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Euphorbia lathyris

National Institutes of Health

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Euphorbia lathyris extract

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2019
2019
Distinct triterpene synthases in the laticifers of Euphorbia lathyris
Euphorbia lathyris was proposed about fifty years ago as a potential agroenergetic crop. The tremendous amounts of triterpenes… 
2019
2019
Synthesis of New Lathyrane Diterpenoid Derivatives from Euphorbia lathyris and Evaluation of Their Anti‐Inflammatory Activities
Euphorbia factor L3, a lathyrane diterpenoid extracted from Euphorbia lathyris, was found to display good anti‐inflammatory… 
2018
2018
Five New Diterpenoids from the Seeds of Euphorbia lathyris
A new premyrsinane‐type diterpenoid, premylanin (1), and four new lathyrane‐type diterpenoids named Euphorbia Factors L30–L33 (2… 
2018
2018
Mechanism of action of cytotoxic compounds from the seeds of Euphorbia lathyris.
2017
2017
Phytochemicals of Euphorbia lathyris L. and Their Antioxidant Activities
The objectives of this study were to characterize the antioxidant capacities and phytochemicals such as phenolics and flavonoids… 
2007
2007
Euphorbia factor L8: a diterpenoid from the seeds of Euphorbia lathyris
The title compound [systematic name: (2S*,3S*,4R*,5R*,9S*,11S*,15R*)-5,15-diacetoxy-3-nicotinoyloxy-14-oxolathyra-6(17),12(E… 
Highly Cited
2003
Highly Cited
2003
A new P-glycoprotein inhibitor from the caper spurge (Euphorbia lathyris).
The macrocyclic lathyrane polyester Euphorbia factor L10 (1a) has been obtained from the seeds of the caper spurge (E. lathyris… 
Highly Cited
1989
Highly Cited
1989
An Antitumor Principle from Euphorbia lathyris
Euphorbia lathyris 
1989
1989
Purification and Characterization of Calmodulins from Papaver somniferum and Euphorbia lathyris.
Calmodulins (CaM) were isolated and characterized from two well-known latex producing plants, Papaver somniferum and Euphorbia… 
1987
1987
Triterpene Biosynthesis in the Latex of Euphorbia lathyris: Effect of Calmodulin Antagonists and Chlorinated Phenoxy Compounds.
Recognized calmodulin antagonists and chlorinated phenoxyalkylamines were tested as inhibitors of mevalonate incorporation into… 
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