CAS 10478-66-7
:Coenzyme A, S-(2-hydroxybenzoate)
Description:
Coenzyme A, S-(2-hydroxybenzoate) is a derivative of coenzyme A, which plays a crucial role in various biochemical processes, particularly in the metabolism of fatty acids and the synthesis of acetyl-CoA. This compound features a 2-hydroxybenzoate moiety, which contributes to its unique properties and biological functions. It is characterized by its ability to participate in acyl transfer reactions, facilitating the transfer of acyl groups to various substrates. The presence of the 2-hydroxybenzoate group may enhance its interaction with specific enzymes or receptors, influencing its reactivity and biological activity. Coenzyme A derivatives are often involved in the regulation of metabolic pathways and can act as cofactors for various enzymatic reactions. The compound is typically soluble in polar solvents, reflecting its polar functional groups. Its applications extend to research in metabolic engineering, drug development, and understanding biochemical pathways, making it a significant compound in both biochemical and pharmaceutical contexts.
Formula:C28H40N7O18P3S
InChI:InChI=1S/C28H40N7O18P3S/c1-28(2,22(39)25(40)31-8-7-18(37)30-9-10-57-27(41)15-5-3-4-6-16(15)36)12-50-56(47,48)53-55(45,46)49-11-17-21(52-54(42,43)44)20(38)26(51-17)35-14-34-19-23(29)32-13-33-24(19)35/h3-6,13-14,17,20-22,26,36,38-39H,7-12H2,1-2H3,(H,30,37)(H,31,40)(H,45,46)(H,47,48)(H2,29,32,33)(H2,42,43,44)/t17-,20-,21-,22+,26-/m1/s1
InChI key:InChIKey=YTKKDFTVSNSVEE-TYHXJLICSA-N
SMILES:O[C@H]1[C@H](N2C=3C(N=C2)=C(N)N=CN3)O[C@H](COP(OP(OCC([C@H](C(NCCC(NCCSC(=O)C4=C(O)C=CC=C4)=O)=O)O)(C)C)(=O)O)(=O)O)[C@H]1OP(=O)(O)O
Synonyms:- Coenzyme A, S-salicylate
- 2-Hydroxybenzoyl-CoA
- Salicyloyl-CoA
- Coenzyme A, S-(2-hydroxybenzoate)
- o-Hydroxybenzoyl-coenzyme A
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