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721-90-4,MFCD00021728
Catalog No.:AA00FCP3

721-90-4 | H-Phe-gly-oh

Pack Size
Purity
Availability
Price(USD)
Quantity
  
100mg
95%
in stock  
$18.00   $13.00
- +
250mg
95%
in stock  
$44.00   $31.00
- +
1g
95%
in stock  
$129.00   $90.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA00FCP3
Chemical Name:
H-Phe-gly-oh
CAS Number:
721-90-4
Molecular Formula:
C11H14N2O3
Molecular Weight:
222.2405
MDL Number:
MFCD00021728
SMILES:
N[C@H](C(=O)NCC(=O)O)Cc1ccccc1
Properties
Computed Properties
 
Complexity:
250  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
16  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
3  
Isotope Atom Count:
0  
Rotatable Bond Count:
5  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
-2.5  

Literature

Title: Prohormone-substrate peptide sequence recognition by peptidylglycine α-amidating monooxygenase and its reflection in increased glycolate inhibitor potency.

Journal: Bioorganic & medicinal chemistry letters 20121201

Title: Hydrogen exchange equilibria in thiols.

Journal: Chemical research in toxicology 20120917

Title: Modulation of fibrillation of hIAPP core fragments by chemical modification of the peptide backbone.

Journal: Biochimica et biophysica acta 20120201

Title: Fragmental modeling of hPepT2 and analysis of its binding features by docking studies and pharmacophore mapping.

Journal: Bioorganic & medicinal chemistry 20110801

Title: Transport and signaling via the amino acid binding site of the yeast Gap1 amino acid transceptor.

Journal: Nature chemical biology 20090101

Title: Human PEPT1 pharmacophore distinguishes between dipeptide transport and binding.

Journal: Journal of medicinal chemistry 20060615

Title: Molecular mechanism of the inhibition of cytochrome c aggregation by Phe-Gly.

Journal: Archives of biochemistry and biophysics 20050301

Title: Intrinsic folding of small peptide chains: spectroscopic evidence for the formation of beta-turns in the gas phase.

Journal: Journal of the American Chemical Society 20050119

Title: Phe-Gly dipeptidomimetics designed for the di-/tripeptide transporters PEPT1 and PEPT2: synthesis and biological investigations.

Journal: Journal of medicinal chemistry 20040212

Title: Translocation of beta-catenin into the nucleus independent of interactions with FG-rich nucleoporins.

Journal: Experimental cell research 20031101

Title: Enhanced transdermal delivery of phenylalanyl-glycine by chemical modification with various fatty acids.

Journal: International journal of pharmaceutics 20030102

Title: Enhanced permeability of phenylalanyl-glycine (Phe-Gly) across the intestinal membranes by chemical modification with various fatty acids.

Journal: Drug metabolism and pharmacokinetics 20030101

Title: Diastereoselective reduction of a chiral N-Boc-protected delta-amino-alpha,beta-unsaturated gamma-keto ester Phe-Gly dipeptidomimetic.

Journal: The Journal of organic chemistry 20021227

Title: In vivo nephrotoxic action of an isomeric mixture of S-(1-phenyl-2-hydroxyethyl)glutathione and S-(2-phenyl-2-hydroxyethyl)glutathione in Fischer-344 rats.

Journal: Toxicology 19910325

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SDS
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Tags:721-90-4 Molecular Formula|721-90-4 MDL|721-90-4 SMILES|721-90-4 H-Phe-gly-oh
Catalog No.: AA00FCP3
721-90-4,MFCD00021728
721-90-4 | H-Phe-gly-oh
Pack Size： 100mg
Purity： 95%
in stock
$18.00 $13.00
Pack Size： 250mg
Purity： 95%
in stock
$44.00 $31.00
Pack Size： 1g
Purity： 95%
in stock
$129.00 $90.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA00FCP3
Chemical Name: H-Phe-gly-oh
CAS Number: 721-90-4
Molecular Formula: C11H14N2O3
Molecular Weight: 222.2405
MDL Number: MFCD00021728
SMILES: N[C@H](C(=O)NCC(=O)O)Cc1ccccc1
Properties
Complexity: 250  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 1  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 16  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 3  
Isotope Atom Count: 0  
Rotatable Bond Count: 5  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: -2.5  
Literature fold

Title: Prohormone-substrate peptide sequence recognition by peptidylglycine α-amidating monooxygenase and its reflection in increased glycolate inhibitor potency.

Journal: Bioorganic & medicinal chemistry letters20121201

Title: Hydrogen exchange equilibria in thiols.

Journal: Chemical research in toxicology20120917

Title: Modulation of fibrillation of hIAPP core fragments by chemical modification of the peptide backbone.

Journal: Biochimica et biophysica acta20120201

Title: Fragmental modeling of hPepT2 and analysis of its binding features by docking studies and pharmacophore mapping.

Journal: Bioorganic & medicinal chemistry20110801

Title: Transport and signaling via the amino acid binding site of the yeast Gap1 amino acid transceptor.

Journal: Nature chemical biology20090101

Title: Human PEPT1 pharmacophore distinguishes between dipeptide transport and binding.

Journal: Journal of medicinal chemistry20060615

Title: Molecular mechanism of the inhibition of cytochrome c aggregation by Phe-Gly.

Journal: Archives of biochemistry and biophysics20050301

Title: Intrinsic folding of small peptide chains: spectroscopic evidence for the formation of beta-turns in the gas phase.

Journal: Journal of the American Chemical Society20050119

Title: Phe-Gly dipeptidomimetics designed for the di-/tripeptide transporters PEPT1 and PEPT2: synthesis and biological investigations.

Journal: Journal of medicinal chemistry20040212

Title: Translocation of beta-catenin into the nucleus independent of interactions with FG-rich nucleoporins.

Journal: Experimental cell research20031101

Title: Enhanced transdermal delivery of phenylalanyl-glycine by chemical modification with various fatty acids.

Journal: International journal of pharmaceutics20030102

Title: Enhanced permeability of phenylalanyl-glycine (Phe-Gly) across the intestinal membranes by chemical modification with various fatty acids.

Journal: Drug metabolism and pharmacokinetics20030101

Title: Diastereoselective reduction of a chiral N-Boc-protected delta-amino-alpha,beta-unsaturated gamma-keto ester Phe-Gly dipeptidomimetic.

Journal: The Journal of organic chemistry20021227

Title: In vivo nephrotoxic action of an isomeric mixture of S-(1-phenyl-2-hydroxyethyl)glutathione and S-(2-phenyl-2-hydroxyethyl)glutathione in Fischer-344 rats.

Journal: Toxicology19910325

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