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(947 products)
- Antifection(27 products)
- DHFR(30 products)
- DNA/RNA Synthesis(808 products)
- HBV(187 products)
- HIV Protease(507 products)
- HSV(99 products)
- Integrase(2 products)
- Ribosome(5 products)
Show 2 more subcategories
Found 6444 products of "Microbiology/Virology"
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
MmpL3-IN-2
CAS:MmpL3-IN-2, an inhibitor targeting MmpL3, exhibits low cytotoxicity and moderate metabolic stability, making it suitable for tuberculosis research [1].Formula:C27H30N2Color and Shape:SolidMolecular weight:382.54Antibacterial 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:344.39Mycobactin-IN-1
CAS:Mycobactin-IN-1, a pyrazoline analogue, inhibits MbtA, key in mycobactin synthesis, targeting mycobacteria.Formula:C15H13ClN2OColor and Shape:SolidMolecular weight:272.73Chitin synthase inhibitor 3
CAS:Compound 2d is a potent chitin synthase inhibitor (IC50: 0.16 mM, MIC: 1 μg/mL vs. Candida albicans) with antifungal properties.Formula:C20H19N3O4Color and Shape:SolidMolecular weight:365.38Fosclevudine alafenamide
CAS:Fosclevudine alafenamide (Compound EIDD-02173) is an antiviral agent that acts against HBV (EC50: 1.71 μM).Formula:C22H29FN3O9PColor and Shape:SolidMolecular weight:529.45PNU-101603
CAS:PNU-101603, a Sutezolid metabolite, effective against TB including drug-resistant strains, works solo or with SQ109.Formula:C16H20FN3O4SColor and Shape:SolidMolecular weight:369.41SARS-CoV-2 Mpro-IN-1
CAS: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].Formula:C15H11FN2O2SColor and Shape:SolidMolecular weight:302.32Antitubercular agent-39
CAS:Antitubercular agent-39 (Compound P1) is a potent agent effective against both drug-resistant strains and drug-susceptible clinical isolates of tuberculosis,Formula:C26H30N4O2Color and Shape:SolidMolecular weight:430.54RYL-552S
CAS:RYL-552S is a drug-resistant strain of Plasmodium falciparum that effectively kills the asexual blood stage of the parasite in vitro.Formula:C24H17F4NOSColor and Shape:SolidMolecular weight:443.46Diethyl 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:329.52Antiviral agent 18
CAS:Compound 5, an antiviral agent, effectively targets murine norovirus, with potential in infectious disease and oncology research.Formula:C11H13ClN4O4Color and Shape:SolidMolecular weight:300.7Crisnatol
CAS:Crisnatol (BWA770U) is an oral anticancer DNA intercalator, toxic to breast cancer cells, not skin fibroblasts.Formula:C23H23NO2Color and Shape:SolidMolecular weight:345.43GAK inhibitor 2
CAS:GAK inhibitor 2, IC50: 0.024μM, strongly blocks GAK; potent against dengue virus, EC50: 1.049μM.Formula:C20H23N3O3SColor and Shape:SolidMolecular weight:385.48Antimicrobial agent-4
CAS:Antimicrobial agent-4 (6a) has potent activity against pathogens; binds target enzyme with 10.0 kcal/mol affinity.Formula:C22H16ClN5O2SColor and Shape:SolidMolecular weight:449.91(Z)-Fluoxastrobin
CAS:(Z)-Fluoxastrobin is a fungicide that exhibits effective control of important seed and soil-borne pathogens.Formula:C21H16ClFN4O5Color and Shape:SolidMolecular weight:458.83Antibacterial agent 131
