FLAVOPIRIDOL HYDROCHLORIDE
- Product Name
- FLAVOPIRIDOL HYDROCHLORIDE
- CAS No.
- 131740-09-5
- Chemical Name
- FLAVOPIRIDOL HYDROCHLORIDE
- Synonyms
- HL 275;CS-976;L-86-8276;NSC 649890;MDL 107826A;Alvocidib HCL;NSC 649890 HCl;Flavopiridol HC;FLAVOPIRIDOL HCL;Flavopiridol HCI
- CBNumber
- CB1972179
- Molecular Formula
- C21H21Cl2NO5
- Formula Weight
- 438.3
- MOL File
- 131740-09-5.mol
FLAVOPIRIDOL HYDROCHLORIDE Property
- Melting point:
- 169.5-170°C
- alpha
- 24D -1.73 to -3.9°
- storage temp.
- 2-8°C
- solubility
- H2O: ~2mg/mL
- form
- powder
- pka
- 5.68 ± 0.06(at 25℃)
- color
- white to light brown
- Stability:
- Stable for 2 years from date of purchase as supplied. Solutions in DMSO or distilled water may be stored at -20°C for up to 1 month
- CAS DataBase Reference
- 131740-09-5
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
- Precautionary statements
-
P280Wear protective gloves/protective clothing/eye protection/face protection.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- F3055
- Product name
- Flavopiridol hydrochloride hydrate
- Purity
- ≥98% (HPLC), powder
- Packaging
- 5mg
- Price
- $156
- Updated
- 2024/03/01
- Product number
- F3055
- Product name
- Flavopiridol hydrochloride hydrate
- Purity
- ≥98% (HPLC), powder
- Packaging
- 25mg
- Price
- $586
- Updated
- 2024/03/01
- Product number
- 10009197
- Product name
- Flavopiridol (hydrochloride)
- Purity
- ≥95%
- Packaging
- 5mg
- Price
- $49
- Updated
- 2024/03/01
- Product number
- 10009197
- Product name
- Flavopiridol (hydrochloride)
- Purity
- ≥95%
- Packaging
- 10mg
- Price
- $73
- Updated
- 2024/03/01
- Product number
- 10009197
- Product name
- Flavopiridol (hydrochloride)
- Purity
- ≥95%
- Packaging
- 25mg
- Price
- $143
- Updated
- 2024/03/01
FLAVOPIRIDOL HYDROCHLORIDE Chemical Properties,Usage,Production
Description
Flavopiridol is an orally bioavailable inhibitor of cyclin dependent kinases (IC50s = ~100, ~100, ~100, and 300 nM for Cdk1, Cdk2, Cdk4, and Cdk7, respectively). It also inhibits TEFb, a complex composed of Cdk9 and cyclin T1, with a Ki value of 3 nM. Flavopiridol inhibits transcription of a CMV promoter in HeLa nuclear extract (IC50 = 34 nM), Tat-stimulated transcription of an HIV-1 promotor (IC50 = 7 nM), and HIV-1 replication in HEK239T cells (IC50 = <10 nM). In vivo, flavopiridol (5 mg/kg, i.p.) induces apoptosis and cyclin D1 depletion and delays tumor growth in an HN-12 head and neck carcinoma mouse xenograft model. It also suppresses synovial hyperplasia and joint destruction in a mouse model of collagen-induced arthritis.
Chemical Properties
Yellow Powder
Uses
An inhibitor of cyclin-dependent kinases; the (-)-cis form induces apoptosis in certain tumor cells.
Uses
Flavopiridol hydrochloride hydrate has been used:
- as a cyclin-dependent kinase 9 (CDK9) inhibitor to study its effects on histone H3 methylation at lysine 36 (H3K36) and deactivation of transcription in porcine fetal fibroblasts
- as an RNA polymerase inhibitor to study its effects on hepatic cells
- as RNA transcription inhibitor to study its effects on euchromatin coarsening in zebrafish embryo
Definition
ChEBI: A hydrochloride salt resulting from the formal reaction of equimolar amounts of alvocidib and hydrogen chloride. A cyclin-dependent kinase 9 (CDK9) inhibitor, it has been studied for the treatment of acute myeloid leukaemia, arthritis and atherosclerotic p aque formation.
Biochem/physiol Actions
Flavopiridol?is a semi-synthetic flavone obtained from Dysoxylum binectariferum that acts as an anti-tumor agent against several cancers. It also shows anti-cancer properties due to which it has been studied in the treatment of acute myeloid leukemia (AML).
storage
Store at +4°C
References
1) Kaur?et al. (1992),?Growth inhibition with reversible cell cycle arrest of carcinoma cells by flavone L86-8275;? J. Natl. Cancer Inst.,?84?1736 2) Cartee?et al. (2002),?Synergistic induction of apoptosis in human myeloid leukemia cells by phorbol 12-myristate 13-acetate and flavopiridol proceeds via activation of both the intrinsic and tumor necrosis factor-mediated extrinsic cell death pathways;? Mol. Pharmacol.,?61?1313 3) Ambrosini?et al. (2008),?The cyclin-dependent kinase inhibitor flavopiridol potentiates the effects of topoisomerase I poisons by suppressing Rad51 expression in a p53-dependent manner;? Cancer Res.?68?2312 4) Schang?et al. (2004),?Effects of pharmacological cyclin-dependent kinase inhibitors on viral transcription and replication;? Biochim. Biophys. Acta,?1697?197
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View Lastest Price from FLAVOPIRIDOL HYDROCHLORIDE manufacturers
- Product
- FLAVOPIRIDOL HYDROCHLORIDE 131740-09-5
- Price
- US $7.00/KG
- Min. Order
- 1KG
- Purity
- 99%
- Supply Ability
- 100KG
- Release date
- 2018-08-15
- Product
- FLAVOPIRIDOL HYDROCHLORIDE 131740-09-5
- Price
- US $7.00/KG
- Min. Order
- 1KG
- Purity
- 99%
- Supply Ability
- 1000KG
- Release date
- 2018-08-15