Benzoyl coenzyme A trilithium
Modify Date: 2024-01-02 11:29:38
Benzoyl coenzyme A trilithium structure
|
Common Name | Benzoyl coenzyme A trilithium | ||
|---|---|---|---|---|
| CAS Number | 102185-37-5 | Molecular Weight | 889.44 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C28H37Li3N7O17P3S | Melting Point | N/A | |
| MSDS | USA | Flash Point | N/A | |
Use of Benzoyl coenzyme A trilithiumBenzoyl coenzyme A (trilithium) is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
| Name | Benzoyl CoA lithium salt |
|---|---|
| Synonym | More Synonyms |
| Description | Benzoyl coenzyme A (trilithium) is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
|---|---|
| Related Catalog | |
| Target |
Microbial Metabolite |
| Molecular Formula | C28H37Li3N7O17P3S |
|---|---|
| Molecular Weight | 889.44 |
| Exact Mass | 877.15000 |
| PSA | 421.19000 |
| LogP | 1.77970 |
| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
|---|---|
| RIDADR | NONH for all modes of transport |
|
Characterisation of two alcohol acyltransferases from kiwifruit (Actinidia spp.) reveals distinct substrate preferences.
Phytochemistry 72 , 700-710, (2011) Volatile esters are key compounds of kiwifruit flavour and are formed by alcohol acyltransferases that belong to the BAHD acyltransferase superfamily. Quantitative RT-PCR was used to screen kiwifruit-... |
|
|
4-Coumarate:CoA ligase family members from elicitor-treated Sorbus aucuparia cell cultures.
J. Plant Physiol. 168 , 944-951, (2011) Sorbus aucuparia cell cultures accumulate biphenyl and dibenzofuran phytoalexins in response to elicitor treatment. These polyketide derivatives arise from the starter substrate benzoyl-CoA, the biosy... |
|
|
Structure and mechanism of the diiron benzoyl-coenzyme A epoxidase BoxB.
J. Biol. Chem. 286 , 29241-29248, (2011) The coenzyme A (CoA)-dependent aerobic benzoate metabolic pathway uses an unprecedented chemical strategy to overcome the high aromatic resonance energy by forming the non-aromatic 2,3-epoxybenzoyl-Co... |
| 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] benzenecarbothioate,lithium |