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Key Documents

SMB00379

Sigma-Aldrich

Schisantherin A

≥98% (HPLC)

同義詞:

Gomisin C, Schizantherin A, Wuweizi ester A

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About This Item

經驗公式(希爾表示法):
C30H32O9
CAS號碼:
分子量::
536.57
分類程式碼代碼:
12352200
PubChem物質ID:
NACRES:
NA.25

化驗

≥98% (HPLC)

形狀

powder

應用

metabolomics
vitamins, nutraceuticals, and natural products

儲存溫度

−20°C

SMILES 字串

CC1(O)C(C)CC2=CC(OCO3)=C3C(OC)=C2C4=C(C=C(OC)C(OC)=C4OC)C1OC(C5=CC=CC=C5)=O

InChI

1S/C30H32O9/c1-16-12-18-13-21-25(38-15-37-21)26(35-5)22(18)23-19(14-20(33-3)24(34-4)27(23)36-6)28(30(16,2)32)39-29(31)17-10-8-7-9-11-17/h7-11,13-14,16,28,32H,12,15H2,1-6H3

InChI 密鑰

UFCGDBKFOKKVAC-UHFFFAOYSA-N

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生化/生理作用

Schisantherin A is a lignan isolated from the fruits of Schisandra chinesi.
Schisantherin A is a mechanism-based inhibitor that competitively inhibits and irreversibly inactivates CYP3A4.
Schisantherin A (StA) has neuroprotective activity and could be potential candidate for the treatment of neuron loss in neurodegenerative diseases including Parkinson′s disease. It inhibits tumor progression and could be a potential drug target for cancer treatment. StA blocks ATP-binding cassette transporters and restores the levels of anti-cancer drugs in cancer cells. It also has anti-inflammatory property.

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


分析證明 (COA)

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存取文件庫

Discovery of novel anti-parkinsonian effect of schisantherin A in in vitro and in vivo.
Sa F, et al.
Neuroscience Letters, 593, 7-12 (2015)
Lignans from Schisandra sphenathera Rehd. et Wils. and semisynthetic schisantherin A analogues: absolute configuration, and their estrogenic and anti-proliferative activity.
Liu H W, et al.
European Journal of Medicinal Chemistry, 59, 265-273 (2013)
Schisantherin A suppresses interleukin-1β-induced inflammation in human chondrocytes via inhibition of NF-κB and MAPKs activation.
Liao S, et al.
European Journal of Pharmacology, 780, 65-70 (2016)
Identification and characterization of potent CYP3A4 inhibitors in Schisandra fruit extract
Iwata H, et al.
Drug Metabolism and Disposition (2004)
Synthesis of the first unnatural schisantherins and their effects in multidrug-resistant cancer cells.
Schobert R, et al.
Tetrahedron Letters, 49(21), 3359-3362 (2008)

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