Comparison

Flavopiridol (Hydrochloride) European Partner

Item no. HY-10006-50mg
Manufacturer MedChem Express
CASRN 131740-09-5
Amount 50 mg
Quantity options 100 mg 10 mM/1 mL 10 mg 50 mg 5 mg
Category
Type Inhibitors
Specific against other
Purity 99.73
Citations [1]Mahoney E, et al. ER stress and autophagy: new discoveries in the mechanism of action and drug resistance of the cyclin-dependent kinase inhibitor flavopiridol.Blood. 2012 Aug 9;120(6):1262-1273.|[2]Keskin H, et al. Complex effects of flavopiridol on the expression of primary response genes. Cell Div. 2012 Mar 29;7:11.|[3]Kim KS, et al.Thio- and oxoflavopiridols, cyclin-dependent kinase 1-selective inhibitors: synthesis and biological effects. J Med Chem. 2000 Nov 2;43(22):4126-34.
Cancer Discov. 2021 Oct 6;candisc.1848.2020.|Cell Commun Signal. 2022 Sep 5;20(1):96.|Nat Commun. 2024 Dec 5;15(1):10594.|Proc Natl Acad Sci U S A. 2021 Nov 16;118(46):e2115667118.|Research Square Preprint. 2024 May 2.|ACS Chem Biol. 2017 May 19;12(5):1245-1256.|Acta Pharm Sin B. 26 February 2022.|Biochem Biophys Res Commun. 2019 Jun 11;513(4):967-973.|Biomaterials. 2014 Aug;35(24):6585-94. |bioRxiv. 2023 Sep 7.|bioRxiv. 2024 July 27.|bioRxiv. 2024 Mar 17.|bioRxiv. 2024 Sep 29:2024.09.28.615444.|Cancers (Basel). 2022 Mar 19;14(6):1575.|Cell Chem Biol. 2018 Feb 15;25(2):135-142.e5.|Cell Chem Biol. 2019 Aug 15;26(8):1067-1080.e8. |Cell Mol Life Sci. 2020 May 21.|Cell Rep. 2020 Apr 28;31(4):107586.|Cell Syst. 2018 Apr 25;6(4):424-443.e7.|Cell. 2021 Apr 15;184(8):2167-2182.e22.|Clin Cancer Res. 2020 Apr 15;26(8):2011-2021. |EMBO Rep. 2022 Apr 11;e53932.|Free University of Berlin. Gedruckt mit Genehmigung des Fachbereichs Veterinärmedizin. 2021 Mar.|Harvard Medical School LINCS LIBRARY|Int J Biol Sci. 2023 Aug 6;19(13):4123-4138.|iScience. 2024 May 16.|J Med Chem. 2021 Mar 11;64(5):2725-2738.|Molecules. 2023 Mar 4.|Nature. 2024 Apr;628(8007):408-415.|PLoS Genet. 2024 Jun 3;20(6):e1011308.|Purdue University. Department of Chemistry.|Research Square Preprint. 2022 Jan.|Research Square Preprint. 2024 Apr 2.|School of Medicine, Department of Pharmacology. 2020 Jun.|Sci Data. 2024 Sep 19.|Sci Rep. 2015 Dec 1;5:17675. |Sci Rep. 2021 Mar 8;11(1):5374.|Sci Rep. 2024 Oct 31;14(1):26239.|Sci Transl Med. 2018 Jul 18;10(450):eaaq1093.|The University of Chicago. Biological Sciences Division Pritzker School of Medicine. 2022 Aug.|Toxicol Lett. 2024 Sep 12:S0378-4274(24)02025-3.|Turk Neurosurg. 2016;26(6):922-929.
Smiles O=C1C2=C(C=C(C([C@]3([H])[C@H](O)CN(C)CC3)=C2OC(C4=CC=CC=C4Cl)=C1)O)O.[H]Cl
ECLASS 10.1 32160490
ECLASS 11.0 32160490
UNSPSC 12000000
Alias Alvocidib (Hydrochloride),L86-8275 (Hydrochloride),HMR-1275 (Hydrochloride)
Shipping Condition Room temperature
Available
Manufacturer - Type
Reference compound
Manufacturer - Applications
Cancer-Kinase/protease
Manufacturer - Targets
Autophagy; CDK; HIV
Shipping Temperature
Room Temperature
Storage Conditions
4°C (Powder, sealed storage, away from moisture)
Molecular Weight
438.30
Product Description
Flavopiridol Hydrochloride (Alvocidib Hydrochloride) is a broad inhibitor of CDK, competing with ATP to inhibit CDKs including CDK1, CDK2, CDK4 with IC50s of 30, 170, 100 nM, respectively.
Manufacturer - Research Area
Cancer
Solubility
DMF: 7.69 mg/mL (ultrasonic)|DMSO: ≥ 20 mg/mL|H2O: ≥ 20 mg/mL
Manufacturer - Pathway
Anti-infection; Autophagy; Cell Cycle/DNA Damage
Isoform
CDK1; CDK2; CDK4
Clinical information
Phase 2

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 50 mg
Available: In stock
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