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Silychristin

Silychristin Structure
CAS No.
33889-69-9
Chemical Name:
Silychristin
Synonyms
SILYCRISTIN;Silicristin;SILICHRISTIN;SILYCHRISTIN;Silymarin II;Christianity;Silychristin A;Silychristin,SC;SILYCHRISTIN hplc;Silicristin USP/EP/BP
CBNumber:
CB8687836
Molecular Formula:
C25H22O10
Molecular Weight:
482.44
MOL File:
33889-69-9.mol
Modify Date:
2024/7/2 8:55:37

Silychristin Properties

Melting point 174~176℃
Boiling point 782.0±60.0 °C(Predicted)
Density 1.578±0.06 g/cm3(Predicted)
storage temp. 2-8°C
solubility Acetone (Slightly), Methanol (Slightly)
pka 7.39±0.60(Predicted)
form Solid
color White to Off-White
Water Solubility practically insoluble in water
Stability Hygroscopic

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P301+P312+P330
Hazard Codes  Xn
Risk Statements  22
Safety Statements  22-45
WGK Germany  3
NFPA 704
0
2 0

Silychristin price More Price(2)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) SML2581 Silychristin Milk Thistle component, ≥95% (HPLC) 33889-69-9 5MG ₹22526.83 2022-06-14 Buy
Sigma-Aldrich(India) 51681 Silychristin analytical standard 33889-69-9 10MG ₹45183.55 2022-06-14 Buy
Product number Packaging Price Buy
SML2581 5MG ₹22526.83 Buy
51681 10MG ₹45183.55 Buy

Silychristin Chemical Properties,Uses,Production

Chemical Properties

Silychristin is the second most abundant flavonolignan in the silymarin complex, which is usually produced by the acetone extraction of Silybum marianum (L.) Gaertn. (milk thistle) fruits. Natural silychristin is a mixture of two diastereomers (silychristin A and B, 95:5). Isosilychristin is a silychristin isomer mainly occurring in wild milk thistle. At the same time, 2,3-dehydrosilychristin is a product of its aerial oxidation detectable in silymarin preparations. In contrast, anhydrosilychristin is a dehydrated product obtained by treating silychristin with hydrochloric acid in hot ethanol[1].

Definition

ChEBI: A flavonolignan isolated from Silybum marianum and has been shown to exhibit inhibitory activities against lipoxygenase and prostaglandin synthetase.

benefits

Like other components of the silymarin complex, silychristin has antioxidant properties. Its potential to scavenge the 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical is nearly 14× higher than that of silybin (considered “the active component of silymarin”) and approximately 1.5× lower than that of its oxidized derivative 2,3-dehydrosilybin. This compound exhibited a higher antioxidant capacity than “traditional” antioxidants.
Silychristin was able to inhibit α-glucosidase, exhibiting a potential in the treatment of diabetes mellitus type II. Furthermore, it increased insulin secretion and decreased glucose content in induced type I diabetic rats and Mesocestoides vogae larvae.
Silychristin also displayed concentration-dependent anti-inflammatory activity and inhibited collagenase much more efficiently than its standard inhibitor 1,10-phenanthroline, thus showing a potential application in cosmeceuticals. In a transdermal study, silychristin penetrated the human skin but did not reach the basolateral side. Both acute cytotoxic and genotoxic doses were higher than 100 μM for blood platelets, peripheral blood mononuclear cells, and alveolar basal epithelial cells. Moreover, at these concentrations, this compound protected mitochondria against spontaneous DNA damage. Moreover, copper and iron chelation was also affected by silychristin, which could have implications for the absorption of these ions in the gastrointestinal tract[1].

in vitro

Silychristin exhibits a strong inhibition of MCT8-mediated T3 uptake with an IC50 of 110 nM in MCT8 overexpressing MDCK1-cells.
It causes no cytotoxic for fibroblasts.
Silychristin (6.5-75 μM; 24 hours) diminishes UVA toxicity and reduces ROS generation, and the protective effect is dose-dependent.
Silychristin (12.5μM, 25μM) reduces the metalloproteinase-1 (MMP-1) level in cells.

target

MCT8

storage

Powder
-20°C 3 years
4°C 2 years
In solvent
-80°C 2 years
-20°C 1 year

References

[1] Simona Dobiasová. “Multidrug Resistance Modulation Activity of Silybin Derivatives and Their Anti-inflammatory Potential.” Antioxidants 9 5 (2020).

Silychristin Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 181)Suppliers
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Apeloa Pharmaceutical Co., Ltd. +86-0571-87635730 +8615858229168 China 1478 58 Inquiry

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Silychristin Spectrum

SILYCHRISTIN SILYCRISTIN SILICHRISTIN Silicristin SILYCHRISTIN hplc 4H-1-Benzopyran-4-one,2-[(2R, 3S)-2,3-dihydro-7- hydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-5-benzofuranyl]-2,3-dihydro-3,5,7-trihydroxy-,(2R,3R)- Silychristin A Silymarin II (2R,3R)-3,5,7-Trihydroxy-2-[(2R,3S)-7-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-2,3-dihydro-1-benzofuran-5-yl]chroman-4-one Silicristin, SilyMarin II 4H-1-Benzopyran-4-one,2-[(2R,3S)-2,3-dihydro-7-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-5-benzofuranyl]-2,3-dihydro-3,5,7-trihydroxy-,(2R,3R)- Silychristin, 98%, from Silybum marianum (L.) Gaertn. Silychristin,SC Silicristin USP/EP/BP Christianity (2R,3R)-3,5,7-Trihydroxy-2-((2R,3S)-7-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-2,3-dihydrobenzofuran-5-yl)chroman-4-one 33889-69-9 chemical reagent pharmaceutical intermediate phytochemical reference standards from Chinese medicinal herbs (TCM). standardized herbal extract Miscellaneous Natural Products