RV-1729

CAS No. 1293915-42-0

RV-1729( RV1729 | RV 1729 )

Catalog No. M11188 CAS No. 1293915-42-0

RV-1729 is a potent, selective PI3Kδ inhibitor with IC50 of 12 nM.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 963 Get Quote
50MG 1962 Get Quote
100MG 2520 Get Quote
200MG Get Quote Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    RV-1729
  • Note
    Research use only, not for human use.
  • Brief Description
    RV-1729 is a potent, selective PI3Kδ inhibitor with IC50 of 12 nM.
  • Description
    RV-1729 is a potent, selective PI3Kδ inhibitor with IC50 of 12 nM, 2-fold selectivity for PI3Kδ relative to PI3Kγ and 16-fold over PI3Kα; inhibits PMA-induced peroxide production in U937 cells and phosphorylation of Akt in MCP1-stimulated THP1 cells with IC50 of 1.1 and 46 nM; significantly inhibits allergen-induced responses in murine models of asthma and COPD.Asthma Phase 1 Clinical.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    RV1729 | RV 1729
  • Pathway
    PI3K/Akt/mTOR signaling
  • Target
    PI3K
  • Recptor
    PI3K
  • Research Area
    Inflammation/Immunology
  • Indication
    Asthma

Chemical Information

  • CAS Number
    1293915-42-0
  • Formula Weight
    735.242
  • Molecular Formula
    C39H39ClN8O5
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    O=C(N(CCOC)CCOC)CCCC#CC1=CC=CC(N=C(CN2N=C(C3=CC=CC(O)=C3)C4=C(N)N=CN=C42)N5CC6=CC=CC=C6Cl)=C1C5=O
  • Chemical Name
    6-(2-((4-amino-3-(3-hydroxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)methyl)-3-(2-chlorobenzyl)-4-oxo-3,4-dihydroquinazolin-5-yl)-N,N-bis(2-methoxyethyl)hex-5-ynamide

Shipping & Storage Information

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

Reference

1. Norman P. Expert Opin Ther Pat. 2014 Apr;24(4):471-5. 2. Respivert Ltd. Crystalline PI3 kinase inhibitors. WO2013136076; 2013
molnova catalog
related products
  • BAY 1082439

    BAY 1082439 is a potent, highly selective, orally available PI3Kα/β inhibitor, selectively inhibits both PI3Kα.

  • AZD8835

    AZD8835 (AZD-8835) is a potent, selective inhibitor of PI3Kα and PI3Kδ with IC50 of 6.2 and 5.7 nM.

  • PF-04979064

    A highly potent and selective, dual PI3K/mTOR inhibitor.