A novel dicyanotriterpenoid, 2-cyano-3,12-dioxooleana-1,9(11)-dien-28-onitrile, active at picomolar concentrations for inhibition of nitric oxide production
- 4 March 2002
- journal article
- research article
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 12 (7) , 1027-1030
- https://doi.org/10.1016/s0960-894x(02)00105-1
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Synthetic Oleanane and Ursane Triterpenoids with Modified Rings A and C: A Series of Highly Active Inhibitors of Nitric Oxide Production in Mouse MacrophagesJournal of Medicinal Chemistry, 2000
- Novel Synthetic Oleanane and Ursane Triterpenoids with Various Enone Functionalities in Ring A as Inhibitors of Nitric Oxide Production in Mouse MacrophagesJournal of Medicinal Chemistry, 2000
- Novel synthetic oleanane triterpenoids: A series of highly active inhibitors of nitric oxide production in mouse macrophagesBioorganic & Medicinal Chemistry Letters, 1999
- Glycosylation of acids under phase transfer conditions. Partial synthesis of saponinsTetrahedron Letters, 1994
- Allyl esters as carboxy protecting groups in the synthesis of O-glycopeptidesThe Journal of Organic Chemistry, 1989
- A simple method for the efficient synthesis of unsaturated .beta.-dicarbonyl compoundsThe Journal of Organic Chemistry, 1981
- A Convenient Procedure for Esterification of Carboxylic AcidsBulletin of the Chemical Society of Japan, 1978
- 1230. Halogenolysis of methyl glycyrrhetate with lithium iodide–dimethylformamideJournal of the Chemical Society, 1965
- Chelation as a Driving Force in Organic Reactions. IV.1 Synthesis of α-Nitro Acids by Control of the Carboxylation-Decarboxylation Equilibrium2Journal of the American Chemical Society, 1963
- Aminoalkohole, III. Nor‐olea‐12‐enol‐17‐amin und Olea‐12‐enol‐28‐aminEuropean Journal of Inorganic Chemistry, 1958