Chemodex

Telmisartan

CHF 34.00
In stock
CDX-T0460-M01010 mgCHF 34.00
CDX-T0460-M05050 mgCHF 102.00
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Product Details
Synonyms BIBR 277; Micardis; Pritor; 4'[(1,4'-Dimethyl-2'-propyl[2,6'-bi-1H-benzimidazol]-1'-yl)methyl][1,1'-biphenyl]-2-carboxylic acid
Product Type Chemical
Properties
Formula C33H30N4O2
MW 514.62
CAS 144701-48-4
RTECS DV2037500
Source/Host Chemicals Synthetic
Purity Chemicals ≥98% (HPLC)
Appearance White to off-white solid.
Solubility Soluble in DMSO, chloroform, DMF or ethanol.
Identity Determined by 1H-NMR.
Declaration Manufactured by Chemodex.
Other Product Data

Click here for Original Manufacturer Product Datasheet
Our product description may differ slightly from the original manufacturers product datasheet.

InChi Key RMMXLENWKUUMAY-UHFFFAOYSA-N
Smiles CN1C2=CC=CC=C2N=C1C3=CC(N(CC4=CC=C(C5=CC=CC=C5C(O)=O)C=C4)C(CCC)=N6)=C6C(C)=C3
Shipping and Handling
Shipping AMBIENT
Short Term Storage +20°C
Long Term Storage +20°C
Handling Advice Protect from light and moisture.
Use/Stability Stable for at least 2 years after receipt when stored at RT.
Documents
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Product Specification Sheet
Datasheet Download PDF
Description

Telmisartan is a nonpeptide angiotensin II receptor antagonist which selectively inhibits the angiotensin II AT1 receptor subtype (Ki=3.7nM). Telmisartan exhibits antihypertensive activity in a renin-dependent model of hypertension. In addition to blocking the renin-angiotensin system (RAS), telmisartan acts as a selective modulator of peroxisome proliferator-activated receptor gamma (PPAR-γ), a central regulator of insulin and glucose metabolism and improving insulin sensitivity. It is believed that telmisartan's dual mode of action may provide protective benefits against the vascular and renal damage caused by diabetes and cardiovascular disease (CVD). Through these actions, telmisartan potently reduces blood pressure in various animal models of hypertension, diminishing cardiac hypertrophy, cardiovascular and renal risk and glomerulosclerosis. Furthermore, telmisartan inhibits proliferation in several cancer models by inducing apoptosis and cell cycle arrest.

Product References

(1) U.J. Ries, et al.; J. Med. Chem. 36, 4040 (1993) | (2) W. Wienen, et al.; Br. J. Pharmacol. 110, 245 (1993) | (3) K.J. McClellan & A. Markham; Drugs 56, 1039 (1998) | (4) S.C. Benson, et al.; Hypertension 43, 993 (2004) | (5) X. Rong, et al.; J. Pharmacol. Exp. Ther. 331, 1096 (2009) | (6) R.E. Schmieder, et al.; J. Nephrol. 24, 263 (2011) | (7) J.E. Frampton; Drugs 71, 651 (2011) (Review) | (8) T. Kozako, et al.; FEBS Open Bio 6, 442 (2016) | (9) E. Samukawa, et al.; Int. J. Oncol. 51, 1674 (2017)

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