
Antivíricos
Foram encontrados 768 produtos de "Antivíricos"
Adefovir dipivoxil 100 µg/mL in Acetonitrile
CAS:Fórmula:C20H32N5O8PCor e Forma:Single SolutionPeso molecular:501.47Arbidol
CAS:Arbidol (Umifenovir) is a broad-spectrum antiviral compound that is a fusion inhibitor and interacts with the SARS-CoV-2 spicin.
Fórmula:C22H25BrN2O3SPureza:99.57%Cor e Forma:White To Off-White Crystalline PowderPeso molecular:477.429-(2,3-Dideoxy-β-D-glycero-pentofuranosyl)-9H-purin-6-amine (2',3'-Dideoxyadenosine)
CAS:Produto ControladoFórmula:C10H13N5O2Cor e Forma:NeatPeso molecular:235.243N4-Isobutylquinoline-3,4-diamine
CAS:Produto ControladoFórmula:C13H17N3Cor e Forma:NeatPeso molecular:215.291H-1,2,4-Triazole-3-carboxylic Acid
CAS:Produto ControladoFórmula:C3H3N3O2Cor e Forma:NeatPeso molecular:113.07Efavirenz USP Related Compound C
CAS:Produto ControladoFórmula:C13H9ClF3NCor e Forma:NeatPeso molecular:271.67Abacavir Sulfate EP Impurity C (Abacavir Related USP Compound A)
CAS:Produto ControladoFórmula:C11H14N6OCor e Forma:NeatPeso molecular:246.279-[4-Acetoxy-3-(acetoxymethyl)butyl]-2-amino-6-chloropurine
CAS:Produto ControladoFórmula:C14H18ClN5O4Cor e Forma:NeatPeso molecular:355.78Nevirapine EP Impurity B
CAS:Produto ControladoFórmula:C12H10N4OCor e Forma:NeatPeso molecular:226.232'-β-C-Methyl inosine
CAS:2'-beta-C-Methyl inosine (2'-C-Methyl inosine) is an HCV RNA polymerase inhibitor with antiviral activity and may be used in studies to treat hcv infections.Fórmula:C11H14N4O5Cor e Forma:SolidPeso molecular:282.25(R)-9-(2-Hydroxypropyl)adenine (Desphosphoryltenofovir)
CAS:Produto ControladoFórmula:C8H11N5OCor e Forma:NeatPeso molecular:193.212-[2-(2-Amino-9H-purin-9-yl)ethyl]propane-1,3-diol Hydrochloride
CAS:Produto ControladoFórmula:C10H15N5O2·ClHCor e Forma:NeatPeso molecular:273.72Paracetamol EP Impurity F (Acetaminophen USP Related Compound F)
CAS:Produto ControladoFórmula:C6H5NO3Cor e Forma:NeatPeso molecular:139.11Ribavirin 100 µg/mL in Acetonitrile:Methanol
CAS:Produto ControladoFórmula:C8H12N4O5Cor e Forma:Single SolutionPeso molecular:244.20Entecavir Monohydrate
CAS:Produto ControladoFórmula:C12H15N5O3·H2OCor e Forma:NeatPeso molecular:295.292-[[(2-(Acetylamino)-6-oxo-1,6-dihydro-9H-purin-9-yl]-methoxy]ethyl Acetate
CAS:Produto ControladoFórmula:C12H15N5O5Cor e Forma:NeatPeso molecular:309.281-(5-O-Benzoyl-2,3-dideoxy-β-D-glycero-pent-2-enofuranosyl)-5-methylpyrimidine-2,4(1H,3H)-dione
CAS:Produto ControladoFórmula:C17H16N2O5Cor e Forma:NeatPeso molecular:328.31934-Nitrophenyl Thiazol-5-ylmethyl Carbonate
CAS:Produto ControladoFórmula:C11H8N2O5SCor e Forma:NeatPeso molecular:280.26Nevirapine 100 µg/mL in Acetonitrile
CAS:Fórmula:C15H14N4OCor e Forma:Single SolutionPeso molecular:266.30N4-Isobutylquinoline-3,4-diamine Hydrochloride
CAS:Produto ControladoFórmula:C13H17N3·ClHCor e Forma:NeatPeso molecular:251.76Arg-AMS
CAS:Arg-AMS is an arginine tRNA synthetase inhibitor with antiviral activity for the study of viral infections and myeloma.Fórmula:C16H26N10O7SPureza:98.00%Cor e Forma:SolidPeso molecular:502.51N,N-Dimethylpyridin-4-amine
CAS:Produto ControladoFórmula:C7H10N2Cor e Forma:NeatPeso molecular:122.17Ganciclovir 100 µg/mL in Acetonitrile:Water
CAS:Fórmula:C9H13N5O4Cor e Forma:Single SolutionPeso molecular:255.23β-Anomer
CAS:β-Anomer shows antiviral properties.Fórmula:C10H13N3O6Pureza:98.68% - 99.81%Cor e Forma:SolidPeso molecular:271.234-Chloro-1-isobutyl-1H-imidazo[4,5-c]quinoline
CAS:Produto ControladoFórmula:C14H14ClN3Cor e Forma:NeatPeso molecular:259.73Anti-RSV-F/HMPV-F Antibody (MPE8)
Anti-RSV-F/HMPV-F Antibody (MPE8) is a CHO-expressed IgG1λ monoclonal antibody that neutralizes RSV-F/HMPV-F, suitable for respiratory virus research.Cor e Forma:Odour LiquidPeso molecular:150 kDaGanciclovir Mono-O-acetate
CAS:Produto ControladoFórmula:C11H15N5O5Cor e Forma:NeatPeso molecular:297.27Efavirenz USP Related Compound A
CAS:Produto ControladoFórmula:C13H11ClF3NOCor e Forma:NeatPeso molecular:289.68Emtricitabine Sulfoxide
CAS:Produto ControladoFórmula:C8H10FN3O4SCor e Forma:NeatPeso molecular:263.25Stavudine 100 µg/mL in Acetonitrile
CAS:Fórmula:C10H12N2O4Cor e Forma:Single SolutionPeso molecular:224.21Rilpivirine Hydrochloride
CAS:Produto ControladoFórmula:C22H18N6·ClHCor e Forma:NeatPeso molecular:402.88Enpatoran hydrochloride
CAS:Enpatoran (M5049) hydrochloride is a strong, oral TLR7/8 inhibitor (IC50: 11.1/24.1 nM), inactive against TLR3/4/9, with good pharmacokinetics.Fórmula:C16H16ClF3N4Pureza:97.44% - 99.88%Cor e Forma:SolidPeso molecular:356.77Isoborneol
