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Immunosuppressive acidic protein

Hashimoto et al. [64] simplified the chip layout without etching the manifolds. The detection point was set at the interface of separation channel and reaction reservoir. They successfully separated and detected dansyl amino acids (glycine and glycine) using peroxyoxalate CL reaction using CL detection-based microchip capillary electrophoresis. They further incorporated an immune reaction with CL detection to determine human serum albumin or immunosuppressive acidic protein as a cancer marker in human serum [72]. [Pg.181]

Fig. 6 Illustration of a microfluidic device incorporating immunoassay, electrophoresis, and chemiluminescence detection for the determination of immunosuppressive acidic protein in serum (Reprinted with permission from Tsukagoshi et al. [13]. Copyright (2005) American Chemical Society)... Fig. 6 Illustration of a microfluidic device incorporating immunoassay, electrophoresis, and chemiluminescence detection for the determination of immunosuppressive acidic protein in serum (Reprinted with permission from Tsukagoshi et al. [13]. Copyright (2005) American Chemical Society)...
Aso H, Tamura K, Yoshie O, Nakamura T, Kikuchi S, Ishida N (1992) Impaired NK response of cancer patients to IFN-alphabut not to IL-2 correlation with serum immunosuppressive acidic protein (lAP) and role of suppressor macrophage. Microbiol Immunol 36 1087-1097... [Pg.351]

Oka M, Mitsunaga H, Hazama S, Yoshino S, Suzuki T (1993) Natural killer activity and serum immunosuppressive acidic protein levels in esophageal and gastric cancers. Surg Today 23 669-674... [Pg.353]

Cortisol, the most important g/ucocorticoid, is synthesized by the adrenal cortex, it is involved in regulating protein and carbohydrate metabolism by promoting protein degradation and the conversion of amino acids into glucose. As a result, the blood glucose level rises (see p. 152). Synthetic glucocorticoids (e.g., dexamethasone) are used in drugs due to their anti-inflammatory and immunosuppressant effects. [Pg.374]

Many antibiotics, which inhibit protein synthesis, do not bind to ribosomes but block any of a variety of vital chemical processes needed for growth. Among them are pseudomonic acid, which inhibits isoleucyl-tRNA synthetase from many gram-positive bacteria.1111/VV Rapamycin, best known as an immunosuppressant (Box 9-F), inhibits phosphoinositide-3-kinase and also phosphorylation of the cap-binding protein 4G, a component of the eukaryotic initiation factor complex (Fig. 29-11 ).ww The bacterial enzyme peptide deformylase, which is absent from the human body, has been suggested as a target for design of synthetic antibiotics. 01... [Pg.1691]

CONTENTS Preface. Bruce E. Maryanoff and Cynthia A. Maryanoft. Novel An-tipsychotics with Unique D /5-HT1A Affinity and Minimal Extrapyramidal Side Effect Liability. Allen B. Reitz and Malcolm K. Scott. Antiplatelet and Antithrombotic Agents From Viper Venom Proteins, to Peptides and Peptidomimetics. to Small Organic Molecules, Peter L. Barker and Robert R. Webb. II. Discovery and Preclinical Development of the Serotonin Reuptake Inhibitor Sertraline, Willard M. Welch. Boronic Acid Inhibitors of Dipeptidyipeptidase IV A New Class of Immunosuppressive Agents, Roger J. Snow. Index. [Pg.324]

The utility of the phenacyl group is exemplified in the C-terminal deprotection [Scheme 6.70] taken from Schmidt s synthesis of the immunosuppressive and antiviral cyclodepsipeptide Didemnin.113 Here, the phenacyl ester was reduc-tively cleaved with zinc in acetic acid. A similar transformation was used in a synthesis of the potent protein serine/threonine phosphatase inhibitor Motupor-in.lM Zinc-copper couple is an attractive alternative that can be used on a large scale [Scheme 6.71 ]J70... [Pg.402]

Extensive studies on the endocannabinoid system have revealed a number of cannabinergic proteins involved in the inactivation and biosynthesis of endocannabinoids. These include fatty acid amide hydrolase (FAAH) (Di Marzo et al. 1994 Gaetani et al. 2003 Piomelli et al. 1999), monoglyceride lipase (MAG) (Dinh et al. 2002), and the anandamide transporter (ANT) (Beltramo et al. 1997 Di Marzo et al. 1994 Fegley et al. 2004 Hillard et al. 1997). The above three proteins and the two cannabinoid receptors have received considerable attention and show great promise as potential targets for the development of novel medications for various conditions, including pain, immunosuppression, peripheral vascular disease, appetite enhancement or suppression, and motor disorders. [Pg.211]


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See also in sourсe #XX -- [ Pg.181 ]




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