color and Shape:SolidMolecular weight:252.26LS-BF1
CAS:<p>LS-BF1: Stable, low-toxic antimicrobial peptide targeting ESKAPE pathogens via cell membrane disruption, effective in mouse infection model.</p>Formula:C107H166N28O15Color and Shape:SolidMolecular weight:2084.64Zika virus-IN-1
CAS:<p>Zika virus-IN-1 is an inhibitor of Zika virus (EC50: 1.56 μM).</p>Formula:C30H37N3O3SiColor and Shape:SolidMolecular weight:515.72BILR-355
CAS:<p>BILR-355 is a reverse transcriptase inhibitor.</p>Formula:C25H23N5O3Purity:98%Color and Shape:SolidMolecular weight:441.48Diazoketone methotrexate
CAS:<p>Diazoketone methotrexate is an analog of methotrexate with potential antitumor activity.</p>Formula:C21H22N10O4Color and Shape:SolidMolecular weight:478.46Antibacterial agent 91
<p>Antibacterial 91: Inhibits aaRS, IC50 2.10μM vs. S. enterica ThrRS, has antibacterial properties. [1]</p>Formula:C33H31BrClN5O4Color and Shape:SolidMolecular weight:676.99RSV L-protein-IN-4
CAS:<p>RSV L-protein-IN-4 (Compound C) is a noncompetitive inhibitor of the RSV polymerase with an IC50 of 0.88 μM.</p>Formula:C32H35N5O6Purity:98%Color and Shape:SolidMolecular weight:585.65SARS-CoV-2-IN-69
CAS:<p>SARS-CoV-2-IN-69 (Compound 7E) is a potent, non-covalent inhibitor of the SARS-CoV-2 main protease (M^pro) with an EC50 of 7.4 μM and also inhibits the papain-</p>Formula:C15H11NO3SPurity:98%Color and Shape:SolidMolecular weight:285.32Debrisoquin
CAS:<p>Debrisoquin (Isocaramidine) is a TMPRSS2 inhibitor that prevents SARS-CoV-2 from entering human lung cells through TMPRSS2-dependent pathways, exhibiting an</p>Formula:C10H13N3Purity:98%Color and Shape:SolidMolecular weight:175.23CcpA-IN-1
CAS:<p>CcpA-IN-1 is a Staphylococcus aureus antibiotic exhibiting significant bactericidal activity (MICs=460 nM) [1].</p>Formula:C77H82F12N8OP3RuPurity:98%Color and Shape:SolidMolecular weight:1557.5Alteconazole
CAS:<p>Alteconazole is an antifungal drug.</p>Formula:C17H12Cl3N3OPurity:98%Color and Shape:SolidMolecular weight:380.66TAS-114
CAS:<p>TAS-114 is a dUTPase and DPD inhibitor that modulates catabolic pathways to improve systemic availability of 5-FU.</p>Formula:C21H29N3O6SPurity:99.76%Color and Shape:SolidMolecular weight:451.54Pencitabine
CAS:<p>Pen is an oral cancer drug that blocks DNA synthesis by inhibiting key enzymes and integrating into DNA.</p>Formula:C15H20F3N3O6Color and Shape:SolidMolecular weight:395.33Teropavimab
CAS:<p>Teropavimab (3BNC117-LS), an antibody, is utilized in the research of HIV infection [1].</p>Color and Shape:LiquidNSC309401 dihydrochloride
CAS:<p>NSC309401 is an E. coli dihydrofolate reductase inhibitor with an IC50 value of 189 nM and a dissociation constant (Kd) of 14.57 nM [1].</p>Formula:C17H18Cl2N6Color and Shape:SolidMolecular weight:377.27HBV-IN-30
CAS:<p>HBV-IN-30, a flavone derivative, inhibits cccDNA in HBV research.</p>Formula:C22H18BrClO6Color and Shape:SolidMolecular weight:493.73Prochloraz manganese
CAS:<p>Prochloraz manganese, an antifungal agent utilized in the agricultural sectors [1], serves to protect crops by inhibiting fungal growth.</p>Formula:C60H64Cl14MnN12O8Color and Shape:SolidMolecular weight:1632.51Sulfachloropyridazine sodium
CAS:<p>Sulfachloropyridazine (sodium) is a sulfonamide antibiotic that impedes bacterial proliferation [1].</p>Formula:C10H8ClN4NaO2SPurity:98%Color and Shape:SolidMolecular weight:306.7Methyl 2-amino-5-bromobenzoate
