LEE011 succinate - 10mM in DMSO , Cyclin-dependent kinase 6 inhibitor, CAS No.1374639-75-4, Cyclin-dependent kinase 6 inhibitor

CAS: 1374639-75-4 Cat. No.: L421422 Formula: C₂₇H₃₆N₈O₅ Peso molecolare: 552.63 Numero EC: 801-486-4

GRADE & PURITY 10mM in DMSO

Synonyms

D10979 | Q27274660 | SB18482 | 7-cyclopentyl-N,N-dimethyl-2-{[5-(piperazin-1-yl)pyridin-2-yl]amino}-7H-pyrrolo[2,3-d]pyrimidine-6-carboxamide; butanedioic acid | SCHEMBL2684999 | 1374639-75-4 | LEE011 succinateLEE011 succinate | 7-Cyclopentyl-N,N-dimethyl

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

Panoramica

Ribociclib (lee011) succeed (kiskali) is a highly specific dual inhibitor for CDK4 and Cdk6, with IC50 values of 10 nm and 39 nm, respectively.

Specifications

Sinonimi

D10979 | Q27274660 | SB18482 | 7-cyclopentyl-N,N-dimethyl-2-{[5-(piperazin-1-yl)pyridin-2-yl]amino}-7H-pyrrolo[2,3-d]pyrimidine-6-carboxamide; butanedioic acid | SCHEMBL2684999 | 1374639-75-4 | LEE011 succinateLEE011 succinate | 7-Cyclopentyl-N,N-dimethyl

Specifiche e purezza

10mM in DMSO

Condizioni di conservazione di stoccaggio

Store at -80°C

Spedito in

Dry ice packs + Cold packs

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Tipo di azione

INHIBITOR

Meccanismo d'azione

Cyclin-dependent kinase 6 inhibitor

Nomi e identificatori

• Pubchem Sid: 528765279
• Sorrisi canonici: CN(C)C(=O)C1=CC2=CN=C(N=C2N1C3CCCC3)NC4=NC=C(C=C4)N5CCNCC5.C(CC(=O)O)C(=O)O
• IUPAC Name: butanedioic acid;7-cyclopentyl-N,N-dimethyl-2-[(5-piperazin-1-ylpyridin-2-yl)amino]pyrrolo[2,3-d]pyrimidine-6-carboxamide
• InChIKey: NHANOMFABJQAAH-UHFFFAOYSA-N
• INCHI: 1S/C23H30N8O.C4H6O4/c1-29(2)22(32)19-13-16-14-26-23(28-21(16)31(19)17-5-3-4-6-17)27-20-8-7-18(15-25-20)30-11-9-24-10-12-30;5-3(6)1-2-4(7)8/h7-8,13-15,17,24H,3-6,9-12H2,1-2H3,(H,25,26,27,28);1-2H2,(H,5,6)(H,7,8)
• Isomeri SMILES: CN(C)C(=O)C1=CC2=CN=C(N=C2N1C3CCCC3)NC4=NC=C(C=C4)N5CCNCC5.C(CC(=O)O)C(=O)O
• Peso molecolare: 552.63
• Reaxy-Rn: 30234406
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=30234406&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Classe Diazinanes
      • Subclass Piperazines

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Classe: Diazinanes
• Subclass: Piperazines
• Intermediate Tree Nodes: Not available
• Direct Parent: Pyridinylpiperazines
• Alternative Parents: N-arylpiperazines Pyrrolo[2,3-d]pyrimidines Pyrimidinecarboxamides Pyrrole carboxamides 2-heteroaryl carboxamides Dialkylarylamines Aminopyrimidines and derivatives Aminopyridines and derivatives Substituted pyrroles Imidolactams Fatty acids and conjugates Dicarboxylic acids and derivatives Tertiary carboxylic acid amides Heteroaromatic compounds Amino acids and derivatives Dialkylamines Azacyclic compounds Carboxylic acids Carbonyl compounds Hydrocarbon derivatives Organic oxides
• Molecular Framework: Not available
• Substituents: Pyridinylpiperazine - N-arylpiperazine - Pyrimidinecarboxamide - Pyrrolopyrimidine - Pyrrolo[2,3-d]pyrimidine - 2-heteroaryl carboxamide - Pyrrole-2-carboxamide - Pyrrole-2-carboxylic acid or derivatives - Dialkylarylamine - Aminopyrimidine - Aminopyridine - Imidolactam - Substituted pyrrole - Fatty acid - Pyrimidine - Dicarboxylic acid or derivatives - Pyridine - Heteroaromatic compound - Tertiary carboxylic acid amide - Pyrrole - Tertiary amine - Carboxamide group - Amino acid or derivatives - Azacycle - Secondary amine - Carboxylic acid derivative - Carboxylic acid - Secondary aliphatic amine - Organic oxide - Hydrocarbon derivative - Organic oxygen compound - Carbonyl group - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Amine - Aromatic heteropolycyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as pyridinylpiperazines. These are compounds containing a pyridinylpiperazine skeleton, which consists of a pyridine linked (not fused) to a piperazine by a bond by a single bond that is not part of a ring.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Proprietà chimiche e fisiche

• Peso molecolare: 552.600 g/mol
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 11
• Rotatable Bond Count: 8
• Exact Mass: 552.281 Da
• Monoisotopic Mass: 552.281 Da
• Topological Polar Surface Area: 166.000 Ų
• Heavy Atom Count: 40
• Formal Charge: 0
• Complexity: 728.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 2

XLogP3