| Weight | 296.41 g/mol |
|---|---|
| Formula | C20H24O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 1 |
Inulavosin (6022-36-2)
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- Inulavosin, a melanogenesis inhibitor, leads to mistargeting of tyrosinase to lysosomes and accelerates its degradation. (Journal of Investigative Dermatology, 2009)
- INULAVOSIN, A NEW THYMOL DIMER WITH PISCICIDAL ACTIVITY FROM INULA NERVOSA (Heterocycles, 1995)
- Inulavosin and its benzo-derivatives, melanogenesis inhibitors, target the copper loading mechanism to the active site of tyrosinase (Pigment Cell & Melanoma Research, 2014)
- PP-06 Inulavosin, a new type of melanogenesis inhibitor, promote tyrosinase degradation (Pigment Cell Research, 2003)
- ChemInform Abstract: Inulavosin, a New Thymol Dimer with Piscicidal Activity from Inula nervosa. (ChemInform, 2010)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC1=CC(=C(C=C1)C2(CC(C3=C(O2)C=C(C=C3)C)(C)C)C)O
-
InChIKeyMXPGQUVVLMPLEC-UHFFFAOYSA-N
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