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(3,423 products)
- Antibiotic(945 products)
- Antifection(27 products)
- DHFR(30 products)
- DNA/RNA Synthesis(808 products)
- HBV(186 products)
- HIV Protease(507 products)
- HSV(99 products)
- Integrase(2 products)
- Ribosome(5 products)
Show 2 more subcategories
Found 6442 products of "Microbiology/Virology"
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
AFN-1252 tosylate
CAS:AFN-1252 tosylate is an enoyl-ACP Reductase inhibitor.Formula:C29H29N3O6SPurity:98%Color and Shape:SolidMolecular weight:547.62MenA-IN-1
MenA IN-1 inhibits MTB's MenA enzyme; IC50=13µM, GIC50=8µM, helps fight tuberculosis spread.Formula:C29H36N2O2Color and Shape:SolidMolecular weight:444.61SCY-078 phosphate
CAS:SCY-078 phosphate is a novel glucan synthesis inhibitor.Formula:C44H70N5O8PColor and Shape:SolidMolecular weight:828.04Docosylferulate
CAS:Docosylferulate is a biochemical that has been studied for its inhibition on Hep G2 cells and anti-tumor activities.Formula:C32H54O4Color and Shape:SolidMolecular weight:502.77Teroxalene hydrochloride
CAS:Teroxalene Hydrochloride is disubstituted piperazine used to treat animals with Schistosoma mansoni.Formula:C28H42Cl2N2OColor and Shape:SolidMolecular weight:493.55Yoshi-864
CAS:Yoshi-864, an alkyl sulfonate, alkylates DNA to hinder replication; potential anti-cancer agent.Formula:C8H20ClNO6S2Color and Shape:SolidMolecular weight:325.83Exeporfinium chloride
CAS:Exeporfinium chloride(XF-73) is an antimicrobial agent that can weaken bacterial cell walls.Formula:C44H50Cl2N6O2Color and Shape:SolidMolecular weight:765.81(R,R)-BAY-Y 3118
CAS:(R,R)-BAY-Y 3118, the R-enantiomer of BAY-Y 3118, exhibits weak bactericidal activity.Formula:C20H21ClFN3O3Color and Shape:SolidMolecular weight:405.85Antimycobacterial agent-1
CAS:Compound 33: antimycobacterial, MIC 1 μg/ml vs M. tuberculosis H37Ra, low toxicity (IC50 143.2 μg/ml in Vero cells).Formula:C18H12N4O5SColor and Shape:SolidMolecular weight:396.38Phosphoglycolohydroxamic acid
CAS:Phosphoglycolohydroxamic acid inhibits aldolase/triose-phosphate isomerase; used in antibacterial/antifungal research.Formula:C2H6NO6PColor and Shape:SolidMolecular weight:171.05AB-506
CAS:AB-506: Oral HBV replication blocker, targets core protein, hinders pgRNA encapsidation, for CHB study.Formula:C21H18ClF2N5O3Color and Shape:SolidMolecular weight:461.85Diamthazole
CAS:Diamthazole (Dimazole) is an antifungal agent that can be used in the infection research[1].Formula:C15H23N3OSColor and Shape:SolidMolecular weight:293.43pUL89 Endonuclease-IN-1
CAS:Compound 13d: potent pUL89 endonuclease inhibitor, IC50 0.88 μM, anti-HCMV activity.Formula:C10H8N2O4SColor and Shape:SolidMolecular weight:252.25SARS-CoV-2 Mpro-IN-6
CAS:SARS-CoV-2 Mpro-IN-6: irreversible Mpro inhibitor, IC50 0.18 μM, selective; doesn't block cathepsins B/F/K/L or caspase 3.Formula:C18H18Cl3N3O2SColor and Shape:SolidMolecular weight:446.78Antibacterial agent 74
CAS:Antibacterial agent 74 (compound 36) has anti-Salmonella activity [1].Formula:C16H20N2O3Color and Shape:SolidMolecular weight:288.34Fungicide4
CAS:Fungicide4 exhibits the high activity against the P. infestans strain.Formula:C14H11N3OColor and Shape:SolidMolecular weight:237.26Ceftobiprole medocaril sodium
