telmisartan

Telmisartan (BIBR 277) is an Angiotensin 2 Receptor Blocker. The mechanism of action of telmisartan is as an Angiotensin 2 Receptor Antagonist.

Telmisartan methyl ester is an impurity that is found in Telmisartan.

Telmisartan-D3 (Standard) is a reference standard of Telmisartan-D3 intended for quantitative analysis, quality control, and related biochemical research applications. Telmisartan-d3 is a deuterated compound of Telmisartan.

Telmisartan-13C-D3 (Standard) is a reference standard of Telmisartan-13C-D3 intended for quantitative analysis, quality control, and related biochemical research applications. Telmisartan-13C-d3 the 13C and deuterated compound of Telmisartan. Telmisartan has a CAS number of 144701-48-4. Telmisartan is an Angiotensin 2 Receptor Blocker. The mechanism of action of telmisartan is as an Angiotensin 2 Receptor Antagonist.

Telmisartan-D3 is a deuterated compound of Telmisartan (T1570).

Telmisartan-D7 is a deuterium-labeled form of Telmisartan. Telmisartan (T1570) serves as a potent antagonist of the angiotensin II type 1 receptor, effectively inhibiting its activity with an IC50 of 9.2 nM.

Telmisartan-D4 is the deuterated form of Telmisartan (T1570), which is a potent antagonist of the angiotensin II type 1 receptor (angiotensin II type 1 receptor). It effectively inhibits the receptor's activity, with an IC50 value of 9.2 nM.

Telmisartan-13C-D3 the 13C and deuterated compound of Telmisartan. Telmisartan (T1570) has a CAS number of 144701-48-4. Telmisartan is an Angiotensin 2 Receptor Blocker. The mechanism of action of telmisartan is as an Angiotensin 2 Receptor Antagonist.

Anticanceragent 259 (Compound 3g) is a telmisartan-based cell death regulator that disrupts the STAT5 signaling pathway, thereby increasing the sensitivity of resistant cells to imatinib, with an SC50 of 1.5 μM.

GSK1820795A is a selective G2A/GPR132a antagonist and a telmisartan analog. GSK1820795A also exhibits angiotensin II receptor antagonist activity and partial PPARγ agonist activity. GSK1820795A effectively blocks the activating effects of N-acylamides on yeast cells expressing hGPR132a.

N1-Methylbenzene-1,2-diamine is a biochemical reagent applied in: one-pot synthesis of 1-methyl-2(hetero)arylbenzimidazoles; preparation of 1-methyl-1H-benzimidazole-2(3H)-thione; total synthesis of telmisartan (an angiotensin II receptor antagonist); and benzimidazole synthesis from ketene dithioacetals.