79923-55-0,MFCD27978232
Catalog No.:AA00G4PC

79923-55-0 | Ticlopidine N-Oxide

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  • Technical Information
  • Properties
  • Literature
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  • Download SDS
Technical Information
Catalog Number:
AA00G4PC
Chemical Name:
Ticlopidine N-Oxide
CAS Number:
79923-55-0
Molecular Formula:
C14H14ClNOS
Molecular Weight:
279.7851
MDL Number:
MFCD27978232
SMILES:
C1C[N+](CC2=C1SC=C2)(CC3=CC=CC=C3Cl)[O-]
Properties
Computed Properties
 
Complexity:
304  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
18  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
0  
Isotope Atom Count:
0  
Rotatable Bond Count:
2  
Undefined Atom Stereocenter Count:
1  
Undefined Bond Stereocenter Count:
0  
XLogP3:
3.1  

Literature

Title: Comparison of in vitro metabolism of ticlopidine by human cytochrome P450 2B6 and rabbit cytochrome P450 2B4.

Journal: Drug metabolism and disposition: the biological fate of chemicals 20110301

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Tags:79923-55-0 Molecular Formula|79923-55-0 MDL|79923-55-0 SMILES|79923-55-0 Ticlopidine N-Oxide
Catalog No.: AA00G4PC
79923-55-0,MFCD27978232
79923-55-0 | Ticlopidine N-Oxide
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: AA00G4PC
Chemical Name: Ticlopidine N-Oxide
CAS Number: 79923-55-0
Molecular Formula: C14H14ClNOS
Molecular Weight: 279.7851
MDL Number: MFCD27978232
SMILES: C1C[N+](CC2=C1SC=C2)(CC3=CC=CC=C3Cl)[O-]
Properties
Complexity: 304  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 18  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 0  
Isotope Atom Count: 0  
Rotatable Bond Count: 2  
Undefined Atom Stereocenter Count: 1  
Undefined Bond Stereocenter Count: 0  
XLogP3: 3.1  
Literature fold

Title: Comparison of in vitro metabolism of ticlopidine by human cytochrome P450 2B6 and rabbit cytochrome P450 2B4.

Journal: Drug metabolism and disposition: the biological fate of chemicals20110301

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