VU0119498
Based on 1 publication(s) in Google Scholar
VU0119498 is a pan Gq mAChR M1, M3, M5 positive allosteric modulator (PAM), with EC50s of 6.04, 6.38, and 4.08 µM, respectively. VU0119498 has antidiabetic activity.
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- Purity: 98.76%
- CAS No.: 79183-37-2
- 화학식: C15H10BrNO2
- 분자량:316.15
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보관:Powder -20°C, 3 years ; In solvent -80°C, 6 months , -20°C, 1 month
Publications Citing Use of MedChemExpress (MCE) VU0119498
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Biological Activity
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mAChR1 |
mAChR3 |
mAChR5 |
|
Cell Line
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Type | Value | Description | References |
|---|---|---|---|---|
| CHO | EC50 |
>30 μM
Compound: 1, VU0119498
|
Positive allosteric modulation of muscarinic M2 receptor expressed in CHO cells co-expressing Gqi5 assessed as effect on acetylcholine-induced intracellular calcium mobilization after 1 hr by FLIPR assay
Positive allosteric modulation of muscarinic M2 receptor expressed in CHO cells co-expressing Gqi5 assessed as effect on acetylcholine-induced intracellular calcium mobilization after 1 hr by FLIPR assay
|
[PMID: 20801651] |
| CHO | EC50 |
>30 μM
Compound: 1, VU0119498
|
Positive allosteric modulation of muscarinic M4 receptor expressed in CHO cells co-expressing Gqi5 assessed as effect on acetylcholine-induced intracellular calcium mobilization after 1 hr by FLIPR assay
Positive allosteric modulation of muscarinic M4 receptor expressed in CHO cells co-expressing Gqi5 assessed as effect on acetylcholine-induced intracellular calcium mobilization after 1 hr by FLIPR assay
|
[PMID: 20801651] |
| CHO | EC50 |
>30 μM
Compound: 1
|
Agonist activity at rat muscarinic M2 expressed in CHO cells assessed as stimulation of calcium mobilization
Agonist activity at rat muscarinic M2 expressed in CHO cells assessed as stimulation of calcium mobilization
|
[PMID: 20004578] |
| CHO | EC50 |
>30 μM
Compound: 1
|
Agonist activity at rat muscarinic M4 expressed in CHO cells assessed as stimulation of calcium mobilization
Agonist activity at rat muscarinic M4 expressed in CHO cells assessed as stimulation of calcium mobilization
|
[PMID: 20004578] |
| CHO | EC50 |
4.08 μM
Compound: 113, (VU0119498)
|
Activation of human muscarinic M5 receptor expressed in CHO cells coexpressing Gq protein assessed as potentiation of acetylcholine-induced intracellular Ca2+ mobilization
Activation of human muscarinic M5 receptor expressed in CHO cells coexpressing Gq protein assessed as potentiation of acetylcholine-induced intracellular Ca2+ mobilization
|
[PMID: 19438238] |
| CHO | EC50 |
4.1 μM
Compound: 1
|
Agonist activity at human muscarinic M5 expressed in CHO cells assessed as stimulation of calcium mobilization
Agonist activity at human muscarinic M5 expressed in CHO cells assessed as stimulation of calcium mobilization
|
[PMID: 20004578] |
| CHO | EC50 |
4.6 μM
Compound: 1, VU0119498
|
Positive allosteric modulation of muscarinic M5 receptor expressed in CHO cells assessed as effect on acetylcholine-induced intracellular calcium mobilization after 1 hr by FLIPR assay
Positive allosteric modulation of muscarinic M5 receptor expressed in CHO cells assessed as effect on acetylcholine-induced intracellular calcium mobilization after 1 hr by FLIPR assay
|
[PMID: 20801651] |
| CHO | EC50 |
6.04 μM
Compound: 113, (VU0119498)
|
Activation of rat muscarinic M1 receptor expressed in CHO cells co-expressing Gq protein assessed as potentiation of acetylcholine-induced intracellular Ca2+ mobilization
Activation of rat muscarinic M1 receptor expressed in CHO cells co-expressing Gq protein assessed as potentiation of acetylcholine-induced intracellular Ca2+ mobilization
|
[PMID: 19438238] |
| CHO | EC50 |
6.1 μM
Compound: 1, VU0119498
|
Positive allosteric modulation of muscarinic M1 receptor expressed in CHO cells assessed as effect on acetylcholine-induced intracellular calcium mobilization after 1 hr by FLIPR assay
Positive allosteric modulation of muscarinic M1 receptor expressed in CHO cells assessed as effect on acetylcholine-induced intracellular calcium mobilization after 1 hr by FLIPR assay
|
[PMID: 20801651] |
| CHO | EC50 |
6.1 μM
Compound: 1
|
Agonist activity at rat muscarinic M1 expressed in CHO cells assessed as stimulation of calcium mobilization
Agonist activity at rat muscarinic M1 expressed in CHO cells assessed as stimulation of calcium mobilization
|
[PMID: 20004578] |
| CHO | EC50 |
6.38 μM
Compound: 113, (VU0119498)
|
Activation of human muscarinic M3 receptor expressed in CHO cells coexpressing Gq protein assessed as potentiation of acetylcholine-induced intracellular Ca2+ mobilization
Activation of human muscarinic M3 receptor expressed in CHO cells coexpressing Gq protein assessed as potentiation of acetylcholine-induced intracellular Ca2+ mobilization
|
[PMID: 19438238] |
| CHO | EC50 |
6.4 μM
Compound: 1, VU0119498
|
Positive allosteric modulation of muscarinic M3 receptor expressed in CHO cells assessed as effect on acetylcholine-induced intracellular calcium mobilization after 1 hr by FLIPR assay
Positive allosteric modulation of muscarinic M3 receptor expressed in CHO cells assessed as effect on acetylcholine-induced intracellular calcium mobilization after 1 hr by FLIPR assay
|
[PMID: 20801651] |
| CHO | EC50 |
6.4 μM
Compound: 1
|
Agonist activity at human muscarinic M3 expressed in CHO cells assessed as stimulation of calcium mobilization
Agonist activity at human muscarinic M3 expressed in CHO cells assessed as stimulation of calcium mobilization
|
[PMID: 20004578] |
VU0119498 (0.01-30 μM; 150 s) potentiates Ach responses in M1, M3, and M5-expressing CHO cells, with EC50s of 6.04, 6.38, and 4.08 µM, respectively[1].