Antibacterial agent 131 is a compound with antibacterial properties.Formula:C24H17ClN4OSPurity:99.63%Color and Shape:SolidMolecular weight:444.94As-358
CAS:As-358 has inhibitory effects against Ebola virus (IC50 = 47.5 μM) and Marburg virus (IC50 = 3.7 μM) [1].Formula:C18H31NO2Color and Shape:SolidMolecular weight:293.4413(S)-HpOTrE
CAS:13(S)-HpOTrE, a fatty acid from soy LO-2 action on α-linolenic acid, forms in soybeans (9:1 ratio). It generates plant defense signals against pests.Formula:C18H30O4Color and Shape:SolidMolecular weight:310.43Urease-IN-4
Urease-IN-4 inhibits urease (IC50: 1.64 µM), targets P. vulgaris (IC50: 15.27 µg/mL), and is low in cytotoxicity.Formula:C16H20N2O3SColor and Shape:SolidMolecular weight:320.41SPR39
SPR39 inhibits SARS-CoV-2 protease (Ki: 0.252µM), with lesser effect on hCatL/B, and has antiviral, cytotoxic properties.Formula:C24H31N3O5Color and Shape:SolidMolecular weight:441.524-((4-((4-Aminophenyl)sulfonyl)phenyl)amino)-4-oxobutanoic acid
CAS:4-((4-((4-Aminophenyl)sulfonyl)phenyl)amino)-4-oxobutanoic acid is a sulfonamide compound that can be used as an anti infective agent [1].Formula:C16H16N2O5SColor and Shape:SolidMolecular weight:348.37HBV-IN-4
CAS:HBV-IN-4, a phthalazinone, inhibits HBV DNA replication orally (IC50: 14 nM), encouraging genome-free capsids with strong anti-HBV effects.Formula:C24H19ClFN5O3Color and Shape:SolidMolecular weight:479.89Stemphyperylenol
CAS:Stemphyperylenol: antifungal, targets Alternaria solani, MIC at 1.57 μM.Formula:C20H16O6Color and Shape:SolidMolecular weight:352.34Haloprogin
CAS:Haloprogin is an antifungal agent with inhibitory activity against dermatophytes, Candida, and some Gram-positive bacteria.Formula:C9H4Cl3IOPurity:98.18%Color and Shape:SolidMolecular weight:361.39Neuraminidase-IN-6
CAS:Neuraminidase-IN-6, a 1,3,4-triazole derivative, is a strong NA inhibitor (IC50 = 0.11 μM) used in anti-influenza drug development.Formula:C16H16N4O2SColor and Shape:SolidMolecular weight:328.39MLAF50
CAS:MLAF50 is an inhibitor of the REV1 UBM2-Ubiquitin interaction.Formula:C15H12I2O4Color and Shape:SolidMolecular weight:510.06Antibacterial agent 26
CAS:Antibacterial agent 26 is an antimicrobial compound that is a potent DHFR inhibitor (S. aureus DHFR Ki of 0.020 nM).
Formula:C19H17N5O2Purity:98.86%Color and Shape:SolidMolecular weight:347.37Antimicrobial agent-8
Antimicrobial agent-8: potent against Gram+ & Gram-, 2-8 μg/mL MIC, anti-inflammatory action.Formula:C39H54N16Color and Shape:SolidMolecular weight:746.95HIV-1 inhibitor-56
CAS:HIV-1 inhibitor-56 (compound 12126065) is a potent non-nucleoside reverse transcriptase inhibitor with significant antiviral activity against wild-type HIV-1,Formula:C22H14ClN7O2SColor and Shape:SolidMolecular weight:475.91Cgp 53820
CAS:CGP 53820 is a pseudosymmetric inhibitor of HIV-1 Protease.Formula:C31H51N5O5Color and Shape:SolidMolecular weight:573.77Antifungal agent 69
CAS:Antifungal agent 69 (compound 13), a eugenol-imidazole derivative, demonstrates targeted activity against Candida albicans with a minimum inhibitoryFormula:C23H23ClN2O4Color and Shape:SolidMolecular weight:426.89INSCoV-600K(1)