CAS:<p>Methyl 2-amino-5-bromobenzoate (Methyl 5-Bromoanthranilate) is an HCV NS5b RNA polymerase inhibitor with antimicrobial activity.</p>Formula:C8H8BrNO2Purity:98.05%Color and Shape:SolidMolecular weight:230.06EHNA hydrochloride
CAS:<p>EHNA hydrochloride is a PDE2 and ADA inhibitor with anticancer activity, increasing intracellular adenosine concentration in a treatment time-dependent manner.</p>Formula:C14H24ClN5OPurity:98%Color and Shape:SolidMolecular weight:313.83SARS-CoV-2 3CLpro-IN-5
CAS:<p>SARS-CoV-2 3CLpro-IN-5 is a covalent inhibitor targeting the 3C-like protease (3CLpro), exhibiting potent inhibitory activity with an IC50 of 3.8 nM and</p>Formula:C22H26ClF2N5O4Purity:98%Color and Shape:SolidMolecular weight:497.92Elastase LasB-IN-1
CAS:<p>Elastase LasB-IN-1 (Compound 4b), a potent and selective inhibitor of elastase LasB, exhibits antibacterial activity and has been determined to possess an IC50</p>Formula:C13H17F3NO4PColor and Shape:SolidMolecular weight:339.25Dup-721
CAS:<p>DuP-721: broad-spectrum, oral antibiotic targeting various bacteria, including M. tuberculosis.</p>Formula:C14H16N2O4Purity:99.84%Color and Shape:SolidMolecular weight:276.29Antifungal agent 49
CAS:<p>Antifungal agent 49 (Example 112) exhibits activity against Cryptococcus neoformans, demonstrating a minimum inhibitory concentration (MIC) of 49 μM [1].</p>Formula:C15H12O4Color and Shape:SolidMolecular weight:256.25NS5A-IN-2
CAS:<p>NS5A-IN-2, a potent inhibitor, is highly effective against HCV 1b and shows increased activity for GT 3a with good metabolic stability.</p>Formula:C46H45N7O7Purity:98%Color and Shape:SolidMolecular weight:807.89AZD-7295
CAS:<p>AZD-7295 (A-689) is an NS5A inhibitor that may be used to treat HCV infection.</p>Formula:C32H35F3N4O5SColor and Shape:SolidMolecular weight:644.7Antiviral agent 35
CAS:<p>Antiviral agent 35 (compound 4d) serves as a potent orally active inhibitor of the influenza virus, targeting early stages of viral replication.</p>Formula:C23H18N2O4SPurity:98%Color and Shape:SolidMolecular weight:418.47SARS-CoV-2-IN-1
CAS:<p>SARS-CoV-2-IN-1 is a potent inhibitor of Mpro(SARS-CoV-2 Mpro, SARS-CoV Mpro and MERS-CoV Mpro with IC50s of 0.67, 0.90 and 0.58 μM, respectively).</p>Formula:C31H39N5O7Purity:98%Color and Shape:SolidMolecular weight:593.67BMS-561390
CAS:<p>BMS-561390, a reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.</p>Formula:C14H12ClF3N2OColor and Shape:SolidMolecular weight:316.71Isotianil
CAS:<p>Isotianil is a plant defense inducer that activates typical plant defense responses without direct antimicrobial effects, serving as a plant protection agent</p>Formula:C11H5Cl2N3OSColor and Shape:SolidMolecular weight:298.15Japonilure
CAS:<p>Japonilure is an agent of insecticide and pheromone.</p>Formula:C14H24O2Purity:98%Color and Shape:SolidMolecular weight:224.34SARS-CoV-2/MERS Mpro-IN-1
<p>SARS-CoV-2/MERS Mpro-IN-1 is a potent inhibitor of the main proteases in SARS-CoV-2 and MERS, exhibiting IC50 values of 0.10 and 0.06 µM, respectively.</p>Formula:C30H36N4O7Color and Shape:SolidMolecular weight:564.63Fervenulin
CAS:<p>Fervenulin, from Streptomyces sp. CMU-MH021, halts egg hatch (MIC: 30 μg/mL) and kills J2 larvae (MIC: 120 μg/mL) of M. incognita.</p>Formula:C7H7N5O2Purity:99.75%Color and Shape:SolidMolecular weight:193.16ZIKV-IN-1
CAS:<p>ZIKV-IN-1 blocks Zika virus effectively (EC50: 2.8 μM, EC90: 6.8 μM), targets the RdRp domain, and is low-toxic.</p>Formula:C21H18BrF2N3O3Color and Shape:SolidMolecular weight:478.29β-Lactamase-IN-8
