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Antifungal rapamycin analogues with reduced immunosuppressive activity
- Source :
- Bioorganic & Medicinal Chemistry Letters. 10:1405-1408
- Publication Year :
- 2000
- Publisher :
- Elsevier BV, 2000.
-
Abstract
- Several 1,2,3,4-tetrahydro- and 7-N-hydroxycarbamate derivatives of the natural product rapamycin were prepared and assayed for their immunosuppressive and antifungal profiles. Substitutions at the 7-position indicate the possibility of a differentiated immunosuppressive to antifungal profile, whereas 40-position variants of the tetrahydro-analogues did not show similar differentiated activity.
- Subjects :
- Antifungal
Antifungal Agents
medicine.drug_class
Stereochemistry
Chemistry, Pharmaceutical
Clinical Biochemistry
Pharmaceutical Science
Microbial Sensitivity Tests
Biochemistry
Biopharmaceutics
chemistry.chemical_compound
Drug Discovery
medicine
Animals
Humans
heterocyclic compounds
Molecular Biology
Candida
Sirolimus
chemistry.chemical_classification
Natural product
Molecular Structure
organic chemicals
Organic Chemistry
Chemical modification
Thiophene derivatives
In vitro
chemistry
Lactam
Molecular Medicine
Immunosuppressive Agents
Lactone
Signal Transduction
medicine.drug
Subjects
Details
- ISSN :
- 0960894X
- Volume :
- 10
- Database :
- OpenAIRE
- Journal :
- Bioorganic & Medicinal Chemistry Letters
- Accession number :
- edsair.doi.dedup.....cbcedd0ca3f58dba80109bd506c1b8d5
- Full Text :
- https://doi.org/10.1016/s0960-894x(00)00184-0