External detection of regional myocardial metabolism with radioiodinated hexadecenoic acid in the dog heart

1981 ◽  
Vol 6 (4) ◽  
pp. 147-151 ◽  
Author(s):  
E. E. van der Wall ◽  
G. Westera ◽  
W. den Hollander ◽  
F. C. Visser
Keyword(s):  
Myocardial Metabolism ◽  
Hexadecenoic Acid ◽  
Dog Heart

A comparison between terminally radioiodinated hexadecenoic acid (*I-HA) and 201Tl-thallium chloride in the dog heart

1980 ◽  
Vol 5 (4) ◽  
pp. 339-343 ◽  
Author(s):  
G. Westera ◽  
E. E. van der Wall ◽  
G. A. K. Heidendal ◽  
G. C. van den Bos
Keyword(s):  
Hexadecenoic Acid ◽  
Dog Heart ◽  
Thallium Chloride

A comparison between terminally radioiodinated hexadecenoic acid (125I-HA) and heptadecanoic acid (131I-H0A) in the dog heart

1981 ◽  
Vol 6 (12) ◽  
pp. 581-584 ◽  
Author(s):  
E. E. van der Wall ◽  
G. Westera ◽  
G. A. K. Heidendal ◽  
W. den Hollander
Keyword(s):  
Hexadecenoic Acid ◽  
Heptadecanoic Acid ◽  
Dog Heart

Effect of tolbutamide on myocardial metabolism and mechanical performance of the diabetic rat

Diabetes ◽  
1984 ◽  
Vol 33 (12) ◽  
pp. 1138-1143 ◽  
Author(s):  
B. H. Tan ◽  
G. L. Wilson ◽  
S. W. Schaffer
Keyword(s):  
Myocardial Metabolism ◽  
Mechanical Performance ◽  
Diabetic Rat

Inotropic Effects of Glyceryl Trinitrate and Spontaneous NO Donors in the Dog Heart

Circulation ◽  
1997 ◽  
Vol 96 (8) ◽  
pp. 2675-2682 ◽  
Author(s):  
Benedikt Preckel ◽  
Georg Kojda ◽  
Wolfgang Schlack ◽  
Dirk Ebel ◽  
Karin Kottenberg ◽  
...  
Keyword(s):  
Glyceryl Trinitrate ◽  
Inotropic Effects ◽  
No Donors ◽  
Dog Heart

Dihydro- and tetrahydroisoquinolines as inhibitors of cyclic nucleotide phosphodiesterases from dog heart

1979 ◽  
Vol 28 (8) ◽  
pp. 1307-1312 ◽  
Author(s):  
Richard G. van Inwegen ◽  
Phyllis Salaman ◽  
Vassil St. Georgiev ◽  
Ira Weinryb
Keyword(s):  
Cyclic Nucleotide ◽  
Dog Heart ◽  
Cyclic Nucleotide Phosphodiesterases ◽  
Nucleotide Phosphodiesterases

scholarly journals Occurrence of Cis-11,12-Methylene-Hexadecanoic Acid in the Red Alga Solieria pacifica (Yamada) Yoshida

Molecules ◽  
2021 ◽  
Vol 26 (8) ◽  
pp. 2286
Author(s):  
Gwang-Woo Kim ◽  
Jae-Man Sim ◽  
Yutaka Itabashi ◽  
Min-Jeong Jung ◽  
Joon-Young Jun
Keyword(s):  
Fatty Acids ◽  
Fatty Acid ◽  
Red Alga ◽  
Proton Nuclear Magnetic Resonance ◽  
Animal Origin ◽  
Monoenoic Acid ◽  
Resonance Spectroscopy ◽  
Hexadecenoic Acid ◽  
Cyclopropane Fatty Acid ◽  
Hexadecanoic Acid

Fatty acids in marine algae have attracted the attention of natural chemists because of their biological activity. The fatty acid compositions of the Solieriaceae families (Rhodophyceae, Gaigartinales) provide interesting information that unusual cyclic fatty acids have been occasionally found. A survey was conducted to profile the characteristic fatty acid composition of the red alga Solieria pacifica (Yamada) Yoshida using gas chromatography-mass spectrometry (GC-MS), infrared spectroscopy (IR), and proton nuclear magnetic resonance spectroscopy (1H-NMR). In S. pacifica, two cyclopentyl fatty acids, 11-cyclopentylundecanoic acid (7.0%), and 13-cyclopentyltridecanoic acid (4.9%), and a cyclopropane fatty acid, cis-11,12-methylene-hexadecanoic acid (7.9%) contributed significantly to the overall fatty acid profile. In particular, this cyclopropane fatty acid has been primarily found in bacteria, rumen microorganisms or foods of animal origin, and has not previously been found in any other algae. In addition, this alga contains a significant amount of the monoenoic acid cis-11-hexadecenoic acid (9.0%). Therefore, cis-11,12-methylene-hexadecanoic acid in S. pacifica was likely produced by methylene addition to cis-11-hexadecenoic acid.

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