CAS:<p>β-Lactamase-IN-8 (compound 20) is a potent and oral bioavailable broad-spectrum cyclic boronate β-lactamase inhibitor that can be used for researching</p>Formula:C10H14BNO4SColor and Shape:SolidMolecular weight:255.1L-696229
CAS:<p>L-696229: specific HIV-1 RT inhibitor, blocks viral spread in various cells.</p>Formula:C17H18N2O2Purity:98%Color and Shape:SolidMolecular weight:282.34β-Lactamase-IN-2
CAS:<p>β-Lactamase-IN-2 is an inhibitor of β-Lactamase with anti-microbial and anti-bacterial effects.</p>Formula:C11H9FO3Purity:99.52%Color and Shape:SolidMolecular weight:208.19WQ 2743
CAS:<p>WQ 2743 is a potent agent of antimicrobial.</p>Formula:C19H15BrF3N5O3Purity:98%Color and Shape:SolidMolecular weight:498.25NVS-SM2
CAS:<p>NVS-SM2 boosts SMN2 splicing, enhances exon 7 inclusion, and raises SMN protein levels orally.</p>Formula:C23H30N6OColor and Shape:SolidMolecular weight:406.52RSV604 (R enantiomer)
CAS:<p>RSV604 R enantiomer is the R-enantiomer of RSV604. RSV604 is a respiratory syncytial virus (RSV) replication inhibitor.</p>Formula:C22H17FN4O2Purity:98%Color and Shape:SolidMolecular weight:388.39Ravidasvir HCl
CAS:<p>Ravidasvir, also known as PPI-668 and ASC16, is a second-generation, orally active, potent and selective HCV NS5A protein inhibitor.</p>Formula:C42H52Cl2N8O6Color and Shape:SolidMolecular weight:835.828EBOV-IN-1
CAS:<p>EBOV-IN-1 is an adamantane dipeptide piperazine inhibitor of Ebola virus (EBOV) that inhibits EBOV infection and suppresses pseudotypic EBOV infection.</p>Formula:C34H43N3O5Purity:98.62% - 98.92%Color and Shape:SolidMolecular weight:573.72Phylloflavan
CAS:<p>Phylloflavan, an antileishmanial compound, exhibits an intracellular half maximal effective concentration (EC50) of 3.2 nM in RAW 264.7 cells and inhibits the</p>Formula:C26H26O10Purity:98%Color and Shape:SolidMolecular weight:498.48Nilofabicin
CAS:<p>Nilofabicin (CG-400549) is a potent inhibitor of enoyl-(acyl-carrier-protein) reductase fall(FabI) and can be used in studies about the treatment of complicated</p>Formula:C19H20N2O2SPurity:98.66%Color and Shape:SolidMolecular weight:340.44AZ-27
CAS:<p>AZ-27 is a respiratory syncytial virus inhibitor which differentially inhibits different polymerase activities at the promoter.</p>Formula:C36H35N5O4SColor and Shape:SolidMolecular weight:633.76Antibiofilm agent-2
CAS:<p>Antibiofilm Agent-2 (Compound 4T) serves as a potent biofilm inhibitor, exhibiting an IC50 of 3.6 μM, and impairs the quorum sensing system along with iron</p>Formula:C17H21NO5Color and Shape:SolidMolecular weight:319.35Antifungal agent 50
CAS:<p>Antifungal agent 50 exhibits minimum inhibitory concentrations (MICs) ranging from less than 0.063 to 1 μg/mL [1].</p>Formula:C25H20ClN5O2SColor and Shape:SolidMolecular weight:489.98UNC2170 maleate
CAS:<p>53BP1-binding protein 1 (53BP1) engages with dimethylated lysine 20 on histone 4 (H4K20me2) through its tandem tudor domains within a homodimer configuration, crucial for the DNA damage response. UNC2170, a micromolar 53BP1 ligand, selectively interacts with this site, demonstrating at least 17-fold preference for 53BP1 over similar proteins. This interaction occurs in a pocket formed by the 53BP1's tudor domains. Moreover, UNC2170 acts as an antagonist to 53BP1 in cellular lysates, effectively inhibiting class switch recombination, a process dependent on the functional 53BP1 tudor domain, thus confirming its cellular activity.</p>Formula:C14H21BrN2OC4H4O4Color and Shape:SolidMolecular weight:429.31BLI-489 Hydrate
