Reaction Details | |||
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Target | Acetyl-CoA carboxylase 2 | ||
Ligand | BDBM307247 | ||
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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BDBM307247 | |||
n/a | |||
Name | BDBM307247 | ||
Synonyms: | US10150728, Example I-460 | ||
Type | Small organic molecule | ||
Emp. Form. | C20H24ClFN4O4 | ||
Mol. Mass. | 438.88 | ||
SMILES | C[C@@H](CO[C@H]1C[C@H](COc2ncnc(OCc3cc(Cl)ccn3)c2F)C1)NC(C)=O |r,wU:4.3,wD:6.6,1.0,(7.61,3.01,;7.61,1.47,;6.28,.7,;4.94,1.47,;3.61,.7,;3.21,-.78,;1.72,-.38,;.39,-1.15,;-.94,-.38,;-2.28,-1.15,;-2.28,-2.69,;-3.61,-3.47,;-4.94,-2.69,;-4.94,-1.15,;-6.28,-.38,;-7.61,-1.15,;-8.95,-.38,;-8.95,1.15,;-10.28,1.93,;-10.28,3.47,;-11.61,1.15,;-11.61,-.38,;-10.28,-1.15,;-3.61,-.38,;-3.61,1.15,;2.12,1.1,;8.95,.7,;10.28,1.47,;11.61,.7,;10.28,3.01,)| | ||
Structure |