GMQ
Based on 1 publication(s) in Google Scholar
GMQ is an acid-sensing ion channel modulator, competitive GABAAR antagonist. GMQ preferentially, potently, competitively inhibits GABAARs. GMQ inhibits α1β2, α1β2γ2, α4β2γ2 and α5β2γ2 GABAARs. GMQ enhances neuronal excitation through inhibition of GABAergic transmission. GMQ has anti-histamine effects in the enteric system, inhibiting gastric acid secretion.
For research use only. We do not sell to patients.
- CAS No.: 716-11-0
- Formula: C10H11N5
- Molecular Weight:201.23
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Publications Citing Use of MedChemExpress (MCE) GMQ
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Biological Activity
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Cell Line
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Type | Value | Description | References |
|---|---|---|---|---|
| Huh-7 | CC50 |
66.41 μM
Compound: GNF-Pf-3515
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NOVARTIS: Cytotoxicity against human hepatocellular carcinoma cell line (Huh7)
NOVARTIS: Cytotoxicity against human hepatocellular carcinoma cell line (Huh7)
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[PMID: 18579783] |
| L6 | CC50 |
>64 μM
Compound: 20
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Cytotoxicity against rat L6 cells
Cytotoxicity against rat L6 cells
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[PMID: 19364854] |
Chemical Information
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CAS No. 716-11-0
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Molecular Weight 201.23
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Formula C10H11N5
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SMILES
NC(NC1=NC(C)=C2C=CC=CC2=N1)=N
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Synonyms
2-Guanidine-4-methylquinazoline
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Publications (1)
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Journal Impact Factor
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Most Recent
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Eur J Pharmacol
2-guanidine-4-methylquinazoline inhibits platelet activation and thrombosis by targeting the acid-sensing ion channel 3. [Abstract]2026 May 30:1030:179005. PMID: 42219052
Purity & Documentation
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)