Reaction Details | |||
---|---|---|---|
Report a problem with these data | |||
Target | Cyclin-T1 | ||
Ligand | BDBM126552 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | IMAP Assay | ||
IC50 | 0.00043±n/a nM | ||
Citation | Barsanti, PA; Hu, C; Jin, J; Keyes, R; Kucejko, R; Lin, X; Pan, Y; Pfister, KB; Sendzik, M; Sutton, J; Wan, L Heteroaryl compounds and their uses US Patent US8778951 Publication Date 7/15/2014 | ||
More Info.: | Get all data from this article, Assay Method | ||
Cyclin-T1 | |||
Name: | Cyclin-T1 | ||
Synonyms: | CCNT1 | CCNT1_HUMAN | CycT | CycT1 | Cyclin T | Cyclin T1 | Cyclin-T | ||
Type: | Enzyme Subunit | ||
Mol. Mass.: | 80712.40 | ||
Organism: | Homo sapiens (Human) | ||
Description: | n/a | ||
Residue: | 726 | ||
Sequence: |
| ||
BDBM126552 | |||
n/a | |||
Name | BDBM126552 | ||
Synonyms: | US8778951, 363 | ||
Type | Small organic molecule | ||
Emp. Form. | C28H37ClN6O2 | ||
Mol. Mass. | 525.085 | ||
SMILES | Clc1cnc(N[C@H]2CC[C@@H](CC2)NC2CCOCC2)cc1-c1cccc(NCC2(CCOCC2)C#N)n1 |r,wU:6.5,wD:9.12,(-7.57,1.92,;-6.23,2.69,;-6.23,4.23,;-4.9,5,;-3.56,4.23,;-2.23,5.01,;-.9,4.24,;.44,5.01,;1.77,4.24,;1.77,2.7,;.44,1.93,;-.9,2.7,;3.1,1.93,;4.59,2.32,;5.68,1.23,;7.17,1.63,;7.57,3.12,;6.48,4.21,;4.99,3.81,;-3.56,2.69,;-4.9,1.92,;-4.9,.38,;-6.23,-.39,;-6.23,-1.93,;-4.9,-2.7,;-3.56,-1.93,;-2.23,-2.7,;-.9,-1.93,;.44,-2.7,;.44,-4.24,;1.77,-5.01,;3.1,-4.24,;3.1,-2.7,;1.77,-1.93,;.44,-1.16,;.44,.38,;-3.56,-.39,)| | ||
Structure |