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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 611460생성일: 2026년 10월 27일

sodium (4R)-4-[(3R,5S,7R,8R,9R,10S,12S,13R,14R,17R)-3,7,12-trihydroxy-8,10,13-trimethyl-1,2,3,4,5,6,7,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]pentanoate → Palmitic Acid

https://huagongshe.com/reaction/611460

반응식

참여 물질

역할이름HCID투입량
반응물sodium (4R)-4-[(3R,5S,7R,8R,9R,10S,12S,13R,14R,17R)-3,7,12-trihydroxy-8,10,13-trimethyl-1,2,3,4,5,6,7,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]pentanoateHCID 44582063—
용매Calcium ChlorideHCID 5284359—
생성물Palmitic AcidHCID 98547%
생성물Stearic AcidHCID 5281—
생성물Oleic AcidHCID 445639—

반응 단계

To 0.5 mL of a cultured cell fraction of Pyrococcus horikoshii JCM 9974 were added 2 mg of each of these substrates, 40 μl of 100 mM sodium cholate and 100 μL of 20 mM calcium chloride. The resultant reaction solution was reacted at 75° C. overnight. From the reaction solution, a fraction containing the fatty acid produced was extracted with isooctane and then subjected to gas chromatography. As a result, a decomposition product including 47-48% of oleic acid, oleic acid, palmitic acid or linolenic acid resulted from the decomposition by phospholipase A2 and 47-48% of palmitic acid, stearic acid, oleic acid or stearic acid resulted from the decomposition by phospholipase A1 was obtained from each of the substrates.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06001626
출처 데이터셋uspto-grants-1999_12
ORD IDord-c8c00cdd1b30490b9b3d5e825036be32
출처 메모uspto-grants-1999_12