CAS 3952-98-5: Sinigrin monohydrate
Formula:C10H17NO9S2·K
InChI:InChI=1S/C10H17NO9S2.K/c1-2-3-6(11-20-22(16,17)18)21-10-9(15)8(14)7(13)5(4-12)19-10;/h2,5,7-10,12-15H,1,3-4H2,(H,16,17,18);/t5-,7-,8+,9-,10+;/m1./s1
InChI key:InChIKey=CRISREJYBIDTLU-XNTWFIRCSA-N
SMILES:S(C(=NOS(=O)(=O)O)CC=C)[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O.[K]
Synonyms:- 1-S-[(1E)-N-(sulfonatooxy)but-3-enimidoyl]-1-thio-beta-D-glucopyranose
- 2-Propenyl glucosinolate
- Allyl glucosinolate potassium
- Glucopyranose, 1-thio-, 1-(3-butenoate), oxime, O-sulfate, potassium salt, β-<span class="text-smallcaps">D</span>-
- Glucopyranose, 1-thio-, 1-(3-butenohydroximate) NO-(hydrogen sulfate), monopotassium salt, β-<span class="text-smallcaps">D</span>-
- NSC 407279
- NSC 90774
- Sinigrin
- Sinigrin monohydrate from horseradish
- Sinigrine
- Tritium
- See more synonyms
Sort by
Found 12 products.
Sinigrin
CAS:Sinigrin is a glucosinolate compound, which is a naturally occurring sulfur-containing chemical found in various cruciferous plants, such as mustard, broccoli, and Brussels sprouts. It is primarily sourced from the seeds of black mustard (Brassica nigra) and related species. Sinigrin serves as a precursor to biologically active compounds that result from the enzyme-mediated hydrolysis process. Upon tissue damage or stress, sinigrin is hydrolyzed by the enzyme myrosinase into allyl isothiocyanate, which exhibits various bioactive properties. The degradation products of sinigrin, particularly allyl isothiocyanate, are known for their antimicrobial, antifungal, and potential anticancer activities. These properties are linked to their ability to interfere with cell proliferation and induce apoptosis in certain cancer cell lines. Due to these attributes, sinigrin and its derivatives are extensively studied in agricultural biotechnology and medical research for their potential use in natural pesticide development and cancer prevention strategies. Additionally, they are explored for their role in promoting human health through dietary consumption. The holistic understanding of sinigrin’s biochemical interactions continues to expand its application possibilities in both scientific research and practical domains.Formula:C10H16NO9S2·KPurity:Min. 95%Color and Shape:PowderMolecular weight:397.47 g/molSinigrine
CAS:Applications Sinigrine, is a glucosinolate which is found naturally in Cruciferae including the genus Brassica. When enzymatically hydrolysed, Sinigrine yields isothiocyanates and give a pungent taste. Both Sinigrine, and isothiocyanates, have been shown to have anticancer activity as well as antifungal and antibacterial properties. References Cools, K., et al.: J. Chromatograohy B., 901, 115 (2012); Okullcz, M., et al.: Materiae Veg., 65 (3), 217 2010;Formula:C10H16NO9S2·KColor and Shape:NeatMolecular weight:397.46Sinigrin potassium salt
CAS:Sinigrin potassium salt analytical standard provided with w/w absolute assay, to be used for quantitative titration.Formula:C10H16NO9S2KPurity:(HPLC) ≥99%Color and Shape:PowderMolecular weight:397.46Sinigrin
CAS:Formula:C10H16KNO9S2Purity:>98.0%(HPLC)Color and Shape:White to Light yellow to Light orange powder to crystalMolecular weight:397.45Sinigrin potassium salt
CAS:Natural glycosideFormula:C10H16NO9S2KPurity:≥ 95.0 % (HPLC)Color and Shape:PowderMolecular weight:397.47Sinigrin
CAS:Sinigrin, a glucosinolate used to test and identify myrosinase enzymes, serves as a reference for isolating glucosinolates.Formula:C10H16KNO9S2Purity:98.92%Color and Shape:White To Beige Crystalline PowderMolecular weight:397.45Sinigrin Potassium Salt Hydrate Reference Standard Grade, 97%
CAS:Formula:C10H16KNO9S2·xH2OPurity:min. 97%Color and Shape:White to off - white, PowderMolecular weight:397.46 (anhy)Sinigrin hydrate
CAS:Formula:C10H16KNO9S2·xH2OPurity:≥ 99%Color and Shape:White to off-white powderMolecular weight:397.46 (anhydrous)