VU0119498 (3-20 μM) augments ACh-mediated increasing in insulin secretion and intracellular calcium levels in MIN6-K8 cells[3].
VU0119498 (20 μM; 90 min) enhances ACh-induced insulin release in mouse and human pancreatic islets[3].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
VU0119498 (0.5 mg/kg; a single i.p.) improves glucose tolerance and insulin secretion in obese, glucose-intolerant mice[3].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:Male WT mice (12 weeks)[3]
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Dosage:0.1, 0.5, 2 mg/kg
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Administration:A single i.p.
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Result:Caused a significant improvement in glucose tolerance at the dose of 0.5 mg/kg.
Significantly augmented GSIS at the dose of 0.5 mg/kg.
Chemical Information
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CAS No. 79183-37-2
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Appearance Solid
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분자량 316.15
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화학식 C15H10BrNO2
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Color Orange to red
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SMILES
O=C1N(C2=C(C1=O)C=CC=C2)CC3=CC=C(C=C3)Br
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선적
Room temperature in continental US; may vary elsewhere.
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보관
Powder -20°C 3 years In solvent -80°C 6 months -20°C 1 month
Publications (1)
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Journal Impact Factor
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Most Recent
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Anal Chem
Exposome-Scale Investigation of Cl-/Br-Containing Chemicals Using High-Resolution Mass Spectrometry, Multistage Machine Learning, and Cloud Computing. [Abstract]2025 Jun 3;97(21):11099-11109. PMID: 40401576
용액&용해도
DMSO : 50 mg/mL (158.15 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
순도&문서
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Data Sheet (278 KB)
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SDS (393 KB)
- English - EN (393 KB)
- Français - FR (393 KB)
- Deutsch - DE (393 KB)
- Norwegian - NO (393 KB)
- Español - ES (393 KB)
- Swedish - SV (393 KB)
- Italian - IT (393 KB)
- Korean - KR (393 KB)
- Portuguese - PT (393 KB)
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Handling Instructions (2659 KB)
References
[1]. Bridges TM, et, al. Discovery of the first highly M5-preferring muscarinic acetylcholine receptor ligand, an M5 positive allosteric modulator derived from a series of 5-trifluoromethoxy N-benzyl isatins. J Med Chem. 2009 Jun 11;52(11):3445-8. [Content Brief]
[2]. Bridges TM, et, al. Chemical lead optimization of a pan Gq mAChR M1, M3, M5 positive allosteric modulator (PAM) lead. Part II: development of a potent and highly selective M1 PAM. Bioorg Med Chem Lett. 2010 Mar 15;20(6):1972-5. [Content Brief]
[3]. Zhu L, et, al. Allosteric modulation of β-cell M 3 muscarinic acetylcholine receptors greatly improves glucose homeostasis in lean and obese mice. Proc Natl Acad Sci U S A. 2019 Sep 10;116(37):18684-18690. [Content Brief]
Complete Stock Solution Preparation Table
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
| Optional Solvent | Concentration Solvent Mass | 1 mg | 5 mg | 10 mg | 25 mg |
|---|---|---|---|---|---|
| DMSO | 1 mM | 3.1631 mL | 15.8153 mL | 31.6306 mL | 79.0764 mL |
| 5 mM | 0.6326 mL | 3.1631 mL | 6.3261 mL | 15.8153 mL | |
| 10 mM | 0.3163 mL | 1.5815 mL | 3.1631 mL | 7.9076 mL | |
| 15 mM | 0.2109 mL | 1.0544 mL | 2.1087 mL | 5.2718 mL | |
| 20 mM | 0.1582 mL | 0.7908 mL | 1.5815 mL | 3.9538 mL | |
| 25 mM | 0.1265 mL | 0.6326 mL | 1.2652 mL | 3.1631 mL | |
| 30 mM | 0.1054 mL | 0.5272 mL | 1.0544 mL | 2.6359 mL | |
| 40 mM | 0.0791 mL | 0.3954 mL | 0.7908 mL | 1.9769 mL | |
| 50 mM | 0.0633 mL | 0.3163 mL | 0.6326 mL | 1.5815 mL | |
| 60 mM | 0.0527 mL | 0.2636 mL | 0.5272 mL | 1.3179 mL | |
| 80 mM | 0.0395 mL | 0.1977 mL | 0.3954 mL | 0.9885 mL | |
| 100 mM | 0.0316 mL | 0.1582 mL | 0.3163 mL | 0.7908 mL |