Results 171 to 180 of about 9,505 (220)
Advancements in the therapeutic potential of sesquiterpenoids for the treatment of hepatocellular carcinoma (Review). [PDF]
Li Y, Du X, Mao J.
europepmc +1 more source
Research advances in natural sesquiterpene lactones: overcoming cancer drug resistance through modulation of key signaling pathways. [PDF]
Teng C+4 more
europepmc +1 more source
Synthesis and Antimicrobial Evaluation of (+)-Neoisopulegol-Based Amino and Thiol Adducts. [PDF]
Moustafa R+5 more
europepmc +1 more source
Some of the next articles are maybe not open access.
Related searches:
Related searches:
Sesquiterpene Lactones as Allelochemicals
Journal of Natural Products, 2006Six new sesquiterpene lactones, annuolide H (3), helivypolides F, H-J (4, 11-13), and helieudesmanolide A (6), together with known compounds, were isolated from polar bioactive fractions of Helianthus annuus cv. SH-222 and Stella fresh leaf water extracts.
Macias, Francisco A.+5 more
openaire +4 more sources
American Journal of Contact Dermatitis, 1996
Sesquiterpene lactones are a large, diverse group of chemicals found in several plant families that cause allergic contact dermatitis. The biological, botanical, allergenic, and structural significance of sesquiterpene lactones is explored as well as the clinical characteristics of cutaneous reactions.
Erin M. Warshaw, Kathryn A. Zug
openaire +3 more sources
Sesquiterpene lactones are a large, diverse group of chemicals found in several plant families that cause allergic contact dermatitis. The biological, botanical, allergenic, and structural significance of sesquiterpene lactones is explored as well as the clinical characteristics of cutaneous reactions.
Erin M. Warshaw, Kathryn A. Zug
openaire +3 more sources
ChemInform Abstract: Sesquiterpene Lactones of the Umbelliferae
ChemInform, 1986Abstract A survey of sesquiterpene lactones from the species of Umbelliferae is presented. The structures based on predominantly undescribed stereostructural types were derived for the majority of these lactones.
M. Budesinsky, M. Holub
openaire +3 more sources
Tetrahedron, 1979
Abstract A novel synthesis of (± )-Vernolepin ( 1 ) is described. A suitably substituted cis -fused 2-oxa-3-decalone precursor ( 29 ) has been constructed starting from 2,5-cyclohexadiene carboxylic acid via an intramolecular cyclopropanation reaction ( 23 to 18 ).
M. Vandewalle+4 more
openaire +2 more sources
Abstract A novel synthesis of (± )-Vernolepin ( 1 ) is described. A suitably substituted cis -fused 2-oxa-3-decalone precursor ( 29 ) has been constructed starting from 2,5-cyclohexadiene carboxylic acid via an intramolecular cyclopropanation reaction ( 23 to 18 ).
M. Vandewalle+4 more
openaire +2 more sources
Metabolism of antimalarial sesquiterpene lactones
Pharmacology & Therapeutics, 1990Metabolism of artemisinin derivatives, which are antimalarial sesquiterpenes, appeared to lead to the production of the more polar metabolites in general. Presence of the endoperoxide moiety in the A/B ring structure seems crucial for the expression of antimalarial activity of these compounds.
Charles D. Hufford, Ik-Soo Lee
openaire +3 more sources
2003
The sesquiterpene lactone mix (SL mix) consists of 3 allergens: alantolactone, costunolide, dehydrocostus lactone.
Paulsen, E., Andersen, K.E.
openaire +3 more sources
The sesquiterpene lactone mix (SL mix) consists of 3 allergens: alantolactone, costunolide, dehydrocostus lactone.
Paulsen, E., Andersen, K.E.
openaire +3 more sources
Tetrahedron, 1983
Abstract Two routes towards (±) quadrone ( 1 ), via an intramolecular Diels-Alder reaction have been studied. The cycloaddition of 5 failed, probably because of prohibitive strain. In the alternative approach, the key step afforded a mixture of the endo- and exo-adducts 6 and 7 .
J.M. Dewanckele+2 more
openaire +2 more sources
Abstract Two routes towards (±) quadrone ( 1 ), via an intramolecular Diels-Alder reaction have been studied. The cycloaddition of 5 failed, probably because of prohibitive strain. In the alternative approach, the key step afforded a mixture of the endo- and exo-adducts 6 and 7 .
J.M. Dewanckele+2 more
openaire +2 more sources