Glucomalcomiin
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.
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- CAS No.: 75331-11-2
- 화학식: C17H23NO11S2
- 분자량:481.49
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보관:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
제품 설명
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
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CAS No. 75331-11-2
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분자량 481.49
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화학식 C17H23NO11S2
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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
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Synonyms
3-Benzoyloxypropyl glucosinolate
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Structure Classification
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Initial Source
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선적
Room temperature in continental US; may vary elsewhere.
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보관
Please store the product under the recommended conditions in the Certificate of Analysis.
Protocol
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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.
순도&문서
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)