TCID - 10mM in DMSO, high purity , CAS No.30675-13-9

Item Number
T423175
Grouped product items
SKUSizeAvailabilityPrice Qty
T423175-1ml
1ml
Available within 8-12 weeks(?)
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$241.90

Potent and selective ubiquitin C-terminal hydrolase-L3 inhibitor

Basic Description

Synonyms30675-13-9 | TCID | 4,5,6,7-Tetrachloro-1H-indene-1,3(2H)-dione | 4,5,6,7-Tetrachloroindan-1,3-dione | UCH-L3 Inhibitor | 4,5,6,7-tetrachloroindene-1,3-dione | 4,5,6,7-Tetrachloroindane-1,3-dione | 1H-Indene-1,3(2H)-dione, 4,5,6,7-tetrachloro- | CHEMBL1241028 | compound 6
Specifications & PurityMoligand™, 10mM in DMSO
Biochemical and Physiological MechanismsTCID is a cell penetrant potent and specific inhibitor of UCH-L3 (Ubiquitin carboxyl-terminal hydrolase isozyme L3). TCID is used to distinguish between UCH-L1 and UCH-L3 activities in cells.
Storage TempStore at -80°C
Shipped InIce chest + Ice pads
GradeMoligand™

Associated Targets(Human)

UCHL3 Tchem Ubiquitin carboxyl-terminal hydrolase isozyme L3 (2 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
UCHL1 Tchem Ubiquitin carboxyl-terminal hydrolase isozyme L1 (107 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UCHL3 Tchem Ubiquitin carboxyl-terminal hydrolase isozyme L3 (50 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Names and Identifiers

IUPAC Name 4,5,6,7-tetrachloroindene-1,3-dione
INCHI InChI=1S/C9H2Cl4O2/c10-6-4-2(14)1-3(15)5(4)7(11)9(13)8(6)12/h1H2
InChi Key IDLAOWFFKWRNHB-UHFFFAOYSA-N
Canonical SMILES C1C(=O)C2=C(C1=O)C(=C(C(=C2Cl)Cl)Cl)Cl
Isomeric SMILES C1C(=O)C2=C(C1=O)C(=C(C(=C2Cl)Cl)Cl)Cl
PubChem CID 2729042
Molecular Weight 283.92

Certificates

Certificate of Analysis(COA)

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Related Documents

Citations of This Product

1. Shaowei Bo, Dong Zhang, Mengjie Ma, Xukai Mo, Julia Stabinska, Michael T. McMahon, Changzheng Shi, Liangping Luo.  (2023)  Acyl Hydrazides and Acyl Hydrazones as High-Performance Chemical Exchange Saturation Transfer MRI Contrast Agents.  Pharmaceuticals,  16  (5): (639).  [PMID:37242423] [10.3390/ph16050639]
2. Wang Qian, He Yuan, Lu Rui, Wang Wen-Ming, Yang Ke-Wu, Fan Hai Ming, Jin Yi, Blackburn G. Michael.  (2018)  Thermokinetic profile of NDM-1 and its inhibition by small carboxylic acids.  BIOSCIENCE REPORTS,  38  (2):   [PMID:29507059] [10.1042/BSR20180244]

References

1. Shaowei Bo, Dong Zhang, Mengjie Ma, Xukai Mo, Julia Stabinska, Michael T. McMahon, Changzheng Shi, Liangping Luo.  (2023)  Acyl Hydrazides and Acyl Hydrazones as High-Performance Chemical Exchange Saturation Transfer MRI Contrast Agents.  Pharmaceuticals,  16  (5): (639).  [PMID:37242423] [10.3390/ph16050639]
2. Wang Qian, He Yuan, Lu Rui, Wang Wen-Ming, Yang Ke-Wu, Fan Hai Ming, Jin Yi, Blackburn G. Michael.  (2018)  Thermokinetic profile of NDM-1 and its inhibition by small carboxylic acids.  BIOSCIENCE REPORTS,  38  (2):   [PMID:29507059] [10.1042/BSR20180244]

Solution Calculators