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A-49816

  Cat. No.:  DC76675  
Chemical Structure
78235-72-0
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More than 5000 active chemicals with high quality for research!
Field of application
A-49816 is an orally active diuretic that increases urine volume and sodium and chloride excretion. A-49816 at high doses (12.5, 15, and 20 mg) caused significant salt and chloride excretion and diuresis in experimental animals.
Cas No.: 78235-72-0
Chemical Name: A-49816
SMILES: O=C(COC1=CC=C(C(Cl)=C1Cl)C(C2=CC=C(C(CN)=C2)O)=O)OCC
Formula: C18H17Cl2NO5
M.Wt: 398.24
Sotrage: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
MSDS
Cat. No. Product name Field of application
DC70087 Desmopressin Desmopressin is a synthetic analogue of the antidiuretic hormone arginine vasopressin.
DC11516 Balovaptan Balovaptan (RG7314, RG-7314) is a potent, selective vasopressin-1 receptor antagonist..
DC76677 Elsovaptan Elsovaptan is the antagonist for vasopressin receptor that can be used in researchs of Alzheimer disease.
DC76676 DM-4111 DM-4111, one of the major monohydroxyl metabolites of Tolvaptan. Obeticholic acid is a potent, selective and orally active FXR agonist.
DC76675 A-49816 A-49816 is an orally active diuretic that increases urine volume and sodium and chloride excretion. A-49816 at high doses (12.5, 15, and 20 mg) caused significant salt and chloride excretion and diuresis in experimental animals.
DC76674 (R)-(+)-Tolvaptan (R)-(+)-Tolvaptan ((R)-(+)-OPC-41061) is the (R)-(+) enantiomer of Tolvaptan.
DC73513 RGH-122 RGH-122 is a potent, selective, and orally bioavailable V1a receptor antagonist with Ki/IC50 of 0.3/0.9 nM (hV1a) respectively, >100-fold selectiive over V2 receptor.
DC73512 OPC-61815 OPC-61815 is a water-soluble phosphate ester pro-drug of Tolvaptan (Cat# PC-45125), which is an orally active vasopressin V2 receptor antagonist.
DC72348 Selepressin Selepressin (FE 202158) is a selective vasopressin V1A receptor agonist. Selepressin is a potent vasopressor. Selepressin can be used in the research of septic shock.
DC48979 TASP0390325 TASP0390325 is a high affinity and orally active arginine vasopressin receptor 1B (V1B receptor) antagonist with antidepressant and anxiolytic activities.
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