Effective <i>in vitro</i> evaluation of the risk of histamine release related to valemetostat tosylate using MRGPRX2-expressing cells
Author:
Affiliation:
1. Medicinal Safety Research Laboratories, Daiichi Sankyo Co., Ltd.
2. Medicinal Safety, Precision Medicine, Daiichi Sankyo, Inc., USA
3. Translational Research Department, Daiichi Sankyo RD Novare Co., Ltd.
Publisher
Japanese Society of Toxicology
Link
https://www.jstage.jst.go.jp/article/jts/49/4/49_163/_pdf
Reference37 articles.
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2. Ennis, M., Lorenz, W., Kapp, B., Lüben, L. and Schmal, A. (1985): Comparison of the histamine-releasing activity of cremophor E1 and some of its derivatives in two experimental models: the in vivo anaesthetized dog and in vitro rat peritoneal mast cells. Agents Actions, 16, 265-268.
3. Ferry, X., Brehin, S., Kamel, R. and Landry, Y. (2002): G protein-dependent activation of mast cell by peptides and basic secretagogues. Peptides, 23, 1507-1515.
4. Foer, D., Wien, M., Karlson, E.W., Song, W., Boyce, J.A. and Brennan, P.J. (2023): Patient characteristics associated with reactions to Mrgprx2-activating drugs in an electronic health record-linked biobank. J. Allergy Clin. Immunol. Pract., 11, 492499.e2.
5. Furuhata, K., Hayakawa, H., Soumi, K., Arai, H., Watanabe, Y. and Narita, H. (1998): Histamine-releasing properties of T-3762, a novel fluoroquinolone antimicrobial agent in intravenous use. I. Effects of doses and infusion rate on blood pressure, heart rate and plasma histamine concentration. Biol. Pharm. Bull., 21, 456-460.
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