19350-66-4,MFCD00417306
Catalog No.:AA0072ZP

19350-66-4 | 2,6-Dimethyl-1,4-dihydro-pyridine-3,4,5-tricarboxylic acid 3,5-diethyl ester

Pack Size
Purity
Availability
Price(USD)
Quantity
  
100mg
97%
in stock  
$23.00   $16.00
- +
1g
97%
in stock  
$183.00   $128.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA0072ZP
Chemical Name:
2,6-Dimethyl-1,4-dihydro-pyridine-3,4,5-tricarboxylic acid 3,5-diethyl ester
CAS Number:
19350-66-4
Molecular Formula:
C14H18NO6-
Molecular Weight:
296.2958
MDL Number:
MFCD00417306
SMILES:
CCOC(=O)C1=C(C)NC(=C(C1C(=O)[O-])C(=O)OCC)C
Properties
Computed Properties
 
Complexity:
492  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
21  
Hydrogen Bond Acceptor Count:
7  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0  
Rotatable Bond Count:
7  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
1.1  

Downstream Synthesis Route

[1]EuropeanJournalofMedicinalChemistry,1994,vol.29,p.325-328

19350-66-4   
sodium2-(2,6-dimethyl-3,5-diethoxycarbonyl-1,4-dihydroisonicotinoyl)aminopropionate 

[1]EuropeanJournalofMedicinalChemistry,1994,vol.29,p.325-328

19350-66-4   
sodium2-(2,6-dimethyl-3,5-diethoxycarbonyl-1,4-dihydropyridine-4-carboxamido)ethanesulfonate 

[1]EuropeanJournalofMedicinalChemistry,1994,vol.29,p.325-328

[2]EuropeanJournalofMedicinalChemistry,1994,vol.29,p.325-328

Literature

Title: Modulation of cellular defense processes in human lymphocytes in vitro by a 1,4-dihydropyridine derivative.

Journal: Mutation research 20090101

Title: Microsphere-based protease assays and screening application for lethal factor and factor Xa.

Journal: Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501

Title: A 1,4-dihydropyridine derivative reduces DNA damage and stimulates DNA repair in human cells in vitro.

Journal: Mutation research 20051110

Title: Nadezhda I Ryabokon, et al. A 1,4-dihydropyridine Derivative Reduces DNA Damage and Stimulates DNA Repair in Human Cells in Vitro. Mutat Res. 2005 Nov 10;587(1-2):52-8.

Title: E Buraka, et al. DNA-binding Studies of AV-153, an Antimutagenic and DNA Repair-Stimulating Derivative of 1,4-dihydropiridine. Chem Biol Interact. 2014 Sep 5;220:200-7.

Title: Lidija Milkovic, et al. Antioxidative 1,4-Dihydropyridine Derivatives Modulate Oxidative Stress and Growth of Human Osteoblast-Like Cells In Vitro. Antioxidants (Basel). 2018 Sep 19;7(9):123.

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SDS
Tags:19350-66-4 Molecular Formula|19350-66-4 MDL|19350-66-4 SMILES|19350-66-4 2,6-Dimethyl-1,4-dihydro-pyridine-3,4,5-tricarboxylic acid 3,5-diethyl ester
Catalog No.: AA0072ZP
19350-66-4,MFCD00417306
19350-66-4 | 2,6-Dimethyl-1,4-dihydro-pyridine-3,4,5-tricarboxylic acid 3,5-diethyl ester
Pack Size: 100mg
Purity: 97%
in stock
$23.00 $16.00
Pack Size: 1g
Purity: 97%
in stock
$183.00 $128.00
Quantity
- +
Add to Card
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bulk Quotation Request
Technical Information
Catalog Number: AA0072ZP
Chemical Name: 2,6-Dimethyl-1,4-dihydro-pyridine-3,4,5-tricarboxylic acid 3,5-diethyl ester
CAS Number: 19350-66-4
Molecular Formula: C14H18NO6-
Molecular Weight: 296.2958
MDL Number: MFCD00417306
SMILES: CCOC(=O)C1=C(C)NC(=C(C1C(=O)[O-])C(=O)OCC)C
Properties
Complexity: 492  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 21  
Hydrogen Bond Acceptor Count: 7  
Hydrogen Bond Donor Count: 2  
Isotope Atom Count: 0  
Rotatable Bond Count: 7  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 1.1  
Downstream Synthesis Route
771-61-9    19350-66-4    92236-40-3 

[1]EuropeanJournalofMedicinalChemistry,1994,vol.29,p.325-328

19350-66-4   
sodium2-(2,6-dimethyl-3,5-diethoxycarbonyl-1,4-dihydroisonicotinoyl)aminopropionate 

[1]EuropeanJournalofMedicinalChemistry,1994,vol.29,p.325-328

19350-66-4   
sodium2-(2,6-dimethyl-3,5-diethoxycarbonyl-1,4-dihydropyridine-4-carboxamido)ethanesulfonate 

[1]EuropeanJournalofMedicinalChemistry,1994,vol.29,p.325-328

[2]EuropeanJournalofMedicinalChemistry,1994,vol.29,p.325-328

Literature fold

Title: Modulation of cellular defense processes in human lymphocytes in vitro by a 1,4-dihydropyridine derivative.

Journal: Mutation research20090101

Title: Microsphere-based protease assays and screening application for lethal factor and factor Xa.

Journal: Cytometry. Part A : the journal of the International Society for Analytical Cytology20060501

Title: A 1,4-dihydropyridine derivative reduces DNA damage and stimulates DNA repair in human cells in vitro.

Journal: Mutation research20051110

Title: Nadezhda I Ryabokon, et al. A 1,4-dihydropyridine Derivative Reduces DNA Damage and Stimulates DNA Repair in Human Cells in Vitro. Mutat Res. 2005 Nov 10;587(1-2):52-8.

Title: E Buraka, et al. DNA-binding Studies of AV-153, an Antimutagenic and DNA Repair-Stimulating Derivative of 1,4-dihydropiridine. Chem Biol Interact. 2014 Sep 5;220:200-7.

Title: Lidija Milkovic, et al. Antioxidative 1,4-Dihydropyridine Derivatives Modulate Oxidative Stress and Growth of Human Osteoblast-Like Cells In Vitro. Antioxidants (Basel). 2018 Sep 19;7(9):123.

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