464-48-2
464-48-2
Chemical Structure
(-)-Camphor
- CAS. Nr.: 464-48-2
- Formula:C10H16O
- Molecular Weight:152.24
IUPAC Name: (1S,4S)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one
InChIKey: DSSYKIVIOFKYAU-OIBJUYFYSA-N
SMILES: O=C1[C@@](C2(C)C)(C)CC[C@@]2([H])C1
Biological Activity: (-)-Camphor is an enantiomer of Camphor (HY-N0808) and belongs to the class of bicyclic monoterpene ketones. Camphor ((±)-Camphor) is a topical anti-infective and antipruritic agent, and exhibits carminative effects when administered orally. However, Camphor is toxic upon ingestion. Camphor possesses antiviral, antitussive and anticancer activities. Camphor acts as a TRPV3 agonist[1].
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(-)-Camphor | 98.0% | (-)-Camphor is an enantiomer of Camphor (HY-N0808) and belongs to the class of bicyclic monoterpene ketones. Camphor ((±)-Camphor) is a topical anti-infective and antipruritic agent, and exhibits carminative effects when administered orally. However, Camphor is toxic upon ingestion. Camphor possesses antiviral, antitussive and anticancer activities. Camphor acts as a TRPV3 agonist. | ||||||||||||||||||||
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