نتایج جستجو برای: substance p analogue

تعداد نتایج: 1475186  

Journal: :Naunyn-Schmiedeberg's Archives of Pharmacology 1974

Journal: :Journal of the Royal Society of Medicine 1980

Journal: :British Journal of Pharmacology 1984

2015
Saeed Mozaffari Mostafa Erfani Davood Beiki Fariba Johari Daha Farzad Kobarfard Saeed Balalaie Babak Fallahi

Neurokinin 1 receptors (NK1R) are overexpressed on several types of important human cancer cells. Substance P (SP) is the most specific endogenous ligand known for NK1Rs. Accordingly,a new SP analogue was synthesized and evaluated for detection of NK1R positive tumors.[6-hydrazinopyridine-3-carboxylic acid (HYNIC)-Tyr(8)-Met(O)(11)-SP] was synthesized and radiolabeled with (99m)Tc using ethylen...

Journal: :Current Opinion in Endocrinology, Diabetes and Obesity 2009

Journal: :Folia Pharmacologica Japonica 1996

Journal: :The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 1992
P J Larsen T Saermark S E Mau

Several lines of anatomic, biochemical, and pharmacological evidence suggest that the neuropeptide substance P has a direct action on cells of the anterior pituitary lobe via a specific neurokinin-1 receptor. In the present study we confirmed this association by combining Bolton-Hunter iodinated substance P-receptor autoradiography with immunocytochemistry on cultured anterior pituitary cells. ...

Journal: :Biochemical Society transactions 1977
D Cannon P Skrabanek D Powell M G Harrington

on the response of bone alkaline phosphatase to parathyrin. The results of a typical experiment showing percentage change in alkaline phosphatase activity compared with the hormone-free control are presented in Fig. 2(b). Tissue from 1-day-old animals was unresponsive to parathyrin, that from the 3-day-old animal showed decreased alkaline phosphatase activity and those from 5and 6-day-old anima...

Journal: :Journal of dental research 1986
E Bobyock E J Barbieri W S Chernick

The intra-arterial infusion of substance P produced dose-related responses of both parotid and submandibular salivary secretion in anesthetized rats. The substance P-induced secretion in both glands was inhibited by the substance P analogues [D-Arg1, D-Trp7.9, Leu11]-substance P and [D-Arg1, D-Pro2, D-Trp7.9, Leu11]-substance P, but not by [D-Pro2, D-Trp7,9]-substance P. The profiles of protein...

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