CI-947
CAS No. 96392-15-3
CI-947( PD-117519 | PD 117519 | PD117519 | CI 947 | CI947 )
Catalog No. M16865 CAS No. 96392-15-3
An orally active adenosine receptor agonist that can induce acute cardiovascular toxicity and coronary vascular injury in vivo.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 52 | In Stock |
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| 2MG | 29 | In Stock |
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| 5MG | 48 | In Stock |
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| 10MG | 79 | In Stock |
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| 25MG | 141 | In Stock |
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| 50MG | 252 | In Stock |
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| 100MG | 369 | In Stock |
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| 200MG | Get Quote | In Stock |
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| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameCI-947
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NoteResearch use only, not for human use.
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Brief DescriptionAn orally active adenosine receptor agonist that can induce acute cardiovascular toxicity and coronary vascular injury in vivo.
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DescriptionAn orally active adenosine receptor agonist that can induce acute cardiovascular toxicity and coronary vascular injury in vivo.
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In Vitro——
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In VivoPD 117519 (2-10 mg/kg; oral administration; 16-24 hours; male beagle dogs) treatment produces significant hemodynamic changes at Tmax (4 hours) follows by acute coronary vascular injury that is evident at 16 hours postdosing.Treatment with 2 or 10 mg/kg of PD 117519 produces significant increases in mean heart rate and decreases in mean indirectsystolic blood pressure at time of highest drug exposure, 4 hours postdosing. Animal Model:24 male beagle dogs (8-12 months old)Dosage:2 mg/kg or 10 mg/kg Administration:Oral administration; 16 hours and 24 hours Result:Increased in mean heart rate and decreased in mean indirectsystolic blood pressure at time of highest drug exposure. Induced acute coronary arteriopathy. The endothelium also appears injured.
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SynonymsPD-117519 | PD 117519 | PD117519 | CI 947 | CI947
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PathwayApoptosis
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TargetAdenosine Receptor
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RecptorAdenosine Receptor
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Research AreaNeurological Disease
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Indication——
Chemical Information
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CAS Number96392-15-3
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Formula Weight383.4012
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Molecular FormulaC19H21N5O4
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Purity>98% (HPLC)
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SolubilityDMSO: ≥ 3.9 mg/mL
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SMILESC1CC2=CC=CC=C2C1NC3=C4C(=NC=N3)N(C=N4)C5C(C(C(O5)CO)O)O
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Chemical NameAdenosine, N-[(1R)-2,3-dihydro-1H-inden-1-yl]-
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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Metipranolol
Metipranolol is a β-adrenergic receptor antagonist that is given orally for the treatment of hypertension and also applied topically to the cornea for treating glaucoma.
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Alloxazine
Alloxazine (Isoalloxazine) is an A2 receptor antagonist, which is approximately 10-fold more selective for the A2B receptor than for the A2A receptor.
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SCH 442416
SCH-442416 is an selective antagonist of adenosine A2A receptor.?SCH-442416 binds to human and rat A2A receptors with high affinity (Ki values are 0.048 and 0.5 nM respectively).The A2A receptor antagonist (SCH 442416) could increase mRNA expression of the Kir 2.1and Kir 4.1 channels in Müller cells to protect the retinal neurons in vitro under hypoxic conditions.
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