2005
DOI: 10.1002/chin.200525180
|View full text |Cite
|
Sign up to set email alerts
|

Studies on the Chemical Constituents of Nardostachys jatamansi DC (Valerianaceae).

Abstract: Terpenes U 0200 Studies on the Chemical Constituents of Nardostachys jatamansi DC (Valerianaceae). -[isolation and structure determination of the new sesquiterpene acid, nardin (I), and the new pyranocoumarin (II)] -(CHATTERJEE*, A.; BASAK, B.; DATTA, U.; BANERJI, J.; NEUMAN, A.; PRANGE, T.; Indian J. Chem., Sect. B: Org. Chem. Incl. Med. Chem. 44 (2005) 2, 430-433; Cent. Adv. Stud. Nat. Prod., Univ. Coll. Sci., Calcutta 700 009, India; Eng.) -A. Forchert 25-180

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

0
17
0

Year Published

2006
2006
2024
2024

Publication Types

Select...
6
1

Relationship

0
7

Authors

Journals

citations
Cited by 16 publications
(17 citation statements)
references
References 0 publications
0
17
0
Order By: Relevance
“…Its structure was confirmed by 1 H‐ and 13 C‐NMR and HR mass analysis. The NMR data were found to exactly match with the reported values of nardin (Chatterjee et al ., 2005; Rao et al ., 2008). The accurate mass calculated for nardin, [M − H] ‐ C 15 H 21 O 2 was 233.1542 and the measured m / z value was 233.1548 (2.5 ppm; Fig.…”
Section: Resultsmentioning
confidence: 99%
“…Its structure was confirmed by 1 H‐ and 13 C‐NMR and HR mass analysis. The NMR data were found to exactly match with the reported values of nardin (Chatterjee et al ., 2005; Rao et al ., 2008). The accurate mass calculated for nardin, [M − H] ‐ C 15 H 21 O 2 was 233.1542 and the measured m / z value was 233.1548 (2.5 ppm; Fig.…”
Section: Resultsmentioning
confidence: 99%
“…Kanshone B (17) differs from 15 only by the presence of an extra oxygen atom that revealed 16 has a hydroxyl group at C-2. Kanshone A (18) has the same carbon framework and stereochemistry as that of 1 and bears (Bagchi, Oshima, & Hikino, 1991;Chatterjee et al, 2005) Roots and rhizomes powder Epilepsy, stress, anxiety, fever, hysteria, mental weakness, menopausal symptoms, intestinal colic, and syncope External application of oil Inflammation of the uterus, eye compounds, and hair fall Hot infusion Melancholic depression Roots powder Epilepsy, heart palpitation, hysteria, and cholera (Dweck, 1996;Rai et al, 2000) External application of roots powder paste Boils, diseases of the eyes, and itch Infusion of roots Flatulence, jaundice, spasmodic hysterical affections, nervous headache, palpitation of the heart, and leprosy (Kapoor, 2000) 2. Islamic Herb powder, decoction, and infusion Cardiotonic, diuretic, hepatic tonic, and analgesic (Ali et al, 2000) 3.…”
Section: Phytochemistrymentioning
confidence: 99%
“…Epilepsy is the condition of recurrent spontaneous seizures arising from abnormal electrical activity within the brain (McCormick & Contreras, 2001). N. chinensis is widely used traditionally for the treatment of seizures, nervous headaches, insomnia, epilepsy, and other convulsive ailments (Chatterjee et al, 2005;Dweck, 1996;Houghton, 1999;Kapoor, 2000). For validation of traditional use of N. chinensis in epilepsy treatment, various animal studies have been conducted.…”
Section: Anticonvulsant Activitymentioning
confidence: 99%
“…Volatile essential oil, resins, sugar, starch, bitter extractive matter, gum, ketone, sesqueterpin ketone, spirojatamol etc 4,5 . Other sesquiterpenes include nardin, nardal, jatamnsic acid, b-maline and patchouli alcohol 6 .…”
Section: Chemical Constituentsmentioning
confidence: 99%