Structure of SCH442416
CAS No.: 316173-57-6
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The BI-3802 was designed by Boehringer Ingelheim and could be obtained free of charge through the Boehringer Ingelheim open innovation portal opnMe.com, associated with its negative control.
SCH-442416 is a selective adenosine A2A receptor antagonist. SCH-442416 binds to human and rat A2A receptors with high affinity (Ki values are 0.048 and 0.5 nM respectively). It displays > 23000-fold selectivity for hA2A over hA1 in vitro with minimal affinity for hA2B and hA3 receptors (IC50 > 10 μM).
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Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
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Batch number can be found on the product's label following the word 'Batch'.
CAS No. : | 316173-57-6 |
Formula : | C20H19N7O2 |
M.W : | 389.41 |
SMILES Code : | NC1=NC(N(CCCC2=CC=C(OC)C=C2)N=C3)=C3C4=NC(C5=CC=CO5)=NN14 |
MDL No. : | MFCD08703126 |
InChI Key : | AEULVFLPCJOBCE-UHFFFAOYSA-N |
Pubchem ID : | 10668061 |
GHS Pictogram: |
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Signal Word: | Warning |
Hazard Statements: | H302-H315-H319-H335 |
Precautionary Statements: | P261-P280-P301+P312-P302+P352-P305+P351+P338 |
In Vitro:
Cell Line
|
Concentration | Treated Time | Description | References |
Müller cells | 100 nM | 2 weeks | SCH442416 significantly increased Kir4.1 and TASK-1 protein expressions and enhanced inward potassium currents in Müller cells | Sci Rep. 2015 Jun 11;5:11294 |
Human subcutaneous fibroblasts (HSCF) | 10 nM | 28 days | SCH442416 blocked the A2A receptor, preventing the pro-fibrotic effects of AMP and CGS21680C on collagen production | Cells. 2020 Mar 7;9(3):651 |
HEK-293T cells | 10 µM | 5 minutes | To evaluate the inhibitory effect of MRS7145 on A2AR-mediated cAMP accumulation, results showed that MRS7145 significantly inhibited CGS21680-induced cAMP accumulation under light conditions | J Control Release. 2018 Aug 10;283:135-142 |
HEK-293T cells | 1 µM | 5 minutes | To evaluate the blocking effect of MRS7145 on A2AR ligand binding, results showed that MRS7145 effectively blocked APEC647 binding to A2AR under light conditions | J Control Release. 2018 Aug 10;283:135-142 |
MDA-MB-231 breast cancer cells | 1 µM | 72 hours | Evaluate the effect of A2AR antagonist on extracellular vesicle production, results showed SCH442416 significantly decreased exosome production. | Purinergic Signal. 2020 Jun;16(2):231-240 |
Mel526 metastatic melanoma cells | 1 µM | 72 hours | Evaluate the effect of A2AR antagonist on extracellular vesicle production, results showed SCH442416 significantly decreased exosome production. | Purinergic Signal. 2020 Jun;16(2):231-240 |
U251 glioblastoma cells | 1 µM | 72 hours | Evaluate the effect of A2AR antagonist on extracellular vesicle production, results showed SCH442416 significantly decreased exosome production. | Purinergic Signal. 2020 Jun;16(2):231-240 |
UMSCC47 cells | 1 µM | 72 hours | Evaluate the effect of A2AR antagonist on extracellular vesicle production, results showed SCH442416 stimulated exosome production under metabolic stress or cisplatin treatment. | Purinergic Signal. 2020 Jun;16(2):231-240 |
CHO cells | 20 nM | at least 2 hours | To assess whether CBD interacts with the orthosteric site of the A2A receptor. Results showed that CBD was unable to significantly compete for the binding of the labeled antagonist to the receptor. | Int J Mol Sci. 2023 Dec 15;24(24):17500 |
Sheep brain striatum membranes | 0.1 nM to 50 μM | To study the role of SCH442416 as an A2AR antagonist in competitive binding experiments, the results showed that SCH442416 could produce bell-shaped competition curves, indicating the existence of a ligand-competitor allosteric interaction. | Pharmacol Res. 2019 Jan;139:337-347 |
In Vivo:
Species
|
Animal Model
|
Administration | Dosage | Frequency | Description | References |
Rat | Rat caudate putamen brain slices | Perfusion | 1 µM | 30 minutes | To test the role of A2A receptors in dopamine release modulation, results showed SCH442416 did not affect dopamine release | J Neurochem. 2015 Jan;132(1):51-60 |
Rats | 6-hydroxydopamine (6-OHDA) hemi-parkinsonian rat model | Micro-pressure administration | 1 µM | Single administration | SCH442416 significantly increased the spontaneous firing rate of pallidal neurons, indicating that endogenous adenosine modulates the activity of pallidal neurons through adenosine A 2A receptors | Front Physiol. 2017 Nov 7;8:897 |
Sprague Dawley rats | Chronic ocular hypertension (COH) model | Intravitreal injection | 100 nM | Single injection, lasting 2 weeks | SCH442416 up-regulated Müller cell Kir4.1, TASK-1, GS and GLAST expressions and enhanced inward potassium currents, while increasing retinal ganglion cell (RGC) count | Sci Rep. 2015 Jun 11;5:11294 |
Mice | Unilateral 6-hydroxydopamine (6-OHDA)-lesioned Parkinson’s disease model | Intraperitoneal injection | 3 mg/kg | Single administration, irradiation for 20 minutes | To evaluate the enhancing effect of MRS7145 on L-DOPA-induced contralateral rotations under light conditions, results showed that MRS7145 significantly potentiated the effect of L-DOPA under light conditions | J Control Release. 2018 Aug 10;283:135-142 |
Mice (C57BL/6) | Wild-type and CB1 receptor knockout mice | Intraperitoneal | 3 mg/kg | Single injection, monitored for 30 min | SCH442416 robustly increased locomotor activity, an effect attenuated by CB1 receptor blockade or knockout | J Neurosci. 2010 Feb 10;30(6):2160-4 |
Rats | Bilateral common carotid artery occlusion (BCCAO) model | Intraperitoneal injection | 3 mg/kg | Administered before BCCAO | To evaluate the effects of A2A receptors on rapid adenosine and oxygen dynamics during I/R. SCH 442416 eliminated the increase in adenosine and oxygen events caused by I/R. | ACS Chem Neurosci. 2019 Apr 17;10(4):1941-1949 |
Rats | Anesthetized rats | Intraperitoneal injection | 3 mg/kg | Single dose, observed for 2 hours | SCH442416 significantly decreased the number of adenosine and oxygen transient events and increased the time interval between each transient release. | J Neurochem. 2017 Jan;140(1):13-23 |
Clinical Trial:
NCT Number | Conditions | Phases | Recruitment | Completion Date | Locations |
NCT00531193 | Healthy | Phase 1 | Completed | - | United Kingdom ... More >> Research Site London, United Kingdom Less << |
NCT02764892 | Parkinson's Disease | Phase 1 | Completed | - | - |
Tags: SCH442416 | SCH 442416 | SCH-442416 | Adenosine Receptor | P1 receptor | adenosine | A2A | imaging | inhibitor | 316173-57-6 |
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