A NEW PENTACYCLIC TRITERPENE FROM THE ROOT BARK OF CRATEVA NURVALA

Planta Medica ◽  
1977 ◽  
Vol 32 (07) ◽  
pp. 214-216 ◽  
Author(s):  
V. Lakshmi ◽  
J. Chauhan
1999 ◽  
Vol 62 (5) ◽  
pp. 764-766 ◽  
Author(s):  
Bong-Sik Yun ◽  
In-Ja Ryoo ◽  
In-Kyoung Lee ◽  
Kyu-Hwan Park ◽  
Dong-Ho Choung ◽  
...  

Planta Medica ◽  
2012 ◽  
Vol 78 (11) ◽  
Author(s):  
SS Teh ◽  
GCL Ee ◽  
YM Lim
Keyword(s):  

Planta Medica ◽  
2007 ◽  
Vol 73 (09) ◽  
Author(s):  
JM Rollinger ◽  
R Spitaler ◽  
M Menz ◽  
P Schneider ◽  
EP Ellmerer ◽  
...  

2017 ◽  
Vol 1 (3) ◽  
pp. 129-132
Author(s):  
Jamilu Ya’u ◽  
◽  
Sani Malami ◽  
Mohammed Abugi ◽  
Hyelnaya Ngura ◽  
...  

2018 ◽  
Vol 2 (11) ◽  
pp. 494-497
Author(s):  
Nahandoo Ichôron ◽  
Terrumun Tor-Anyiin ◽  
John Igoli

Author(s):  
Pradeep Deshmukh ◽  
Tanaji Nandgude ◽  
Mahendra Singh Rathode ◽  
Anil Midha ◽  
Nitin Jaiswal

The suspensions of alcoholic extract of root bark of the plant Calotropis gigantea in 0.6% carboxy methyl cellulose (CMC) were evaluated for hepatoprotective activity in Wistar albino rats by inducing hepatic injury with D-galactosamine (400 mg/kg). Alcoholic extract of root bark of the plant Calotropis gigantea at an oral dose of 200 mg/kg and 400 mg/kg exhibited a significant (P<0.001, P<0.01 and P<0.05) protection effect by normalizing the levels of aspartate amino transferase (ASAT/ GOT), alanine amino transferase (ALAT/GPT), alkaline phosphatase (ALP), total bilirubin (TB), lactate dehydrogenase (LDH), which were significantly (P<0.001) increased in rats by treatment with 400 mg/kg i.p. of D-galactosamine. Silymarin (25 mg/kg), a known hepatoprotective drug used for comparison exhibited significant activity (P<0.001).


2009 ◽  
Vol 38 (10) ◽  
pp. 1444-1451 ◽  
Author(s):  
So-Young Yoon ◽  
Jung-Soo Choi ◽  
So-Young Lee ◽  
Koth-Bong-Woo-Ri Kim ◽  
Eu-Jin Song ◽  
...  

Author(s):  
Justyna Żwawiak ◽  
Anna Pawełczyk ◽  
Dorota Olender ◽  
Lucjusz Zaprutko

: Triterpenes are a wide and important group of compounds that have several promising pharmacological properties, such as hepatoprotective, anti-inflammatory, anti-HIV, antioxidant, or anticancer activities. Such potent substances can be successfully incorporated in more complex chemical systems e.g. codrugs or pro-drugs that have better pharmacological profile. The codrug is connected with a drug formation pathway to chemically cohere at least two drug molecules to improve positive therapeutic efficiency or decrease side effects. The codrug can be cleaved in the organism to generate effective compounds previously used as substrates. This article presents an overview of codrugs that consist of pentacyclic triterpene moiety that is chosen as a basic codrug moiety due to their wide range of vital activities and another drug molecule fragment. It was found that triterpenoid codrugs are characterized by a wide range of biological activities. However, most of them have anticancer potency.


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