Co-Target(s) Information
Target General Information | Top | ||||
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Target ID | T15497 | Target Info | |||
Target Name | Prostaglandin E2 receptor EP1 (PTGER1) | ||||
Synonyms |
Prostanoid EP1 receptor; Prostaglandin E2 receptor EP1 subtype; PGE2 receptor EP1 subtype; PGE receptor, EP1 subtype; PGE receptor EP1 subtype; EP1 receptor
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Target Type | Clinical trial Target | ||||
Gene Name | PTGER1 | ||||
Biochemical Class | GPCR rhodopsin | ||||
UniProt ID |
Co-Targets of This Target | Top | |||||
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Co-Target Name | Thromboxane A2 receptor (TBXA2R) | Successful Target | ||||
UniProt ID | TA2R_HUMAN | |||||
Gene Name | TBXA2R | |||||
Synonyms |
TXA2-R; TXA2 receptor; Prostanoid TP receptor
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Representative Drug(s) | PGF2alpha | Drug Info | IC50 ~ 0.001 nM | [1] | ||
Co-Target Name | Prostaglandin F2-alpha receptor (PTGFR) | Successful Target | ||||
UniProt ID | PF2R_HUMAN | |||||
Gene Name | PTGFR | |||||
Synonyms |
Prostanoid FP receptor; PGF2-alpha receptor; PGF2 alpha receptor; PGF receptor; FP prostanoid receptor; FP prostaglandin receptor
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Representative Drug(s) | PGF2alpha | Drug Info | IC50 = 2.5 nM | [2] | ||
Co-Target Name | Prostaglandin E2 receptor EP3 (PTGER3) | Clinical trial Target | ||||
UniProt ID | PE2R3_HUMAN | |||||
Gene Name | PTGER3 | |||||
Synonyms |
Prostanoid EP3 receptor; Prostaglandin E2 receptor EP3 subtype; PGE2-R; PGE2 receptor EP3 subtype; PGE receptor, EP3 subtype; PGE receptor EP3 subtype
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Representative Drug(s) | PGF2alpha | Drug Info | IC50 = 110 nM | [1] | ||
Co-Target Name | Prostaglandin transporter (SLC21A2) | Patented-recorded Target | ||||
UniProt ID | SO2A1_HUMAN | |||||
Gene Name | SLCO2A1 | |||||
Synonyms |
Solute carrier organic anion transporter family member 2A1; Solute carrier family 21 member 2; PGT; OATP2A1
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Representative Drug(s) | PGF2alpha | Drug Info | Ki = 23 nM | [3] |
References | Top | ||||
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REF 1 | Synthesis and biological evaluation of prostaglandin-F alkylphosphinic acid derivatives as bone anabolic agents for the treatment of osteoporosis. J Med Chem. 2001 Nov 22;44(24):4157-69. | ||||
REF 2 | Synthesis and in vitro evaluation of human FP-receptor selective prostaglandin analogues. Bioorg Med Chem Lett. 2000 Jul 17;10(14):1519-22. | ||||
REF 3 | Cloning of mouse prostaglandin transporter PGT cDNA: species-specific substrate affinities. Am J Physiol. 1999 Sep;277(3):R734-41. |
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