Wikidata

(Q27149238)

English

lankacidin c

chemical compound

In more languages

Statements

mass
459.226±0 dalton
1 reference
stated in
PubChem
PubChem CID
6440871
language of work or name
English
title
Lankacidins (English)
retrieved
19 October 2016
chemical formula
C₂₅H₃₃NO₇
1 reference
stated in
PubChem
PubChem CID
6440871
language of work or name
English
title
Lankacidins (English)
retrieved
20 November 2016
canonical SMILES
CC1C2CC(C=CC(=CCC(C=CC(=CC(C(C1=O)(C(=O)O2)C)NC(=O)C(=O)C)C)O)C)O
1 reference
stated in
PubChem
PubChem CID
6440871
language of work or name
English
title
Lankacidins (English)
retrieved
20 November 2016
isomeric SMILES
C[C@@H]1[C@H]2C[C@@H](/C=C/C(=C/C[C@@H](/C=C/C(=C/[C@H]([C@@](C1=O)(C(=O)O2)C)NC(=O)C(=O)C)/C)O)/C)O
1 reference
stated in
PubChem
PubChem CID
6440871
language of work or name
English
title
Lankacidins (English)
retrieved
20 November 2016
found in taxon
Streptomyces rochei
12 references
stated in
Studies on lankacidin-group (T-2636) antibiotics. VII. Structure-activity relationships of lankacidin-group antibiotics
stated in
Identification of two polyketide synthase gene clusters on the linear plasmid pSLA2-L in Streptomyces rochei
stated in
Gamma-butyrolactone-dependent expression of the Streptomyces antibiotic regulatory protein gene srrY plays a central role in the regulatory cascade leading to lankacidin and lankamycin production in Streptomyces rochei
stated in
Extensive mutational analysis of modular-iterative mixed polyketide biosynthesis of lankacidin in Streptomyces rochei.
stated in
Giant linear plasmids in Streptomyces: a treasure trove of antibiotic biosynthetic clusters
stated in
Genetic and biochemical analysis of the antibiotic biosynthetic gene clusters on the Streptomyces linear plasmid.
stated in
The genome sequence of Streptomyces rochei 7434AN4, which carries a linear chromosome and three characteristic linear plasmids
stated in
Isolation and characterization of linear plasmids from lankacidin-producing Streptomyces species
stated in
Isolation, structural elucidation, and biosynthesis of 15-norlankamycin derivatives produced by a type-II thioesterase disruptant of Streptomyces rochei
stated in
Quinoprotein dehydrogenase functions at the final oxidation step of lankacidin biosynthesis in Streptomyces rochei 7434AN4
stated in
The large linear plasmid pSLA2-L of Streptomyces rochei has an unusually condensed gene organization for secondary metabolism.
stated in
Isolation and Biosynthesis of an Azoxyalkene Compound Produced by a Multiple Gene Disruptant of Streptomyces rochei.

Identifiers

ChemSpider ID
4945111
1 reference
stated in
ChemSpider
ChemSpider ID
4945111
language of work or name
English
title
N-[(1S,2R,3E,5E,7S,9E,11E,13S,15R,19R)-7,13-Dihydroxy-1,4,10,19-tetramethyl-17,18-dioxo-16-oxabicyclo[13.2.2]nonadeca-3,5,9,11-tetraen-2-yl]-2-oxopropanamide (English)
retrieved
20 November 2016
NSC number
145118
0 references
KNApSAcK ID
C00018701
1 reference
stated in
ChEBI
ChEBI ID
80085
language of work or name
English
title
Lankacidin C (English)
retrieved
19 October 2016
KEGG ID
C15758
1 reference
stated in
ChEBI
ChEBI ID
80085
language of work or name
English
title
Lankacidin C (English)
retrieved
19 October 2016
PDB ligand ID
LC2
0 references
 
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