Basic information Safety Supplier Related

VU0155041

Basic information Safety Supplier Related

VU0155041 Basic information

Product Name:
VU0155041
Synonyms:
  • VU0155041
  • cis-2-[[(3,5-Dichlorophenyl)amino]carbonyl]cyclohexanecarboxylicacid
  • UV0155041
  • (1R,2S)-2-[(3,5-dichlorophenyl)carbamoyl]cyclohexane-1-carboxylic acid
  • (±)-cis-2-(3,5-DichlorophenylcarbaMoy)cyclohexanecarboxylic Acid
  • (±)-cis-2-(3,5-Dicholorphenylcarbamoyl)cyclohexanecarboxylic acid
  • rel-(1R,2S)-2-[[(3,5-Dichlorophenyl)amino]carbonyl]cyclohexanecarboxylic acid
  • VU0155041;VU-0155041
CAS:
1093757-42-6
MF:
C14H15Cl2NO3
MW:
316.18
Product Categories:
  • Glutamate
Mol File:
1093757-42-6.mol
More
Less

VU0155041 Chemical Properties

Boiling point:
540.2±50.0 °C(Predicted)
Density 
1.429±0.06 g/cm3(Predicted)
storage temp. 
Store at RT
solubility 
Soluble to 100 mM in 1eq. NaOH and to 100 mM in DMSO
form 
white powder
pka
4.48±0.44(Predicted)
color 
Pale purple to purple
More
Less

Safety Information

Hazard Codes 
Xn
Risk Statements 
22
WGK Germany 
3
More
Less

VU0155041 Usage And Synthesis

Uses

Acts as an allosteric modulator (PAM) of mGluR4, part of the class of receptors influencing Parkinson’s disease and it’s expression.

Biological Activity

VU0155041 is a mixed allosteric agonist/positive allosteric modulator (PAM) of mGluR4. VU0155041 is approximately 8-fold more potent than PHCCC and does not show any significant potentiator or antagonist activity at other mGluR subtypes. It is soluble in an aqueous vehicle and intracerebroventricular administration of 31-316 nmol of VU0155041 dose-dependently decreased haloperidol-induced catalepsy and reserpine-induced akinesia in rats. VU0155041 exhibits selectivity for mGluR4 relative to 67 different targets and does not affect the function of striatal NMDA receptors.', 'VU0155041 is a positive allosteric modulator of the metabotropic glutamate receptor subtype 4. It also shows some direct agonist activity, but at a site different from the glutamate binding site. /VU0155041 is approximately 8-fold more potent than PHCCC and enhances the activity of glutamate also about 8-fold. It shows promising anti-Parkinsonian effects in animal models of Parkinsonμs disease.

in vivo

VU0155041 (31 nmol, 93 nmol; i.c.v.) reverses catalepsy induced by the dopamine D2 receptor antagonist Haloperidol (1.5 mg/kg, i.p.) in rats[1].
VU0155041 (93 nnmol, 316 nmol; i.c.v.) reverses Reserpine (HY-N0480)-induced akinesia in rats[1].

Animal Model:Third ventricle cannulated (TVC) Male Sprague-Dawley rats (225-255 g)[1]
Dosage:31 nmol, 93 nmol (10 μL)
Administration:Intracerebroventrical injection, after the Haloperidol (1.5 mg/kg) treatment 2 hours
Result:Decreased the cataleptic effects of Haloperidol, and the effects still presented 30 min after infusion.

IC 50

Human mGlu4: 798 nM (EC50); Rat mGlu4: 693 nM (EC50)

VU0155041Supplier

J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Email
jkinfo@jkchemical.com
Tel
821-50328103-801 18930552037
Email
3bsc@sina.com
Ascent Scientific
Tel
4401179829988
Email
customerservice@ascentscientific.co.uk
Shanghai JiYi Biotechnology Co. Ltd.
Tel
13621943973
Email
sales@shjiyipharmatech.com
EMMX Biotechnology LLC
Tel
888-539-0666
Email
info@emmx.com