Cas no 38665-10-0 (Validoxylamine A)

Validoxylamine A is a potent trehalase inhibitor derived from Validamycin A, a natural compound produced by Streptomyces hygroscopicus. It exhibits high specificity for trehalase enzymes, making it a valuable tool for studying trehalose metabolism in insects, fungi, and plants. Its competitive inhibition mechanism disrupts trehalose hydrolysis, which is critical for energy storage in many organisms. Validoxylamine A is particularly useful in agricultural research for investigating pest control strategies, as trehalase inhibition can impair insect growth and survival. The compound is also employed in biochemical studies to elucidate trehalose-related pathways. Its stability and selectivity make it a reliable reagent for both in vitro and in vivo applications.
Validoxylamine A structure
Validoxylamine A structure
Product Name:Validoxylamine A
CAS No:38665-10-0
MF:C14H25NO8
MW:335.350205183029
CID:923820
PubChem ID:11450478
Update Time:2025-05-27

Validoxylamine A Chemical and Physical Properties

Names and Identifiers

    • Validoxylamine A
    • 4-(Hydroxymethyl)-6-{[2,3,4-trihydroxy-5-(hydroxymethyl)cyclohexy l]amino}-4-cyclohexene-1,2,3-triol
    • 4-(Hydroxymethyl)-6-((2,3,4-trihydroxy-5-(hydroxymethyl)cyclohexyl)amino)-4-cyclohexene-1,2,3-triol
    • NCI60_008244
    • FT-0630904
    • 82309-75-9
    • CHEMBL2006788
    • SCHEMBL5160235
    • DTXSID00959504
    • 4-(hydroxymethyl)-6-[[2,3,4-trihydroxy-5-(hydroxymethyl)cyclohexyl]amino]cyclohex-4-ene-1,2,3-triol
    • 4-(hydroxymethyl)-6-{[2,3,4-trihydroxy-5-(hydroxymethyl)cyclohexyl]amino}cyclohex-4-ene-1,2,3-triol
    • NSC626095
    • NSC-626095
    • (+)-Validoxylamine-A
    • (1s,2s,3r,6s)-4-(Hydroxymethyl)-6-{[(1s,2s,3s,4r,5r)-2,3,4-Trihydroxy-5-(Hydroxymethyl)cyclohexyl]amino}cyclohex-4-Ene-1,2,3-Triol
    • CHEMBL1236649
    • vinylpelargonate
    • Q27225311
    • C17700
    • CHEBI:131941
    • VALIDOXYLAMINE
    • (1S,2S,3R,6S)-4-(hydroxymethyl)-6-[[(1S,2S,3S,4R,5R)-2,3,4-trihydroxy-5-(hydroxymethyl)cyclohexyl]amino]cyclohex-4-ene-1,2,3-triol
    • D-chiro-Inositol, 1,5,6-trideoxy-5-(hydroxymethyl)-1-((4,5,6-trihydroxy-3-(hydroxymethyl)-2-cyclohexen-1-yl)amino)-, (1S-(1alpha,4alpha,5beta,6alpha))-
    • (1S,2S,3R,6S)-4-(hydroxymethyl)-6-((1S,2S,3S,4R,5R)-2,3,4-trihydroxy-5-(hydroxymethyl)cyclohexylamino)cyclohex-4-ene-1,2,3-triol
    • (+)-Validoxylamine A
    • D-chiro-Inositol, 5-(hydroxymethyl)-1,5,6-trideoxy-1-((4,5,6-trihydroxy-3-(hydroxymethyl)-2-cyclohexen-1-yl)amino)-, (1S-(1-alpha,4-alpha,5-beta,6-alpha))-
    • 38665-10-0
    • 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; (+)-Validoxylamine A;
    • 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： YCJYNBLLJHFIIW-MBABXGOBSA-N
    • SMILES： O[C@@H]1[C@H]([C@@H]([C@@H](CO)C[C@@H]1N[C@H]1C=C(CO)[C@H]([C@@H]([C@H]1O)O)O)O)O

