Microbiologia/Virologia
Os inibidores de microbiologia e virologia são compostos que têm como alvo microrganismos, incluindo bactérias, vírus e fungos, interrompendo seu crescimento, replicação ou sobrevivência. Esses inibidores são essenciais para estudar a patogênese microbiana, entender os mecanismos de resistência e desenvolver novas terapias antimicrobianas e antivirais. Os inibidores nessa categoria são usados para combater doenças infecciosas, explorar a ecologia microbiana e investigar as interações hospedeiro-patógeno. Na CymitQuimica, oferecemos uma ampla seleção de inibidores de alta qualidade para microbiologia e virologia para apoiar sua pesquisa em doenças infecciosas, microbiologia e virologia.
Subcategorias de "Microbiologia/Virologia"
- Antibacteriano(2.968 produtos)
- Antibiótico(922 produtos)
- Antifecção(23 produtos)
- DHFR(33 produtos)
- Síntese de DNA/RNA(711 produtos)
- HBV(177 produtos)
- HIV Protease(451 produtos)
- HSV(91 produtos)
- Integrase(2 produtos)
- Ribossomo(13 produtos)
Exibir 2 mais subcategorias
Foram encontrados 5863 produtos de "Microbiologia/Virologia"
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Grepafloxacin, (S)-
CAS:<p>Grepafloxacin, (S)- is an oral broad-spectrum fluoroquinolone antibacterial used for the treatment of bacterial infections.</p>Fórmula:C19H22FN3O3Cor e Forma:SolidPeso molecular:359.39DNAC-1
CAS:<p>DNAC-1 is against Gram-positive and Gram-negative pathogens potentiator of β-lactam activity.</p>Fórmula:C11H9BrN2S2Pureza:98%Cor e Forma:SolidPeso molecular:313.24Acaterin
CAS:Acaterin, an inhibitor of acyl-CoA: cholesterol acyltransferase (ACAT), inhibits synthesis of cholesteryl ester in macrophage J774.Fórmula:C13H22O3Cor e Forma:SolidPeso molecular:226.31Benthiavalicarb isopropyl
CAS:Benthiavalicarb isopropyl is a fungicide, specifically targeting downy mildew and blight.Fórmula:C18H24FN3O3SPureza:98%Cor e Forma:SolidPeso molecular:381.465-Et-ddU
CAS:5-Et-ddU: A pyrimidine nucleoside with anti-HIV-1 activity in human blood cells.Fórmula:C11H16N2O4Pureza:98%Cor e Forma:SolidPeso molecular:240.26BMS-199945
CAS:<p>BMS-199945 is an Influenza H1N1 Virus inhibitor.</p>Fórmula:C18H27NO2Pureza:98%Cor e Forma:SolidPeso molecular:289.41DVR-23
CAS:<p>DVR-23 is a potent inhibitor of HBV virus.</p>Fórmula:C17H17F3N2O3SCor e Forma:SolidPeso molecular:386.39Picoplatin
CAS:<p>Picoplatin, an anti-cancer agent overcoming platinum resistance, alkylates DNA to block replication, transcription, and induce apoptosis.</p>Fórmula:C6H10Cl2N2PtPureza:98%Cor e Forma:SolidPeso molecular:376.14Amphotalide
CAS:<p>Amphotalide is an anthelminthic agent.</p>Fórmula:C19H20N2O3Pureza:98%Cor e Forma:SolidPeso molecular:324.37JX040
CAS:<p>JX040 inhibits enterovirus replication, strong against non-polio strains, weak on polioviruses.</p>Fórmula:C19H17N5OSCor e Forma:SolidPeso molecular:363.44Iprovalicarb
CAS:<p>Iprovalicarb is a fungicide aimed at oomycetes.</p>Fórmula:C18H28N2O3Pureza:98%Cor e Forma:SolidPeso molecular:320.43Linatine
CAS:<p>Linatine is used as a bacterial inhibitor.</p>Fórmula:C10H17N3O5Pureza:98%Cor e Forma:SolidPeso molecular:259.26HIPP
