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1-Hydroxyphenazine

CAS No.:
528-71-2
Catalog Number:
AG003EF5
Molecular Formula:
C12H8N2O
Molecular Weight:
196.2047
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
100mg
>95.0%(GC)
1 week
United States
$167
- +
1g
1 week
United States
$316
- +
5g
1 week
United States
$1055
- +
Product Description
Catalog Number:
AG003EF5
Chemical Name:
1-Hydroxyphenazine
CAS Number:
528-71-2
Molecular Formula:
C12H8N2O
Molecular Weight:
196.2047
MDL Number:
MFCD00059692
IUPAC Name:
phenazin-1-ol
InChI:
InChI=1S/C12H8N2O/c15-11-7-3-6-10-12(11)14-9-5-2-1-4-8(9)13-10/h1-7,15H
InChI Key:
SVRNCBGWUMMBQB-UHFFFAOYSA-N
SMILES:
Oc1cccc2c1nc1ccccc1n2
UNII:
0D51M21IXN
NSC Number:
88882
Properties
Complexity:
234  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
196.064g/mol
Formal Charge:
0
Heavy Atom Count:
15  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
196.209g/mol
Monoisotopic Mass:
196.064g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
46A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.3  
Literature
Title Journal
Generation of Reactive Oxygen Species Mediated by 1‑Hydroxyphenazine, a Virulence Factor of Pseudomonas aeruginosa. Chemical research in toxicology 20150216
Production, purification, and characterization of antifungal metabolite from Pseudomonas aeruginosa SD12, a new strain obtained from tannery waste polluted soil. Journal of microbiology and biotechnology 20120501
Inhibition of autophagy by 3-methyladenine protects 1321N1 astrocytoma cells against pyocyanin- and 1-hydroxyphenazine-induced toxicity. Archives of toxicology 20120201
Chromophenazines from the terrestrial Streptomyces sp. Ank 315. Journal of natural products 20120127
Metabolic profiling and biological activities of bioactive compounds produced by Pseudomonas sp. strain ICTB-745 isolated from Ladakh, India. Journal of microbiology and biotechnology 20120101
Tasco®: a product of Ascophyllum nodosum enhances immune response of Caenorhabditis elegans against Pseudomonas aeruginosa infection. Marine drugs 20120101
Quantifying the dynamics of bacterial secondary metabolites by spectral multiphoton microscopy. ACS chemical biology 20110916
Izumiphenazine D, a new phenazoquinoline N-oxide from Streptomyces sp. IFM 11204. Chemical & pharmaceutical bulletin 20110101
Bioactive pigments from marine bacteria: applications and physiological roles. Evidence-based complementary and alternative medicine : eCAM 20110101
Metabolism and function of phenazines in bacteria: impacts on the behavior of bacteria in the environment and biotechnological processes. Applied microbiology and biotechnology 20100501
Scarless and sequential gene modification in Pseudomonas using PCR product flanked by short homology regions. BMC microbiology 20100101
Inflammatory mechanisms in the lung. Journal of inflammation research 20090101
Cell wall glycans and soluble factors determine the interactions between the hyphae of Candida albicans and Pseudomonas aeruginosa. FEMS microbiology letters 20081001
Redox reactions of phenazine antibiotics with ferric (hydr)oxides and molecular oxygen. Environmental science & technology 20080401
Widespread pyocyanin over-production among isolates of a cystic fibrosis epidemic strain. BMC microbiology 20070101
State of the art: why do the lungs of patients with cystic fibrosis become infected and why can't they clear the infection? Respiratory research 20030101
Induction of neutrophil apoptosis by the Pseudomonas aeruginosa exotoxin pyocyanin: a potential mechanism of persistent infection. Journal of immunology (Baltimore, Md. : 1950) 20020215
Properties