Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C10H16O |
| Molecular Weight | 152.2334 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@]12CC[C@](C)(C(=O)C1)C2(C)C
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
| Molecular Formula | C10H16O |
| Molecular Weight | 152.2334 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
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) |
|||
Target ID: Q8NER1 Gene ID: 7442.0 Gene Symbol: TRPV1 Target Organism: Homo sapiens (Human) |
|||
Target ID: O75762 Gene ID: 8989.0 Gene Symbol: TRPA1 Target Organism: Homo sapiens (Human) |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Osmitopsis asteriscoides (Asteraceae)-the antimicrobial activity and essential oil composition of a Cape-Dutch remedy. | 2003 Oct |
|
| Stereoisomer composition of the chiral UV filter 4-methylbenzylidene camphor in environmental samples. | 2005 May 1 |
|
| Composition, enantiomeric distribution, and antimicrobial activity of Tanacetum argenteum subsp. flabellifolium essential oil. | 2007 Dec 21 |
|
| Synthesis, structure and chiroptical study of chiral macrocyclic imine nickel(II) coordination compounds derived from camphor. | 2010 Apr 7 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 09:28:23 GMT 2023
by
admin
on
Sat Dec 16 09:28:23 GMT 2023
|
| Record UNII |
213N3S8275
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Code | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
464-48-2
Created by
admin on Sat Dec 16 09:28:23 GMT 2023 , Edited by admin on Sat Dec 16 09:28:23 GMT 2023
|
PRIMARY | |||
|
DTXSID8022036
Created by
admin on Sat Dec 16 09:28:23 GMT 2023 , Edited by admin on Sat Dec 16 09:28:23 GMT 2023
|
PRIMARY | |||
|
1648124
Created by
admin on Sat Dec 16 09:28:23 GMT 2023 , Edited by admin on Sat Dec 16 09:28:23 GMT 2023
|
PRIMARY | RxNorm | ||
|
15397
Created by
admin on Sat Dec 16 09:28:23 GMT 2023 , Edited by admin on Sat Dec 16 09:28:23 GMT 2023
|
PRIMARY | |||
|
444294
Created by
admin on Sat Dec 16 09:28:23 GMT 2023 , Edited by admin on Sat Dec 16 09:28:23 GMT 2023
|
PRIMARY | |||
|
207-354-7
Created by
admin on Sat Dec 16 09:28:23 GMT 2023 , Edited by admin on Sat Dec 16 09:28:23 GMT 2023
|
PRIMARY | |||
|
m3004
Created by
admin on Sat Dec 16 09:28:23 GMT 2023 , Edited by admin on Sat Dec 16 09:28:23 GMT 2023
|
PRIMARY | Merck Index | ||
|
213N3S8275
Created by
admin on Sat Dec 16 09:28:23 GMT 2023 , Edited by admin on Sat Dec 16 09:28:23 GMT 2023
|
PRIMARY | |||
|
213N3S8275
Created by
admin on Sat Dec 16 09:28:23 GMT 2023 , Edited by admin on Sat Dec 16 09:28:23 GMT 2023
|
PRIMARY | |||
|
26351
Created by
admin on Sat Dec 16 09:28:23 GMT 2023 , Edited by admin on Sat Dec 16 09:28:23 GMT 2023
|
PRIMARY |