CAS:<p>BLI-489 hydrate is a penicillin β-lactamase inhibitor that acts on classes A and C and some class D β-lactamases.</p>Formula:C13H10N3NaO4SColor and Shape:SolidMolecular weight:327.29G4/HDAC-IN-1
<p>G4/HDAC-IN-1, a G4/HDAC dual inhibitor, IC50 1.1 µM, blocks TNBC growth, useful in cancer research.</p>Formula:C36H49ClFN7O4Color and Shape:SolidMolecular weight:698.27MurA-IN-4
CAS:<p>MurA-IN-4 exhibits antibacterial properties as a MurA inhibitor, impeding the synthesis of bacterial cell walls [1].</p>Formula:C8H12ClNO3Color and Shape:SolidMolecular weight:205.64OM173-αA
CAS:<p>OM173-αA is a quinone bacterial metabolite that inhibits the growth of the bacteria M.</p>Formula:C17H16O6Color and Shape:SolidMolecular weight:316.31Δ2-trans Eicosenoic Acid
CAS:<p>Δ2-transEicosenoic acid, an α,β-unsaturated fatty acid, emerges as a by-product during the synthesis of Δ2-ciseicosenoic acid, which along with its salts, shows promise in diabetes treatment and lipid metabolism enhancement. Additionally, the compound 2-octadecenoic acid is recognized for its ability to enhance liver function and reduce blood sugar levels in streptozocin-induced diabetic rats.</p>Formula:C20H38O2Color and Shape:SolidMolecular weight:310.5Lagociclovir valactate
CAS:<p>Lagociclovir valactate is a prodrug of Lagociclovir . Lagociclovir valactate is an orally active anti- HBV agent [1] .</p>Formula:C18H25FN6O6Color and Shape:SolidMolecular weight:440.43GS-6620
CAS:<p>GS-6620 is a HCV nonstructural protein 5B (NS5B) inhibitor.</p>Formula:C29H37N6O9PColor and Shape:SolidMolecular weight:644.61(E)-LHF-535
CAS:<p>(E)-LHF-535, an E-isomer antiviral, EC50 <1 μM vs Lassa/Machupo/Junin, 1-10 μM vs VSVg.</p>Formula:C27H28N2O2Purity:98%Color and Shape:SolidMolecular weight:412.52Oxynitidine
CAS:<p>Oxynitidine, an HBV inhibitor (ID50 = 30.8 µg/mL), effectively suppresses HBV DNA replication and may be utilized in viral infection research [1].</p>Formula:C21H17NO5Purity:98%Color and Shape:SolidMolecular weight:363.36LY 173013
CAS:<p>LY 173013 is a bicyclic pyrazolidinone, it has antibacterial properties.</p>Formula:C15H16N6O7SPurity:98%Color and Shape:SolidMolecular weight:424.39SARS-CoV-2 Mpro-IN-12
CAS:<p>SARS-CoV-2 Mpro-IN-12 (compound D026) serves as an inhibitor of the main protease (Mpro) of SARS-CoV-2, exhibiting antiviral properties [1].</p>Formula:C20H17NO3Purity:98%Color and Shape:SolidMolecular weight:319.35Caerulomycin A
CAS:<p>Caerulomycin A (Caerulomycin) (Cerulomycin; Caerulomycin) is an antifungal compound.</p>Formula:C12H11N3O2Purity:99.28%Color and Shape:SolidMolecular weight:229.23Clazuril
CAS:<p>Clazuril, a phenylacetonitrile derivative, treats coccidiosis in poultry by killing Eimeria species.</p>Formula:C17H10Cl2N4O2Color and Shape:SolidMolecular weight:373.19Zndm19
CAS:<p>Zndm19 is an inhibitor of New Delhi Metallo-β-lactamase-1 (NDM-1), utilized in researching drug-resistant bacterial infections [1].</p>Formula:C13H13N3OS2Color and Shape:SolidMolecular weight:291.39RSV L-protein-IN-5
CAS:<p>RSV L-protein-IN-5 (Compound E) serves as a potent inhibitor of the Respiratory Syncytial Virus (RSV), with an EC50 value of 0.1 μM.</p>Formula:C31H36N6O4Purity:98%Color and Shape:SolidMolecular weight:556.66Y18501
CAS:<p>Y18501, an oxysterol-binding protein (OSBPI) inhibitor structurally akin to Oxathiapiprolin, demonstrates potent inhibition against Phytophthora spp.</p>Formula:C27H26F2N6O2SColor and Shape:SolidMolecular weight:536.6HIV-IN-8
