2010
DOI: 10.1080/10286020903505057
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New triterpenoids from Arisaema jacquemontii

Abstract: Phytochemical investigation of the roots of Arisaema jacquemontii led to the isolation of two new triterpenoids, which were characterized by NMR, IR, and MS spectra as 30-nor-lanost-5-ene-3beta-ol (1) and 30-norlanost-5-ene-3-one (2).

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Cited by 14 publications
(8 citation statements)
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“…The antioxidant activities of extracts were evaluated using DPPH free radical scavenging assay, total reducing power and total antioxidant capacity assays. The reported DPPH quenching potential of EtOH extract of A. jaquamontii was significantly ( P < 0.05) higher than reported earlier [7, 10]. Other extracts also showed significant DPPH based free radical scavenging activity.…”
Section: Discussioncontrasting
confidence: 54%
See 1 more Smart Citation
“…The antioxidant activities of extracts were evaluated using DPPH free radical scavenging assay, total reducing power and total antioxidant capacity assays. The reported DPPH quenching potential of EtOH extract of A. jaquamontii was significantly ( P < 0.05) higher than reported earlier [7, 10]. Other extracts also showed significant DPPH based free radical scavenging activity.…”
Section: Discussioncontrasting
confidence: 54%
“…It is a deciduous perennial herb that grows to a height of about 1–2 m [6] and is further distributed in many parts of East Asia, Afghanistan to South East Tibet, upper and lower alpine zones in the dried areas of Himalayas. Various constituents of this plant, especially tuber lectins are being used for medicinal purposes [7]. A tuber lectin purified from this plant has been reported to exhibit potent anti-insect and anti-proliferative activities [8].…”
Section: Introductionmentioning
confidence: 99%
“…The tested phytoconstituents chemical structures were collected from the literature (Scifinder, Pubmed, Google Scholar). [7][8][9][10][11][12][13][14][15][16][17][18][19][20][21][22][23][24]…”
Section: Methodsmentioning
confidence: 99%
“…25 The structure of abiesatrine A 20 was confirmed by X-ray analysis. 32 The 30-nor derivatives 35 and 36 have been known synthetically for many years. 26 Other new lanostanes include oenotheralanosterols A 28 and B 29 from the roots of Oenothera biennis, 27 the 24-methyl lanostane derivatives 30 and 31 from the bulbs of the orchid Prosthechea michuacana, 28 sexangulic acid 32 from the Chinese mangrove Bruguiera sexangula, 29 pisticialanstenoic acid 33 from the galls of Pistacia integerrima, 30 scolopianate A (which is methyl lucidenate N) 34 from the stems of Scolopia chinensis 31 and 30-norlanost-5-en-3bol 35 and the corresponding 3-ketone 36 from Arisaema jacquemontii.…”
Section: The Lanostane Groupmentioning
confidence: 99%