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Target5-hydroxytryptamine receptor 1E
LigandBDBM50267555
Substrate/Competitorn/a
Meas. Tech.ChEMBL_563488 (CHEMBL961036)
Ki>10000±n/a nM
Citation Herth, MMKramer, VPiel, MPalner, MRiss, PJKnudsen, GMRösch, F Synthesis and in vitro affinities of various MDL 100907 derivatives as potential 18F-radioligands for 5-HT2A receptor imaging with PET. Bioorg Med Chem17:2989-3002 (2009) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
5-hydroxytryptamine receptor 1E
Name:5-hydroxytryptamine receptor 1E
Synonyms:5-HT-1E | 5-HT1E | 5-Hydroxytryptamine Receptor Subtype 1E (5HT1E) | 5-hydroxytryptamine receptor 1E | 5-hydroxytryptamine receptor 1E (5-HT-1E) (S31) | 5-hydroxytryptamine receptor 1E (5-HT-1E) (Serotonin receptor 1E) (5-HT1E) (S31). | 5HT1E_HUMAN | HTR1E | S31 | Serotonin (5-HT) receptor | Serotonin 1e (5-HT1e) receptor | Serotonin Receptor 1E
Type:G Protein-Coupled Receptor (GPCR)
Mol. Mass.:41697.80
Organism:Homo sapiens (Human)
Description:gi_112822
Residue:365
Sequence:
MNITNCTTEASMAIRPKTITEKMLICMTLVVITTLTTLLNLAVIMAIGTTKKLHQPANYL
ICSLAVTDLLVAVLVMPLSIIYIVMDRWKLGYFLCEVWLSVDMTCCTCSILHLCVIALDR
YWAITNAIEYARKRTAKRAALMILTVWTISIFISMPPLFWRSHRRLSPPPSQCTIQHDHV
IYTIYSTLGAFYIPLTLILILYYRIYHAAKSLYQKRGSSRHLSNRSTDSQNSFASCKLTQ
TFCVSDFSTSDPTTEFEKFHASIRIPPFDNDLDHPGERQQISSTRERKAARILGLILGAF
ILSWLPFFIKELIVGLSIYTVSSEVADFLTWLGYVNSLINPLLYTSFNEDFKLAFKKLIR
CREHT
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  Blast E-value cutoff:
BDBM50267555
n/a
NameBDBM50267555
Synonyms:(3-(2-Fluoroethoxy)-2-methoxyphenyl)-(1-(2-p-methoxyphenylethyl)-piperidine-4-yl)-methanol | CHEMBL490633
TypeSmall organic molecule
Emp. Form.C24H32FNO4
Mol. Mass.417.5136
SMILESCOc1ccc(CCN2CCC(CC2)C(O)c2cccc(OCCF)c2OC)cc1
Structure
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