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Telmisartan amide

CAS# 915124-86-6

Telmisartan amide

Catalog No. BCN9634----Order now to get a substantial discount!

Product Name & Size Price Stock
Telmisartan amide: 5mg $288 In Stock
Telmisartan amide: 10mg Please Inquire In Stock
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Quality Control of Telmisartan amide

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Chemical structure

Telmisartan amide

3D structure

Chemical Properties of Telmisartan amide

Cas No. 915124-86-6 SDF Download SDF
PubChem ID 11978018 Appearance Powder
Formula C33H31N5O M.Wt 513.6
Type of Compound Impurities Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 2-[4-[[4-methyl-6-(1-methylbenzimidazol-2-yl)-2-propylbenzimidazol-1-yl]methyl]phenyl]benzamide
SMILES CCCC1=NC2=C(N1CC3=CC=C(C=C3)C4=CC=CC=C4C(=O)N)C=C(C=C2C)C5=NC6=CC=CC=C6N5C
Standard InChIKey YAIWQMXHIQDCFT-UHFFFAOYSA-N
Standard InChI InChI=1S/C33H31N5O/c1-4-9-30-36-31-21(2)18-24(33-35-27-12-7-8-13-28(27)37(33)3)19-29(31)38(30)20-22-14-16-23(17-15-22)25-10-5-6-11-26(25)32(34)39/h5-8,10-19H,4,9,20H2,1-3H3,(H2,34,39)
General tips For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.
We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months.
Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it.
About Packaging 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial.
2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial.
3. Try to avoid loss or contamination during the experiment.
Shipping Condition Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request.

Telmisartan amide Dilution Calculator

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Telmisartan amide Molarity Calculator

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Preparing Stock Solutions of Telmisartan amide

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.947 mL 9.7352 mL 19.4704 mL 38.9408 mL 48.676 mL
5 mM 0.3894 mL 1.947 mL 3.8941 mL 7.7882 mL 9.7352 mL
10 mM 0.1947 mL 0.9735 mL 1.947 mL 3.8941 mL 4.8676 mL
50 mM 0.0389 mL 0.1947 mL 0.3894 mL 0.7788 mL 0.9735 mL
100 mM 0.0195 mL 0.0974 mL 0.1947 mL 0.3894 mL 0.4868 mL
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations.

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References on Telmisartan amide

Identification and development of non-cytotoxic cell death modulators: Impact of sartans and derivatives on PPARgamma activation and on growth of imatinib-resistant chronic myelogenous leukemia cells.[Pubmed:32272420]

Eur J Med Chem. 2020 Jun 1;195:112258.

4'-((2-Propyl-1H-benzo[d]imidazol-1-yl)methyl)-[1,1'-biphenyl]-2-carboxylic acid derived from telmisartan was identified as lead for the design of cell death modulators. In this study, we evaluated the efficacy of telmisartan itself and other sartans in combination with imatinib against K562-resistant cells. The findings were directly used to further optimize the lead structure. Telmisartan and candesartan cilexetil represented the most effective sartans, thus the influence of carboxyl/methyl carboxylate groups at positions 7 (compounds 6, 7) or 4 (compounds 12-14) at the benzimidazole core was studied. Additionally, according to the results of a former structure-activity study, telmisartan was transformed to the related amide (1). Telmisartan amide 1, as well as the esters 6 and 12 markedly sensitized the resistant CML cells to imatinib treatment. Correlation with their potency to activate PPARgamma is not given. Candesartan cilexetil, telmisartan and 1 showed the profile of partial agonists at PPARgamma with EC50 values of 4.2, 4.3 and 9.1 muM, respectively, while 6 and 12 caused only marginal intrinsic activation at 10 muM (Amax = 22% and 13%). However, the repression of the STAT5 phosphorylation relates with the possibility to sensitize K562-resistant CML cells to imatinib treatment. It is worth mentioning that all compounds were per se non-cytotoxic at relevant concentrations.

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