Reaction Details |
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Target | Acetylcholinesterase |
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Ligand | BDBM50570980 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_2304347 |
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Ki | 3.3±n/a nM |
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Citation | Nehra, B; Rulhania, S; Jaswal, S; Kumar, B; Singh, G; Monga, V Recent advancements in the development of bioactive pyrazoline derivatives. Eur J Med Chem205:0 (2020) [PubMed] |
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More Info.: | Get all data from this article, Assay Method |
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Acetylcholinesterase |
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Name: | Acetylcholinesterase |
Synonyms: | ACES_HUMAN | ACHE | Acetylcholinesterase (AChE) | Acetylcholinesterase (human AChE) |
Type: | Enzyme |
Mol. Mass.: | 67792.70 |
Organism: | Homo sapiens (Human) |
Description: | P22303 |
Residue: | 614 |
Sequence: | MRPPQCLLHTPSLASPLLLLLLWLLGGGVGAEGREDAELLVTVRGGRLRGIRLKTPGGPV
SAFLGIPFAEPPMGPRRFLPPEPKQPWSGVVDATTFQSVCYQYVDTLYPGFEGTEMWNPN
RELSEDCLYLNVWTPYPRPTSPTPVLVWIYGGGFYSGASSLDVYDGRFLVQAERTVLVSM
NYRVGAFGFLALPGSREAPGNVGLLDQRLALQWVQENVAAFGGDPTSVTLFGESAGAASV
GMHLLSPPSRGLFHRAVLQSGAPNGPWATVGMGEARRRATQLAHLVGCPPGGTGGNDTEL
VACLRTRPAQVLVNHEWHVLPQESVFRFSFVPVVDGDFLSDTPEALINAGDFHGLQVLVG
VVKDEGSYFLVYGAPGFSKDNESLISRAEFLAGVRVGVPQVSDLAAEAVVLHYTDWLHPE
DPARLREALSDVVGDHNVVCPVAQLAGRLAAQGARVYAYVFEHRASTLSWPLWMGVPHGY
EIEFIFGIPLDPSRNYTAEEKIFAQRLMRYWANFARTGDPNEPRDPKAPQWPPYTAGAQQ
YVSLDLRPLEVRRGLRAQACAFWNRFLPKLLSATDTLDEAERQWKAEFHRWSSYMVHWKN
QFDHYSKQDRCSDL
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BDBM50570980 |
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n/a |
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Name | BDBM50570980 |
Synonyms: | CHEMBL4847624 |
Type | Small organic molecule |
Emp. Form. | C23H21F2N3O4S |
Mol. Mass. | 473.492 |
SMILES | COc1ccc(C2CC(=NN2c2ccc(cc2)S(N)(=O)=O)c2cc(F)ccc2F)c(OC)c1 |c:8| |
Structure |
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