CAS:<p>HIPP is a highly selective inhibitor of antineoplastic CtBP.</p>Fórmula:C9H9NO3Cor e Forma:SolidPeso molecular:179.17LP10
CAS:<p>LP10 is a reverse type I inhibitor of Mycobacterium tuberculosis CYP125A1 and a Potent type II inhibitor of Trypanosoma cruzi CYP51.</p>Fórmula:C24H28N4O2Cor e Forma:SolidPeso molecular:404.5Urease-IN-7
CAS:<p>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.</p>Fórmula:C16H10BrFN4SCor e Forma:SolidPeso molecular:389.24Influenza virus-IN-5
CAS:<p>Influenza virus-IN-5 (Compound 5f) is an influenza virus hemagglutinin (HA) inhibitor that acts on the A/H3N2 virus (EC50: 1 nM).</p>Fórmula:C21H26ClN3O2SCor e Forma:SolidPeso molecular:419.97Azosulfamide
CAS:<p>Azosulfamide is an azo compound with similar antibacterial effect as sulfanilamide.</p>Fórmula:C18H16N4Na2O10S3Cor e Forma:SolidPeso molecular:590.5Mollugogenol A
CAS:<p>Mollugogenol A: a Gammacerane saponin from Mollugo pentaphylla with antifungal and spermatocidal properties; damages sperm membrane.</p>Fórmula:C30H52O4Cor e Forma:SolidPeso molecular:476.73BMS-663749 lysine
CAS:<p>BMS-663749 lysine is used as a phosphonooxymethyl prodrug 4 for HIV-1 attachment inhibitor.</p>Fórmula:C29H39N6O11PPureza:98%Cor e Forma:SolidPeso molecular:678.63HIV-1 inhibitor-33
CAS:<p>HIV-1 inhibitor-33, potent against HIV-1 (EC50: 8.6 nM), low toxicity to MT-4 cells (CC50: 18 μM), useful for AIDS research.</p>Fórmula:C25H28N6OCor e Forma:SolidPeso molecular:428.53Buclosamide
CAS:<p>Buclosamide is a topical antimycotic agent that can be used in dermatomycoses [1].</p>Fórmula:C11H14ClNO2Cor e Forma:SolidPeso molecular:227.69INSCoV-614(1B)
CAS:<p>INSCoV-614(1B), a potent Mpro inhibitor, may help fight SARS-CoV-2, per patent WO2021219089A1.</p>Fórmula:C23H21ClF3N5O3Cor e Forma:SolidPeso molecular:507.89NPD9948
CAS:<p>NPD9948 is a competitive inhibitor of MTH1.</p>Fórmula:C13H14N6Cor e Forma:SolidPeso molecular:254.29Mtb-IN-2
CAS:<p>Mtb-IN-2 is a Mycobacterium tuberculosis (Mtb) compound with antimicrobial activity and low toxicity for the study of tuberculosis.</p>Fórmula:C17H12N2O4Pureza:99.27%Cor e Forma:SolidPeso molecular:308.29116-9e
CAS:<p>116-9e (MAL2-11B) is an Hsp70 chaperone DNAJA1 inhibitor with antiviral properties, inhibits SV40 replication, and can be used to study cancer drug resistance.</p>Fórmula:C31H32N2O5Pureza:99.55%Cor e Forma:SolidPeso molecular:512.6Niridazole
CAS:<p>Niridazole (Ambilhar) is an antiparasitic compound belonging to nitroimidazoles.</p>Fórmula:C6H6N4O3SPureza:98.26% - 99.55%Cor e Forma:Yellow Crystals From Dimethylformamide/Methanol SolidPeso molecular:214.2TH1217
CAS:<p>TH1217: potent dCTPase inhibitor, IC50=47 nM; boosts cytidine analogues in leukemia, may affect COVID-19.</p>Fórmula:C20H17BCl2N4O6Pureza:99.3%Cor e Forma:SolidPeso molecular:491.09Trofosfamide
CAS:<p>Trofosfamide is a derivative of oxazaphosphorine with antineoplastic potency.</p>Fórmula:C9H18Cl3N2O2PPureza:98.5% - >99.99%Cor e Forma:SolidPeso molecular:323.58Enzaplatovir
