ChemicalBook--->CAS DataBase List--->1293915-42-0

1293915-42-0

1293915-42-0 Structure

1293915-42-0 Structure
IdentificationBack Directory
[Name]

5-HexynaMide, 6-[2-[[4-aMino-3-(3-hydroxyphenyl)-1H-pyrazolo[3,4-d]pyriMidin-1-yl]Methyl]-3-[(2-chlorophenyl)Methyl]-3,4-dihydro-4-oxo-5-quinazolinyl]-N,N-bis(2-Methoxyethyl)-
[CAS]

1293915-42-0
[Synonyms]

RV-1729
RV-1729;RV 1729;RV1729
6-[2-[[4-Amino-3-(3-hydroxyphenyl)pyrazolo[3,4-d]pyrimidin-1-yl]methyl]-3-[(2-chlorophenyl)met
6-[2-[[4-Amino-3-(3-hydroxyphenyl)pyrazolo[3,4-d]pyrimidin-1-yl]methyl]-3-[(2-chlorophenyl)methyl]-4-oxo-quinazolin-5-yl]-N,N-bis(2-methoxyethyl)hex-5-ynamide
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
5-HexynaMide, 6-[2-[[4-aMino-3-(3-hydroxyphenyl)-1H-pyrazolo[3,4-d]pyriMidin-1-yl]Methyl]-3-[(2-chlorophenyl)Methyl]-3,4-dihydro-4-oxo-5-quinazolinyl]-N,N-bis(2-Methoxyethyl)-
[Molecular Formula]

C39H39ClN8O5
[MDL Number]

MFCD27987097
[MOL File]

1293915-42-0.mol
[Molecular Weight]

735.23
Chemical PropertiesBack Directory
[storage temp. ]

Store at 0-8 °C
[Appearance]

white powder
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Hazard InformationBack Directory
[Uses]

RV-1729 is an inhibitor of the phosphatidylinositol 3-kinase-δ (PI3Kδ). RV-1729 identifies inhibition of the PI3K isotype by quantifying the release of phosphatidylinositol 3,4, 5-triphosphate (PIP3) (IC50=12 nM), showing twice the selectivity for PI3Kδ relative to PI3Kγ. RV-1729 is also 16 times more selective to PI3Kα. RV-1729 regulates immune and inflammatory responses by inhibiting PI3Kδ. RV-1729 can be used in studies of asthma and chronic obstructive pulmonary disease (COPD)[1].
[References]

[1] Norman P. Evaluation of WO2013136076: two crystalline forms of the phosphatidylinositol 3-kinase-δ inhibitor RV-1729[J]. Expert Opinion on Therapeutic Patents, 2014, 24(4): 471-475. DOI:10.1517/13543776.2014.865725
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