CAS:Isoborneol (DL-Isoborneol) is a monoterpene alcohol, with neuroprotective and antiviral activitiesFórmula:C10H18OPureza:≥95%Cor e Forma:White Solid PelletslargecrystalsPeso molecular:154.25ITMN4077
CAS:ITMN4077 is an antiviral that inhibits Hepatitis C replication in HuH7 cells, with an EC50 of 2.131μM.Fórmula:C26H40N4O8SPureza:99.78%Cor e Forma:SolidPeso molecular:568.68Lopinavir
CAS:Fórmula:C37H48N4O5Pureza:≥ 98.0% (anhydrous basis)Cor e Forma:White crystalline powderPeso molecular:628.80pocapavir
CAS:Pocapavir (SCH-48973) is an investigational enterovirus (EV) capsid inhibitor.Fórmula:C21H17Cl3O3Pureza:98.05%Cor e Forma:SolidPeso molecular:423.72Pirodavir
CAS:Pirodavir (R77975) (R 77975), the prototype of broad-spectrum anti-picornavirus compounds, is a potent human rhinovirus (HRV) capsid-binding inhibitor.Fórmula:C21H27N3O3Pureza:98.43% - 99.47%Cor e Forma:SolidPeso molecular:369.46Ref: TM-T1750
2mg42,00€5mg62,00€1mL*10mM (DMSO)71,00€10mg96,00€25mg210,00€50mg334,00€100mg474,00€200mg642,00€Adefovir
CAS:Adefovir: acyclic nucleoside phosphonate, reverse transcriptase inhibitor for hepatitis B and herpes treatment.Fórmula:C8H12N5O4PPureza:99% - 99.56%Cor e Forma:White To Off-White PowderPeso molecular:273.19Rose Bengal sodium
CAS:Rose Bengal sodium is a potent inhibitor of VGlut and vesicular monoamine transporter (VMAT) (Ki of 19 and 64 nM for VGlut andVMAT, respectively)Fórmula:C20H2Cl4I4Na2O5Pureza:91.6%Cor e Forma:Bordeux SolidPeso molecular:1017.64Lycorine
CAS:Lycorine (Narcissine) inhibits protein synthesis and may inhibit ascorbic acid biosynthesis, although studies on the latter are controversial and inconclusive.Fórmula:C16H17NO4Pureza:98.60% - 99.95%Cor e Forma:SolidPeso molecular:287.311-Deoxynojirimycin
CAS:1-Deoxynojirimycin (Moranoline) is a potent α-glucosidase inhibitor, suppressing postprandial blood glucose, thereby possibly preventing diabetes mellitus.Fórmula:C6H13NO4Pureza:99.65% - 99.98%Cor e Forma:White-Beige Solid CrystallinePeso molecular:163.17Ref: TM-T3675
2mg43,00€1mL*10mM (DMSO)57,00€5mg58,00€10mg74,00€25mg140,00€50mg248,00€100mg321,00€500mg773,00€Telaprevir
CAS:Fórmula:C36H53N7O6Pureza:≥ 99.0%Cor e Forma:White to light yellow powderPeso molecular:679.85Cidofovir
CAS:Cidofovir ((S)-HPMPC) 通过特异性抑制病毒 DNA 合成来抑制病毒复制。Fórmula:C8H14N3O6PPureza:99.24% - 99.76%Cor e Forma:Fluffy White PowderPeso molecular:279.19Pleconaril
CAS:Pleconaril (VP 63843) is a capsid inhibitor used previously to treat enterovirus infections. Pleconaril is effective in inhibiting replication (IC50: 50 nM).Fórmula:C18H18F3N3O3Pureza:98.21% - 99.09%Cor e Forma:SolidPeso molecular:381.35Ref: TM-T4536
1mg35,00€2mg50,00€5mg71,00€1mL*10mM (DMSO)71,00€10mg98,00€25mg200,00€50mg306,00€100mg444,00€200mg647,00€Dodecyl gallate
CAS:Dodecyl gallate (Progallin LA) is the ester of gallic acid and dodecanol. As a food additive, it is used as a preservative and antioxidant.Fórmula:C19H30O5Pureza:99.74%Cor e Forma:White Or Creamy-White Odourless SolidPeso molecular:338.445-Fluorocytidine
CAS:5-Fluorocytidine with antiviral activityFórmula:C9H12FN3O5Pureza:99.23%Cor e Forma:White PowderPeso molecular:261.213-Methoxyflavone
CAS:3-Methoxyflavone is a Flavonoids, with antiviral activityFórmula:C16H12O3Pureza:99.29% - 99.97%Cor e Forma:SolidPeso molecular:252.26Chelidonine
CAS:Chelidonine from Chelidonium majus triggers HeLa cell apoptosis, may reverse MDR, boost chemotherapeutics against leukemia, and inhibit cancer cell metastasis.Fórmula:C20H19NO5Pureza:98% - 99.61%Cor e Forma:SolidPeso molecular:353.37Alovudine
CAS:3'-Fluoro-3'-deoxythymidine (3'-Deoxy-3'-fluorothymidine) is a marker of DNA synthesis,which is less susceptible to inflammatory changes than FDG.Fórmula:C10H13FN2O4Pureza:99.41%Cor e Forma:Less Solid Colourless SolidPeso molecular:244.22Elvitegravir
CAS:Fórmula:C23H23ClFNO5Pureza:≥ 98.0%Cor e Forma:White to off-white powder or solidPeso molecular:447.88Direct Violet 1
CAS:Direct Violet 1 (CCRIS 2413) is an agent of dye.Fórmula:C32H22N6Na2O8S2Pureza:≥98%Cor e Forma:SolidPeso molecular:728.66Sodium Camptothecin
CAS:Sodium Camptothecin: plant-derived, antitumor, inhibits RNA/DNA synthesis, disrupts viral DNA.Fórmula:C20H18N2NaO5Pureza:98.93%Cor e Forma:SolidPeso molecular:389.36Boceprevir
CAS:Fórmula:C27H45N5O5Pureza:≥ 98.0%Cor e Forma:White to light-yellow powderPeso molecular:519.68T-1105
CAS:T-1105 is a broad-spectrum antiviral inhibitor.Fórmula:C5H5N3O2Pureza:99.57%Cor e Forma:SolidPeso molecular:139.11CBS1117
CAS:CBS1117: influenza A entry inhibitor; blocks HA fusion, IC50=70 nM for H1N1.Fórmula:C15H20Cl2N2OPureza:99.8%Cor e Forma:SolidPeso molecular:315.24Ref: TM-T8793
