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T3615315(S)-15-methyl Prostaglandin D2；15(S)-15-methyl Prostaglandin D215(S)-15-methyl Prostaglandin D2；15
15(S)-15-methyl Prostaglandin D2 (15(S)-15-methyl PGD2) is a metabolically stable synthetic analog of PGD2 . In contrast to PGD2, 15(S)-15-methyl PGD2 induces vasoconstriction and increases systemic blood pressure with much reduced inhibitory activity on ADP-induced platelet aggregation. It also exhibits strong antifertility activity in hamsters (200-fold more potent than PGD2).
价 格：￥电议型 号：T36153产 地：中国大陆
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T3614813,14-dihydro-15-keto Prostaglandin F1α；13,14-dihydro-15-keto Prostaglandin F1α13,14-dihydro-15-keto
13,14-dihydro-15-keto Prostaglandin F1α (13,14-dihydro-15-keto PGF1α) is a metabolite of PGF1α that has been reported in the rat stomach. The measurement of 13,14-dihydro-15-keto PGF1α can be used as a marker of the in vivo production of PGF1α.
价 格：￥电议型 号：T36148产 地：中国大陆
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T3614713,14-dihydro-15-keto Prostaglandin E1；13,14-dihydro-15-keto Prostaglandin E113,14-dihydro-15-keto P
13,14-dihydro-15-keto Prostaglandin E1 inhibits ADP-induced platelet aggregation in human isolated platelet-rich plasma (IC50=14.8 μg/mL) and is a PGE1 metabolite.
价 格：￥电议型 号：T36147产 地：中国大陆
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T3614613,14-dihydro Prostaglandin F2α；13,14-dihydro Prostaglandin F2α13,14-dihydro Prostaglandin F2α|||13,
13,14-dihydro Prostaglandin F2α (13,14-dihydro PGF2α) is the analog of PGF2α which has no unsaturation in the lower side chain. It causes luteolysis in hamsters with a potency five times higher than PGF2α. The ED50 value for 13,14-dihydro PGF2α as a luteolytic agent in hamsters is 1.5 µg/100 g.[1]
价 格：￥电议型 号：T36146产 地：中国大陆
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T3614411β-Prostaglandin E2；11β-Prostaglandin E211β-PGE2|||11β-Prostaglandin E2；11β-PGE2|||11β-Prostaglandi
11β-PGE2 is the C-11 epimer of PGE2. It is a moderate inhibitor of PGE2 binding to rat hypothalamic membranes with a Ki value of 53 nM.[1] 11β-PGE2 also stimulates bone resorption in rats at concentrations of 10-8 to 10-6 M which is similar to PGE2.2 11β-PGE2 inhibits PGE2 binding to the prostaglandin transporter protein with a Ki of 56 nM.[3]
价 格：￥电议型 号：T36144产 地：中国大陆
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T360451a,1b-dihomo Prostaglandin E2；1a,1b-dihomo Prostaglandin E21a,1b-dihomo Prostaglandin E2；1a,1b-dihom
1a,1b-dihomo Prostaglandin E2 (PGE2) is a rare polyunsaturated fatty acid first identified in extracts of sheep vesicular gland microsomes, known to contain COX, incubated with adrenic acid . 1a,1b-dihomo PGE2 has also been identified in conditioned media of RAW 264.7 macrophages stimulated with endotoxin and arachidonic acid . This product is thought to be produced by elongation of AA to adrenic acid, which is then metabolized sequentially by COX and PGE synthase.
价 格：￥电议型 号：T36045产 地：中国大陆
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T3604116,16-dimethyl Prostaglandin A2；16,16-dimethyl Prostaglandin A216,16-dimethyl Prostaglandin A2；16,16
16,16-dimethyl PGA2 is a metabolism-resistant analog of PGA2 with a prolonged in vivo half-life. It inhibits the proliferation of Sendai virus in cultured African green monkey kidney cells by >90% at a concentration of 4 μg/ml. Daily infusion of 10 μg of 16,16-dimethyl PGA2 methyl ester into mice infected with influenza A virus increased survival by 40%. Similar treatment of mice inoculated with erythroleukemia cells delayed tumor growth and increased survival time.
价 格：￥电议型 号：T36041产 地：中国大陆
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T3604016,16-dimethyl Prostaglandin A1；16,16-dimethyl Prostaglandin A116,16-dimethyl Prostaglandin A1；16,16
16,16-dimethyl Prostaglandin A1 是一种前列腺素类似物，可以抑制 Lewis 肺癌和 B 16无黑色素瘤细胞中的 DNA 合成 (DNA synthesis)，以及抑制 HSV 和 HIV-1的病毒复制。
价 格：￥电议型 号：T36040产 地：中国大陆
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T35992ent-Prostaglandin F2α；ent-Prostaglandin F2αent-Prostaglandin F2α；ent-Prostaglandin F2α
ent-Prostaglandin F2α is the enantiomer of PGF2α and is found in urine.
