Determine the necessary mass, volume, or concentration for preparing a solution.
Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
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SKU | Size | Availability | Price | Qty |
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F124946-1mg | 1mg | Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding. | $16.90 | |
F124946-5mg | 5mg | Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience! | $64.90 | |
F124946-25mg | 25mg | In stock | $292.90 | |
F124946-100mg | 100mg | In stock | $469.90 | |
F124946-250mg | 250mg | In stock | $1,057.90 |
Synonyms | L868275 | ALVOCIDIB [MART.] | AS-74761 | Q4063441 | 2-(2-chlorophenyl)-5,7-dihydroxy-8-[(3S,4R)-3-hydroxy-1-methyl-4-piperidyl]chromen-4-one | 4H-1-Benzopyran-4-one, 2-(2-chlorophenyl)-5,7-dihydroxy-8-((3R,4S)-3-hydroxy-1-methyl-4-piperidinyl)-, rel-(-)- |
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Specifications & Purity | Moligand™, ≥99% |
Biochemical and Physiological Mechanisms | Flavopiridol is a synthetic flavone compound that inhibits the phosphorylation of cyclin-dependent kinases (Cdks) and suppresses expression of cyclin D1 and D3, interrupting the central role of Cdks in the regulation of the cell cycle and consequently pro |
Storage Temp | Store at 2-8°C,Argon charged |
Shipped In | Wet ice |
Grade | Moligand™ |
Action Type | INHIBITOR |
Mechanism of action | Cyclin-dependent kinase 7 inhibitor |
Product Description | Flavopiridol competes with ATP to inhibit CDKs including CDK1, CDK2, CDK4 and CDK6 with IC50 of ~ 40 nM. It is 7.5-fold more selective for CDK1/2/4/6 than CDK7. Flavopiridol is initially found to inhibit EGFR and PKA |
ALogP | 3.3 |
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Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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IUPAC Name | 2-(2-chlorophenyl)-5,7-dihydroxy-8-[(3S,4R)-3-hydroxy-1-methylpiperidin-4-yl]chromen-4-one |
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INCHI | InChI=1S/C21H20ClNO5/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/t12-,17+/m0/s1 |
InChi Key | BIIVYFLTOXDAOV-YVEFUNNKSA-N |
Canonical SMILES | CN1CCC(C(C1)O)C2=C(C=C(C3=C2OC(=CC3=O)C4=CC=CC=C4Cl)O)O |
Isomeric SMILES | CN1CC[C@@H]([C@@H](C1)O)C2=C(C=C(C3=C2OC(=CC3=O)C4=CC=CC=C4Cl)O)O |
PubChem CID | 5287969 |
Molecular Weight | 401.85 |
CAS Registry No. | 146426-40-6 |
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DrugBank Ligand | DB03496 |
DiscoveRx TREEspot | Flavopiridol| |
PubChem CID | 5287969 |
ChEMBL Ligand | CHEMBL428690 |
Wikipedia | Alvocidib |
RCSB PDB Ligand | CPB |
Enter Lot Number to search for COA:
Find and download the COA for your product by matching the lot number on the packaging.
Lot Number | Certificate Type | Date | Item |
---|---|---|---|
L2201264 | Certificate of Analysis | Sep 12, 2024 | F124946 |
L2201265 | Certificate of Analysis | Sep 12, 2024 | F124946 |
L2201423 | Certificate of Analysis | Sep 12, 2024 | F124946 |
L2202103 | Certificate of Analysis | Sep 12, 2024 | F124946 |
G1521054 | Certificate of Analysis | Jan 09, 2023 | F124946 |
Solubility | DMSO ≥14mg/mL Water <1.2mg/mL Ethanol ≥7.8mg/mL;Soluble in chloroform, and water (slightly soluble). |
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Pictogram(s) | GHS07 |
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Signal | Warning |
Hazard Statements | H302:Harmful if swallowed |
Precautionary Statements | P501:Dispose of contents/container to ... P264:Wash hands [and …] thoroughly after handling. P270:Do not eat, drink or smoke when using this product. P330:Rinse mouth. P301+P317:IF SWALLOWED: Get medical help. |
1. Mengling Huang, Abrar Ahmed, Wei Wang, Xue Wang, Cui Ma, Haowei Jiang, Wei Li, Lili Jing. (2022) Negative Elongation Factor (NELF) Inhibits Premature Granulocytic Development in Zebrafish. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 23 (7): (3833). [PMID:35409193] [10.3390/ijms23073833] |
1. Kaur G, Stetler-Stevenson M, Sebers S, Worland P, Sedlacek H, Myers C, Czech J, Naik R, Sausville E. (1992) Growth inhibition with reversible cell cycle arrest of carcinoma cells by flavone L86-8275.. J Natl Cancer Inst, 84 (22): (1736-40). [PMID:1279187] [10.1021/op500134e] |
2. Bose P, Simmons GL, Grant S. (2013) Cyclin-dependent kinase inhibitor therapy for hematologic malignancies.. Expert Opin Investig Drugs, 22 (6): (723-38). [PMID:23647051] [10.1021/op500134e] |
3. Worland PJ, Kaur G, Stetler-Stevenson M, Sebers S, Sartor O, Sausville EA. (1993) Alteration of the phosphorylation state of p34cdc2 kinase by the flavone L86-8275 in breast carcinoma cells. Correlation with decreased H1 kinase activity.. Biochem Pharmacol, 46 (10): (1831-40). [PMID:8250970] [10.1021/op500134e] |
4. Carlson BA, Dubay MM, Sausville EA, Brizuela L, Worland PJ. (1996) Flavopiridol induces G1 arrest with inhibition of cyclin-dependent kinase (CDK) 2 and CDK4 in human breast carcinoma cells.. Cancer Res, 56 (13): (2973-8). [PMID:8674031] [10.1021/op500134e] |
5. Mengling Huang, Abrar Ahmed, Wei Wang, Xue Wang, Cui Ma, Haowei Jiang, Wei Li, Lili Jing. (2022) Negative Elongation Factor (NELF) Inhibits Premature Granulocytic Development in Zebrafish. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 23 (7): (3833). [PMID:35409193] [10.3390/ijms23073833] |