Computed Properties

  • Exact Mass: 335.15805
  • Monoisotopic Mass: 335.15801676g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 9
  • Hydrogen Bond Acceptor Count: 9
  • Heavy Atom Count: 23
  • Rotatable Bond Count: 4
  • Complexity: 433
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 9
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: -4.1
  • Topological Polar Surface Area: 174?2

Experimental Properties

  • Density: 1.6±0.1 g/cm3
  • Boiling Point: 602.6±55.0 °C at 760 mmHg
  • Flash Point: 222.6±22.1 °C
  • PSA: 173.87
  • Vapor Pressure: 0.0±3.9 mmHg at 25°C

Validoxylamine A Security Information

Validoxylamine A Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
TRC
V943450-25mg
Validoxylamine A
 38665-10-0
25mg
 165.00 2021-07-15
TRC
V943450-100mg
Validoxylamine A
 38665-10-0
100mg
 655.00 2021-07-15
TRC
V943450-250mg
Validoxylamine A
 38665-10-0
250mg
 1320.00 2021-07-15
TRC
V943450-1mg
Validoxylamine A
 38665-10-0
1mg
 $ 207.00 2023-09-05
TRC
V943450-5mg
Validoxylamine A
 38665-10-0
5mg
 $ 816.00 2023-09-05
TRC
V943450-10mg
Validoxylamine A
 38665-10-0
10mg
 $ 1642.00 2023-09-05

Validoxylamine A Related Literature

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Additional information on Validoxylamine A

Comprehensive Guide to Validoxylamine A (CAS No. 38665-10-0): Properties, Applications, and Market Insights

Validoxylamine A (CAS No. 38665-10-0) is a naturally occurring compound that has garnered significant attention in the fields of biochemistry and pharmaceuticals. Known for its unique structural properties, this compound is often studied for its potential applications in enzyme inhibition and metabolic pathways. Researchers and industry professionals are increasingly interested in Validoxylamine A due to its role in modulating biological processes, making it a hot topic in scientific discussions.

The chemical structure of Validoxylamine A features a distinctive amine group attached to a validated sugar moiety, which contributes to its biological activity. This structural uniqueness has led to extensive research into its mechanism of action, particularly in the context of glycosidase enzymes. Scientists are exploring how Validoxylamine A can be utilized to develop novel therapeutic agents, especially for conditions related to carbohydrate metabolism disorders.

One of the most frequently asked questions about Validoxylamine A is its potential role in drug development. Recent studies suggest that this compound could serve as a lead molecule for designing inhibitors targeting specific enzymes involved in diseases like diabetes and certain viral infections. The ability of Validoxylamine A to interfere with enzymatic activity makes it a promising candidate for further investigation in preclinical and clinical settings.

In addition to its pharmaceutical applications, Validoxylamine A is also being studied for its use in agricultural biotechnology. Researchers are examining its potential as a natural pesticide or growth regulator, leveraging its ability to disrupt metabolic pathways in pests without harming beneficial organisms. This aligns with the growing demand for eco-friendly agricultural solutions, a trend that has gained momentum in recent years.

The market for Validoxylamine A is expected to grow as more discoveries about its applications emerge. Currently, the compound is primarily available for research purposes, with suppliers offering it in various purity grades. However, as its therapeutic and agricultural potential becomes more evident, the demand for Validoxylamine A is likely to increase, prompting more companies to enter the market.

For those looking to purchase Validoxylamine A, it is essential to consider factors such as purity, supplier reputation, and intended use. High-purity grades are typically required for pharmaceutical research, while lower grades may suffice for agricultural studies. Additionally, researchers should stay updated on the latest advancements related to Validoxylamine A, as new findings could open up additional avenues for its application.

In summary, Validoxylamine A (CAS No. 38665-10-0) is a versatile compound with significant potential in both pharmaceuticals and agriculture. Its unique properties and mechanisms of action make it a valuable subject of study, and ongoing research is likely to uncover even more uses for this intriguing molecule. Whether you are a scientist, a biotech professional, or an industry stakeholder, keeping an eye on developments related to Validoxylamine A could prove highly beneficial.

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