CAS:Enzaplatovir is an inhibitor of Respiratory Syncytial Virus (RSV), can be used as a viral fusion protein inhibitor.Fórmula:C20H19N5O3Pureza:98.54% - 99.72%Cor e Forma:SolidPeso molecular:377.4Chlamydia pneumoniae-IN-1
CAS:Chlamydia pneumoniae-IN-1 (compound 55), a benzimidazole derivative, exhibits potent antibacterial activity, inhibiting 99% of C.Fórmula:C19H15N3OSPureza:97.71%Cor e Forma:SolidPeso molecular:333.41Trimetozine
CAS:<p>Trimetozine (Sedoxazine) is a sedative that has been marketed in Europe since 1959. It has mild tranquilizing effects and has been used to treat anxiety.</p>Fórmula:C14H19NO5Pureza:99.83%Cor e Forma:SolidPeso molecular:281.3BAY-43-9695
CAS:<p>BAY-43-9695 is a non-nucleoside compound with anti-human cytomegalovirus (HCMV) activity. It is the major metabolite of BAY-38-4766.</p>Fórmula:C22H25N3O4SPureza:99.50% - 99.65%Cor e Forma:SolidPeso molecular:427.52MP265
CAS:<p>MP265 disrupts the MreB cytoskeleton and has antiproliferative effects.</p>Fórmula:C8H10Cl2N2SPureza:99.55%Cor e Forma:SolidPeso molecular:237.15Isatin-β-thiosemicarbazone
CAS:<p>Isatin-β-thiosemicarbazone is a potent inhibitor of herpes simplex virus (HSV).</p>Fórmula:C9H8N4OSPureza:98.23%Cor e Forma:SolidPeso molecular:220.25Isatoribine
CAS:<p>Isatoribine(ANA245) free base is a potent TLR7 receptor agonist with anti-hepatitis C virus infection activity for the study of HCV infection.</p>Fórmula:C10H12N4O6SPureza:98.99% - 99.75%Cor e Forma:SolidPeso molecular:316.29SARS-CoV-2-IN-38
CAS:SARS-CoV-2-IN-38, also known as compound 24, is an inhibitor of SARS-CoV-2 that demonstrates favorable oral bioavailability in mice, with an absorption fractionFórmula:C18H14ClF4NO4Pureza:99.37%Cor e Forma:SolidPeso molecular:419.76Nortopixantrone HCl
CAS:<p>Nortopixantrone HCl (BBR 3438) is a novel 9-azacyclonopyrazole that shows antitumor activity in a human prostate cancer model.</p>Fórmula:C20H26Cl2N6O2Pureza:99.08% - 99.74%Cor e Forma:SolidPeso molecular:453.36MK-8325
CAS:<p>MK-8325 is a potent and orally available HCV NS5A inhibitor with replicative activity against a wide range of genotypes.MK-8325 has demonstrated bioavailability</p>Fórmula:C43H54Cl2F2N8O6SiPureza:>99.99%Cor e Forma:SolidPeso molecular:915.93Galocitabine
CAS:<p>Galocitabine (Neofrutulon), a thymidylate synthase inhibitor, is used potentially for the treatment of cancer.</p>Fórmula:C19H22FN3O8Pureza:99.89%Cor e Forma:SolidPeso molecular:439.39BILB-1941
CAS:<p>BILB-1941 (BILB-1941ZW) is an inhibitor of HCV NS5B polymerase and can be used in studies about HCV infection.</p>Fórmula:C34H34N4O4Pureza:99.51% - 99.65%Cor e Forma:SolidPeso molecular:562.66SARS-CoV-2-IN-14
CAS:<p>SARS-CoV-2-IN-14 is a potent and oral inhibitor of SARS-CoV-2 (IC50:0.39 μM), which is an analogue of niclosamide.</p>Fórmula:C13H9Cl2NO2Pureza:99.78%Cor e Forma:SolidPeso molecular:282.12NITD-916
CAS:<p>NITD-916: oral Mycobacterium InhA inhibitor (IC50: 570 nM), lipophilic 4-hydroxy-2-pyridone with antituberculosis action.</p>Fórmula:C20H25NO2Pureza:99.01% - 99.78%Cor e Forma:SolidPeso molecular:311.42NIOCH 14
