Name | SB 3CT |
Synonyms | SB 3CT CS-860 SB-3CT [[(4-Phenoxyphenyl)sulfonyl]methyl]thiirane 2-[[(4-phenoxyphenyl)sulfonyl]methyl]-thiirane SB-3CT (This product is only available in Japan.) |
CAS | 292605-14-2 |
Molecular Formula | C15H14O3S2 |
Molar Mass | 306.4 |
Melting Point | 92-96°C |
Solubility | DMSO: 30.6 mg/mL (100 mM)Ethanol: 6.1 mg/mL (20 mM)( < 1 mg/ml refers to the product slightly soluble or insoluble) |
Appearance | powder |
Color | white to off-white |
Storage Condition | -20°C |
Use | SB-3CT is an effective competitive metalloproteinase MMP-2 and MMP-9 inhibitor with Ki values of 13.9 nM and 600 nM respectively. SB-3CT has high selectivity to gelatinase. SB-3CT can penetrate the blood-brain barrier and have neuroprotective and anti-cancer effects. |
Target | MMP-2; MMP-9 |
In vitro study | SB-3CT direct inhibition of bone marrow endothelial cell infiltration and tubule formation in vitro. SB-3CT inhibited bone marrow endothelial cell infiltration and tubule formation directly in the artificial basement membrane in vitro. |
In vivo study | In the L-CI.5sT-cell lymphatic model, SB-3CT (5-50 mg/kg/day, I. P.) effectively inhibited the metastasis of liver cancer cells and improved the survival rate of mice. SB-3CT (50 mg/kg/day, I. P.) inhibited human prostate cancer cell growth, osteolysis, and angiogenesis in a bone metastasis model. In a mouse model of "permanent" cerebral ischemia caused by emboli, SB-3CT blocked the degeneration of neuronal laminin, protecting neurons from ischemic cell death, and improve the outcome of neurological behavior after embolic MCA occlusion. In a L-CI.5sT-cell lymphoid model, SB-3CT (5-50 mg/kg/day, I. P.) effectively inhibited liver cancer cell metastasis and increased survival in mice. SB-3CT (50 mg/kg/day, I. P.) inhibited human prostate cancer cell growth, osteolysis, and angiogenesis in a bone metastasis model. In a mouse model of "permanent" cerebral ischemia caused by emboli, SB-3CT blocked the degeneration of neuronal laminin, protecting neurons from ischemic cell death, and improve the outcome of neurological behavior after embolic MCA occlusion. |
Hazard Symbols | Xi - Irritant |
Risk Codes | 36 - Irritating to the eyes |
Safety Description | 26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. |
WGK Germany | 3 |
HS Code | 29349990 |
1mg | 5mg | 10mg | |
---|---|---|---|
1 mM | 3.264 ml | 16.319 ml | 32.637 ml |
5 mM | 0.653 ml | 3.264 ml | 6.527 ml |
10 mM | 0.326 ml | 1.632 ml | 3.264 ml |
5 mM | 0.065 ml | 0.326 ml | 0.653 ml |
biological activity | SB-3CT is a highly potent and selective gelatinase inhibitor, its Ki for MMP-2 and MMP-9 was 13.9 nM and 600 nM, respectively. SB-3CT is a highly selective gelatinase inhibitor with a Ki of 13.9 nM and 600 nM for MMP-2 and MMP-9, respectively. |
in vitro study | SB-3CT directly inhibits bone marrow endothelial cell infiltration and tubule formation in an in vitro artificial basement membrane. SB-3CT inhibited bone marrow endothelial cell infiltration and tubule formation directly in the artificial basement membrane in vitro. |
in vivo study | L-CI.5sT (5-50 mg/kg/day, I. P.) in a SB-3CT-cell lymphoid model effectively inhibit the metastasis of liver cancer cells and improve the survival rate of mice. SB-3CT (50 mg/kg/day, I. P.) inhibited human prostate cancer cell growth, osteolysis, and angiogenesis in a bone metastasis model. In a mouse model of "permanent" cerebral ischemia caused by emboli, SB-3CT blocked the degeneration of neuronal laminin, protecting neurons from ischemic cell death, and improve the outcome of neurological behavior after embolic MCA occlusion. In a L-CI.5sT-cell lymphoid model, SB-3CT (5-50 mg/kg/day, I. P.) effectively inhibited liver cancer cell metastasis and increased survival in mice. SB-3CT (50 mg/kg/day, I. P.) inhibited human prostate cancer cell growth, osteolysis, and angiogenesis in a bone metastasis model. In a mouse model of "permanent" cerebral ischemia caused by emboli, SB-3CT blocked the degeneration of neuronal laminin, protecting neurons from ischemic cell death, and improve the outcome of neurological behavior after embolic MCA occlusion. |
Target | TargetValue MMP-2 (Cell-free assay) 13.9 nM(Ki) MMP-9 (Cell-free assay) 600 nM(Ki) |
Target | Value |
MMP-2 (Cell-free assay) | 13.9 nM(Ki) |
MMP-9 (Cell-free assay) | 600 nM(Ki) |