Phenazoviridin
Basic information
- CAS
155233-15-1- Standard SMILES
CC(C)=CCc1cccc2nc3c(C(=O)O[C@@H]4O[C@@H](C)[C@@H](O)[C@@H](O)[C@H]4O)cccc3nc12- InChIKey
YYAZCIFRQFQQRH-PQILALKLSA-N- Molecular formula
- C24H26N2O6
- Average molar mass
- 438.5 g/mol
- Monoisotopic mass
- 438.17908655
Overview
Phenazoviridin is a member of phenazines.
Names & identifiers
- Preferred name
- Phenazoviridin
- IUPAC
- [(2S,3R,4R,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl] 6-(3-methylbut-2-enyl)phenazine-1-carboxylate
- English name
- α-L-Talopyranose, 6-deoxy-, 1-[6-(3-methyl-2-buten-1-yl)-1-phenazinecarboxylate]
- Molecular formula
- C24H26N2O6
- Molecular weight
- 438.48
Names & synonyms
Phenazoviridin155233-15-1HL3PYH7JDC[(2S,3R,4R,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl] 6-(3-methylbut-2-enyl)phenazine-1-carboxylateDTXSID601658616-(3-methyl-2-butenyl)phenazine-1-carboxylic acid 6-deoxy-alpha-L-talopyranose ester((2S,3R,4R,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl) 6-(3-methylbut-2-enyl)phenazine-1-carboxylateRefChem:172648DTXCID3088352alpha-L-Talopyranose, 6-deoxy-, 1-(6-(3-methyl-2-butenyl)-1-phenazinecarboxylate)orb1701803CHEBI:212199
Show more names
α-L-Talopyranose, 6-deoxy-, 1-[6-(3-methyl-2-buten-1-yl)-1-phenazinecarboxylate]
HR-04AKOS040747269DA-66659HY-114651CS-0063656T259436-Deoxy-1-O-[6-(3-methylbut-2-en-1-yl)phenazine-1-carbonyl]-alpha-L-talopyranosealpha-L-Talopyranose, 6-deoxy-, 1-[6-(3-methyl-2-buten-1-yl)-1-phenazinecarboxylate]
Database identifiers
- CAS
155233-15-1
Properties
Computed structural properties
- XLogP
- 2.8
- Topological polar surface area
- 122 Ų
- Hydrogen bond donors
- 3
- Hydrogen bond acceptors
- 8
- Rotatable bonds
- 5
- Heavy atoms
- 32
- Formal charge
- 0
- Complexity
- 698
Physicochemical properties
- Boiling point
- 661.1 · 661.1±55.0 °C(Predicted)
- Density
- 1.38 · 1.38±0.1 g/cm3(Predicted)
- pka
- 12.52 · 12.52±0.70(Predicted)
Chemistry & industry
Applications
DescriptionPhenazoviridin is an antihypoxic agent.
UsesPhenazoviridin is a free radical scavenger. Phenazoviridin shows strong inhibitory activity against lipid peroxidation in rat brain homogenate and exhibits antihypoxic activity in mice[1].
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Compound notes
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