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Merck

SML0786

Sigma-Aldrich

Decursin

≥97% (HPLC)

别名:

(+)-Decursin, (7S)-7,8-Dihydro-8,8-dimethyl-2-oxo-2H,6H-benzo[1,2-b:5,4-b′]dipyran-7-yl 3-methyl-2-butenoate, 3-Methyl-2-butenoic acid (7S)-7,8-dihydro-8,8-dimethyl-2-oxo-2H,6H-pyrano[3,2-g]-1-benzopyran-7-yl ester

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About This Item

经验公式(希尔记法):
C19H20O5
CAS号:
分子量:
328.36
MDL號碼:
分類程式碼代碼:
12352200
NACRES:
NA.77

生物源

Radix peucedani

品質等級

化驗

≥97% (HPLC)

形狀

powder

光學活性

[α]/D +120 to +160°, c = 0.5 in chloroform-d

顏色

white to beige

溶解度

DMSO: 5 mg/mL, clear

運輸包裝

wet ice

儲存溫度

−20°C

InChI

1S/C19H20O5/c1-11(2)7-18(21)23-16-9-13-8-12-5-6-17(20)22-14(12)10-15(13)24-19(16,3)4/h5-8,10,16H,9H2,1-4H3/t16-/m0/s1

InChI 密鑰

CUKSFECWKQBVED-INIZCTEOSA-N

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生化/生理作用

Decursin is a cumarin isolated from Radix peucedani that exhibits a number of physiological actions including anticancer, antibacterial, antinematodal and antioxidant. Decursin is potent anti-angiogenic agent targeting the VEGFR-2 signaling pathway. Decursin exhibits potent neuroprotective activity against glutamate and Ab- induced neurotoxicity. Apparently, decursin stimulates activation of Nerf2. Also, decursin inhibits androgen stimulated AR translocation to the nucleus in LNCaP prostate cancer cells.

特點和優勢

This compound is featured on the Nuclear Receptors (Steroids) page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

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


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Jin-Taek Hwang et al.
Phytotherapy research : PTR, 26(5), 633-638 (2011-10-06)
Decursin (De), an active component of Angelica gigas, is known to exert anticancer and neuroprotective effects. However, its antiobesity and antidiabetic potential has not yet been investigated. This study evaluated the antiobesity effect of decursin, particularly focusing on its ability
Tariq A Bhat et al.
Indian journal of experimental biology, 49(11), 848-856 (2011-12-01)
The present study was undertaken to observe the inhibition of angiogenesis by decursin. It was the first time to show that decursin offered strong anti-angiogenic activities under the biologically relevant growth (with serum) conditions. Decursin significantly inhibited human umbilical vein
Seung Hwa Son et al.
Phytotherapy research : PTR, 25(7), 959-964 (2010-12-21)
The principal objective of the present study was to evaluate the antimetastatic activity of decursin and decursinol isolated from Angelica gigas. Decursin and decursinol inhibited the proliferation and invasion of CT-26 colon carcinoma cells. The expressions of matrix metalloproteinase (MMP)-2
Bimit Mahat et al.
Drug development and industrial pharmacy, 39(10), 1523-1530 (2012-09-26)
Angelica gigas Nakai and its components are known to have neuroprotective, antiplatelet, and anticancer activities. The present study evaluated the in vitro and in vivo biopharmaceutical characterization of Angelica gigas component substances, including decursin (the main substance), decursinol angelate (decursin
Jung-woo Chae et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 50(10), 3666-3672 (2012-07-10)
Herb-drug interactions represent a serious problem as herbal medicine is used extensively in the modern world. This study investigated the effects of decursinol angelate on the pharmacokinetics of theophylline, a typical substrate of the cytochrome P450 1A2 enzyme, in rats.

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