Reaction Details | |||
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Target | Acetyl-CoA carboxylase 2 | ||
Ligand | BDBM307223 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | Inhibitory Activity on Human ACC1 and the ACC2 | ||
IC50 | 4.00±n/a nM | ||
Citation | Kobayashi, N; Asahi, K; Tomida, Y; Ohdan, M; Fumoto, M; Sasaki, Y; Kurahashi, K; Inoue, T; Urabe, T; Nishiura, Y; Iwatsu, M; Miyazaki, K; Ohyabu, N; Wada, T; Katou, M Alkylene derivatives US Patent US10150728 Publication Date 12/11/2018 | ||
More Info.: | Get all data from this article, Assay Method | ||
Acetyl-CoA carboxylase 2 | |||
Name: | Acetyl-CoA carboxylase 2 | ||
Synonyms: | ACACB | ACACB_HUMAN | ACC-beta | ACC2 | ACCB | Acetyl-CoA carboxylase | Acetyl-CoA carboxylase 2 | Acetyl-CoA carboxylase 2 (ACC) | Acetyl-CoA carboxylase 2 (ACC2) | ||
Type: | Protein | ||
Mol. Mass.: | 276535.21 | ||
Organism: | Homo sapiens (Human) | ||
Description: | O00763 | ||
Residue: | 2458 | ||
Sequence: |
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BDBM307223 | |||
n/a | |||
Name | BDBM307223 | ||
Synonyms: | US10150728, Example I-436 | ||
Type | Small organic molecule | ||
Emp. Form. | C20H25ClN4O4 | ||
Mol. Mass. | 420.89 | ||
SMILES | C[C@@H](CO[C@@H]1C[C@H](COc2ncnc(OCc3ccccn3)c2Cl)C1)NC(C)=O |r,wU:6.6,4.3,wD:1.0,(7.61,3.24,;7.61,1.7,;6.28,.93,;4.94,1.7,;3.61,.93,;2.12,1.33,;1.72,-.16,;.39,-.93,;-.94,-.16,;-2.28,-.93,;-2.28,-2.47,;-3.61,-3.24,;-4.94,-2.47,;-4.94,-.93,;-6.28,-.16,;-7.61,-.93,;-8.95,-.16,;-8.95,1.38,;-10.28,2.15,;-11.61,1.38,;-11.61,-.16,;-10.28,-.93,;-3.61,-.16,;-3.61,1.38,;3.21,-.56,;8.95,.93,;10.28,1.7,;11.61,.93,;10.28,3.24,)| | ||
Structure |