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22976-86-9 | β-D-Allofuranuronic acid, 5-[[2-amino-5-O-(aminocarbonyl)-2-deoxy-L-xylonoyl]amino]-1-(5-carboxy-3,4-dihydro-2,4-dioxo-1(2H)-pyrimidinyl)-1,5-dideoxy-
CAS No: 22976-86-9 Catalog No: AG002LRJ MDL No:
Product Description
Catalog Number:
AG002LRJ
Chemical Name:
β-D-Allofuranuronic acid, 5-[[2-amino-5-O-(aminocarbonyl)-2-deoxy-L-xylonoyl]amino]-1-(5-carboxy-3,4-dihydro-2,4-dioxo-1(2H)-pyrimidinyl)-1,5-dideoxy-
CAS Number:
22976-86-9
Molecular Formula:
C17H23N5O14
Molecular Weight:
521.3896
IUPAC Name:
1-[(2R,3R,4S,5R)-5-[(S)-[[(2S,3S,4S)-2-amino-5-carbamoyloxy-3,4-dihydroxypentanoyl]amino]-carboxymethyl]-3,4-dihydroxyoxolan-2-yl]-2,4-dioxopyrimidine-5-carboxylic acid
InChI:
InChI=1S/C17H23N5O14/c18-5(7(24)4(23)2-35-16(19)33)12(28)20-6(15(31)32)10-8(25)9(26)13(36-10)22-1-3(14(29)30)11(27)21-17(22)34/h1,4-10,13,23-26H,2,18H2,(H2,19,33)(H,20,28)(H,29,30)(H,31,32)(H,21,27,34)/t4-,5-,6-,7+,8-,9+,10+,13+/m0/s1
InChI Key:
JPFWJDMDPLEUBD-ITJAGOAWSA-N
SMILES:
NC(=O)OC[C@@H]([C@H]([C@@H](C(=O)N[C@@H]([C@H]1O[C@H]([C@@H]([C@@H]1O)O)n1cc(C(=O)O)c(=O)[nH]c1=O)C(=O)O)N)O)O
UNII:
A2468O1N7D
Properties
Complexity:
971
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
8
Defined Bond Stereocenter Count:
0
Exact Mass:
521.124g/mol
Formal Charge:
0
Heavy Atom Count:
36
Hydrogen Bond Acceptor Count:
15
Hydrogen Bond Donor Count:
10
Isotope Atom Count:
0
Molecular Weight:
521.392g/mol
Monoisotopic Mass:
521.124g/mol
Rotatable Bond Count:
11
Topological Polar Surface Area:
322A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
-7.5
Literature
| Title | Journal |
|---|---|
| Can a chitin-synthesis-inhibiting turfgrass fungicide enhance black cutworm susceptibility to a baculovirus? | Pest management science 20120301 |
| Comparative studies on effects of three chitin synthesis inhibitors on common malaria mosquito (Diptera: Culicidae). | Journal of medical entomology 20071101 |
| Inhibition of chitin synthases and antifungal activities by 2'-benzoyloxycinnamaldehyde from Pleuropterus ciliinervis and its derivatives. | Biological & pharmaceutical bulletin 20070301 |
| In vitro activity of polyoxin D and nikkomycin Z against Encephalitozoon cuniculi. | Parasitology research 20020501 |
| Inhibition of chitin synthetase from Saccharomyces cerevisiae by a new UDP-GlcNAc analogue. | Journal of enzyme inhibition 20010101 |
| Phellinsin A, a novel chitin synthases inhibitor produced by Phellinus sp. PL3. | The Journal of antibiotics 20000901 |
| Synthesis and anticandidal properties of polyoxin L analogues containing alpha-amino fatty acids. | Journal of medicinal chemistry 19880301 |
| Cell wall of pathogenic yeasts and implications for antimycotic therapy. | Drugs under experimental and clinical research 19860101 |
| Synthesis and biological activity of tripeptidyl polyoxins as antifungal agents. | Antimicrobial agents and chemotherapy 19831101 |
| Design of anticandidal agents: synthesis and biological properties of analogues of polyoxin L. | Journal of medicinal chemistry 19831001 |
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