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Cat. No. Product Name Target Signaling Pathways
T2868 Evodiamine

d-Evodiamine,Isoevodiamine,(+)-Evodiamine,吴茱萸碱

Prostaglandin Receptor GPCR/G Protein; Immunology/Inflammation
Evodiamine (d-Evodiamine) 是一种生物碱,从萱草的果实中分离得到,具有多种生物活性,包括抗炎,抗肥胖和抗肿瘤。
T75424 (±)-Evodiamine

(±)-Evodiamine,一种天然生物碱,作为Top1的抑制剂,展现了抗炎、抗肥胖及抗肿瘤特性。(±)-Evodiamine能够通过诱导细胞凋亡来抑制多种肿瘤细胞的增殖。
T5721 Dehydroevodiamine hydrochloride

AChE Neuroscience
Dehydroevodiamine hydrochloride 是分离自吴茱萸叶中,能够抑制 AChE。 它能够调节一氧化氮的产生,具有降压和神经保护作用。
T2S2335 Dehydroevodiamine

DHED,去氢吴茱萸碱

Others; NF-κB; COX; PGE Synthase; NO Synthase Immunology/Inflammation; Neuroscience; NF-κB; Others
Dehydroevodiamine (DHED) 是从吴茱萸中分离出的一种喹唑啉生物碱,可抑制 LPS 诱导的小鼠巨噬细胞中iNOS、COX-2、PGE2和NF-κB 的表达,对豚鼠心室肌细胞具有抗心律失常作用。
TN1752 Hydroxyevodiamine

Others Others
Hydroxyevodiamine is a natural product
TN2553 1-Methyl-2-undecyl-4(1H)-quinolone

1-Methyl-2-undecylquinolin-4(1H)-one

MAO Metabolism; Neuroscience
1-Methyl-2-undecyl-4(1H)-quinolone, and dihydroevocarpine should also be served as the chemical markers together with evodiamine for the quality control of Evodia rutaecarpa (Juss.) Benth. 1-Methyl-2-undecyl-4(1H)-quinolone shows a selective inhibition of type B MAO (MAO-B) activity with the IC(50) value of 15.3 microM using a substrate kynuramine, but does not inhibit type A MAO (MAO-A) activity.It can mitigate high phosphate-induced human aortic valve interstitial cells (HAVICs) calcification ...

天然产物

Evodiamine
Cat.No: T2868
Synonym: d-Evodiamine,Isoevodiamine,(+)-Evodiamine,吴茱萸碱
Target: Prostaglandin Receptor
(±)-Evodiamine
Cat.No: T75424
Synonym:
Target:
Dehydroevodiamine hydrochloride
Cat.No: T5721
Synonym:
Target: AChE
Dehydroevodiamine
Cat.No: T2S2335
Synonym: DHED,去氢吴茱萸碱
Target: Others, NF-κB, COX, PGE Synthase, NO Synthase
Hydroxyevodiamine
Cat.No: TN1752
Synonym:
Target: Others
1-Methyl-2-undecyl-4(1H)-quinolone
Cat.No: TN2553
Synonym: 1-Methyl-2-undecylquinolin-4(1H)-one
Target: MAO
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