Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C10H16O4 |
| Molecular Weight | 200.2316 |
| Optical Activity | ( + ) |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1(C)[C@H](CC[C@@]1(C)C(O)=O)C(O)=O
InChI
InChIKey=LSPHULWDVZXLIL-LDWIPMOCSA-N
InChI=1S/C10H16O4/c1-9(2)6(7(11)12)4-5-10(9,3)8(13)14/h6H,4-5H2,1-3H3,(H,11,12)(H,13,14)/t6-,10+/m1/s1
Camphoric acid is a product of oxidation of camphor, naturally occurring in rosemary. In the early twentieth century, camphoric acid was used in the night-sweats of phthisis and was also employed in solution as a local antiseptic to the nose, throat, and bladder. Camphoric acid was found to induce the expression of glutamate receptors NMDAR1, GluR3/4, and mGluR8.
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| (1R,3S)-Camphoramic acid. | 2002 Feb |
|
| 2-Amino-pyrimidinium picrate. | 2007 Dec 6 |
|
| Synthesis of (1R,4S,6R)-5,5,6-trimethyl-2-phosphabicyclo[2.2.2]octane and derivatives. | 2010 Apr 28 |
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| Progresses in TCM metal-based antitumour agents. | 2010 Jun |
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| Poly[(μ(3)-camphorato-κO:O':O'')(2-methyl-1H-imidazole-κN)zinc(II)]. | 2010 Mar 3 |
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| Multifunctional homochiral lanthanide camphorates with mixed achiral terephthalate ligands. | 2010 Oct 18 |
|
| Chiral gels derived from secondary ammonium salts of (1R,3S)-(+)-camphoric acid. | 2010 Sep 21 |
Patents
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| Code System | Code | Type | Description | ||
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DTXSID60883316
Created by
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C45678
Created by
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CONCEPT | Industrial Aid | ||
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2264361
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124-83-4
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204-715-0
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C029077
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m3005
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PRIMARY | Merck Index | ||
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30193
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PRIMARY | RxNorm | ||
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101807
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C87496
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W77RM1CSD5
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W77RM1CSD5
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PRIMARY |
SALT/SOLVATE (PARENT)
SUBSTANCE RECORD
