CAS 1346574-57-9

N-[(1,2-Dihydro-4,6-dimethyl-2-oxo-3-pyridinyl)methyl]-3-methyl-1-[(1S)-1-methylpropyl]-6-[6-(1-piperazinyl)-3-pyridinyl]-1H-indole-4-carboxamide

Description:

The chemical substance N-[(1,2-Dihydro-4,6-dimethyl-2-oxo-3-pyridinyl)methyl]-3-methyl-1-[(1S)-1-methylpropyl]-6-[6-(1-piperazinyl)-3-pyridinyl]-1H-indole-4-carboxamide, with CAS number 1346574-57-9, is a complex organic compound characterized by its multi-ring structure, which includes indole and pyridine moieties. This compound features various functional groups, including amides and ketones, contributing to its potential biological activity. The presence of piperazine suggests possible interactions with biological targets, making it of interest in medicinal chemistry. Its molecular structure indicates potential lipophilicity, which may influence its pharmacokinetic properties, such as absorption and distribution in biological systems. The compound's synthesis and characterization would typically involve advanced organic chemistry techniques, and its stability, solubility, and reactivity would be critical for applications in drug development or research. Overall, this substance represents a class of compounds that may exhibit significant therapeutic potential, warranting further investigation into its biological effects and mechanisms of action.

Formula: C₃₁H₃₈N₆O₂

InChI: InChI=1S/C31H38N6O2/c1-6-22(5)37-18-20(3)29-25(30(38)34-17-26-19(2)13-21(4)35-31(26)39)14-24(15-27(29)37)23-7-8-28(33-16-23)36-11-9-32-10-12-36/h7-8,13-16,18,22,32H,6,9-12,17H2,1-5H3,(H,34,38)(H,35,39)/t22-/m0/s1

InChI key: InChIKey=FKSFKBQGSFSOSM-QFIPXVFZSA-N

SMILES: [C@@H](CC)(C)N1C=2C(=C(C(NCC3=C(C)C=C(C)NC3=O)=O)C=C(C2)C=4C=CC(=NC4)N5CCNCC5)C(C)=C1

Synonyms:

• GSK 2816126A
• N-[(1,2-Dihydro-4,6-dimethyl-2-oxo-3-pyridinyl)methyl]-3-methyl-1-[(1S)-1-methylpropyl]-6-[6-(1-piperazinyl)-3-pyridinyl]-1H-indole-4-carboxamide
• 1H-Indole-4-carboxamide, N-[(1,2-dihydro-4,6-dimethyl-2-oxo-3-pyridinyl)methyl]-3-methyl-1-[(1S)-1-methylpropyl]-6-[6-(1-piperazinyl)-3-pyridinyl]-
• N-[(4,6-Dimethyl-2-oxo-1,2-dihydro-3-pyridinyl)methyl]-3-methyl-1-((1S)-1-methylpropyl)-6-[6-(1-piperazinyl)-3-pyridinyl]-1H-indole-4-carboxamide
• GSK 126
• 1-[(2S)-butan-2-yl]-N-[(4,6-dimethyl-2-oxo-1H-pyridin-3-yl)methyl]-3-methyl-6-(6-piperazin-1-ylpyridin-3-yl)indole-4-carboxamide
• GSK-2816126
• 1-(S)-sec-butyl-N-((4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-3-methyl-6-(6-(piperazin-1-yl)pyridin-3-yl)-1H-indole-4-carboxamide
• GSK126, >=98%
• S)-1-(sec-butyl)-N-((4,6-diMethyl-2-oxo-1,2-dihydropyridin-3-yl)Methyl)-3-Methyl-6-(6-(piperazin-1-yl)pyridin-3-yl)-1H-indole-4-carboxaMide
• N-[(4,6-Dimethyl-2-oxo-1,2-dihydro-3-pyridinyl)methyl]-3-methyl-1-((1S)-1-methylpropyl)-6-[6-(1-piperazinyl)-3-pyridinyl]-1H-indole-4-carboxamide GSK126

GSK126

CAS: 1346574-57-9

GSK126

Purity: ≥98%

Molecular weight: 526.67g/mol

Ref: 54-BUP15338

GSK126

CAS: 1346574-57-9

GSK126

Purity: 98%

Molecular weight: 526.67g/mol

Ref: 54-BISN0124

GSK126

CAS: 1346574-57-9

GSK126 (GSK2816126A) is a excellently specific EZH2 methyltransferase inhibitor ( IC50=9.9 nM).

Formula: C₃₁H₃₈N₆O₂

Purity: 98% - 99.67%

Color and Shape: Solid

Molecular weight: 526.67

Ref: TM-T2079

GSK 126

CAS: 1346574-57-9

GSK-126 is a potent inhibitor of histone lysine methyl transferase 2, which is encoded by the enhancer of zeste homolog 2 gene (EZH2). The EZH2 protein regulates cell cycle as it represses the Polycomb-Repressive Complex 2 (PRC2), allowing cells to divide actively. GSK-126 inhibits the EZH2 by targeting the catalytic domain (SET) of the enzyme and therefore blocks the PCR2 repression mechanism, resulting in cell proliferation arrest. The compound has shown therapeutic potential for a variety of cancers.

Formula: C₃₁H₃₈N₆O₂

Purity: Min. 95%

Color and Shape: White To Yellow Solid

Molecular weight: 526.30562

Ref: 3D-FB43076

GSK126

CAS: 1346574-57-9

Applications GSK126 is a potent and highly selective S-adenosyl-methionine-competitive small molecule inhibitor of EZH2 methyltransferase enzyme activity. The inhibition activity of GSK126 on EZH2 activity may provide a promising treatment for EZH2 mutant lymphoma.
References McCabe, M.T., et al.: Nature., 492, 108 (2012);

Formula: C₃₁H₃₈N₆O₂

Color and Shape: Neat

Molecular weight: 526.67

Ref: TR-G797650