✦ LIBER ✦

5α-Cholest-8(14)-en-3β-ol-15-one. In vivo conversion to cholesterol upon oral administration to a nonhuman primate

✍ Scribed by George J. Schroepfer Jr.; Thomas N. Pajewski; Mark Hylarides; Alemka Kisic

Book ID: 115760456
Publisher: Elsevier Science
Year: 1987
Tongue: English
Weight: 408 KB
Volume: 146
Category: Article
ISSN: 0006-291X
DOI: 10.1016/0006-291x(87)90750-9

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

The biological conversion of 5α-cholest-

The biological conversion of 5α-cholest-8-en-3β-ol to 5α-cholest-7-en-3β-ol in the biosynthesis of cholesterol

✍ L. Canonica; A. Fiecchi; M. Galli Kienle; A. Scala; G. Galli; E. Grossi Paoletti 📂 Article 📅 1968 🏛 Elsevier Science 🌐 English ⚖ 456 KB

5α-Cholest-8(14)-EN-3β-OL-15-one. A comp

5α-Cholest-8(14)-EN-3β-OL-15-one. A competitive substrate for acyl coenzyme a:Cholesterol acyl transferase

✍ Larry R. Miller; Dolores H. Needleman; John S. Brabson; Ker-Shi Wang; George J. 📂 Article 📅 1987 🏛 Elsevier Science 🌐 English ⚖ 372 KB

Inhibition of hepatic sterol synthesis a

Inhibition of hepatic sterol synthesis and reduction of serum cholesterol in rats by 5α-cholest-8(14)-en-3β-ol-15-one

✍ Dwight L. Raulston; Clifford O. Mishaw; Edward J. Parish; George J. Schroepfer J 📂 Article 📅 1976 🏛 Elsevier Science 🌐 English ⚖ 267 KB

Inhibitors of sterol synthesis. Dietary

Inhibitors of sterol synthesis. Dietary administration of 5α-cholest-8(14)-en-3β-ol-15-one inhibits the intestinal absorption of cholesterol in lymph-cannulated rats

✍ George J. Schroepfer Jr.; Armand Christophe; Dolores H. Needleman; Alemka Kisic; 📂 Article 📅 1987 🏛 Elsevier Science 🌐 English ⚖ 333 KB

Crystal structure of 3β-benzoyloxy-6α-ch

Crystal structure of 3β-benzoyloxy-6α-chloro-5α-cholest-7-ene, a key intermediate in the chemical synthesis of 5α-cholest-8(14)-en-3β-ol-15-one

✍ David K. Wilson; William K. Wilson; Florante A. Quiocho; George J. Schroepfer Jr 📂 Article 📅 1988 🏛 Elsevier Science 🌐 English ⚖ 441 KB

The X-ray crystal structure of 3~-benzoyloxy-6a-chloro-5a-cholest-7-ene (IV) was determined by the heavy atom method and ref'med to R ---0.063 (space group P2s, a --11.364, b = 11.089, c --12.232,/~ = 99.43 °, Z ---2). IV was previously shown to be an important intermediate in the acid-catalyzed iso

Inhibitors of sterol synthesis. Oleate e

Inhibitors of sterol synthesis. Oleate ester of 5α-cholest-8(14)-en-3β-ol-15-one as a substrate for pancreatic cholesterol esterase

✍ Thomas W. Stephens; George J. Schroepfer Jr. 📂 Article 📅 1988 🏛 Elsevier Science 🌐 English ⚖ 645 KB