CAS:Ceftobiprole medocaril sodium (BAL5788) is a prodrug of broad-spectrum cephalosporin active against MRSA, VRSA, and resistant streptococci.Formula:C26H25N8NaO11S2Color and Shape:SolidMolecular weight:712.64Diazaborine
CAS:Diazaborine disrupts large ribosome formation by inhibiting rRNA maturation and AAA-ATPase Drg1, leading to rapid protein redistribution.Formula:C14H13BN2O3SPurity:98%Color and Shape:SolidMolecular weight:300.14Antitubercular agent-12
CAS:Compound 2c, an effective antitubercular, MIC 1.439 μg/mL, low toxicity with CC50 57.34 μg/mL.Formula:C13H7BrN4O5Color and Shape:SolidMolecular weight:379.12Salifluor
CAS:Salifluor is a broad spectrum antimicrobial agent that has been investigated for its abilities to inhibit dental plaque formation.Formula:C22H24F3NO3Color and Shape:SolidMolecular weight:407.43HIV-1 inhibitor-9
CAS:HIV-1 inhibitor-9 potently blocks WT and NNRTI-resistant HIV strains at low nanomolar levels.Formula:C24H21N5OColor and Shape:SolidMolecular weight:395.46HIV-1 inhibitor-47
CAS:HIV-1 Inhibitor-47 blocks Vif-APOBEC3G interaction, has 14.33 μM IC50, and may yield antianxiety and antipsychotic derivatives.Formula:C12H14N6Color and Shape:SolidMolecular weight:242.28Antibacterial agent 124
CAS:Antibacterial agent 124 inhibits Sa ProRS with an IC50 of 0.18 μM.Formula:C16H17ClFN3O2Color and Shape:SolidMolecular weight:337.78BI-10
CAS:BI-10, paired with fluconazole, hinders fungal growth, increases ROS, decreases MMP, and changes membrane permeability.Formula:C23H17BrN2OColor and Shape:SolidMolecular weight:417.3SSAA09E1
CAS:SSAA09E1 blocks SARS-CoV entry, lowers ACE2-mediated HEK293T cell infection (EC50 = 6.7 μM), and inhibits cathepsin L (IC50 = 5.33 μM).Formula:C7H9N3S2Color and Shape:SolidMolecular weight:199.3Pamaqueside
CAS:Pamaqueside is an anti-atherosclerotic agent.Formula:C39H62O14Purity:98%Color and Shape:SolidMolecular weight:754.9Goitrin
CAS:Goitrin, from glucosinolate reactions, blocks thyroid peroxidase and iodine use, and fights H1N1.Formula:C5H7NOSColor and Shape:SolidMolecular weight:129.18Anti-infective agent 1
CAS:Compound 3a: potent, selective antiprotozoal/antimycobacterial. IC50: P. falciparum 10.95 μM, T. brucei 0.06 μM. MIC against M. smegmatis: 8 μg/mL.Formula:C16H10O2Color and Shape:SolidMolecular weight:234.25ZINC04177596
CAS:ZINC04177596 is a novel Nef Protein Inhibitor with anti-HIV activity.Formula:C22H16N6O4Color and Shape:SolidMolecular weight:428.4Antimalarial agent 20
CAS:Antimalarial agent 20, exhibiting potent efficacy with an IC50 value of 0.6 nM against the P.Formula:C31H38N4O3Color and Shape:SolidMolecular weight:514.66SARS-CoV-2-IN-16
CAS:SARS-CoV-2-IN-16 strongly inhibits NPro, with EC50 of 3.69 μM and Kd of 7.82 μM, suggesting effective binding and antiviral properties.Formula:C17H20N2O2Color and Shape:SolidMolecular weight:284.35Antileishmanial agent-8
CAS:Compound 18: Antileishmanial, IC50=5.64 μM for L. donovani, low toxicity in L-6 cells, IC50=73.9 μM.Formula:C18H16O4Color and Shape:SolidMolecular weight:296.32Antibacterial agent 97
CAS:Antibacterial agent 97 is potent; MIC: 16 μg/mL for E. coli and S. aureus.Formula:C19H23N5SColor and Shape:SolidMolecular weight:353.48Antitubercular agent-26
CAS:Compound 32: oral antitubercular, acts on M. tuberculosis, IC50 ~0.50μM, stable, low cardiotoxicity, non-genotoxic.Formula:C22H23N5O3S2Color and Shape:SolidMolecular weight:469.58RyRs activator 1
