Prostaglandin Receptor(前列腺素受体)
Prostaglandin receptors are a group of g-protein coupled receptor that exhibited a variety of functions in regulation of blood pressure and renal function; smooth muscle contraction; inhibition of plate aggregation; immune response etc.
- Cat.No. 产品名称 Information
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GC67982
Treprostinil palmitil
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GC67726
ONO-8711 dicyclohexylamine
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GC65987
EP3 antagonist 3
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GC65317
EP2 receptor antagonist-1
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GC64958
BAY-1316957
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GC64921
Pexopiprant
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GC64765
Ridogrel
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GC64435
Aganepag isopropyl
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GC63148
Pizuglanstat
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GC62867
BGC-20-1531 free base
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GC62667
KW-8232
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GC62493
MF-766
An EP4 receptor antagonist
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GC61805
Cefminox sodium
Cefminox Sodium (Meicelin, MT-141) is the sodium salt form of cefminox, a semi-synthetic, second-generation, beta-lactamase-stable cephalosporin with antibacterial activity.
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GC61581
BAY 73-1449
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GC50722
ER 819762
ER 817692 是一种具有口服活性的高选择性前列腺素 E2 (PGE2) EP4 受体拮抗剂,对人 EP4 受体的 EC50 为 70 nM。
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GC61234
Rebamipide D4
An internal standard for the quantification of rebamipide
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GC60611
AZ12672857
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GC60248
Misoprostol acid D5
Internal standard for the quantification of misoprostol (free acid)
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GC60225
Licarin A
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GC60152
Epibetulinic acid
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GC39632
Laflunimus
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GC50450
Carboprost tromethamine
卡前列素氨丁三醇是合成的前列腺素 F2α 的 15-甲基类似物。
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GC50393
DG 041
DG 041 是一种有效的、高亲和力和选择性的 EP3 受体拮抗剂,在结合和 FLIPR 试验中的 IC50 分别为 4.6 nM 和 8.1 nM。
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GC50240
AMG 853
AMG 853 (AMG 853) 是一种苯乙酸衍生物。
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GC50055
Ro 1138452 hydrochloride
Selective prostacyclin IP receptor antagonist
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GC39053
Saikogenin D
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GC38902
Dazoxiben
Dazoxiben hydrochloride (HCl) is a potent, selevtive and orally active inhibitor of thromboxane (TX) synthase. Dazoxiben inhibits TXB2 production in clotting human whole blood with IC50 of 0.3 μM and causes parallel enhancement of PGE2 production.
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GC38891
Beraprost sodium
A stable, orally active analog of prostacyclin
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GC38827
NTP42
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GC38764
Darbufelone
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GC38763
Daltroban
A TP antagonist
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GC38379
Furprofen
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GC37822
Travoprost
A PGF2α analog and prodrug form of (+)-fluprostenol
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GC37795
Timapiprant sodium
Timapiprant sodium (OC000459 sodium), a potent, selective, and orally active D prostanoid receptor 2 (DP2, also known as CRTH2) antagonist, potently displaces [3H]PGD2 from human recombinant DP2, rat recombinant DP2, and human native DP2 with Ki values of 13, 3 and 4 nM, respectively.
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GC37794
Timapiprant
A potent, selective DP2 antagonist
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GC36624
MK-7246 S enantiomer
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GC36623
MK-2894 sodium salt
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GC36379
KAG-308
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GC35620
CAY10471 Racemate
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GC45259
(+)-Cloprostenol (sodium salt)
The active isomer of cloprostenol, a potent IP receptor agonist
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GC44360
Nedocromil (sodium salt)
A mast cell stabilizer
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GC44021
L-826,266
A selective EP3 antagonist
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GC42927
BGC 20-1531 (hydrochloride)
A potent and selective EP4 receptor antagonist
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GC41442
Misoprostol (free acid)
An EP2, EP3, and EP4 receptor agonist
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GC41229
Latanoprost (free acid)
Potent FP receptor agonist
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GC40854
Latanoprost Lactone Diol
An intermediate in the synthesis of latanoprost
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GC40750
Agnuside
An iridoid glycoside with diverse biological activities
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GC40591
Prostaglandin F2β
The 9β-hydroxy stereoisomer of PGF2α
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GC34015
MRE-269 (ACT-333679)
Selective IP receptor agonist
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GC33550
LCB-2853