2mg42,00€5mg62,00€1mL*10mM (DMSO)78,00€10mg92,00€25mg166,00€50mg241,00€100mg358,00€200mg500,00€ML-SA1
CAS:ML-SA1 (Mucolipin synthetic agonist 1) is a selective TRPML agonist, inhibits DENV2 and ZIKV by promoting lysosomal acidification and protease activity.Fórmula:C22H22N2O3Pureza:99.34% - 99.71%Cor e Forma:SolidPeso molecular:362.42Ref: TM-T23004
2mg34,00€5mg49,00€1mL*10mM (DMSO)55,00€10mg77,00€25mg142,00€50mg230,00€100mg344,00€200mg520,00€zapnometinib
CAS:Zapnometinib (ATR-002) is a MEK inhibitor.Fórmula:C13H7ClF2INO2Pureza:99.67%Cor e Forma:SolidPeso molecular:409.55BMS-707035
CAS:BMS-707035 is a specific HIV-I integrase (IN) inhibitor with IC50 of 15 nM. Phase 2.Fórmula:C17H19FN4O5SPureza:99.78%Cor e Forma:SolidPeso molecular:410.421-Deoxynojirimycin hydrochloride
CAS:1-Deoxynojirimycin hydrochloride (Moranoline) is a potent and selective inhibitor of alpha-glucosidase, most commonly found in mulberry leaves.Fórmula:C6H14ClNO4Pureza:99.88%Cor e Forma:SolidPeso molecular:199.63Curcumol
CAS:Curcumol ((-)-Curcumol), a pure monomer isolated extracted from Rhizoma Curcumaeis, has antitumor activities.Fórmula:C15H24O2Pureza:98.99% - 99.87%Cor e Forma:SolidPeso molecular:236.35Bemnifosbuvir
CAS:Bemnifosbuvir (AT-511) is a novel phosphoramidate prodrug of 2'-fluoro-2'-C-methylguanosine-5'-monophosphate that has potent in vitro activity against HCV.Fórmula:C24H33FN7O7PPureza:99.35% - 99.54%Cor e Forma:SolidPeso molecular:581.53Amantadine
CAS:Amantadine (1-Aminoadamantane), an antiviral, is a weak antagonist of the NMDA-type glutamate receptor, increases dopamine release and blocks dopamine reuptake.Fórmula:C10H17NPureza:99.73% - 99.94%Cor e Forma:Hexakistetrahedral Crystals By Sublimation SolidPeso molecular:151.25Azvudine hydrochloride
CAS:Azvudine hydrochloride (RO-0622 hydrochloride) is an NRTI inhibitor with antiviral activity, inhibiting HIV, HBV and HCV.Fórmula:C9H12ClFN6O4Pureza:99.06%Cor e Forma:SolidPeso molecular:322.68HIV-1 Nef-IN-1
CAS:HIV-1 Nef-IN-1 is an inhibitor of HIV-1 Nef protein. It efficiently competes for Nef-SH3Hck interactions(Kd : 6.7 μM).Fórmula:C18H16O2Pureza:99.90%Cor e Forma:SolidPeso molecular:264.32Inarigivir ammonium
CAS:Inarigivir ammonium, an antiviral dinucleotide, lowers HBV DNA and activates innate immunity via RIG-I agonism.Fórmula:C20H29N8O10PSPureza:99.91%Cor e Forma:SolidPeso molecular:604.53Ref: TM-T9518
1mg54,00€5mg114,00€1mL*10mM (DMSO)152,00€10mg177,00€25mg334,00€50mg557,00€100mg893,00€200mg1.198,00€Daclatasvir dihydrochloride
CAS:Daclatasvir dihydrochloride is an oral antiviral that treats chronic hepatitis C by inhibiting HCV's NS5A; rare liver enzyme elevation, seldom causes jaundice.Fórmula:C40H52Cl2N8O6Pureza:99.67%Cor e Forma:SolidPeso molecular:811.8Ref: TM-T1786
5mg39,00€10mg48,00€1mL*10mM (DMSO)49,00€25mg57,00€50mg67,00€100mg77,00€500mg161,00€1g230,00€Gossypin
CAS:Gossypin exhibits multiple medicinal properties and inhibits NF-kappaB, reducing inflammation, cancer growth, and angiogenesis.Fórmula:C21H20O13Pureza:97.57% - 98.97%Cor e Forma:SolidPeso molecular:480.38EIDD-2801
CAS:Fórmula:C13H19N3O7Pureza:≥ 98.0%Cor e Forma:White to off-white solidPeso molecular:329.31Vebicorvir
CAS:Vebicorvir (ABI-H0731) is a first-generation hepatitis B virus (HBV) core protein inhibitor, has demonstrated effective antiviral activity.Fórmula:C19H12F3N3O4S2Pureza:99.51% - 99.64%Cor e Forma:SolidPeso molecular:467.44Robinetin
CAS:Robinetin (3,3',4',5',7-Pentahydroxyflavone) has antioxidant and antiradical activities, inhibits EYPC membrane lipid peroxidation and HbA glycosylation withFórmula:C15H10O7Pureza:98.95% - 99.61%Cor e Forma:SolidPeso molecular:302.24Bemnifosbuvir hemisulfate
CAS:Bemnifosbuvir hemisulfate (AT-527) is a potent inhibitor of HCV virus replication.Fórmula:C48H68F2N14O18P2SPureza:99.98%Cor e Forma:SolidPeso molecular:1261.15Rilpivirine
CAS:Rilpivirine (R278474) is a diarylpyrimidine derivative and reverse transcriptase inhibitor with antiviral activity against HIV-1 that is used in the treatmentFórmula:C22H18N6Pureza:97.22% - 98.83%Cor e Forma:SolidPeso molecular:366.42Ref: TM-T2330
2mg35,00€5mg52,00€1mL*10mM (DMSO)58,00€10mg84,00€25mg138,00€50mg230,00€100mg319,00€200mg474,00€Riamilovir
CAS:Riamilovir (7-methylsulfanyl-3-nitro-6H-[1,2,4]triazolo[5,1-c][1,2,4]triazin-4-one) is a broad-spectrum antiviral drug candidate.Fórmula:C5H4N6O3SPureza:99.84%Cor e Forma:SolidPeso molecular:228.19Ref: TM-T8904
1mg34,00€5mg63,00€1mL*10mM (DMSO)64,00€10mg96,00€25mg168,00€50mg241,00€100mg335,00€200mg462,00€2,2'-Anhydrouridine
CAS:2,2'-Anhydrouridine (2,2'-Cyclouridine) is a research tool for antiviral and anticancer studies.Fórmula:C9H10N2O5Pureza:98.45%Cor e Forma:SolidPeso molecular:226.19Mbx2329
