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TCID - 10mM in DMSO, high purity , CAS No.30675-13-9, Inhibitor of ubiquitin C-terminal hydrolase L3

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T423175
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T423175-1ml
1ml
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$241.90

Potent and selective ubiquitin C-terminal hydrolase-L3 inhibitor

Basic Description

Synonyms 30675-13-9 | 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 & Purity Moligand™, 10mM in DMSO
Biochemical and Physiological Mechanisms TCID 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 Temp Store at -80°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Grade Moligand™
Action Type INHIBITOR
Mechanism of action Inhibitor of ubiquitin C-terminal hydrolase L3

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Benzenoids
Class Indanes
Subclass Indanones
Intermediate Tree Nodes Not available
Direct Parent Indanediones
Alternative Parents Aryl alkyl ketones  Beta-diketones  Aryl chlorides  Vinylogous halides  Organochlorides  Organic oxides  Hydrocarbon derivatives  
Molecular Framework Aromatic homopolycyclic compounds
Substituents Indanedione - Aryl ketone - Aryl alkyl ketone - 1,3-diketone - Aryl chloride - Aryl halide - 1,3-dicarbonyl compound - Vinylogous halide - Ketone - Organooxygen compound - Organochloride - Organohalogen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Aromatic homopolycyclic compound
Description This compound belongs to the class of organic compounds known as indanediones. These are compounds containing an indane ring bearing two ketone groups.
External Descriptors Not available

Associated Targets(Human)

UCHL3 Tchem Ubiquitin carboxyl-terminal hydrolase isozyme L3 (2 Activities)
Activity Type Activity Value -log(M) Mechanism of Action Activity Reference Publications (PubMed IDs)
UCHL1 Tchem Ubiquitin carboxyl-terminal hydrolase isozyme L1 (107 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
UCHL3 Tchem Ubiquitin carboxyl-terminal hydrolase isozyme L3 (50 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Hdac6 Histone deacetylase 6 (222 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

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
InChIKey IDLAOWFFKWRNHB-UHFFFAOYSA-N
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(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Chemical and Physical Properties

Molecular Weight 283.900 g/mol
XLogP3 3.900
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 2
Rotatable Bond Count 0
Exact Mass 283.878 Da
Monoisotopic Mass 281.881 Da
Topological Polar Surface Area 34.100 Ų
Heavy Atom Count 15
Formal Charge 0
Complexity 289.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

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). 
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):  
3. Guiying Zhu, Chaozheng Liu, Changli Zhang, Jiangtao Shi, Changtong Mei, Mingzhu Pan, Zhipeng Liu.  (2024)  Activating the Room-Temperature Phosphorescence of Organic Dyes through the Confinement Effect of Delignified Wood.  ACS Sustainable Chemistry & Engineering,  12  (9): (3726-3735). 
4. Binhao Wang, Yu Shen, Ruonan Hao, Shuheng Pan, Ruizhi Han, Ye Ni.  (2025)  Novel Approach for Efficient Separation of Primary Amines Using Supercritical Fluid Chromatography.  CHIRALITY,  37  (1): (e70012). 

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