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BMN 673

BMN 673 Structure
CAS No.
1207456-01-6
Chemical Name:
BMN 673
Synonyms
LT-673;CS-750;BMN 673;MDV3800);Talazoparib;BMN 673, >=98%;(8S,9R)-BMN 673;BMN 673 USP/EP/BP;BMN-673, TALAZOPARIB;Talazoparib (BMN 673)
CBNumber:
CB22615112
Molecular Formula:
C19H14F2N6O
Molecular Weight:
380.35
MOL File:
1207456-01-6.mol
Modify Date:
2024/1/3 15:56:48

BMN 673 Properties

Melting point 247 - 249°C
Density 1.63
storage temp. Hygroscopic, -20°C Freezer, Under inert atmosphere
solubility DMSO (Slightly), Methanol (Slightly)
form Solid
pka 10.14±0.60(Predicted)
color White to Off-White

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS08
Signal word  Danger
Hazard statements  H360-H372-H341
Precautionary statements  P260-P264-P270-P314-P501-P201-P202-P281-P308+P313-P405-P501

BMN 673 Chemical Properties,Uses,Production

Enzyme inhibitor

This novel, orally bioavailable poly(ADP-ribose) polymerase, or PARP, inhibitor (FW = 380.35 g/mol; CAS 1207456-01-6), also known as (8S,9R)- 5-fluoro-8-(4-fluorophenyl)-9-(1-methyl-1H-1,2,4-triazol-5-yl)-8,9-dihydro- 2H-pyrido[4,3,2-de]phthalazin-3(7H)-one, targets PARP-mediated DNA repair (IC50 = 0.58 nM) of single-strand DNA breaks by the base-excision repair pathway. By enhancing the accumulation of DNA strand breaks, BMN 673 promotes genomic instability, eventually leading to apoptosis. BMN 673 exhibits selective anti-tumor cytotoxicity and elicits DNA repair biomarkers at much lower concentrations than earlier generation PARP1/2 inhibitors, including olaparib, rucaparib and veliparib. BMN 673 shows remarkable anti-tumor activity in vivo, with strong action against xenografted tumors carrying defects in DNA repair due to BRCA mutations or PTEN deficiency. Synergistic or additive anti-tumor effects are observed, when BMN 673 was combined with temozolomide, SN38 or platinum drugs.

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Related articles

BMN 673 Spectrum

1207456-01-6(BMN 673)Related Search:

BMN 673 LT-673 (8S,9R)-5-Fluoro-8-(4-fluorophenyl)-2,7,8,9-tetrahydro-9-(1-methyl-1H-1,2,4-triazol-5-yl)-3H-pyrido[4,3,2-de]phthalazine-3-one (8S,9R)-5-fluoro-8-(4-fluorophenyl)-9-(1-Methyl-1H-1,2,4-triazol-5-yl)-8,9-dihydro-2H-pyrido[4,3,2-de]phthalazin-3(7H)-one Talazoparib 3H-Pyrido[4,3,2-de]phthalazin-3-one, 5-fluoro-8-(4-fluorophenyl)-2,7,8,9-tetrahydro-9-(1-methyl-1H-1,2,4-triazol-5-yl)-, (8S,9R)- Talazoparib (BMN 673) (8S,9R)-5-Fluoro-8-(4-fluorophenyl)-2,7,8,9-tetrahydro-9-(1-methyl-1H-1,2,4-triazol-5-yl)-3H-pyrido[4,3,2-de]phthalazine-3-one BMN673 BMN 673, >=98% (8S,9R)-5-Fluoro-8-(4-fluorophenyl)-9-(1-methyl-1H-1,2,4-triazol-5-yl)-8,9-dihydro-2H-pyrido[4 BMN 673 USP/EP/BP LT-673;BMN673;LT673;TALAZOPARIB; BMN 673 Talazoparib - BMN 673 | LT 00673 CS-750 LT-673;BMN673;LT673;BMN-673;BMN 673 (8S,9R)-BMN 673 BMN-673, TALAZOPARIB (8S,9R)-5-fluoro-8-(4-fluorophenyl)-9-(1-methyl-1H-1,2,4-triazol-5-yl)- 2,7,8,9-tetrahydro-3H-pyrido[4,3,2-de]phthalazin-3-one MDV3800) (8S,9R)-5-Fluoro-8-(4-fluorophenyl)-2,7,8,9-tetrahydro-9-(1-... inhibit,LT673,BRCA1/2,MX-1,PARP-mediated,Talazoparib,poly ADP ribose polymerase,BMN 673,breast cancer,BMN673,Inhibitor,PARylation,anticancer,LT 673,PARP BMN-673 (TALAZOPARIB) (MDV-3800) (LT 00673) Brotizolam Impurity 4 1207456-01-6 C19H14F2N6O Inhibitors API