CAS:MBX2329 is a specific inhibitor of HA-mediated viral entry that inhibits H1N1 virus strain high pathogenic avian influenza H5N1 virus strain.Fórmula:C16H26ClNOPureza:99.82%Cor e Forma:SolidPeso molecular:283.84OSS_128167
CAS:OSS_128167 (SIRT6-IN-1) is a specific SIRT6 inhibitor, and for SIRT6(IC50=89 μM), SIRT1(IC50=1578 μM) and SIRT2(IC50=751 μM).Fórmula:C19H14N2O6Pureza:97.47% - 98.6%Cor e Forma:SolidPeso molecular:366.32Brincidofovir
CAS:Brincidofovir (HDP-CDV) is an orally active, lipophilic form of cidofovir.Fórmula:C27H52N3O7PPureza:98% - 99.62%Cor e Forma:SolidPeso molecular:561.69Sisunatovir hydrochloride
CAS:Sisunatovir hydrochloride (RV521 HCl) is an orally available inhibitor of the RSV-F protein that has exhibited potent efficacy against a panel of clinicalFórmula:C23H23ClF4N4OPureza:99.49%Cor e Forma:SolidPeso molecular:482.9Diphyllin
CAS:Diphyllin could be characterized as a new V-ATPase inhibitor in treating gastric cancer and inhibiting the phosphorylation of LRP6 in Wnt/β-catenin signaling.Fórmula:C21H16O7Pureza:99.76% - 99.98%Cor e Forma:SolidPeso molecular:380.35Cidofovir dihydrate
CAS:Cidofovir dihydrate: Injectable anti-CMV; suppresses CMV by inhibiting viral DNA polymerase; treats CMV retinitis in AIDS.Fórmula:C8H18N3O8PPureza:99.44%Cor e Forma:SolidPeso molecular:315.22Remdesivir
CAS:Remdesivir (GS-5734) is a nucleoside analog, a broad-spectrum antiviral compound that exerts its activity by inhibiting the RNA-dependent RNA polymerase ofFórmula:C27H35N6O8PPureza:97.62% - 99.98%Cor e Forma:SolidPeso molecular:602.58Ref: TM-T7766
1mg108,00€5mg205,00€1mL*10mM (DMSO)268,00€10mg326,00€25mg497,00€50mg663,00€100mg1.063,00€FIT-039
CAS:FIT-039 is a selective and ATP-competitive, orally active inhibitor of CDK9( IC50 : 5.8 μM;CDK9/cyclin T1).Fórmula:C17H18FN3SPureza:98.61%Cor e Forma:SolidPeso molecular:315.41ML188
CAS:ML188 is a selective noncovalent SARS-CoV 3CLpro inhibitor(IC50 : 1.5 μM), with moderate MW and good enzyme and antiviral inhibitory activity.Fórmula:C26H31N3O3Pureza:99.69%Cor e Forma:SolidPeso molecular:433.54Cobicistat
CAS:Cobicistat (GS-9350): A carbamate, thiazole derivative, and CYP3A inhibitor used to boost anti-HIV drugs for treating HIV.Fórmula:C40H53N7O5S2Pureza:97.36% - 99.62%Cor e Forma:SolidPeso molecular:776.02Ref: TM-T6246
1mg43,00€2mg56,00€5mg88,00€1mL*10mM (DMSO)105,00€10mg117,00€25mg200,00€50mg333,00€100mg477,00€Nirmatrelvir
CAS:PF-07321332 is a potent and orally active inhibitor of SARS-CoV 3C-like protease (3CLPRO) .Fórmula:C23H32F3N5O4Pureza:98.66% - 99.93%Cor e Forma:SolidPeso molecular:499.53Ref: TM-T9351
1mg55,00€2mg78,00€5mg114,00€1mL*10mM (DMSO)127,00€10mg177,00€25mg314,00€50mg485,00€100mg627,00€200mg895,00€500mg1.341,00€Amitivir
CAS:Amitivir (LY 217896)—an IMP dehydrogenase inhibitor that blocks MDCK cell division and may increase uric acid without affecting flu A.Fórmula:C3H2N4SPureza:97.35%Cor e Forma:SolidPeso molecular:126.14Ref: TM-T26619
1mg84,00€1mL*10mM (DMSO)119,00€5mg168,00€10mg241,00€25mg399,00€50mg532,00€100mg745,00€LY2334737
CAS:LY2334737 is an orally available prodrug of gemcitabine with antineoplastic activity.Fórmula:C17H25F2N3O5Pureza:98.82%Cor e Forma:SolidPeso molecular:389.39Ref: TM-T4061
1mg35,00€5mg79,00€1mL*10mM (DMSO)94,00€10mg111,00€25mg215,00€50mg319,00€100mg442,00€200mg583,00€Daclatasvir
CAS:Daclatasvir (EBP 883/BMS-790052) is a potent HCV NS5A inhibitor with EC50 9-50 pM across various genotypes. Phase 3.Fórmula:C40H50N8O6Pureza:99.81% - 99.99%Cor e Forma:SolidPeso molecular:738.886-AZATHYMINE
CAS:6-azathymine inhibits D-3-aminoisobutyrate-pyruvate aminotransferase; 6-azauracil competes with beta-alanine, uncompetitive with pyruvic acid, Ki ~8.9 mM.Fórmula:C4H5N3O2Pureza:99.47%Cor e Forma:SolidPeso molecular:127.1Triazavirin
CAS:Triazavirin is a nucleoside analogue of nucleic acid and an antiviral agent.Fórmula:C5H7N6NaO5SPureza:99.55%Cor e Forma:SolidPeso molecular:286.2Arctigenin
CAS:(-)-Arctigenin ((-)-Arctigenin) is found in burdock.Fórmula:C21H24O6Pureza:98% - 99.51%Cor e Forma:SolidPeso molecular:372.41Didecyldimethylammonium chloride, 50% solution
CAS:Fórmula:C22H48ClNCor e Forma:Clear, colourless to pale yellow liquidPeso molecular:362.08AG-1478
CAS:AG-1478 (NSC-693255) (Tyrphostin AG-1478) is a selective EGFR inhibitor.
Fórmula:C16H14ClN3O2Pureza:99.03% - 99.71%Cor e Forma:SolidPeso molecular:315.75Glaucine
CAS:Glaucine: antitussive, antioxidative, antiviral, may fight arthritis, boosts IL-10, hinders breast cancer cell spread by inhibiting MMP-9 and NF-κB.
