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ChemicalBook--->CAS DataBase List--->1859053-21-6

1859053-21-6

1859053-21-6 Structure

1859053-21-6 Structure
IdentificationBack Directory
[Name]

Rucaparib Camsylate
[CAS]

1859053-21-6
[Synonyms]

Rucaparib Camsylate
Rucaparib Camphosulfonate
8‐Fluoro‐2‐(4‐methylaminomethyl‐phenyl)‐1,3,4,5‐tetrahydro‐azepino[5,4,3‐cd] indol‐6‐one (S)‐camphorsulfonate Salt
Bicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S,4R)-, compd. with 8-fluoro-1,3,4,5-tetrahydro-2-[4-[(methylamino)methyl]phenyl]-6H-pyrrolo[4,3,2-ef][2]benzazepin-6-one (1:1)
[Molecular Formula]

C29H34FN3O5S
[MOL File]

1859053-21-6.mol
[Molecular Weight]

555.661
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

DMSO:79.63(Max Conc. mg/mL);143.31(Max Conc. mM)
[form ]

Solid
[color ]

Light yellow to gray
Safety DataBack Directory
[Symbol(GHS) ]


GHS08
[Signal word ]

Warning
[Hazard statements ]

H361-H341
[Precautionary statements ]

P201-P202-P281-P308+P313-P405-P501-P201-P202-P281-P308+P313-P405-P501
Hazard InformationBack Directory
[Uses]

Rucaparib Camsylate is a novel DNA repair enzyme poly-ADP ribose polymerase-1 (PARP-1) inhibitor.
[Definition]

ChEBI:Rucaparib camsylate is a camphorsulfonate salt obtained by reaction of rucaparib with one molar equivalent of (1S,4R)-camphorsulfonic acid. It is an inhibitor of poly (ADP-ribose) polymerase and is used as monotherapy for advanced ovarian cancer and deleterious germline or somatic BRCA mutation. It has a role as an EC 2.4.2.30 (NAD(+) ADP-ribosyltransferase) inhibitor. It is a camphorsulfonate salt and an azepinoindole. It contains a (S)-camphorsulfonate and a rucaparib(1+).
[Biological Activity]

Rucaparib is an inhibitor of the DNA repair enzyme poly-ADP ribose polymerase-1 (PARP-1). It has been found to have anticancer activity in a number of cancers and has been approved for treatment of previously treatedBRCA-mutant ovarian cancer.
[storage]

Store at -20°C
Spectrum DetailBack Directory
[Spectrum Detail]

Rucaparib Camsylate(1859053-21-6)1HNMR
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