Z-Phe-OHCAS# 1161-13-3 |
2D Structure
- Dihydroberberine
Catalog No.:BCN2573
CAS No.:483-15-8
- Sesamolin
Catalog No.:BCN1289
CAS No.:526-07-8
- Carnosol
Catalog No.:BCN1055
CAS No.:5957-80-2
- Harpagide
Catalog No.:BCN4996
CAS No.:6926-08-5
Quality Control & MSDS
3D structure
Package In Stock
Number of papers citing our products
Cas No. | 1161-13-3 | SDF | Download SDF |
PubChem ID | 70878 | Appearance | Powder |
Formula | C17H17NO4 | M.Wt | 299.3 |
Type of Compound | N/A | Storage | Desiccate at -20°C |
Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
Chemical Name | (2S)-3-phenyl-2-(phenylmethoxycarbonylamino)propanoic acid | ||
SMILES | C1=CC=C(C=C1)CC(C(=O)O)NC(=O)OCC2=CC=CC=C2 | ||
Standard InChIKey | RRONHWAVOYADJL-HNNXBMFYSA-N | ||
Standard InChI | InChI=1S/C17H17NO4/c19-16(20)15(11-13-7-3-1-4-8-13)18-17(21)22-12-14-9-5-2-6-10-14/h1-10,15H,11-12H2,(H,18,21)(H,19,20)/t15-/m0/s1 | ||
General tips | For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months. We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months. Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it. |
||
About Packaging | 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial. 2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial. 3. Try to avoid loss or contamination during the experiment. |
||
Shipping Condition | Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request. |
Z-Phe-OH Dilution Calculator
Z-Phe-OH Molarity Calculator
1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
1 mM | 3.3411 mL | 16.7056 mL | 33.4113 mL | 66.8226 mL | 83.5282 mL |
5 mM | 0.6682 mL | 3.3411 mL | 6.6823 mL | 13.3645 mL | 16.7056 mL |
10 mM | 0.3341 mL | 1.6706 mL | 3.3411 mL | 6.6823 mL | 8.3528 mL |
50 mM | 0.0668 mL | 0.3341 mL | 0.6682 mL | 1.3365 mL | 1.6706 mL |
100 mM | 0.0334 mL | 0.1671 mL | 0.3341 mL | 0.6682 mL | 0.8353 mL |
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations. |
Calcutta University
University of Minnesota
University of Maryland School of Medicine
University of Illinois at Chicago
The Ohio State University
University of Zurich
Harvard University
Colorado State University
Auburn University
Yale University
Worcester Polytechnic Institute
Washington State University
Stanford University
University of Leipzig
Universidade da Beira Interior
The Institute of Cancer Research
Heidelberg University
University of Amsterdam
University of Auckland
TsingHua University
The University of Michigan
Miami University
DRURY University
Jilin University
Fudan University
Wuhan University
Sun Yat-sen University
Universite de Paris
Deemed University
Auckland University
The University of Tokyo
Korea University
Z-Phe-OH
- RETF-4NA
Catalog No.:BCC6073
CAS No.:1160928-63-1
- IDE 1
Catalog No.:BCC7841
CAS No.:1160927-48-9
- Dehydromiltirone
Catalog No.:BCN5357
CAS No.:116064-77-8
- Piperolactam C
Catalog No.:BCN4818
CAS No.:116064-76-7
- Pyr3
Catalog No.:BCC7771
CAS No.:1160514-60-2
- MLN4924 HCl salt
Catalog No.:BCC1773
CAS No.:1160295-21-5
- VU 0238429
Catalog No.:BCC7729
CAS No.:1160247-92-6
- 1-Amino-4-hydroxyanthraquinone
Catalog No.:BCC8452
CAS No.:116-85-8
- 4-Amino-3-hydroxy-1-naphthalenesulfonic acid
Catalog No.:BCC8680
CAS No.:116-63-2
- Aldicarb
Catalog No.:BCC5475
CAS No.:116-06-3
- TC-I 2000
Catalog No.:BCC6244
CAS No.:1159996-20-9
- Caulophine
Catalog No.:BCN7990
CAS No.:1159989-19-1
- Phenamil
Catalog No.:BCC7673
CAS No.:1161-94-0
- G-15
Catalog No.:BCC6058
CAS No.:1161002-05-6
- VU 0361737
Catalog No.:BCC4596
CAS No.:1161205-04-4
- Brevicolline
Catalog No.:BCN2459
CAS No.:20069-02-7
- Alexine
Catalog No.:BCN2054
CAS No.:116174-63-1
- Complanatoside
Catalog No.:BCN8213
CAS No.:116183-66-5
- Aflatoxin B1
Catalog No.:BCC9212
CAS No.:1162-65-8
- Levobetaxolol HCl
Catalog No.:BCC4671
CAS No.:116209-55-3
- MCB-613
Catalog No.:BCC3982
CAS No.:1162656-22-5
- Pyrroside B
Catalog No.:BCN4042
CAS No.:116271-35-3
- 6-Aldehydoisoophiopogonanone A
Catalog No.:BCN2860
CAS No.:116291-82-8
- Clemizole hydrochloride
Catalog No.:BCC1486
CAS No.:1163-36-6
Unraveling the molecular recognition of amino acid derivatives by a pseudopeptidic macrocycle: ESI-MS, NMR, fluorescence, and modeling studies.[Pubmed:19606887]
J Org Chem. 2009 Aug 21;74(16):6130-42.
The binding between a pseudopeptidic macrocyclic naphthalenophane and different N-protected amino acid derivatives has been thoroughly studied by ESI-MS, NMR, fluorescence, and molecular modeling. Careful NMR titration experiments led to the characterization of the intermolecular noncovalent interactions, reflecting a slight side chain and l-stereoselectivity of the host-guest complexes. The data suggest the formation of an intimate ionic pair after the proton transfer from the carboxylic substrate to the amino macrocycle. Additional intermolecular interactions like H-bonding and pi-pi contacts are also important. This receptor shows a stronger interaction with substrates bearing aromatic rings, either in the side chain or in the N-protecting group. Besides, for N-Z-Phe-OH, a moderate enantioselectivity has been observed. Mass spectrometry suggests the formation of supramolecular complexes with stoichiometries higher than 1:1. The dual nature of the fluorescence emission of the macrocyclic receptor allowed determining binding constants and pertinent thermodynamic parameters. On the basis of the experimental data (NMR titrations, intermolecular ROESY, VT-NMR) and with the help of molecular modeling, a reasonable structure for the supramolecular complexes can be proposed, in which the interactions with the naphthyl ring of the receptor play a fundamental role in the strength and selectivity of the molecular recognition event.