## Abstract ^1^H and ^13^C NMR data for 1‐cyano‐, 4‐cyano‐, 4‐bromo‐ and 4‐bromo‐5‐nitro‐substituted isoquinolines, isoquinoline N‐oxides and N‐methoxy and N‐ethyl salts in different solvents are reported. The substituent chemical shifts are discussed with regard to the reactivity of the N‐methoxy
13C and 1H NMR Study of the Metabolic Degradation of 4-Pentenoate in Different Dog Nephron Segments
✍ Scribed by Yvan Boulanger; Hong Wong; Angelica Fleser; Fernando Commodari; Patrick Vinay
- Publisher
- John Wiley and Sons
- Year
- 1992
- Tongue
- English
- Weight
- 384 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0740-3194
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The metabolism of 4‐pentenoate in isolated kidney tubules has been investigated by ^1^H and ^13^C NMR. The 4‐pentenoate metabolite, 3‐keto‐4‐pentenoyl‐CoA, accumulated in proximal tubules only and its formation could be competitively inhibited by octanoate. 4‐Pentenoate was metabolized in thick ascending limbs but not in papillary collecting ducts.© 1992 Academic Press,Inc.
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