CAS:<p>NIOCH 14 is an orally available antiviral compound that inhibits exocorticoviruses, poxviruses, and smallpox viruses.</p>Fórmula:C19H17F3N2O4Pureza:98%Cor e Forma:SolidPeso molecular:394.35Molnupiravir
CAS:<p>Molnupiravir (EIDD-2801) is an isopropyl ester prodrug of the ribonucleoside analog EIDD-1931 with oral bioavailability.Cost-effective and quality-assured.</p>Fórmula:C13H19N3O7Pureza:99.81% - 99.98%Cor e Forma:SolidPeso molecular:329.31Uprifosbuvir
CAS:Uprifosbuvir is an inhibitor of uridine nucleotide analog HCV NS5B polymerase.Fórmula:C22H29ClN3O9PPureza:99.73% - >99.99%Cor e Forma:SolidPeso molecular:545.91VP-4604
CAS:<p>VP-4604: potent anti-MRSA, inhibits S. aureus growth (MIC 4-8 μg/mL), >95% effective against MRSA.</p>Fórmula:C11H14N2O4SPureza:99.76%Cor e Forma:SolidPeso molecular:270.3Flaviviruses-IN-2
CAS:<p>Flaviviruses-IN-2 is a potent flaviviruses inhibitor. Flaviviruses-IN-2 reduces West Nile virus (WNV) protease activity and inhibits WNV by 56%.</p>Fórmula:C21H20N2O3SPureza:99.68%Cor e Forma:SoildPeso molecular:380.46QPX7728-OH disodium
CAS:<p>QPX7728 disodium (Xeruborbactam disodium) is a cyclic boronate inhibitor of many serine and metal-β-lactamases, exhibiting antibacterial activity.</p>Fórmula:C10H8BFNa2O5Pureza:>99.99%Cor e Forma:SolidPeso molecular:283.96TBT1
CAS:<p>TBT1 is a first-gen MsbA ATPase activator and LPS transport blocker in Acinetobacter, EC50 at 13 μM.</p>Fórmula:C16H14ClNO3SPureza:99.27%Cor e Forma:SolidPeso molecular:335.81Ferroquine
CAS:Ferroquine, a ferrocenyl variant of Chloroquine, exhibits antimalarial properties through oxidative stress induction, destroying Plasmodium membranes.Fórmula:C23H24ClFeN3Pureza:99.97%Cor e Forma:SolidPeso molecular:433.76MtUng-IN-1
CAS:<p>MtUng-IN-1 acts as an inhibitor of Mycobacterium uracil DNA glycosylase (MtUng).MtUng-IN-1 is indicated for use in cancer and infectious disease research.</p>Fórmula:C14H12N2O6Pureza:99.88%Cor e Forma:SolidPeso molecular:304.25AP-C5
CAS:<p>AP-C5 inhibits cGKII with a Pic50 of 7.2, useful in diarrheal disease research.</p>Fórmula:C16H13N5Pureza:99.82%Cor e Forma:SolidPeso molecular:275.31ERCC1-XPF-IN-2
CAS:<p>ERCC1-XPF-IN-2: Nucleotide repair active, boosts cisplatin, inhibits ERCC1-XPF (IC50: 0.6 μM).</p>Fórmula:C15H13Cl2NO3Pureza:98.21%Cor e Forma:SolidPeso molecular:326.17ClpB-IN-1
CAS:<p>ClpB-IN-1 is a potential antimicrobial agent.ClpB-IN-1 is a potent ClpB inhibitor.</p>Fórmula:C14H10N2O2S2Pureza:98.68%Cor e Forma:SolidPeso molecular:302.37SARS-CoV-2 Mpro-IN-2
CAS:SARS-CoV-2 MPro-IN-2, selective non-covalent inhibitor, IC50 0.40 μM, low toxicity, anti-COVID-19 with EC50 1.1 μM.Fórmula:C22H20Cl2N4O2SPureza:99.87% - 99.97%Cor e Forma:SolidPeso molecular:475.39Quinupristin
CAS:<p>Quinupristin, a macrolide-lincosamide-streptogramin antibiotic, inhibits protein synthesis in bacteria.</p>Fórmula:C53H67N9O10SPureza:98.05% - 98.16%Cor e Forma:SolidPeso molecular:1022.22NS1-IN-1
CAS:<p>NS1-IN-1: Potent NS1 inhibitor, antiviral, reduces viral proteins by inhibiting mTORC1 via TSC1-TSC2, limits replication.</p>Fórmula:C23H26N2O4Pureza:98.71%Cor e Forma:SolidPeso molecular:394.46Pramiconazole
