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Gomisin A

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Gomisin A manufacturers

  • Gomisin A
  • Gomisin A pictures
  • 2026-09-11
  • CAS:58546-54-6
  • Min. Order: 20mg
  • Purity: 98% HPLC
  • Supply Ability: 100kg
  • Schisandrol B
  • Schisandrol B pictures
  • $65.00
  • 2026-06-02
  • CAS:58546-54-6
  • Purity: 99.95%
  • Supply Ability: 10g
  • Gomisin A
  • Gomisin A pictures
  • 2023-02-24
  • CAS:58546-54-6
  • Min. Order: 5mg
  • Purity: ≥98%(HPLC)
  • Supply Ability: 10 g
Gomisin A Basic information
Product Name:Gomisin A
Synonyms:2,3,13-tetramethoxy-l-stereoisomer;benzo(3,4)cycloocta(1,2-f)(1,3)benzodioxol-6-ol,5,6,7,8-tetrahydro-6,7-dimethy;wuweizialcoholb;wuweizichunb;BESIGOMISIN;GOMISIN A;SCHIZANDROL B;Besigomsin
CAS:58546-54-6
MF:C23H28O7
MW:416.47
EINECS:
Product Categories:chemical reagent;pharmaceutical intermediate;phytochemical;reference standards from Chinese medicinal herbs (TCM).;standardized herbal extract;Miscellaneous Natural Products
Mol File:58546-54-6.mol
Gomisin A Structure
Gomisin A Chemical Properties
Melting point 88.5°C
Boiling point 454.79°C (rough estimate)
density 1.1772 (rough estimate)
refractive index 1.5300 (estimate)
storage temp. Sealed in dry,Store in freezer, under -20°C
solubility DMSO : 50 mg/mL (120.06 mM; Need ultrasonic)H2O : < 0.1 mg/mL (insoluble)
pka14.58±0.40(Predicted)
form powder to crystal
color White to Light yellow
biological sourceSchisandra chinensis
InChI1S/C23H28O7/c1-12-7-13-8-16-20(30-11-29-16)22(28-6)17(13)18-14(10-23(12,2)24)9-15(25-3)19(26-4)21(18)27-5/h8-9,12,24H,7,10-11H2,1-6H3/t12-,23-/m0/s1
InChIKeyZWRRJEICIPUPHZ-MYODQAERSA-N
SMILESC[C@]1([H])[C@@](C)(O)CC2=C(C(OC)=C(OC)C(OC)=C2)C3=C(OC)C4=C(OCO4)C=C3C1
LogP4.770 (est)
Safety Information
Safety Statements 24/25
WGK Germany WGK 3
HS Code 29329990
Storage Class11 - Combustible Solids
MSDS Information
Gomisin A Usage And Synthesis
DescriptionSchisandrol B is a lignan originally isolated from S. chinensis that has hepatoprotective activity. It increases the expression of pregnane X receptor (PXR) target genes involved in bile acid metabolism, including Cyp3a11, Ugt1a1, Oatp2, and Mrp3 in mouse liver and CYP3A4, UGT1A1, and OATP2 in HEK293T cells. It also protects against lithocholic acid-induced hepatic necrosis and intrahepatic cholestasis in wild-type, but not Pxr-null, mice and decreases mortality in a mouse model of cholestasis when administered at a dose of 100 mg/kg twice per day. It also promotes liver regeneration following partial hepatectomy and protects against hepatotoxicity induced by acetaminophen .
Chemical PropertiesWhite powder
UsesSchizandrol B exhibits potent protective effects of on ET-1-induced dysfunctional human-induced pluripotent stem cell-derived cardiomyocytes (hiPS-CMs). Anti-cholestasis effect.
in vivo

Schisandrol B (12.5-200mg/kg; oral administration; seven times with an interval of 12hours) pretreatment significantly attenuates the increases in alanine aminotransferase and aspartate aminotransferase activity, and prevents elevated hepatic malondialdehyde formation and the depletion of GSH in a dose-dependent manner. Schisandrol B abrogates APAP-induced activation of p53 and p21, and increases expression of liver regeneration and antiapoptotic-related proteins such as cyclin D1 (CCND1), PCNA, and BCL-2[1].

Animal Model:Male C57BL/6 mice (6-8 weeks old, 20-22g) injected with Acetaminophen (APAP)[1]
Dosage:12.5mg/kg, 12.5mg/kg and 200mg/kg
Administration:Oral administration; seven times with an interval of 12hours
Result:Showed a protective effect against APAP-induced liver injury in mice.
IC 50CYP2; CYP3A
References[1] H. TAGUCHI Y I. The Constituents of Schizandra chinensis BAILL. I. The Structures of Gomisin A, B and C[J]. Chemical & pharmaceutical bulletin, 1975, 114 1: 3296-3298. DOI: 10.1248/cpb.23.3296
[2] HANG ZENG. Schisandrol B protects against cholestatic liver injury through pregnane X receptors[J]. British Journal of Pharmacology, 2017, 174 8: 672-688. DOI: 10.1111/bph.13729
[3] XI LI . Schisandrol B promotes liver regeneration after partial hepatectomy in mice[J]. European journal of pharmacology, 2018, 818: Pages 96-102. DOI: 10.1016/j.ejphar.2017.10.044
[4] YI-MING JIANG. Schisandrol B protects against acetaminophen-induced acute hepatotoxicity in mice via activation of the NRF2/ARE signaling pathway[J]. Acta Pharmacologica Sinica, 2016, 37 3: 382-389. DOI: 10.1038/aps.2015.120
Gomisin A Preparation Products And Raw materials
Tag:Gomisin A(58546-54-6) Related Product Information
Schisandrin A Nortropine GOMISIN N Schisandrin Silybin Ginkgo biloba extract WUWEIZISU C (5S)-6α,7β-Dimethyl-1,2,3,11,12-pentamethoxy(5,6,7,8-tetrahydrodibenzo[a,c]cyclooctene)-5α,6β,10-triol 5-benzoate Benzo(3,4)cycloocta(1,2-f)(1,3)benzodioxol-1-ol, 5,6,7,8-tetrahydro-2, 3,13-trimethoxy-6,7-dimethyl-, stereoisomer SCHISANTHERIN C 98+% HPLC Schisantherin A 2-Butenoic acid, 2-methyl-, (5S,6S,7S,13aS)-5,6,7,13a-tetrahydro-6-hydroxy-1,2,3,13-tetramethoxy-6,7-dimethylbenzo[3,4]cycloocta[1,2-f][1,3]benzodioxol-5-yl ester, (2Z)- schisanhenol Gomisin B(Schisantherin B) Masoprocol SCHISANDROL B (GOMISIN A)(P),SCHISANDROL B(GOMISIN A) SNAP-N-SHOOT 0.1mg/mL(P),Gomisin A(Schisandrol B) SCHISANTHERIN A Dihydromyristicin