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BMS-265246

CAS No.
582315-72-8
Chemical Name:
BMS-265246
Synonyms
CS-984;BMS-265246;BMS-265246, >=98%;BMS-265246 USP/EP/BP;BMS265246; BMS 265246;(4-Butoxy-1H-pyrazolo[3,4-b]pyridin-5-yl)(2,6-difluoro-4-methylphenyl)-methanone;Methanone, (4-butoxy-1H-pyrazolo[3,4-b]pyridin-5-yl)(2,6-difluoro-4-methylphenyl)-;(4-Butoxy-1H-pyrazolo[3,4-b]pyridin-5-yl)(2,6-difluoro-4-methylphenyl)-methanone BMS265246
CBNumber:
CB32624100
Molecular Formula:
C18H17F2N3O2
Molecular Weight:
345.34
MDL Number:
MFCD22420825
MOL File:
582315-72-8.mol
MSDS File:
SDS
Last updated:2024-07-02 08:55:06

BMS-265246 Properties

Boiling point 552.9±50.0 °C(Predicted)
Density 1.304±0.06 g/cm3(Predicted)
storage temp. Store at -20°C
solubility insoluble in H2O; insoluble in EtOH; ≥17.25 mg/mL in DMSO
form solid
pka 8.50±0.40(Predicted)
color White to pink
FDA UNII 4GF4A623RF

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H319
Precautionary statements  P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313

BMS-265246 price More Price(27)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 19168 BMS-265246 ≥95% 582315-72-8 1mg $62 2024-03-01 Buy
Cayman Chemical 19168 BMS-265246 ≥95% 582315-72-8 5mg $270 2024-03-01 Buy
Tocris 5654 BMS265246 ≥97%(HPLC) 582315-72-8 10 $189 2021-12-16 Buy
Tocris 5654 BMS265246 ≥97%(HPLC) 582315-72-8 50 $794 2021-12-16 Buy
Usbiological 004336 BMS-265246 582315-72-8 5mg $566 2021-12-16 Buy
Product number Packaging Price Buy
19168 1mg $62 Buy
19168 5mg $270 Buy
5654 10 $189 Buy
5654 50 $794 Buy
004336 5mg $566 Buy

BMS-265246 Chemical Properties,Uses,Production

Uses

BMS-265246 is a potent and selective pyra-zolopyridine based inhibitor of cdk2/cyclinE, cdk1/cyclinB and cdk4/ cyclinD.

Biological Activity

bms265246 is a potent and selective inhibitor for cdk1 and cdk2 (ic50= 6 nm and 9 nm)cyclin-dependent kinases (cdk) are a group of serine/threonine kinases. they are activated by coupling to cyclin and participate in the regulation of cell cycle.bms265246 inhibited the cdk4/cycd activity and prevented a2780 cytox (ic50 = 0.23 μm and 0.76 μm) [1]. in hct-116 cells, bms-265246 blocked the cell proliferation (ec50= 0.293 μm—0.492 μm). following the treatment of bms-265246, low dna intensity, large round nuclei and 4n dna content were observed in the dominant cell population –g2 arrested cells. [2]

storage

Store at -20°C

References

1. misra rn, xiao hy, rawlins db et al. 1h-pyrazolo[3,4-b]pyridine inhibitors of cyclin-dependent kinases: highly potent 2,6-difluorophenacyl analogues. bioorgmed chem lett. 2003 jul 21;13(14):2405-8.2. sutherland jj, low j, blosser w et al. a robust high-content imaging approach for probing the mechanism of action and phenotypic outcomes of cell-cycle modulators. mol cancer ther. 2011 feb;10(2):242-54.

BMS-265246 Preparation Products And Raw materials

Raw materials

Preparation Products

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BMS-265246 BMS-265246, >=98% (4-Butoxy-1H-pyrazolo[3,4-b]pyridin-5-yl)(2,6-difluoro-4-methylphenyl)-methanone (4-Butoxy-1H-pyrazolo[3,4-b]pyridin-5-yl)(2,6-difluoro-4-methylphenyl)-methanone BMS265246 BMS265246; BMS 265246 CS-984 Methanone, (4-butoxy-1H-pyrazolo[3,4-b]pyridin-5-yl)(2,6-difluoro-4-methylphenyl)- BMS-265246 USP/EP/BP 582315-72-8 Inhibitors