Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C10H16O |
| Molecular Weight | 152.2334 |
| Optical Activity | ( - ) |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1(C)[C@H]2CC[C@]1(C)C(=O)C2
InChI
InChIKey=DSSYKIVIOFKYAU-OIBJUYFYSA-N
InChI=1S/C10H16O/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7H,4-6H2,1-3H3/t7-,10+/m0/s1
Camphor, -/- is a bicyclic monoterpene ketone found widely in plants, especially Cinnamomum camphora. Camphor has anti-inflammatory and analgesic properties. It is also used for its aromatic properties as an insect repellant and in embalming fluids. It is used topically as a skin antipruritic (itch relief) and as an anti-infective agent.
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: Q8NET8 Gene ID: 162514.0 Gene Symbol: TRPV3 Target Organism: Homo sapiens (Human) |
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Target ID: Q8NER1 Gene ID: 7442.0 Gene Symbol: TRPV1 Target Organism: Homo sapiens (Human) |
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Target ID: O75762 Gene ID: 8989.0 Gene Symbol: TRPA1 Target Organism: Homo sapiens (Human) |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Synthesis, structure and chiroptical study of chiral macrocyclic imine nickel(II) coordination compounds derived from camphor. | 2010-04-07 |
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| Composition, enantiomeric distribution, and antimicrobial activity of Tanacetum argenteum subsp. flabellifolium essential oil. | 2007-12-21 |
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| Spectrophotometric and calorimetric titration studies on molecular recognition of camphor and borneol by nucleobase-modified beta-cyclodextrins. | 2007-10-25 |
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| In vitro metabolism of (-)-camphor using human liver microsomes and CYP2A6. | 2007-02 |
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| Vapor phase toxicity of marjoram oil compounds and their related monoterpenoids to Blattella germanica (Orthoptera: Blattellidae). | 2005-10-05 |
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| Stereoisomer composition of the chiral UV filter 4-methylbenzylidene camphor in environmental samples. | 2005-05-01 |
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| Osmitopsis asteriscoides (Asteraceae)-the antimicrobial activity and essential oil composition of a Cape-Dutch remedy. | 2003-10 |
Patents
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464-48-2
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DTXSID8022036
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1648124
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444294
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207-354-7
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m3004
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213N3S8275
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213N3S8275
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26351
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SUBSTANCE RECORD
