Olmesartan
CAS No. 144689-24-7
Olmesartan( RNH 6270 | CS 088 )
Catalog No. M11905 CAS No. 144689-24-7
An angiotensin II receptor antagonist which has been used for the treatment of high blood pressure.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 41 | In Stock |
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| 25MG | 37 | In Stock |
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| 50MG | 60 | In Stock |
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| 100MG | 91 | In Stock |
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| 200MG | Get Quote | In Stock |
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| 500MG | 244 | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameOlmesartan
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NoteResearch use only, not for human use.
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Brief DescriptionAn angiotensin II receptor antagonist which has been used for the treatment of high blood pressure.
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DescriptionAn angiotensin II receptor antagonist which has been used for the treatment of high blood pressure. Hypertension Discontinued(In Vitro):Olmesartan (0.7-5 mM; 24, 48 and 72 h) inhibits the growth of HeLa cells as a concentration- and time-dependent mode.(In Vivo):Repeated dosing of olmesartan (1 mg/kg, 2 mg/kg, p.o.) dose-dependently decreases mean arterial blood pressure (MAP) in SHR without significant influence on body weight and food intake during 10 weeks. Olmesartan (5 mg/kg/d, p.o.) and Hyd treatments lower systolic blood pressure to the same degree in mice. Olmesartan treatment inhibits cardiac hypertrophy, evaluated by echocardiography, heart weight, cross-sectional area of cardiomyocytes, and gene expression. Olmesartan treatment reverses decreased gene expressions of ACE2 and Mas receptor of Ren-Tg mice and inhibits enhanced NADPH oxidase (Nox)4 expression and reactive oxygen species.
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In VitroOlmesartan (0.7-5 mM; 24, 48 and 72?h) inhibits the growth of HeLa cells as a concentration- and time-dependent mode. Cell Viability Assay Cell Line:Human cervical cancer cell line (HeLa) Concentration:0.7- 5 mM Incubation Time:24, 48 and 72?h Result:IC50s against HeLa cell line are 4.685 and 1.651 mM for 48 and 72 h, respectively.
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In VivoRepeated dosing of olmesartan (1 mg/kg, 2 mg/kg, p.o.) dose-dependently decreases mean arterial blood pressure (MAP) in SHR without significant influence on body weight and food intake during 10 weeks. Olmesartan (5 mg/kg/d, p.o.) and Hyd treatments lower systolic blood pressure to the same degree in mice. Olmesartan treatment inhibits cardiac hypertrophy, evaluated by echocardiography, heart weight, cross-sectional area of cardiomyocytes, and gene expression. Olmesartan treatment reverses decreased gene expressions of ACE2 and Mas receptor of Ren-Tg mice and inhibits enhanced NADPH oxidase (Nox)4 expression and reactive oxygen species.
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SynonymsRNH 6270 | CS 088
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PathwayGPCR/G Protein
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TargetAngiotensin Receptor
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RecptorAngiotensin Receptor
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Research AreaCardiovascular Disease
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IndicationHypertension
Chemical Information
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CAS Number144689-24-7
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Formula Weight446.5016
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Molecular FormulaC24H26N6O3
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Purity>98% (HPLC)
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SolubilityDMSO: ≥ 55 mg/mL
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SMILESO=C(C1=C(C(C)(O)C)N=C(CCC)N1CC2=CC=C(C3=CC=CC=C3C4=NN=NN4)C=C2)O
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Chemical Name1H-Imidazole-5-carboxylic acid, 4-(1-hydroxy-1-methylethyl)-2-propyl-1-[[2'-(2H-tetrazol-5-yl)[1,1'-biphenyl]-4-yl]methyl]-
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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Valsartan
An angiotensin II receptor antagonist for treatment of high blood pressure and heart failure.
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Angiotensin II (1-4)...
Angiotensin II is a potent direct vasoconstrictor, causing arteries and veins to constrict, so leading to an increase in blood pressure. Angiotensin also potentiates the release of norepinephrine by a direct action on postganglionic sympathetic fibers.
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C-Type Natriuretic P...
CNP, a member of the natriuretic peptide family, was first identified in porcine brain and later found in other mammals as well as non-mammals. Processing of the CNP precursor gives rise to CNP-22 and its N-terminally elongated form, CNP-53. The CNPs share considerable sequence homology with ANP and BNP within the disulfide loop and exert similar pharmacological actions, although with different relative potencies.
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