Flavopiridol HCl - ≥99% , CAS No.131740-09-5

CAS: 131740-09-5 Cat. No.: F129964 Peso molecular: 438.3 Número EC: 634-346-4
Disponible para pedir
GRADE & PURITY ≥99%
Synonyms
4H-1-BENZOPYRAN-4-ONE, 2-(2-CHLOROPHENYL)-5,7-DIHYDROXY-8-((3S,4R)-3-HYDROXY-1-METHYL-4-PIPERIDINYL)-, HYDROCHLORIDE (1:1) | BCP9000688 | rel-(-)-2-(2-Chlorophenyl)-5,7-dihydroxy-8-[(3S,4R)-3-hydroxy-1-methyl-4-piperidinyl]-4H-1-benzopyran-4-one Hydrochlo
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
5mg
F129964-5mg
3

53,90US$

80,90US$
Guardar 27,00 US$ (33.37%)
10mg
F129964-10mg
3

86,90US$

130,90US$
Guardar 44,00 US$ (33.61%)
25mg
F129964-25mg
3

195,90US$

293,90US$
Guardar 98,00 US$ (33.34%)
50mg
F129964-50mg
2

206,90US$

310,90US$
Guardar 104,00 US$ (33.45%)
100mg
F129964-100mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

360,90US$

541,90US$
Guardar 181,00 US$ (33.40%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Product Describtion:

Alvocidib Hydrochloride is a synthetic N-methylpiperidinyl chlorophenyl flavone compound. As an inhibitor of cyclin-dependent kinase, alvocidib induces cell cycle arrest by preventing phosphorylation of cyclin-dependent kinases (CDKs) and by down-regulating cyclin D1 and D3 expression, resulting in G1 cell cycle arrest and apoptosis. This agent is also a competitive inhibitor of adenosine triphosphate activity.

Specifications

Sinónimos
4H-1-BENZOPYRAN-4-ONE, 2-(2-CHLOROPHENYL)-5, 7-DIHYDROXY-8-((3S, 4R)-3-HYDROXY-1-METHYL-4-PIPERIDINYL)-, HYDROCHLORIDE (1:1) | BCP9000688 | rel-(-)-2-(2-Chlorophenyl)-5, 7-dihydroxy-8-[(3S, 4R)-3-hydroxy-1-methyl-4-piperidinyl]-4H-1-benzopyran-4-one Hydrochlo
Especificaciones y pureza
≥99%
Mecanismos bioquímicos y fisiológicos
Flavopiridol hydrochloride is a pan-cdk inhibitor.Potent ATP-competitive CDK and CDC25 phosphatase inhibitor (IC 50 values are 40, 40, 40, 40 and 300 nM for CDK1, 2, 4, 6 and 7 respectively). Inhibits EGFR and PKA (IC 50 values are 21 and 122 μM respectively
Condiciones de almacenamiento de almacenamiento
Store at -20°C
Enviado en
Ice chest + Ice pads
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Nota
Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Pureza
≥99%
Nombres e identificadores
Pubchem Sid504765078
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504765078
Sonrisas canónicasCN1CCC(C(C1)O)C2=C(C=C(C3=C2OC(=CC3=O)C4=CC=CC=C4Cl)O)O.Cl
IUPAC Name2-(2-chlorophenyl)-5,7-dihydroxy-8-[(3S,4R)-3-hydroxy-1-methylpiperidin-4-yl]chromen-4-one;hydrochloride
InChIKeyLGMSNQNWOCSPIK-LWHGMNCYSA-N
INCHI1S/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
Isómeros SMILES CN1CC[C@@H]([C@@H](C1)O)C2=C(C=C(C3=C2OC(=CC3=O)C4=CC=CC=C4Cl)O)O.Cl
Peso molecular 438.3
Reaxy-Rn 25500302
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=25500302&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassPhenylpropanoids and polyketides
ClaseFlavonoids
SubclassFlavones
Intermediate Tree Nodes Not available
Direct ParentFlavones
Alternative Parents 5-hydroxyflavonoids  7-hydroxyflavonoids  Phenylpiperidines  Chromones  Pyranones and derivatives  1-hydroxy-2-unsubstituted benzenoids  Aralkylamines  Chlorobenzenes  Aryl chlorides  Vinylogous acids  Heteroaromatic compounds  Trialkylamines  Secondary alcohols  1,2-aminoalcohols  Oxacyclic compounds  Azacyclic compounds  Hydrochlorides  Organic oxides  Organochlorides  Hydrocarbon derivatives  Organopnictogen compounds  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents 5-hydroxyflavonoid - 7-hydroxyflavonoid - Flavone - Hydroxyflavonoid - Phenylpiperidine - Chromone - Benzopyran - 1-benzopyran - 1-hydroxy-2-unsubstituted benzenoid - Chlorobenzene - Halobenzene - Pyranone - Aralkylamine - Benzenoid - Pyran - Piperidine - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Heteroaromatic compound - Vinylogous acid - Tertiary aliphatic amine - Tertiary amine - Secondary alcohol - 1,2-aminoalcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Alcohol - Organic oxide - Organopnictogen compound - Organic nitrogen compound - Organic oxygen compound - Hydrocarbon derivative - Organohalogen compound - Organochloride - Organonitrogen compound - Organooxygen compound - Amine - Hydrochloride - Aromatic heteropolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as flavones. These are flavonoids with a structure based on the backbone of 2-phenylchromen-4-one (2-phenyl-1-benzopyran-4-one).
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
Caco-2 (12174 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

5 results found

Lot NumberCertificate TypeFechaArticulo
B2318057Certificate of AnalysisDec 05, 2024 F129964
B2318062Certificate of AnalysisDec 05, 2024 F129964
B2318070Certificate of AnalysisDec 05, 2024 F129964
B2318083Certificate of AnalysisDec 05, 2024 F129964
B23171122Certificate of AnalysisJan 14, 2023 F129964
Propiedades químicas y físicas
SolubilidadDMSO 88 mg/mL Water <1 mg/mL Ethanol <1 mg/mL
SensibilidadMoisture sensitive
Peso molecular438.300 g/mol
XLogP3
Hydrogen Bond Donor Count4
Hydrogen Bond Acceptor Count6
Rotatable Bond Count2
Exact Mass437.08 Da
Monoisotopic Mass437.08 Da
Topological Polar Surface Area90.200 Ų
Heavy Atom Count29
Formal Charge0
Complexity628.000
Isotope Atom Count0
Defined Atom Stereocenter Count2
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count2
Calculadoras de soluciones
Reseñas

Reseñas de cliente

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.