Drug General Information
Drug ID
D04TQO
Former ID
DNCL003361
Drug Name
AZD1722
Drug Type
Small molecular drug
Indication Renal disease [ICD10:N00-N29] Phase 2 [524182]
Company
AstraZeneca
Structure
Download
2D MOL
Formula
C50H66Cl4N8O10S2
InChI
InChI=1S/C50H66Cl4N8O10S2/c1-61-31-43(41-27-37(51)29-47(53)45(41)33-61)35-7-5-9-39(25-35)73(65,66)59-15-19-71-23-21-69-17-13-57-49(63)55-11-3-4-12-56-50(64)58-14-18-70-22-24-72-20-16-60-74(67,68)40-10-6-8-36(26-40)44-32-62(2)34-46-42(44)28-38(52)30-48(46)54/h5-10,25-30,43-44,59-60H,3-4,11-24,31-34H2,1-2H3,(H2,55,57,63)(H2,56,58,64)/t43-,44-/m0/s1
InChIKey
DNHPDWGIXIMXSA-CXNSMIOJSA-N
PubChem Compound ID
PubChem Substance ID
Target and Pathway
Target(s) Sodium/hydrogen exchanger 3 Target Info Modulator [550792]
KEGG Pathway Proximal tubule bicarbonate reclamation
Protein digestion and absorption
Bile secretion
Mineral absorption
Pathway Interaction Database Endothelins
RhoA signaling pathway
WikiPathways SIDS Susceptibility Pathways
References
Ref 524182ClinicalTrials.gov (NCT01764854) Pharmacodynamic Study of AZD1722 in End-stage Renal Disease Patients on Hemodialysis. U.S. National Institutes of Health.
Ref 550792RDX5791, a First-in-Class Minimally Systemic NHE3 Inhibitor in Clinical Development for CIC and IBS-C, Increases Intestinal Sodium Leading to Enhanced Intestinal Fluid Volume and Transit. Gastroenterology. 2011;140(suppl 1):S99.

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