CAS:Pramiconazole (R126638), an oral antifungal, treats dermatophyte and yeast infections in seborrheic dermatitis.Fórmula:C35H39F2N7O4Pureza:98.1% - 98.59%Cor e Forma:SolidPeso molecular:659.73Sivelestat sodium tetrahydrate
CAS:<p>Sivelestat sodium tetrahydrate (ONO5046 sodium tetrahydrate) is a competitive inhibitor of human neutrophil elastase, with an IC50 of 44 nM and a Ki of 200 nM.</p>Fórmula:C20H29N2NaO11SPureza:99.68%Cor e Forma:SolidPeso molecular:528.51Bithionol sulfoxide
CAS:<p>Bithionol sulfoxide (Bithionoloxide) is a compound with inhibitory effects against parasites, inhibiting Fasciola hepatica and Schistosoma mansoni.</p>Fórmula:C12H6Cl4O3SPureza:98.76%Cor e Forma:Off White To Tinch Pink Crystalline PowderPeso molecular:372.05Caracemide
CAS:<p>Caracemide (NSC-253272) inhibits the enzyme ribonucleotide reductase of Escherichia coli. Caracemide can be used in anticancer studies.</p>Fórmula:C6H11N3O4Pureza:99.8%Cor e Forma:SolidPeso molecular:189.17Artelinic acid
CAS:Artelinic acid is an artemisinin analog with antimalarial activity and is used for the treatment of multi-drug resistant strains of Plasmodium falciparum.Fórmula:C23H30O7Pureza:97.49% - 97.69%Cor e Forma:SolidPeso molecular:418.48Clofoctol
CAS:<p>Clofoctol is a bacteriostatic antibiotic with activity against Gram-positive bacteria, used in the treatment of upper and lower respiratory tract infections.</p>Fórmula:C21H26Cl2OPureza:98% - 99.87%Cor e Forma:SolidPeso molecular:365.34SQ609
CAS:<p>SQ609 is a dipiperidine-based drug candidate with notable in vitro anti-tuberculosis effects in mouse macrophages.</p>Fórmula:C22H38N2OPureza:99.84%Cor e Forma:SolidPeso molecular:346.55ABMA
CAS:<p>ABMA is a broad-spectrum inhibitor shielding cells from viruses, bacteria, and parasites, acting in late endosomes.</p>Fórmula:C18H24BrNOPureza:99.866%Cor e Forma:SolidPeso molecular:350.29Setrobuvir
CAS:<p>Setrobuvir (ANA-598) is an orally active non-nucleoside HCV NS5B polymerase inhibitor with inhibitory effects on de novo RNA synthesis and primer extension with</p>Fórmula:C25H25FN4O6S2Pureza:98.92% - >99.99%Cor e Forma:SolidPeso molecular:560.62MAC13243 HCl
CAS:MAC13243 HCl inhibits LolA chaperone, targeting Gram-negative bacteria as a specific antimicrobial agent.Fórmula:C20H25Cl2N3O2SPureza:99.75%Cor e Forma:SolidPeso molecular:442.4Cytembena
CAS:<p>Cytembena is a cytostatic and a carcinogenic compound that may increase the incidence of fibroadenomas.Cytembena broadly inhibits DNA biosynthesis.</p>Fórmula:C11H8BrNaO4Pureza:99.35%Cor e Forma:White PowderPeso molecular:307.07Morinidazole
CAS:<p>Morinidazole has antibacterial properties for researching anaerobic infections like appendicitis and PID.</p>Fórmula:C11H18N4O4Pureza:98.92% - 99.82%Cor e Forma:SolidPeso molecular:270.29RP-6685
CAS:<p>RP-6685 is a potent, selective DNA Polθ inhibitor with strong oral efficacy, an IC50 of 5.8 nM, and marked antitumor effects in mice.</p>Fórmula:C22H14F7N5OPureza:99.65%Cor e Forma:SoildPeso molecular:497.37Bofutrelvir