CAS:<p>HIV-IN-8 (Compound 9) acts as an HIV inhibitor, suppressing HIV replication with an effective concentration (EC50) of 13 μg/mL [1].</p>Formula:C36H30O16Color and Shape:SolidMolecular weight:718.61WRNA10
CAS:<p>WRNA10 is a potent binding agent for HIV-1TAR RNA (IC50: 10 μM, CC50: 40 μM).</p>Formula:C25H32N4O4Color and Shape:SolidMolecular weight:452.55BMY-43748
CAS:<p>BMY-43748 is an antibacterial compound with great in vitro and in vivo antibacterial activity.</p>Formula:C20H17F3N4O3Purity:98%Color and Shape:SolidMolecular weight:418.37MPI8
CAS:<p>MPI8 is a SARS-CoV-2 Protease inhibitor (IC50 = 105 nM).</p>Formula:C32H48N4O7Color and Shape:SolidMolecular weight:600.75SARS-CoV-2-IN-66
CAS:<p>SARS-CoV-2-IN-66 (1), a derivative of vitamin K, functions as an inhibitor of SARS-CoV-2, exhibiting an effective concentration (EC50) of 70.8 μM in VeroE6/</p>Formula:C28H30O2Purity:98%Color and Shape:SolidMolecular weight:398.54Antifungal agent 24
CAS:<p>Antifungal agent 24 (Compound 6) is an antifungal agent that inhibits Candida albicans (MIC: 0.03 μg/ml).</p>Formula:C24H18F2N4OColor and Shape:SolidMolecular weight:416.42Bio-AMS
CAS:<p>Bio-AMS is a potent inhibitor of bacterial biotin protein ligase, exhibiting selective activity against Mycobacterium tuberculosis (Mtb) and disrupting fatty</p>Formula:C20H29N9O7S2Color and Shape:SolidMolecular weight:571.63Antimalarial agent 10
CAS:<p>Compound 17b, an amino alcohol-quinoline, targets Pf3D7 (IC50: 14.9 nM) and PfW2 (IC50: 11 nM) with selectivity index >770.</p>Formula:C23H22F6N2O2Color and Shape:SolidMolecular weight:472.42GSK3839919A
CAS:<p>GSK3839919A is a potent allosteric inhibitor of HIV-1 integrase [1].</p>Formula:C36H46ClN3O3Color and Shape:SolidMolecular weight:604.22U 104489
CAS:<p>U 104489 (PNU-104489) is a novel specific inhibitor of human immunodeficiency virus 1 (HIV-1), showing effective activity against BHA-P-resistant HIV-1MF.</p>Formula:C26H36N6O3SColor and Shape:SolidMolecular weight:512.67RO-7
CAS:<p>RO-7 is a next-generation polymerase (PA) endonuclease influenza A and B viruses inhibitor.</p>Formula:C24H20F3N3O3SPurity:98%Color and Shape:SolidMolecular weight:487.49L 687908
CAS:<p>L 687908 is a potent inhibitor of hydroxyethylene-containing HIV protease.</p>Formula:C40H51N5O5Purity:98%Color and Shape:SolidMolecular weight:681.86Fenpropidin
CAS:<p>Fenpropidin (Ro-12-3049), a fungicide, is a specific inhibitor of sterol 14-reductase and biosynthesis.</p>Formula:C19H31NPurity:98.58% - 99.54%Color and Shape:SolidMolecular weight:273.46Myrrhterpenoid O
CAS:<p>Unfortunately, you did not provide the description of the chemical compound that needs to be rewritten.</p>Formula:C16H20O3Purity:98%Color and Shape:SolidMolecular weight:260.33D1N52
CAS:<p>D1N52 is a potent inhibitor of the SARS-CoV-2 3CL protease, demonstrating an inhibitory concentration half-maximal (IC50) value of 0.53 μM [1].</p>Formula:C20H13F4N5O3Purity:98%Color and Shape:SolidMolecular weight:447.34NEU-730
CAS:<p>NEU-730, a novel inhibitor of TbrPDEB1, shows modest inhibition of T. brucei proliferation.</p>Formula:C25H29NO5Purity:98%Color and Shape:SolidMolecular weight:423.5MK-3281
CAS:<p>MK-3281: Oral, potent HCV NS5B inhibitor with promising properties and efficacy in replication trials, suitable for clinical use.</p>Formula:C29H37N3O3Color and Shape:SolidMolecular weight:475.62Capravirine
