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GPCR

NameUrotensin-2 receptor
SpeciesRattus norvegicus (Rat)
GeneUts2r
SynonymUT receptor
urotensin II receptor
UR-II-R
UR-2-R
UII-R1
[ Show all ]
DiseaseN/A for non-human GPCRs
Length386
Amino acid sequenceMALSLESTTSFHMLTVSGSTVTELPGDSNVSLNSSWSGPTDPSSLKDLVATGVIGAVLSAMGVVGMVGNVYTLVVMCRFLRASASMYVYVVNLALADLLYLLSIPFIIATYVTKDWHFGDVGCRVLFSLDFLTMHASIFTLTIMSSERYAAVLRPLDTVQRSKGYRKLLVLGTWLLALLLTLPMMLAIQLVRRGSKSLCLPAWGPRAHRTYLTLLFGTSIVGPGLVIGLLYVRLARAYWLSQQASFKQTRRLPNPRVLYLILGIVLLFWACFLPFWLWQLLAQYHEAMPLTPETARIVNYLTTCLTYGNSCINPFLYTLLTKNYREYLRGRQRSLGSSCHSPGSPGSFLPSRVHLQQDSGRSLSSSSQQATETLMLSPVPRNGALL
UniProtP49684
Protein Data BankN/A
GPCR-HGmod modelN/A
3D structure modelNo available structures or models
BioLiPN/A
Therapeutic Target DatabaseN/A
ChEMBLCHEMBL4921
IUPHAR365
DrugBankN/A

Ligand

NameCHEMBL501579
Molecular formulaC56H70N10O10S2
IUPAC name(2S)-2-[[(4R,7S,10S,13R,16S,19S)-19-[[(2S)-2-amino-3-phenylpropanoyl]amino]-10-(3-aminopropyl)-16-benzyl-7-[(4-hydroxyphenyl)methyl]-13-(1H-indol-3-ylmethyl)-20,20-dimethyl-6,9,12,15,18-pentaoxo-1,2-dithia-5,8,11,14,17-pentazacycloicosane-4-carbonyl]amino]-3-methylbutanoic acid
Molecular weight1107.36
Hydrogen bond acceptor14
Hydrogen bond donor12
XlogP2.1
SynonymsBDBM50413765
Inchi KeyGYCUZIHFIHIAHM-UVTBRFMXSA-N
Inchi IDInChI=1S/C56H70N10O10S2/c1-32(2)46(55(75)76)65-53(73)45-31-77-78-56(3,4)47(66-48(68)39(58)26-33-14-7-5-8-15-33)54(74)63-43(27-34-16-9-6-10-17-34)50(70)62-44(29-36-30-59-40-19-12-11-18-38(36)40)52(72)60-41(20-13-25-57)49(69)61-42(51(71)64-45)28-35-21-23-37(67)24-22-35/h5-12,14-19,21-24,30,32,39,41-47,59,67H,13,20,25-29,31,57-58H2,1-4H3,(H,60,72)(H,61,69)(H,62,70)(H,63,74)(H,64,71)(H,65,73)(H,66,68)(H,75,76)/t39-,41-,42-,43-,44+,45-,46-,47-/m0/s1
PubChem CID44574147
ChEMBLCHEMBL501579
IUPHARN/A
BindingDB50413765
DrugBankN/A

Structure

SDF download

2D structure
Lipinski's druglikenessThis ligand has more than 5 hydrogen bond donor.
This ligand has more than 10 hydrogen bond acceptor.
This ligand is heavier than 500 daltons.

Experimental Data

ParameterValueReferenceDatabase source
pKb8.68 -PMID19432421ChEMBL

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