| MDL | MFCD00864464 |
|---|---|
| Molecular Weight | 428.53 |
| Molecular Formula | C25H28N6O |
| SMILES | O=C1N(CC2=CC=C(C3=C(C4=NN=NN4)C=CC=C3)C=C2)C(CCCC)=NC15CCCC5 |
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] .
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. |
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. |
| 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 |
| NCT00352560 | Bristol-Myers Squibb|Sanofi |
Atrial Fibrillation
|
July 2006 | Phase 3 |
| NCT00517322 | Università degli Studi dell´Insubria |
Left Atrial Volume|Hypertensive Heart Disease|Antihypertensive Drugs|Diastolic Function|Renin Angiotensin System
|
August 2007 | Phase 4 |
| NCT03016832 | Jiangsu Famous Medical Technology Co., Ltd. |
Diabetic Kidney Disease
|
January 2017 | Early Phase 1 |
| NCT00529750 | Sanofi |
Hypertension
|
July 2002 | Phase 4 |
| NCT00708344 | Sanofi |
Hypertension
|
June 2008 | Phase 4 |
| NCT00389168 | Karolinska Institutet|Bristol-Myers Squibb|Sanofi|Swedish Heart Lung Foundation |
Hypertension
|
April 1995 | Phase 2|Phase 3 |
| NCT00347087 | Charite University, Berlin, Germany|Bristol-Myers Squibb |
Chronic Heart Failure
|
July 2004 | Phase 4 |
| NCT00350038 | Sanofi|Bristol-Myers Squibb |
Hypertension|Dyslipidemia
|
February 2005 | Phase 4 |
| NCT00564187 | Sanofi|Bristol-Myers Squibb |
Hypertension
|
February 2003 | Phase 4 |
| NCT00362037 | Sanofi|Bristol-Myers Squibb |
Hypertension
|
March 2006 | Phase 4 |
| NCT03476603 | Norwegian University of Science and Technology|St. Olavs Hospital|Volvat Medisinsk Senter Stokkan|Namsos Hospital|Alesund Hospital |
Obesity, Morbid
|
November 2, 2016 | |
| NCT02380625 | Clinical Research Management, Inc.|Bill and Melinda Gates Foundation|Duke University|University of Sierra Leone|Syneos Health|University of North Carolina |
Ebola Virus Disease
|
April 2015 | Phase 1|Phase 2 |
| NCT03762850 | Travere Therapeutics, Inc. |
Immunoglobulin A Nephropathy
|
December 11, 2018 | Phase 3 |
| NCT00443612 | Sanofi |
Hypertension
|
September 2006 | Phase 4 |
| NCT05476354 | Handok Inc. |
Essential Hypertension
|
August 2022 | Phase 3 |
| NCT00263003 | Sanofi |
Hypertension
|
June 2005 | Phase 3 |
| NCT00110422 | Bristol-Myers Squibb|Sanofi |
Metabolic Syndrome|Hypertension
|
November 2005 | Phase 4 |
| NCT01238705 | LanZhou University |
Hypertension|Sexual Dysfunction
|
April 2008 | Phase 4 |
| NCT00283036 | Sanofi|Bristol-Myers Squibb |
Hypertension
|
April 2005 | Phase 4 |
| NCT03147677 | The Third Xiangya Hospital of Central South University |
Type 2 Diabetic Nephropathy
|
July 28, 2016 | Phase 4 |
| NCT00660309 | Novartis |
Type 2 Diabetes Mellitus
|
April 2008 | Phase 4 |
| NCT00561964 | Sanofi|Bristol-Myers Squibb |
Hypertension
|
January 2004 | Phase 3 |
| NCT00095394 | Bristol-Myers Squibb|Sanofi |
Hypertension
|
September 2004 | Phase 3 |
| NCT00152698 | University of Erlangen-Nürnberg Medical School|Bristol-Myers Squibb |
Hypercholesterolemia
|
November 2009 | Phase 3 |
| NCT00185055 | Daiichi Sankyo, Inc. |
Healthy
|
