Isobutyryl-CoA
Names | |
---|---|
IUPAC name 3′-O-Phosphonoadenosine 5′-[(3R)-3-hydroxy-2,2-dimethyl-4-{[3-({2-[(2-methylpropanoyl)sulfanyl]ethyl}amino)-3-oxopropyl]amino}-4-oxobutyl dihydrogen diphosphate] | |
Systematic IUPAC name O1-{[(2R,3S,4R,5R)-5-(6-Amino-9H-purin-9-yl)-4-hydroxy-3-(phosphonooxy)oxolan-2-yl]methyl} O3-[(3R)-3-hydroxy-2,2-dimethyl-4-{[3-({2-[(2-methylpropanoyl)sulfanyl]ethyl}amino)-3-oxopropyl]amino}-4-oxobutyl] dihydrogen diphosphate | |
Other names Isobutyryl-coenzyme A | |
Identifiers | |
CAS Number |
|
3D model (JSmol) |
|
ChEBI |
|
MeSH | Isobutyryl-coenzyme+A |
PubChem CID |
|
CompTox Dashboard (EPA) |
|
InChI
| |
| |
Properties | |
Chemical formula | C25H42N7O17P3S |
Molar mass | 837.62 g/mol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N verify (what is YN ?) Infobox references |
Chemical compound
Isobutyryl-coenzyme A is a starting material for many natural products derived from Poly-Ketide Synthase (PKS) assembly lines, as well as PKS-NRPS hybrid assembly lines. These products can often be used as antibiotics. Notably, it is also an intermediate in the metabolism of the amino acid Valine, and structurally similar to intermediates in the catabolism of other small amino acids.
See also
- Isobutyryl-CoA mutase
- Isobutyryl-coenzyme A dehydrogenase deficiency
- v
- t
- e
Amino acid metabolism metabolic intermediates
lysine→ | |
---|---|
leucine→ | |
tryptophan→alanine→ |
G→pyruvate→ citrate |
| ||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|
G→glutamate→ α-ketoglutarate |
| ||||||||||
G→propionyl-CoA→ succinyl-CoA |
| ||||||||||
G→fumarate |
| ||||||||||
G→oxaloacetate |
|
Cysteine metabolism |
---|
This article about an organic compound is a stub. You can help Wikipedia by expanding it. |
- v
- t
- e