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兔血浆前列腺素A异构酶抑制剂。

Inhibitors of rabbit plasma prostaglandin A isomerase.

作者信息

Jones R L

出版信息

Biochem J. 1974 May;139(2):381-9. doi: 10.1042/bj1390381.

Abstract
  1. The potent inhibitory activities of three groups of prostaglandin analogues on the prostaglandin A isomerase of rabbit plasma were demonstrated. 2. Six of the compounds were prepared by NaBH(4) reduction of the C-9 oxo groups of prostaglandin A(2) and prostaglandin C(2) and their C-15 epimers. The remaining four were racemates and were synthesized in another laboratory. Unknown configurations at C-9 and at C-15 were assigned. 3. All the compounds were found to be competitive inhibitors of the isomerase in vitro. K(m)/K(i) ratios were determined and it was found that both the 15(S) and 15(R) epimers have potent inhibitory activity. 4. One of the inhibitors was used to study the reversibility of the isomerase. 5. It is suggested that these compounds may be useful for determining the biological significance of prostaglandin A isomerase. In view of its weak biological activity and possibly extended half-life in vivo, the reduction product of 15-epiprostaglandin C(2) may be the most suitable agent for this purpose.
摘要
  1. 已证实三组前列腺素类似物对兔血浆中的前列腺素A异构酶具有强大的抑制活性。2. 其中六种化合物是通过用硼氢化钠还原前列腺素A₂和前列腺素C₂的C-9羰基及其C-15差向异构体而制备的。其余四种为外消旋体,是在另一个实验室合成的。确定了C-9和C-15处的未知构型。3. 发现所有化合物在体外均为该异构酶的竞争性抑制剂。测定了Kₘ/Kᵢ比值,发现15(S)和15(R)差向异构体均具有强大的抑制活性。4. 其中一种抑制剂被用于研究该异构酶的可逆性。5. 有人提出,这些化合物可能有助于确定前列腺素A异构酶的生物学意义。鉴于其较弱的生物活性以及在体内可能延长的半衰期,15-表前列腺素C₂的还原产物可能是用于此目的的最合适试剂。

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Cardiovascular effect of a prostaglandin isolated from a gorgonian Plexaura homomalla.
J Pharm Pharmacol. 1969 Nov;21(11):782-3. doi: 10.1111/j.2042-7158.1969.tb08172.x.

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