Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Pachycarpine"'
Autor:
B. A. Abdusalamov
Publikováno v:
Chemistry of Natural Compounds. 16:46-49
The dynamics of the accumulation of free amino acids and the main alkaloids have been determined, and 15 free amino acids have been detected and identified, 11 having been determined quantitatively. The amounts of the main alkaloids have also been de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4a5e7f846aee05708c323c36a132ceec
https://doi.org/10.1007/bf00564877
https://doi.org/10.1007/bf00564877
Publikováno v:
Chemistry of Natural Compounds. 12:692-695
A chromatographic method has been developed for the quantitative determination of the alkaloids ofAnabasis aphylla — anabasine, aphylline, lupinine, aphyllidine, and anabasamine — and also pachycarpine in the mixture of reduction products of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::73be7b007c4b64ccc4715db4139aa333
https://doi.org/10.1007/bf00564961
https://doi.org/10.1007/bf00564961
Publikováno v:
Archiv der Pharmazie. 322:399-403
Pachycarpin (4), der optische Antipode des Lupinenalkaloids (−)-Spartein (1), wurde aus (−)-Lupanin synthetisiert und sein Metabolismus in der Ratte untersucht. Als Urinhauptmetabolit konnte nach chromatographischer Reinigung stereochemisch einhe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fed9c2babc97d810da17444ff11f1b91
https://doi.org/10.1002/ardp.19893220704
https://doi.org/10.1002/ardp.19893220704
Publikováno v:
Chemistry of Natural Compounds. 13:207-210
The interconversions of the alkaloids of Sophora alopecuroides L. have been studied by feeding the plants with tritium-labelled alkaloids ([3H]sophoridine, [3H]pachycarpine, [3H]cytisine, [3H]isosophoridine, [3H]allomatrine, and [3H]N-methylcytisine)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::84039247bc255684b826cf60414e7564
https://doi.org/10.1007/bf00563949
https://doi.org/10.1007/bf00563949
Publikováno v:
Chemistry of Heterocyclic Compounds. 10:221-229
The low- and high-resolution mass spectra of pachycarpine, tetrahydrodesoxocytisine, matridine, α-isolupanine, tetrahydrocytisine, matrine, d-thermopsine, cytisine, and isosophoramine, as well as some of their stereoisomers and deutero analogs, make
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::404908758ba17d6b3b37c767edf00c29
https://doi.org/10.1007/bf00487790
https://doi.org/10.1007/bf00487790
Publikováno v:
Chemistry of Natural Compounds. 12:696-699
The biosynthesis of the alkaloids ofAmmothamnus lehmannii Bge. have been studied by supplying the plants with [1,5-14C2] cadaverine. It has been shown that cadaverine is a precursor of sophocarpidine, sophocarpine, and pachycarpine. Possible routes o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cf77720d6da90d6d88a333d53cdb7ccb
https://doi.org/10.1007/bf00564962
https://doi.org/10.1007/bf00564962
Publikováno v:
Organic Magnetic Resonance. 4:837-846
The INDOR homonuclear PMR spectra of three quinolizidine alkaloids—pachycarpine (d-sparteine), lupanine and 13-hydroxylupanine—have been studied. The molecular conformations including the boat-structure of the ring C have been established.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b1fb89e661233d1b739b0d3182a19549
https://doi.org/10.1002/mrc.1270040608
https://doi.org/10.1002/mrc.1270040608
Publikováno v:
Chemistry of Natural Compounds. 7:160-164
1. The epigeal part ofThermopsis alterniflora at the beginning of flowering contains 3.35% of combined alkaloids. The separation of the combined bases yielded cytisine, N-methylcytisine, pachycarpine, thermopsine, and the new alkaloid alteramine.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::46da8afcf728477800bda5b558fccf16
https://doi.org/10.1007/bf00568689
https://doi.org/10.1007/bf00568689
Publikováno v:
BJOG: An International Journal of Obstetrics and Gynaecology. 66:939-945
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c350333003cabc55a309cf738e54d09c
https://doi.org/10.1111/j.1471-0528.1959.tb01964.x
https://doi.org/10.1111/j.1471-0528.1959.tb01964.x
Publikováno v:
Chemistry of Natural Compounds. 13:210-212
The biosynthesis of the alkaloids ofAmmodendron karelinii Fisch. et Mey has been studied by feeding the plant with labelled [1,5-14C]cadaverine. It has been shown that cadaverine is a precursor of anagyrine, pachycarpine, ammodendrine, N-methylcytisi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4b1ff56ebc0e17f67adb2e80ee334a1f
https://doi.org/10.1007/bf00563950
https://doi.org/10.1007/bf00563950