ODQ
Based on 11 publication(s) in Google Scholar
ODQ is a potent and selective soluble guanylyl cyclase (sGC, nitric oxide-activated enzyme) inhibitor. ODQ enhances the pro-apoptotic effects of Cisplatin in human mesothelioma cells.
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研究用途以外に使用した場合、当社は一切の責任を負いかねます。
- 純度: 99.75%
- CAS 番号: 41443-28-1
- 分子式: C9H5N3O2
- 分子量:187.16
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保管条件:Powder -20°C, 3 years , 4°C, 2 years ; In solvent -80°C, 2 years , -20°C, 1 year
MedChemExpress(MCE)の使用を引用している文献 ODQ
More- Nature. 2025 Sep;645(8079):244-253. [Abstract]
- EMBO J. 2024 Apr;43(8):1519-1544. [Abstract]
- Int J Mol Med. 2024 Aug;54(2):67. [Abstract]
- J Ethnopharmacol. 2026 Jun 12:364:121498. [Abstract]
- Pharmaceuticals (Basel). 2025 Sep 21;18(9):1420. [Abstract]
- Eur J Pharmacol. 2025 Nov 5:1006:178190. [Abstract]
- J Biol Chem. 2026 Jan 23;302(3):111202. [Abstract]
- Acad Radiol. 2025 Jul;32(7):4121-4133. [Abstract]
- J Virol. 2026 Feb 17;100(2):e0165625. [Abstract]
- Microbiol Spectr. 2024 Apr 2;12(4):e0322023. [Abstract]
- In Vitro Model. 2025 Oct 28.
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In Vivo Efficacy Study
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In Vivo Efficacy Study
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In Vivo Efficacy Study
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Flow Cytometry
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WB
生物活性
At 30 and 50 μM, ODQ causes significant induction of apoptosis in the NCI-H2452 cells, elevating apoptotic levels by 12 fold and 15 fold, respectively. At 10μM, a concentration below the threshold for induction of apoptosis by ODQ, ODQ in combination with Cisplatin enhanced (in fact, doubled) the pro-apoptotic effects of Cisplatin at 1 μM[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:Anesthetized, male Wistar rats[2]
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Dosage:2 mg/kg
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Administration:I.p.
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Result:Attenuated the renal dysfunction, lung injury, and hepatocellular injury caused by lipoteichoic acid/peptidoglycan or lipopolysaccharide.
| NCT Number | Sponsor | Condition | Start Date |
Phase
|
|---|---|---|---|---|
| NCT01329991 | Plexxikon| | 2011-05 | PHASE1 |
化学情報
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CAS 番号 41443-28-1
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性状 Solid
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分子量 187.16
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分子式 C9H5N3O2
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Color Off-white to yellow
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SMILES
O=C1ON=C2N1C3=C(C=CC=C3)N=C2
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輸送条件
Room temperature in continental US; may vary elsewhere.
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保管条件
Powder -20°C 3 years 4°C 2 years In solvent -80°C 2 years -20°C 1 year
Publications (11)
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Journal Impact Factor
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Most Recent
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Nature
2025 Sep;645(8079):244-253. PMID: 40562926 -
EMBO J
Pericyte signaling via soluble guanylate cyclase shapes the vascular niche and microenvironment of tumors. [Abstract]2024 Apr;43(8):1519-1544. PMID: 38528180
ODQ purchased from MedChemExpress. Usage Cited in: EMBO J. 2024 Apr;43(8):1519-1544. [Abstract]
Schematic depiction of the experimental design. Wild-type mice were subcutaneously inoculated with LLC cells at 8 weeks of age, and then received oral administration of 2.5 mg/kg Fruquintinib or corresponding vehicle and intraperitoneal injection of 6 mg/kg ODQ or corresponding vehicle, both starting from day 6 post-tumor inoculation, with tumor analysis at day 14 post inoculation.
ODQ purchased from MedChemExpress. Usage Cited in: EMBO J. 2024 Apr;43(8):1519-1544. [Abstract]
Plot depicting the growth curves of LLC tumors in wild-type mice with Fruquintinib or ODQ (6 mg/kg, ip) treatment.
ODQ purchased from MedChemExpress. Usage Cited in: EMBO J. 2024 Apr;43(8):1519-1544. [Abstract]
Macroscope images of LLC tumors isolated from wild-type mice with Fruquintinib or ODQ (6 mg/kg, ip) treatment. Scale bars, 10 mm.
ODQ purchased from MedChemExpress. Usage Cited in: EMBO J. 2024 Apr;43(8):1519-1544. [Abstract]
Plot showing the CD31-positive area, pericyte coverage, and vessel diameter of wild-type mice with Fruquintinib or ODQ (6 mg/kg, ip) treatment.
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Int J Mol Med
Naringenin modulates the NO‑cGMP‑PKG signaling pathway by binding to AKT to enhance osteogenic differentiation in hPDLSCs. [Abstract]2024 Aug;54(2):67. PMID: 38940332
ODQ purchased from MedChemExpress. Usage Cited in: Int J Mol Med. 2024 Aug;54(2):67. [Abstract]
Upon addition of ODQ (an sGC inhibitor), the NAR + ODQ (20 μM) group exhibited decreased expression of the osteogenesis-related factors, RUNX2 and OPN, at both the gene and protein levels.
