Deacetylcephalosporin-C
General
Type : Natural, Antibiotic, Azabicyclo
Chemical_Nomenclature : (6R,7R)-7-[[(5R)-5-amino-5-carboxypentanoyl]amino]-3-(hydroxymethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
Canonical SMILES : C1C(=C(N2C(S1)C(C2=O)NC(=O)CCCC(C(=O)O)N)C(=O)O)CO
InChI : InChI=1S\/C14H19N3O7S\/c15-7(13(21)22)2-1-3-8(19)16-9-11(20)17-10(14(23)24)6(4-18)5-25-12(9)17\/h7,9,12,18H,1-5,15H2,(H,16,19)(H,21,22)(H,23,24)\/t7-,9-,12-\/m1\/s1
InChIKey : XWCFYHBHOFBVIV-JWKOBGCHSA-N
Other name(s) : Deacetylcephalosporin C || (6R,7R)-7-{[(5R)-5-amino-5-carboxypentanoyl]amino}-3-(hydroxymethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid || AC1L4NVC || SCHEMBL11534966 || CHEBI:18065
MW : 373.38
Formula : C14H19N3O7S
CAS_number : 1476-46-6
PubChem : 160577
UniChem : XWCFYHBHOFBVIV-JWKOBGCHSA-N
Target
Structures : 2VAV
Families : Homoserine_transacetylase
References (1)
| Title : The last step in cephalosporin C formation revealed: crystal structures of deacetylcephalosporin C acetyltransferase from Acremonium chrysogenum in complexes with reaction intermediates - Lejon_2008_J.Mol.Biol_377_935 |
| Author(s) : Lejon S , Ellis J , Valegard K |
| Ref : Journal of Molecular Biology , 377 :935 , 2008 |
| Abstract : |
| PubMedSearch : Lejon_2008_J.Mol.Biol_377_935 |
| PubMedID: 18279889 |
| Gene_locus related to this paper: cepac-cefg |