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DKM 2-93 - 10mM in DMSO, high purity , CAS No.65836-72-8

    Grade & Purity:
  • 10mM in DMSO
In stock
Item Number
D425322
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D425322-1ml
1ml
Available within 8-12 weeks(?)
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$69.90

E1 Activating Inhibitors

Basic Description

Synonyms 2-chloro-N-(3,4-dimethoxybenzyl)acetamide | 65836-72-8 | DKM 2-93 | 2-chloro-N-[(3,4-dimethoxyphenyl)methyl]acetamide | Acetamide, 2-chloro-N-((3,4-dimethoxyphenyl)methyl)- | 2-Chloro-N-((3,4-dimethoxyphenyl)methyl)acetamide | 2-Chloro-N-(3,4-dimethoxy-benzyl)-acetam
Specifications & Purity 10mM in DMSO
Biochemical and Physiological Mechanisms DKM 2-93 is a relatively selective lead inhibitor of ubiquitin-like modifier activating enzyme 5 (UBA5).
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.
Product Description

Information

DKM 2-93 DKM 2-93 is a relatively selective lead inhibitor of ubiquitin-like modifier activating enzyme 5 (UBA5) .

Targets

UBA5

In vitro

DKM 2-93 not only impairs pancreatic cancer cell survival in PaCa2, but also Panc1 cells with 50 % effective concentration values of 90 and 30 μM, respectively.

In vivo

DKM 2-93 daily treatment significantly impairs tumor growth of PaCa2 cells in vivo in tumor xenograft studies in immune-deficient mice without causing any weight loss or overt toxicity.

Cell Research(from reference)

Cell lines:PaCa2 and Panc1 pancreatic cancer cells 

Incubation Time:48 h 

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Benzenoids
Class Benzene and substituted derivatives
Subclass Methoxybenzenes
Intermediate Tree Nodes Not available
Direct Parent Dimethoxybenzenes
Alternative Parents Phenoxy compounds  Anisoles  Alkyl aryl ethers  Chloroacetamides  Secondary carboxylic acid amides  Organopnictogen compounds  Organonitrogen compounds  Organochlorides  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  Alkyl chlorides  
Molecular Framework Aromatic homomonocyclic compounds
Substituents O-dimethoxybenzene - Dimethoxybenzene - Phenoxy compound - Anisole - Phenol ether - Alkyl aryl ether - Chloroacetamide - Carboxamide group - Secondary carboxylic acid amide - Carboxylic acid derivative - Ether - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Organochloride - Organohalogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Carbonyl group - Organic oxygen compound - Alkyl halide - Alkyl chloride - Aromatic homomonocyclic compound
Description This compound belongs to the class of organic compounds known as dimethoxybenzenes. These are organic aromatic compounds containing a monocyclic benzene moiety carrying exactly two methoxy groups.
External Descriptors Not available

Names and Identifiers

IUPAC Name 2-chloro-N-[(3,4-dimethoxyphenyl)methyl]acetamide
INCHI InChI=1S/C11H14ClNO3/c1-15-9-4-3-8(5-10(9)16-2)7-13-11(14)6-12/h3-5H,6-7H2,1-2H3,(H,13,14)
InChIKey CETPWRGZGWGPSV-UHFFFAOYSA-N
Smiles COC1=C(C=C(C=C1)CNC(=O)CCl)OC
Isomeric SMILES COC1=C(C=C(C=C1)CNC(=O)CCl)OC
Molecular Weight 243.69
Reaxy-Rn 2857211
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2857211&ln=

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

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

Chemical and Physical Properties

Molecular Weight 243.680 g/mol
XLogP3 1.200
Hydrogen Bond Donor Count 1
Hydrogen Bond Acceptor Count 3
Rotatable Bond Count 5
Exact Mass 243.066 Da
Monoisotopic Mass 243.066 Da
Topological Polar Surface Area 47.600 Ų
Heavy Atom Count 16
Formal Charge 0
Complexity 225.000
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

Solution Calculators

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