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Cat. No.: HY-N21951

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Glucomalcomiin

Name: Glucomalcomiin
Brand: MedChemExpress
SKU: HY-N21951
Availability: PreOrder

(Synonyms: 3-Benzoyloxypropyl glucosinolate)

Glucomalcomin (3-Benzoyloxypropyl glucosinolate) is an aliphatic, side-chain benzoylated hydroxyalkyl derivative of 3-hydroxypropyl glucosinolate. Glucomalcomin is one of the most abundant glucosinolates induced to accumulate by high temperature during seed development of Arabidopsis thaliana, and its content is closely correlated with the expression of the AOP3 gene.

For research use only. We do not sell to patients.

CAS No.: 75331-11-2
Formula: C₁₇H₂₃NO₁₁S₂
Molecular Weight:481.49

Storage:

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

Glucomalcomiin Chemical Structure

CAS No.: 75331-11-2

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Fluorescent Dye

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

Biological Activity
- Description
- In Vitro
Chemical Information
Protocols (1)
Purity & Documentation
References
Calculators
Help & FAQs
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Biological Activity

Description

In Vitro

Overexpression of AtNSP2 in Arabidopsis thaliana Col-0 and C24 seeds redirects the hydrolysis of endogenous Glucomalcomiin from its isothiocyanate to its nitrile product^[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only. Further protocols information, click here.

Chemical Information

CAS No. 75331-11-2
Molecular Weight 481.49
Formula C₁₇H₂₃NO₁₁S₂
SMILES

O=C(C1=CC=CC=C1)OCCC/C(S[C@@H]2O[C@@H]([C@H]([C@@H]([C@H]2O)O)O)CO)=N/OS(=O)(O)=O
Synonyms

3-Benzoyloxypropyl glucosinolate
Structure Classification
- Saccharides
- Monosaccharides
Initial Source
Shipping

Room temperature in continental US; may vary elsewhere.
Storage

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

Protocols

All Molecular Biology

RNA extraction experimental
By lysing cells, releasing RNA, and removing impurities such as proteins and DNA, high-purity RNA products are finally obtained. The commonly used traditional method is the guanidine isothiocyanate/phenol/chloroform method (Trizol), which is suitable for a variety of animal materials including animal tissues, microorganisms, cultured cells, etc., and most plant materials.

Purity & Documentation

Handling Instructions (2659 KB)

References

[1]. Kissen R, et al. Nitrile-specifier proteins involved in glucosinolate hydrolysis in Arabidopsis thaliana. The Journal of biological chemistry. 2009 May 01;284(18):12057-70.

[2]. Barreda L, et al. Elevated temperature drives the biosynthesis of novel acylated glucosinolates in Arabidopsis thaliana seeds[J]. bioRxiv, 2026: 2026.06. 03.729804.

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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.

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