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TargetApelin receptor
LigandBDBM50571376
Substrate/Competitorn/a
Meas. Tech.ChEMBL_2114593 (CHEMBL4823534)
EC50>10000±n/a nM
Citation Narayanan, SWang, SVasukuttan, VVyas Devambatla, RKDai, DJin, CSnyder, RLaudermilk, LRunyon, SPMaitra, R Pyrazole Agonist of the Apelin Receptor Improves Symptoms of Metabolic Syndrome in Mice. J Med Chem64:3006-3025 (2021) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Apelin receptor
Name:Apelin receptor
Synonyms:AGTRL1 | APJ | APJ_HUMAN | APLNR | Angiotensin receptor-like 1 | Apelin receptor | Apelin receptor (APJ) | G-protein coupled receptor APJ | G-protein coupled receptor HG11
Type:Enzyme Catalytic Domain
Mol. Mass.:42664.06
Organism:Homo sapiens (Human)
Description:P35414
Residue:380
Sequence:
MEEGGDFDNYYGADNQSECEYTDWKSSGALIPAIYMLVFLLGTTGNGLVLWTVFRSSREK
RRSADIFIASLAVADLTFVVTLPLWATYTYRDYDWPFGTFFCKLSSYLIFVNMYASVFCL
TGLSFDRYLAIVRPVANARLRLRVSGAVATAVLWVLAALLAMPVMVLRTTGDLENTTKVQ
CYMDYSMVATVSSEWAWEVGLGVSSTTVGFVVPFTIMLTCYFFIAQTIAGHFRKERIEGL
RKRRRLLSIIVVLVVTFALCWMPYHLVKTLYMLGSLLHWPCDFDLFLMNIFPYCTCISYV
NSCLNPFLYAFFDPRFRQACTSMLCCGQSRCAGTSHSSSGEKSASYSSGHSQGPGPNMGK
GGEQMHEKSIPYSQETLVVD
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  Blast E-value cutoff:
BDBM50571376
n/a
NameBDBM50571376
Synonyms:CHEMBL4869477
TypeSmall organic molecule
Emp. Form.C26H39ClN4O5
Mol. Mass.523.065
SMILESCl.CCN(CC)CC[C@@H](CC(O)=O)NC(=O)c1cc(-c2c(OC)cccc2OC)n(n1)C1CCCC1 |r,wU:8.6,(26.45,-12.76,;25.46,-3.21,;26.08,-4.61,;25.17,-5.86,;23.65,-5.7,;23.02,-4.29,;25.8,-7.27,;24.9,-8.51,;25.52,-9.92,;27.06,-10.08,;27.96,-8.83,;29.49,-8.99,;27.33,-7.42,;24.62,-11.17,;23.09,-11.01,;22.46,-9.6,;22.19,-12.25,;20.65,-12.26,;20.17,-13.72,;18.72,-14.2,;17.57,-13.17,;17.89,-11.66,;16.75,-10.63,;16.11,-13.64,;15.79,-15.15,;16.95,-16.18,;18.4,-15.7,;19.55,-16.73,;19.24,-18.23,;21.42,-14.63,;22.66,-13.72,;21.43,-16.16,;20.19,-17.07,;20.66,-18.53,;22.2,-18.53,;22.68,-17.07,)|
Structure
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