Terrein
Modify Date: 2025-08-25 17:24:30
Terrein structure
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Common Name | Terrein | ||
|---|---|---|---|---|
| CAS Number | 582-46-7 | Molecular Weight | 154.16300 | |
| Density | 1.449g/cm3 | Boiling Point | 327.2ºC at 760mmHg | |
| Molecular Formula | C8H10O3 | Melting Point | N/A | |
| MSDS | Chinese USA | Flash Point | 165.9ºC | |
Use of TerreinTerrein is a melanogenesis inhibitor[1]. Terrein induces apoptosis in breast cancer cell lines [2]. Terrein is an inhibitor of quorum sensing and c-di-GMP in Pseudomonas aeruginosa[3]. |
| Name | 2-Cyclopenten-1-one, 4,5-dihydroxy-3-(1-propenyl) |
|---|---|
| Synonym | More Synonyms |
| Description | Terrein is a melanogenesis inhibitor[1]. Terrein induces apoptosis in breast cancer cell lines [2]. Terrein is an inhibitor of quorum sensing and c-di-GMP in Pseudomonas aeruginosa[3]. |
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| Related Catalog | |
| In Vitro | Treatment of Mel-Ab cells with Terrein (10-100 µM) for 4 days significantly reduces melanin levels in a dose-dependent manner. Terrein reduces melanin synthesis by reducing tyrosinase production via ERK activation[1]. Terrein (5-500 µM; 24 and 48 hours) reduces the viability of these cells in concentration- and time-dependent manners[2]. Terrein (150, 250, 500µM; 24 hours) induces programmed cell death in both invasive and non-invasive breast cancer cell lines. Thus, the optimal non-toxic concentrations of Terrein (25 and 75 µM) were used for subsequent experiments[2]. Terrein (25 and 75 µM) significantly decrease the mRNA levels of both MMP-2 and MMP-9 in MDA-MB-231 cells. Terrein (75 µM) significantly decrease the mRNA levels of both MMP-2 and MMP-9 in MCF-7 cells[2]. Terrein (75 µM) inhibits the expression of RhoA, RhoB, p-Rac1 in MCF-7 cells. Terrein (75 µM) inhibits the expression of RhoB, p-Rac1 in MDA-MB-231 cells[2]. Terrein (10, 30, and 100 μM) inhibits the production of virulence factors such as elastase, pyocyanin, and rhamnolipid, as well as biofilm formation in P. aeruginosa PAO1 and PA14 strains[3]. Cell Viability Assay[2] Cell Line: MCF-7 and MDA-MB-231 cells Concentration: 5, 25, 50, 75, 100, 150, 250, 500 µM Incubation Time: 24 and 48 hours Result: The IC50s for MCF-7 and MDA-MB-231 cells after 24 h of incubation were 2.34 mM and 700 µM, respectively. After 48 h of incubation, the IC50s are 244.3 µM for MCF-7 and 244.5 µM for MDA-MB-231 cells. Apoptosis Analysis[2] Cell Line: MCF-7 and MDA-MB-231 cells Concentration: 25, 75, 150, 250, 500 µM Incubation Time: 24 hours Result: The percentages of apoptotic cells after 25 and 75 µM treatment were 7.52 and 5.82%, respectively for MCF-7 cells (9.94% for the control), and 15.77 and 15.82%, respectively for MDA-MB-231 cells (8.79% for the control). RT-PCR[2] Cell Line: MCF-7 and MDA-MB-231 cells Concentration: 25, 75 µM Incubation Time: Result: Decreased the mRNA levels of both MMP-2 and MMP-9 in a concentration-dependent manner. Western Blot Analysis[2] Cell Line: MCF-7 and MDA-MB-231 cells Concentration: 75 µM Incubation Time: 6, 12 and 24 hours Result: RhoA and RhoB protein levels were significantly decreased after 6 h of 75 µM treatment in MCF-7 cells. Phosphorylated (p)-Rac1 was also slightly decreased at 12 h. However, RhoC and Cdc42 levels remained unchanged. RhoB protein levels and Rac1 phosphorylation were also decreased in MDA-MB-231 cells at 12 and 24 h, respectively. |
| References |
| Density | 1.449g/cm3 |
|---|---|
| Boiling Point | 327.2ºC at 760mmHg |
| Molecular Formula | C8H10O3 |
| Molecular Weight | 154.16300 |
| Flash Point | 165.9ºC |
| Exact Mass | 154.06300 |
| PSA | 57.53000 |
| Index of Refraction | 1.713 |
| RIDADR | NONH for all modes of transport |
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| Precursor 0 | |
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| DownStream 1 | |
CAS#:64-18-6|
Name: USP8 deubiquitinase inhibition: Primary qHTS
Source: 24642
Target: ubiquitin specific peptidase 8
External Id: USP8 FAST DUB HTS Primary
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Name: USP17 deubiquitinase inhibition: Primary qHTS
Source: 24642
Target: ubiquitin specific peptidase 17 like family member 5
External Id: USP17 FAST DUB HTS Primary
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Name: USP7 deubiquitinase inhibition: Primary qHTS
Source: 24642
Target: ubiquitin specific peptidase 7
External Id: USP7 FAST DUB HTS Primary
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Name: Primary high throughput screening by co-culture imaging for identification hits as a ...
Source: 23209
Target: N/A
External Id: UIHTS20180925
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Name: Discovering small molecule activators of G protein-gated inwardly-rectifying potassiu...
Source: 15621
Target: G protein-activated inward rectifier potassium channel 2
External Id: VANDERBILT_HTS_GIRK2_MPD
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Name: Cytotoxicity against HGF cells assessed as reduction in cell proliferation at >50 uM ...
Source: ChEMBL
Target: N/A
External Id: CHEMBL3373792
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Name: Cytotoxicity against HGF cells assessed as cell proliferation at <10 uM incubated for...
Source: ChEMBL
Target: N/A
External Id: CHEMBL3373791
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Name: Inhibition of IL-6/soluble IL-6 receptor signaling-induced STAT3 phosphorylation in H...
Source: ChEMBL
Target: N/A
External Id: CHEMBL3373794
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Name: Inhibition of IL-6/soluble IL-6 receptor signaling-induced VEGF secretion in HGF cell...
Source: ChEMBL
Target: N/A
External Id: CHEMBL3373793
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Name: USP28 deubiquitinase inhibition: Primary qHTS
Source: 24642
Target: ubiquitin specific peptidase 28
External Id: USP28 FAST DUB HTS Primary
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| trans-(4S,5R)-4,5-dihydroxy-3-[(E)-1-propenyl]-2-cyclopenten-1-one |
| trans-4,5-dihydroxy-3-propenyl-2-cylopenten-1-one |
| (4S)-4r,5t-dihydroxy-3-trans-propenyl-cyclopent-2-enone |
| (4S,5R)-4,5-Dihydroxy-3-[(E)-1-propenyl]-2-cyclopenten-1-one |
| trans-2,3-dihydroxy-4-propenylcyclopent-4-enone |
| TERREIN |