CAS:INSCoV-600K(1) is a potent inhibitor of Mpro (3CLpro), key in viral replication, with potential against SARS-CoV-2 (Patent WO2021219089A1).Formula:C23H22ClF2N5O2SColor and Shape:SolidMolecular weight:505.97Caprochlorone
CAS:Caprochlorone fights orthopoxvirus, lowers influenza in mice lungs, blocks virus entry, and delays its release from cells.Formula:C19H19ClO3Color and Shape:SolidMolecular weight:330.81Anti-infective agent 5
CAS:Orally active compound 74 targets Trypanosoma cruzi with 0.10 μM IC50, reducing in vivo parasite load.Formula:C18H13N5O3Color and Shape:SolidMolecular weight:347.33HIV-1 inhibitor-33
CAS:HIV-1 inhibitor-33, potent against HIV-1 (EC50: 8.6 nM), low toxicity to MT-4 cells (CC50: 18 μM), useful for AIDS research.Formula:C25H28N6OColor and Shape:SolidMolecular weight:428.53Influenza 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:389.24F594-1001
CAS:F594-1001 (compound 6) serves as a potent, highly selective inhibitor of SARS-CoV-2 Mac1-ADP-ribose, displaying IC 50 values of 8.5 μM, 68 μM, and 45 μM in AS, FP, and FRET assays, respectively. It binds directly to SARS-CoV-2 Mac1 and demonstrates dose-dependent inhibition of Mac1 ADP-ribosylhydrolase activity.Formula:C23H28ClN3O4Color and Shape:SolidMolecular weight:445.94Dutacatib
CAS:Dutacatib is an inhibitor of SARS-CoV-2 3CLpro and cathepsin K, offering antiviral properties and potential benefits in treating cancer-induced bone disease.Formula:C23H31N7OColor and Shape:SolidMolecular weight:421.54Succinate dehydrogenase-IN-1
CAS:Succinate dehydrogenase-IN-1 (Compound 34) acts as an inhibitor of succinate dehydrogenase (SDH), exhibiting an IC50 value of 0.94 μM and a KD of 22.4 μM. This compound also demonstrates antifungal activity, with EC50 values against Rhizoctonia solani, Sclerotinia sclerotiorum, Monilinia fructicola, and Botrytis cinerea measured at 0.04 μM, 1.13 μM, 1.61 μM, and 1.21 μM, respectively.Formula:C20H13F6N3OColor and Shape:SolidMolecular weight:425.33Sulfasymazine
CAS:Sulfasymazine is a sulfonamide drug.Formula:C13H17N5O2SPurity:98%Color and Shape:SolidMolecular weight:307.37FGF22-IN-1
CAS:FGF22-IN-1 is a CD4 N-terminal immunoglobulin variable region-like structural domain (CD4 D1) inhibitor that suppresses the immune response.Formula:C14H11N3OSPurity:99.18%Color and Shape:SolidMolecular weight:269.32Zelpolib
CAS:Zelpolib is a specific inhibitor of DNA polymerase δ (Pol δ), inhibiting DNA replication. antiproliferative.Formula:C22H21N3O5S2Purity:98.79%Color and Shape:SolidMolecular weight:471.55InhA-IN-3
CAS:InhA-IN-3 (TU13) is a Mycobacterium tuberculosis InhA (enoyl ACP reductase) inhibitor for the study of Mycobacterium tuberculosis infection.Formula:C14H12ClN3O2SPurity:99.48%Color and Shape:SolidMolecular weight:321.78InhA-IN-4
CAS:InhA-IN-4 (TU14) is a Mycobacterium tuberculosis InhA (enoyl ACP reductase) inhibitor for the study of Mycobacterium tuberculosis infection.Formula:C14H12BrN3O2SPurity:>99.99%Color and Shape:SolidMolecular weight:366.23Lagociclovir
