(E)-Methyl caffeate
(E)-Methyl caffeate is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
For research use only. We do not sell to patients.
- CAS No.: 67667-67-8
- Formula: C10H10O4
- Molecular Weight:194.18
-
Storage:
4°C, stored under nitrogen
* In solvent : -80°C, 6 months; -20°C, 1 month (stored under nitrogen)
Biological Activity
|
Cell Line
|
Type | Value | Description | References |
|---|---|---|---|---|
| A-431 | IC50 |
1.79 μg/mL
Compound: 4a
|
Inhibitory concentration required against A 431 human epidermoid carcinoma cell line
Inhibitory concentration required against A 431 human epidermoid carcinoma cell line
|
[PMID: 11354370] |
| A549 | IC50 |
7.54 μM
Compound: 2a
|
Cytotoxicity against human A549 cells after 72 hrs by alamar blue assay
Cytotoxicity against human A549 cells after 72 hrs by alamar blue assay
|
[PMID: 22954735] |
| B16 | IC50 |
2.96 μg/mL
Compound: 4a
|
Inhibitory concentration against B16 murine melanoma cell line
Inhibitory concentration against B16 murine melanoma cell line
|
[PMID: 11354370] |
| BeWo | IC50 |
17.27 μM
Compound: I-1
|
Antitumor activity against human Bewo cells assessed as inhibition of cell growth by MTT assay
Antitumor activity against human Bewo cells assessed as inhibition of cell growth by MTT assay
|
[PMID: 25160837] |
| Calu-1 | IC50 |
5.5 μM
Compound: 2a
|
Cytotoxicity against human Calu1 cells after 72 hrs by alamar blue assay
Cytotoxicity against human Calu1 cells after 72 hrs by alamar blue assay
|
[PMID: 22954735] |
| HCT-116 | IC50 |
3.01 μg/mL
Compound: 4a
|
Inhibitory concentration against HCT 116 human colon cancer cell line
Inhibitory concentration against HCT 116 human colon cancer cell line
|
[PMID: 11354370] |
| HeLa | IC50 |
3.77 μM
Compound: 2a
|
Cytotoxicity against human HeLa cells after 72 hrs by alamar blue assay
Cytotoxicity against human HeLa cells after 72 hrs by alamar blue assay
|
[PMID: 22954735] |
| HeLa | IC50 |
52.53 μM
Compound: I-1
|
Antitumor activity against human HeLa cells assessed as inhibition of cell growth by MTT assay
Antitumor activity against human HeLa cells assessed as inhibition of cell growth by MTT assay
|
[PMID: 25160837] |
| HepG2 | IC50 |
81.55 μM
Compound: I-1
|
Antitumor activity against human HepG2 cells assessed as inhibition of cell growth by MTT assay
Antitumor activity against human HepG2 cells assessed as inhibition of cell growth by MTT assay
|
[PMID: 25160837] |
| HL-60 | IC50 |
12.32 μM
Compound: I-1
|
Antitumor activity against human HL60 cells assessed as inhibition of cell growth by MTT assay
Antitumor activity against human HL60 cells assessed as inhibition of cell growth by MTT assay
|
[PMID: 25160837] |
| HL-60 | IC50 |
7.5 μM
Compound: 4
|
Cytotoxicity against human HL60 cells after 72 hrs by MTT assay
Cytotoxicity against human HL60 cells after 72 hrs by MTT assay
|
[PMID: 15387667] |
| HOP-62 | IC50 |
3.86 μM
Compound: 2a
|
Cytotoxicity against human HOP62 cells after 72 hrs by alamar blue assay
Cytotoxicity against human HOP62 cells after 72 hrs by alamar blue assay
|
[PMID: 22954735] |
| HT-1080 | IC50 |
11.1 μM
Compound: 4
|
Cytotoxicity against human HT1080 cells after 72 hrs by MTT assay
Cytotoxicity against human HT1080 cells after 72 hrs by MTT assay
|
[PMID: 15387667] |
| KB | IC50 |
>200 μM
Compound: 1d
|
Antitumor activity against KB cells by MTT assay
Antitumor activity against KB cells by MTT assay
|
[PMID: 17387015] |
| LNCaP | IC50 |
>100 μM
Compound: 3
|
Cytotoxicity against human LNCAP cells assessed as reduction in cell viability after 24 hrs by WST-1 assay
Cytotoxicity against human LNCAP cells assessed as reduction in cell viability after 24 hrs by WST-1 assay
|
[PMID: 24080105] |
| LoVo | IC50 |
>40 μM
Compound: 4
|
Cytotoxicity against human doxorubicin-resistant LoVo cells after 72 hrs by MTT assay
Cytotoxicity against human doxorubicin-resistant LoVo cells after 72 hrs by MTT assay
|
[PMID: 15387667] |
| LoVo | IC50 |
5.8 μM
Compound: 4
|
Cytotoxicity against human LoVo cells after 72 hrs by MTT assay
Cytotoxicity against human LoVo cells after 72 hrs by MTT assay
|
[PMID: 15387667] |
| LOX IMVI | IC50 |
21.8 μM
Compound: 2a
|
Cytotoxicity against human LOXIMVI cells after 72 hrs by alamar blue assay
Cytotoxicity against human LOXIMVI cells after 72 hrs by alamar blue assay
|
[PMID: 22954735] |
| M14 | IC50 |
8.86 μM
