F3055

Flavopiridol hydrochloride hydrate

≥98% (HPLC), CDK and CDC25 phosphatase family inhibitor, powder

• Synonim(y): (−)-2-(2-Chlorophenyl)-5,7-dihydroxy-8-[(3S,4R)-3-hydroxy-1-methyl-4-piperidinyl]-4H-1-benzopyran-4-one hydrochloride, L-86-8276, NSC-649890
• Wzór empiryczny (zapis Hilla): C₂₁H₂₀ClNO₅ ·HCl · xH₂O
• Numer CAS: 131740-09-5
• Masa cząsteczkowa: 438.30 (anhydrous basis)
• UNSPSC Code: 12352200
• PubChem Substance ID: 24724481
• NACRES: NA.77
• MDL number: MFCD26792554
• Assay: ≥98% (HPLC)
• Form: powder
• Storage condition: desiccated

Właściwości

• Nazwa produktu: Flavopiridol hydrochloride hydrate, ≥98% (HPLC), powder
• Quality Segment: 100
• assay: ≥98% (HPLC)
• form: powder
• storage condition: desiccated
• color: white to light brown
• solubility: H₂O: ~2 mg/mL, DMSO: >5 mg/mL
• storage temp.: 2-8°C
• SMILES string: OC1=C(C(C=C(C2=C(Cl)C=CC=C2)O3)=O)C3=C([C@H]4CCN(C)C[C@H]4O)C(O)=C1.Cl
• InChI: 1S/C21H20ClNO5.ClH/c1-23-7-6-12(17(27)10-23)19-14(24)8-15(25)20-16(26)9-18(28-21(19)20)11-4-2-3-5-13(11)22;/h2-5,8-9,12,17,24-25,27H,6-7,10H2,1H3;1H/t12-,17+;/m0./s1
• InChI key: LGMSNQNWOCSPIK-LWHGMNCYSA-N
• Gene Information: human ... CDK1(983), CDK2(1017), CDK4(1019), CDK6(1021), CDK7(1022), CDK9(1025)

Opis

Application

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[1]
• as an RNA polymerase inhibitor to study its effects on hepatic cells[2]
• as RNA transcription inhibitor to study its effects on euchromatin coarsening in zebrafish embryo[3]

Biochem/physiol Actions

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

Flavopiridol is a semi-synthetic flavone obtained from Dysoxylum binectariferum that acts as an anti-tumor agent against several cancers.[4] It also shows anti-cancer properties due to which it has been studied in the treatment of acute myeloid leukemia (AML).[5]

Features and Benefits

This compound is featured on the CDKs page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

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Informacja o środkach bezpieczeństwa

• pictograms: GHS07
• signalword: Warning
• hcodes: H302
• pcodes: P264 - P270 - P301 + P312 - P501
• Hazard Classifications: Acute Tox. 4 Oral
• Klasa składowania: 11 - Combustible Solids
• wgk: WGK 3
• flash_point_f: Not applicable
• flash_point_c: Not applicable
• ppe: dust mask type N95 (US), Eyeshields, Gloves