Fórmula:C21H25NO4Pureza:99.42% - 99.56%Cor e Forma:SolidPeso molecular:355.43BVDV-IN-1
CAS:BVDV-IN-1 is a non-nucleoside inhibitor (NNI) of bovine viral diarrhea virus (BVDV), with an EC50 of 1.8 μM.Fórmula:C20H22N4OPureza:98.43%Cor e Forma:SolidPeso molecular:334.41Ref: TM-T9103
1mg38,00€5mg86,00€1mL*10mM (DMSO)95,00€10mg124,00€25mg241,00€50mg355,00€100mg507,00€200mg687,00€Voxilaprevir
CAS:Voxilaprevir is an inhibitor of hepatitis C virus (HCV) nonstructural (NS) protein 3/4A protease.Fórmula:C40H52F4N6O9SPureza:99.83% - 99.98%Cor e Forma:SolidPeso molecular:868.93Ref: TM-T19862
1mg75,00€5mg295,00€1mL*10mM (DMSO)394,00€10mg423,00€25mg708,00€50mg954,00€100mg1.288,00€200mg1.738,00€DL-Serine
CAS:DL-Serine is a non-essential amino acid and a natural ligand and allosteric activator of pyruvate kinase M2.Fórmula:C3H7NO3Pureza:97.57%Cor e Forma:Hexagonal Plates Or Prisms White CrystalsPeso molecular:105.09Bonafton
CAS:Bonafton (Bonaphthone) is an antiviral agent.Fórmula:C10H5BrO2Pureza:97.16%Cor e Forma:SolidPeso molecular:237.05Ref: TM-T8877
1mg56,00€1mL*10mM (DMSO)92,00€5mg118,00€10mg167,00€25mg281,00€50mg421,00€100mg605,00€200mg845,00€Norwogonin
CAS:Norwogonin (5,7,8-Trihydroxyflavone), isolated from Scutellaria baicalensis Georgi, possesses antiviral activity against Enterovirus 71 (IC50: 31.83 μg/ml).Fórmula:C15H10O5Pureza:98.17% - 98.84%Cor e Forma:SolidPeso molecular:270.24Ref: TM-T8205
1mg58,00€1mL*10mM (DMSO)158,00€5mg167,00€10mg245,00€25mg434,00€50mg620,00€100mg865,00€200mg1.161,00€AKOS B018304
CAS:AKOS B018304 is an arylalkylidene derivative with polar substitution at para-position.Fórmula:C10H6N2O3S2Pureza:99.19%Cor e Forma:SolidPeso molecular:266.3Sofosbuvir
CAS:Fórmula:C22H29FN3O9PPureza:≥ 98.0%Cor e Forma:White to off-white crystalline powderPeso molecular:529.45L-Chicoric Acid
CAS:L-Chicoric Acid (trans-Caffeoyltartaric acid) has been shown to inhibit hyaluronidase and HIV-1 integrase, and to possess phagoeytosis stimulatory activity.Fórmula:C22H18O12Pureza:98.33% - 99%Cor e Forma:SolidPeso molecular:474.37Ref: TM-T6S2391
2mg39,00€5mg58,00€1mL*10mM (DMSO)64,00€10mg93,00€25mg138,00€50mg197,00€100mg294,00€200mg437,00€Dryocrassin ABBA
CAS:Dryocrassin ABBA (Dryocrassin) is a flavonoid natural product derived from Dryopteris crassirhizoma, with antiviral and antibacterial activities.Fórmula:C43H48O16Pureza:98.43%Cor e Forma:SolidPeso molecular:820.83Aplidine
CAS:Aplidine possesses antiviral activity against SARS-CoV-2(IC90 = 0.88 nM).Fórmula:C57H87N7O15Pureza:99.86%Cor e Forma:SolidPeso molecular:1110.34Ref: TM-T9715
1mg235,00€5mg588,00€10mg787,00€1mL*10mM (DMSO)938,00€25mg1.216,00€50mg1.568,00€100mg2.527,00€Adapalene Methyl Ester
CAS:Impurity Adapalene USP Related Compound B
Applications Adapalene intermediate, an ester of Adapalene. Adapalene USP Related Compound B.
References Charpentier, B., et al.: J. Med. Chem., 38, 4993 (1995),Fórmula:C29H30O3Cor e Forma:NeatPeso molecular:426.55(2R,3S)-3-(tert-Boc)amino-1,2-epoxy-4-phenylbutane
CAS:Produto ControladoImpurity Atazanavir Impurity C
Applications Atazanavir intermediate. Enantiomer R. Atazanavir Impurity C
References Vassar, R., et al.: Science, 286, 735 (1999), Maillard, M., et al.: J. Med. Chem., 50, 776 (2007), Stauffer, S., et al.: Bioorg. Med. Chem. Lett., 17, 1788 (2007),Fórmula:C15H21NO3Cor e Forma:NeatPeso molecular:263.332'-C-β-Methylguanosine
CAS:2'-C-beta-Methylguanosine (2'-C-Methylguanosine), with antiviral activity, inhibits dengue virus 2.Fórmula:C11H15N5O5Pureza:99.37%Cor e Forma:SolidPeso molecular:297.27Braco-19
CAS:Braco-19 is a telomerase/telomere inhibitor and an inhibitor of HAdV viral replication with antiviral activity that reduces lipid vacuolization in adipocytes, inhibits proliferation and decreases telomerase activity in human glioblastoma cells.Fórmula:C35H43N7O2Pureza:97.01%Cor e Forma:SolidPeso molecular:593.76Elenolic Acid (>90%)
CAS:Applications Elenolic Acid is an antiviral agent that inhibits reverse transcriptases, inhibited the growth of chicken embryo fibroblast cells as well as Escherichia coli and Bacillus subtilis strains.
References Heinze, J.E., et al.: Antimicrob. Agents Chemother., 8, 421 (1975); Renis, H,E..: Antimicrob. Agents Chemother., 8, 149 (1975)Fórmula:C11H14O6Pureza:>90%Cor e Forma:NeatPeso molecular:242.231,2,4-Triazole-3-carboxylic Acid
CAS:Impurity Ribavirin EP Impurity C
Applications 1,2,4-Triazole-3-carboxylic Acid (Ribavirin EP Impurity C) is a major metabolite of the antiviral agent Ribavirin (R414475).
References Miller, J.P. et al.: Ann. N.Y. Acad. Sci., 284, 211 (1977); Catlin, D. et al.: Ribavirin: Broad Spec. Antivir. Ag., 83 (1980); Lin, C.C. et al.: Antimicrob. Ag. Chemother., 50, 2368 (2006);Fórmula:C3H3N3O2Cor e Forma:White SolidPeso molecular:113.072-[(1S,3R)-3-Hydroxycyclopentyl]-9-methoxy-1,8-dioxo-N-[(2,4,6-trifluorophenyl)methyl]pyrido[1,2-a]pyrazine-7-carboxamide
CAS:Fórmula:C22H20F3N3O5Cor e Forma:NeatPeso molecular:463.41(2S,3S,5S)-2-Amino-3-hydroxy-5-(tert-butyloxycarbonylamino)-1,6-diphenylhexane
CAS:Produto ControladoFórmula:C23H32N2O3Cor e Forma:NeatPeso molecular:384.51N2-Acetyl Acyclovir Methyl Acetate
Produto ControladoApplications N2-Acetyl Acyclovir Methyl Acetate is an intermediate in the synthesis of Acyclovir (A192400), an orally active acyclic nucleoside with inhibitory activity towards several herpes viruses. Antiviral.
