1988
DOI: 10.1016/0031-9422(88)80790-8
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Components from Santolina rosmarinifolia, subspecies rosmarinifolia and canescens

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Cited by 25 publications
(15 citation statements)
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“…The carbonyl group was detected at 167.76 ppm and the methyl signal at 20.06 ppm. The structure of Var ID 1 was confirmed to be acetylmycosinol by a comparison of the NMR data with the literature, 33,34) and was confirmed by heteronuclear multiple bond coherence (HMBC) NMR analysis (Fig. S3).…”
Section: Resultssupporting
confidence: 52%
“…The carbonyl group was detected at 167.76 ppm and the methyl signal at 20.06 ppm. The structure of Var ID 1 was confirmed to be acetylmycosinol by a comparison of the NMR data with the literature, 33,34) and was confirmed by heteronuclear multiple bond coherence (HMBC) NMR analysis (Fig. S3).…”
Section: Resultssupporting
confidence: 52%
“…cereus activity of six compounds isolated from F. pinicola are presented. This phytochemical study resulted in the identification of one new lanostane triterpenoid, 3-oxo-24-methyl-5α-lanost-8,25-dien-21-oic acid (1); four known lanostane triterpenoids, 3-oxo-5α-lanost-8,24-dien-21-oic acid (pinicolic acid, 2) [6], 16α-hydroxy-24-methylene-3-oxo-5α-lanost-7,9(11)-dien-21oic acid (polyporenic acid, 3) [6], 16α-hydroxy-24-methylene-3oxo-5α-lanost-8-en-21-oic acid (4) [7], and 16α-acetyloxy-24methylene-3-oxo-5α-lanost-7,9(11)-dien-21-oic acid (5) [6]; and one ergostane steroid, 22E-5α-ergost-7,9(11),22-trien-3β-ol (6) [8] (l " Fig. 1).…”
Section: Abstract Antibacterial Activity • Fomitopsis Pinicola (Polymentioning
confidence: 99%
“…xanthioides [4]. In our continuing study of this source, we further isolated three new terpene glycosides (1-3), in addition to four known compounds (4)(5)(6)(7), from the MeOH extract of this plant and tested the cytotoxicities of the isolates (l " Fig. 1).…”
mentioning
confidence: 99%
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“…Phytochemical investigations on Santolina species revealed the presence of several classes of constituents. Eudesmane-type sesquiterpenes [23][24][25][26][27], germacrane-type sesquiterpenes [2,[23][24][25][26], dammarane-type triterpenes [4], acetylene heterocycles [4,28,29], spiroketalenol ether-type acetylenes [4,24,[27][28][29], flavonoids [5,6], and coumarins [6,7,27] have been identified as common secondary metabolites from the genus. Several Santolina species have been studied for their essential oil composition.…”
Section: Phytochemicalsmentioning
confidence: 99%