Ki Summary

Reaction Details

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Target

5-hydroxytryptamine receptor 1A

Ligand

BDBM50157767

Substrate/Competitor

n/a

Meas. Tech.

ChEMBL_2091048 (CHEMBL4772311)

254±n/a nM

Citation

Jankowska, A; Sata?a, G; Ko?aczkowski, M; Bucki, A; G?uch-Lutwin, M; ?wierczek, A; Pociecha, K; Partyka, A; Jastrz?bska-Wi?sek, M; Lubelska, A; Latacz, G; Gawalska, A; Bojarski, AJ; Wyska, E; Ch?o?-Rzepa, G Novel anilide and benzylamide derivatives of arylpiperazinylalkanoic acids as 5-HT Eur J Med Chem201:0 (2020) [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

BDBM50157767

n/a

Name

BDBM50157767

Synonyms:

CHEMBL376662 | N-(5-methoxy-1,2,3,4-tetrahydronaphthalen-1-yl)-4-(2-methoxyphenyl)-1-piperazinebutanamide

Type

Small organic molecule

Emp. Form.

C26H35N3O3

Mol. Mass.

437.5744

SMILES

COc1cccc2C(CCCc12)NC(=O)CCCN1CCN(CC1)c1ccccc1OC

Structure