36207-49-5,MFCD00057761
Catalog No.:AA00COBK

36207-49-5 | AMINO ACID HYDROXAMATES DL-NORVALINE HYDROXAMATE

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  • Technical Information
  • Properties
  • Literature
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Technical Information
Catalog Number:
AA00COBK
Chemical Name:
AMINO ACID HYDROXAMATES DL-NORVALINE HYDROXAMATE
CAS Number:
36207-49-5
Molecular Formula:
C5H12N2O2
Molecular Weight:
132.1610
MDL Number:
MFCD00057761
SMILES:
CCCC(C(=NO)O)N
Properties
Computed Properties
 
Complexity:
95  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
3  
Isotope Atom Count:
0  
Rotatable Bond Count:
3  
Undefined Atom Stereocenter Count:
1  
Undefined Bond Stereocenter Count:
0  
XLogP3:
-0.6  

Literature

Title: Design and evaluation of hydroxamate derivatives as metal-mediated inhibitors of a protein tyrosine kinase.

Journal: Journal of medicinal chemistry 20061214

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Tags:36207-49-5 Molecular Formula|36207-49-5 MDL|36207-49-5 SMILES|36207-49-5 AMINO ACID HYDROXAMATES DL-NORVALINE HYDROXAMATE
Catalog No.: AA00COBK
36207-49-5,MFCD00057761
36207-49-5 | AMINO ACID HYDROXAMATES DL-NORVALINE HYDROXAMATE
This product is typically in stock,please click "Inquire" below or contact us at [email protected]for pricing and availability information.
Inquire
Technical Information
Catalog Number: AA00COBK
Chemical Name: AMINO ACID HYDROXAMATES DL-NORVALINE HYDROXAMATE
CAS Number: 36207-49-5
Molecular Formula: C5H12N2O2
Molecular Weight: 132.1610
MDL Number: MFCD00057761
SMILES: CCCC(C(=NO)O)N
Properties
Complexity: 95  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 9  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 3  
Isotope Atom Count: 0  
Rotatable Bond Count: 3  
Undefined Atom Stereocenter Count: 1  
Undefined Bond Stereocenter Count: 0  
XLogP3: -0.6  
Literature fold

Title: Design and evaluation of hydroxamate derivatives as metal-mediated inhibitors of a protein tyrosine kinase.

Journal: Journal of medicinal chemistry20061214

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