247580-43-4,MFCD16618397
Catalog No.:AA002P9X

247580-43-4 | L-Phenylalanine, N-(1-naphthalenylcarbonyl)-4-nitro-, methyl ester

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1mg
≥98%
in stock  
$49.00   $34.00
- +
5mg
≥98%
in stock  
$159.00   $111.00
- +
10mg
≥98%
in stock  
$289.00   $202.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA002P9X
Chemical Name:
L-Phenylalanine, N-(1-naphthalenylcarbonyl)-4-nitro-, methyl ester
CAS Number:
247580-43-4
Molecular Formula:
C21H18N2O5
Molecular Weight:
378.3780
MDL Number:
MFCD16618397
SMILES:
COC(=O)[C@@H](NC(=O)c1cccc2c1cccc2)Cc1ccc(cc1)[N+](=O)[O-]
Properties
Computed Properties
 
Complexity:
568  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Heavy Atom Count:
28  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
6  
XLogP3:
4.2  

Literature

Title: Graft-versus-host disease reduces regulatory T-cell migration into the tumour tissue.

Journal: Immunology 20120901

Title: What is the role of CCR3 in choroidal neovascularization?

Journal: Advances in experimental medicine and biology 20120101

Title: Pulmonary epithelial CCR3 promotes LPS-induced lung inflammation by mediating release of IL-8.

Journal: Journal of cellular physiology 20110901

Title: CCR3 and choroidal neovascularization.

Journal: PloS one 20110101

Title: Selective suppression of Th2-mediated airway eosinophil infiltration by low-molecular weight CCR3 antagonists.

Journal: International immunology 20070801

Title: Design and synthesis of novel CCR3 antagonists.

Journal: Bioorganic & medicinal chemistry letters 20031020

Title: Discovery of potent and selective phenylalanine derived CCR3 antagonists. Part 1.

Journal: Bioorganic & medicinal chemistry letters 20010604

Title: Discovery of potent and selective phenylalanine derived CCR3 receptor antagonists. Part 2.

Journal: Bioorganic & medicinal chemistry letters 20010604

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Related Products of 247580-43-4
Tags:247580-43-4 Molecular Formula|247580-43-4 MDL|247580-43-4 SMILES|247580-43-4 L-Phenylalanine, N-(1-naphthalenylcarbonyl)-4-nitro-, methyl ester
Catalog No.: AA002P9X
247580-43-4,MFCD16618397
247580-43-4 | L-Phenylalanine, N-(1-naphthalenylcarbonyl)-4-nitro-, methyl ester
Pack Size: 1mg
Purity: ≥98%
in stock
$49.00 $34.00
Pack Size: 5mg
Purity: ≥98%
in stock
$159.00 $111.00
Pack Size: 10mg
Purity: ≥98%
in stock
$289.00 $202.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA002P9X
Chemical Name: L-Phenylalanine, N-(1-naphthalenylcarbonyl)-4-nitro-, methyl ester
CAS Number: 247580-43-4
Molecular Formula: C21H18N2O5
Molecular Weight: 378.3780
MDL Number: MFCD16618397
SMILES: COC(=O)[C@@H](NC(=O)c1cccc2c1cccc2)Cc1ccc(cc1)[N+](=O)[O-]
Properties
Complexity: 568  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 1  
Heavy Atom Count: 28  
Hydrogen Bond Acceptor Count: 5  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 6  
XLogP3: 4.2  
Literature fold

Title: Graft-versus-host disease reduces regulatory T-cell migration into the tumour tissue.

Journal: Immunology20120901

Title: What is the role of CCR3 in choroidal neovascularization?

Journal: Advances in experimental medicine and biology20120101

Title: Pulmonary epithelial CCR3 promotes LPS-induced lung inflammation by mediating release of IL-8.

Journal: Journal of cellular physiology20110901

Title: CCR3 and choroidal neovascularization.

Journal: PloS one20110101

Title: Selective suppression of Th2-mediated airway eosinophil infiltration by low-molecular weight CCR3 antagonists.

Journal: International immunology20070801

Title: Design and synthesis of novel CCR3 antagonists.

Journal: Bioorganic & medicinal chemistry letters20031020

Title: Discovery of potent and selective phenylalanine derived CCR3 antagonists. Part 1.

Journal: Bioorganic & medicinal chemistry letters20010604

Title: Discovery of potent and selective phenylalanine derived CCR3 receptor antagonists. Part 2.

Journal: Bioorganic & medicinal chemistry letters20010604

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