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TecadenosonTecadenoson (CVT 510) is a selective A1 adenosine receptor agonist. Product information CAS Number: 204512 90 3 Molecular Weight: 337. 33 Formula: C14H19N5O5 Chemical Name: (2R,3S,4R,5R) 2 (hydroxymethyl) 5 (6 {[(3R) oxolan 3 yl]amino} 9H purin 9 yl)oxolane 3,4 diol Smiles: OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2C(N[C@H]3COCC3)=NC=NC1=2 InChiKey: OESBDSFYJMDRJY BAYCTPFLSA N InChi: InChI=1S C14H19N5O5 c20 3 8 10(21)11(22)14(24 8)19 6 17 9 12(15 5 16
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Tecadenoson (CVT-510) is a selective A1 adenosine receptor agonist.

Product information

CAS Number: 204512-90-3

Molecular Weight: 337.33

Formula: C14H19N5O5

Chemical Name: (2R,3S,4R,5R)-2-(hydroxymethyl)-5-(6-{[(3R)-oxolan-3-yl]amino}-9H-purin-9-yl)oxolane-3,4-diol

Smiles: OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2C(N[C@H]3COCC3)=NC=NC1=2

InChiKey: OESBDSFYJMDRJY-BAYCTPFLSA-N

InChi: InChI=1S/C14H19N5O5/c20-3-8-10(21)11(22)14(24-8)19-6-17-9-12(15-5-16-13(9)19)18-7-1-2-23-4-7/h5-8,10-11,14,20-22H,1-4H2,(H,15,16,18)/t7-,8-,10-,11-,14-/m1/s1

Technical Data

Appearance: Solid Power

Purity: ≥98% (or refer to the Certificate of Analysis)

Solubility: DMSO : ≥ 155 mg/mL (459.49 mM).

Shipping Condition: Shipped under ambient temperature as non-hazardous chemical or refer to Certificate of Analysis

Storage Condition: Dry, dark and -20 oC for 1 year or refer to the Certificate of Analysis.

Shelf Life: ≥12 months if stored properly.

Stock Solution Storage: 0 - 4 oC for 1 month or refer to the Certificate of Analysis.

Drug Formulation: To be determined

HS Tariff Code: 382200

How to use

In Vitro:

In the atrial-paced isolated heart, Tecadenoson is approximately 5 fold more potent to prolong the stimulus-to-His bundle (S-H interval), a measure of slowing AV nodal conduction (EC50=41 nM) than to increase coronary conductance (EC50=200 nM). At concentrations of Tecadenoson (40 nM) and diltiazem (1 μM) that causes equal prolongation of S-H interval (∼10 ms), diltiazem, but not Tecadenoson, significantly reduces left ventricular developed pressure (LVP) and markedly increases coronary conductance. Tecadenoson shortens atrial (EC50=73 nM) but not the ventricular monophasic action potentials (MAP).

In Vivo:

In atrial-paced anaesthetized guinea-pigs, intravenous infusions of Tecadenoson and diltiazem causes nearly equal prolongations of P-R interval. Tecadenoson (2, 5, 20 μg/kg i.p.) causes a rapid and sustained dose-dependent decrease in NEFA at doses that do not cause bradycardia. Tecadenoson given at 50 μg/kg causes a significant bradycardia (50% decrease in heart rate at 25 min.

Products are for research use only. Not for human use.

Tecadenoson

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