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Lipoprotein Lipase Activator - 10mM in DMSO, high purity , CAS No.133208-93-2

    Grade & Purity:
  • 10mM in DMSO
In stock
Item Number
L421258
Grouped product items
SKU Size
Availability
Price Qty
L421258-1ml
1ml
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$241.90

an inducer of lipoprotein lipase mRNA

Basic Description

Synonyms Ibrolipim | 133208-93-2 | NO-1886 | Lipoprotein Lipase Activator | OPF 009 | OPF-009 | Diethyl (4-((4-bromo-2-cyanophenyl)carbamoyl)benzyl)phosphonate | Phosphonic acid, [[4-[[(4-bromo-2-cyanophenyl)amino]carbonyl]phenyl]methyl]-, diethyl ester | Phosphonic acid, ((4-(((
Specifications & Purity 10mM in DMSO
Biochemical and Physiological Mechanisms Lipoprotein lipase activator. Overexpression of lipoprotein lipase in transgenic rabbits leads to increased small dense LDL in plasma and promotes atherosclerosis. Long-term administration of NO-1886 protects against the development of experimental athero
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

Lipoprotein Lipase Activator is a cell-permeable benzylphosphonate derivative that selectively induces lipoprotein lipase (LPL) mRNA and protein levels, but does not exhibit PPARα or PPARγ agonistic activities. Lipoprotein Lipase Activator lowers serum lipid levels and plasma triglycerides with concomitant elevation in high-density lipoprotein cholesterol (HDL-C) in animal models. Lipoprotein Lipase Activator also induces fatty acid oxidation related enzymes, lowers free fatty acids (FFA), and minimizes fat accumulation. Also reported to suppress the plasma levels of TNF-a and COX-2 and displays anti-tumor properties.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Benzenoids
Class Benzene and substituted derivatives
Subclass Anilides
Intermediate Tree Nodes Aromatic anilides
Direct Parent Benzanilides
Alternative Parents Benzamides  Benzoyl derivatives  Benzonitriles  Dialkyl alkylphosphonates  Bromobenzenes  Phosphonic acid esters  Aryl bromides  Secondary carboxylic acid amides  Nitriles  Organopnictogen compounds  Organophosphorus compounds  Organooxygen compounds  Organobromides  Organic oxides  Hydrocarbon derivatives  
Molecular Framework Aromatic homomonocyclic compounds
Substituents Benzanilide - Benzamide - Benzoic acid or derivatives - Benzonitrile - Benzoyl - Dialkyl alkylphosphonate - Bromobenzene - Halobenzene - Phosphonic acid diester - Phosphonic acid ester - Aryl bromide - Aryl halide - Organophosphonic acid derivative - Secondary carboxylic acid amide - Carboxamide group - Carboxylic acid derivative - Nitrile - Carbonitrile - Hydrocarbon derivative - Organohalogen compound - Organobromide - Organonitrogen compound - Organooxygen compound - Organopnictogen compound - Organic oxygen compound - Organophosphorus compound - Organic nitrogen compound - Organic oxide - Aromatic homomonocyclic compound
Description This compound belongs to the class of organic compounds known as benzanilides. These are aromatic compounds containing an anilide group in which the carboxamide group is substituted with a benzene ring. They have the general structure RNC(=O)R', where R,R'= benzene.
External Descriptors Not available

Product Properties

pKa pKa: 11.51 (Predicted)

Associated Targets(Human)

LPL Tchem Lipoprotein lipase (101 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
RPTEC (172 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Rattus norvegicus (775804 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 N-(4-bromo-2-cyanophenyl)-4-(diethoxyphosphorylmethyl)benzamide
INCHI InChI=1S/C19H20BrN2O4P/c1-3-25-27(24,26-4-2)13-14-5-7-15(8-6-14)19(23)22-18-10-9-17(20)11-16(18)12-21/h5-11H,3-4,13H2,1-2H3,(H,22,23)
InChIKey KPRTURMJVWXURQ-UHFFFAOYSA-N
Smiles CCOP(=O)(CC1=CC=C(C=C1)C(=O)NC2=C(C=C(C=C2)Br)C#N)OCC
Isomeric SMILES CCOP(=O)(CC1=CC=C(C=C1)C(=O)NC2=C(C=C(C=C2)Br)C#N)OCC
WGK Germany 3
Molecular Weight 451.25
Reaxy-Rn 7497256
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=7497256&ln=

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

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

Chemical and Physical Properties

Refractive Index n20D1.59 (Predicted)
Boil Point(°C) 512.47° C at 760 mmHg (Predicted)
Melt Point(°C) 90.27° C (Predicted)
Molecular Weight 451.200 g/mol
XLogP3 3.500
Hydrogen Bond Donor Count 1
Hydrogen Bond Acceptor Count 5
Rotatable Bond Count 8
Exact Mass 450.034 Da
Monoisotopic Mass 450.034 Da
Topological Polar Surface Area 88.400 Ų
Heavy Atom Count 27
Formal Charge 0
Complexity 576.000
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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