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T38197Prostaglandin F2α Alcohol；Prostaglandin F2α AlcoholProstaglandin F2α Alcohol
Prostaglandin F2α Alcohol is a PGF2α (T15133) analogue. Prostaglandin F2α Alcohol is an orally active prostaglandin F receptor (FP receptor) agonist.
价 格：￥电议型 号：T38197产 地：中国大陆
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T38196Prostaglandin F2α isopropyl ester；Prostaglandin F2α isopropyl esterProstaglandin F2α isopropyl ester
PGF2α isopropyl ester is an ester prodrug of PGF2α with enhanced lipid solubility. Due to better membrane penetration, PGF2α isopropyl ester is more suitable than PGF2α or PGF2α tromethamine salt for topical application in studies on intraocular pressure. The ester functionality is readily hydrolyzed in vivo to release the active compound PGF2α. When administered topically to the eyes of cynomolgus monkeys, a 5 μg dose reduces intraocular pressure by 68% after the fourth day of treatment.
价 格：￥电议型 号：T38196产 地：中国大陆
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T38195Prostaglandin F2α Ethanolamide；Prostaglandin F2α EthanolamideProstaglandin F2α Ethanolamide；Prostagl
Prostaglandin F2α ethanolamide (PGF2α-EA) is produced by COX-2 metabolism of the endogenous cannabinoid, arachidonoyl ethanolamide (AEA), found in brain, liver, and other mammalian tissues. AEA can be metabolized directly by the sequential action of COX-2 and specific PG synthases to produce ethanolamide congeners of the classical PGs. PGF2α-EA has also been reported to be biosynthesized by this mechanism when AEA was infused into the lung and liver of living mice. PGF2α-EA is a potent dilator (
价 格：￥电议型 号：T38195产 地：中国大陆
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T38194Prostaglandin E3；Prostaglandin E3PGE3；PGE3
Prostaglandin E3 (PGE3) is formed via the cyclooxygenase (COX) metabolism of eicosapentaenoic acid. [1] In human ocular tissue, it comprises 2.4% of the COX products formed. [1] When applied to the eyes of a rabbit, a 1 µg dose of PGE3 decreases intraocular pressure from 21 mmHg to about 17 mmHg.[2]
价 格：￥电议型 号：T38194产 地：中国大陆
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T38139Orexin receptor antagonist 2；Orexin receptor antagonist 2Orexin receptor antagonist 2
Orexin Receptor Antagonist 2 (compound 30), characterized by its potent antagonistic activity with pKis of 7.69 and 9.78, holds promise for insomnia research[1].
价 格：￥电议型 号：T38139产 地：中国大陆
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T3799617-phenyl trinor Prostaglandin E2 ethyl amide；17-phenyl trinor Prostaglandin E2 ethyl amide17-phenyl
17-phenyl trinor PGE2 ethyl amide is derived from 17-phenyl trinor PGE2, a synthetic analog of PGE2 that acts as an agonist of EP1 and EP3 receptors in mice (Ki = 14 and 3.7 nM, respectively) and EP1, EP3, and EP4 in rats (Ki = 25, 4.3, and 54 nM, respectively). 17-phenyl trinor PGE2 causes contraction of guinea pig ileum at a concentration of 11 μM and is 4.4 times more potent than PGE2 as an antifertility agent in hamsters. Modification of the C-1 carboxyl group to an ethyl amide serves to inc
价 格：￥电议型 号：T37996产 地：中国大陆
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T3799516-phenoxy tetranor Prostaglandin F2α；16-phenoxy tetranor Prostaglandin F2α16-phenoxy tetranor Prost
16-phenoxy PGF2α is a metabolically stable analog of PGF2α. It binds to the FP receptor on ovine luteal cells with much greater affinity (440%) than PGF2α.
价 格：￥电议型 号：T37995产 地：中国大陆
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T3799316,16-dimethyl Prostaglandin F2α；16,16-dimethyl Prostaglandin F2α16,16-dimethyl Prostaglandin F2α；16
16,16-dimethyl Prostaglandin F2α can be used in related research in the field of life sciences. Its product number is T37993 and CAS number is 39746-23-1.