价 格：￥电议型 号：T35992产 地：中国大陆
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T35991ent-Prostaglandin E2；ent-Prostaglandin E2ent-Prostaglandin E2；ent-Prostaglandin E2
Enzymatically-derived prostaglandin E2 (PGE2) is an optically pure compound whereas PGE2 derived from the free radical-catalyzed peroxidation of arachidonate is a racemic mixture. Ent-PGE2 is the opposite enantiomer of PGE2. Significant amounts of racemic PGE2 (rac-PGE2) are generated in vitro and in vivo in settings of oxidative stress via the isoprostane pathway. A proposed mechanism for the formation of rac-PGE2 involves the base catalyzed equilibration from 15-E2t-isoprostane (8-iso-PGE2), g
价 格：￥电议型 号：T35991产 地：中国大陆
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T35990ent-8-iso-15(S)-Prostaglandin F2α；ent-8-iso-15(S)-Prostaglandin F2αent-8-iso-15(S)-Prostaglandin F2α
Isoprostanes are produced by the non-enzymatic, free radical peroxidation of phospholipid-esterified arachidonic acid. They have been used as biomarkers of oxidative stress, but they also have been found to have potent biological activity. ent-8-iso-15(S)-Prostaglandin F2α (ent-8-iso-15(S)-PGF2α) is a potent vasoconstrictor of porcine retinal and brain microvessels with EC50 values of 15 and 24 nM, respectively. This isoprostane is about ten-fold more potent than 8-iso-PGF2α in a whole blood pla
价 格：￥电议型 号：T35990产 地：中国大陆
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T35961Prostaglandin Bx；Prostaglandin BxProstaglandin Bx
PGBx is a mixture of oligomers of PGB1 with a molecular weight of 1,000-1,500. It has antioxidant and free radical trapping activity that was first studied in isolated mitochondria.1 PGBx has anti-inflammatory and cytoprotective activity which may be attributed to inhibition of the 14 kDa sPLA2.2,3 At a dose of 1 mg/kg, PGBx significantly reduces the incidence of ulcers in rats.2
价 格：￥电议型 号：T35961产 地：中国大陆
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T3594415-keto-17-phenyl trinor Prostaglandin F2α ethyl amide；15-keto-17-phenyl trinor Prostaglandin F2α et
Bimatoprost is the Allergan trade name for 17-phenyl trinor prostaglandin F2α ethyl amide (17-phenyl trinor PGF2α ethyl amide), an F-series PG analog which has been approved for use as an ocular hypotensive drug. Oxidation of the C-15 hydroxyl group produces 15-keto-17-phenyl trinor PGF2α ethyl amide. 15-keto-17-phenyl trinor PGF2α ethyl amide is a potential metabolite of 17-phenyl trinor PGF2α ethyl amide when 17-phenyl trinor PGF2α ethyl amide is administered to intact animals. No pharmacologi
价 格：￥电议型 号：T35944产 地：中国大陆
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T35830Dehydro Olmesartan；Dehydro OlmesartanDehydro Olmesartan
Dehydro Olmesartan, deriving from Olmesartan, acts as an angiotensin II receptor (AT1R) antagonist and exhibits potential for the study of high blood pressure [1][2].
价 格：￥电议型 号：T35830产 地：中国大陆
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T35790Palmitic acid-1,2,3,4-13C4；Palmitic Acid-13C (C1, C2, C3, and C4 labeled)Palmitic Acid-13C (C1, C2,
Palmitic acid-13C (C1, C2, C3, and C4 labeled) is intended for use as an internal standard for the quantification of palmitic acid by GC- or LC-MS. Palmitic acid is a common 16-carbon saturated fat that represents 10-20% of human dietary fat intake and comprises approximately 25 and 65% of human total plasma lipids and saturated fatty acids, respectively.1,2Acylation of palmitic acid to proteins facilitates anchoring of membrane-bound proteins to the lipid bilayer and trafficking of intracellula
价 格：￥电议型 号：T35790产 地：中国大陆
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T35298Zelandopam hydrochloride；化合物 T35298YM 435|||YM435|||YM-435；YM 435|||YM435|||YM-435
Zelandopam hydrochloride is a biochemical.
价 格：￥电议型 号：T35298产 地：中国大陆
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T35132Wieland-gumlich aldehyde；化合物 T35132Desacetyldiaboline|||Caracurine VII|||Deacetyldiaboline；Desacetyl
Wieland-Gumlich aldehyde is an indoline derived by chemical degradation from strychnine.
价 格：￥电议型 号：T35132产 地：中国大陆
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T35037Vanilmandelic acid, L-(+)-；化合物 T35037Vanilmandelic acid L-form|||(+)-Vanilmandelic acid；Vanilmandeli
Vanilmandelic acid, L-(+)- is a chemical intermediate in the synthesis of artificial vanilla flavorings and is an end-stage metabolite of the catecholamines, epinephrine, and norepinephrine. It is produced via intermediary metabolites.
价 格：￥电议型 号：T35037产 地：中国大陆
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T34574Schisandronic acid；化合物 T34574Schizandronic acid|||Ganwuweizic acid；Schizandronic acid|||Ganwuweizic
Schisandronic acid is a triterpenoid acid isolated from the stems of Schisandra propinqua.
价 格：￥电议型 号：T34574产 地：中国大陆
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T34511Sandosaponin B；化合物 T34511Sandosaponin B
Sandosaponin B is a olean-12-ene-type triterpene oligoglycoside isolated from kidney bean, the seed of Phaseolus vulgaris L.
价 格：￥电议型 号：T34511产 地：中国大陆