CAS:RyRs activator 1 triggers ranibulin receptors; 100% larvicidal at 0.5 mg/L, 90% at 0.01 mg/L.Formula:C21H14ClF3N6O4Color and Shape:SolidMolecular weight:506.82SARS-CoV-2-IN-20
CAS:SARS-CoV-2-IN-20 inhibits virus effectively with 6.5 μM EC50, promising for disease research.Formula:C24H30N2O2Color and Shape:SolidMolecular weight:378.51gp120-IN-2
CAS:gp120-IN-2 is a potent HIV-1 inhibitor (IC50 = 7.5 μM) with low cytotoxicity (CC50 = 112.93 μM).Formula:C15H18N2O5Color and Shape:SolidMolecular weight:306.31(±)-Hydnocarpin
CAS:(±)-Hydnocarpin, a flavonolignan, demonstrates inhibitory activity against S.Formula:C25H20O9Color and Shape:SolidMolecular weight:464.42Antimicrobial agent-22
CAS:Antimicrobial agent-22 (THI 6c) constitutes a broad-spectrum, multi-target antibacterial with notable rapid bactericidal efficacy and effective anti-biofilmFormula:C15H16N4OSPurity:97.86%Color and Shape:SolidMolecular weight:300.38Neuraminidase-IN-9
CAS:Neuraminidase-IN-9 inhibits flu virus neuraminidase H5N1 (IC50: 0.12 μM), H5N2 (IC50: 0.049 μM), H5N6 (IC50: 0.16 μM).Formula:C24H33BrN6O3Color and Shape:SolidMolecular weight:533.46RmlA-IN-1
CAS:RmlA-IN-1 inhibits RmlA enzyme with 0.073 μM IC50, affecting l-Rhamnose synthesis and bacterial wall permeability.Formula:C18H18N4O4SColor and Shape:SolidMolecular weight:386.42Antifungal agent 32
CAS:Antifungal 32 (1a) strongly inhibits Candida albicans growth, filamentation, biofilm, and adhesion.Formula:C25H28N2OColor and Shape:SolidMolecular weight:372.5HCV-IN-33
CAS:HCV-IN-33 (Compound (S)-3i) is an inhibitor of HCV entry.Formula:C31H36ClN5Color and Shape:SolidMolecular weight:514.1ZINC36617540
CAS:ZINC36617540 is a novel Nef Protein Inhibitor with anti-HIV activity.Formula:C21H17N5OColor and Shape:SolidMolecular weight:355.39MC4
CAS:MC4 is a first-in-class inhibitor of ribosomal RNA synthesis with antimicrobial activity against Staphylococcus aureus.Formula:C15H10N2O3Color and Shape:SolidMolecular weight:266.25Antitubercular agent-27
CAS:Antitubercular agent-27: IC50=3.2 μM, MIC=7.8 μM, IC90=7.0 μM; effective against resistant Mycobacterium tuberculosis, low toxicity.Formula:C14H8BrN3O3Color and Shape:SolidMolecular weight:346.14BPH-715
CAS:BPH-715 inhibits the liver-stage growth of P. falciparum with an IC50 of 10 μM for P. falciparum exoerythrocytic forms in HepG2 cells.Formula:C17H31NO7P2Purity:98.91%Color and Shape:SolidMolecular weight:423.38SQ109
CAS: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.Formula:C22H38N2Purity:99.70% - 99.91%Color and Shape:SolidMolecular weight:330.55Ref: TM-T16925
1mg63.00€5mg133.00€1mL*10mM (DMSO)148.00€10mg205.00€25mg439.00€50mg642.00€100mg888.00€500mg1,783.00€Vebufloxacin
CAS:Vebufloxacin (OPC-7251) shows potent antibacterial activity against gram-positive and -negative bacteria, including Staphylococcus aureus and PseudomonasFormula:C19H22FN3O3Purity:98%Color and Shape:SolidMolecular weight:359.39Influenza virus-IN-4
CAS: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.Formula:C23H31FN2O4Color and Shape:SolidMolecular weight:418.5Mt KARI-IN-5
CAS:Mt KARI-IN-5 inhibits MtbKARI with Ki 4.72 μM, has MIC 1.56 μM against MtbH37Rv, and is low in cytotoxicity with IC50 >64 μg/mL in HEK.Formula:C14H10N4O5S3Color and Shape:SolidMolecular weight:410.45RMI 10874
