[CAS NO. 138402-11-6]  Irbesartan

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PRODUCTS SPECIFICATIONS [138402-11-6]

Store
Catalog
HY-B0202
Brand
MCE
CAS
138402-11-6

DESCRIPTION [138402-11-6]

Overview

MDLMFCD00864464
Molecular Weight428.53
Molecular FormulaC25H28N6O
SMILESO=C1N(CC2=CC=C(C3=C(C4=NN=NN4)C=CC=C3)C=C2)C(CCCC)=NC15CCCC5

For research use only. We do not sell to patients.


Summary

Irbesartan (SR-47436) is an orally active Ang II type 1 (AT1) receptor blocker (ARB) . Irbesartan can relax the blood vessels, low blood pressure and increase the supply of blood and oxygen to the heart. Irbesartan can be used for the research of high blood pressure, heart failure, and diabetic kidney disease [1] .


In Vitro

Irbesartan (20 μM, 3 h) reduces Th22 cells chemotaxis in vitro [1] .
Irbesartan (0 μM, 20 μM, 40 μM and 60 μM) suppresses Th22 cells differentiation in vitro [1] .
Irbesartan (20 μM) inhibits Th22 cells related proinflammatory response of TECs in vitro [1] .

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Viability Assay [1]

Cell Line: CD4+ T cells
Concentration: 0, 20, 40 and 60 μM
Incubation Time: 48 h
Result: Exerted no obvious effect on viability of CD4 + T cells.

In Vivo

Irbesartan (oral gavage; 50 mg/kg/d; once daily) reduces Th22 lymphocytosis and serum IL-22 level in Ang II-infused mice [1] .
Irbesartan (oral gavage; 50 mg/kg/d; once daily) exerts obvious renoprotective effects [1] .
Irbesartan (oral gavage; 50 mg/kg/d; once daily) relieves systemic inflammation and renal fibrosis in hypertension mice induced by Ang II [1] .
Irbesartan hydrochloride (20 μM; for 3 h) can attenuate Th22 cells recruitment and IL-22 secretion, which might be through inhibiting chemotaxis in hypertensive renal injury mice [1] .

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: C57BL/6 mice [1]
Dosage: 50 mg/kg
Administration: oral gavage; 50 mg/kg/d; once daily
Result: Displayed low Th22 cells and IL-22, exerted similar inhibitory effect on Th1 cell proportion and displayed decreased IL-22 level in kidney.
Prevented BP elevation markedly and decreased urinary albumin/creatinine ratio, BUN and Scr.
Repressed the expression of IL-1β, IL-6, TNF-α, α-SMA, FN and Col I and diminished the extent of fibrosis.
Animal Model: C57BL/6 mice [1]
Dosage: 20 μM
Administration: 20 μM; for 3 h
Result: Downregulated renal CCL20, CCL22 and CCL27 concentrations.

Clinical Trial

NCT Number Sponsor Condition Start Date Phase
NCT01968759 Mario Negri Institute for Pharmacological Research
Chronic Kidney Disease
October 2013 Phase 2
NCT00657059 Sun Yat-sen University
IgA Nephropathy
September 2007 Phase 3
NCT05243199 Ruijin Hospital
CKD5 Stage Dialysis|Heart Failure
August 1, 2020 Phase 4

Appearance

Solid


Shipping

Room temperature in continental US; may vary elsewhere.


Storage

Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month

Solvent & Solubility

In Vitro:

DMSO : 100 mg/mL ( 233.36 mM ; Need ultrasonic)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 2.3336 mL 11.6678 mL 23.3356 mL
5 mM 0.4667 mL 2.3336 mL 4.6671 mL
10 mM 0.2334 mL 1.1668 mL 2.3336 mL
* Please refer to the solubility information to select the appropriate solvent.
In Vivo:
  • 1.

    Add each solvent one by one: 10% DMSO >> 40% PEG300 >> 5% Tween-80 >> 45% saline

    Solubility: ≥ 2.5 mg/mL (5.83 mM); Clear solution

  • 2.

    Add each solvent one by one: 10% DMSO >> 90% (20% SBE-β-CD in saline)

    Solubility: ≥ 2.5 mg/mL (5.83 mM); Clear solution

  • 3.

    Add each solvent one by one: 10% DMSO >> 90% corn oil

    Solubility: ≥ 2.5 mg/mL (5.83 mM); Clear solution

* All of the co-solvents are available by MCE.


Synonyms

1,3-Diazaspiro[4.4]non-1-en-4-one, 2-butyl-3-[[2′-(2H-tetrazol-5-yl)[1,1′-biphenyl]-4-yl]methyl]-
1,3-Diazaspiro[4.4]non-1-en-4-one, 2-butyl-3-[[2′-(1H-tetrazol-5-yl)[1,1′-biphenyl]-4-yl]methyl]-
2-Butyl-3-[[2′-(2H-tetrazol-5-yl)[1,1′-biphenyl]-4-yl]methyl]-1,3-diazaspiro[4.4]non-1-en-4-one
SR 47436
2-Butyl-3-[p-(o-1H-tetrazol-5-ylphenyl)benzyl]-1,3-diazaspiro[4.4]non-1-en-4-one
Irbesartan
BMS 186295
Avapro
Aprovel
Karvea
2-Butyl-3-[[2′-(tetrazol-5-yl)biphenyl-4-yl]-methyl]-1,3-diazaspiro[4.4]non-1-en-4-one
Irbetan
Irbest
Kansartan
X-Tension
3-Butyl-2-[[4-[2-(2H-tetrazol-5-yl)phenyl]phenyl]methyl]-2,4-diazaspiro[4.4]non-3-en-1-one
2-Butyl-3-[[4-[2-(2H-tetrazol-5-yl)phenyl]phenyl]methyl]-1,3-diazaspiro[4.4]non-1-en-4-one
2-Butyl-3-[2′-(2H-tetrazol-5-yl)-biphenyl-4-ylmethyl]-1,3-diaza-spiro[4.4]non-1-en-4-one
Sabervel