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Target5-hydroxytryptamine receptor 1A
LigandBDBM50558338
Substrate/Competitorn/a
Meas. Tech.ChEMBL_2063306 (CHEMBL4718559)
Ki 366±n/a nM
Citation Stefanowicz, JS?owi?ski, TWróbel, MZHerold, FGomó?ka, AEWeso?owska, AJastrz?bska-Wi?sek, MPartyka, AAndres-Mach, MCzuczwar, SJ?uszczki, JJZagaja, MSiwek, ANowak, G?o?nierek, MB?czek, TUlenberg, SBelka, MTur?o, J Synthesis and biological investigation of new equatorial (?) stereoisomers of 3-aminotropane arylamides with atypical antipsychotic profile. Bioorg Med Chem24:3994-4007 (2016) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
5-hydroxytryptamine receptor 1A
Name:5-hydroxytryptamine receptor 1A
Synonyms:5-HT-1A | 5-HT1 | 5-HT1A | 5-Hydroxytryptamine receptor 1A (5-HT1A) | 5-hydroxytryptamine receptor 1A (5HT1A) | 5HT1A_RAT | 5ht1a | G-21 | Htr1a | Serotonin 1 (5-HT1) receptor | Serotonin 1a (5-HT1a) receptor/Adrenergic receptor alpha-1 | Serotonin receptor 1A
Type:G Protein-Coupled Receptor (GPCR)
Mol. Mass.:46445.29
Organism:Rattus norvegicus (rat)
Description:Binding assays were performed using rat hippocampal membranes.
Residue:422
Sequence:
MDVFSFGQGNNTTASQEPFGTGGNVTSISDVTFSYQVITSLLLGTLIFCAVLGNACVVAA
IALERSLQNVANYLIGSLAVTDLMVSVLVLPMAALYQVLNKWTLGQVTCDLFIALDVLCC
TSSILHLCAIALDRYWAITDPIDYVNKRTPRRAAALISLTWLIGFLISIPPMLGWRTPED
RSDPDACTISKDHGYTIYSTFGAFYIPLLLMLVLYGRIFRAARFRIRKTVRKVEKKGAGT
SLGTSSAPPPKKSLNGQPGSGDWRRCAENRAVGTPCTNGAVRQGDDEATLEVIEVHRVGN
SKEHLPLPSESGSNSYAPACLERKNERNAEAKRKMALARERKTVKTLGIIMGTFILCWLP
FFIVALVLPFCESSCHMPALLGAIINWLGYSNSLLNPVIYAYFNKDFQNAFKKIIKCKFC
RR
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50558338
n/a
NameBDBM50558338
Synonyms:CHEMBL4757614
TypeSmall organic molecule
Emp. Form.C25H25FN2O
Mol. Mass.388.4772
SMILESFc1ccccc1CN1C2CCC1CC(C2)NC(=O)c1ccc2ccccc2c1 |TLB:7:8:14.15.13:10.11|
Structure
Search PDB for entries with ligand similarity:Similarity to this molecule at least: