✦ LIBER ✦

Deuterium- and tritium-labeled (±)-7α-hydroxy-5,11-diketotetranorprostane-1,16-dioic acid

✍ Scribed by A. Rosegay; D. Taub

Book ID: 119048167
Publisher: Elsevier Science
Year: 1976
Tongue: English
Weight: 128 KB
Volume: 12
Category: Article
ISSN: 0090-6980
DOI: 10.1016/0090-6980(76)90052-6

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Capillary column gas—liquid chromatograp

Capillary column gas—liquid chromatographic—mass spectrometric assay for 7α-hydroxy-5,11-diketotetranorprostane-1,16-dioic acid, the major human urinary metabolite of prostaglandins E1 and E2

✍ R.W. Walker; V.F. Gruber; J. Pile; K. Yabumoto; A. Rosegay; D. Taub; M. L'E. Orm 📂 Article 📅 1980 🏛 Elsevier Science ⚖ 370 KB

Stereoselective total synthesis of 7α-hy

Stereoselective total synthesis of 7α-hydroxy-5,11-diketotetranor-prostane-1,16-dioic acid, the major human urinary metabolite of PGE1 and PGE2

✍ D. Taub; Z.S. Zelawski; N.L. Wendler 📂 Article 📅 1975 🏛 Elsevier Science 🌐 French ⚖ 193 KB

The identification of 5β,7α-dihydroxy-11

The identification of 5β,7α-dihydroxy-11-oxotetranor-prostane-1, 16-dioic acid as a urinary metabolite of prostaglandin F2α in the rat

✍ Alan R. Brash; Thomas A. Baillie 📂 Article 📅 1979 🏛 Elsevier Science 🌐 English ⚖ 481 KB

A urinary metabolite of Δ1-tetrahydrocan

A urinary metabolite of Δ1-tetrahydrocannabinol. The first synthesis of 4″,5″-bisnor-Δ1-tetrahydrocannabinol-7,3″-dioic acid, and a deuterium labelled analogue

✍ Maria Szirmai; Magnus M. Halldin 📂 Article 📅 1995 🏛 Elsevier Science 🌐 English ⚖ 807 KB

The f'LrSt synthesis of unlabelled and [2Hs]-labelled 4",5"-bisnor-ALTHC-7,3"-dioic acid, the major dicarboxylated urinary metabolite of At-THC in man, is presented (preliminary results of this work have been presented in part at the Melbourne Symposium on Cannabis, Australia, September 1987, Ref. 1

On the conformational equilibrium of 16α

On the conformational equilibrium of 16α-acetoxy-13, 1 7-seco-5α-androstan- 13ξ-hydroxy- 1 7-carboxylic acid lactone molecule in the crystalline state: X-ray study and MMX calculations

✍ Gy. Argay; A. K'a1mán; L. Párkányi; B. Ribár; Z. Ďjarmati 📂 Article 📅 1991 🏛 Elsevier Science 🌐 English ⚖ 679 KB

Labeled bile acids VI: [22,23,24-13C3]-m

Labeled bile acids VI: [22,23,24-13C3]-methyl 3α,7α-diacetoxy 5β-cholan-24-oate, [22,23,24-13c3]-methyl 3β-acetoxychol-5-en-24-oate, and [16,17,22,23-3h4]-methyl 3β-acetoxychol-5-en-24-oate (1)

✍ Chee Kong Lai; Chang Yon Byon; Warren G. Anderson; Marcel Gut 📂 Article 📅 1986 🏛 John Wiley and Sons 🌐 French ⚖ 204 KB