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Tenapanor

Tenapanor Suppliers list
Company Name: Nanjing Becas pharmatech Ltd.  Gold
Tel: +86-13912903754 13912903754
Email: info@becaspharma.com
Company Name: WUHAN SUN-SHINE BIO-TECHNOLOGY Co., Ltd.  
Tel: 17702719238
Email: sales@sun-shinechem.com
Company Name: MedChemexpress LLC  
Tel: 021-58955995
Email: sales@medchemexpress.cn
Company Name: ShangHai Caerulum Pharma Discovery Co., Ltd.  
Tel: 18149758185 18149758185
Email: sales-cpd@caerulumpharma.com
Company Name: AdooQ Bioscience CHINA  
Tel: 025-58849295
Email: info@adooq.cn

Tenapanor manufacturers

  • Tenapanor
  • Tenapanor pictures
  • $31.00
  • 2026-07-17
  • CAS:1234423-95-0
  • Purity: 99.85%
  • Supply Ability: 10g
  • Tenapanor
  • Tenapanor pictures
  • 2026-06-30
  • CAS:1234423-95-0
  • Min. Order: 1kg
  • Purity: 98%
  • Supply Ability: 1000kg
  • Tenapanor
  • Tenapanor pictures
  • 2024-10-31
  • CAS:1234423-95-0
  • Min. Order: 10g
  • Purity: 0.99
  • Supply Ability: 1KG
Tenapanor Basic information
Product Name:Tenapanor
Synonyms:Tenapanor;Rovatirelin Hydrate;Tenapanor(free base);AZD-1722; AZD 1722; AZD1722; RDX 5791; RDX-5791; RDX5791; TENAPANOR FREE BASE; IBSRELA.;Ibsrela.;Tenapanor (AZD1722,RDX5791);CS-2459;AZD1722
CAS:1234423-95-0
MF:C50H66Cl4N8O10S2
MW:1145.04
EINECS:
Product Categories:
Mol File:1234423-95-0.mol
Tenapanor Structure
Tenapanor Chemical Properties
storage temp. Store at -20°C
solubility DMSO : 50 mg/mL (43.67 mM);Water : < 0.1 mg/mL (insoluble)
form Solid
color White to off-white
InChIKeyDNHPDWGIXIMXSA-KQPQOZEFNA-N
SMILESClC1C=C(Cl)C=C2[C@H](C3C=CC=C(S(=O)(=O)NCCOCCOCCNC(=O)NCCCCNC(=O)NCCOCCOCCNS(C4C=CC=C([C@@H]5CN(C)CC6=C(C=C(Cl)C=C56)Cl)C=4)(=O)=O)C=3)CN(C)CC=12 |&1:7,52,r|
Safety Information
MSDS Information
Tenapanor Usage And Synthesis
UsesTenapanor is a medicine. This drug targets Nsp16 protein may corroborates a promising approach to combat SARS-CoV-2 virus.
in vivo

Tenapanor (0.15, 0.5 mg/kg; p.o.) reduces passive paracellular phosphate absorption in rats[1].
Tenapanor (0.15 mg/kg; p.o.; twice-daily for 11 consecutive days) increases the reduction in urinary phosphorus excretion in rats[2].

Animal Model:Rats (intestinal loop model)[1]
Dosage:0.15, 0.5 mg/kg
Administration:P.o.
Result:Reduced passive paracellular phosphate absorption by reduced urinary phosphate and sodium excretion after the high-phosphate meal and increased sodium and phosphate delivery to the cecum.
Animal Model:8 weeks, 250 g male Sprague–Dawley rats[2]
Dosage:0.15 mg/kg in combination with sevelamer (0%, 0.75%, 1.5%, and 3% (wt/wt))
Administration:Oral gavage; twice-daily for 11 consecutive days
Result:Significantly augmented the reduction in urinary phosphorus excretion.
Tenapanor Preparation Products And Raw materials
Tag:Tenapanor(1234423-95-0) Related Product Information
N,N'-(10,17-dioxo-3,6,21,24-tetraoxa-9,11,16,18-tetraazahexacosane-1,26-diyl)bis(3-(6,8-dichloro-2-methyl-1,2,3,4-tetrahydroisoquinolin-4-yl)benzenesulfonamide) Tenapanor hydrochloride Tenapanor BIIB 513 BMS-284640 Zoniporide hydrochloride hydrate