CAS:<p>Capravirine, a non-nucleoside reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.</p>Formula:C20H20Cl2N4O2SPurity:98%Color and Shape:SolidMolecular weight:451.37Ibuzatrelvir
CAS:<p>Ibuzatrelvir (PF-07817883) is an antiviral compound designed to inhibit the SARS-CoV-2 3CL protease, and is utilized in the treatment of COVID-19 [1].</p>Formula:C21H30F3N5O5Purity:98%Color and Shape:SolidMolecular weight:489.49WRN inhibitor 5
CAS:<p>WRN Inhibitor 5 (Example 157), a cyclic vinyl sulfone-based compound, serves as an inhibitor of Werner Syndrome ATP-dependent helicase enzyme (WRN).</p>Formula:C23H20N2O6SColor and Shape:SolidMolecular weight:452.48Cefteram
CAS:<p>Cefteram (T-2525), an orally active ester of the cephalosporin class, is the free acid form of Cefteram pivoxil.</p>Formula:C16H17N9O5S2Color and Shape:SolidMolecular weight:479.49Sulfisoxazole acetyl
CAS:<p>Sulfisoxazole acetyl (Gantrisin) is an agent with antibacterial activity.</p>Formula:C13H15N3O4SPurity:99.85%Color and Shape:SolidMolecular weight:309.34Anti-MRSA agent 5
CAS:<p>Potent anti-MRSA compound, MIC50: 0.38 μg/mL, minimal hERG activity (IC50: 40 μM), low toxicity, and resistance unlikely.</p>Formula:C25H22N4O4Color and Shape:SolidMolecular weight:442.47JTK-853
CAS:<p>JTK-853: novel non-nucleoside HCV polymerase inhibitor with strong antiviral activity (EC50: 0.38 μM genotype 1a, 0.035 μM 1b).</p>Formula:C28H23F7N6O4S2Purity:98%Color and Shape:SolidMolecular weight:704.64TH-Z145
CAS:<p>TH-Z145 is a potent FPPS inhibitor for the study of myeloma and lung cancer.</p>Formula:C16H28O7P2Purity:98.29%Color and Shape:SolidMolecular weight:394.34Urease-IN-6
CAS:<p>Urease-IN-6, a potent Urease inhibitor, exhibits an IC50 value of 14.2 μM and is utilized in the research of peptic and gastric ulcers [1].</p>Formula:C18H19N3OSColor and Shape:SolidMolecular weight:325.43N,O-Diacetyltyramine
CAS:<p>N,O-Diacetyltyramine, isolated from the actinomycete Pseudonocardia endophytica VUK-10, exhibits both antibacterial activity against Gram-positive and Gram-negative bacteria, alongside fungi, and demonstrates cytotoxicity towards MDA-MB-231, HeLa, MCF-7, and OAW-42 cells [1].</p>Formula:C12H15NO3Color and Shape:SolidMolecular weight:221.25VT-1598
CAS:<p>VT-1598 is a novel, selective, orally active fungal CYP51 inhibitor. VT-1598 exhibits antifungal effects against Candida albicans.</p>Formula:C31H20F4N6O2Color and Shape:SolidMolecular weight:584.52DDD85646
CAS:<p>DDD85646 is an inhibitor of T. brucei N-myristoyltransferase with a Ki of 1.44 nM, an IC50 of 2 nM and an EC50 of 2 nM. The IC50 of hNMT is 4 nM.</p>Formula:C21H24Cl2N6O2SPurity:97.8% - 99.76%Color and Shape:SolidMolecular weight:495.43Propiolactone
CAS:<p>Propiolactone (β-propiolactone; 2-Oxetanone), a chemosterilant, effectively inactivates viruses, rendering them non-infectious.</p>Formula:C3H4O2Purity:98%Color and Shape:SolidMolecular weight:72.06KY386
CAS:<p>KY386 is a potent and selective DHX33 helicase inhibitor with an IC50 value of 19 nM.</p>Formula:C21H19N5O2SColor and Shape:SolidMolecular weight:405.478-NH2-ATP tetrasodium
CAS:<p>8-NH2-ATP tetrasodium, an inactive ATP variant, originates from 8-NH2-Ado tetrasodium, which triggers the apoptosis-associated cleavage of poly (ADP-ribose) polymerase [1] [2].</p>Formula:C10H13N6Na4O13P3Color and Shape:SolidMolecular weight:610.12Micronomicin
