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线性分子式:
[HOC6H3(OCH3)CH=CHCO]2CH2
化学文摘社编号:
分子量:
368.38
EC Number:
207-280-5
UNSPSC Code:
41115710
NACRES:
NA.21
PubChem Substance ID:
MDL number:
Colour Index Number:
75300
Beilstein/REAXYS Number:
2306965
产品名称
姜黄素, suitable for matrix substance for MALDI-MS, ≥99.5% (HPLC)
InChI key
VFLDPWHFBUODDF-FCXRPNKRSA-N
InChI
1S/C21H20O6/c1-26-20-11-14(5-9-18(20)24)3-7-16(22)13-17(23)8-4-15-6-10-19(25)21(12-15)27-2/h3-12,24-25H,13H2,1-2H3/b7-3+,8-4+
SMILES string
COc1cc(\C=C\C(=O)CC(=O)\C=C\c2ccc(O)c(OC)c2)ccc1O
vapor density
13 (vs air)
assay
≥99.5% (HPLC)
form
powder
technique(s)
MALDI-MS: suitable
mp
183-188 °C
cation traces
Na: ≤50 mg/kg
suitability
suitable for matrix substance for MALDI-MS
storage temp.
2-8°C
Quality Level
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Application
- Hybrid Ethylcellulose Polymeric Films: Ag(I)-Based Components and Curcumin as Reinforcing Ingredients for Enhanced Food Packaging Properties:本文开发一种掺入姜黄素的杂化乙基纤维素膜来改进食品包装,说明本品在组分相容性和性能评估方面的分析化学应用(Crispini A et al., 2024)。
- Intelligent double-layer film based on gellan gum/modified anthocyanin/curcumin/sodium alginate/zinc oxide for monitoring shrimp freshness:本文制造一种含有姜黄素的智能膜用于实时监测虾新鲜度,体现姜黄素在食品安全和保质期延长中的实用性(Li C et al., 2024)。
- Cyclodextrin-grafted redox-responsive hydrogel mediated by disulfide bridges for regulated drug delivery:本文研究一种含姜黄素的环糊精水凝胶,说明姜黄素开发先进给药系统的作用,体现靶向治疗应用潜力(Xu X et al., 2024)。
Biochem/physiol Actions
一种天然酚类化合物。它是有效的抗肿瘤剂,具有抗炎和抗氧化活性。除了具有化疗活性外,姜黄素还被认为是潜在的化学预防剂。它能够诱导癌细胞凋亡并抑制佛波酯诱导的蛋白激酶C(PKC)活性。据报道,它能抑制外周血单核细胞和肺泡巨噬细胞产生炎性细胞因子。它是EGFR酪氨酸激酶和IκB激酶的有效抑制剂。它能抑制诱导型一氧化氮合酶(iNOS)、环加氧酶和脂氧合酶。它易于渗透到细胞质中,在质膜、内质网和核膜等膜结构中积累。
它是一种天然酚类化合物,是姜黄的黄色来源。它是有效的抗肿瘤剂,作用于高度多样化的肿瘤特异性通路。它具有抗炎和抗氧化活性。它能够诱导癌细胞凋亡并抑制佛波酯诱导的蛋白激酶C(PKC)活性。据报道,它能抑制外周血单核细胞和肺泡巨噬细胞产生炎性细胞因子。它是EGFR酪氨酸激酶和IκB激酶的有效抑制剂。它能抑制诱导型一氧化氮合酶(iNOS)、环加氧酶(COX-2)和5-脂氧合酶(5-LOX)。
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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The anticarcinogenic and anti-inflammatory properties of curcumin have been extensively investigated, identifying prostaglandin E2 synthase (mPGES)-1 and 5-lipoxygenase (5-LO), key enzymes linking inflammation with cancer, as high affinity targets. A comparative structure-activity study revealed three modifications dissecting mPGES-1/5-LO inhibition, namely
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