POLYOXORIM

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C17H23N5O14
Molecular Weight	521.3896
Optical Activity	UNSPECIFIED
Defined Stereocenters	8 / 8
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

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(C(O)=O)C(=O)NC2=O)C(O)=O

InChI

InChIKey=JPFWJDMDPLEUBD-ITJAGOAWSA-N

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

HIDE SMILES / InChI

Molecular Formula	C17H23N5O14
Molecular Weight	521.3896
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	8 / 8
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

PubMed

Title	Date	PubMed
Phellinsin A, a novel chitin synthases inhibitor produced by Phellinus sp. PL3.	2000-09	11099223
Synthesis and anticandidal properties of polyoxin L analogues containing alpha-amino fatty acids.	1988-03	3279209
Cell wall of pathogenic yeasts and implications for antimycotic therapy.	1986	3527633
Synthesis and biological activity of tripeptidyl polyoxins as antifungal agents.	1983-11	6362556
Design of anticandidal agents: synthesis and biological properties of analogues of polyoxin L.	1983-10	6352943

Substance Class	Chemical Created by `admin` on `Mon Mar 31 22:11:07 GMT 2025` Edited by `admin` on `Mon Mar 31 22:11:07 GMT 2025`
Record UNII	A2468O1N7D
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

POLYOXIN D

Preferred Name

English

POLYOXORIM

Common Name

English

.BETA.-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-

Common Name

English

POLYOXORIM [ISO]

Common Name

English

Code System Code Type Description

FDA UNII

A2468O1N7D