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经验公式(希尔记法):
C20H18O5
化学文摘社编号:
分子量:
338.35
UNSPSC Code:
12352205
PubChem Substance ID:
NACRES:
NA.77
MDL number:
产品名称
去甲氧基姜黄素, ≥98% (HPLC)
SMILES string
COc1cc(\C=C\C(=O)CC(=O)\C=C\c2ccc(O)cc2)ccc1O
InChI key
HJTVQHVGMGKONQ-LUZURFALSA-N
InChI
1S/C20H18O5/c1-25-20-12-15(6-11-19(20)24)5-10-18(23)13-17(22)9-4-14-2-7-16(21)8-3-14/h2-12,21,24H,13H2,1H3/b9-4+,10-5+
assay
≥98% (HPLC)
form
powder
storage condition
protect from light
color
orange
solubility
DMSO: ≥10 mg/mL
storage temp.
2-8°C
Quality Level
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相关类别
Biochem/physiol Actions
脱甲氧基姜黄素 (DMC) 是一种衍生物或姜黄素,是从 姜黄中分离得到的姜黄素产品的主要活性成分之一。DMC通过阻止NF-kB激活来抑制LPS诱导的一氧化氮(NO)产生以及RAW264.7细胞中iNOS和COX2的表达。在LPS处理的大鼠小胶质细胞中,DMC也抑制NF-kB对iNOS,TNFα和IL-1β的表达。DMC通过抑制NF-kB抑制MDA-MB-231人乳腺癌细胞中MMP和ICAM-1的表达。
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Hye Jin Kim et al.
Phytochemical analysis : PCA, 20(5), 372-377 (2009-06-18)
The new ion source technique, direct analysis in real time (DART) atmospheric pressure ionisation, allows high resolution mass measurements of gas, liquid and solid samples. As DART-MS produces [M + H](+) molecular ions of most compounds, relatively simple and clear
T Ahmed et al.
Neuroscience, 169(3), 1296-1306 (2010-06-12)
Alzheimer's disease (AD) is a neurodegenerative disease. There are a limited number of therapeutic options available for the treatment of AD. Curcuminoids (a mixture of bisdemethoxycurcumin, demethoxycurcumin and curcumin) is the main chemical constituent found in turmeric, a well known
Supachai Yodkeeree et al.
European journal of pharmacology, 627(1-3), 8-15 (2009-10-13)
Demethoxycurcumin (DMC) is one of the main active compounds of curcuminoids found in turmeric powder, which is used as a spice in Asian cooking and traditional medicine. Recent studies reveal that DMC has several biological activities including anti-inflammation and anti-cancer
Lijia Zhang et al.
International immunopharmacology, 10(3), 331-338 (2009-12-19)
Our previous report has showed that demethoxycurcumin (DMC), a natural derivative of curcumin (Cur), exhibited stronger inhibitory activity on nitric oxide (NO) and tumor necrosis factor-alpha (TNF-alpha) production compared with Cur in lipopolysaccharide (LPS) activated rat primary microglia. In the
Reactions of reactive oxygen species (ROS) with curcumin analogues: Structure-activity relationship.
Umang Singh et al.
Free radical research, 45(3), 317-325 (2010-11-03)
Three curcumin analogues viz., bisdemethoxy curcumin, monodemethoxy curcumin, and dimethoxycurcumin that differ at the phenolic substitution were synthesized. These compounds have been subjected for free radical reactions with DPPH radicals, superoxide radicals (O(2)(•-)), singlet oxygen ((1)O(2)) and peroxyl radicals (CCl(3)O(2)(•))
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