Compound: 2a
|
Cytotoxicity against human M14 cells after 72 hrs by alamar blue assay
Cytotoxicity against human M14 cells after 72 hrs by alamar blue assay
|
[PMID: 22954735] |
| NCI-H1299 | IC50 |
3.53 μM
Compound: 2a
|
Cytotoxicity against human NCI-H1299 cells after 72 hrs by alamar blue assay
Cytotoxicity against human NCI-H1299 cells after 72 hrs by alamar blue assay
|
[PMID: 22954735] |
| NCI-H157 | IC50 |
6.25 μM
Compound: 2a
|
Cytotoxicity against human NCI-H157 cells after 72 hrs by alamar blue assay
Cytotoxicity against human NCI-H157 cells after 72 hrs by alamar blue assay
|
[PMID: 22954735] |
| NCI-H1792 | IC50 |
6.09 μM
Compound: 2a
|
Cytotoxicity against human NCI-H1792 cells after 72 hrs by alamar blue assay
Cytotoxicity against human NCI-H1792 cells after 72 hrs by alamar blue assay
|
[PMID: 22954735] |
| NCI-H460 | IC50 |
14.8 μM
Compound: 2a
|
Cytotoxicity against human H460 cells after 72 hrs by alamar blue assay
Cytotoxicity against human H460 cells after 72 hrs by alamar blue assay
|
[PMID: 22954735] |
| Oocyte | IC50 |
388 μM
Compound: Caf-COOMe, methyl caffeate
|
Antagonist activity at Gloeobacter violaceus ligand-gated ion channel expressed in Xenopus oocytes assessed as inhibition of MES buffer pH 5.5 -induced currents after 30 secs by voltage clamp technique
Antagonist activity at Gloeobacter violaceus ligand-gated ion channel expressed in Xenopus oocytes assessed as inhibition of MES buffer pH 5.5 -induced currents after 30 secs by voltage clamp technique
|
[PMID: 23682762] |
| RAW264.7 | EC50 |
3.199 μM
Compound: 2, methyl caffeate
|
Inhibition of LPS-induced nitric oxide production in mouse RAW264.7 cells assessed as nitrite accumulation administered 1 hr before LPS challenge and measured after 24 hrs by Griess reagent assay
Inhibition of LPS-induced nitric oxide production in mouse RAW264.7 cells assessed as nitrite accumulation administered 1 hr before LPS challenge and measured after 24 hrs by Griess reagent assay
|
[PMID: 18667320] |
| RAW264.7 | EC50 |
367.5 μM
Compound: 2, methyl caffeate
|
Cytotoxicity against mouse RAW264.7 cells assessed as cell survival after 24 hrs by MTT assay
Cytotoxicity against mouse RAW264.7 cells assessed as cell survival after 24 hrs by MTT assay
|
[PMID: 18667320] |
| RAW264.7 | IC50 |
>0.3 μM/mL
Compound: 31
|
Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-induced nitric oxide production after 24 hrs
Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-induced nitric oxide production after 24 hrs
|
[PMID: 18986199] |
| RAW264.7 | IC50 |
3.9 μM
Compound: 29
|
Antiinflammatory activity against LPS-stimulated mouse RAW264.7 cells assessed as decrease in PGE2 production preincubated for 1 hr followed by LPS stimulation and measured after 24 hrs by ELISA
Antiinflammatory activity against LPS-stimulated mouse RAW264.7 cells assessed as decrease in PGE2 production preincubated for 1 hr followed by LPS stimulation and measured after 24 hrs by ELISA
|
[PMID: 31747281] |
| SGC-7901 | IC50 |
>100 μM
Compound: I-1
|
Antitumor activity against human SGC7901 cells assessed as inhibition of cell growth by MTT assay
Antitumor activity against human SGC7901 cells assessed as inhibition of cell growth by MTT assay
|
[PMID: 25160837] |
| SiHa | IC50 |
60.26 μM
Compound: I-1
|
Antitumor activity against human SiHa cells assessed as inhibition of cell growth by MTT assay
Antitumor activity against human SiHa cells assessed as inhibition of cell growth by MTT assay
|
[PMID: 25160837] |
Chemical Information
-
CAS No. 67667-67-8
-
Appearance Solid
-
Molecular Weight 194.18
-
Formula C10H10O4
-
Color White to off-white
-
SMILES
COC(/C=C/C1=CC(O)=C(C=C1)O)=O
-
Shipping
Room temperature in continental US; may vary elsewhere.
-
Storage
4°C, stored under nitrogen
* In solvent : -80°C, 6 months; -20°C, 1 month (stored under nitrogen)
Purity & Documentation
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Data Sheet (239 KB)
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SDS (252 KB)
- Français - FR (252 KB)
- Deutsch - DE (252 KB)
- Norwegian - NO (252 KB)
- Español - ES (252 KB)
- Swedish - SV (252 KB)
- Italian - IT (252 KB)
- Korean - KR (252 KB)
- Portuguese - PT (252 KB)
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Handling Instructions (2659 KB)
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)