200,000+ products from a single source!
sales@angenechem.com
Home > Other Building Blocks > 114289-47-3
114289-47-3 | Dodecanamide, 2,2-dimethyl-N-(2,4,6-trimethoxyphenyl)-
CAS No: 114289-47-3 Catalog No: AG000AZK MDL No:
Product Description
Catalog Number:
AG000AZK
Chemical Name:
Dodecanamide, 2,2-dimethyl-N-(2,4,6-trimethoxyphenyl)-
CAS Number:
114289-47-3
Molecular Formula:
C23H39NO4
Molecular Weight:
393.5601
IUPAC Name:
2,2-dimethyl-N-(2,4,6-trimethoxyphenyl)dodecanamide
InChI:
InChI=1S/C23H39NO4/c1-7-8-9-10-11-12-13-14-15-23(2,3)22(25)24-21-19(27-5)16-18(26-4)17-20(21)28-6/h16-17H,7-15H2,1-6H3,(H,24,25)
InChI Key:
WAFNZAURAWBNDZ-UHFFFAOYSA-N
SMILES:
CCCCCCCCCCC(C(=O)Nc1c(OC)cc(cc1OC)OC)(C)C
UNII:
8653IQ20EA
Properties
Complexity:
413
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
393.288g/mol
Formal Charge:
0
Heavy Atom Count:
28
Hydrogen Bond Acceptor Count:
4
Hydrogen Bond Donor Count:
1
Isotope Atom Count:
0
Molecular Weight:
393.568g/mol
Monoisotopic Mass:
393.288g/mol
Rotatable Bond Count:
14
Topological Polar Surface Area:
56.8A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
7.1
Literature
| Title | Journal |
|---|---|
| Inhibition of Acyl-CoA: cholesterol acyltransferase (ACAT), overexpression of cholesterol transporter gene, and protection of amyloid β (Aβ) oligomers-induced neuronal cell death by tricyclic pyrone molecules. | Journal of medicinal chemistry 20121025 |
| Pyripyropenes, fungal sesquiterpenes conjugated with alpha-pyrone and pyridine moieties, exhibits anti-angiogenic activity against human umbilical vein endothelial cells. | Biological & pharmaceutical bulletin 20090701 |
| The lysophospholipid acyltransferase antagonist CI-976 inhibits a late step in COPII vesicle budding. | Traffic (Copenhagen, Denmark) 20080501 |
| Use of acyltransferase inhibitors to block vesicular traffic between the ER and Golgi complex. | Methods in enzymology 20050101 |
| Molecular cloning and biochemical characterization of Candida albicans acyl-CoA:sterol acyltransferase, a potential target of antifungal agents. | Biochemical and biophysical research communications 20040702 |
| Sustained ER Ca2+ depletion suppresses protein synthesis and induces activation-enhanced cell death in mast cells. | The Journal of biological chemistry 20020419 |
| Cholesterol esterification by host and parasite is essential for optimal proliferation of Toxoplasma gondii. | The Journal of biological chemistry 20010914 |
| Preferential pharmacological inhibition of macrophage ACAT increases plaque formation in mouse and rabbit models of atherogenesis. | Atherosclerosis 20010401 |
| Pharmacological properties of R-755, a novel acyl-CoA:cholesterol acyltransferase inhibitor, in cholesterol-fed rats, hamsters and rabbits. | Japanese journal of pharmacology 20010401 |
| [ACAT inhibitors]. | Nihon rinsho. Japanese journal of clinical medicine 20010301 |
| Molecular cloning and characterization of two isoforms of Saccharomyces cerevisiae acyl-CoA:sterol acyltransferase. | The Journal of biological chemistry 19960927 |
Related Products
Featured Products
© 2019 Angene International Limited. All rights Reserved.