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BioAssay: AID 1965

Summary of Image-based HTS for Selective Agonists of GPR55

Assay Provider: Dr. Mary Abood, California Pacific Medical Center Research Institute (currently Temple University) ..more
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 Tested Compounds
 Tested Compounds
All(3)
 
 
Probe(3)
 
 
Active(3)
 
 
 Tested Substances
 Tested Substances
All(3)
 
 
Probe(3)
 
 
Active(3)
 
 
AID: 1965
Data Source: Burnham Center for Chemical Genomics (BCCG-A223-GPR55-Agonist-Summary-Assay)
BioAssay Type: Summary, Candidate Probes/Leads with Supporting Evidence
Depositor Category: NIH Molecular Libraries Probe Production Network
BioAssay Version:
Deposit Date: 2009-10-05
Modify Date: 2011-06-22

Data Table ( Complete ):           View Active Data    View All Data
Target
BioActive Compounds: Chemical Probe: 3    Active: 3
Related Experiments
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AIDNameTypeComment
1961Image-based HTS for Selective Agonists of GPR55Confirmatorydepositor-specified cross reference: Image-based HTS for Selective Agonists of GPR55
2338SAR analysis of Antagonists of the GPR35 Receptor using an Image-Based AssayConfirmatorydepositor-specified cross reference: SAR analysis of Antagonists of the GPR35 Receptor using an Image-Based Assay
2339SAR analysis of antagonists of the Cannabinoid Receptor 1 using an Image-Based AssayConfirmatorydepositor-specified cross reference
2340SAR analysis of Agonists of the GPR35 Receptor using an Image-Based AssayConfirmatorydepositor-specified cross reference
2341SAR analysis of agonists of the Cannabinoid Receptor 1 using an Image-Based AssayConfirmatorydepositor-specified cross reference
2347SAR analysis of selective Agonists of GPR55 using an Image-Based AssayConfirmatorydepositor-specified cross reference
2843SAR analysis of selective Agonists of GPR55 using an Image-Based Assay - Set 2Confirmatorydepositor-specified cross reference
2844SAR analysis of agonists of the Cannabinoid Receptor 1 using an Image-Based Assay - Set 3Confirmatorydepositor-specified cross reference
434922SAR analysis of antagonists of the Cannabinoid Receptor 2 using an Image-Based Assay - Set 2Confirmatorydepositor-specified cross reference
434924SAR analysis of Agonists of the GPR35 Receptor using an Image-Based Assay - Set 3Confirmatorydepositor-specified cross reference
434925SAR analysis of Antagonists of the GPR35 Receptor using an Image-Based Assay - Set 4Confirmatorydepositor-specified cross reference
434928SAR analysis of agonists of the Cannabinoid Receptor 2 using an Image-Based Assay - Set 2Confirmatorydepositor-specified cross reference
434929SAR analysis of antagonists of the Cannabinoid Receptor 1 using an Image-Based Assay - Set 3Confirmatorydepositor-specified cross reference
463192SAR Analysis for the identification of Selective Agonists of GPR55 using an Image-Based ScreenOtherdepositor-specified cross reference
485279SAR analysis of Agonists of GPR55 using MAPK Activation AssayOtherdepositor-specified cross reference
2397SAR Analysis of Selective Antagonists of GPR55 using an Image-Based AssayConfirmatorysame project related to Summary assay
2480SAR analysis of Antagonists of the GPR35 Receptor using an Image-Based Assay - Set 2Confirmatorysame project related to Summary assay
2809SAR analysis of Agonists of the GPR35 Receptor using an Image-Based Assay - Set 2Confirmatorysame project related to Summary assay
2814SAR analysis of agonists of the Cannabinoid Receptor 1 using an Image-Based Assay - Set 2Confirmatorysame project related to Summary assay
2820SAR Analysis of Selective Antagonists of GPR55 using an Image-Based Assay - Set 2Confirmatorysame project related to Summary assay
2822SAR analysis of antagonists of the Cannabinoid Receptor 1 using an Image-Based Assay - Set 2Confirmatorysame project related to Summary assay
463227SAR analysis of Antagonists of the GPR35 Receptor using an Image-Based Assay - Set 5Confirmatorysame project related to Summary assay
Description:
Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG)
Source Affiliation: Sanford-Burnham Medical Research Institute (SBMRI, San Diego, CA)
Network: NIH Molecular Libraries Probe Production Centers Network (MLPCN)
Grant Proposal Number: 1X01 DA026205-01
Assay Provider: Dr. Mary Abood, California Pacific Medical Center Research Institute (currently Temple University)

