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(-)-Menthone

$52

  • Brand : BIOFRON

  • Catalogue Number : BD-D1267

  • Specification : 94%(HPLC)

  • CAS number : 14073-97-3

  • Formula : C10H18O

  • Molecular Weight : 154.253

  • Volume : 0.2ML

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Catalogue Number

BD-D1267

Analysis Method

HPLC,NMR,MS

Specification

94%(HPLC)

Storage

-20℃

Molecular Weight

154.253

Appearance

Botanical Source

Structure Type

Monoterpenoids

Category

SMILES

Synonyms

IUPAC Name

Applications

Density

0.89

Solubility

Flash Point

72ºC

Boiling Point

207-210ºC

Melting Point

-6ºC

InChl

InChl Key

WGK Germany

RID/ADR

HS Code Reference

2914290000

Personal Projective Equipment

Correct Usage

For Reference Standard and R&D, Not for Human Use Directly.

Meta Tag

provides coniferyl ferulate(CAS#:14073-97-3) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. Articles of coniferyl ferulate are included as well.>> amp version: coniferyl ferulate

No Technical Documents Available For This Product.

PMID

31910241

Abstract

Research organism: Mouse

Title

Color discrimination and gas chromatography-mass spectrometry fingerprint based on chemometrics analysis for the quality evaluation of Schizonepetae Spica

Author

Xindan Liu, Data curation, Formal analysis, Writing - original draft, Writing - review & editing, Ying Zhang, Resources, Writing - review & editing, Menghua Wu, Methodology, Writing - review & editing, Zhiguo Ma, Methodology, Writing - review & editing, and Hui Cao, Conceptualization, Funding acquisition, Project administration, Writing - original draft, Writing - review & editing* Joseph Banoub, Editor

Publish date

2020;

PMID

16958095

Abstract

As part of our ongoing effort to relate stimulus to response in the olfactory system, we tested the hypothesis that the unique chemical structures and odors of various cyclic odorants would be associated with unique spatial response patterns in the glomerular layer of the rat olfactory bulb. To this end, rats were exposed to sets of odorants including monocyclic hydrocarbons, bicyclic compounds, and various heterocyclic structures containing oxygen or nitrogen in the ring. Relative activity across the entire layer was assessed by mapping uptake of 2-deoxyglucose into anatomically standardized data matrices. Whereas monocyclic hydrocarbons evoked patterns similar to those evoked by open-chained hydrocarbon odorants, a set of bicyclic compounds with structures and odors similar to camphor evoked uptake in paired ventral domains not previously associated with any other odorant chemical structures. Despite their unique odors as judged by humans, heterocyclic odorants either evoked uptake in previously characterized areas corresponding to their functional groups or stimulated weak or patchy patterns involving isolated glomeruli. While the patchiness of the patterns may be partly related to the rigidity of the compounds, which would be expected to restrict their interactions to only a few receptors, the weakness of the patterns suggests the possibility of species-specific odorant representations. We conclude that whereas some of the novel cyclic structures indeed were represented by unique patterns in the rat bulb, other unique structures were poorly represented, even when they evoked intense and unique odors in humans.

Title

Differential specificity in the glomerular response profiles for alicyclic, bicyclic and heterocyclic odorants

Author

Brett A. Johnson,1,* Zhe Xu,1 Paige Pancoast,1 Jennifer Kwok,1 Joan Ong,1 and Michael Leon1

Publish date

2008 Jan 27.

PMID

32685798

Abstract

Nowadays, crop protection is a major concern and how to proceed is a delicate point of contention. New products must be safe and ecofriendly in accordance with the actual legislation. In this context, we present a quantitative structure-activity relationship strategy based on molecular topology as a tool for generating natural products as potential fungicides following a mechanism of action based on the synthesis of chitin inhibition (chitinase inhibition). Two discriminant equations using statistical linear discriminant analysis were used to identify three potential candidates (1-methylxanthine, hematommic acid, and antheraxanthin). The equations showed accuracy and specificity levels above 80%, minimizing the risk of selecting false active compounds.

Title

Molecular Topology QSAR Strategy for Crop Protection: New Natural Fungicides with Chitin Inhibitory Activity

Author

Maria Galvez-Llompart,†§ Riccardo Zanni,‡§ Jorge Galvez,§ and Ramon Garcia-Domenechcorresponding author*§

Publish date

2020 Jul 14