CasNo: 763113-22-0
MF: C24H23FN4O3
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Many of the products generated by alkylating agents on DNA can be efficiently repaired by normal base excision repair (BER). Some poly(ADP-ribose) polymerases (PARPs) assist in the repair of single-strand DNA nicks, an important step in BER. Olaparib is a potent inhibitor of PARP1 and PARP2 (IC50 = 5 and 1 nM, respectively) but is less effective against the PARP tankyrase-1 (IC50 = 1.5 μM). It can be used in cells and in animals, alone or in combination therapy with alkylating agents, to block BER and increase cancer cell death.
Many of the products generated by alkylating agents on DNA can be efficiently repaired by normal base excision repair (BER). Some poly(ADP-ribose) polymerases (PARPs) assist in the repair of single-strand DNA nicks, an important step in BER. Olaparib is a potent inhibitor of PARP1 and PARP2 (IC50 = 5 and 1 nM, respectively) but is less effective against the PARP tankyrase-1 (IC50 = 1.5 μM). It can be used in cells and in animals, alone or in combination therapy with alkylating agents, to block BER and increase cancer cell death.[Cayman Chemical]
The CAS number of Olaparib is 763113-22-0.
More information of Olaparib 763113-22-0 are:
CAS Number |
763113-22-0 |
Density |
1.43 g/cm3 |
Refractive Index |
1.702 |
HS CODE |
29339900 |
PSA |
86.37000 |
LogP |
2.22320 |
Pka |
12.07±0.40(Predicted) |
The chemical formula of Olaparib is C24H23FN4O3 which containing 24 Carbon atoms,23 Hydrogen atoms,1 Fluorine atoms,4 Nitrogen atoms and 3 Oxygen atoms,and the molecular weight, and the molecular weight of Olaparib is 434.47
Many of the products generated by alkylating agents on DNA can be efficiently repaired by normal base excision repair (BER). Some poly(ADP-ribose) polymerases (PARPs) assist in the repair of single-strand DNA nicks, an important step in BER. Olaparib is a potent inhibitor of PARP1 and PARP2 (IC50 = 5 and 1 nM, respectively) but is less effective against the PARP tankyrase-1 (IC50 = 1.5 μM). It can be used in cells and in animals, alone or in combination therapy with alkylating agents, to block BER and increase cancer cell death.
InChI:InChI=1/C24H23FN4O3/c25-20-8-5-15(14-21-17-3-1-2-4-18(17)22(30)27-26-21)13-19(20)24(32)29-11-9-28(10-12-29)23(31)16-6-7-16/h1-5,8,13,16H,6-7,9-12,14H2,(H,27,30)
Relevant articles related to Olaparib:
Article |
Source |
Novel synthesis method of olaparib bulk drug |
- , (2021/06/22) |
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