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15(S)-15-methyl Prostaglandin E2 Sale

(Synonyms: 15(S)15methyl PGE2) 目录号 : GC41167

A potent, metabolically stable analog of PGE2

15(S)-15-methyl Prostaglandin E2 Chemical Structure

Cas No.:35700-27-7

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500μg
¥1,181.00
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1mg
¥2,244.00
现货

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Sample solution is provided at 25 µL, 10mM.

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产品描述

15(S)-15-methyl PGE2 is a potent, metabolically stable analog of PGE2. It is a potent gastric antisecretory and antiulcer compound. 15(S)-15-methyl PGE2 binds to human myometrium with twice the affinity of PGE2 and is ten times more potent than PGE1 in contracting uterine smooth muscle.

Chemical Properties

Cas No. 35700-27-7 SDF
别名 15(S)15methyl PGE2
Canonical SMILES O[C@H]1[C@H](/C=C/[C@](O)(C)CCCCC)[C@@H](C/C=C\CCCC(O)=O)C(C1)=O
分子式 C21H34O5 分子量 366.5
溶解度 DMF: >100 mg/ml (from PGE2),DMSO: >100 mg/ml (from PGE2),Ethanol: >100 mg/ml (from PGE2),PBS pH 7.2: >5 mg/ml (from PGE2) 储存条件 Store at -20°C
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储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。
为了提高溶解度,请将管子加热至37℃,然后在超声波浴中震荡一段时间。
Shipping Condition 评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备RT,或根据请求配备蓝冰。

溶解性数据

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1 mg 5 mg 10 mg
1 mM 2.7285 mL 13.6426 mL 27.2851 mL
5 mM 0.5457 mL 2.7285 mL 5.457 mL
10 mM 0.2729 mL 1.3643 mL 2.7285 mL
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Research Update

Effects of 15(S)-15-methyl Prostaglandin E2 methyl ester on phospholipid metabolism in rat gastric mucosa

Biochem Pharmacol 1989 Mar 15;38(6):955-60.PMID:2930596DOI:10.1016/0006-2952(89)90286-4.

The effects of 15(S)-15-methyl Prostaglandin E2 (PGE2) methyl ester on gastric mucosal metabolism of phospholipids in intact rats and rats injured by intragastric instillation of acidified taurocholic acid were examined by using radioisotope-labeled precursors. The incorporation of palmitic, oleic and arachidonic acids into phosphatidylcholine (PC) and phosphatidylethanolamine (PE) was reduced by treatment with 15(S)-15-methyl PGE2 methyl ester in the intact rats, but the incorporation of glycerol was unaffected or affected only slightly. Instillation of acidified taurocholic acid resulted in decreased incorporation of palmitic acid and glycerol into PC and PE, whereas pretreatment with 15(S)-15-methyl PGE2 methyl ester caused the incorporations of these precursors to be maintained after acidified taurocholic acid treatment. These results suggest that 15(S)-15-methyl PGE2 methyl ester may reduce the incorporation of fatty acids into PC and PE by inhibition of the deacylation-reacylation cycle either directly or indirectly, whereas acidified taurocholic acid decreases de novo synthesis of PC and PE, and probably also the reacylation of fatty acid into phospholipids. Pretreatment with 15(S)-15-methyl PGE2 methyl ester protected the PC- and PE-synthesizing activity against the injury induced by acidified taurocholic acid, and this effect may be involved in the prevention of mucosal damage.