CAS:RMI 10874 is a tilorone analogue. Tilorone is an orally bioavailable antiviral agent.Formula:C21H26N2O4Purity:98%Color and Shape:SolidMolecular weight:370.44Polyketide synthase 13-IN-2
CAS:Comp 42 is a potent PKS13 inhibitor in M. tuberculosis with MIC of 0.25 μg/mL.Formula:C22H21NO5Color and Shape:SolidMolecular weight:379.41BAY-707
CAS:BAY-707: tolerable in mice, no anticancer efficacy; potent, selective MTH1 inhibitor, IC50 = 2.3 nM; good PK profile.Formula:C15H20N4O2Purity:98%Color and Shape:SolidMolecular weight:288.34Antiviral agent 10
CAS:Antiviral agent 10 effectively inhibits the respiratory syncytial virus (RSV) [1], serving as a potent anti-viral compound.Formula:C22H24N2O5Color and Shape:SolidMolecular weight:396.443-Chlorogentisyl alcohol
CAS:3-Chlorogentisyl alcohol: E. coli β-glucuronidase inhibitor (IC50=0.74µM, Ki=0.58µM), antiproliferative, for anti-cancer/inflammatory research.Formula:C7H7ClO3Color and Shape:SolidMolecular weight:174.58Antiparasitic agent-6
CAS:Compound 5b: antiparasitic against L. infantum (IC50 = 3.89 μM), cytotoxic to HepG2 cells (CC50 = 13.64 μM).Formula:C19H15N3O3Color and Shape:SolidMolecular weight:333.34SJ-3366
CAS:SJ3366 is a unique and highly potent nonnucleoside reverse transcriptase human immunodeficiency virus type 1 and HIV-2 inhibitor.Formula:C21H24N2O3Color and Shape:SolidMolecular weight:352.43F8-S40
CAS:F8-S40 is a SARS-CoV-2 main protease inhibitor (IC 50 = 10.88 μM) [1].Formula:C13H11N3O3SColor and Shape:SolidMolecular weight:289.31Cholic Acid anilide
CAS:Cholic acid anilide is a synthetic bile acid derivative that prevents C. difficile R20291 spore germination (IC50 = 1.8 μM).Formula:C30H45NO4Color and Shape:SolidMolecular weight:483.68BPH-1086
CAS:BPH-1086 inhibits IspH, which with RPS1 binds mRNA or integrates into bacterial ribosomes.Formula:C4H8O7P2Color and Shape:SolidMolecular weight:230.05Globosuxanthone A
CAS:Globosuxanthone A: a dihydroxanthenone with anticancer and antifungal properties (MIC: F. graminearum 4, F. solani 8, B. cinerea 16 μg/mL).Formula:C15H12O7Color and Shape:SolidMolecular weight:304.25INSCoV-601I(1)
CAS:INSCoV-601I(1) is a strong 3CLpro inhibitor, key in SARS-CoV-2 replication; potential for research use - WO2021219089A1.Formula:C23H22ClF2N5O2SColor and Shape:SolidMolecular weight:505.97EGFR/HER2/TS-IN-2
CAS: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).Formula:C26H21N7OS2Color and Shape:SolidMolecular weight:511.62Cap-dependent endonuclease-IN-16
CAS:Cap-dependent endonuclease-IN-16, a pyridone derivative, inhibits CEN, showing promise for flu research.Formula:C28H25F2N3O7SColor and Shape:SolidMolecular weight:585.58Anti-infective agent 2
CAS:Compound 3k is antiprotozoal/antimycobacterial, with IC50s: P. falciparum 0.07 μM, T. brucei 2.20 μM; MIC: M. smegmatis 32 μg/mL.Formula:C15H8ClNO2Color and Shape:SolidMolecular weight:269.68HBV-IN-25
CAS:HBV-IN-25: oral HBV cccDNA reducer, anti-HBeAg, anti-HBV (IC50: 0.58/1.15 μM), soluble (>452 μg/mL), non-toxic.Formula:C18H14ClNO4Color and Shape:SolidMolecular weight:343.76MmpL3-IN-1
CAS:MmpL3-IN-1 (compound 32) inhibits MmpL3 with <0.016 μg/mL MIC against M. tuberculosis, aiding drug-resistant TB research.Formula:C20H21F2N3OColor and Shape:SolidMolecular weight:357.4Cap-dependent endonuclease-IN-23
CAS:Cap-dependent endonuclease-IN-23 hinders influenza virus replication by inhibiting CEN, with potential for flu research.Formula:C26H23F2N3O7Color and Shape:SolidMolecular weight:527.47LpxH-IN-AZ1
