OPN-IN-1
Based on 9 publication(s) in Google Scholar
OPN-IN-1 is an osteopontin (OPN) expression inhibitor. OPN-IN-1 has potential anti-breast cancer cell metastasis activity and can be used in the study of cancer.
For research use only. We do not sell to patients.
- Purity: 99.98%
- CAS No.: 2257492-95-6
- Formula: C25H33N3O5
- Molecular Weight:455.55
-
Storage:Powder -20°C, 3 years , 4°C, 2 years ; In solvent -80°C, 6 months , -20°C, 1 month
Publications Citing Use of MedChemExpress (MCE) OPN-IN-1
More- Cancer Commun (Lond). 2025 Dec 26.
- Adv Sci (Weinh). 2024 Dec 5:e2410360. [Abstract]
- J Neuroinflammation. 2023 Dec 9;20(1):294. [Abstract]
- J Inflamm (Lond). 2025 Jan 24;22(1):4. [Abstract]
- Int Immunopharmacol. 2025 Mar 24:153:114538. [Abstract]
- Biol Direct. 2025 Mar 14;20(1):30. [Abstract]
- Brain Res Bull. 2025 Oct 27:232:111607. [Abstract]
- Mol Biol Rep. 2024 Jun 1;51(1):720. [Abstract]
- Research Square Preprint. 2024 Dec 16.
-
WB
-
Cell Migration/Invasion Assay
-
Cell Proliferation/Viability Assay
-
In Vivo Efficacy Study
-
IF
Biological Activity
OPN-IN-1 (Compound 11) (50 μM; 24 h) can inhibit the expression of osteopontin (OPN) in MDA-MB-435 cells[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
-
Cell Line:MDA-MB-435
-
Concentration:50 μM
-
Incubation Time:24 h
-
Result:Decreased OPN expression by ~ 0.3 fold.
Chemical Information
-
CAS No. 2257492-95-6
-
Appearance Solid
-
Molecular Weight 455.55
-
Formula C25H33N3O5
-
Color White to yellow
-
SMILES
[H][C@@]12CC[C@]3(OO[C@]14[C@@H](O3)OC([C@@H]([C@@]4(CC[C@H]2C)[H])C)OCC5=CN(N=N5)CC6=CC=CC=C6)C
-
Shipping
Room temperature in continental US; may vary elsewhere.
-
Storage
Powder -20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month
Publications (9)
-
Journal Impact Factor
-
Most Recent
-
OPN-IN-1 purchased from MedChemExpress. Usage Cited in: Cancer Commun (Lond). 2025 Dec 26.
OPNi-1 (50 μM, 24 h) decreased the protein expression of YKL40, EFEMP-1, and CD44 in BNI_2-4 cells after culture with hypoxic conditioned medium derived from THP-1 and U937.
OPN-IN-1 purchased from MedChemExpress. Usage Cited in: Cancer Commun (Lond). 2025 Dec 26.
OPNi-1 (50 μM, 48 h) decreased cell migration in BNI_2-4 cells after culture with hypoxic conditioned medium derived from THP-1 (L) and U937.
OPN-IN-1 purchased from MedChemExpress. Usage Cited in: Cancer Commun (Lond). 2025 Dec 26.
OPNi-1 (50 μM, 48 h) inhibited cell growth of BNI_2-4 cells following culture with hypoxic conditioned medium from THP-1 (L) and U937.
OPN-IN-1 purchased from MedChemExpress. Usage Cited in: Cancer Commun (Lond). 2025 Dec 26.
OPNi-1 (0.5 mg/kg, intraperitoneal injections, 5 consecutive days followed by a 2-day drug holiday, and repeat the cycle) inhibited tumor growth compared with the control treatment in an orthotopic mouse model of GBM using GL261 cells in C57BL/6J mice.
OPN-IN-1 purchased from MedChemExpress. Usage Cited in: Cancer Commun (Lond). 2025 Dec 26.
OPNi-1 (0.5 mg/kg, intraperitoneal injections, 5 consecutive days followed by a 2-day drug holiday, and repeat the cycle) reduced PD-L1 expression in an orthotopic mouse model of GBM using GL261 cells in C57BL/6J mice.