价 格：￥电议型 号：T37993产 地：中国大陆
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T3799115-keto Prostaglandin F2α；化合物15-keto Prostaglandin F2α15-keto Prostaglandin F2α|||15-keto PGF2α；15-k
15-keto Prostaglandin F2α is a metabolite of Prostaglandin F2α that lowers intraocular pressure in rabbits.
价 格：￥电议型 号：T37991产 地：中国大陆
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T3799015-keto Prostaglandin F1α；15-keto Prostaglandin F1α15-keto Prostaglandin F1α；15-keto Prostaglandin F
15-keto PGF1α is the initial metabolite of PGF1α via 15-hydroxy PGDH. In mammals, oxidation of C-15 markedly attenuates receptor binding and activity. In fish, the 15-keto compounds serve as post-ovulatory pheromones and are more active than the parent prostaglandins.
价 格：￥电议型 号：T37990产 地：中国大陆
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T3794817-trifluoromethylphenyl-13,14-dihydro trinor Prostaglandin F2α；17-trifluoromethylphenyl-13,14-dihyd
A number of 17-phenyl trinor prostaglandin F2α(17-phenyl trinor PGF2α) derivatives have been approved for the treatment of glaucoma.1,2,3Of these, the ones wherein the 13,14-double bond has been hydrogenated retain relatively good potency, but show a significantly reduced incidence of local irritant side effects.417-trifluoromethylphenyl-13,14-dihydro trinor PGF2αbears an aromatic ring which is reminiscent of the trifluoromethyl-phenoxy ring of travoprost ((+)-fluprostenol isopropyl ester). As a
价 格：￥电议型 号：T37948产 地：中国大陆
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T3794717-trifluoromethylphenyl trinor Prostaglandin F2α methyl ester；17-trifluoromethylphenyl trinor Prost
Prostaglandin F2α (PGF2α), acting through the FP receptor, causes smooth muscle contraction and exhibits potent luteolytic activity. 17-trifluoromethylphenyl trinor PGF2α is an analog of PGF2α that shares the meta-trifluoromethyl group of travoprost with the 17-phenyl trinor modification of latanoprost. It is anticipated to be a potent and selective agonist of the FP receptor, with potential applications in glaucoma and luteolysis. 17-trifluoromethylphenyl trinor PGF2α methyl ester is a lipophil
价 格：￥电议型 号：T37947产 地：中国大陆
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T3794617-trifluoromethylphenyl trinor Prostaglandin F2α；17-trifluoromethylphenyl trinor Prostaglandin F2α1
A number of 17-phenyl trinor prostaglandin F2α (17-phenyl trinor PGF2α) derivatives have been approved for the treatment of glaucoma. Of these, the unsubstituted or meta-substituted aromatic derivatives are the most potent FP receptor agonists. 17-trifluoromethylphenyl trinor PGF2α bears an aromatic ring which is reminiscent of the trifluoromethyl-phenoxy ring of travoprost ((+)-fluprostenol isopropyl ester). As an ocular hypotensive agent, it would be expected that 17-trifluoromethylphenyl trin
价 格：￥电议型 号：T37946产 地：中国大陆
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T37945Bimatoprost methyl ester；化合物 Bimatoprost methyl ester17-phenyl trinor Prostaglandin F2α methyl ester
Prostaglandin F2α (PGF2α) drives luteolysis and smooth muscle contraction by activating the FP receptor. Bimatoprost methyl ester is a lipophilic analog of 17-phenyl trinor PGF2α, a potent agonist for the FP receptor. 17-phenyl trinor PGF2α binds the FP receptor on ovine luteal cells with a relative potency of 756% compared to that of PGF2α. Esters of PGs serve as prodrugs, as they are efficiently hydrolyzed in certain tissues to generate the bioactive free acid.