CAS:<p>Micronomicin (Gentamicin C2b) is an antibiotic exhibiting antibacterial and bactericidal capacity.</p>Formula:C20H41N5O7Purity:97.05% - 99.79%Color and Shape:SolidMolecular weight:463.57WRN inhibitor 2
CAS:<p>WRN Inhibitor 2 (example 118), a potent inhibitor of the WRN (Werner Syndrome ATP-dependent helicase enzyme), exhibits a pIC50 value of 7.0 or greater [1].</p>Formula:C15H11F3N2O5S2Purity:98%Color and Shape:SolidMolecular weight:420.38Inz-5
CAS:<p>Inz-5 is a fungal-selective inhibitor of mitochondrial cytochrome bc1. Inz-5 impairs fungal virulence. It also prevents the evolution of drug resistance.</p>Formula:C18H14F4N6Color and Shape:SolidMolecular weight:390.34Variculanol
CAS:<p>Variculanol, a compound with antimicrobial, anticancer, and anti-HCV NS3/4A protease properties, is derived from the marine fungus Aspergillus versicolor [1].</p>Formula:C25H40O2Color and Shape:SolidMolecular weight:372.58Aminoacyl tRNA synthetase-IN-1
CAS:<p>Aminoacyl tRNA synthetase-IN-1 is an inhibitor of bacterial aminoacyl tRNA synthetase (aaRS).</p>Formula:C16H25N7O7SPurity:98%Color and Shape:SolidMolecular weight:459.48NCI-B16
CAS:<p>NCI-B16 is a small-molecule RNA binder that inhibits HCV (hepatitis C virus) replication [1].</p>Formula:C27H26N8O4Color and Shape:SolidMolecular weight:526.55Daldinone A
CAS:<p>Daldinone A (Compound 4), isolated from Nigrospora oryzae, exhibits antibacterial properties, specifically demonstrating antimicrobial potential against P. aeruginosa [1].</p>Formula:C20H16O5Color and Shape:SolidMolecular weight:336.34HBV-IN-8
CAS:<p>HBV-IN-6 is a potent inhibitor of HBV (EC50: 287.9 nM).</p>Formula:C21H25ClFN5O5S2Color and Shape:SolidMolecular weight:546.04Ro 31-8588
CAS:<p>Talviraline (HBY 097) inhibits HIV-1 replication and reduces cell death in various cells and immune cells.</p>Formula:C33H56N4O5Color and Shape:SolidMolecular weight:588.82Zoxamide
CAS:<p>Zoxamide (RH-7281) is an oomycete-specific fungicide that impedes nuclear division in Phytophthora capsici germlings and disrupts the microtubule cytoskeleton [</p>Formula:C14H16Cl3NO2Color and Shape:SolidMolecular weight:336.64Antibacterial agent 93
<p>Antibacterial agent 93: potent aaRS inhibitor; effective against certain gram-positive and negative bacteria.</p>Formula:C29H28Cl3N5O4Color and Shape:SolidMolecular weight:616.92Mtb-IN-4
CAS:<p>Mtb-IN-4 (compound 17h) is a non-toxic isoxazole that exhibits anti-Mycobacterium tuberculosis (Mtb) activity, with an IC50 value of 0.70 μM.</p>Formula:C24H18N2O4SColor and Shape:SolidMolecular weight:430.48Tuberculosis inhibitor 6
CAS:<p>Tuberculosis inhibitor 6 (compound 2c), a 3-methoxy-2-phenylimidazo[1,2-b]pyridazine derivative, is highly active against Mycobacterium tuberculosis (MIC 90 of</p>Formula:C21H19N3O2SColor and Shape:SolidMolecular weight:377.46DQn-1
CAS:<p>DQn-1, a potent antifolate, demonstrates efficacy against Mycobacterium tuberculosis (Mtb) with an MIC 90 of 0.03 µM.</p>Formula:C16H14ClN5O2Color and Shape:SolidMolecular weight:343.77A 33853
CAS:<p>A 33853 is an antibiotic isolated from culture broth of Streptomyces sp.</p>Formula:C20H13N3O6Color and Shape:SolidMolecular weight:391.33Droxinavir HCl
CAS:<p>Droxinavir HCl is an antiviral agent and HIV protease inhibitor.</p>Formula:C29H52ClN5O4Purity:98%Color and Shape:SolidMolecular weight:570.22β-Gal-NONOate
CAS:<p>Beta-gal-nonoate, a β-galactosidase dependent nitric oxide (NO) donor, releases NO upon activation by β-galactosidase. It exhibits bactericidal activity, thus serving as an effective bactericide [1].</p>Formula:C10H19N3O7Color and Shape:SolidMolecular weight:293.27EDI048
