ChemicalBook > CAS DataBase List > P276

P276

Product Name
P276
CAS No.
920113-03-7
Chemical Name
P276
Synonyms
P276;CS-996;P276 USP/EP/BP;Riviciclib HCl;Riviciclib hydrochloride;Riviciclib HCl (P276-00);RIVICICLIB HYDROCHLORIDE (P276-00);inhibit,Inhibitor,Riviciclib,CDK,Riviciclib hydrochloride,Cyclin dependent kinase,Apoptosis;2-(2-chlorophenyl)-5,7-dihydroxy-8-[(2R,3S)-2-(hydroxymethyl)-1-methylpyrrolidin-3-yl]chromen-4-one:hydrochloride;2-(2-chlorophenyl)-5,7-dihydroxy-8-((2R,3S)-2-(hydroxymethyl)-1-methylpyrrolidin-3-yl)-4H-chromen-4-one hydrochloride
CBNumber
CB32668296
Molecular Formula
C21H21Cl2NO5
Formula Weight
438.3
MOL File
920113-03-7.mol
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P276 Property

storage temp. 
Store at -20° C
solubility 
Soluble in DMSO
form 
Solid
color 
Off-white to light yellow
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

ChemScene
Product number
CS-0006648
Product name
Riviciclibhydrochloride
Purity
98.33%
Packaging
5mg
Price
$180
Updated
2021/12/16
ChemScene
Product number
CS-0006648
Product name
Riviciclibhydrochloride
Purity
98.33%
Packaging
10mg
Price
$300
Updated
2021/12/16
Medical Isotopes, Inc.
Product number
60932
Product name
P276-00
Packaging
1mg
Price
$650
Updated
2021/12/16
Crysdot
Product number
CD11014532
Product name
P276-00(RivicilibHydrocloride)
Purity
95+%
Packaging
25mg
Price
$327
Updated
2021/12/16
Crysdot
Product number
CD11014532
Product name
P276-00(RivicilibHydrocloride)
Purity
95+%
Packaging
5mg
Price
$107
Updated
2021/12/16
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P276 Chemical Properties,Usage,Production

Uses

P276-00 is a cyclin-dependent kinase (CDK) inhibitor. P276-00 has shown to be highly selective for cancer cells and has shown to produce potent inhibition of Cdk4-D1 activity. P276-00 also induces apoptosis in human promyelocytic leukemia (HL-60) cells.

Enzyme inhibitor

This cell cycle-inhibiting flavone and anticancer agent (FW = 438.30 g/mol; CAS 920113-03-7), also named 2-(2-chlorophenyl)-5,7-dihydroxy-8- [(2R,3S)-2-(hydroxymethyl)-1-methyl-3-pyrrolidinyl]-4H-1-benzopyran-4- one, targets the Cyclin-Dependent Kinases CDK1 (IC50 = 79 nM), CDK4 (IC50 = 63 nM) and CDK9 (IC50 = 20 nM). p276-00 showed potent antiproliferative effects against various human cancer cell lines (IC50 values ranging from 300 to 800 nmol/L), but has little effect on cultured fibroblasts. A significant down-regulation of cyclin D1 and Cdk4 and a decrease in Cdk4-specific pRb Ser(780) phosphorylation is observed. P276-00 produces potent inhibition of Cdk4-D1 activity that is competitive with ATP, and not with retinoblastoma protein. The compound also induced apoptosis in human promyelocytic leukemia (HL-60) cells, as evidenced by the induction of caspase-3 and DNA ladder studies. In 22 human cancer xenografts, P276-00 is approximately 26x more potent than cisplatin, and is also active against cisplatin-resistant tumors of central nervous system, melanoma, prostate, and renal cancers. Synchronized human non-small cell lung carcinoma (H-460) and human normal lung fibroblast (WI-38) cells are arrested in G1

P276 Preparation Products And Raw materials

Raw materials

Preparation Products

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P276 Suppliers

J & K SCIENTIFIC LTD.
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920113-03-7, P276Related Search:


  • P276
  • 4H-1-Benzopyran-4-one, 2-(2-chlorophenyl)-5,7-dihydroxy-8-[(2R,3S)-2-(hydroxymethyl)-1-methyl-3-pyrrolidinyl]-, hydrochloride (1:1)
  • Riviciclib hydrochloride
  • CS-996
  • Riviciclib HCl
  • RIVICICLIB HYDROCHLORIDE (P276-00)
  • P276-00 4H-1-Benzopyran-4-one, 2-(2-chlorophenyl)-5,7-dihydroxy-8-((2R,3S)-2-(hydroxymethyl)-1-methyl-3-pyrrolidinyl)-, hydrochloride (1:1)
  • 2-(2-chlorophenyl)-5,7-dihydroxy-8-[(2R,3S)-2-(hydroxymethyl)-1-methylpyrrolidin-3-yl]chromen-4-one:hydrochloride
  • 2-(2-chlorophenyl)-5,7-dihydroxy-8-((2R,3S)-2-(hydroxymethyl)-1-methylpyrrolidin-3-yl)-4H-chromen-4-one hydrochloride
  • P276 USP/EP/BP
  • Riviciclib HCl (P276-00)
  • inhibit,Inhibitor,Riviciclib,CDK,Riviciclib hydrochloride,Cyclin dependent kinase,Apoptosis
  • 920113-03-7
  • Inhibitors