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T4S0794(R)-(+)-Corypalmine；D-四氢药根碱Corypalmine|||(+)-Corypalmine；D-四氢药根碱|||Corypalmine|||(+)-Corypalmine
1. (R)-(+)-Corypalmine ((+)-Corypalmine) shows strong papaverine-like activity.
价 格：￥电议型 号：T4S0794产 地：中国大陆
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T4794Glutaric acid；戊二酸Glutaric acid
Glutaric acid is a simple five-carbon linear dicarboxylic acid. Glutaric acid is naturally produced in the body during the metabolism of some amino acids, including lysine and tryptophan
价 格：￥电议型 号：T4794产 地：中国大陆
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T40794HEPPSO；HEPPSOHEPPSO
HEPPSO is a zwitterionic buffer with a working pH range of 7.1-8.5. It exhibits strong copper(II) binding capability and a pK value of 7.84 at a concentration of 2.0 mM.
价 格：￥电议型 号：T40794产 地：中国大陆
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T39794Bisabolone oxide A；Bisabolone oxide ABisabolone oxide A
Bisabolone oxide A is an α-glucosidase inhibitor.
价 格：￥电议型 号：T39794产 地：中国大陆
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T39611EnuvaptanEnuvaptanEnuvaptan|||BAY-2327949
Enuvaptan is a vasopressin receptor antagonist and has the potential for research into renal and cardiovascular diseases.
价 格：￥电议型 号：T39611产 地：中国大陆
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T38794LLLO (91-99) acetate；化合物LLO (91-99) acetateLLO (91-99) acetate(137856-41-8 free base)；LLO (91-99) ace
LLO (91-99) acetate is an exotoxin and a class I MHC-restricted T-cell epitopes of listeriolysin. LLO (91-99) acetate is essential for the induction of T-cell mediated immunity in vivo.
价 格：￥电议型 号：T38794L产 地：中国大陆
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T38794LLO (91-99)；LLO (91-99)LLO (91-99)|||Listeriolysin O (91-99)；LLO (91-99)|||Listeriolysin O (91-99)
LLO (91-99), also known as Listeriolysin O (91-99), is a class I MHC-restricted T-cell epitope derived from listeriolysin (LLO), an exotoxin. It plays a vital role as an antigen in the induction of T-cell mediated immunity in vivo.
价 格：￥电议型 号：T38794产 地：中国大陆
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T379492,4-Dihydroxyphenylacetyl-L-asparagine；2,4-Dihydroxyphenylacetyl-L-asparagine2,4-Dihydroxyphenylacet
2,4-Dihydroxyphenylacetyl-L-asparagine is a natural product for research related to life sciences. The catalog number is T37949 and the CAS number is 111872-98-1.
价 格：￥电议型 号：T37949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
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T37794Rec 15/2615 (hydrochloride)；Rec 15/2615 (hydrochloride)Rec 15/2615 (hydrochloride)
Rec 15/2615 is an antagonist of α1B-adrenergic receptors (α1B-ARs; Ki = 0.45 nM for the recombinant human receptor).1 It selectively inhibits α1B-ARs over α1A-, α1D-, and α1L-ARs (Kis = 7.59, 10.23, and 49 nM, respectively). Rec 15/2615 inhibits norepinephrine-induced contractions of isolated rabbit prostate and urethral strips (Kis = 100 and 316.2 nM, respectively), as well as reduces norepinephrine-induced contractions of chloroethylclonidine-precontracted isolated rabbit aortic rings (Ki = 50
价 格：￥电议型 号：T37794产 地：中国大陆
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T36794Dolutegravir O-β-D-Glucuronide；Dolutegravir O-β-D-GlucuronideDolutegravir O-β-D-Glucuronide
Dolutegravir O-β-D-glucuronide is a metabolite of the HIV integrase inhibitor dolutegravir .1It is formed from dolutegravir primarily by the UDP-glucuronosyltransferase (UGT) isoform UGT1A1in vivobut is also metabolized by UGT1A9 in human liver and kidney microsomes and UGT1A3 in human intestinal microsomes.2,1
价 格：￥电议型 号：T36794产 地：中国大陆
