ChemicalBook > CAS DataBase List > Schisantherin A

Schisantherin A

Product Name
Schisantherin A
CAS No.
58546-56-8
Chemical Name
Schisantherin A
Synonyms
Gomisin C(P);Schisantherin A;Schisantherin A-RM;SCHISANTHERINGOMISIN;Gomisin C(Schisantherin A);Schisantherin A (Gomisin-C;SCHISANTHERIN A 98.0% BY HPLC;Gomisin, 98%, from Schisandra chinensis;(5S,6S,7S,13aS)-5,6,7,8-Tetrahydro-1,2,3,13-tetramethoxy-6,7-dimethylbenzo[3,4]cycloocta[1,2-f];Benzo[3,4]cycloocta[1,2-f][1,3]benzodioxole-5,6-diol, 5,6,7,8-tetrahydro-1,2,3,13-tetramethoxy-6,7-dimethyl-, 5-benzoate, (5S,6S,7S,13aS)-
CBNumber
CB5462083
Molecular Formula
C30H32O9
Formula Weight
536.57
MOL File
58546-56-8.mol
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Schisantherin A Property

Melting point:
110~112℃
Boiling point:
675.6±55.0 °C(Predicted)
Density 
1.33±0.1 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Store in freezer, under -20°C
solubility 
Chloroform (Slightly), Methanol (Slightly, Sonicated)
form 
Solid
pka
13.70±0.60(Predicted)
color 
White to Off-White
Water Solubility 
insoluble in water
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Safety

Safety Statements 
24/25
HS Code 
29329990
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

TCI Chemical
Product number
G0538
Product name
Gomisin C
Packaging
25MG
Price
$71
Updated
2025/07/31
TCI Chemical
Product number
G0538
Product name
Gomisin C
Packaging
100MG
Price
$214
Updated
2025/07/31
Cayman Chemical
Product number
18643
Product name
Gomisin C
Purity
≥98%
Packaging
5mg
Price
$32
Updated
2024/03/01
Cayman Chemical
Product number
18643
Product name
Gomisin C
Purity
≥98%
Packaging
10mg
Price
$61
Updated
2024/03/01
Cayman Chemical
Product number
18643
Product name
Gomisin C
Purity
≥98%
Packaging
25mg
Price
$116
Updated
2024/03/01
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Schisantherin A Chemical Properties,Usage,Production

Chemical Properties

Rectangular crystals (ethanol), mp 122°C-124°C, [α]D23 -175° (c=0.12, chloroform). Soluble in benzene, chloroform, acetone, soluble in methanol, ethanol, insoluble in petroleum ether, insoluble in water. Seven biphenyl cyclooctenoid lignans with transaminase-lowering activity were isolated from the ethanol extract of Schisandra chinensis kernels, including deoxyschisandrin, schisandrin, schisandrin, schisandrin, schisandrin, schisandrinol ethyl, schisandrin ester A and schisandrin ester ethyl. All seven components have the effect of lowering SGPT, promoting hepatic gluconeogenesis and prolonging pentobarbital sleep time. Schisandra chinensis ester B had the strongest SGPT-lowering effect, Schisandra chinensis alcohol B had the most significant effect in promoting hepatic gluconeogenesis, and Schisandra chinensis prolonged pentobarbital sleep time most prominently.

Uses

Schisantherin A?is a ligand from Schisandra chinensis. It is capable of?suppressing interleukin-1β-induced inflammation in human chondrocytes by inhibiting NF-κB and MAPKs activation.

Definition

ChEBI: Schisantherin A is a tannin.

in vivo

Schisantherin A, a dibenzocyclooctadiene lignan isolated from the fruit of Schisandra sphenanthera, has been reported to possess varied beneficial pharmacological effects. Schisantherin A protects lipopolysaccharide-induced acute respiratory distress syndrome in mice through inhibiting NF-κB and MAPKs signaling pathways. Pretreatment with Schisantherin A markedly ameliorates LPS-induced histopathologic changes and decreases the levels of TNF-α, IL-6 and IL-1β in the BALF. In addition, the phosphorylation of NF-κB p65, IκB-α, JNK, ERK and p38 induced by LPS are suppressed by Schisantherin A. The lung wet/dry weight ratio is evaluated at 7 h after the intranasal instillation of LPS. The results show that there are no differences between control group and Schisantherin A (40 mg/kg) group (p>0.05). LPS causes a significant increase in lung wet/dry weight ratio (p<0.01) compared with the control group. Schisantherin A dose-dependently decreases the lung wet/dry weight ratio (p<0.05) compared to those in the LPS group[1].

target

ROS | NO | NOS | MAPK | PI3K | GSK-3 | IL Receptor | PGE | TNF-α | COX | ERK | p38MAPK | JNK | NF-kB | Beta Amyloid | Akt

IC 50

p65

Schisantherin A Preparation Products And Raw materials

Raw materials

Preparation Products

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View Lastest Price from Schisantherin A manufacturers

Shanghai Standard Technology Co., Ltd.
Product
Schisantherin A 58546-56-8
Price
US $0.00/mg
Min. Order
5mg
Purity
≥98%(HPLC)
Supply Ability
10 g
Release date
2019-10-23
Shanghai Standard Technology Co., Ltd.
Product
Schisantherin A 58546-56-8
Price
US $0.00/mg
Min. Order
5mg
Purity
Analytical Standard
Supply Ability
10 g
Release date
2019-10-23
Career Henan Chemical Co
Product
Schisantherin A 58546-56-8
Price
US $1.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
Customized
Release date
2019-05-25

58546-56-8, Schisantherin ARelated Search:


  • SCHISANTHERIN A 98.0% BY HPLC
  • Schisantherin A (Gomisin-C
  • Gomisin C(Schisantherin A)
  • Schisantherin A
  • SCHISANTHERINGOMISIN
  • Gomisin, 98%, from Schisandra chinensis
  • Benzo[3,4]cycloocta[1,2-f][1,3]benzodioxole-5,6-diol, 5,6,7,8-tetrahydro-1,2,3,13-tetramethoxy-6,7-dimethyl-, 5-benzoate, (5S,6S,7S,13aS)-
  • (5S,6S,7S,13aS)-5,6,7,8-Tetrahydro-1,2,3,13-tetramethoxy-6,7-dimethylbenzo[3,4]cycloocta[1,2-f]
  • (5S,6S,7S)-6-Hydroxy-1,2,3,13-tetramethoxy-6,7-dimethyl-5,6,7,8-tetrahydrobenzo[3',4']cycloocta[1',2':4,5]benzo[1,2-d][1,3]dioxol-5-yl benzoate
  • Gomisin C(P)
  • Schisantherin A-RM
  • 58546-56-8
  • Inhibitors
  • chemical reagent
  • pharmaceutical intermediate
  • phytochemical
  • reference standards from Chinese medicinal herbs (TCM).
  • standardized herbal extract
  • Heterocycles