Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C8H10O2 |
| Molecular Weight | 138.1638 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OCC(O)C1=CC=CC=C1
InChI
InChIKey=PWMWNFMRSKOCEY-UHFFFAOYSA-N
InChI=1S/C8H10O2/c9-6-8(10)7-4-2-1-3-5-7/h1-5,8-10H,6H2
| Molecular Formula | C8H10O2 |
| Molecular Weight | 138.1638 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Metabolism of styrene to styrene oxide and vinylphenols in cytochrome P450 2F2- and P450 2E1-knockout mouse liver and lung microsomes. | 2014-01-21 |
|
| Modification of the metabolism and toxicity of styrene and styrene oxide in hepatic cytochrome P450 reductase deficient mice and CYP2F2 deficient mice. | 2012-04-11 |
|
| Highly enantioselective reduction of 2-hydroxy-1-phenylethanone to enantiopure (R)-phenyl-1,2-ethanediol using Saccharomyces cerevisiae of remarkable reaction stability. | 2010-11 |
|
| Enhancement of Candida parapsilosis catalyzing deracemization of (R,S)-1-phenyl-1,2-ethanediol to its (S)-enantiomer by a highly productive "two-in-one" resin-based in situ product removal strategy. | 2010-11 |
|
| Biotransformation of α-bromoacetophenones by the marine fungus Aspergillus sydowii. | 2010-10 |
|
| Characterization of the epoxide hydrolase NcsF2 from the neocarzinostatin biosynthetic gene cluster. | 2010-09-03 |
|
| Enhancement of substrate concentration in microbial stereoinversion through one-pot oxidation and reduction by aqueous two-phase system. | 2010-03 |
|
| Improved production of (R)-1-phenyl-1,2-ethanediol by a codon-optimized R-specific carbonyl reductase from Candida parapsilosis in Escherichia coli. | 2010-03 |
|
| [Gene cloning and expression of a novel (S)-specific carbonyl reductase]. | 2010-01 |
|
| [Improved expression and catalytic efficiency of (R)-carbonyl reductase in Escherichia coli by secondary structure optimization of mRNA translation initiation region]. | 2009-12 |
|
| Using a water-immiscible ionic liquid to improve asymmetric reduction of 4-(trimethylsilyl)-3-butyn-2-one catalyzed by immobilized Candida parapsilosis CCTCC M203011 cells. | 2009-10-22 |
|
| Cloning and characterization of an epoxide hydrolase from Novosphingobium aromaticivorans. | 2009-04 |
|
| [Construction of an enzyme-coupled system consisting of (R)- and (S)-specific carbonyl reductases for one-step preparation of (S)-1-phenyl-1,2-ethanediol]. | 2009-02 |
|
| A new strategy to improve the efficiency and sustainability of Candida parapsilosis catalyzing deracemization of (R,S)-1-phenyl-1,2-ethanediol under non-growing conditions: increase of NADPH availability. | 2009-01 |
|
| [Co-expression of formate dehydrogenase from Candida boidinii and (R)-specific carbonyl reductase from Candida parapsilosis CCTCC M203011 in Escherichia coli]. | 2008-12 |
|
| Crystal structure of a carbonyl reductase from Candida parapsilosis with anti-Prelog stereospecificity. | 2008-08 |
|
| Biosynthesis of (R)-phenyl-1,2-ethanediol from racemic styrene oxide by using bacterial and marine fish epoxide hydrolases. | 2008-01 |
|
| A catalytic one-step process for the chemo- and regioselective acylation of monosaccharides. | 2007-10-24 |
|
| Screening enantioselective epoxide hydrolase activities from marine microorganisms: detection of activities in Erythrobacter spp. | 2007-08-21 |
|
| A novel NADH-dependent carbonyl reductase with unusual stereoselectivity for (R)-specific reduction from an (S)-1-phenyl-1,2-ethanediol-producing micro-organism: purification and characterization. | 2007-05 |
|
| New phenyl-ethanediols from the culture broth of Boletus edulis. | 2007-04 |
|
| Polymer supported vanadium and molybdenum complexes as potential catalysts for the oxidation and oxidative bromination of organic substrates. | 2006-08-07 |
|
| Enantioconvergent production of (R)-1-phenyl-1,2-ethanediol from styrene oxide by combining the Solanum tuberosum and an evolved Agrobacterium radiobacter AD1 epoxide hydrolases. | 2006-06-20 |
|
| Enzymatic resolution of racemic phenyloxirane by a novel epoxide hydrolase from Aspergillus niger SQ-6 and its fed-batch fermentation. | 2006-04 |
|
| Synthesis, characterisation, reactivity and in vitro antiamoebic activity of hydrazone based oxovanadium(IV), oxovanadium(V) and mu-bis(oxo)bis{oxovanadium(V)} complexes. | 2006-02-21 |
|
| Preparation and evaluation of a chiral stationary phase covalently bound with chiral pseudo-1 8-crown-6 ether having 1-phenyl-1,2-cyclohexanediol as a chiral unit. | 2005-06-17 |
|
| Determination of absolute configuration of acyclic 1,2-diols with [Mo2(OAc)4], part 2: new structural evidence toward a rationale of the method: what remains of [Mo2(OAc)4] in DMSO solution? | 2004-03-05 |
|
| Synthesis, biological, and chiroptical activity of 3-phenyl-clavams. | 2004-01-15 |
|
| Liquid chromatography/electrospray tandem mass spectrometry characterization of styrene metabolism in man and in rat. | 2002 |
|
| Trospium chloride--an effective drug in the treatment of overactive bladder and detrusor hyperreflexia. | 2001-11 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:29:24 GMT 2025
by
admin
on
Mon Mar 31 22:29:24 GMT 2025
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| Record UNII |
2ZAC511UK8
|
| Record Status |
Validated (UNII)
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| Record Version |
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202-258-1
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7149
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DTXSID8042422
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406601
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2ZAC511UK8
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m10261
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93-56-1
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