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10211-09-3

10211-09-3 | Acetamide, N-[2-(4-hydroxy-3-methoxyphenyl)ethyl]-

CAS No: 10211-09-3 Catalog No: AG0006ND MDL No:

Product Description

Catalog Number:
AG0006ND
Chemical Name:
Acetamide, N-[2-(4-hydroxy-3-methoxyphenyl)ethyl]-
CAS Number:
10211-09-3
Molecular Formula:
C11H15NO3
Molecular Weight:
209.2417
IUPAC Name:
N-[2-(4-hydroxy-3-methoxyphenyl)ethyl]acetamide
InChI:
InChI=1S/C11H15NO3/c1-8(13)12-6-5-9-3-4-10(14)11(7-9)15-2/h3-4,7,14H,5-6H2,1-2H3,(H,12,13)
InChI Key:
LPMUFBLEYLSXFN-UHFFFAOYSA-N
SMILES:
COc1cc(CCNC(=O)C)ccc1O

Properties

Complexity:
208  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
209.105g/mol
Formal Charge:
0
Heavy Atom Count:
15  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
209.245g/mol
Monoisotopic Mass:
209.105g/mol
Rotatable Bond Count:
4  
Topological Polar Surface Area:
58.6A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.5  

Literature

Title Journal
Enhanced ERK dependent CREB activation reduces apoptosis in staurosporine-treated human neuroblastoma SK-N-BE(2)C cells. Neuroscience letters 20060710
Syntheses of NAMDA derivatives inhibiting NO production in BV-2 cells stimulated with lipopolysaccharide. Bioorganic & medicinal chemistry letters 20050715
A neuroprotective role of extracellular signal-regulated kinase in N-acetyl-O-methyldopamine-treated hippocampal neurons after exposure to in vitro and in vivo ischemia. Neuroscience 20040101
Early c-Fos induction after cerebral ischemia: a possible neuroprotective role. Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism 20010501
Repression of proinflammatory cytokine and inducible nitric oxide synthase (NOS2) gene expression in activated microglia by N-acetyl-O-methyldopamine: protein kinase A-dependent mechanism. Glia 20010315

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