CHEBI:61781 - tripalmitoyl-S-glyceryl-cysteinyl-seryl-serine

Main

ChEBI Ontology

Automatic Xrefs

Reactions

Pathways

Models

ChEBI Name tripalmitoyl-S-glyceryl-cysteinyl-seryl-serine ChEBI ID CHEBI:61781 ChEBI ASCII Name tripalmitoyl-S-glyceryl-cysteinyl-seryl-serine Definition A triacyl lipopeptide consisting of the tripeptide L-cysteinyl-L-seryl-L-serine with the cysteinyl residue carrying N-palmitoyl and S-2,3-bis(palmitoyloxy)propyl groups. Stars This entity has been manually annotated by the ChEBI Team. Supplier Information Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Formula C60H113N3O11S Net Charge 0 Average Mass 1084.61800 Monoisotopic Mass 1083.80958 InChI InChI=1S/C60H113N3O11S/c1-4-7-10-13-16-19-22-25-28-31-34-37-40-43-55(66)61-54(59(70)62-52(46-64)58(69)63-53(47-65)60(71)72)50-75-49-51(74-57(68)45-42-39-36-33-30-27-24-21-18-15-12-9-6-3)48-73-56(67)44-41-38-35-32-29-26-23-20-17-14-11-8-5-2/h51-54,64-65H,4-50H2,1-3H3,(H,61,66)(H,62,70)(H,63,69)(H,71,72)/t51?,52-,53-,54-/m0/s1 InChIKey XVQKZSLOGHBCET-INVHGPFASA-N SMILES CCCCCCCCCCCCCCCC(=O)N[C@@H](CSCC(COC(=O)CCCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCC)C(=O)N[C@@H](CO)C(=O)N[C@@H](CO)C(O)=O Roles Classification Chemical Role(s): Bronsted base A molecular entity capable of accepting a hydron from a donor (Bronsted acid). (via organic amino compound ) View more via ChEBI Ontology ChEBI Ontology Outgoing tripalmitoyl-S-glyceryl-cysteinyl-seryl-serine (CHEBI:61781) is a triacyl lipopeptide (CHEBI:60192) IUPAC Name S-[2,3-bis(hexadecanoyloxy)propyl]-N-hexadecanoyl-L-cysteinyl-L-seryl-L-serine Synonyms Sources N-Palmitoyl-5,6-dipalmitoyl-S-glycerylcysteinyl-seryl-serine ChemIDplus N-palmitoyl-S-[2,3-bis(palmitoyloxy)propyl]-cysteinyl-seryl-serine ChEBI P3CSS ChEBI S-[2,3-bis(palmitoyloxy)propyl]-N-palmitoyl-L-cysteinyl-L-seryl-L-serine ChEBI tripalmitoyl-S-glyceryl-Cys-Ser-Ser ChEBI Registry Numbers Types Sources 15383379 Reaxys Registry Number Reaxys 98633-82-0 CAS Registry Number ChemIDplus Citation Type Source 2470437 PubMed citation Europe PMC Last Modified 05 April 2011