References Collins, P., et al.: J. Antimicrob. Chemother., 5, 431 (1979); Matsumoto, H., et al.: Chem. Pharm. Bull., 36, 1153 (1988); Whitley, R.J., et al.: N. Engl. J. Med., 327, 782 (1992)Fórmula:C13H17N5O6Cor e Forma:NeatPeso molecular:339.3(+)-Bornyl Acetate
CAS:Produto ControladoFórmula:C12H20O2Cor e Forma:Colourless OilyPeso molecular:196.29Peramivir
CAS:Peramivir is a neuraminidase inhibitor used to treat influenza by preventing virus release from cells.Fórmula:C15H28N4O4Pureza:99.82%Cor e Forma:SolidPeso molecular:328.413-Methyloxazinane Arbidol
CAS:Produto ControladoFórmula:C22H24BrN2O3SCor e Forma:NeatPeso molecular:476.407Indinavir Sulfate
CAS:Applications Indinavir Sulfate is a member of the novel hydroxyaminopentane amide class of HIV-1 protease inhibitors. Antiviral. It is a COVID19-related research product.
References Vacca, J.P., et al.: Proc. Nat. Acad. Sci. USA, 91, 4096 (1994), Dorsey, B. D., et al.: J. Med. Chem., 37, 3443 (195), Balani, S.K., et al.: Drug Metab. Dispos., 23, 266 (1995)Fórmula:C36H47N5O4·H2O4SCor e Forma:White SolidPeso molecular:711.874-Acetylamino-3-hydroxybenzoic Acid Ethyl Ester, 100 mg
CAS:Impurity Oseltamivir EP Impurity D
Applications 4-Acetylamino-3-hydroxybenzoic Acid Ethyl Ester (Oseltamivir EP Impurity D) is an impurity in the antiviral drug Oseltamivir (O700100).Fórmula:C11N13NO4Cor e Forma:NeatPeso molecular:223.234-(2-Pyridinyl)benzoic Acid
CAS:Produto ControladoImpurity Atazanavir Impurity (Pyridinyl Benzoic Acid)
Applications Reactive metabolite of Atazanavir (A790051). Atazanavir Impurity (Pyridinyl Benzoic Acid)
References Li, F. et al. Drug Metab. Disp., 39, 294 (2011);Fórmula:C12H9NO2Cor e Forma:NeatPeso molecular:199.21cis 5-Fluoro-1-[2-(hydroxymethyl)-1,3-oxathiolan-5-yl]-2,4(1H,3H)- pyrimidinedione
CAS:Produto ControladoApplications Antiviral nucleoside analog, also an impurity found in emtricitabine (E525000).
References Jeong, L., et al.: J. Med. Chem., 36, 181 (1993),Fórmula:C8H9FN2O4SCor e Forma:Off-WhitePeso molecular:248.23BMS 806
CAS:BMS 806 is an antiretroviral agent and is used for the treatment of HIV. It inhibits the fusion of the HIV virus with the host cell membrane.Fórmula:C22H22N4O4Pureza:Min. 98 Area-%Cor e Forma:PowderPeso molecular:406.43 g/molPeramivir trihydrate
CAS:Selective and potent inhibitor of sialidases (neuraminidases) in influenza A and B viruses. The compound binds tightly to the viral neuraminidase active site in late stages of viral life-cycle. It inhibits shedding sialic acids from host cell surface glycans, which interact with viral hemagglutinin, and consequently prevents release of new viral particles from the host cell surface.
Fórmula:C15H28N4O4·3H2OPureza:Min. 95%Cor e Forma:PowderPeso molecular:382.45 g/molRaltegravir - Bio-X ™
CAS:Raltegravir is an antiretroviral agent used for the treatment of HIV infections in conjunction with other antiretrovirals. It inhibits the activity of HIV-1 integrase, which impedes the insertion of HIV-1 DNA into the host cell genome. Raltegravir also inhibits resistant mutants of HIV-1 that are associated with disease activity and progression.
Fórmula:C20H21FN6O5Pureza:Min. 98 Area-%Cor e Forma:PowderPeso molecular:444.42 g/molFilociclovir
CAS:Filociclovir is a novel antiviral agent, which is synthesized from small-molecule pharmaceutical compounds. It functions primarily by inhibiting viral DNA polymerase, thereby halting viral replication within infected host cells. This mechanism of action is particularly effective against certain herpesviruses, as it targets the polymerase enzyme that is critical for viral DNA synthesis and proliferation.
Fórmula:C11H13N5O3Pureza:Min. 95%Peso molecular:263.25 g/molGanciclovir - Bio-X ™
CAS:Ganciclovir is an acyclovir analog that is used in the treatment of cytomegalovirus and herpetic keratitis of the eye. This drug is a DNA polymerase inhibitor and exhibits its anti-viral properties by inhibiting viral replication.
Fórmula:C9H13N5O4Pureza:Min. 95%Cor e Forma:PowderPeso molecular:255.23 g/molOseltamivir acid
CAS:Inhibitor of viral neuraminidase enzyme, effective against influenza A and B viruses. This antiviral compound inhibits neuraminidase-mediated cleavage of host cell sialic acids, which interact with newly synthesised virions from the host cell. This prevents virion budding from the host, resulting in inhibition of virion release and viral infection overall.Fórmula:C14H24N2O4Pureza:Min. 95 Area-%Cor e Forma:White PowderPeso molecular:284.35 g/molRaltegravir
CAS:Raltegravir is an antiretroviral agent, which is a synthetic integrase inhibitor sourced from pharmaceutical research. Its mode of action involves the inhibition of the HIV-1 integrase enzyme, which is essential for the viral replication process. By blocking the strand transfer step of the integration of viral DNA into the host cell genome, Raltegravir prevents the proliferation of the virus within the host.
