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GLASS

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GPCR

Name	Prostaglandin E2 receptor EP4 subtype
Species	Homo sapiens (Human)
Gene	PTGER4
Synonym	Prostanoid EP4 receptor PGE2 receptor EP4 subtype PGE receptor EP4 subtype EP4 receptor EP2
Disease	Ulcerative colitis Glaucoma Inflammatory disease Migraine Osteoarthritis Osteoarthritis; Pain Pain Fracture Asthma Acute heart failure [ Show all ]
Length	488
Amino acid sequence	MSTPGVNSSASLSPDRLNSPVTIPAVMFIFGVVGNLVAIVVLCKSRKEQKETTFYTLVCGLAVTDLLGTLLVSPVTIATYMKGQWPGGQPLCEYSTFILLFFSLSGLSIICAMSVERYLAINHAYFYSHYVDKRLAGLTLFAVYASNVLFCALPNMGLGSSRLQYPDTWCFIDWTTNVTAHAAYSYMYAGFSSFLILATVLCNVLVCGALLRMHRQFMRRTSLGTEQHHAAAAASVASRGHPAASPALPRLSDFRRRRSFRRIAGAEIQMVILLIATSLVVLICSIPLVVRVFVNQLYQPSLEREVSKNPDLQAIRIASVNPILDPWIYILLRKTVLSKAIEKIKCLFCRIGGSRRERSGQHCSDSQRTSSAMSGHSRSFISRELKEISSTSQTLLPDLSLPDLSENGLGGRNLLPGVPGMGLAQEDTTSLRTLRISETSDSSQGQDSESVLLVDEAGGSGRAGPAPKGSSLQVTFPSETLNLSEKCI
UniProt	P35408
Protein Data Bank	5ywy, 5yhl
GPCR-HGmod model	P35408
3D structure model	This structure is from PDB ID 5ywy.
BioLiP	BL0434347, BL0434289
Therapeutic Target Database	T18876
ChEMBL	CHEMBL1836
IUPHAR	343
DrugBank	BE0003522

