α5β1 integrin-IN-1
α5β1 integrin-IN-1 is a potent and selective α5β1 integrin inhibitor with an IC50 value of approximately 0.4 nM (pIC50 = 9.4 M). α5β1 integrin-IN-1 disrupts the interaction between α5β1 integrin and fibronectin, thereby blocking smooth muscle tension transmission and α5β1 integrin-mediated cell adhesion. α5β1 integrin-IN-1 can be used in the research of asthma and allergic asthma.
For research use only. We do not sell to patients.
- CAS No.: 2649899-08-9
- Formula: C29H27Cl2FN6O5
- Molecular Weight:629.47
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
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α5β1 0.4 nM (IC50) |
αvβ3 5500 mM (pIC50) |
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Cell Line
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Type | Value | Description | References |
|---|---|---|---|---|
| SW480 | IC50 |
0.4 nM
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Inhibition of α5β1-mediated cell adhesion to fibronectin in human SW480 colon adenocarcinoma cells via crystal violet staining assay with 15 min pre-incubation and 1 h adhesion incubation.
Inhibition of α5β1-mediated cell adhesion to fibronectin in human SW480 colon adenocarcinoma cells via crystal violet staining assay with 15 min pre-incubation and 1 h adhesion incubation.
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41427225 |
α5β1 integrin-IN-1 (Compound 65) at 30 μM exhibits only extremely weak inhibitory activity against hERG channels in hERG-expressing cells, with an inhibition rate of 6.11%.
α5β1 integrin-IN-1 (30 μM) does not inhibit hERG ion channel activity at concentrations up to 30 μM.
α5β1 integrin-IN-1 (up to 1000 μg/well) shows no mutagenicity in the Ames test.
α5β1 integrin-IN-1 (10 μM; 5-45 min) does not inhibit the activity of CYP subtypes at a concentration of 10 μM.
α5β1 integrin-IN-1 (pre-incubated at 4°C for 15 min, followed by incubation at 37°C for 1 h) exhibits high α5β1 receptor selectivity in β3-transfected SW480 cells plated on fibrinogen, HT1080 cells plated on rat tail collagen I, SW480 cells plated on vitronectin, and human α4-transfected SW480 cells plated on VCAM-1, with an IC50 of approximately 0.4 nM (pIC50 = 9.4 M).
α5β1 integrin-IN-1 (100 µM) exhibits specific transmembrane permeability and efflux effects in the Caco-2 cell model.
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
| Species | Dose | Route | Tmax | Cmax | T1/2 | AUCinf | F |
|---|---|---|---|---|---|---|---|
| Mice[1] | 2 mg/kg | i.n. | 0.083 h | 916 ng/mL | 1.01 h | 326 ng/mL·h | 122 % |
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:C57BL/6 (sex-matched, 7 weeks old, ovalbumin-sensitized and challenged)[1]
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Dosage:1 mg/kg
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Administration:i.n.; single dose
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Result:Significantly reduced respiratory system resistance compared to the ovalbumin/vehicle group (P < 0.01).
Showed no significant differences in inflammatory markers, including BAL cell count and differential, serum IgE level, histology, or PAS score, compared to vehicle-treated mice.
Chemical Information
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CAS No. 2649899-08-9
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Molecular Weight 629.47
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Formula C29H27Cl2FN6O5
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SMILES
ClC1=C(C(N[C@@H](CNC(CNC(C2=CC(NC3=NCC(F)CN3)=CC=C2)=O)=O)C(O)=O)=O)C(Cl)=CC(C4=CC=CC=C4)=C1
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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.
Purity & Documentation
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)