CAS:<p>MProinhibitor 11a: SARS-CoV-2 MPro blocker, IC50=0.053μM; cuts viral yield/RNA in Vero E6 cells, EC50=0.53μM, effective 1.85-50μM.</p>Fórmula:C25H32N4O4Pureza:99.92% - >99.99%Cor e Forma:SolidPeso molecular:452.55CHD1Li 6.11
CAS:<p>CHD1Li 6.11 inhibits CHD1L protein (IC50: 3.3 µM), shrinks CRC tumors in vivo, and is orally active.</p>Fórmula:C21H22BrN5OSPureza:99.04%Cor e Forma:SolidPeso molecular:472.4SARS-CoV-2-IN-13
CAS:<p>SARS-CoV-2-IN-13, a stable niclosamide analogue, enhances oral bioavailability and inhibits SARS-CoV-2 (IC50: 0.057 μM).</p>Fórmula:C13H8Cl2N2O4Pureza:98.54%Cor e Forma:SolidPeso molecular:327.12Flutrimazole
CAS:Flutrimazole: a dual-action imidazole with anti-inflammatory and antifungal effects; ideal for topical use due to limited skin penetration.Fórmula:C22H16F2N2Pureza:98.56%Cor e Forma:SolidPeso molecular:346.37N-(2-Hydroxypropyl)methacrylamide
CAS:N-(2-Hydroxypropyl)methacrylamide is used in the synthesis of copolymers for the targeted delivery of antileishmanial agents in Visceral leishmaniasis.Fórmula:C7H13NO2Pureza:99.87%Cor e Forma:SolidPeso molecular:143.18BB-78485
CAS:BB-78485 is an inhibitor of LpxC metalloenzymes with antibacterial activity. BB-78485 can be used for the study of Gram-negative bacterial infections.Fórmula:C23H20N2O4SPureza:99.49%Cor e Forma:SolidPeso molecular:420.486-Hydroxy-DOPA
CAS:<p>6-Hydroxy-DOPA is an allosteric inhibitor of RAD52, it inhibits proliferation of BRCA-deficient cancer cells in vitro and also inhibits APE1.</p>Fórmula:C9H11NO5Pureza:97.78% - 97.95%Cor e Forma:SolidPeso molecular:213.192'-C-Methyladenosine
CAS:<p>2'-C-Methyladenosine from C. renalis inhibits HCV, NS5B RNA synthesis (IC50: 0.3, 1.9µM), and LRV1 in L. guyanensis, L. braziliensis.</p>Fórmula:C11H15N5O4Pureza:99.85%Cor e Forma:SolidPeso molecular:281.27Antimalarial agent 30
CAS:<p>Antimalarial agent 30 has anti-Plasmodium berghei liver stage parasite activity and antimalarial activity for the study of malarial infections.</p>Fórmula:C18H11F3N2Pureza:99.83% - 99.90%Cor e Forma:SolidPeso molecular:312.29ZIM
CAS:<p>ZIM, from 4-Aminoantipyrine, induces DNA and chromosomal damage, cell death, and phagocytosis, with potential in cancer therapy.</p>Fórmula:C20H19N3O3Pureza:99.85%Cor e Forma:SolidPeso molecular:349.38JPD447
CAS:JPD447, a derivative of MAC-0547630, represents a new class of UppS inhibitors designed to enhance the efficacy of β-lactam antibiotics.Fórmula:C20H23FN4Pureza:99.69%Cor e Forma:SolidPeso molecular:338.42Azidamfenicol
CAS:<p>Azidamfenicol inhibits ribosomal peptidyltransferase with a Ki of 22 µM. Azidamfenicol is a broad-spectrum chloramphenicol-like antibiotic.</p>Fórmula:C11H13N5O5Pureza:99.61%Cor e Forma:SolidPeso molecular:295.25Anticancer agent 73
CAS:<p>Anticancer agent 73 inhibits TRBP, disrupting TRBP-Dicer, and hinders HCC growth and spread by altering HCC miRNA and protein expression.</p>Fórmula:C14H15NO4Pureza:99.19%Cor e Forma:SolidPeso molecular:261.27Sovaprevir
CAS:<p>Sovaprevir is a non-structural 3 (NS3) protease inhibitor with antiviral activity for the treatment of HCV infection.</p>Fórmula:C43H53N5O8SPureza:99.11%Cor e Forma:SolidPeso molecular:799.97Tenofovir alafenamide fumarate