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J Ethnopharmacol
Exploring the molecular mechanism of Shenling baizhu formula in the treatment of ulcerative colitis via the cGMP-PKG signaling pathway. [Abstract]2026 Jun 12:364:121498. PMID: 41796620 -
Pharmaceuticals (Basel)
2025 Sep 21;18(9):1420. PMID: 41011287 -
Eur J Pharmacol
HEC95468, a novel soluble guanylate cyclase stimulator, shows protection in the Dahl model of cardiorenal disorder. [Abstract]2025 Nov 5:1006:178190. PMID: 40998191 -
J Biol Chem
Nitric oxide mediates ET-1-induced-inhibition of NPPB-sensitive Cl- currents in the early distal convoluted tubule of the mouse kidney. [Abstract]2026 Jan 23;302(3):111202. PMID: 41581878 -
Acad Radiol
Ultrasound-Stimulated Microbubbles Cavitation Combined with Nitric Oxide Signaling Pathway to Alleviate Tumor Hypoperfusion and Hypoxia in MC38 Tumor Model. [Abstract]2025 Jul;32(7):4121-4133. PMID: 40234163 -
J Virol
Seneca Valley virus 3C protease targets the Nrf2/HO-1 pathway to antagonize its antiviral activity. [Abstract]2026 Feb 17;100(2):e0165625. PMID: 41489372 -
Microbiol Spectr
Heme oxygenase-1 is an equid alphaherpesvirus 8 replication restriction host protein and suppresses viral replication via the PKCβ/ERK1/ERK2 and NO/cGMP/PKG pathway. [Abstract]2024 Apr 2;12(4):e0322023. PMID: 38441979 -
溶剤 & 溶解度
DMSO : 100 mg/mL (534.31 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, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.
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, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.
濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)
Select the appropriate dissolution method based on your experimental animal and administration route.
- For the following dissolution methods, please ensure to first prepare a clear stock solution using an In Vitro approach and then sequentially add co-solvents:
- To ensure reliable experimental results, the clarified stock solution can be appropriately stored based on storage conditions. As for the working solution for In Vivo experiments, it is recommended to prepare freshly and use it on the same day.
- The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.
Please enter the basic information of animal experiments:
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Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Please enter your animal formula composition:
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%DMSO +
Recommended: Keep the proportion of DMSO in working solution below 2% if your animal is weak.
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%+
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+%Tween-80 + +
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%Saline +
The co-solvents required include: DMSO, . All of co-solvents are available by MedChemExpress (MCE). , Tween 80. All of co-solvents are available by MedChemExpress (MCE).
Working solution concentration: 0.22 mg/mL
Method for preparing stock solution: mg drug dissolved in μL DMSO. Stock solution concentration: mg/mL.
1. Take μL DMSO stock solution;
2. Add μL .
μL , mix evenly;
3. Then add μL Tween 80, mix evenly;
4. Then add μL
Please ensure that the stock solution in the first step is dissolved to a clear state, and add co-solvents in sequence. You can use ultrasonic heating (ultrasonic cleaner, recommended frequency 20-40 kHz), vortexing, etc. to assist dissolution.
純度とドキュメンテーション
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データシート (281 KB)
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SDS (394 KB)
- English - EN (394 KB)
- Français - FR (394 KB)
- Deutsch - DE (394 KB)
- Norwegian - NO (394 KB)
- Español - ES (394 KB)
- Swedish - SV (394 KB)
- Italian - IT (394 KB)
- Korean - KR (394 KB)
- Portuguese - PT (394 KB)
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取扱説明書 (2659 KB)
参考文献
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, 2 years; -20°C, 1 year. When stored at -80°C, please use it within 2 years. When stored at -20°C, please use it within 1 year.
| Optional Solvent | Concentration Solvent Mass | 1 mg | 5 mg | 10 mg | 25 mg |
|---|---|---|---|---|---|
| DMSO | 1 mM | 5.3431 mL | 26.7154 mL | 53.4308 mL | 133.5770 mL |
| 5 mM | 1.0686 mL | 5.3431 mL | 10.6862 mL | 26.7154 mL | |
| 10 mM | 0.5343 mL | 2.6715 mL | 5.3431 mL | 13.3577 mL | |
| 15 mM | 0.3562 mL | 1.7810 mL | 3.5621 mL | 8.9051 mL | |
| 20 mM | 0.2672 mL | 1.3358 mL | 2.6715 mL | 6.6788 mL | |
| 25 mM | 0.2137 mL | 1.0686 mL | 2.1372 mL | 5.3431 mL | |
| 30 mM | 0.1781 mL | 0.8905 mL | 1.7810 mL | 4.4526 mL | |
| 40 mM | 0.1336 mL | 0.6679 mL | 1.3358 mL | 3.3394 mL | |
| 50 mM | 0.1069 mL | 0.5343 mL | 1.0686 mL | 2.6715 mL | |
| 60 mM | 0.0891 mL | 0.4453 mL | 0.8905 mL | 2.2263 mL | |
| 80 mM | 0.0668 mL | 0.3339 mL | 0.6679 mL | 1.6697 mL | |
| 100 mM | 0.0534 mL | 0.2672 mL | 0.5343 mL | 1.3358 mL |