
CAS 122021-74-3: Magnesium tanshinoate B
Formula:C36H28MgO16
InChI:InChI=1S/C36H30O16.Mg/c37-20-6-1-16(11-24(20)41)13-27(34(45)46)50-29(44)10-5-18-3-9-23(40)33-30(18)31(32(52-33)19-4-8-22(39)26(43)15-19)36(49)51-28(35(47)48)14-17-2-7-21(38)25(42)12-17;/h1-12,15,27-28,31-32,37-43H,13-14H2,(H,45,46)(H,47,48);/q;+2/p-2
InChI key:InChIKey=ANUBYMNVOPVATP-UHFFFAOYSA-L
SMILES:OC1=C2C=3C(C4=O[Mg+2]5(O=C(C=CC3C=C1)OC(CC6=CC(O)=C(O)C=C6)C(=O)[O-]5)[O-]C(=O)C(CC7=CC(O)=C(O)C=C7)O4)C(O2)C8=CC(O)=C(O)C=C8
Synonyms:- 3-Benzofurancarboxylic acid, 4-[3-[1-carboxy-2-(3,4-dihydroxyphenyl)ethoxy]-3-oxo-1-propenyl]-2-(3,4-dihydroxyphenyl)-2,3-dihydro-7-hydroxy-, 1-carboxy-2-(3,4-dihydroxyphenyl)ethyl ester, magnesium complex, [2S-[2α,3β(S*),4[E(S*)]]]-
- Lithospermate B
- Lithospermic acid B Mg complex
- Magnesium tanshinoate B
- Magnesium, ((1R)-1-(carboxy-kappaO)-2-(3,4-dihydroxyphenyl)ethyl (2S,3S)-4-((1E)-3-((1R)-1-(carboxy-kappaO)-2-(3,4-dihydroxyphenyl)ethoxy)-3-(oxo-kappaO)-1-propenyl)-2-(3,4-dihydroxyphenyl)-2,3-dihydro-7-hydroxy-3-benzofurancarboxylato(2-)-kappaO3')-, (T-4)-
- Magnesium, (1-carboxy-2-(3,4-dihydroxyphenyl)ethyl 4-(3-(1-carboxy-2-(3,4-dihydroxyphenyl)ethoxy)-3-oxo-1-propenyl)-2-(3,4-dihydroxyphenyl)-2,3-dihydro-7-hydroxy-3-benzofurancarboxylato(2-))-, (T-4-(2S-(2alpha,3beta(S*),4(E(S*)))))-
- Magnesium, [(1R)-1-(carboxy-κO)-2-(3,4-dihydroxyphenyl)ethyl (2S,3S)-4-[(1E)-3-[(1R)-1-(carboxy-κO)-2-(3,4-dihydroxyphenyl)ethoxy]-3-(oxo-κO)-1-propenyl]-2-(3,4-dihydroxyphenyl)-2,3-dihydro-7-hydroxy-3-benzofurancarboxylato(2-)-κO<sup>3′</sup>]-, (T-4)-
- Magnesium, [1-(carboxy-κO)-2-(3,4-dihydroxyphenyl)ethyl 4-[3-[1-(carboxy-κO)-2-(3,4-dihydroxyphenyl)ethoxy]-3-(oxo-κO)-1-propenyl]-2-(3,4-dihydroxyphenyl)-2,3-dihydro-7-hydroxy-3-benzofurancarboxylato(2-)-κO<sup>3′</sup>]-, [T-4-[2S-[2α,3β(S*),4[E(S*)]]]]-
- Magnesium, [1-carboxy-2-(3,4-dihydroxyphenyl)ethyl 4-[3-[1-carboxy-2-(3,4-dihydroxyphenyl)ethoxy]-3-oxo-1-propenyl]-2-(3,4-dihydroxyphenyl)-2,3-dihydro-7-hydroxy-3-benzofurancarboxylato(2-)]-, [T-4-[2S-[2α,3β(S*),4[E(S*)]]]]-
- magnesium 2-({(2E)-3-[3-{[1-carboxylato-2-(3,4-dihydroxyphenyl)ethoxy]carbonyl}-2-(3,4-dihydroxyphenyl)-7-hydroxy-2,3-dihydro-1-benzofuran-4-yl]prop-2-enoyl}oxy)-3-(3,4-dihydroxyphenyl)propanoate
- Magnesium, [(1R)-1-(carboxy-κO)-2-(3,4-dihydroxyphenyl)ethyl (2S,3S)-4-[(1E)-3-[(1R)-1-(carboxy-κO)-2-(3,4-dihydroxyphenyl)ethoxy]-3-(oxo-κO)-1-propenyl]-2-(3,4-dihydroxyphenyl)-2,3-dihydro-7-hydroxy-3-benzofurancarboxylato(2-)-κO3′]-, (T-4)-
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Found 4 products.
Magnesium Salvianolate B
CAS:Formula:C36H28MgO16Purity:95%~99%Color and Shape:PowderMolecular weight:740.909Monomethyl lithospermate B
CAS:Monomethyl lithospermate B is a small molecule belonging to the class of compounds known as polyphenolic esters, which is derived from the plant Salvia miltiorrhiza, commonly known as Danshen. This compound acts primarily through its anti-oxidative and anti-inflammatory properties, influencing various cellular pathways and modulating oxidative stress responses. Monomethyl lithospermate B has garnered significant interest for its potential applications in the field of cardiovascular and neuroprotective research. Its ability to inhibit lipid peroxidation and scavenge free radicals underlies its role in mitigating oxidative damage. Additionally, it has been studied for its potential to improve endothelial function and offer neuroprotective effects, making it a compound of interest for the treatment of cardiovascular diseases and neurodegenerative disorders. Current research is exploring its detailed mechanisms of action and therapeutic potential in various models, indicating promising directions for future clinical applications.Formula:C36H28MgO16Purity:Min. 95%Molecular weight:740.9 g/molMagnesium Lithospermate B
CAS:Magnesium Lithospermate B is a derivative of caffeic acid tetramer. Magnesium Lithospermate B inhibits neuroinflammation and reduces neurodegeneration.Formula:C36H28MgO16Purity:97.50% - 99.87%Color and Shape:SolidMolecular weight:740.9