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Published TCIMAIL newest issue No.197 | Notice of Discontinuing the Use of Password-Protected Compressed Files | Various analytical charts can be searched on each product detail page and Product Document Search (The kinds of analytical charts differ by product)
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CAS RN: 144701-48-4 | 產品號碼: T2861
產品規格
| Appearance | White to Almost white powder to crystal |
| Purity(HPLC) | min. 98.0 area% |
| Purity(Neutralization titration) | min. 98.0 % |
性質
| 熔點 | 269 °C |
GHS
| 危險性說明 | H413 : May cause long lasting harmful effects to aquatic life. |
| 防範說明 | P501 : Dispose of contents/ container to an approved waste disposal plant. P273 : Avoid release to the environment. |
相關法規
| RTECS # | DV2037500 |
運輸資料
| HS編碼* | 2933.99-000 |
Application
Telmisartan: An Angiotensin II Receptor Type 1 (AT1) Antagonist
Telmisartan is an angiotensin II receptor type 1 (AT1) antagonist. Angiotensin II is formed from angiotensin I in a reaction catalyzed by angiotensin-converting enzyme (ACE). Angiotensin II, a vasoconstrictor substance, is the principal pressor agent of the renin-angiotensin system. Telmisartan blocks the effects of angiotensin II by selectively blocking the binding of angiotensin II to the AT1 receptor in many tissues. Thereby, telmisartan reduces peripheral vascular resistance and blood pressure. There is also an AT2 receptor found in many tissues, but AT2 is not known to be associated with cardiovascular homeostasis. Telmisartan has much greater affinity for the AT1 receptor than for the AT2 receptor. For your reference, our product [D5079] is a key synthetic intermediate of telmisartan. (The product is for research purpose only.)
References
- Identification of Telmisartan as a Unique Angiotensin II Receptor Antagonist With Selective PPARγ-Modulating Activity
- Angiotensin Type 1 Receptor Blockers Induce Peroxisome Proliferator-Activated Receptor-γ Activity
- A review on telmisartan: A novel, long-acting angiotensin II-receptor antagonist
- W. Wienen, M. Entzeroth, J. C. A. Van Meel, J. Stangier, U. Busch, T. Ebner, J. Schmid, H. Lehmann, K. Matzek, J. Kempthorne-Rawson, et al., Cardiovasc. Drug Rev. 2000, 18, 127.
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