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GPCR

Name	Somatostatin receptor type 4
Species	Homo sapiens (Human)
Gene	SSTR4
Synonym	SS4R SS4-R SS-4-R SRIF2B SST4 receptor
Disease	N/A
Length	388
Amino acid sequence	MSAPSTLPPGGEEGLGTAWPSAANASSAPAEAEEAVAGPGDARAAGMVAIQCIYALVCLVGLVGNALVIFVILRYAKMKTATNIYLLNLAVADELFMLSVPFVASSAALRHWPFGSVLCRAVLSVDGLNMFTSVFCLTVLSVDRYVAVVHPLRAATYRRPSVAKLINLGVWLASLLVTLPIAIFADTRPARGGQAVACNLQWPHPAWSAVFVVYTFLLGFLLPVLAIGLCYLLIVGKMRAVALRAGWQQRRRSEKKITRLVLMVVVVFVLCWMPFYVVQLLNLFVTSLDATVNHVSLILSYANSCANPILYGFLSDNFRRFFQRVLCLRCCLLEGAGGAEEEPLDYYATALKSKGGAGCMCPPLPCQQEALQPEPGRKRIPLTRTTTF
UniProt	P31391
Protein Data Bank	N/A
GPCR-HGmod model	P31391
3D structure model	This predicted structure model is from GPCR-EXP P31391.
BioLiP	N/A
Therapeutic Target Database	N/A
ChEMBL	CHEMBL1853
IUPHAR	358
DrugBank	BE0009273

Ligand

Name	SOMATOSTATIN
Molecular formula	C76H104N18O19S2
IUPAC name	(4R,7S,10S,13S,16S,19S,22S,25S,28S,31S,34S,37R)-19,34-bis(4-aminobutyl)-31-(2-amino-2-oxoethyl)-37-[[2-[[(2S)-2-aminopropanoyl]amino]acetyl]amino]-13,25,28-tribenzyl-10,16-bis[(1R)-1-hydroxyethyl]-7-(hydroxymethyl)-22-(1H-indol-3-ylmethyl)-6,9,12,15,18,21,24,27,30,33,36-undecaoxo-1,2-dithia-5,8,11,14,17,20,23,26,29,32,35-undecazacyclooctatriacontane-4-carboxylic acid
Molecular weight	1637.9
Hydrogen bond acceptor	24
Hydrogen bond donor	22
XlogP	-3.1
Synonyms	MolPort-006-823-896 Somatostatin acetate Somatostatine Synthetic growth hormone release-inhibiting hormone 51110-01-1 (Parent) Ala-Gly-cyclo-[Cys-Lys-Asn-Phe-Phe-Trp-Lys-Thr-Phe-Thr-Ser-Cys] Growth hormone-release inhibiting factor: L-alanylglycyl-L-cysteinyl-L-lysyl-L-asparaginyl-L-phenylalanyl-L-phenylalanyl-L-tryptophyl-L-lysyl-L-threonyl-L-phenylalanyl-L-threonyl-L-seryl-L-cysteine cyclic (3-14) disulfide Somatostatin, cyclic Somatostatinum [INN-Latin] UNII-F6R2N217HS 6E20216Q0L C76H104N18O19S2 D0T5RO HS-2027 Somatostatin (rat) Somatostatina SRIF 15-28-Somatostatin-28 AK552885 CCRIS 3629 F6R2N217HS LS-174755 NCGC00167137-01 Somatostatin [BAN:INN] Somatostatine [INN-French] Synthetic somatostatin-14 52769-04-7 BDBM81767 CHEMBL1823872 Growth hormone-release inhibiting factor: L-alanylglycyl-L-cysteinyl-L-lysyl-L-asparaginyl-L-phenylalanyl-L-phenylalanyl-L-tryptophyl-L-lysyl-L-threonyl-L-phenylalanyl-L-threonyl-L-seryl-L-cysteine cyclic (3->14) disulfide Somatostatin (human) Somatostatin-1 Somatotropin release inhibiting factor CAS_38916-34-6 L-alanyl-N-[(4R,7S,10S,13S,16S,19S,22S,25S,28S,31S,34S,37R)-19,34-bis(4-aminobutyl)-31-(2-amino-2-oxoethyl)-13,25,28-tribenzyl-4-carboxy-10,16-bis[(1R)-1-hydroxyethyl]-7-(hydroxymethyl)-22-(1H-indol-3-ylmethyl)-6,9,12,15,18,21,24,27,30,33,36-undecaoxo-1,2 Somatostatin (sheep) Somatostatina [INN-Spanish] Synthetic cyclic growth hormone release-inhibiting factor 38916-34-6 AKOS015994634 CHEBI:64628 Growth hormone release inhibiting factor MFCD00076762 NHXLMOGPVYXJNR-ATOGVRKGSA-N Somatostatin [INN:BAN] Somatostatinum UNII-6E20216Q0L 55914-64-2 BRD-K14681867-015-01-6 Cyclic Somatostatin H664 Somatostatin (pigeon) Somatostatin-14 SR 9357 916S346 CB6417646 EINECS 254-186-5 L-alanylglycyl-L-cysteinyl-L-lysyl-L-asparaginyl-L-phenylalanyl-L-phenylalanyl-L-tryptophyl-L-lysyl-L-threonyl-L-phenylalanyl-L-threonyl-L-seryl-L-cysteine cyclic (3-14) disulfide [ Show all ]
Inchi Key	NHXLMOGPVYXJNR-ATOGVRKGSA-N
Inchi ID	InChI=1S/C76H104N18O19S2/c1-41(79)64(100)82-37-61(99)83-58-39-114-115-40-59(76(112)113)92-72(108)57(38-95)91-75(111)63(43(3)97)94-71(107)54(33-46-23-11-6-12-24-46)90-74(110)62(42(2)96)93-66(102)51(28-16-18-30-78)84-69(105)55(34-47-36-81-49-26-14-13-25-48(47)49)88-68(104)53(32-45-21-9-5-10-22-45)86-67(103)52(31-44-19-7-4-8-20-44)87-70(106)56(35-60(80)98)89-65(101)50(85-73(58)109)27-15-17-29-77/h4-14,19-26,36,41-43,50-59,62-63,81,95-97H,15-18,27-35,37-40,77-79H2,1-3H3,(H2,80,98)(H,82,100)(H,83,99)(H,84,105)(H,85,109)(H,86,103)(H,87,106)(H,88,104)(H,89,101)(H,90,110)(H,91,111)(H,92,108)(H,93,102)(H,94,107)(H,112,113)/t41-,42+,43+,50-,51-,52-,53-,54-,55-,56-,57-,58-,59-,62-,63-/m0/s1
PubChem CID	16129706
ChEMBL	CHEMBL1823872
IUPHAR	N/A
BindingDB	81767
DrugBank	DB09099
Structure SDF download
Lipinski's druglikeness	This 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