价 格：￥电议型 号：T37945产 地：中国大陆
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T3794417-phenyl trinor Prostaglandin F2α methyl amide；17-phenyl trinor Prostaglandin F2α methyl amide17-ph
17-phenyl trinor Prostaglandin F2α (17-phenyl trinor PGF2α) is a metabolically stable analog of PGF2α and is a potent agonist for the FP receptor, binding with a relative potency of 756% compared to that of PGF2α. The ethyl amide of 17-phenyl trinor PGF2α bimatoprost has been approved for use as an ocular hypotensive drug. 17-phenyl trinor PGF2α methyl amide is an analog of bimatoprost. Its biological and toxicological properties have not been evaluated.
价 格：￥电议型 号：T37944产 地：中国大陆
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T3794317-phenyl trinor Prostaglandin F2α isopropyl ester；17-phenyl trinor Prostaglandin F2α isopropyl este
17-phenyl trinor PGF2α N-ethyl amide is an F-series prostaglandin analog which has been approved for use as an ocular hypotensive drug, sold under the Allergan trade name Bimatoprost. The N-ethyl amide prostaglandin prodrugs are converted to the active free acid more slowly than the analogous prostaglandin ester prodrugs such as latanoprost. This product is the isopropyl ester of the free acid prostaglandin which corresponds to Bimatoprost. The free acid, 17-phenyl trinor PGF2α, is a potent FP r
价 格：￥电议型 号：T37943产 地：中国大陆
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T3794217-phenyl trinor Prostaglandin F2α dimethyl amide；17-phenyl trinor Prostaglandin F2α dimethyl amide1
17-phenyl trinor Prostaglandin F2αdimethyl amide is an isomer of 17-phenyl trinor prostaglandin F2αethyl amide.
价 格：￥电议型 号：T37942产 地：中国大陆
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T3794117-phenyl trinor Prostaglandin F2α cyclopropyl methyl amide；17-phenyl trinor Prostaglandin F2α cyclo
Prostaglandin F2α (PGF2α) activates the FP receptor, promoting smooth muscle contraction and luteolysis. 17-phenyl trinor PGF2α binds the FP receptor on ovine luteal cells with a relative potency of 756% compared to that of PGF2α. It is produced in vivo by the hydrolysis of 17-phenyl trinor PGF2α ethyl amide. 17-phenyl trinor PGF2α ethyl amide is used to reduce intraocular pressure related to glaucoma. 17-phenyl trinor PGF2α cyclopropyl methyl amide is a lipophilic analog of 17-phenyl trinor PGF
价 格：￥电议型 号：T37941产 地：中国大陆
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T3794017-phenyl trinor Prostaglandin F2α cyclopropyl amide；17-phenyl trinor Prostaglandin F2α cyclopropyl
17-phenyl trinor Prostaglandin F2α cyclopropyl amide (17-phenyl trinor PGF2α cyclopropyl amide) is a novel analog of 17-phenyl trinor PGF2α ethyl amide. There are no published reports on the biological activity of 17-phenyl trinor PGF2α cyclopropyl amide.
价 格：￥电议型 号：T37940产 地：中国大陆
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T3794Pentagalloylglucose；1,2,3,4,6-五没食子酰葡萄糖Penta-O-galloyl-β-D-glucose|||1,2,3,4,6-O-Pentagalloylglucose|
1, 2, 3, 4, 6-Pentagalloylglucose (Penta-O-galloyl-β-D-glucose) and gallic acid from Pistacia lentiscus have antimutagenic and antioxidant activities. 2. 1, 2, 3, 4, 6-Penta-O-galloyl-beta-D-glucose (PGG) possesses potent anti-proliferative and anti-invasive effects, it also has inhibition of inducible nitric oxide synthase and cyclooxygenase-2 activity. 3. PGG may serve as a model for the development of new types of anti-diabetic and anti-metabolic syndrome therapeutics. 4. 1, 2, 3, 4, 6-Penta-
价 格：￥电议型 号：T3794产 地：中国大陆
