S-[2-[3-[[4-[[[5-(6-aminopurin-9-yl)-4-hydroxy-3-phosphonooxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-hydroxyphosphoryl]oxy-2-hydroxy-3,3-dimethylbutanoyl]amino]propanoylamino]ethyl] 2-phenylethanethioate,lithium

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Names

[ CAS No. ]:
108321-26-2

[ Name ]:
S-[2-[3-[[4-[[[5-(6-aminopurin-9-yl)-4-hydroxy-3-phosphonooxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-hydroxyphosphoryl]oxy-2-hydroxy-3,3-dimethylbutanoyl]amino]propanoylamino]ethyl] 2-phenylethanethioate,lithium

[Synonym ]:
Phenylacetyl coenzyme A lithium salt

Chemical & Physical Properties

[ Molecular Formula ]:
C29H42LiN7O17P3S

[ Molecular Weight ]:
892.60800

[ Exact Mass ]:
892.17300

[ PSA ]:
425.34000

[ LogP ]:
2.16920

MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

Articles

Structural and functional studies of the Escherichia coli phenylacetyl-CoA monooxygenase complex.

J. Biol. Chem. 286 , 10735-10743, (2011)

The utilization of phenylacetic acid (PA) in Escherichia coli occurs through a hybrid pathway that shows features of both aerobic and anaerobic metabolism. Oxygenation of the aromatic ring is performe...

The TetR family of transcriptional repressors.

Microbiol. Mol. Biol. Rev. 69 , 326-356, (2005)

We have developed a general profile for the proteins of the TetR family of repressors. The stretch that best defines the profile of this family is made up of 47 amino acid residues that correspond to ...

Phenylacetyl coenzyme A is an effector molecule of the TetR family transcriptional repressor PaaR from Thermus thermophilus HB8.

J. Bacteriol. 193 , 4388-4395, (2011)

Phenylacetic acid (PAA) is a common intermediate in the catabolic pathways of several structurally related aromatic compounds. It is converted into phenylacetyl coenzyme A (PA-CoA), which is degraded ...


More Articles


Related Compounds

  • Tert-butyl 3-methyl-4-(nitromethyl)piperidine-1-carboxylate
  • (2S)-1-(1-benzylpiperidin-2-yl)propan-2-ol
  • (1S)-1-(1-benzylpiperidin-2-yl)ethan-1-ol
  • 1-[3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-2,2-dimethylpropanoyl]-4,4-dimethylpyrrolidine-3-carboxylic acid
  • tert-butyl N-[2-(3,5-dichlorophenyl)-1-oxopropan-2-yl]carbamate
  • 1-[3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-methylbutanoyl]-4,4-dimethylpyrrolidine-3-carboxylic acid
  • tert-butyl N-{4-[(1S)-2-amino-1-hydroxyethyl]-2-hydroxyphenyl}carbamate
  • tert-butyl N-{[1-(aminomethyl)cyclopentyl]methyl}-N-(propan-2-yl)carbamate
  • 1-[3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)pentanoyl]-4,4-dimethylpyrrolidine-3-carboxylic acid
  • tert-butyl 3-[(3S)-3-hydroxybutyl]piperidine-1-carboxylate
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