Flavopiridol hydrochloride hydrate

• Catalog No.: F3055
• M. F.: C21H21Cl2NO5
• M. W.: 438.30114
• Purity: ≥98% (HPLC)
• Storage: desiccated

SYNONYMS

• Title: Flavopiridol 盐酸盐
• IUPAC name: 2-(2-chlorophenyl)-5,7-dihydroxy-8-[(3S,4R)-3-hydroxy-1-methylpiperidin-4-yl]-4H-chromen-4-one hydrochloride
• IUPAC Traditional name: flavopiridol hydrochloride
• Synonyms: (-)-2-(2-chlorophenyl)-5,7-dihydroxy-8-[(3s,4r)-3-hydroxy-1-methyl-4-piperidinyl]-4h-1-benzopyran-4-one 盐酸盐; NSC-649890; L-86-8276; (-)-2-(2-Chlorophenyl)-5,7-dihydroxy-8-[(3S,4R)-3-hydroxy-1-methyl-4-piperidinyl]-4H-1-benzopyran-4-one hydrochloride

DATABASE IDS

• PubChem SID: 24724481

PROPERTIES

• Empirical Formula (Hill Notation): C21H20ClNO5 ·HCl · xH2O
• Purity: ≥98% (HPLC)
• Apperance: white to light brown powder
• Solubility: H2O: ~2 mg/mL
• Solubility: DMSO: >5 mg/mL
• GHS Signal Word: Warning
• GHS Hazard statements: H302
• European Hazard Symbols: Harmful (Xn)
• Personal Protective Equipment: dust mask type N95 (US), Eyeshields, Gloves
• Risk Statements: 22
• Storage Condition: desiccated
• Storage Temperature: 2-8°C
• German water hazard class: 3

DETAILS

Description (English)

Biochem/physiol Actions
Flavopiridol hydrochloride is a potent CDK (cyclin-dependent kinase), and a CDC25 phosphatase family inhibitor.

Description (简体中文)

Biochem/physiol Actions
Flavopiridol hydrochloride is a potent CDK (cyclin-dependent kinase), and a CDC25 phosphatase family inhibitor.