CAS:LpxH-IN-AZ1: Strong LpxH inhibitor, antimicrobial; IC50 0.36 μM against Klebsiella pneumoniae.Formula:C21H22F3N3O3SPurity:99.84%Color and Shape:SolidMolecular weight:453.48Antibacterial agent 111
CAS:Compound 3: potent against B. cereus & K. pneumonia; MICs: 3.90 & 0.49 μg/mL; targets tyrosyl-tRNA synthetase.Formula:C18H12N6SColor and Shape:SolidMolecular weight:344.39SJ000025081
CAS:SJ000025081, a dihydropyridine, shows potent antimalarial action against P. yoelii in mice.Formula:C28H30FNO5Color and Shape:SolidMolecular weight:479.54Diethyl butylmalonate
CAS:Diethyl butylmalonate shows toxicity to T. pyriformis, with a log(IGC50 -1 ) of 0.557 [1].Formula:C11H20O4Color and Shape:SolidMolecular weight:216.27Dodicin
CAS:Dodicin is a potent disinfectant exhibiting broad-spectrum antimicrobial activity [1].Formula:C18H39N3O2Color and Shape:SolidMolecular weight:329.52BMH-23
CAS:BMH-23 is an RNA polymerase I inhibitor that acts by causing nucleolar stress and showing potent anticancer activity across many tumor types.Formula:C15H15N3Purity:98%Color and Shape:SolidMolecular weight:237.3DHX9-IN-1
CAS:DHX9-IN-1 is a potent ATP-dependent RNA helicase A (DHX9) inhibitor, exhibiting an IC50 of 9.45 nM and demonstrating antitumor activity [1].Formula:C21H21F2N5O3SColor and Shape:SolidMolecular weight:461.49Ref: TM-T82569
1mg205.00€5mg528.00€1mL*10mM (DMSO)537.00€10mg782.00€25mg1,161.00€50mg1,558.00€100mg2,322.00€Exalamide
CAS:Exalamide (2-(Hexyloxy)benzamide) is an aromatic amide with antifungal activity used in the study of dermatophytes.Formula:C13H19NO2Purity:99.61%Color and Shape:White PowderMolecular weight:221.3PknB-IN-2
CAS:PknB-IN-2 (Compound 10) is an inhibitor of Mycobacterium tuberculosis protein kinase B (PknB) (IC50: 12.1 μM).Formula:C28H32N2O4Color and Shape:SolidMolecular weight:460.56S.pombe lumazine synthase-IN-1
CAS:S.pombe lumazine synthase-IN-1 inhibits lumazine synthases: Ki of 243μM for S.pombe, 9.6μM for M.tuberculosis.Formula:C14H13N3O6Color and Shape:SolidMolecular weight:319.27HSV-1/HSV-2-IN-2
CAS:HSV-1/HSV-2-IN-2 is a compound that acts as an inhibitor of HSV-1, HSV-2, and VV, demonstrating antiviral activity with EC50 values of 6.8, 8.9, and 8.9 μM,Formula:C17H14ClFN4OSColor and Shape:SolidMolecular weight:376.84Pirlindole free base
CAS:Pirlindole is a reversible inhibitor of monoamine oxidase A (RIMA). It is structurally and pharmacologically related to metralindole.Formula:C15H18N2Color and Shape:SolidMolecular weight:226.32INSCoV-614(1B)
CAS:INSCoV-614(1B), a potent Mpro inhibitor, may help fight SARS-CoV-2, per patent WO2021219089A1.Formula:C23H21ClF3N5O3Color and Shape:SolidMolecular weight:507.89Helioxanthin derivative 5-4-2
CAS:Helioxanthin derivative 5-4-2 （Helioxanthin 5-4-2） is an analogue of helioxanthin that shows anti-HBV activity in vitro and can be used to study HBV.Formula:C20H13NO5Purity:99.91% - 99.92%Color and Shape:SolidMolecular weight:347.32Influenza virus-IN-5
CAS:Influenza virus-IN-5 (Compound 5f) is an influenza virus hemagglutinin (HA) inhibitor that acts on the A/H3N2 virus (EC50: 1 nM).Formula:C21H26ClN3O2SColor and Shape:SolidMolecular weight:419.97Urease-IN-7
