| Weight | 352.77 g/mol |
|---|---|
| Formula | C17H17ClO6 |
| Hydrogen Acceptors | 6 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 3 |
Polygris (6915-11-3)
Griseofulvin · Grisactin · Grifulvin V
Score:
#185 in Microbiology
,
#675 in Biochemistry
,
#1894 in Biology
,
#2283 in Chemistry
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- Preparation and Dissolution Characteristics of Several Fast-Release Solid Dispersions of Griseofulvin (Journal of Pharmaceutical Sciences, 1969)
- Studies in the biochemistry of micro-organisms: Griseofulvin, C17H17O6Cl, a metabolic product of Penicillium griseo-fulvum Dierckx (Biochemical Journal, 1939)
- Vinblastine and griseofulvin reversibly disrupt the living mitotic spindle. (Science, 1968)
- Experimental ringworm in Guinea Pigs: oral treatment with griseofulvin. (Nature, 1958)
- CHO mutants resistant to colchicine, colcemid or griseofulvin have an altered -tubulin (Cell, 1980)
- Human Pharmacology of Griseofulvin: The Effect of Fat Intake on Gastrointestinal Absorption1 (Journal of Investigative Dermatology, 1961)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Griseofulvin
- Grisactin
- Grifulvin V
- Grisefuline
- Gris-PEG
- FulvicinUF
- Fulvicin U F
- Fulvicin-U-F
- Gris PEG
- GrisPEG
-
SMILESCC1CC(=O)C=C(C12C(=O)C3=C(O2)C(=C(C=C3OC)OC)Cl)OC
-
InChIKeyDDUHZTYCFQRHIY-UHFFFAOYSA-N
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