CAS 1716-06-9

S-oleoylcoenzyme A

Description:

S-oleoylcoenzyme A, with the CAS number 1716-06-9, is a derivative of coenzyme A that features an oleoyl group, which is a long-chain unsaturated fatty acid. This compound plays a crucial role in various biochemical processes, particularly in lipid metabolism and the synthesis of fatty acids. It is characterized by its amphipathic nature, possessing both hydrophilic and hydrophobic properties, which allows it to interact with both water and lipid environments. S-oleoylcoenzyme A is involved in the acylation of proteins and the formation of lipid molecules, serving as a substrate for various enzymatic reactions. Its structure includes a coenzyme A backbone, which is essential for its function in transferring acyl groups in metabolic pathways. Additionally, the presence of the oleoyl group contributes to its role in cellular signaling and membrane dynamics. Overall, S-oleoylcoenzyme A is vital for maintaining cellular homeostasis and energy balance within biological systems.

Formula: C₃₉H₆₈N₇O₁₇P₃S

InChI: InChI=1/C39H68N7O17P3S/c1-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-30(48)67-23-22-41-29(47)20-21-42-37(51)34(50)39(2,3)25-60-66(57,58)63-65(55,56)59-24-28-33(62-64(52,53)54)32(49)38(61-28)46-27-45-31-35(40)43-26-44-36(31)46/h11-12,26-28,32-34,38,49-50H,4-10,13-25H2,1-3H3,(H,41,47)(H,42,51)(H,55,56)(H,57,58)(H2,40,43,44)(H2,52,53,54)/b12-11-/t28-,32-,33-,34?,38-/m1/s1

InChI key: InChIKey=XDUHQPOXLUAVEE-BPMMELMSSA-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(CCCCCCC/C=C\CCCCCCCC)=O)=O)=O)O)(C)C)(=O)O)(=O)O)[C@H]1OP(=O)(O)O

Synonyms:

• 9-Octadecenoyl-CoA
• 9-Octadecenoyl-coenzyme A
• Coenzyme A cis-9-octadecenoate
• Coenzyme A oleate
• Coenzyme A, S-(9Z)-9-octadecenoate
• Coenzyme A, S-9-octadecenoate, (Z)-
• Coenzyme A, S-oleate
• Oleoyl-CoA
• Oleoyl-coenzyme A
• Oleyl coenzyme A
• Oleyl-CoA
• S-{17-[(2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-4-hydroxy-3-(phosphonooxy)tetrahydrofuran-2-yl]-9,13,15-trihydroxy-10,10-dimethyl-13,15-dioxido-4,8-dioxo-12,14,16-trioxa-3,7-diaza-13,15-diphosphaheptadec-1-yl} (9Z)-octadec-9-enethioate (non-preferred name)
• cis-9-Octadecenoyl-CoA
• S-Oleoylcoenzyme A
• Adenosine 3'-phosphoric acid 5'-[diphosphoric acid P2-[(R)-3-hydroxy-4-[[3-[[2-[(Z)-9-octadecenoylthio]ethyl]amino]-3-oxopropyl]amino]-2,2-dimethyl-4-oxobutyl]] ester
• OLEOYL COENZYME A POTASSIUM SALT
• coenzyme A oleoyl derivative, dihydrate
• Coenzyme A (Z)-S-9-octadecenoate
• [5-(6-aminopurin-9-yl)-4-hydroxy-2-[[hydroxy-[hydroxy-[3-hydroxy-2,2-dimethyl-3-[2-(2-octadec-9-enoylsulfanylethylcarbamoyl)ethylcarbamoyl]propoxy]-phosphoryl]oxy-phosphoryl]oxymethyl]oxolan-3-yl]oxyphosphonic aci
• CIS-9-OCTADECENOYL COENZYME A
• Oleoyl coenzyme A dipotassium salt
• CIS-9-OCTADECENOYL COENZYME A POTASSIUM SALT

Oleoyl coenzyme A

CAS: 1716-06-9

Oleoyl coenzyme A is an acyl-coa that is synthesized from oleic acid. Its synthesis is regulated by transcriptional factors. The enzyme ATP-binding cassette transporter transports the oleoyl coenzyme A to the endoplasmic reticulum, where it is converted to caprylic acid by synthetase. Caprylic acid is then transported back to the cytosol, where it can be converted into other compounds. Oleoyl CoA has been shown to regulate cellular metabolism and energy production in the liver, which may be related to its ability to prevent hepatic steatosis and reduce cancer tissues. Oleoyl CoA also has a role in regulating the activity of various enzymes in cells through a polymerase chain reaction (PCR) technique.

Formula: C₃₉H₆₈N₇O₁₇P₃S

Purity: Min. 95%

Molecular weight: 1,031.98 g/mol

Ref: 3D-NO47203