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Submit ReviewCompetitive non-selective angiotensin II antagonist.
M. Wt | 912 |
Formula | C42H65N13O10 |
Sequence |
XRVYVHPA (Modifications: X = Sar) |
Storage | Desiccate at -20°C |
CAS Number | 34273-10-4 |
PubChem ID | 6324663 |
InChI Key | PFGWGEPQIUAZME-NXSMLHPHSA-N |
Smiles | [H]N(C)CC(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC1=CNC=N1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C)C(O)=O |
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
References are publications that support the biological activity of the product.
Steinhausen et al (1986) Angiotensin II control of the renal microcirculation: effect of blockade by saralasin. Kidney Int. 30 56 PMID: 3747343
Thomas et al (1995) Saralasin suppresses arrhythmias in an isolated guinea-pig ventricular free wall model of simulated ischemia and reperfusion. J.Pharmacol.Exp.Ther. 274 1379 PMID: 7562511
Keywords: Saralasin, Saralasin supplier, Non-Selective, angiotensin, II, antagonist, AT, Receptors, Non-selective, 1163, Tocris Bioscience
Citations are publications that use Tocris products. Selected citations for Saralasin include:
Mayama et al (2008) Remodelling of cardiac gap junction connexin 43 and arrhythmogenesis. Exp Clin Cardiol 12 67 PMID: 18650985
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