Found 1 publication.
Displayed publication 1
Expand all publications
Collapse all publications
Show all as text (SweetDB notation)
Show all graphically (SNFG notation)
1. (Article ID: 5554)
Bormann C, Huhn W, Zähner H, Rathmann R, Hahn H, Konig WA
Metabolic products of microorganisms. 228. New nikkomycins produced by mutants of Streptomyces tendae
The Journal of Antibiotics 38(1) (1985)
9-16
Four new dipeptidyl nikkomycins of the Z- and the X-series with a variation in the amino acid moiety of the molecule were isolated from the mutant Streptomyces tendae 901/395 and characterized. Nikkomycins Kz and Kx contain 2-amino-4-hydroxy-4-(2-pyridyl)butyric acid, and nikkomycins Oz and Ox 2-amino-4-hydroxy-4-(5-hydroxy-2-pyridyl)butyric acid. In contrast to nikkomycins Z and X, nikkomycins Kx and Ox are quite stable at alkaline pH and exhibit a lower biological activity against various test organisms. From the mutant S. tendae 901/C37, which is auxotrophic for methionine and threonine, enhanced amounts of two tripeptidyl nikkomycins, Qz and Qx, were produced which are analogues of nikkomycins J and I and contain a homoserine residue instead of glutamic acid. These nikkomycins exhibit a high pH instability
antibiotics, nikkomycins, Streptomyces tendae
NCBI PubMed ID: 3972731Publication DOI: 10.7164/antibiotics.38.9Journal NLM ID: 0151115Publisher: London: Nature Publishing Group
Institutions: Institute of Biology II, University Tübingen, Tübingen, Germany, Institute of Organic Chemistry, University Hamburg, Hamburg, Germany
Methods: biological assays, HPLC, extraction, hydrolysis, cell growth, mutagenesis, evaporation
The publication contains the following compound(s):
- Compound ID: 14064
|
Subst-(1-5)-b-D-Allf1N5NA-(1-1)-Subst1
All1N5NA = 1,5-diamino-1,5-deoxy-alluronic acid;
Subst = SMILES NC(CC(O)c1ccccn1){1}C(=O)O;
Subst1 = uracil = SMILES O=c1{5}cc{1}[nH]c(=O)[nH]1 |
Show graphically |
Structure type: monomer
Trivial name: nikkomycin Kz
Compound class: glycoside
- Compound ID: 14065
|
Subst-(1-5)-b-D-Allf1N5NA-(1-1)-Subst1
All1N5NA = 1,5-diamino-1,5-deoxy-alluronic acid;
Subst = SMILES NC(CC(O)c1ccccn1){1}C(=O)O;
Subst1 = 4-formyl-4-imidazolin-2-one = SMILES O=Cc1c{1}[nH]c(=O)[nH]1 |
Show graphically |
Structure type: monomer
Trivial name: nikkomycin Kx
Compound class: glycoside
- Compound ID: 14066
|
Subst-(1-5)-b-D-Allf1N5NA-(1-1)-Subst1
All1N5NA = 1,5-diamino-1,5-deoxy-alluronic acid;
Subst = SMILES NC(CC(O)c1ccc(O)cn1){1}C(=O)O;
Subst1 = uracil = SMILES O=c1{5}cc{1}[nH]c(=O)[nH]1 |
Show graphically |
Structure type: monomer
Trivial name: nikkomycin Oz
Compound class: glycoside
- Compound ID: 14067
|
Subst-(1-5)-b-D-Allf1N5NA-(1-1)-Subst1
All1N5NA = 1,5-diamino-1,5-deoxy-alluronic acid;
Subst = SMILES NC(CC(O)c1ccc(O)cn1){1}C(=O)O;
Subst1 = 4-formyl-4-imidazolin-2-one = SMILES O=Cc1c{1}[nH]c(=O)[nH]1 |
Show graphically |
Structure type: monomer
Trivial name: nikkomycin Ox
Compound class: glycoside
- Compound ID: 14068
|
L-Glu-(2-6)-+
|
Subst-(1-5)-b-D-Allf1N5NA-(1-1)-Subst1
All1N5NA = 1,5-diamino-1,5-deoxy-alluronic acid;
Subst = SMILES NC(CC(O)c1ccc(O)cn1){1}C(=O)O;
Subst1 = uracil = SMILES O=c1{5}cc{1}[nH]c(=O)[nH]1 |
Show graphically |
Structure type: monomer
Trivial name: nikkomycin Qz
Compound class: glycoside
- Compound ID: 14069
|
L-Glu-(2-6)-+
|
Subst-(1-5)-b-D-Allf1N5NA-(1-1)-Subst1
All1N5NA = 1,5-diamino-1,5-deoxy-alluronic acid;
Subst = SMILES NC(CC(O)c1ccc(O)cn1){1}C(=O)O;
Subst1 = 4-formyl-4-imidazolin-2-one = SMILES O=Cc1c{1}[nH]c(=O)[nH]1 |
Show graphically |
Structure type: monomer
Trivial name: nikkomycin Qx
Compound class: glycoside
Expand this publication
Collapse this publication
Total list of publication IDs on all result pages of the current query:
Total list of corresponding CSDB IDs (permanent record IDs):
Execution: <1 sec