Synthetic C3a analogs as specific inhibitors of C3a activity
β Scribed by S. Meuer; U. Hadding; R. Andreatta; D. Bitter-Suermann
- Publisher
- Elsevier Science
- Year
- 1981
- Tongue
- English
- Weight
- 356 KB
- Volume
- 3
- Category
- Article
- ISSN
- 0162-3109
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
A series of KRIBB3 analogs were synthesized by modifying substituents at aryl moieties of KRIBB3 for examining structure-activity relationships, and their inhibitory activities on microtubule polymerization were evaluated. The presence of free phenolic hydrogens in aryl moieties of KRIBB3 analogs pl
The title compound and its Cdpivaloyloxy methyl (PGM) ester have been synthesized by converting zaragozic acid A to the key intermediate of the protected C3-hydroxymethyl compound 6. Subsequent radical deoxygcnation via the Barton-McCombie procedure. followed by dqnvtection, affarded the product 11