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ICCB-19 hydrochloride - 10mM in DMSO, high purity , CAS No.1803605-68-6

    Grade & Purity:
  • 10mM in DMSO
In stock
Item Number
I422211
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I422211-1ml
1ml
Available within 8-12 weeks(?)
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$196.90

RIP kinase Inhibitors

Basic Description

Synonyms 1803605-68-6 | ICCB-19 hydrochloride | N-cycloheptyl-2-(4,5-dihydro-1H-imidazol-2-ylsulfanyl)acetamide hydrochloride | ICCB-19 (hydrochloride) | N-cycloheptyl-2-(4,5-dihydro-1H-imidazol-2-ylsulfanyl)acetamide;hydrochloride | EX-A6564 | s6078 | AKOS034638069 | MS-24169 | HY
Specifications & Purity 10mM in DMSO
Biochemical and Physiological Mechanisms ICCB-19 hydrochloride is an inhibitor of TNFRSF1A Associated Via Death Domain (TRADD) with IC50 of 1.12 μM and 2.01 μM for protecting Velcade-induced apoptosis in Jurkat cells and protecting RDA in MEFs, respectively. ICCB-19 indirectly inhibits Receptor-
Storage Temp Store at -80°C
Shipped In
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Product Description

Information

ICCB-19 hydrochloride ICCB-19 hydrochloride is an inhibitor of TNFRSF1A Associated Via Death Domain (TRADD) with IC50 of 1.12 μM and 2.01 μM for protecting Velcade-induced apoptosis in Jurkat cells and protecting RDA in MEFs, respectively. ICCB-19 indirectly inhibits Receptor-interacting serine/threonine-protein kinase 1 (RIPK1) . ICCB-19 effectively induces autophagy .

Targets

TRADD ; RIPK1

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organoheterocyclic compounds
Class Azolines
Subclass Imidazolines
Intermediate Tree Nodes Not available
Direct Parent Imidazolines
Alternative Parents Secondary carboxylic acid amides  Isothioureas  Sulfenyl compounds  Propargyl-type 1,3-dipolar organic compounds  Carboximidamides  Azacyclic compounds  Organic oxides  Hydrochlorides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular Framework Aliphatic heteromonocyclic compounds
Substituents 2-imidazoline - Carboxamide group - Isothiourea - Secondary carboxylic acid amide - Carboxylic acid derivative - Carboximidamide - Sulfenyl compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Azacycle - Hydrocarbon derivative - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Carbonyl group - Organic nitrogen compound - Organic oxygen compound - Hydrochloride - Organic oxide - Aliphatic heteromonocyclic compound
Description This compound belongs to the class of organic compounds known as imidazolines. These are organic compounds containing an imidazoline ring, which is an unsaturated ring (derived from imidazole) with two nitrogen atoms at positions 1 and 3 respectively, and containing only one CN double bond.
External Descriptors Not available

Names and Identifiers

IUPAC Name N-cycloheptyl-2-(4,5-dihydro-1H-imidazol-2-ylsulfanyl)acetamide;hydrochloride
INCHI InChI=1S/C12H21N3OS.ClH/c16-11(9-17-12-13-7-8-14-12)15-10-5-3-1-2-4-6-10;/h10H,1-9H2,(H,13,14)(H,15,16);1H
InChIKey TZICOTBZKPHMMK-UHFFFAOYSA-N
Smiles C1CCCC(CC1)NC(=O)CSC2=NCCN2.Cl
Isomeric SMILES C1CCCC(CC1)NC(=O)CSC2=NCCN2.Cl
PubChem CID 91654402
Molecular Weight 291.84

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

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

Chemical and Physical Properties

Molecular Weight 291.840 g/mol
XLogP3
Hydrogen Bond Donor Count 3
Hydrogen Bond Acceptor Count 3
Rotatable Bond Count 4
Exact Mass 291.117 Da
Monoisotopic Mass 291.117 Da
Topological Polar Surface Area 78.800 Ų
Heavy Atom Count 18
Formal Charge 0
Complexity 285.000
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 2

Solution Calculators

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