P13207
Phenazine
98%
Synonym(s):
Dibenzo[b,e]pyrazine
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About This Item
Empirical Formula (Hill Notation):
C12H8N2
CAS Number:
Molecular Weight:
180.21
UNSPSC Code:
12352103
NACRES:
NA.23
PubChem Substance ID:
EC Number:
202-193-9
Beilstein/REAXYS Number:
126500
MDL number:
Product Name
Phenazine, 98%
InChI key
PCNDJXKNXGMECE-UHFFFAOYSA-N
InChI
1S/C12H8N2/c1-2-6-10-9(5-1)13-11-7-3-4-8-12(11)14-10/h1-8H
SMILES string
c1ccc2nc3ccccc3nc2c1
assay
98%
form
crystals
mp
172-176 °C (lit.)
fluorescence
λex 426 nm; λem 471 nm in ethyl acetate
Quality Level
Gene Information
human ... PRNP(5621)
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Related Categories
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Ruilian Yao et al.
Biotechnology for biofuels, 11, 130-130 (2018-05-15)
Glycerol, an inevitable byproduct of biodiesel, has become an attractive feedstock for the production of value-added chemicals due to its availability and low price. Pseudomonas chlororaphis HT66 can use glycerol to synthesize phenazine-1-carboxamide (PCN), a phenazine derivative, which is strongly
Lucas William Mendes et al.
Frontiers in microbiology, 10, 2252-2252 (2019-10-22)
The taxonomically diverse rhizosphere microbiome contributes to plant nutrition, growth and health, including protection against soil-borne pathogens. We previously showed that breeding for Fusarium-resistance in common bean changed the rhizosphere microbiome composition and functioning. Here, we assessed the impact of
Raghvendra K Dubey et al.
Phytotherapy research : PTR, 31(12), 1868-1874 (2017-09-28)
We previously reported that piperine, an active alkaloidal principal of black and long peppers, enhances drug bioavailability by inhibiting drug metabolism. Another mechanism influencing drug availability/uptake is its free fraction. Since piperine is highly lipophilic, we hypothesize that it could
Steven Higgins et al.
Frontiers in cellular and infection microbiology, 8, 252-252 (2018-08-08)
The Pseudomonas aeruginosa quorum sensing (QS) network plays a key role in the adaptation to environmental changes and the control of virulence factor production in this opportunistic human pathogen. Three interlinked QS systems, namely las, rhl, and pqs, are central
Daniel W Watkins et al.
Nature communications, 8(1), 358-358 (2017-08-27)
Although catalytic mechanisms in natural enzymes are well understood, achieving the diverse palette of reaction chemistries in re-engineered native proteins has proved challenging. Wholesale modification of natural enzymes is potentially compromised by their intrinsic complexity, which often obscures the underlying
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