Reaction Details |
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Target | Cholinesterase |
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Ligand | BDBM50205673 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1628516 (CHEMBL3871101) |
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IC50 | >10000±n/a nM |
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Citation | Horton, W; Sood, A; Peerannawar, S; Kugyela, N; Kulkarni, A; Tulsan, R; Tran, CD; Soule, J; LeVine, H; Török, B; Török, M Synthesis and application ofß-carbolines as novel multi-functional anti-Alzheimer's disease agents. Bioorg Med Chem Lett27:232-236 (2017) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Cholinesterase |
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Name: | Cholinesterase |
Synonyms: | Acylcholine acylhydrolase | BCHE | Butyrylcholine esterase (BChE) | Butyrylcholinesterase (BChE) | Butyrylcholinesterase (BuChE) | CHE1 | CHLE_HUMAN | Choline esterase II | Cholinesterases | Cholinesterases; ACHE & BCHE | Pseudocholinesterase |
Type: | Homotetramer |
Mol. Mass.: | 68422.27 |
Organism: | Homo sapiens (Human) |
Description: | P06276 |
Residue: | 602 |
Sequence: | MHSKVTIICIRFLFWFLLLCMLIGKSHTEDDIIIATKNGKVRGMNLTVFGGTVTAFLGIP
YAQPPLGRLRFKKPQSLTKWSDIWNATKYANSCCQNIDQSFPGFHGSEMWNPNTDLSEDC
LYLNVWIPAPKPKNATVLIWIYGGGFQTGTSSLHVYDGKFLARVERVIVVSMNYRVGALG
FLALPGNPEAPGNMGLFDQQLALQWVQKNIAAFGGNPKSVTLFGESAGAASVSLHLLSPG
SHSLFTRAILQSGSFNAPWAVTSLYEARNRTLNLAKLTGCSRENETEIIKCLRNKDPQEI
LLNEAFVVPYGTPLSVNFGPTVDGDFLTDMPDILLELGQFKKTQILVGVNKDEGTAFLVY
GAPGFSKDNNSIITRKEFQEGLKIFFPGVSEFGKESILFHYTDWVDDQRPENYREALGDV
VGDYNFICPALEFTKKFSEWGNNAFFYYFEHRSSKLPWPEWMGVMHGYEIEFVFGLPLER
RDNYTKAEEILSRSIVKRWANFAKYGNPNETQNNSTSWPVFKSTEQKYLTLNTESTRIMT
KLRAQQCRFWTSFFPKVLEMTGNIDEAEWEWKAGFHRWNNYMMDWKNQFNDYTSKKESCV
GL
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BDBM50205673 |
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n/a |
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Name | BDBM50205673 |
Synonyms: | CHEMBL3947464 |
Type | Small organic molecule |
Emp. Form. | C18H14N2 |
Mol. Mass. | 258.3172 |
SMILES | Cc1ccccc1-c1nccc2c3ccccc3[nH]c12 |
Structure |
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