Tenapanor Hydrochloride
Tenapanor hydrochloride is the hydrochloride salt form of tenapanor, an NHE3 inhibitor that reduces intestinal sodium and phosphate absorption. See tenapanor for complete pharmacological details. This salt formulation is used in approved oral tablet preparations for IBS-C and hyperphosphatemia in dialysis patients.
Peso Molecular
1218,0000 g/mol
TPSA
235,00 Ų
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Estrutura 2D
Cite this structure
Embed this structure
SMILES
CN1Cc2c(Cl)cc(Cl)cc2[C@H](c2cccc(S(=O)(=O)NCCOCCOCCNC(=O)NCCCCNC(=O)NCCOCCOCCNS(=O)(=O)c3cccc([C@@H]4CN(C)Cc5c(Cl)cc(Cl)cc54)c3)c2)C1.Cl.Cl
InChI
InChI=1S/C50H66Cl4N8O10S2.2ClH/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);2*1H/t43-,44-;;/m0../s1
Molecular Formula
C50H68Cl6N8O10S2
HBD / HBA
8 / 14
Ligações Rotacionáveis
29
Átomos Pesados
76
No targets recorded
Target interaction data is not yet available for this drug.
No interactions recorded
Drug interaction data is not yet available for this compound.
No side effects recorded
Side effect data is not yet available for this drug.
Perguntas frequentes
Tenapanor hydrochloride is the hydrochloride salt form of tenapanor, an NHE3 inhibitor that reduces intestinal sodium and phosphate absorption. See tenapanor for complete pharmacological details. This salt formulation is used in approved oral tablet preparations for IBS-C and hyperphosphatemia in dialysis patients.
Yes, Tenapanor Hydrochloride is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL3301627. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 78131177. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.
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