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Z-Ser-OH

CAS No.:
1145-80-8
Catalog Number:
AG000EKT
Molecular Formula:
C11H13NO5
Molecular Weight:
239.2246
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
96%
In Stock USA
United States
$13
- +
25g
96%
In Stock USA
United States
$25
- +
100g
96%
In Stock USA
United States
$63
- +
500g
96%
In Stock USA
United States
$250
- +
Product Description
Catalog Number:
AG000EKT
Chemical Name:
Z-Ser-OH
CAS Number:
1145-80-8
Molecular Formula:
C11H13NO5
Molecular Weight:
239.2246
MDL Number:
MFCD00002662
IUPAC Name:
(2S)-3-hydroxy-2-(phenylmethoxycarbonylamino)propanoic acid
InChI:
InChI=1S/C11H13NO5/c13-6-9(10(14)15)12-11(16)17-7-8-4-2-1-3-5-8/h1-5,9,13H,6-7H2,(H,12,16)(H,14,15)/t9-/m0/s1
InChI Key:
GNIDSOFZAKMQAO-VIFPVBQESA-N
SMILES:
OC[C@@H](C(=O)O)NC(=O)OCc1ccccc1
EC Number:
214-546-4
Properties
Complexity:
263  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Defined Bond Stereocenter Count:
0
Exact Mass:
239.079g/mol
Formal Charge:
0
Heavy Atom Count:
17  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
3  
Isotope Atom Count:
0
Molecular Weight:
239.227g/mol
Monoisotopic Mass:
239.079g/mol
Rotatable Bond Count:
6  
Topological Polar Surface Area:
95.9A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.4  
Literature
Title Journal
N-(2-oxo-3-oxetanyl)carbamic acid esters as N-acylethanolamine acid amidase inhibitors: synthesis and structure-activity and structure-property relationships. Journal of medicinal chemistry 20120524
Biochemical and mass spectrometric characterization of human N-acylethanolamine-hydrolyzing acid amidase inhibition. PloS one 20120101
From polyesters to polyamides via O-N acyl migration: an original multi-transfer reaction. Macromolecular rapid communications 20110616
Development of miracle medicines from sialic acids. Proceedings of the Japan Academy. Series B, Physical and biological sciences 20110610
Predicting binding to p-glycoprotein by flexible receptor docking. PLoS computational biology 20110601
Analyte separation by OMNiMIPs imprinted with multiple templates. Biosensors & bioelectronics 20091115
Transport and signaling via the amino acid binding site of the yeast Gap1 amino acid transceptor. Nature chemical biology 20090101
Synthesis and anticonvulsant evaluation of 6-amino-1,4-oxazepane-3,5-dione derivatives. Archives of pharmacal research 20080701
A short and efficient synthesis of L-5,5,5,5',5',5'-hexafluoroleucine from N-Cbz-L-serine. Organic letters 20021128
Beta-lactones as a new class of cysteine proteinase inhibitors: inhibition of hepatitis A virus 3C proteinase by N-Cbz-serine beta-lactone. Organic letters 19990909
Properties