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product name SB-3CT


Description: SB-3CT is a potent, effective and selective gelatinase inhibitor with Ki of 13.9 nM and 600 nM for MMP-2 and MMP-9, respectively. SB-3CT is a 2-[(arylsulfonyl)methyl]thiirane that achieves potent inhibition, by a thiirane-opening mechanism, of the MMP2 and MMP9 zinc metalloproteases. SB-3CT attenuates behavioral impairments and hippocampal loss after traumatic brain injury in rat.

References: Cancer Res. 2005 May 1;65(9):3523-6.



Molecular Weight (MW)

306.40
Formula

C15H14O3S2
CAS No.

292605-14-2
Storage

-20℃ for 3 years in powder form
-80℃ for 2 years in solvent
Solubility (In vitro)

DMSO: 61 mg/mL (199.1 mM)
Water: <1 mg/mL
Ethanol: 10 mg/mL (32.6 mM)
Solubility (In vivo)

4% DMSO+corn oil: 10 mg/mL
Synonyms

 

other peoduct :

In Vitro

In vitro activity: SB-3CT directly inhibits bone marrow endothelial cell invasion and tubule formation in Matrigel in vitro.


Kinase Assay:


Cell Assay:

In Vivo In L-CI.5s T-cell lymphoma model, SB-3CT (5-50 mg/kg/d i.p.) potently inhibit liver metastasis and increases survival of mice. SB-3CT (50 mg/kg/d i.p.) inhibits human prostate cancer growth, osteolysis and angiogenesis in a bone metastasis model. In a mouse model of embolus-induced “permanent” focal cerebral ischemia, SB-3CT counteracts degradation of neuronal laminin, protects neurons from ischemic cell death, and ameliorates neurobehavioral outcomes after embolic MCA occlusion.
Animal model Mouse L-CI.5s T-cell lymphoma model
Formulation & Dosage Dissolved in 10% DMSO.; 50 mg/kg; i.p. injection
References Cancer Res. 2005 May 1;65(9):3523-6; Int J Cancer. 2006 Jun 1;118(11):2721-6.

CX-4947

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Author: Sodium channel