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Cat. No.: HY-N18193

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Prunasinamide

Prunasinamide is a catabolite of Prunasin (HY-N1548) and can be found in senescent leaves of Prunus laurocerasus. Prunasinamide can be generated from Prunasin via the Radziszewski reaction.

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CAS No.: 151649-54-6
Formule: C₁₄H₁₉NO₇
Masse moléculaire:313.30

Stockage:

Please store the product under the recommended conditions in the Certificate of Analysis.

Data Sheet (270 KB)

Prunasinamide Chemical Structure

CAS No.: 151649-54-6

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Use of MCE Products

Strong Fluorescence Signal / Multi-Disciplinary Applications / High Fluorescence Specificity

Activité biologique
- Description
- In Vitro
Chemical Information
Pureté et documentation
Références
Calculators
Help & FAQs
Classifications
Bioz

Activité biologique

Description

Prunasinamide is a catabolite of Prunasin (HY-N1548) and can be found in senescent leaves of Prunus laurocerasus. Prunasinamide can be generated from Prunasin via the Radziszewski reaction^[1].

In Vitro

The endogenous concentration of Prunasinamide in senescent Prunus laurocerasus leaves is significantly higher than that in green leaves, while only a small and stable amount of this substance exists in freeze-dried green leaves^[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Chemical Information

CAS No. 151649-54-6
Masse moléculaire 313.30
Formule C₁₄H₁₉NO₇
SMILES

NC([C@@H](C1=CC=CC=C1)O[C@@H]2O[C@@H]([C@H]([C@@H]([C@H]2O)O)O)CO)=O
Structure Classification
- Phenylpropanoids
- Other Phenylpropanoids
Initial Source
Livraison

Room temperature in continental US; may vary elsewhere.
Stockage

Please store the product under the recommended conditions in the Certificate of Analysis.

Pureté et documentation

Select Batch:

Pureté: 99.98%

Assay: 99.98%

ee.: 99.98%

Fiche technique (270 KB)
COA (2659 KB)
Elemental Analysis Report (2659 KB)
HNMR (2659 KB)
CNMR (2659 KB)
RP-HPLC (2659 KB)
NP-HPLC (2659 KB)
MS (2659 KB)
LCMS (2659 KB)
IR (2659 KB)
GC (2659 KB)
OR (2659 KB)
SDS-PAGE (2659 KB)
SEC-HPLC (2659 KB)
Other Report (2659 KB)
Instruction de manipulation (2659 KB)

Références

[1]. Sendker J, et al. Occurrence of Benzoic Acid Esters as Putative Catabolites of Prunasin in Senescent Leaves of Prunus laurocerasus. J Nat Prod. 2016;79(7):1724-1729. [Content Brief]

Calculators

Calculateur de molarité

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass Mass

Concentration Concentration

Volume Volume

Molecular Weight Molecular Weight

Calculateur de dilution

Concentration _(start) × Volume _(start) = Concentration _(final) × Volume _(final)

Concentration _(start) Concentration _(start)

Volume _(start) Volume _(start)

Concentration _(final) Concentration _(final)

Volume _(final) Volume _(final)

Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

Bioz

Keywords

MOQ

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100 mg

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