November 2004 | Phase 4 |
| NCT05056727 | AstraZeneca |
Renal Insufficiency, Chronic|Hyperkalemia
|
September 30, 2021 | Phase 3 |
| NCT02644486 | Zhi-Hong Liu, M.D.|Nanjing University School of Medicine |
Obesity and Glomerulopathy
|
January 2016 | Not Applicable |
| NCT00317915 | Steno Diabetes Center Copenhagen|Bristol-Myers Squibb|Sanofi-Synthelabo |
Type 2 Diabetes|Microalbuminuria|Hypertension
|
Phase 3 | |
| NCT05297929 | The Affiliated Hospital of Qingdao University |
Irbesartan Tablets (0.15g+Tablet)|Under Fasted Condition|Under Fed Condition|Bioequivalence
|
February 17, 2022 | Phase 1 |
| NCT00334581 | Sanofi|Bristol-Myers Squibb |
Hypertension
|
May 2006 | Phase 4 |
| NCT00320879 | Steno Diabetes Center Copenhagen |
Type 2 Diabetes|Microalbuminuria
|
September 2003 | Phase 4 |
| NCT00249795 | Sanofi|Bristol-Myers Squibb |
Atrial Fibrillation|Cardiovascular Disease
|
June 2003 | Phase 3 |
| NCT01613118 | Travere Therapeutics, Inc. |
Focal Segmental Glomerulosclerosis
|
March 2014 | Phase 2 |
| NCT00549133 | Sanofi |
Hypertension|Diabetes Mellitus Type 2
|
October 2003 | Phase 4 |
| NCT01712100 | Roxane Laboratories|West-Ward Pharmaceutical |
Hypertension
|
August 2007 | Not Applicable |
| NCT00095550 | Bristol-Myers Squibb|Sanofi |
Hypertension
|
October 2004 | Phase 3 |
| NCT05475665 | Handok Inc. |
Essential Hypertension
|
July 14, 2022 | Phase 3 |
| NCT01712139 | Roxane Laboratories|West-Ward Pharmaceutical |
Hypertension
|
September 2007 | Not Applicable |
| NCT00095290 | Bristol-Myers Squibb|Sanofi |
Albuminuria
|
September 2004 | Phase 4 |
| NCT00847834 | Sanofi |
Hypertension
|
December 2003 | Phase 4 |
| NCT02386293 | Augusta University |
Hypertension|Obesity|Stress, Psychological|Blood Pressure
|
April 2014 | Phase 2 |
| NCT01360710 | Baker Heart and Diabetes Institute |
Abdominal Obesity|Hypertension
|
January 2012 | Phase 4 |
| NCT00613496 | University of Magdeburg|Sanofi |
Persistent Atrial Fibrillation
|
May 2009 | Phase 4 |
| NCT00180024 | Technische Universität Dresden |
Healthy Subjects
|
January 2002 | Not Applicable |
| NCT00933231 | Astellas Pharma Inc|Astellas Pharma Canada, Inc. |
Kidney Transplantation
|
August 17, 2009 | Phase 3 |
| NCT02721342 | Mario Negri Institute for Pharmacological Research |
Chronic Kidney Disease
|
June 2009 | |
| NCT01949233 | University of Oxford|Oxford University Hospitals NHS Trust |
Marfan Syndrome
|
October 2013 | Phase 2 |
| NCT01825850 | LG Life Sciences |
Healthy
|
June 2013 | Phase 1 |
| NCT01992796 | University of Salerno|Federico II University |
Severe Sepsis
|
January 2014 | Phase 3 |
| NCT00791830 | University of Aarhus |
Kidney Failure, Chronic
|
April 2009 | Phase 3 |
| NCT00957554 | Sanofi |
Hypertension
|
July 2009 | Phase 3 |
| NCT00950066 | Sanofi |
Hypertension
|
July 2009 | Phase 2 |
| NCT02842359 | Sanofi |
Type 2 Diabetes Mellitus
|
August 23, 2016 | Phase 4 |
| NCT00362258 | Sanofi|Bristol-Myers Squibb |
Hypertension
|
February 2006 | Phase 4 |
| NCT00794963 | Northwell Health |
Metabolic Syndrome
|