CAS:Tenofovir alafenamide fumarate (GS-7340) is an oral anti-HIV drug that prevents infection.Fórmula:C25H33N6O9PPureza:99.99%Cor e Forma:SolidPeso molecular:592.54GSK2556286
CAS:<p>GSK2556286 (GSK286) is an oral Mycobacterium tuberculosis inhibitor effective against MDR, XDR, and DS strains with an IC50 of 0.07 μM.</p>Fórmula:C18H23N3O3Pureza:98.17% - 99.59%Cor e Forma:SolidPeso molecular:329.39Bersacapavir
CAS:<p>Bersacapavir (JNJ-56136379) is an in vitro modulator of hepatitis B virus capsid assembly that inhibits HBV replication.</p>Fórmula:C16H14F4N4O3SPureza:98.53%Cor e Forma:SolidPeso molecular:418.37Besifovir PM
<p>Besifovir PM (LB80331 PM) is an analogue of Besifovir, a novel orally available acyclic nucleotide phosphonate for the treatment of chronic hepatitis B</p>Fórmula:C11H15N5OPureza:98.48% - 99.90%Cor e Forma:SoildPeso molecular:233.27BMS-929075
CAS:BMS-929075 is an orally active HCV NS5B replicase (HCV NS5B replicase) palm site variant inhibitor with potency, high oral bioavailability and pharmacokineticFórmula:C31H24F2N4O3Pureza:99.81% - 99.94%Cor e Forma:SolidPeso molecular:538.54CCR-11
CAS:<p>CCR-11 is a bypassed tannin derivative with antimicrobial activity that inhibits bacterial proliferation and can be used in the study of breast cancer.</p>Fórmula:C15H8F3NO2S2Pureza:98%Cor e Forma:SolidPeso molecular:355.35N-phenylacetyl-L-Homoserine lactone
CAS:N-phenylacetyl-L-Homoserine lactone attenuates the group sensing of the pathogen Acinetobacter baumannii and can be used to study bacterial infections.Fórmula:C12H13NO3Pureza:98.99%Cor e Forma:SolidPeso molecular:219.24Tivicilovir
CAS:Tivicilovir (AM188) is a hepatitis B virus inhibitor. tiviclovir is a guanine-related acyclic 2'-deoxyguanine analogue with anti-herpesvirus activity.Fórmula:C9H13N5O3Pureza:99.94%Cor e Forma:SolidPeso molecular:239.23TTP-8307
CAS:TTP-8307 is an antiviral compound that inhibits the replication of rhinoviruses and enteroviruses and is used in the study of viral infections.Fórmula:C27H21FN4OPureza:98.95%Cor e Forma:SolidPeso molecular:436.48B220
CAS:<p>B220, an antiviral agent, inhibits the growth of HSV-1, HSV-2, and human cytomegalovirus (CMV).</p>Fórmula:C20H22N4Pureza:99.61% - 99.9%Cor e Forma:SolidPeso molecular:318.42JCP174
CAS:<p>JCP174 is a depalmitoylase inhibitor that enhances Toxoplasma host-cell invasion by targeting TgPPT1.</p>Fórmula:C12H12ClNO3Pureza:97.05%Cor e Forma:SolidPeso molecular:253.68SMN-C2
CAS:<p>SMN-C2, a SMN2 gene splicing regulator, is an RNA-binding ligand that regulates pre-mRNA splicing and has potential for studying spinal muscular atrophy.</p>Fórmula:C24H27N5O2Pureza:99.14%Cor e Forma:SolidPeso molecular:417.5DDRI-18
CAS:DDRI-18 is an inhibitor that regulates the DNA damage response, has anticancer activity, and inhibits non-homologous end-joining (NHEJ) DNA repair.Fórmula:C26H20N6Pureza:98%Cor e Forma:SolidPeso molecular:416.48anti-TB agent 1
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