货号:A202087
同义名:
3-苯基-2-丙烯酸甲酯
/ Methyl 3-phenylpropenoate
Methyl cinnamate是肉桂酸的甲基酯,广泛存在于多种植物中,可用于香料和香水工业。


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| 产品名称 | diphenolase ↓ ↑ | monophenolase ↓ ↑ | tyrosinase ↓ ↑ | 其他靶点 | 纯度 | ||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Hexylresorcinol |
+++
diphenolase, IC50: 0.85 μM |
++
monophenolase, IC50: 1.24 μM |
+++
diphenolase, IC50: 0.85 μM monophenolase, IC50: 0.85 μM |
99%+ | |||||||||||||||
| Aloin | ✔ | 98% (mixture of A&B) | |||||||||||||||||
| Arbutin |
+
tyrosinase, IC50: 1.09 mM |
98% | |||||||||||||||||
| Monobenzone | ✔ | 98% | |||||||||||||||||
| Deoxyarbutin |
++++
tyrosinase, IC50: 50 nM |
98% | |||||||||||||||||
| 1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。 | |||||||||||||||||||
| Concentration | Treated Time | Description | References | |
| Pre-osteoblast MC3T3-E1 | 10 and 30 µM | 7 days | To investigate the effect of EMC on pre-osteoblast differentiation. EMC inhibited osteoblast differentiation induced by OS, reducing ALP staining and activity. | Int J Mol Sci. 2020 May 24;21(10):3700 |
| Pre-osteoblast MC3T3-E1 | 10 and 30 µM | 24 hours | To investigate the effect of EMC on pre-osteoblast migration. EMC significantly suppressed the cell migration rate. | Int J Mol Sci. 2020 May 24;21(10):3700 |
| Pre-osteoblast MC3T3-E1 | 10 and 30 µM | 24 hours | To investigate the effect of EMC on pre-osteoblast apoptosis. EMC significantly increased the cleaved forms of PARP and caspase-3 and decreased the expression levels of Survivin and Bcl-2. | Int J Mol Sci. 2020 May 24;21(10):3700 |
| Pre-osteoblast MC3T3-E1 | 1, 10, 30, 100 µM | 24 and 48 hours | To evaluate the effect of EMC on pre-osteoblast survival. EMC significantly inhibited cellular proliferation in a time- and dose-dependent manner. | Int J Mol Sci. 2020 May 24;21(10):3700 |
| Peritoneal elucidated macrophages (PEMs) | 25, 50, 100 μM | 24 hours | To evaluate the inhibitory effect of methyl cinnamate on LPS-induced inflammatory response. Results showed that methyl cinnamate significantly reduced the expression levels of TNF-α, IL-1β, and IL-6. | Acta Biochim Biophys Sin (Shanghai). 2023 Nov 25;55(11):1806-1818 |
| RAW264.7 cells | 25, 50, 100 μM | 24 hours | To evaluate the inhibitory effect of methyl cinnamate on LPS-induced inflammatory response. Results showed that methyl cinnamate significantly reduced the expression levels of TNF-α, IL-1β, and IL-6. | Acta Biochim Biophys Sin (Shanghai). 2023 Nov 25;55(11):1806-1818 |
| HepG2 cells | 100μM | 24 hours | To study the effect of MC on lipid accumulation in HepG2 cells, results showed MC significantly reduced FFAs-induced lipid accumulation. | Diabetes Metab Syndr Obes. 2024 Mar 7;17:1183-1197 |
| HepG2 cells | 12.5, 25, 50, 100, 200, 400, 800μM | 24, 48, 72 hours | To assess cell viability, results showed no significant changes in cell viability after 24 and 48 hours, but a significant decrease at 400μM and 800μM concentrations after 72 hours. | Diabetes Metab Syndr Obes. 2024 Mar 7;17:1183-1197 |
| Administration | Dosage | Frequency | Description | References | ||
| C57BL/6 mice | DSS-induced colitis model | Oral | 20 mg/kg, 40 mg/kg | Once daily for 14 days | To evaluate the therapeutic effects of methyl cinnamate on DSS-induced colitis. Results showed that methyl cinnamate significantly alleviated symptoms such as weight loss, increased disease activity index score, and colon shortening, and inhibited the overexpression of pro-inflammatory cytokines. | Acta Biochim Biophys Sin (Shanghai). 2023 Nov 25;55(11):1806-1818 |
| 计算器 | ||||
| 存储液制备 | ![]() |
1mg | 5mg | 10mg |
|
1 mM 5 mM 10 mM |
6.17mL 1.23mL 0.62mL |
30.83mL 6.17mL 3.08mL |
61.66mL 12.33mL 6.17mL |
|
| CAS号 | 103-26-4 |
| 分子式 | C10H10O2 |
| 分子量 | 162.19 |
| SMILES Code | O=C(OC)/C=C/C1=CC=CC=C1 |
| MDL No. | MFCD00008458 |
| 别名 | 3-苯基-2-丙烯酸甲酯 ;Methyl 3-phenylpropenoate |
| 运输 | 蓝冰 |
| InChI Key | CCRCUPLGCSFEDV-BQYQJAHWSA-N |
| Pubchem ID | 637520 |
| 存储条件 |
In solvent -20°C:3-6个月-80°C:12个月 |
| 溶解方案 |
DMSO: 105 mg/mL(647.41 mM),注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO H2O: 1 mg/mL(6.17 mM),配合低频超声助溶 以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
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