Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C17H25N5O13 |
| Molecular Weight | 507.4061 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 8 / 8 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
N[C@@H]([C@H](O)[C@@H](O)COC(N)=O)C(=O)N[C@@H]([C@H]1O[C@H]([C@H](O)[C@@H]1O)N2C=C(CO)C(=O)NC2=O)C(O)=O
InChI
InChIKey=YFZNSPMAOIVQRP-YVKGXWRCSA-N
InChI=1S/C17H25N5O13/c18-6(8(25)5(24)3-34-16(19)32)13(29)20-7(15(30)31)11-9(26)10(27)14(35-11)22-1-4(2-23)12(28)21-17(22)33/h1,5-11,14,23-27H,2-3,18H2,(H2,19,32)(H,20,29)(H,30,31)(H,21,28,33)/t5-,6-,7-,8+,9-,10+,11+,14+/m0/s1
| Molecular Formula | C17H25N5O13 |
| Molecular Weight | 507.4061 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 8 / 8 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Polyoxins are antifungal antibiotics produced by Streptomycetes that were discovered through programs searching for new fungicides and insecticides for agricultural use. The polyoxins, first reported in the 1960s, were isolated from Streptomyces cacaoi. As inhibitors of chitin synthetase, they exhibit antifungal activity, but lack antibacterial activity. Since they also lack mammalian toxicity, they represent potentially useful models for the development of effective agents for the treatment of opportunistic fungal infections.The inhibitory effectiveness of polyoxin B (Polar) makes it a good candidate for the control of powdery mildews on grapevines, apple, and especially on nectarine trees. Polyoxin B is a chitin synthase (CHS) inhibitor with IC50 of 0.16 mM.
Originator
Approval Year
Sample Use Guides
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/24856180
Polyoxin B inhibited Candida albicans with MIC 16 mg/L.
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:55:07 GMT 2025
by
admin
on
Mon Mar 31 22:55:07 GMT 2025
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| Record UNII |
UP481S7UOD
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| Record Status |
Validated (UNII)
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