sales@angenesci.com
Login | Register
logo
Structures Search
Home Other Building Blocks 4'-Carbamoyl-[1,1'-biphenyl]-4-yl methyl(3-(pyridin-4-yl)benzyl)carbamate

4'-Carbamoyl-[1,1'-biphenyl]-4-yl methyl(3-(pyridin-4-yl)benzyl)carbamate

CAS No.:
947669-91-2
Catalog Number:
AG003VBX
Molecular Formula:
C27H23N3O3
Molecular Weight:
437.4898
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5mg
99%
1 week
United States
$207
- +
10mg
99%
1 week
United States
$290
- +
25mg
99%
1 week
United States
$523
- +
50mg
99%
1 week
United States
$857
- +
100mg
99%
1 week
United States
$1190
- +
200mg
99%
1 week
United States
$1640
- +
Product Description
Catalog Number:
AG003VBX
Chemical Name:
4'-Carbamoyl-[1,1'-biphenyl]-4-yl methyl(3-(pyridin-4-yl)benzyl)carbamate
CAS Number:
947669-91-2
Molecular Formula:
C27H23N3O3
Molecular Weight:
437.4898
MDL Number:
MFCD10567112
IUPAC Name:
[4-(4-carbamoylphenyl)phenyl] N-methyl-N-[(3-pyridin-4-ylphenyl)methyl]carbamate
InChI:
InChI=1S/C27H23N3O3/c1-30(18-19-3-2-4-24(17-19)22-13-15-29-16-14-22)27(32)33-25-11-9-21(10-12-25)20-5-7-23(8-6-20)26(28)31/h2-17H,18H2,1H3,(H2,28,31)
InChI Key:
QTWNORFUQILKJL-UHFFFAOYSA-N
SMILES:
O=C(N(Cc1cccc(c1)c1ccncc1)C)Oc1ccc(cc1)c1ccc(cc1)C(=O)N
Properties
Complexity:
635  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
437.174g/mol
Formal Charge:
0
Heavy Atom Count:
33  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
437.499g/mol
Monoisotopic Mass:
437.174g/mol
Rotatable Bond Count:
7  
Topological Polar Surface Area:
85.5A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
4.2  
Literature
Title Journal
WWL70 attenuates PGE(2) production derived from 2-arachidonoylglycerol in microglia by ABHD6-independent mechanism. Journal of neuroinflammation 20170101
Selective blockade of 2-arachidonoylglycerol hydrolysis produces cannabinoid behavioral effects. Nature chemical biology 20090101
A functional proteomic strategy to discover inhibitors for uncharacterized hydrolases. Journal of the American Chemical Society 20070808
Properties