Parameter	Value	Reference	Database source
	N/A	N/A	DrugBank
IC50	0.08 nM	PMID9216843	ChEMBL
IC50	0.08 nM	PMID9216843	BindingDB
IC50	1.6 nM	PMID24378707, PMID15658865	ChEMBL
IC50	1.7 nM	PMID21806016	BindingDB,ChEMBL
Ki	0.3 nM	PMID10433861	BindingDB
Ki	0.53 nM	PMID7988476	BindingDB
Ki	0.59 nM	PMID11327607	ChEMBL
Ki	0.59 nM	PMID11327607	BindingDB
Ki	0.63 nM	PMID11520208	ChEMBL
Ki	0.74 nM	PMID24342240	ChEMBL
Ki	1.2 nM	PMID10818260	BindingDB
Ki	1.23 nM	PMID10598788, PMID9650799	BindingDB
Ki	1.259 nM	PMID12773038	ChEMBL
Ki	1.26 nM	PMID9290757	BindingDB
Ki	1.34 nM	PMID10598788	BindingDB
Ki	1.4 nM	PMID9822540	ChEMBL
Ki	1.7 nM	PMID16220980	ChEMBL
Ki	1.76 nM	PMID9600011, PMID9724791, PMID12477342	BindingDB,ChEMBL
Ki	>2.0 nM	MedChemComm, (2014) 5:8:1150	ChEMBL
Ki	4.07 nM	PMID10598788, PMID9650799	BindingDB
pKD	8.39 -	PMID11448228	ChEMBL