Ligand

Name	prostaglandin D2
Molecular formula	C20H32O5
IUPAC name	(Z)-7-[(1R,2R,5S)-5-hydroxy-2-[(E,3S)-3-hydroxyoct-1-enyl]-3-oxocyclopentyl]hept-5-enoic acid
Molecular weight	352.471
Hydrogen bond acceptor	5
Hydrogen bond donor	3
XlogP	2.6
Synonyms	11-Dehydroprostaglandin F2-alpha 41598-07-6 5179-EP2305640A2 BHMBVRSPMRCCGG-OUTUXVNYSA-N D0H8QQ HMS1989K08 NCGC00161284-02 RXY07S6CZ2 (5Z,13E)-(15S)-9a,15-Dihydroxy-11-oxoprosta-5,13-dienoic acid [3H]PGD2 (5Z,13E,15S)-9alpha,15-Dihydroxy-11-oxoprosta-5,13-dienoate (5Z,9alpha,13E,15S)-9,15-dihydroxy-11-oxo-prosta-5,13-dien-1-oate 5179-EP2281563A1 9S,15S-dihydroxy-11-oxo-5Z,13E-prostadienoate BSPBio_001486 E8965369-341A-46F4-8677-2CEB4F9432BA IDI1_033956 Prosta-5,13-dien-1-oic acid, 9,15-dihydroxy-11-oxo-, (5Z,9-alpha,13E,15S)- (5Z,13E)-(15S)-9,15-dihydroxy-11-oxoprosta-5,13-dienoate SR-01000946237-1 (5Z,13E,15S)-9-alpha,15-dihydroxy-11-oxoprosta-5,13-dienoate (Z)-7-[(1R,2R,5S)-5-hydroxy-2-[(E,3S)-3-hydroxyoct-1-enyl]-3-oxocyclopentyl]hept-5-enoic acid 198163-EP2272827A1 5179-EP2295409A1 AKOS032954030 CHEMBL1235252 HMS1361K08 MFCD00077857 Prostaglandin D2, >=95%, synthetic (5z,13e)-(15s)-9-alpha,15-dihydroxy-11-oxoprosta-5,13-dienoic acid [3H]-PGD2 (5Z,13E,15S)-9a,15-dihydroxy-11-oxoprosta-5,13-dien-1-oic acid 11-Dehydroprostaglandin F2alpha 5179-EP2272832A1 5179-EP2316459A1 BML1-F05 HMS3402K08 NCGC00161284-03 (5E,13E)-9,15-DIHYDROXY-11-OXOPROSTA-5,13-DIEN-1-OIC ACID SCHEMBL2508829 (5Z,13E)-(15S)-9alpha,15-Dihydroxy-11-oxoprosta-5,13-dienoate [3H]prostaglandin D2 (5Z,9-alpha,13E,15S)-9,15-dihydroxy-11-oxo-Prosta-5,13-dien-1-oate (5Z,9alpha,13E,15S)-9,15-dihydroxy-11-oxo-prosta-5,13-dien-1-oic acid 198163-EP2270004A1 5179-EP2281813A1 9S,15S-dihydroxy-11-oxo-5Z,13E-prostadienoic acid C00696 GTPL1881 LMFA03010004 prosta-glandin d2 (5Z,13E)-(15S)-9,15-dihydroxy-11-oxoprosta-5,13-dienoic acid UNII-RXY07S6CZ2 (5Z,13E,15S)-9-alpha,15-dihydroxy-11-oxoprosta-5,13-dienoic acid 11-Dehydroprostaglandin F2 alpha 2004AH 5179-EP2301937A1 BDBM21544 D06KBO HMS1791K08 NCGC00161284-01 Prostaglandin D2, cell culture tested (5Z,13E)-(15S)-9a,15-Dihydroxy-11-oxoprosta-5,13-dienoate [3H]11-dehydroprostaglandin F2-alpha (5Z,13E,15S)-9alpha,15-dihydroxy-11-oxoprosta-5,13-dien-1-oic acid 5179-EP2280006A1 5179-EP2316824A1 BRN 2170623 DB02056 HMS3648M03 PGD2 (5Z)-7-[(1R,2R,5S)-5-hydroxy-2-[(1E,3S)-3-hydroxyoct-1-en-1-yl]-3-oxocyclopentyl]hept-5-enoic acid SR-01000946237 (5Z,13E)-(15S)-9alpha,15-Dihydroxy-11-oxoprosta-5,13-dienoic acid (5Z,9-alpha,13E,15S)-9,15-dihydroxy-11-oxo-Prosta-5,13-dien-1-oic acid (5Z,9alpha,13E,15S)-9,15-Dihydroxy-11-oxoprosta-5,13-dien-1-oic-acid 198163-EP2272825A2 5179-EP2281815A1 AC1L9LZD CHEBI:15555 GTPL1891 LS-125822 (5z,13e)-(15s)-9-alpha,15-dihydroxy-11-oxoprosta-5,13-dienoate ZINC85994848 (5Z,13E,15S)-9a,15-dihydroxy-11-oxoprosta-5,13-dien-1-oate [ Show all ]
Inchi Key	BHMBVRSPMRCCGG-OUTUXVNYSA-N
Inchi ID	InChI=1S/C20H32O5/c1-2-3-6-9-15(21)12-13-17-16(18(22)14-19(17)23)10-7-4-5-8-11-20(24)25/h4,7,12-13,15-18,21-22H,2-3,5-6,8-11,14H2,1H3,(H,24,25)/b7-4-,13-12+/t15-,16+,17+,18-/m0/s1
PubChem CID	448457
ChEMBL	N/A
IUPHAR	1891, 1881
BindingDB	N/A
DrugBank	DB02056
Structure SDF download
Lipinski's druglikeness	This ligand satisfies Lipinski's rule of five.

Experimental Data

Parameter	Value	Reference	Database source
EC50	1.7 nM	PMID19584306	IUPHAR
Ki	1.0 - 2.0 nM	PMID10462542, PMID10952683	IUPHAR

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