SGC stimulator 2
SGC stimulator 2 is an orally active soluble guanylyl cyclase (sGC) stimulator with an EC50 of 44 nM. SGC stimulator 2 exhibits inhibitory activity against the CB2 receptor, with an IC50 of 2.7 μM. SGC stimulator 2 activates native (Fe2+) sGC in a heme-dependent manner. SGC stimulator 2 produces sustained hypotensive effects in animal models. SGC stimulator 2 can be used for the research of hypertension.
For research use only. We do not sell to patients.
- CAS No.: 1350852-88-8
- Formula: C24H18ClF5N6O
- Molecular Weight:536.88
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
Description
In Vitro
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
In Vivo
SGC stimulator 2 (0.1 mg/kg; p.o.; single dose) produces sustained blood pressure lowering in conscious telemetered beagle dogs[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:spontaneously hypertensive rats (male)[1]
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Dosage:0.03 mg/kg (chronic); 0.03, 0.1, 0.3 and 1 mg/kg (acute single dose)
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Administration:p.o.; once daily; 15 days (chronic); p.o.; single dose (acute)
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Result:Reduced systolic blood pressure by 85 mmHg at 4 hours after single 1 mg/kg oral dose.
Produced dose-dependent reductions in mean, systolic, diastolic, and pulse pressures, with effects sustained for >24 hours following single oral doses of 0.03-1 mg/kg.
Achieved consistent systolic blood pressure reductions of ~15-20 mmHg with full 24-hour coverage and no tachyphylaxis during once-daily oral administration of 0.03 mg/kg for 15 days.
Diminished modest reflex tachycardia (HR ~40 beats/min) observed on day 1 by days 4-5, and maintained stable plasma exposures (C_max ~2.5 nM; C_trough ~0.5 nM) during chronic dosing.
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Animal Model:beagle dogs (male)[1]
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Dosage:0.1 mg/kg
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Administration:p.o.; single dose
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Result:Reduced systolic blood pressure by 20 mmHg at 6 hours after single 0.1 mg/kg oral dose.
Maintained a sustained ~10 mmHg systolic blood pressure decrease through 36 hours post-dose.
Sustained a maximal ~20 beats/min reflexogenic increase in heart rate out to 36 hours post-dose.
Chemical Information
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CAS No. 1350852-88-8
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Molecular Weight 536.88
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Formula C24H18ClF5N6O
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SMILES
ClC1=CC2=C(C=C1)C(C3=NC(NC([C@@]4(C)C5=CC=CC=C5)=O)=C4C(N)=N3)=NN2CCC(F)(F)C(F)(F)F
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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)