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Chemical Structure| 2829282-00-8 Chemical Structure| 2829282-00-8

Structure of LY367385 HCl
CAS No.: 2829282-00-8

Chemical Structure| 2829282-00-8

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LY367385 HCl is a potent and selective mGluR1a antagonist with an IC50 of 8.8 μM for quinoline-induced phosphoinositide hydrolys is and an IC50 greater than 100 μM for mGlu5a. It has neuroprotective, anticonvulsant, and antiepileptic effects.

Synonyms: LY367385 hydrochloride

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Product Details of LY367385 HCl

CAS No. :2829282-00-8
Formula : C10H12ClNO4
M.W : 245.66
SMILES Code : O=C(O)C1=CC=C([C@H](N)C(O)=O)C(C)=C1.[H]Cl
Synonyms :
LY367385 hydrochloride
MDL No. :MFCD17215678
InChI Key :IGKQWSUZDKTEPR-QRPNPIFTSA-N
Pubchem ID :122360845

Safety of LY367385 HCl

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Related Pathways of LY367385 HCl

GPCR

Isoform Comparison

Biological Activity

In Vitro:

Cell Line
Concentration Treated Time Description References
CA1 pyramidal cells 100 and 300 µM increased the sIPSC frequency and amplitude Cells. 2022 Sep 27;11(19):3015
Mouse cortical glutamatergic synaptosomes 0.1 μM 90 seconds LY367385 significantly reinforced the inhibitory effect exerted by 1 mM (RS)-baclofen on the 12 mM KCl-evoked overflow of preloaded [3H]D-aspartate Front Mol Neurosci. 2018 Sep 18;11:324
Mouse cortical GABAergic synaptosomes 0.03–1 μM 90 seconds LY367385 significantly amplified the 3 mM (RS)-baclofen-induced inhibition of [3H]GABA overflow evoked by 12 mM KCl Front Mol Neurosci. 2018 Sep 18;11:324
CA1 pyramidal cells 300 µM increased the sIPSC frequency and amplitude, effects reverted by CB1 receptor agonists Cells. 2022 Sep 27;11(19):3015

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
Mice CA1 O-LM interneurons Brain slice pre-incubation 100 μM 15-30 min pre-incubation LY367385 significantly attenuated the peak amplitude of DHPG-induced depolarization and the number of slow oscillations, indicating that mGluR1 plays a major role in slow oscillations in CA1 O/A interneurons. Neuropharmacology. 2018 Sep 1;139:150-162
Rats Cocaine self-administration model In vitro tissue culture 50 µM 1 hour LY367385 did not influence overall translation Biol Psychiatry. 2018 Aug 1;84(3):223-232
Mongolian gerbils (Meriones unguiculatus) Global ischemia model Transdialytic perfusion 1 mM Increased the hippocampal release of GABA and protected CA1 pyramidal cells against post-ischemic injury Cells. 2022 Sep 27;11(19):3015
Rats Pentylenetetrazole-induced status epilepticus model Intracerebroventricular injection 320 nmol/10 μL Single dose LY367385 alleviated the severity of pentylenetetrazole-induced status epilepticus Neural Regen Res. 2023 Mar;18(3):594-602
Japanese quail Castrated, testosterone-treated males Intracerebroventricular injections 100 μg Single injection, 30 min before testing LY367385 significantly inhibited male sexual motivation in Japanese quail, while mGluR2/3 and mGluR5 antagonists were ineffective. Additionally, LY367385 blocked the behavioral restoration induced by E2 or DPN, providing functional evidence that ERβ interacts with metabotropic glutamate receptor 1a (mGluR1a) signaling to acutely regulate male sexual motivation. J Neurosci. 2015 Sep 23;35(38):13110-23

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

4.07mL

0.81mL

0.41mL

20.35mL

4.07mL

2.04mL

40.71mL

8.14mL

4.07mL

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