CAS:Lagociclovir (MIV-210), a nucleoside analogue antiviral, treats HBV by inhibiting its replication in liver cancer cells.Formula:C10H12FN5O3Purity:99.18% - 99.74%Color and Shape:SolidMolecular weight:269.23MMV006833
CAS:MMV006833 is an inhibitor of Plasmodium falciparum. It targets the lipid transfer protein PfSTART1, inhibiting the ring-stage development of Plasmodium falciparum.Formula:C19H27ClN2O4SColor and Shape:SolidMolecular weight:414.95Jobosic acid
CAS:Jobosic acid is a saturated fatty acid and a selective inhibitor of SARS-CoV-2. It inhibits the Mpro and the interaction between spike-RBD/ACE-2 with IC50 values of 7.5 μg/mL and 3 μg/mL, respectively. Jobosic acid also exhibits viral entry inhibition against the omicron variant of SARS-CoV-2.Formula:C16H32O2Color and Shape:SolidMolecular weight:256.42Aliconazole
CAS:Aliconazole is an imidazole derivative with antifungal activity for the study of skin infections.Formula:C18H13Cl3N2Purity:99.21% - 99.79%Color and Shape:SolidMolecular weight:363.67Lipoxamycin 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€Germination-IN-2
CAS:Germination-IN-2 (compound 15) is a potent germination inhibitor (IC50: 1.3 μM) with anti-germination effects (germination rate = 3%).Formula:C30H45NO3Color and Shape:SolidMolecular weight:467.68Chalcone 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€Quinfamide
CAS:Quinfamide is a compound with the potential to treat tropical parasitic infections such as Amoebiasis and Helminthiasis.Formula:C16H13Cl2NO4Purity:99.92%Color and Shape:SolidMolecular weight:354.18Ref: TM-T16705
1mg52.00€5mg100.00€1mL*10mM (DMSO)105.00€10mg147.00€25mg241.00€50mg349.00€100mg479.00€200mg657.00€Datelliptium chloride
CAS:Datelliptium chloride is a DNA-intercalating agent derived from ellipticine. Datelliptium chloride shows anti-tumor activities.Formula:C23H28ClN3OPurity:98%Color and Shape:SolidMolecular weight:397.94DDD01035881
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:404.3Tuberculosis inhibitor 3
CAS:Tuberculosis inhibitor 3 is a highly potent and oral anti-tuberculosis drug against both drug-sensitive and drug-resistant Mycobacterium , H37RV & MDR-TB.Formula:C21H22F6N4O3SPurity:98.8%Color and Shape:SolidMolecular weight:524.48Ref: TM-T38298
1mg71.00€5mg152.00€1mL*10mM (DMSO)170.00€10mg236.00€25mg485.00€50mg713.00€100mg1,063.00€NSC-670224
CAS:NSC-670224 blocks HDAC6 and NF-κB, is toxic to yeast at low µM concentrations, similar to tamoxifen's action.Formula:C21H34Cl3NOPurity:98%Color and Shape:SolidMolecular weight:422.86Nitrobenzofuroxan
CAS:Nitrobenzofuroxan, is a HIV-1 and IDO1 inhibitor.Formula:C6H3N3O4Purity:98%Color and Shape:SolidMolecular weight:181.11REV7/REV3L-IN-1
CAS:REV7/REV3L-IN-1 is a inhibitor of REV7/REV3L interaction(IC50 of 78 μM),Formula:C19H21N3O3SPurity:98%Color and Shape:SolidMolecular weight:371.45DprE1-IN-377790
CAS:DprE1-IN-377790 is a novel DprE1 inhibitor, killing M. tuberculosis.Formula:C13H16N4O2Color and Shape:SolidMolecular weight:260.29Grepafloxacin, (S)-
