MedKoo Cat#: 574896 | Name: TCID
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Description:

WARNING: This product is for research use only, not for human or veterinary use.

TCID is a tetrachloro indandione that acts as a potent inhibitor of Ubiquitin carboxyl-terminal hydrolase isozyme L3 (UCH-L3). UCH-L3 is a eubiquitinating enzyme and thiol-dependent hydrolase.

Chemical Structure

TCID
TCID
CAS#30675-13-9

Theoretical Analysis

MedKoo Cat#: 574896

Name: TCID

CAS#: 30675-13-9

Chemical Formula: C9H2Cl4O2

Exact Mass: 281.8809

Molecular Weight: 283.91

Elemental Analysis: C, 38.07; H, 0.71; Cl, 49.94; O, 11.27

Price and Availability

Size Price Availability Quantity
5mg USD 240.00 2 Weeks
10mg USD 385.00 2 Weeks
25mg USD 665.00 2 Weeks
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Related CAS #
No Data
Synonym
TCID; UCH-L3 Inhibitor
IUPAC/Chemical Name
4,5,6,7-tetrachloro-1H-indene-1,3(2H)-dione
InChi Key
IDLAOWFFKWRNHB-UHFFFAOYSA-N
InChi Code
InChI=1S/C9H2Cl4O2/c10-6-4-2(14)1-3(15)5(4)7(11)9(13)8(6)12/h1H2
SMILES Code
O=C(CC1=O)C2=C1C(Cl)=C(Cl)C(Cl)=C2Cl
Appearance
Solid powder
Purity
>95% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
Soluble in DMSO
Shelf Life
>3 years if stored properly
Drug Formulation
This drug may be formulated in DMSO
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 283.91 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
1. Mason, D.E., Ek, J., Peters, E.C., et al. Substrate profiling of deubiquitin hydrolases with a positional scanning library and mass spectrometry. Biochemistry 43(21), 6535-6544 (2004). 2. Setsuie, R., Sakurai, M., Sakaguchi, Y., et al. Ubiquitin dimers control the hydrolase activity of UCH-L3. Neurochemistry International 54(5-6), 314-321 (2009). 3. Wada, H., Kito, K., Caskey, L.S., et al. Cleavage of the C-terminus of NEDD8 by UCH-L3. Biochemical and Biophysical Research Communications 251(3), 668-692 (1998). 4. Iphöfer, A., Kummer, A., Nimtz, M., et al. Profiling ubiquitin linkage specificities of deubiquitinating enzymes with branched ubiquitin isopeptide probes. ChemBioChem 13(10), 1416-1420 (2012). 5. Liu, Y., Lashuel, H.A., Choi, S., et al. Discovery of inhibitors that elucidate the role of UCH-L1 activity in the H1299 lung cancer cell line. Chemistry & Biology 10(9), 837-846 (2003).