November 2008 | Not Applicable |
| NCT00296218 | Sanofi|Bristol-Myers Squibb |
Myocardial Ischemia|Hypertension
|
February 2006 | Phase 3 |
| NCT00154024 | Technische Universität Dresden |
Healthy Subjects
|
March 2003 | Not Applicable |
| NCT00742066 | Maastricht University Medical Center |
Hypertension|Insulin Resistance|Microcirculation
|
March 2008 | Not Applicable |
| NCT00987662 | Aristotle University Of Thessaloniki |
Obesity|Hypertension
|
January 2012 | Phase 4 |
| NCT00335673 | Sanofi|Bristol-Myers Squibb |
Hypertension
|
February 2006 | Phase 4 |
| NCT01519297 | Brigham and Women´s Hospital |
Preeclampsia|Pregnancy Induced Hypertension
|
May 2012 | Not Applicable |
| NCT00265642 | ANRS, Emerging Infectious Diseases|Sanofi |
Hepatitis C, Chronic
|
October 2006 | Phase 3 |
| NCT03493685 | Travere Therapeutics, Inc. |
Focal Segmental Glomerulosclerosis
|
April 17, 2018 | Phase 3 |
| NCT01442987 | Hanmi Pharmaceutical Company Limited |
Hypertension|Hyperlipidemia
|
May 2011 | Phase 3 |
| NCT00125645 | University of Southern Denmark|Bristol-Myers Squibb |
Myocardial Infarction
|
March 1, 2005 | Phase 4 |
| NCT00005010 | National Institute of Allergy and Infectious Diseases (NIAID) |
End-Stage Renal Disease|Chronic Allograft Nephropathy
|
Phase 3 | |
| NCT00265967 | Sanofi|Bristol-Myers Squibb |
Hypertension
|
September 2005 | Phase 4 |
| NCT03934307 | Alnylam Pharmaceuticals |
Hypertension
|
May 1, 2019 | Phase 1 |
| NCT02597361 | Assistance Publique - Hôpitaux de Paris|Ministry of Health, France |
Ehlers-Danlos Syndrome, Vascular Type
|
January 2016 | Phase 3 |
| NCT01712113 | Roxane Laboratories|West-Ward Pharmaceutical |
Hypertension
|
August 2007 | Not Applicable |
| NCT00225667 | Connolly, Stuart, M.D.|Sanofi|Bristol-Myers Squibb |
Atrial Fibrillation|Hypertension
|
December 2005 | Phase 3 |
| NCT00535925 | University of Campania Luigi Vanvitelli |
Diabetic Nephropathy
|
October 2005 | Phase 4 |
| NCT01712126 | Roxane Laboratories|West-Ward Pharmaceutical |
Hypertension
|
September 2007 | Not Applicable |
| NCT00562809 | Sanofi|Bristol-Myers Squibb |
Hypertension
|
July 2003 | Phase 4 |
| NCT00635232 | Ligand Pharmaceuticals |
Hypertension
|
March 2008 | Phase 2 |
| NCT00106561 | Melbourne Health |
Kidney Disease|Diabetic Nephropathy|Glomerulonephritis|Proteinuria
|
January 2002 | Phase 2|Phase 3 |
| NCT00264212 | Sanofi|Bristol-Myers Squibb |
Hypertension
|
August 2004 | Phase 4 |
| NCT00095238 | Bristol-Myers Squibb|Sanofi |
Congestive Heart Failure
|
June 2002 | Phase 3 |
| NCT01858610 | Damanhour University |
Healthy
|
March 2013 | Not Applicable |
| NCT01447797 | Hanmi Pharmaceutical Company Limited |
Healthy
|
September 2011 | Phase 1 |
| NCT00171080 | Novartis |
Hypertension
|
April 2004 | Phase 3 |
Solid
Room temperature in continental US; may vary elsewhere.
| Powder | -20°C | 3 years |
|---|---|---|
| 4°C | 2 years | |
| In solvent | -80°C | 6 months |
| -20°C | 1 month |
DMSO : 100 mg/mL ( 233.36 mM ; Need ultrasonic)
| 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 |