CAS:Grepafloxacin, (S)- is an oral broad-spectrum fluoroquinolone antibacterial used for the treatment of bacterial infections.Formula:C19H22FN3O3Color and Shape:SolidMolecular weight:359.39INF55
CAS:INF55 inhibits NorA efflux pump.Formula:C14H10N2O2Purity:98%Color and Shape:SolidMolecular weight:238.24HCV-086
CAS:HCV-086, a RNA-directed RNA polymerase (NS5B) inhibitor, is used for the treatment of HCV infection.Formula:C20H21FN2O5SPurity:98%Color and Shape:SolidMolecular weight:420.45A 30641
CAS:A 30641, an epidithioketopiperazine, has in vitro activity against Gram-positive bacteria and fungi.Formula:C12H9ClN2O5S2Purity:98%Color and Shape:SolidMolecular weight:360.79AB-182
CAS:AB-182 is an aziridine derivative with antitumor activity.Formula:C11H22N3O4PColor and Shape:SolidMolecular weight:291.28LY 215891
CAS:LY 215891 is a compound that exhibits potent Gram-negative and Gram-positive antibacterial activity.Formula:C12H10ClN5O5S2Purity:98%Color and Shape:SolidMolecular weight:403.82AHU1
CAS:AHU1 is a blocker of Shiga Toxin expression in Escherichia coli O157:H7.Formula:C14H14N2O3Color and Shape:SolidMolecular weight:258.27BP13944
CAS:BP13944 is used as a potential dengue virus NS2B/NS3 protease inhibitor.Formula:C20H44BrNO2Color and Shape:SolidMolecular weight:410.47DNAC-1
CAS:DNAC-1 is against Gram-positive and Gram-negative pathogens potentiator of β-lactam activity.Formula:C11H9BrN2S2Purity:98%Color and Shape:SolidMolecular weight:313.24R78206
CAS:R 78206 is a pyridazinamine derivative that suppresses the formation of poliovirus eclipse particles.Formula:C22H29N3O3Purity:98%Color and Shape:SolidMolecular weight:383.48GSK951A
CAS:GSK951A blocks EchA6 and FAS-II, halts mycolic acid formation and MAMES in M. bovis BCG; FAMEs stay mostly unchanged.Formula:C24H23F3N4O3Purity:98%Color and Shape:SolidMolecular weight:472.46GSK1829820A
CAS:GSK1829820A is a Mycobacterium tuberculosis H37Rv non-cytotoxic inhibitor.Formula:C15H15N3OSPurity:98%Color and Shape:SolidMolecular weight:285.36GSK5750
CAS:GSK5750 is the ribonuclease H activity inhibitor.Formula:C16H12N4O2SColor and Shape:SolidMolecular weight:324.36Cefcanel daloxate
CAS:Cefcanel daloxate is a pro-drug of KY-087.Formula:C27H27N5O9S3Purity:98%Color and Shape:SolidMolecular weight:661.73MBX2546
CAS:MBX2546, an influenza A inhibitor, stops HA-induced membrane fusion by binding and stabilizing HA. Resistant virus mutations occur near HA2 start.Formula:C18H21N3O5SPurity:98%Color and Shape:SolidMolecular weight:391.44Acaterin
CAS:Acaterin, an inhibitor of acyl-CoA: cholesterol acyltransferase (ACAT), inhibits synthesis of cholesteryl ester in macrophage J774.Formula:C13H22O3Color and Shape:SolidMolecular weight:226.31Benthiavalicarb isopropyl
CAS:Benthiavalicarb isopropyl is a fungicide, specifically targeting downy mildew and blight.Formula:C18H24FN3O3SPurity:98%Color and Shape:SolidMolecular weight:381.465-Et-ddU
CAS:5-Et-ddU: A pyrimidine nucleoside with anti-HIV-1 activity in human blood cells.Formula:C11H16N2O4Purity:98%Color and Shape:SolidMolecular weight:240.26BMS-199945
CAS:BMS-199945 is an Influenza H1N1 Virus inhibitor.Formula:C18H27NO2Purity:98%Color and Shape:SolidMolecular weight:289.41DSM74
