| Literature DB >> 21731373 |
Rakesh P Prajapati1, Manisha Kalariya, Sachin K Parmar, Navin R Sheth.
Abstract
Lagenaria siceraria (Molina) standley (LS) (Family: Cucurbitaceae) is an annual herbaceous climbing plant with a long history of traditional medicinal uses in many countries, especially in tropical and subtropical regions. Since ancient times the climber has been known for its curative properties, and has been utilized for treatment of various ailments, including jaundice, diabetes, ulcer, piles, colitis, insanity, hypertension, congestive cardiac failure (CCF), and skin diseases. Its fruit pulp is used both as an emetic and purgative, and for its cooling, diuretic, antibilious, and pectoral properties. Boiled in oil this pulp is used to treat rheumatism and insomnia. A wide range of chemical compounds including sterols, terpenoids, flavonoids, and saponins have been isolated from the species. Its extracts have been found to possess various pharmacological activities. Below, we give a comprehensive review of its ethnomedical uses, chemical constituents, and pharmacological profile as a medicinal plant. Particular attention is given to its analgesic, anti-inflammatory, antihyperlipidemic, diuretic, hepatoprotective, anthelmintic, and antibacterial effects so that its potential uses in pharmaceutics can be better evaluated.Entities:
Keywords: Chemical constituents; Lagenaria siceraria; cucurbitaceae; ethnomedical uses; pharmacological profile
Year: 2010 PMID: 21731373 PMCID: PMC3117318 DOI: 10.4103/0975-9476.74431
Source DB: PubMed Journal: J Ayurveda Integr Med ISSN: 0975-9476
Figure 1Lagenaia siceraria plant
Figure 2Structure of triterpenoids (22-deoxocurcubitacin-D and 22-deoxoisocurcubitacin-D) isolated form L. siceraria
Structural variation in flavone C-glycosides isolated from L. siceraria
| Compound | R1 | R2 | R3 | R4 | R5 |
|---|---|---|---|---|---|
| Vitexin | H | Glucose | H | H | H |
| Isovitexin | Glucose | H | H | H | H |
| Saponarin | Glucose | H | Glucose | H | H |
| Saponarin | Glucose | H | Glucose | H | Glucose |
| Saponarin Caffiec ester | Glucose | H | Caffioyl glucose | H | H |
| Isoorientin | Glucose | H | H | OH | H |
| Lutonarin | Glucose | H | Glucose | OH | H |
Figure 3Structure of flavone C-glycosides from L. siceraria
Figure 4Structures of triterpenes isolated from L. siceraria
Structural variation in various triterpenes isolated from L. siceraria
| Sr. No | R1 | R2 | R3 | Sr. No. | R1 | R2 | R3 | R4 | R5 |
|---|---|---|---|---|---|---|---|---|---|
| 1 | H | CH2OH | 6 | H | OH | OH | COOCH3 | CH3 | |
| 2 | H | CH2OH | 7 | H | OH | H | CH2OH | CH3 | |
| 3 | H | COOH | 8 | --- | =O | H | COOH | CH3 | |
| 4 | H | OH | CH2OH | 9 | H | OH | H | CH3 | CH3 |
| 5 | --- | =O | COOH | 10 | H | OH | H | COOCH3 | CH3 |
| A | B | C |