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Target5-hydroxytryptamine receptor 1A
LigandBDBM50316682
Substrate/Competitorn/a
Meas. Tech.ChEMBL_632233 (CHEMBL1110095)
Ki 0.61±n/a nM
Citation Childers, WEHavran, LMAsselin, MBicksler, JJChong, DCGrosu, GTShen, ZAbou-Gharbia, MABach, ACHarrison, BLKagan, NKleintop, TMagolda, RMarathias, VRobichaud, AJSabb, ALZhang, MYAndree, THAschmies, SHBeyer, CComery, TADay, MGrauer, SMHughes, ZARosenzweig-Lipson, SPlatt, BPulicicchio, CSmith, DESukoff-Rizzo, SJSullivan, KMAdedoyin, AHuselton, CHirst, WD The synthesis and biological evaluation of quinolyl-piperazinyl piperidines as potent serotonin 5-HT1A antagonists. J Med Chem53:4066-84 (2010) [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-HT1A | 5-hydroxytryptamine receptor 1A (5-HT-1A) | 5HT1A_HUMAN | ADRB2RL1 | ADRBRL1 | Dopamine D2 receptor and serotonin 1a receptor | G-21 | HTR1A | Serotonin receptor 1A
Type:n/a
Mol. Mass.:46122.49
Organism:Homo sapiens (Human)
Description:n/a
Residue:422
Sequence:
MDVLSPGQGNNTTSPPAPFETGGNTTGISDVTVSYQVITSLLLGTLIFCAVLGNACVVAA
IALERSLQNVANYLIGSLAVTDLMVSVLVLPMAALYQVLNKWTLGQVTCDLFIALDVLCC
TSSILHLCAIALDRYWAITDPIDYVNKRTPRRAAALISLTWLIGFLISIPPMLGWRTPED
RSDPDACTISKDHGYTIYSTFGAFYIPLLLMLVLYGRIFRAARFRIRKTVKKVEKTGADT
RHGASPAPQPKKSVNGESGSRNWRLGVESKAGGALCANGAVRQGDDGAALEVIEVHRVGN
SKEHLPLPSEAGPTPCAPASFERKNERNAEAKRKMALARERKTVKTLGIIMGTFILCWLP
FFIVALVLPFCESSCHMPTLLGAIINWLGYSNSLLNPVIYAYFNKDFQNAFKKIIKCKFC
RQ
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50316682
n/a
NameBDBM50316682
Synonyms:6-Bromo-8-{4-[4-(6-methoxyquinolin-8-yl)piperazin-1-yl]piperidin-1-yl}Quinoline | CHEMBL1096529
TypeSmall organic molecule
Emp. Form.C28H30BrN5O
Mol. Mass.532.475
SMILESCOc1cc(N2CCN(CC2)C2CCN(CC2)c2cc(Br)cc3cccnc23)c2ncccc2c1
Structure
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