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A-966492

CAS No.
934162-61-5
Chemical Name:
A-966492
Synonyms
CS-903;A-966492;A-966492, >=98%;A-966492 USP/EP/BP;A-966492(A 966492);A966492;A 966492;A-966492;A-966492 PARP inhibitor A966492;2-[2-Fluoro-4-[(2S)-2-pyrrolidinyl]phenyl]-1H-benzimidazole-7-carboxamide;2-[2-fluoro-4-[(2S)-pyrrolidin-2-yl]phenyl]-1H-benzimidazole-4-carboxamide;1H-Benzimidazole-7-carboxamide, 2-[2-fluoro-4-[(2S)-2-pyrrolidinyl]phenyl]-
CBNumber:
CB42522977
Molecular Formula:
C18H17FN4O
Molecular Weight:
324.35
MDL Number:
MFCD17215207
MOL File:
934162-61-5.mol
MSDS File:
SDS
Last updated:2023-06-08 09:02:57

A-966492 Properties

Boiling point 605.5±65.0 °C(Predicted)
Density 1.335
storage temp. Store at -20°C
solubility ≥32.4 mg/mL in DMSO; ≥16.53 mg/mL in H2O with ultrasonic; ≥3.16 mg/mL in EtOH with gentle warming and ultrasonic
form solid
pka 9.33±0.30(Predicted)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS07,GHS09
Signal word  Warning
NFPA 704
0
2 0

A-966492 price More Price(27)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 26378 A-966492 934162-61-5 1mg $32 2024-03-01 Buy
Cayman Chemical 26378 A-966492 934162-61-5 25mg $533 2024-03-01 Buy
Cayman Chemical 26378 A-966492 934162-61-5 5mg $139 2024-03-01 Buy
Cayman Chemical 26378 A-966492 934162-61-5 10mg $261 2024-03-01 Buy
ApexBio Technology A4160 A-966492 934162-61-5 50mg $590 2021-12-16 Buy
Product number Packaging Price Buy
26378 1mg $32 Buy
26378 25mg $533 Buy
26378 5mg $139 Buy
26378 10mg $261 Buy
A4160 50mg $590 Buy

A-966492 Chemical Properties,Uses,Production

Uses

A-966492 effectively inhibits PARP-1 with an EC50 of 1 nM and a Ki value of 1 nM. When it acts on PARP-2, the Ki value is 1.5 nM. It has excellent efficacy on PARP enzyme, especially on C41 cells. A-966492 significantly enhanced the effect of TMZ in a dose-dependent manner.

Biological Activity

a-966492 is an inhibitor of parp-1 with ki value of 1nm [1].parp-1 belongs to the poly(adp-ribose) polymerases (parps) family, it contributes to the resistance happened after cancer therapy. a-966492 is a potent inhibitor of both parp-1 and parp-2 (ki value of 1.5nm) with good potency in c41 whole cells (ec50 value of 1nm). a-966492 shows excellent pharmaceutical properties with oral bioavailabilities of 34-72% and half-lives of 1.7-1.9 h. additionally, a-966492 can crosses the blood-brain barrier. a-966492 is proved potent in a murine b16f10 syngeneic melanoma model and a brca1-deficient mx-1 breast carcinoma model. meanwhile, it can enhance the efficacy of tmz and carboplatin in these models [1].

Synthesis

A-966492 is prepared by reacting 3-Carboxamido-1,2-phenylenediamine with benzoic acid in a solution(methanol:water=1:1) at 50 °C for 2 hours.

References

[1] penning td, zhu gd, gong j, thomas s, gandhi vb, liu x, shi y, klinghofer v, johnson ef, park ch, fry eh, donawho ck, frost dj, buchanan fg, bukofzer gt, rodriguez le, bontcheva-diaz v, bouska jj, osterling dj, olson am, marsh kc, luo y, giranda vl. optimization of phenyl-substituted benzimidazole carboxamide poly(adp-ribose) polymerase inhibitors: identification of (s)-2-(2-fluoro-4-(pyrrolidin-2-yl)phenyl)-1h-benzimidazole-4-carboxamide (a-966492), a highly potent and efficacious inhibitor. j med chem. 2010 apr 22;53(8):3142-53.

A-966492 Preparation Products And Raw materials

Raw materials

Preparation Products

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A-966492 Spectrum

A-966492 2-[2-Fluoro-4-[(2S)-2-pyrrolidinyl]phenyl]-1H-benzimidazole-7-carboxamide A-966492(A 966492) 2-{2-fluoro-4-[(2S)-pyrrolidin-2-yl]phenyl}-1H-1,3-benzodiazole-7-carboxaMide 2-[2-Fluoro-4-[(2S)-2-pyrrolidinyl]phenyl]-1H-benzimidazole-7-carboxamide A-966492 A-966492, >=98% A966492;A 966492;A-966492 CS-903 1H-Benzimidazole-7-carboxamide, 2-[2-fluoro-4-[(2S)-2-pyrrolidinyl]phenyl]- A-966492 USP/EP/BP A-966492 PARP inhibitor A966492 2-[2-fluoro-4-[(2S)-pyrrolidin-2-yl]phenyl]-1H-benzimidazole-4-carboxamide (S)-2-(2-Fluoro-4-(pyrrolidin-2-yl)phenyl)-1H-benzo[d]imidazole-7-carboxamide 934162-61-5 931462-61-5 Inhibitor Inhibitors APIs