CAS 38665-10-0
:Validoxylamine A
Description:
Validoxylamine A is a naturally occurring compound classified as an alkaloid, primarily derived from certain species of the Validomyces genus. It is known for its structural complexity, featuring a bicyclic framework that contributes to its biological activity. The compound exhibits notable antimicrobial properties, making it of interest in pharmaceutical research, particularly for its potential applications in treating infections. Validoxylamine A has been studied for its mechanism of action, which may involve interference with cellular processes in target organisms. Its solubility characteristics can vary, influencing its bioavailability and efficacy. Additionally, the compound's stability under various conditions is a critical factor in its potential use in medicinal formulations. As research continues, Validoxylamine A may reveal further insights into its therapeutic potential and mechanisms, contributing to the development of new antimicrobial agents. Overall, its unique chemical structure and biological activity make it a subject of interest in the field of natural product chemistry and drug discovery.
Formula:C14H25NO8
InChI:InChI=1S/C14H25NO8/c16-3-5-1-7(11(20)13(22)9(5)18)15-8-2-6(4-17)10(19)14(23)12(8)21/h1,6-23H,2-4H2/t6-,7+,8+,9-,10-,11+,12+,13+,14+/m1/s1
InChI key:InChIKey=YCJYNBLLJHFIIW-MBABXGOBSA-N
SMILES:N([C@H]1C[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)[C@H]2C=C(CO)[C@@H](O)[C@H](O)[C@H]2O
Synonyms:- 1,5,6-Trideoxy-5-(hydroxymethyl)-1-[[(1S,4R,5S,6S)-4,5,6-trihydroxy-3-(hydroxymethyl)-2-cyclohexen-1-yl]amino]-<span class="text-smallcaps">D</span>-chiro-inositol
- 4-(Hydroxymethyl)-6-((2,3,4-trihydroxy-5-(hydroxymethyl)cyclohexyl)amino)-4-cyclohexene-1,2,3-triol
- <span class="text-smallcaps">D</span>-chiro-Inositol, 1,5,6-trideoxy-5-(hydroxymethyl)-1-[[(1S,4R,5S,6S)-4,5,6-trihydroxy-3-(hydroxymethyl)-2-cyclohexen-1-yl]amino]-
- <span class="text-smallcaps">D</span>-chiro-Inositol, 1,5,6-trideoxy-5-(hydroxymethyl)-1-[[4,5,6-trihydroxy-3-(hydroxymethyl)-2-cyclohexen-1-yl]amino]-, [1S-(1α,4α,5β,6α)]-
- validoxylamine A
- D-chiro-Inositol, 1,5,6-trideoxy-5-(hydroxymethyl)-1-[[(1S,4R,5S,6S)-4,5,6-trihydroxy-3-(hydroxymethyl)-2-cyclohexen-1-yl]amino]-
- 1,5,6-Trideoxy-5-(hydroxymethyl)-1-[[(1S,4R,5S,6S)-4,5,6-trihydroxy-3-(hydroxymethyl)-2-cyclohexen-1-yl]amino]-D-chiro-inositol
- D-chiro-Inositol, 1,5,6-trideoxy-5-(hydroxymethyl)-1-[[4,5,6-trihydroxy-3-(hydroxymethyl)-2-cyclohexen-1-yl]amino]-, [1S-(1α,4α,5β,6α)]-
- 1,5,6-Trideoxy-5-hydroxymethyl-1-[[(1S)-4β,5α,6β-trihydroxy-3-hydroxymethyl-2-cyclohexen-1β-yl]amino]-D-chiro-inositol
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Found 4 products.
Validoxylamine A
CAS:Controlled ProductFormula:C14H25NO8Color and Shape:Off-WhiteMolecular weight:335.35Validoxylamine A
CAS:<p>Validoxylamine A is an antibiotic, which is a secondary metabolite produced by certain strains of the Actinomyces species. It functions as a potent inhibitor of the enzyme glucose isomerase, which plays a crucial role in the isomerization of glucose to fructose, an important biochemical reaction in various microbial and plant systems.</p>Formula:C14H25NO8Purity:Min. 95%Molecular weight:335.35 g/molValidoxylamine A
CAS:<p>Validoxylamine A is a natural compound, which is an aminocyclitol isolated from microbial sources, particularly from certain strains of actinobacteria. This compound acts as a glycosidase inhibitor, disrupting the enzymatic processes that hydrolyze glycosidic bonds in carbohydrates. By inhibiting these enzymes, Validoxylamine A can effectively interfere with carbohydrate metabolism.</p>Formula:C14H25NO8Purity:Min. 95%Molecular weight:335.35 g/mol


