4-quinolone

Modify Date: 2024-01-02 13:14:07

4-quinolone Structure
4-quinolone structure
Common Name 4-quinolone
CAS Number 611-36-9 Molecular Weight 145.158
Density 1.3±0.1 g/cm3 Boiling Point 313.0±15.0 °C at 760 mmHg
Molecular Formula C9H7NO Melting Point 200-202 °C(lit.)
MSDS Chinese USA Flash Point 143.1±20.4 °C
Symbol GHS07
GHS07
Signal Word Warning

 Use of 4-quinolone


4-Quinolone (Kynurine) is a quinoline derivative. Kynurine pathway modulates tryptophan metabolism and involves in neuroprotective effect. Kynurine promotes tumor cell survival and motility by suppressing antitumor immune[1][2].

 Names

Name quinolin-4-ol
Synonym More Synonyms

 4-quinolone Biological Activity

Description 4-Quinolone (Kynurine) is a quinoline derivative. Kynurine pathway modulates tryptophan metabolism and involves in neuroprotective effect. Kynurine promotes tumor cell survival and motility by suppressing antitumor immune[1][2].
Related Catalog
In Vitro 4-Quinolone (Kynurine) promotes tumor cell survival and motility by suppressing antitumor immune responses through AhR in an autocrine/paracrine fashion. This system is particularly active in human brain tumors where the activation of AhR enhances the expression of TDO producing more kynurine and kynurinic acid. In the healthy human brain, very low levels of TDO exist, whereas, in human brain tumors, the TDO protein levels increase with malignancy[3].
References

[1]. Pellicciari R, et al. Modulation of the kynurine pathway of tryptophan metabolism in search for neuroprotective agents. Focus on kynurenine-3-hydroxylase. Adv Exp Med Biol. 2003;527:621-8.

[2]. Marija Pinne, et al. Cytochrome P450 Gene Regulation: Reporter Assays to Assess Aryl Hydrocarbon Receptor (HLHE76, AhR) Activation and Antagonism. Cytochrome P450. pp 157-174.

[3]. Opitz CA, et al. An endogenous tumour-promoting ligand of the human aryl hydrocarbon receptor. Nature. 2011 Oct 5;478(7368):197-203.

 Chemical & Physical Properties

Density 1.3±0.1 g/cm3
Boiling Point 313.0±15.0 °C at 760 mmHg
Melting Point 200-202 °C(lit.)
Molecular Formula C9H7NO
Molecular Weight 145.158
Flash Point 143.1±20.4 °C
Exact Mass 145.052765
PSA 33.12000
LogP 2.45
Vapour Pressure 0.0±0.7 mmHg at 25°C
Index of Refraction 1.691

 Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
VC4070000
CHEMICAL NAME :
4-Quinolinol
CAS REGISTRY NUMBER :
611-36-9
LAST UPDATED :
199709
DATA ITEMS CITED :
1
MOLECULAR FORMULA :
C9-H7-N-O
MOLECULAR WEIGHT :
145.17

 Safety Information

Symbol GHS07
GHS07
Signal Word Warning
Hazard Statements H315-H319-H335
Precautionary Statements P261-P305 + P351 + P338
Personal Protective Equipment dust mask type N95 (US);Eyeshields;Gloves
Hazard Codes Xi:Irritant
Risk Phrases R36/37/38
Safety Phrases S26-S36-S37/39
RIDADR NONH for all modes of transport
WGK Germany 3
RTECS VC4070000
HS Code 2933499090

 Synthetic Route

 Customs

HS Code 2933499090
Summary 2933499090. other compounds containing in the structure a quinoline or isoquinoline ring-system (whether or not hydrogenated), not further fused. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 Articles21

More Articles
Synergistic antidepressant-like effect of ferulic acid in combination with piperine: involvement of monoaminergic system.

Metab. Brain Dis. 30 , 1505-14, (2015)

The lifetime prevalence rate for major depressive disorder (MDD) is approximately 17 % for most developed countries around the world. Dietary polyphenols are currently used as an adjuvant therapy to a...

Evolution from a natural flavones nucleus to obtain 2-(4-Propoxyphenyl)quinoline derivatives as potent inhibitors of the S. aureus NorA efflux pump.

J. Med. Chem. 54 , 5722-36, (2011)

Overexpression of efflux pumps is an important mechanism by which bacteria evade the effects of substrate antimicrobial agents. Inhibition of such pumps is a promising strategy to circumvent this resi...

Antioxidant properties of 4-quinolones and structurally related flavones.

Bioorg. Med. Chem. 20 , 809-18, (2012)

Neurodegenerative disorders are frequently associated with increased oxidative damage to the brain as a result of free radicals produced by cellular respiration. The onset and progression of neurodege...

 Synonyms

4-Quinolinol
Chinolin-4-ol
p-hydroxyquinoline
4-quinolone
4(1H)-QUINOLINONE
Chinolin-4(1H)-on
Quinolin-4(1H)-one
quinolin-4-one
1,4-Dihydroquinoline-4-one
HYDROXYQUINOLINE,4
4-hydroxyquinoline acid
KYNURINE
4-Hydroxyquinoline
4-oxo-1,4-dihydroquinoline
4-hydroxy-quinolin
EINECS 210-268-2
quinolin-4-ol
quinoline-4-ol
MFCD00006777
Top Suppliers:I want be here





Get all suppliers and price by the below link:

4-quinolone suppliers

4-quinolone price