Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C10H12O2 |
| Molecular Weight | 164.2011 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)C1=CC=C(C=C1)C(O)=O
InChI
InChIKey=CKMXAIVXVKGGFM-UHFFFAOYSA-N
InChI=1S/C10H12O2/c1-7(2)8-3-5-9(6-4-8)10(11)12/h3-7H,1-2H3,(H,11,12)
| Molecular Formula | C10H12O2 |
| Molecular Weight | 164.2011 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Microsomal metabolism and enzyme kinetics of the terpene p-cymene in the common brushtail possum (Trichosurus vulpecula), koala (Phascolarctos cinereus) and rat. | 2002 May |
|
| Antifungal constituents of the stem bark of Bridelia retusa. | 2003 Feb |
|
| Expansion of growth substrate range in Pseudomonas putida F1 by mutations in both cymR and todS, which recruit a ring-fission hydrolase CmtE and induce the tod catabolic operon, respectively. | 2003 Mar |
|
| Identification and expression of the cym, cmt, and tod catabolic genes from Pseudomonas putida KL47: expression of the regulatory todST genes as a factor for catabolic adaptation. | 2006 Apr |
|
| A study of chemical composition and antimicrobial activity of Bulgarian propolis. | 2007 |
|
| Functional identification of p-cumate operons in the terpene-degrading Rhodococcus sp. strain T104. | 2007 Jan |
|
| High-level recombinant protein production in CHO cells using an adenoviral vector and the cumate gene-switch. | 2007 Jan-Feb |
|
| A new classification system for bacterial Rieske non-heme iron aromatic ring-hydroxylating oxygenases. | 2008 Apr 3 |
|
| The study of some polyphenolic compounds from Melissa officinalis L. (Lamiaceae). | 2008 Apr-Jun |
|
| High-level recombinant protein production in CHO cells using lentiviral vectors and the cumate gene-switch. | 2010 Jun 1 |
|
| Production of functionalized polyhydroxyalkanoates by genetically modified Methylobacterium extorquens strains. | 2010 Sep 16 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 19:46:30 GMT 2023
by
admin
on
Fri Dec 15 19:46:30 GMT 2023
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| Record UNII |
6LP0WTM1JB
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| Record Status |
Validated (UNII)
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| Record Version |
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536-66-3
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6LP0WTM1JB
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DTXSID6060210
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m3878
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10820
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C055607
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208-642-5
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