The orphan G protein coupled receptor, GPR55, has gained notoriety because of its putative identification as a cannabinoid receptor subtype. The significance of this assignment should not be underestimated given the importance of cannabinoids to drug abuse and the potential utility of cannabinoid ligands in treating behavioral disorders leading to conditions such as obesity. The validity of assigning GPR55 to the cannabinoid family is problematic based upon the discovery that endogenous compounds not related to cannabinoid receptor ligands also bind and signal through GPR55. As a consequence, it is important to identify GPR55-selective ligands that can precisely define GPR55's role in regulating addictive behaviors. Lysophosphatidylinositol (LPI; 1.2 uM) is representative of the recently identified endogenous GPR55 ligands and the CB1 inverse agonist/antagonists SR141716A (3.9 uM) and AM251 (9.6 uM), that are also GPR55 agonists, are representative of the cannabinoid receptor ligands that were screened against GPR55 when selectivity was not a consideration. The availability of high potency selective GPR55 agonists will therefore facilitate the study of this receptor's signaling. We have identified 3 potent and selective agonists for GPR55, which represent 3 different chemical scaffolds: 1) a morpholinosulfonylphenylamide, ML186 (CID15945391) with 305 nM potency for GPR55 and >100-fold selectivity against GPR35, CB1 and CB2 (as agonist and antagonists); 2) a tricyclic triazoloquinoline, ML185 (CID1374043) with 658 nM potency for GPR55 and >48-fold selectivity against GPR35, CB1 and CB2 (as agonists and antagonists); and 3) a piperazine, ML184 (2440433) with 263 nM potency for GPR55 and >120-fold, 83-fold, and 57-fold selectivity against GPR35, CB1 and CB2 as antagonists, and >120-fold selective against all 3 counter receptors as agonists. All three probes also are active in activating the downstream responses of ERK phosphorylation and PKC beta II translocationas increased local concentrations of fluorescent arrestins.
Protocol
Please see pertinent AIDs: 1961, 2338, 2339, 2340, 2341, 2347, 2843, 2844, 434922, 434924, 434925, 434929, 434928,485279, 463192
Comment
Probe molecules are defined as the positives of this assay and assigned a score of 100. Compound SIDs 87225730, 87225724 and 87225729 have been identified as probe molecules.
Categorized Comment - additional comments and annotations
From MLP Probe Report:
Probe count: 3
MLP Probe ML# for probe 1: ML186
PubChem Substance ID (SID) for probe 1: 87225730
PubChem Compound ID (CID) for probe 1: 15945391
IC50/EC50 (nM) for probe 1: 305
Target for probe 1: GPR55 Agonist (gi: 33695107)
Anti-target for probe 1: GPR35, CB1, CB2 agonist and antagonist
Fold selectivity for probe 1: >100
NCBI Book chapter link for probe 1: http://www.ncbi.nlm.nih.gov/books/NBK66152/ (ID: 2647588)
Grant number for probe 1: DA026205-01
MLP Probe ML# for probe 2: ML184
PubChem Substance ID (SID) for probe 2: 87225729
PubChem Compound ID (CID) for probe 2: 2440433
IC50/EC50 (nM) for probe 2: 263
Target for probe 2: GPR55 Agonist
Anti-target for probe 2: GPR35, CB1, CB2 agonist and antagonist
Fold selectivity for probe 2: >57
MLP Probe ML# for probe 3: ML185
PubChem Substance ID (SID) for probe 3: 87225724
PubChem Compound ID (CID) for probe 3: 1374043
IC50/EC50 (nM) for probe 3: 658
Target for probe 3: GPR55 Agonist
Anti-target for probe 3: GPR35, CB1, CB2 agonist and antagonist
Fold selectivity for probe 3: >48
NCBI Book chapter title for probe 1: Screening for Selective Ligands for GPR55 - Agonists
Result Definitions
TIDNameDescriptionHistogramTypeUnit
OutcomeThe BioAssay activity outcomeOutcome
ScoreThe BioAssay activity ranking scoreInteger
1ML#ML# for the compoundString
Additional Information
Grant Number: 1X01 DA026205-01

Data Table (Concise)
Data Table ( Complete ):     View Active Data    View All Data
Classification
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