-
Adv Sci (Weinh)
Targeted SPP1 Inhibition of Tumor-Associated Myeloid Cells Effectively Decreases Tumor Sizes. [Abstract]2024 Dec 5:e2410360. PMID: 39639496 -
J Neuroinflammation
Lateralized response of skull bone marrow via osteopontin signaling in mice after ischemia reperfusion. [Abstract]2023 Dec 9;20(1):294. PMID: 38071333 -
J Inflamm (Lond)
2025 Jan 24;22(1):4. PMID: 39856697 -
Int Immunopharmacol
USP22/BRD4 mediated hedgehog pathway activation contributes to airway remodeling in asthma. [Abstract]2025 Mar 24:153:114538. PMID: 40132456 -
Biol Direct
Macrophage-derived SPP1 exacerbate myocardial injury by interacting with fibroblasts in viral myocarditis. [Abstract]2025 Mar 14;20(1):30. PMID: 40087693 -
Brain Res Bull
Osteopontin inhibitor alleviates neuroinflammation after subarachnoid hemorrhage in rats via TLR4/NF-κB pathway. [Abstract]2025 Oct 27:232:111607. PMID: 41161421 -
Mol Biol Rep
Study on the mechanism of heterogeneous tumor-associated macrophages in three subtypes of breast cancer through the integration of single-cell RNA sequencing and in vitro experiments. [Abstract]2024 Jun 1;51(1):720. PMID: 38824268 -
Solvent & Solubility
DMSO : 100 mg/mL (219.51 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)
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.
Add each solvent one by one: 10% DMSO 40% PEG300 5% Tween-80 45% Saline
Solubility: ≥ 2.5 mg/mL (5.49 mM); Clear solution
This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown).
Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 400 μL PEG300, and mix evenly; then add 50 μL Tween-80 and mix evenly; then add 450 μL Saline to adjust the volume to 1 mL.
Preparation of Saline: Dissolve 0.9 g sodium chloride in ddH₂O and dilute to 100 mL to obtain a clear Saline solution.
Add each solvent one by one: 10% DMSO 90% (20% SBE-β-CD in Saline)
Solubility: ≥ 2.5 mg/mL (5.49 mM); Suspended solution
This protocol yields a suspended solution of ≥ 2.5 mg/mL (saturation unknown). Suspended solution can be used for oral and intraperitoneal injection.
Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 900 μL 20% SBE-β-CD in Saline, and mix evenly.
Preparation of 20% SBE-β-CD in Saline (4°C, storage for one week): 2 g SBE-β-CD powder is dissolved in 10 mL Saline, completely dissolve until clear.
Please enter the basic information of animal experiments:
-
-
-
-
Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Please enter your animal formula composition:
-
%DMSO +
Recommended: Keep the proportion of DMSO in working solution below 2% if your animal is weak.
-
%+
-
+%Tween-80 + +
-
%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.
Purity & Documentation
-
Data Sheet (277 KB)
-
SDS (251 KB)
- English - EN (251 KB)
- Français - FR (251 KB)
- Deutsch - DE (251 KB)
- Norwegian - NO (251 KB)
- Español - ES (251 KB)
- Swedish - SV (251 KB)
- Italian - IT (251 KB)
- Korean - KR (251 KB)
- Portuguese - PT (251 KB)
-
Handling Instructions (2659 KB)
References
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 | 2.1951 mL | 10.9757 mL | 21.9515 mL | 54.8787 mL |
| 5 mM | 0.4390 mL | 2.1951 mL | 4.3903 mL | 10.9757 mL | |
| 10 mM | 0.2195 mL | 1.0976 mL | 2.1951 mL | 5.4879 mL | |
| 15 mM | 0.1463 mL | 0.7317 mL | 1.4634 mL | 3.6586 mL | |
| 20 mM | 0.1098 mL | 0.5488 mL | 1.0976 mL | 2.7439 mL | |
| 25 mM | 0.0878 mL | 0.4390 mL | 0.8781 mL | 2.1951 mL | |
| 30 mM | 0.0732 mL | 0.3659 mL | 0.7317 mL | 1.8293 mL | |
| 40 mM | 0.0549 mL | 0.2744 mL | 0.5488 mL | 1.3720 mL | |
| 50 mM | 0.0439 mL | 0.2195 mL | 0.4390 mL | 1.0976 mL | |
| 60 mM | 0.0366 mL | 0.1829 mL | 0.3659 mL | 0.9146 mL | |
| 80 mM | 0.0274 mL | 0.1372 mL | 0.2744 mL | 0.6860 mL | |
| 100 mM | 0.0220 mL | 0.1098 mL | 0.2195 mL | 0.5488 mL |