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Key Documents

SCP0143

Sigma-Aldrich

ET Antagonist PD 145065

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About This Item

經驗公式(希爾表示法):
C52H67N7O10
分子量::
950.13
分類程式碼代碼:
12352200
NACRES:
NA.32

化驗

≥95% (HPLC)

形狀

lyophilized

成份

Peptide Content, ≥75%

儲存條件

protect from light

儲存溫度

−20°C

Amino Acid Sequence

Ac-Bhg-Leu-Asp-Ile-Ile-Trp

應用

PD-145065 is used as an endothelin-A/endothelin-B (ETA/ETB) receptor antagonist.

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


分析證明 (COA)

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Paulo Castro-Chaves et al.
European journal of pharmacology, 544(1-3), 91-96 (2006-07-18)
We analyzed the influence of endothelin-1 and endocardial endothelium on the myocardial effects of angiotensin-II. Angiotensin-II (10(-9)-10(-5) M) was tested in rabbit right papillary muscles in absence (Protocol-A) or presence of PD-145065 (10(-7) M; Protocol-B), BQ-123 (10(-7) M; Protocol-C) or
Comparison of 2 endothelin-receptor antagonists on in vitro responses of equine palmar digital arterial and venous rings to endothelin-1.
Stokes AM, Venugopal CS, Hosgood G, et al.
Canadian Journal of Veterinary Research = Revue Canadienne De Recherche Veterinaire, 7-, 197-205 (2006)
K E Todd et al.
Surgery, 122(2), 443-449 (1997-08-01)
Endothelin peptides are polykines with strong vasoconstrictor properties. We have previously shown that endothelin antagonism (PD145065) reduces the local severity of acute pancreatitis. We now investigated the effect of endothelin antagonism on systemic inflammation in a model of acute hemorrhagic
Francesca Ceccarelli et al.
Biochemical pharmacology, 65(5), 783-793 (2003-03-12)
Expression and pharmacological properties of endothelin receptors (ETRs) were investigated in H9c2 cardiomyoblasts. The mechanism of receptor-mediated modulation of intracellular Ca(2+) concentration ([Ca(2+)](i)) was examined by measuring fluorescence increase of Fluo-3-loaded cells with flow cytometry. Binding assays showed that [125I]endothelin-1

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