CAS:Urease-IN-7 (Compound 5k) acts as a competitive inhibitor of the enzyme urease, exhibiting an IC50 value of 3.33 μM and a K_i of 3.62 μM.Formula:C16H10BrFN4SColor and Shape:SolidMolecular weight:389.24MMV687807
CAS:MMV687807: potent anthelmintic, IC50 0.15 μM, CC50 1.69 μM against T. gondii.Formula:C15H8ClF6NO2Color and Shape:SolidMolecular weight:383.67(S)-BI-1001
CAS:(S)-BI-1001 is an active S-enantiomer of BI-1001. (S)-BI-1001 has antiviral potency against HIV-1 integrase (IC50: 28 nM, and EC50: 450 nM and a Kd: 4.7 μM).Formula:C19H15BrClNO3Purity:98%Color and Shape:SolidMolecular weight:420.68Navuridine
CAS:Navuridine (AZdU) is an oral active inhibitor of HIV reverse transcriptase with a relatively short half-life.Formula:C9H11N5O4Purity:99.83%Color and Shape:SolidMolecular weight:253.22RDEA-806 free acid
CAS:RDEA-806, a reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.Formula:C24H18BrClN4O3SColor and Shape:SolidMolecular weight:557.85Antiparasitic agent-2
CAS:Compound 8a: potent against L. infantum (IC50=7.28μM) & T. cruzi (IC50=2.30μM); mildly toxic to HepG2 (CC50=26.79μM).Formula:C20H17N3O3Color and Shape:SolidMolecular weight:347.37Dapabutan
CAS:Dapabutan is an antimicrobial agent active against Gram-positive bacteria.Formula:C19H40N2O2Color and Shape:SolidMolecular weight:328.53Lipoxamycin hemisulfate
CAS:Lipoxamycin hemisulfate (Lipoxamycin) is an inhibitor of serine palmitoyltransferase (IC50 = 21 nM) with antifungal activity.Formula:C38H74N4O14SPurity:99.14% - 99.93%Color and Shape:SolidMolecular weight:843.08Ref: TM-T26308
1mg55.00€2mg79.00€5mg116.00€1mL*10mM (DMSO)126.00€10mg188.00€25mg424.00€50mg723.00€100mg1,225.00€200mg1,644.00€Stampidine
CAS:Stampidine prevents HIV-1, effective against resistant strains at subnanomolar levels.Formula:C20H23BrN3O8PPurity:98%Color and Shape:SolidMolecular weight:544.29Chalcone 4 hydrate
CAS:Chalcone 4 hydrate, an anti-parasite compound, inhibits the growth of Theileria and Babesia.Formula:C16H15ClO4Purity:99.54%Color and Shape:SolidMolecular weight:306.74AS-136A
CAS:AS-136A is an orally active MV RdRp inhibitor with antiviral activity that inhibits measles virus and blocks viral RNA synthesis.Formula:C17H19F3N4O3SPurity:98.52%Color and Shape:SolidMolecular weight:416.42Ref: TM-T62160
1mg215.00€5mg537.00€1mL*10mM (DMSO)590.00€10mg802.00€25mg1,369.00€50mg1,783.00€100mg2,395.00€MK-2048
CAS:MK-2048 is a potent inhibitor of integrase (IN) and INR263K with IC50 of 2.6 nM and 1.5 nM, respectively.Formula:C21H21ClFN5O4Purity:98%Color and Shape:SolidMolecular weight:461.87Lufotrelvir
CAS:Lufotrelvir (PF-07304814), a prodrug of PF-00835231, is a potent SARS-CoV-2 3CL protease inhibitor with antiviral properties, Ki 174nM.Formula:C24H33N4O9PPurity:99.43% - >99.99%Color and Shape:SolidMolecular weight:552.51DDD01035881
CAS:DDD01035881 is a anti-malarial drug that blocks parasite-to-mosquito transmission by targeting the Plasmodium vesicle membrane protein Pfs16.Formula:C14H14BrNO4S2Purity:99.78%Color and Shape:SolidMolecular weight:404.3AP-C5
CAS:AP-C5 inhibits cGKII with a Pic50 of 7.2, useful in diarrheal disease research.Formula:C16H13N5Purity:99.82%Color and Shape:SolidMolecular weight:275.31Chlamydia pneumoniae-IN-1
CAS:Chlamydia pneumoniae-IN-1 (compound 55), a benzimidazole derivative, exhibits potent antibacterial activity, inhibiting 99% of C.Formula:C19H15N3OSPurity:97.71%Color and Shape:SolidMolecular weight:333.41
