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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1434491생성일: 2026년 10월 26일

5'-Atp → (R)-3-hydroxyoctanoyl-CoA

https://huagongshe.com/reaction/1434491

반응식

참여 물질

역할이름HCID투입량
반응물5'-AtpHCID 5957—
반응물Coenzyme AHCID 87642—
반응물Magnesium ChlorideHCID 5360315—
반응물(R)-3-hydroxyoctanoateHCID 86308678—
반응물(R)-3-Hydroxy-5-(4-fluorophenyl)valeryl-CoAHCID 86588297—
생성물(R)-3-hydroxyoctanoyl-CoAHCID 11966193—

반응 단계

(R)-3-hydroxyoctanoyl-CoA was synthesized according to Rehm B H A, Kruger N, Steinbuchel A (1998) Journal of Biological Chemistry 273 pp 24044-24051 with certain changes. Acyl-CoA synthetase (Sigma Co.) was dissolved in trishydrochloric acid buffer (50 mM, pH 7.5) containing 2 mM ATP, 5 mM MgCl2, 2 mM coenzyme A and 2 mM (R)-3-hydroxyoctanoate to a concentration of 0.1 mU/μL. It was retained in a bath of 37° C. and was sampled suitably and the proceeding of reaction was analyzed by HPLC. After the enzyme reaction was terminated by adding sulfuric acid to 0.02 N to the sampled reaction liquid, the unreacted substrate (R)-3-hydroxyoctganoate was removed by extraction with n-heptane. The HPLC analysis employed RP18 column (nucleosil C18, 7 μm, Knauser), and elusion was made under a linear concentration slope of acetonitrile, utilizing 25 mM phosphoric acid buffer (pH 5.3) as the moving phase, and the thioester compound generated by the enzymatic reaction was detected by monitoring the absorption spectrum of 200 to 500 nm with a diode array detector. (R)-3-hydroxy-5-phenylvaryl CoA and (R)-3-hydroxy-5-(4-fluorophenyl)valeryl CoA were also synthesized in a similar manner.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07615233B2
출처 데이터셋uspto-grants-2009_11
ORD IDord-48431586237a4b14b9107c0f4f03c510
출처 메모uspto-grants-2009_11