Fórmula:C20H21FN6O5Pureza:Min. 98 Area-%Cor e Forma:White Off-White PowderPeso molecular:444.42 g/mol3- Phenyl- N- [1- (phenylmethyl) - 4- piperidinyl] -tricyclo[3.3.1.13, 7] decane- 1- carboxamide
CAS:A compound with antiviral activity against Ebola virus that targets the surface-exposed glycoprotein and inhibits viral entry into host cells. In vitro studies in Vero cells revealed the compound inhibits the viral replication with EC50 of 0.38 µM.Fórmula:C29H36N2OPureza:Min. 95%Cor e Forma:Off-White To Yellow SolidPeso molecular:428.61 g/molFosamprenavir calcium
Fosamprenavir calcium is an antiretroviral medication, which is derived from the prodrug of amprenavir. It is synthesized through chemical processes to enhance oral bioavailability and improve pharmacokinetic properties. Through its mode of action, fosamprenavir is converted in vivo to amprenavir, which acts as an inhibitor of the HIV-1 protease enzyme. By inhibiting this enzyme, it prevents the cleavage of the Gag-Pol polyprotein, disrupting viral replication and processing, ultimately leading to the production of immature, non-infectious viral particles.Fórmula:C25H34CaN3O9PSPureza:Min. 95%Peso molecular:623.67 g/molPleconaril
CAS:Anti-viral; capsid inhibitorFórmula:C18H18F3N3O3Pureza:Min. 98 Area-%Cor e Forma:White PowderPeso molecular:381.35 g/molCabotegravir
CAS:Anti-viral; HIV integrase inhibitorFórmula:C19H17F2N3O5Pureza:Min. 95%Cor e Forma:White/Off-White SolidPeso molecular:405.35 g/molL-Valacyclovir HCl - Bio-X ™
CAS:Valacyclovir is a guanine nucleoside antiviral drug that is used to treat herpes exacerbations. This drug inhibits DNA polymerase and prevents viral DNA synthesis. Valacyclovir is the L-valine ester of acyclovir.Fórmula:C13H20N6O4·HClPureza:Min. 95%Cor e Forma:PowderPeso molecular:360.8 g/molTenofovir - Bio-X ™
CAS:Tenofovir is an acyclic nucleoside phosphonate that exhibits anti-viral properties through its inhibition of reverse transcriptases. In particular, Tenofovir is a potent inhibitor of Human Immunodeficiency Virus (HIV) and chronic Hepatitis B Virus (HBV) reverse transcriptases, thus preventing the replication of genetic viral material. This property is beneficial in virus research areas and developing antiviral treatments. Once inside the body tenofovir is metabolized into its active form, tenofovir diphosphate, by the lysosomal protease cathepsin A, nucleotide kinases and adenylate kinases.
Tenofovir is part of our Bio-X ™ Range. These products are aimed at life science researchers who need high quality ready to use products for assay development, screening or other R&D work. With a solubility datasheet and convenient vials, all of our Bio-X ™ products are in stock across our global warehouses for rapid delivery and ease of use.Fórmula:C9H14N5O4PPureza:Min. 98.5 Area-%Cor e Forma:White To Off-White SolidPeso molecular:287.21 g/molN-[5-[3-[(4-Hydroxyphenyl)sulfamoyl]-4-methoxyphenyl]-4-methyl-1,3-thiazol-2-yl]-2,2-dimethylpropanamide
CAS:PI4KIII beta inhibitorFórmula:C22H25N3O5S2Pureza:Min. 98 Area-%Cor e Forma:White PowderPeso molecular:475.58 g/molLopinavir - Bio-X ™
CAS:Chemically derived from ritonavir, Lopinavir belongs to the amphetamines. Lopinavir is clinically used in the prevention and treatment of HIV infections as it acts as HIV-1 protease inhibitor. In 2020, lopinavir was tested to treat COVID-19 patients and although it led to a higher rate of gastrointestinal side effects, the Lopinavir-treated group had a lower incidence of severe complications. Overall it was deemed not to work as a treatment.Fórmula:C37H48N4O5Pureza:Min. 98 Area-%Cor e Forma:PowderPeso molecular:628.8 g/molDarunavir
CAS:Darunavir is a HIV-1 protease inhibitor used orally in the treatment of patients with multi-drug resistant HIV-1 infection (Ghosh, 2007). It has also been shown to be effective against other infectious diseases such as hepatitis C virus and SARS coronavirus. Metabolized by cytochrome P450 3A (CYP3A) isoenzymes, darunavir is often administered together with ritonavir that prolongs its bioavaiability, giving a terminal elimination half-life (t1/2) of 15 hours (Back, 2008). The effect of darunavir on natural compounds such as matrix proteins and toll-like receptor activity has also been studied via high performance liquid chromatography (HPLC) experiments.
Fórmula:C27H37N3O7SPureza:Min. 95%Cor e Forma:White PowderPeso molecular:547.66 g/molCytarabine hydrochloride - Bio-X ™
CAS:Cytarabine is a pyrimidine nucleoside analogue that is used to treat leukaemia especially, non-lymphocytic leukaemia. This drug also has anti-viral and immunosuppressant properties. Cytarabine is cytotoxic and acts through direct DNA damage. Although its mechanism of action is not fully understood, it is said to inhibit DNA polymerase.Fórmula:C9H13N3O5•HClPureza:Min. 95%Cor e Forma:PowderPeso molecular:279.68 g/molDoravirine
CAS:Non-nucleoside inhibitor of reverse transcriptase; anti-viral
Fórmula:C17H11ClF3N5O3Pureza:Min. 97 Area-%Cor e Forma:White PowderPeso molecular:425.75 g/molAtazanavir - Bio-X ™
CAS:Atazanavir is an antiviral protease inhibitor, used in the anti-retroviral therapy of adult and sometimes paediatric patients infected with HIV. This drug inhibits the processing of viral Gag and Gag-pol polyproteins in HIV-1 infected cells by binding to the HIV-1 protease active site.
Fórmula:C38H52N6O7Pureza:Min. 95%Cor e Forma:PowderPeso molecular:704.86 g/molCidofovir anhydrous - Bio-X ™
CAS:Cidofovir is an anti-viral agent that is used to treat Cytomegalovirus (CMV) retinitis in patients with AIDS. This drug suppresses CMV replication by inhibiting viral DNA synthesis.Fórmula:C8H14N3O6PPureza:Min. 95%Cor e Forma:PowderPeso molecular:279.19 g/molSaquinavir mesylate
CAS:Anti-viral; HIV protease inhibitorFórmula:C38H50N6O5•CH4O3SPureza:Min. 95%Cor e Forma:PowderPeso molecular:766.95 g/molGS 441524
CAS:Nucleoside analog with antiviral activity against zoonotic feline infectious peritonitis virus (FIPV) and severe acute respiratory syndrome (SARS) virus from Coronaviridae family. The compound is a pro-drug and undergoes intracellular phosphorylation resulting in the active triphosphate metabolite. The triphosphorylated GS 441524 analog competes with natural nucleoside triphosphates and interferes with viral RNA synthesis. In previous studies it was tested in vitro as well as in experimental animals and showed good safety profile.Fórmula:C12H13N5O4Pureza:Min. 98 Area-%Cor e Forma:PowderPeso molecular:291.26 g/molBrivudine
CAS:Anti-viral; thymidine analogue; DNA plymerase inhibitorFórmula:C11H13BrN2O5Pureza:Min. 95%Cor e Forma:White PowderPeso molecular:333.14 g/molRitonavir - Bio-X ™
CAS:Ritonavir is a HIV protease inhibitor. It has an anti-retroviral activity as it inhibits the protease enzymes specific of both HIV-1 and HIV-2 and has been shown to be effective in controlling virus replication in humans and animals. Ritonavir works by preventing the HIV viral protease enzyme from cleaving the structural and replicative proteins produced by HIV genes such as gag and pol.
