1987
DOI: 10.1016/s0031-9422(00)81839-7
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Diterpenoids from Nepeta tuberosa subsp. reticulata

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Cited by 51 publications
(15 citation statements)
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“…Based on the foregoing spectral studies, the structure of com pound 1 was characterized as 7-phenyl-hepta-4,6-diyne-2-ol. The known compounds obtained were identified as l-phenyl-hept-5t-ene-l,3-diyne (2), 7 l-phenyl-hepta-1,3,5triyne (3), 8 cx-tocopherylchinon (4), 9 2-phenyl-ethanol (5), 10 linolenic acid (6), 11 methyl linolenate (7), 12 13 2-butoxyethyl Imolenate (9), 14 lmoleic acid (10), 15 ethyl linoleate (ll), 1 6 2-butoxyethyl linoleate (12), 14 2-butoxyethyl oleate (13)," 2-butoxy ethanol (14), 18 phytol (15), 19 phytenic acid (16), 20 squalene (17), 21 ß-sitosterol (18), 22 stigmasterol (19), 22 5oc-stigmasta-7-en-3ß-ol (20), 22 and 5a-stigmasta-7,22t-dien-3ß-ol (21), 22 by the comparison of their spectral data (IR, NMR and MS) with those found in the literature and by direct comparison with authentic samples.…”
Section: Resultsmentioning
confidence: 99%
“…Based on the foregoing spectral studies, the structure of com pound 1 was characterized as 7-phenyl-hepta-4,6-diyne-2-ol. The known compounds obtained were identified as l-phenyl-hept-5t-ene-l,3-diyne (2), 7 l-phenyl-hepta-1,3,5triyne (3), 8 cx-tocopherylchinon (4), 9 2-phenyl-ethanol (5), 10 linolenic acid (6), 11 methyl linolenate (7), 12 13 2-butoxyethyl Imolenate (9), 14 lmoleic acid (10), 15 ethyl linoleate (ll), 1 6 2-butoxyethyl linoleate (12), 14 2-butoxyethyl oleate (13)," 2-butoxy ethanol (14), 18 phytol (15), 19 phytenic acid (16), 20 squalene (17), 21 ß-sitosterol (18), 22 stigmasterol (19), 22 5oc-stigmasta-7-en-3ß-ol (20), 22 and 5a-stigmasta-7,22t-dien-3ß-ol (21), 22 by the comparison of their spectral data (IR, NMR and MS) with those found in the literature and by direct comparison with authentic samples.…”
Section: Resultsmentioning
confidence: 99%
“…umbelliferone (2) [8], scopoletin (3) [9], phellodenol-A (4) [10], six furanocoumarins, i.e., psoralen (5) [11], bergapten (6) [11], S-(þ)-marmesin (7) [12], (þ)-(S)-rutaretin methyl ether (8) [13], (þ)-(S)-rutaretin (9) [14] [15], 2',3'-dehydromarmesin (10) [16], one pyranocoumarin, i.e., xanthyletin (11) [17], three chalcones, i.e., isobavachalcone (12) [18], kanzonol C (13) [19] [20], (E)-1-[2,4-dihydroxy-3-(3-methylbut-2-enyl)phenyl]-3-(2,2-dimethyl-8-hydroxy-2H-benzopyran-6-yl)prop-2-en-1-one (23) [19] [20], one benzenoid, i.e., syringaldehyde (14) [21], one quinone, i.e., a-tocopheryl quinone (15) [22], one triterpenoid, i.e., lupeol (16) [23], two steroids, i.e., a mixture of b-sitosterol (17) and stigmasterol (18) [24], were readily identified by comparison with authentic samples and by comparison with the literature data.…”
mentioning
confidence: 99%
“…Some species of this genus are important medical plants and they have euphoric effects on cats [2]. Many species of the genus have been investigated and found to contain monoterpenoids, diterpenoids and triterpenoids [3][4][5] N. cataria L. (catnip), the most thoroughly studied species, is used in folk medicine as diuretic, carminative, antispasmodic, emmenagogue and sedative [6,7]. N. argolica Bory et chaub.…”
mentioning
confidence: 99%