Atazanavir sulfate
CAS No. 229975-97-7
Atazanavir sulfate( BMS 232632 sulfate | BMS-232632 sulfate | BMS232632 sulfate )
Catalog No. M13641 CAS No. 229975-97-7
A highly potent HIV-1 protease inhibitor that exhibits potent anti-HIV activity EC50 of 2.6-5.3 nM and EC90 of 9-15 nM in cell culture.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 35 | In Stock |
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| 10MG | 57 | In Stock |
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| 25MG | 88 | In Stock |
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| 50MG | 113 | In Stock |
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| 100MG | 194 | In Stock |
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| 200MG | 291 | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameAtazanavir sulfate
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NoteResearch use only, not for human use.
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Brief DescriptionA highly potent HIV-1 protease inhibitor that exhibits potent anti-HIV activity EC50 of 2.6-5.3 nM and EC90 of 9-15 nM in cell culture.
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DescriptionA highly potent HIV-1 protease inhibitor that exhibits potent anti-HIV activity EC50 of 2.6-5.3 nM and EC90 of 9-15 nM in cell culture; shows synergistic antiviral effects in HIV-infected PBMCs; used to treat and prevent HIV/AIDS.HIV Infection Approved.
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In Vitro——
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In Vivo——
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SynonymsBMS 232632 sulfate | BMS-232632 sulfate | BMS232632 sulfate
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PathwayMicrobiology/Virology
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TargetHIV
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RecptorHIVprotease
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Research AreaInfection
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IndicationHIV Infection
Chemical Information
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CAS Number229975-97-7
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Formula Weight802.934
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Molecular FormulaC38H54N6O11S
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Purity>98% (HPLC)
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SolubilityDMSO; H2O: < 0.1 mg/mL
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SMILESCC(C)(C)[C@@H](C(=O)N[C@@H](CC1=CC=CC=C1)[C@H](CN(CC2=CC=C(C=C2)C3=CC=CC=N3)NC(=O)[C@H](C(C)(C)C)NC(=O)OC)O)NC(=O)OC.OS(=O)(=O)O
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Chemical Name2,5,6,10,13-Pentaazatetradecanedioic acid, 3,12-bis(1,1-dimethylethyl)-8-hydroxy-4,11-dioxo-9-(phenylmethyl)-6-[[4-(2-pyridinyl)phenyl]methyl]-, 1,14-dimethyl ester, (3S,8S,9S,12S)-, sulfate
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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BMS-538203
A chemical intermidate of BMS-626529, a HIV-1 attachment inhibitor that targets gp120,
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Helichrysetin
Helichrysetin has mild anti-HIV-1 PR activity. Helichrysetin has great potentials for development as an anticancer agent, it has cytotoxic effect on four selected cancer cell lines, A549, MCF-7, Ca Ski, and HT-29.Searching for anti-HIV-1 protease (PR) inhibitors of Thai medicinal plants led to the isolation of a new cyclohexenyl chalcone named panduratin C and chalcone derivatives (2-6) from the methanol extract of Boesenbergia pandurata rhizomes.
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Punicalin
Punicalin exerts anti-inflammatory antioxidative and anti-hepatotoxic activities it shows inhibitory activity on HIV-1 reverse transcriptase in a dose-dependent manner with an IC50 of 0.11 microg/ml (0.14 microM).
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