InChI
1S/C28H33N7O3/c1-6-23(36)29-20-14-12-19(13-15-20)26(37)31-25-21-16-35(28(2,3)24(21)32-33-25)27(38)30-22(17-34(4)5)18-10-8-7-9-11-18/h6-15,22H,1,16-17H2,2-5H3,(H,29,36)(H,30,38)(H2,31,32,33,37)/t22-/m1/s1
InChI key
KPABJHHKKJIDGX-JOCHJYFZSA-N
SMILES string
CN(C)C[C@@H](NC(N1CC(C(NC(C2=CC=C(NC(C=C)=O)C=C2)=O)=NN3)=C3C1(C)C)=O)C4=CC=CC=C4
assay
≥98% (HPLC)
form
powder
color
white to beige
solubility
DMSO: 2 mg/mL, clear
storage temp.
2-8°C
Quality Level
Biochem/physiol Actions
YKL-5-124 is a potent and highly selective covalent inhibitor of cyclin-dependent kinase 7 (CDK7) that induces cell cycle arrest at the G1/S transition.
potent and highly selective covalent inhibitor of cyclin-dependent kinase 7 (CDK7)
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
新产品
此项目有
Calla M Olson et al.
Cell chemical biology, 26(6), 792-803 (2019-03-25)
Cyclin-dependent kinase 7 (CDK7) regulates both cell cycle and transcription, but its precise role remains elusive. We previously described THZ1, a CDK7 inhibitor, which dramatically inhibits superenhancer-associated gene expression. However, potent CDK12/13 off-target activity obscured CDK7s contribution to this phenotype.
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