Darunavir ethanolate

CAS No. 635728-49-3

Darunavir ethanolate ( TMC-114;UIC-94017 )

Catalog No. M15408 CAS No. 635728-49-3

A potent, selective HIV-1 protease inhibitor that is extremely potent against laboratory HIV-1 strains and primary clinical isolates with IC50 of 3 nM, IC90 of 9 nM.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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5MG 35 In Stock
10MG 50 In Stock
25MG 87 In Stock
50MG 147 In Stock
100MG 237 In Stock
200MG 354 In Stock
500MG 581 In Stock
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Biological Information

  • Product Name
    Darunavir ethanolate
  • Note
    Research use only, not for human use.
  • Brief Description
    A potent, selective HIV-1 protease inhibitor that is extremely potent against laboratory HIV-1 strains and primary clinical isolates with IC50 of 3 nM, IC90 of 9 nM.
  • Description
    A potent, selective HIV-1 protease inhibitor that is extremely potent against laboratory HIV-1 strains and primary clinical isolates with IC50 of 3 nM, IC90 of 9 nM; blockes the infectivity and replication of HIV-1(NL4-3) variants with IC50 of 3-29 nM, also potent against multi-PI-resistant clinical HIV-1 variants isolated from patients; used to treat and prevent HIV/AIDS.HIV Infection Approved
  • Synonyms
    TMC-114;UIC-94017
  • Pathway
    Microbiology/Virology
  • Target
    HIV
  • Recptor
    WTHIV-1protease
  • Research Area
    Infection
  • Indication
    HIV Infection

Chemical Information

  • CAS Number
    635728-49-3
  • Formula Weight
    593.73
  • Molecular Formula
    C29H43N3O8S
  • Purity
    >98% (HPLC)
  • Solubility
    10 mM in DMSO
  • SMILES
    CCO.CC(C)CN(C[C@H]([C@H](CC1=CC=CC=C1)NC(=O)O[C@H]2CO[C@@H]3[C@H]2CCO3)O)S(=O)(=O)C4=CC=C(C=C4)N
  • Chemical Name
    Carbamic acid, N-[(1S,2R)-3-[[(4-aminophenyl)sulfonyl](2-methylpropyl)amino]-2-hydroxy-1-(phenylmethyl)propyl]-, (3R,3aS,6aR)-hexahydrofuro[2,3-b]furan-3-yl ester, compd. with ethanol (1:1)

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Surleraux DL, et al. J Med Chem. 2005 Mar 24;48(6):1813-22.
2. Koh Y, et al. Antimicrob Agents Chemother. 2003 Oct;47(10):3123-9.
3. King NM, et al. J Virol. 2004 Nov;78(21):12012-21.
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