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TCID
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
TCID图片
CAS NO:30675-13-9
规格:≥98%
包装与价格:
包装价格(元)
2mg询价
5mg询价
10mg询价
25mg询价
50mg询价
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理化性质和储存条件
Molecular Weight (MW)283.92
FormulaC9H2Cl4O2
CAS No.30675-13-9
Storage-20℃ for 3 years in powder form
-80℃ for 2 years in solvent
Solubility (In vitro)DMSO: 23 mg/mL (81.0 mM)
Water:<1 mg/mL
Ethanol: <1 mg/mL
SMILESO=C(CC1=O)C2=C1C(Cl)=C(Cl)C(Cl)=C2Cl
Synonyms4,5,6,7-tetrachloro-1H-indene-1,3(2H)-dione
实验参考方法
In Vitro

In vitro activity: TCID is selective for UCH-L3 over UCH-L1 by over 100-fold. NU6027 (10 μM) does not promote YFP-GLT-1 accumulation in intracellular vesicles in transfected MDCK cells, while LDN-57444 (10 μM) promotes YFP-GLT-1 accumulation. NU6027 (10 μM) does not produce long-term lysosomal degradation of GLT-1, while LDN-57444 (10 μM) has such effect. TCID (10 μM) diminishes GlyT2 ubiquitination in brainstem and spinal cord primary neurons, which is more pronounced when UCHL1 is inhibited and when cells are exposed to these inhibitors for longer periods.


Cell Assay: In transfected MDCK cells, TCID (10 μm for 30 mins) was not able to affect the UCH-L1 inhibitor promoted accumulation of YFP-GLT-1 in intracellular vesicles.

In Vivo
Animal model
Formulation & Dosage
References

Chem Biol. 2003 Sep;10(9):837-46; Glia. 2012 Sep;60(9):1356-65.

 
 
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