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LY2794193

Product Name
LY2794193
CAS No.
2173037-97-1
Chemical Name
LY2794193
Synonyms
LY2794193;LY-2794193,LY2794193;Bicyclo[3.1.0]hexane-2,6-dicarboxylic acid, 2-amino-4-[(3-methoxybenzoyl)amino]-, (1S,2S,4S,5R,6S)-
CBNumber
CB45419777
Molecular Formula
C16H18N2O6
Formula Weight
334.32
MOL File
2173037-97-1.mol
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LY2794193 Property

Boiling point:
598.6±50.0 °C(Predicted)
Density 
1.50±0.1 g/cm3(Predicted)
storage temp. 
Store at -20°C
form 
Solid
pka
1.78±0.60(Predicted)
color 
White to off-white
Water Solubility 
Water : 2 mg/mL (5.98 mM; ultrasonic and adjust pH to 14 with NaOH)
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

ChemScene
Product number
CS-0077322
Product name
LY2794193
Purity
99.88%
Packaging
5mg
Price
$550
Updated
2021/12/16
ChemScene
Product number
CS-0077322
Product name
LY2794193
Purity
99.88%
Packaging
10mg
Price
$850
Updated
2021/12/16
ChemScene
Product number
CS-0077322
Product name
LY2794193
Purity
99.88%
Packaging
50mg
Price
$2850
Updated
2021/12/16
ChemScene
Product number
CS-0077322
Product name
LY2794193
Purity
99.88%
Packaging
100mg
Price
$3950
Updated
2021/12/16
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LY2794193 Chemical Properties,Usage,Production

Biological Activity

LY2794193 is a potent and selective mGlu3 receptor agonist (hmGlu3 Ki=0.927 nM, EC50=0.47 nM; hmGlu2 Ki=412 nM, EC50=47.5 nM).

in vitro

LY2794193 exhihits inhibition of spontaneous Ca 2+ oscillations in cultured rat cortical neurons with an EC 50 of 43.6 nM.
In the rat cortical neuron Ca 2+ oscillation assay, LY2794193 exhibits a biphasic inhibition of spontaneous Ca 2+ transients (high affinity EC 50 =0.44 nM; 48% of the total agonist response; low affinity EC 50 =43.6 nM; 52% of the total agonist response) with combined maximal agonist efficacy (E max ) of 66%. < /p>

in vivo

LY2794193 (1-30 mg/kg, sc), given 30 min prior to PCP (5 mg/kg, sc) leads a dose-related reduction in ambulations.
LY2794193 (1 mg/ kg; iv) exhibits moderate clearance (18.3 mL/min per kg) and volume of distribution (1.17 L/kg) with a calculated plasma half-life (T 1/2 ) of 3.1 h in Male Sprague-Dawley rats.
LY2794193 (3 mg/kg; sc) leads to the rapid appearance in the plasma (AUC=9.9 μM; C max =6.78 μM; T max =0.44 h) and a calculated bioavailability of 121% in male Sprague-Dawley rats.

< /tr>
Animal Model: Male Sprague-Dawley rats
Dosage: 1, 3, 10, or 30 mg/kg < /td>
Administration: Administrated sc; given 30 min prior to PCP (5 mg/kg, sc)
Result: A dose-related reduction in ambulations was observed, with the 10 and 30 mg/kg dose groups found to be statistically significant.

target

mGluR3

0.47 nM (EC 50 )

mGluR3

0.927 nM (Ki)

mGluR2

47.5 (EC 50 )

mGluR2

412 (Ki)

LY2794193 Preparation Products And Raw materials

Raw materials

Preparation Products

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LY2794193 Suppliers

TargetMol Chemicals Inc.
Tel
+1-781-999-5354 +1-00000000000
Email
marketing@targetmol.com
Country
United States
ProdList
32161
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58
Aladdin Scientific
Tel
+1-+1(833)-552-7181
Email
sales@aladdinsci.com
Country
United States
ProdList
52924
Advantage
58
MedChemExpress
Tel
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Fax
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Email
sales@medchemexpress.com
Country
United States
ProdList
6398
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58

2173037-97-1, LY2794193Related Search:


  • LY2794193
  • Bicyclo[3.1.0]hexane-2,6-dicarboxylic acid, 2-amino-4-[(3-methoxybenzoyl)amino]-, (1S,2S,4S,5R,6S)-
  • LY-2794193,LY2794193
  • 2173037-97-1