Fórmula:C37H48N6O5S2Pureza:Min. 98 Area-%Cor e Forma:White PowderPeso molecular:720.95 g/molDelavirdine mesylate
CAS:Non-nucleoside reverse transcriptase inhibitor; antiviral agent against HIV
Fórmula:C23H32N6O6S2Pureza:Min. 95%Cor e Forma:White To Yellow SolidPeso molecular:552.18248Nelfinavir mesylate
CAS:Anti-viral; HIV protease inhibitorFórmula:C33H49N3O7S2Cor e Forma:White PowderPeso molecular:663.89 g/mol6-Fluoro-3-hydroxypyrazine-2-carboxamide
CAS:6-Fluoro-3-hydroxypyrazine-2-carboxamide is a potent RNA polymerase inhibitor, active against both RNA viruses in vitro and in vivo. A four-step approach to the synthesis of 6-Fluoro-3-hydroxypyrazine-2-carboxamide was reported in 2014. 6-Fluoro-3-hydroxypyrazine-2-carboxamide is commercialized and has recently been suggested for the treatment of mild cases of COVID-19.Fórmula:C5H4FN3O2Pureza:Min. 97 Area-%Cor e Forma:PowderPeso molecular:157.1 g/molZanamivir hydrate - Bio-X ™
CAS:Potent and selective inhibitor of influenza A and B sialidases. Zanamivir belongs to the class of drugs known as neuraminidase inhibitors. This compound is a sialic acid analogue that occupies viral neuraminidase active site, inhibits enzyme’s hydrolytic activity and cleavage of sialic acid residues from host cell surface glycans. It therefore prevents shedding newly produced virions from infected cell surface and reduces infection of surrounding cells. In in vitro studies with influenza A and B virus isolates, zanamivir inhibited the plaque formation by 50% in canine cells (MDCK) with concentrations between 0.004 and 0.014 μM and 0.02 and 16 μM, respectively. Zanamivir hydrate is part of our Bio-X ™ Range. These products are aimed at life science researchers who need high quality ready to use products for assay development, screening or other R&D work. With a solubility datasheet and convenient vials, all of our Bio-X ™ products are in stock across our global warehouses for rapid delivery and ease of use.Fórmula:C12H22N4O8Pureza:(%) Min. 98%Cor e Forma:PowderPeso molecular:350.33 g/molDasabuvir
CAS:Dasabuvir is a non-nucleoside NS5B polymerase inhibitor with action on hepatitis C virus RNA replication and is used for treating hepatitis C in combination therapies.Fórmula:C26H27N3O5SPureza:Min. 95%Cor e Forma:Off-White PowderPeso molecular:493.58 g/molN-Boc-protected -Guanidino Oseltamivir
CAS:N-Boc-protected -Guanidino Oseltamivir is a fine chemical that belongs to the group of versatile building blocks. It is a complex compound that has been used in research as a reagent and speciality chemical. N-Boc-protected -Guanidino Oseltamivir is an important intermediate for the synthesis of a variety of useful compounds, such as pharmaceuticals and natural products. This compound is also used as a reaction component in organic syntheses, especially for the preparation of high quality and useful scaffolds.
Fórmula:C26H44N4O8Pureza:Min. 95%Cor e Forma:PowderPeso molecular:540.31591Letermovir
CAS:Anti-viral; inhibitor of cytomegalovirus-terminase complex
Fórmula:C29H28F4N4O4Pureza:Min. 98 Area-%Cor e Forma:Yellow PowderPeso molecular:572.55 g/molLedipasvir
CAS:Anti-viral; inhibitor of NS5A proteinFórmula:C49H54F2N8O6Pureza:Min. 98 Area-%Cor e Forma:Off-White PowderPeso molecular:889.00 g/molAtazanavir sulfate
CAS:Anti-viral; HIV protease inhibitor
Fórmula:C38H52N6O7·H2SO4Pureza:Min. 95%Cor e Forma:PowderPeso molecular:802.94 g/molZalcitabine - Bio-X ™
CAS:Zalcitabine (also known as dideoxycytidine or ddC) is a nucleoside analogue reverse transcriptase inhibitor (NRTI) medication used in the treatment of human immunodeficiency virus (HIV) infections. It works by blocking reverse transcriptase, an enzyme essential for replication of the HIV virus, thereby preventing the virus from multiplying and spreading. Zalcitabine is often used in combination with other antiretroviral drugs to effectively treat HIV/AIDS.Fórmula:C9H13N3O3Pureza:Min. 95%Cor e Forma:PowderPeso molecular:211.22 g/molSofosbuvir
CAS:Potent inhibitor of viral RNA polymerase called non-structural protein 5B (NS5B). This nucleotide analog is effective against Hepatitis C virus (HCV) infection since it inhibits viral RNA replication. Sofosbuvir is a prodrug and gets triphosphorylated in the liver cells, generating biologically active compound with anti-viral activity.Fórmula:C22H29FN3O9PPureza:Min. 95%Cor e Forma:Off-White PowderPeso molecular:529.45 g/molGS 331007
CAS:Anti-viral; RNA polymerase inhibitor; sofosbuvir metaboliteFórmula:C10H13FN2O5Pureza:Min. 95%Cor e Forma:Off-White PowderPeso molecular:260.22 g/molRupintrivir
CAS:Rupintrivir is a peptidomimetic antiviral with action on rhinovirus 3C protease to inhibit viral replication and is used for research on rhinovirus and other viral infections.
Fórmula:C31H39FN4O7Pureza:Min. 98 Area-%Cor e Forma:PowderPeso molecular:598.28028Lersivirine
CAS:Anti-viral; non-nucleoside reverse transcriptase inhibitorFórmula:C17H18N4O2Pureza:Min. 95%Cor e Forma:SolidPeso molecular:310.14298EIDD-1931
CAS:Nucleoside analog with antiviral activity against coronaviruses, hepatitis and influenzas viruses. EIDD 1931 inhibited the Middle East Respiratory Syndrome coronavirus (MERS-CoV) and the murine hepatitis virus (MHV) replication in vitro at submicromolar concentrations. EIDD 1931 is able to evade the proofreading exonuclease ExoN and presents with high barrier to development of drug resistance.
Fórmula:C9H13N3O6Pureza:Min. 98 Area-%Cor e Forma:White Off-White PowderPeso molecular:259.22 g/molSimeprevir
CAS:Anti-viral; NS3/4A protease inhibitor_x000D_Fórmula:C38H47N5O7S2Pureza:Min. 95%Cor e Forma:PowderPeso molecular:749.94 g/mol