CAS:<p>EDI048, also known as compound 1.16, is an orally active inhibitor of Cryptosporidium PI4K, utilized in the study of cryptosporidiosis [1].</p>Formula:C25H21ClN4O4Purity:98%Color and Shape:SolidMolecular weight:476.91Antimicrobial photosensitizer-1
CAS:<p>Photosensitizer-1 shows promise in treating infections, effective against S. aureus in mouse wounds.</p>Formula:C19H19BF2I3N3Color and Shape:SolidMolecular weight:718.9Influenza virus-IN-6
CAS:<p>Influenza virus-IN-6 (Compound 35) serves as a potent inhibitor targeting the N-terminal domain of the polymerase acidic protein (PA N ) endonuclease subunit of</p>Formula:C27H26ClNO7Purity:98%Color and Shape:SolidMolecular weight:511.95Brevicompanine B
CAS:<p>Brevicompanine B: fungal metabolite, regulates plant growth/circadian rhythm, inhibits Arabidopsis roots, affects gene transcription, anti-P. falciparum.</p>Formula:C22H29N3O2Color and Shape:SolidMolecular weight:367.48ThrRS-IN-3
<p>ThrRS-IN-3: Potent inhibitor of Salmonella enterica ThrRS, IC50 = 19 nM, Kd = 34 nM, with antibacterial effects.</p>Formula:C31H30Cl2N6O5Color and Shape:SolidMolecular weight:637.51LtaS-IN-1
CAS:<p>LtaS-IN-1 inhibits LTA synthesis in MDR E. faecium; alters cell walls; MIC: 0.5-64 μg/mL for 28 Enterococcus strains.</p>Formula:C24H17N3O5Purity:93.44%Color and Shape:SolidMolecular weight:427.41Hinokinin
CAS:<p>Hinokinin (Cubebinolide), a bioactive lignan, exhibits a broad spectrum of pharmacological activities.</p>Formula:C20H18O6Color and Shape:SolidMolecular weight:354.35SARS-CoV-2 3CLpro-IN-2
CAS:<p>SARS-CoV-2 3CLpro-IN-2 is a potent inhibitor of the 3CL protease pair and has shown research potential for SARS-CoV-2 disease.</p>Formula:C21H18F5N5O4Color and Shape:SolidMolecular weight:499.39(1R,4S)-Yimitasvir diphosphate
CAS:<p>Yimitasvir diphosphate, also known as Emitasvir, is an orally-administered inhibitor of the hepatitis C virus (HCV) nonstructural protein 5A (NS5A).</p>Formula:C49H64N8O14P2Color and Shape:SolidMolecular weight:1051.03CPFX2090
CAS:<p>CPFX2090, a cephalosporin antibacterial compound.</p>Formula:C28H28ClNO6Purity:98%Color and Shape:SolidMolecular weight:509.98CDD-1733
CAS:<p>CDD-1733 is a potent, non-covalent, and non-peptide inhibitor of the SARS-CoV-2 main protease (Mpro) with an inhibition constant (K i) of 12 nM.</p>Formula:C34H32F3N5O2Purity:98%Color and Shape:SolidMolecular weight:599.65Antibacterial compound 1
CAS:<p>Antibacterial compound 1 is an antibacterial compound.</p>Formula:C14H16FN3O4Purity:98%Color and Shape:SolidMolecular weight:309.29Valtorcitabine dihydrochloride
CAS:<p>Valtorcitabine dihydrochloride, a DNA polymerase inhibitor, is used potentially for the treatment of HBV infection.</p>Formula:C14H24Cl2N4O5Color and Shape:SolidMolecular weight:399.27SA09-Cu
CAS:<p>SA09-Cu is a potent, noncompetitive inhibitor of NDM-1, with an IC50 of 9.6 nM.</p>Formula:C8H16CuN2O2S4Color and Shape:SolidMolecular weight:364.03SPR38
<p>SPR38: SARS-CoV-2 protease inhibitor with Ki 0.260 μM; also blocks hCatL (Ki 1.92 μM) and hCatB (Ki 11.1 μM).</p>Formula:C24H33N3O5Color and Shape:SolidMolecular weight:443.54(S)-Mosnodenvir
CAS:<p>(S)-Mosnodenvir, a pan-serotype dengue antiviral agent, exhibits picomolar to low nanomolar in vitro activity with a high barrier to resistance and is</p>Formula:C26H22ClF3N2O6SPurity:98%Color and Shape:SolidMolecular weight:582.98