CAS:DSM74 is a metabolically stable dihydroorotate dehydrogenase inhibitor that has antimalarial activity.Formula:C13H10F3N5Purity:98%Color and Shape:SolidMolecular weight:293.25Aminoanfol
CAS:Aminoanfol is an antifolic acid agent.Formula:C18H18N8O5Purity:98%Color and Shape:SolidMolecular weight:426.39CID21480113
CAS:CID21480113, an antibacterial agent, is effective in treating dapsone resistant leprosy.Formula:C12H10FNO2SPurity:98%Color and Shape:SolidMolecular weight:251.28BDM31827
CAS:BDM31827 is an EthR inhibitor.Formula:C22H18N2O3SPurity:98%Color and Shape:SolidMolecular weight:390.45FMDP
CAS:FMDP is a glucosamine-6-phosphate synthase inhibitor.Formula:C8H12N2O5Purity:98%Color and Shape:SolidMolecular weight:216.19Isometamidium chloride
CAS:Isometamidium chloride is an antiprotozoal agent. It is also used in veterinary medicine.Formula:C28H26ClN7Purity:98%Color and Shape:SolidMolecular weight:496.01HEPT
CAS:HEPT is a non-nucleoside inhibitor of HIV-1 reverse transcription.Formula:C14H16N2O4SPurity:98%Color and Shape:SolidMolecular weight:308.35L-Ristosamine nucleoside
CAS:L-Ristosamine nucleoside shows antiviral activity.Formula:C21H21N3O7Color and Shape:SolidMolecular weight:427.41Acrisorcin
CAS:Acrisorcin is a topical anti-infective typically used as a fungicide.Formula:C25H28N2O2Purity:98%Color and Shape:SolidMolecular weight:388.5PPT
CAS:PPT is a modulator of water-heme interactions of CYP2C9d and CYP125A1 in low-spin P450 complexes.Formula:C11H13N3Purity:98%Color and Shape:SolidMolecular weight:187.24KSK-120
CAS:KSK-120 is a potent Chlamydia trachomatis inhibitor, it targets the glucose-6-phosphate (G-6P) metabolism pathway of Chlamydia trachomatis.Formula:C28H22N2O2SColor and Shape:SolidMolecular weight:450.55Suberosol
CAS:Suberosol possesses anti-HIV replication activity.Formula:C31H50O2Purity:98%Color and Shape:SolidMolecular weight:454.73Tedizolid phosphate disodium salt
CAS:Tedizolid phosphate: novel prodrug antibiotic targeting MRSA, VRE, and other Gram-positive bacteria.Formula:C17H16FN6Na2O6PPurity:98%Color and Shape:SolidMolecular weight:496.3032-Mc-1,4-NHQ
CAS:2-Mc-1,4-NHQ, an inhibitor of the Cdc42-PBD interaction, blocks the association of Cdc42 with the PBD.Formula:C12H10O3Purity:98%Color and Shape:SolidMolecular weight:202.21DVR-23
CAS:DVR-23 is a potent inhibitor of HBV virus.Formula:C17H17F3N2O3SColor and Shape:SolidMolecular weight:386.39Picoplatin
CAS:Picoplatin, an anti-cancer agent overcoming platinum resistance, alkylates DNA to block replication, transcription, and induce apoptosis.Formula:C6H10Cl2N2PtPurity:98%Color and Shape:SolidMolecular weight:376.14Amphotalide
CAS:Amphotalide is an anthelminthic agent.Formula:C19H20N2O3Purity:98%Color and Shape:SolidMolecular weight:324.37JX040
CAS:JX040 inhibits enterovirus replication, strong against non-polio strains, weak on polioviruses.Formula:C19H17N5OSColor and Shape:SolidMolecular weight:363.44HHL-6
CAS:HHL-6 is a c-Fos and BDNF protein expression modulator.Formula:C19H26N2O3Color and Shape:SolidMolecular weight:330.42
