606-59-7,MFCD18379297
Catalog No.:AA00EF69

606-59-7 | 2-Amino-3-oxo-3H-phenoxazine-1,9-dicarboxylic acid

Pack Size
Purity
Availability
Price(USD)
Quantity
  
10mg
≥98%
in stock  
$192.00   $134.00
- +
50mg
≥98%
in stock  
$853.00   $597.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA00EF69
Chemical Name:
2-Amino-3-oxo-3H-phenoxazine-1,9-dicarboxylic acid
CAS Number:
606-59-7
Molecular Formula:
C14H8N2O6
Molecular Weight:
300.2231
MDL Number:
MFCD18379297
SMILES:
OC(=O)c1c2nc3c(oc2cc(=O)c1N)cccc3C(=O)O
Properties
Properties
 
Storage:
Keep in dry area;2-8℃;  

Computed Properties
 
Complexity:
675  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
22  
Hydrogen Bond Acceptor Count:
8  
Hydrogen Bond Donor Count:
3  
Isotope Atom Count:
0  
Rotatable Bond Count:
2  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
0.8  

Literature

Title: Cinnabarinic acid, an endogenous metabolite of the kynurenine pathway, activates type 4 metabotropic glutamate receptors.

Journal: Molecular pharmacology 20120501

Title: Development of a fluorimetric detection method for cinnabarinic acid using ortho-tolyl hydrazine as the derivatization reagent.

Journal: Biomedical chromatography : BMC 20100301

Title: HPLC and NMR studies of phenoxazone alkaloids from Pycnoporus cinnabarinus.

Journal: Natural product communications 20090401

Title: Cinnabarinic acid generated from 3-hydroxyanthranilic acid strongly induces apoptosis in thymocytes through the generation of reactive oxygen species and the induction of caspase.

Journal: Journal of cellular biochemistry 20080101

Title: F Fazio, et al. Cinnabarinic acid, an endogenous metabolite of the kynurenine pathway, activates type 4 metabotropic glutamate receptors.Mol Pharmacol. 2012 May;81(5):643-56.

Title: Martina Ulivieri, et al. The Trace Kynurenine, Cinnabarinic Acid, Displays Potent Antipsychotic-Like Activity in Mice and Its Levels Are Reduced in the Prefrontal Cortex of Individuals Affected by Schizophrenia. Schizophr Bull. 2020 Jun 7;sbaa074.

Title: Francesco Fazio, et al. Cinnabarinic acid and xanthurenic acid: Two kynurenine metabolites that interact with metabotropic glutamate receptors. Neuropharmacology. 2017 Jan;112(Pt B):365-372.

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Tags:606-59-7 Molecular Formula|606-59-7 MDL|606-59-7 SMILES|606-59-7 2-Amino-3-oxo-3H-phenoxazine-1,9-dicarboxylic acid
Catalog No.: AA00EF69
606-59-7,MFCD18379297
606-59-7 | 2-Amino-3-oxo-3H-phenoxazine-1,9-dicarboxylic acid
Pack Size: 10mg
Purity: ≥98%
in stock
$192.00 $134.00
Pack Size: 50mg
Purity: ≥98%
in stock
$853.00 $597.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA00EF69
Chemical Name: 2-Amino-3-oxo-3H-phenoxazine-1,9-dicarboxylic acid
CAS Number: 606-59-7
Molecular Formula: C14H8N2O6
Molecular Weight: 300.2231
MDL Number: MFCD18379297
SMILES: OC(=O)c1c2nc3c(oc2cc(=O)c1N)cccc3C(=O)O
Properties
Storage: Keep in dry area;2-8℃;  
Complexity: 675  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 22  
Hydrogen Bond Acceptor Count: 8  
Hydrogen Bond Donor Count: 3  
Isotope Atom Count: 0  
Rotatable Bond Count: 2  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 0.8  
Literature fold

Title: Cinnabarinic acid, an endogenous metabolite of the kynurenine pathway, activates type 4 metabotropic glutamate receptors.

Journal: Molecular pharmacology20120501

Title: Development of a fluorimetric detection method for cinnabarinic acid using ortho-tolyl hydrazine as the derivatization reagent.

Journal: Biomedical chromatography : BMC20100301

Title: HPLC and NMR studies of phenoxazone alkaloids from Pycnoporus cinnabarinus.

Journal: Natural product communications20090401

Title: Cinnabarinic acid generated from 3-hydroxyanthranilic acid strongly induces apoptosis in thymocytes through the generation of reactive oxygen species and the induction of caspase.

Journal: Journal of cellular biochemistry20080101

Title: F Fazio, et al. Cinnabarinic acid, an endogenous metabolite of the kynurenine pathway, activates type 4 metabotropic glutamate receptors.Mol Pharmacol. 2012 May;81(5):643-56.

Title: Martina Ulivieri, et al. The Trace Kynurenine, Cinnabarinic Acid, Displays Potent Antipsychotic-Like Activity in Mice and Its Levels Are Reduced in the Prefrontal Cortex of Individuals Affected by Schizophrenia. Schizophr Bull. 2020 Jun 7;sbaa074.

Title: Francesco Fazio, et al. Cinnabarinic acid and xanthurenic acid: Two kynurenine metabolites that interact with metabotropic glutamate receptors. Neuropharmacology. 2017 Jan;112(Pt B):365-372.

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