✦ LIBER ✦

Pharmacological properties of the calcimimetic compound NPS R-568 in vitro and in vivo

✍ Scribed by Y. Murakami; Y. Furuya; M. Wada; T. Sakai; N. Nagano

Publisher: Springer
Year: 2000
Tongue: English
Weight: 165 KB
Volume: 4
Category: Article
ISSN: 1342-1751
DOI: 10.1007/s101570070004

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Acute cardiovascular effects of the calc

Acute cardiovascular effects of the calcimimetic R-568 and its enantiomer S-568 in rats

✍ Kumiko Nakagawa; Niru Parekh; Nadezda Koleganova; Eberhard Ritz; Franz Schaefer; 📂 Article 📅 2009 🏛 Springer 🌐 English ⚖ 173 KB

Residue 826 in the Calcium-Sensing Recep

Residue 826 in the Calcium-Sensing Receptor Is Implicated in the Response to Calcium and to R-568 Calcimimetic Compound

✍ Daniel Álvarez-Hernández; Ignacio González-Suárez; José L. Fernández-Martín; Isa 📂 Article 📅 2010 🏛 Springer 🌐 English ⚖ 293 KB

Pharmacological evidence in vitro and in

Pharmacological evidence in vitro and in vivo for functional beta1receptors in the cerebral circulation

✍ R. Sercombe; P. Aubineau; L. Edvinsson; H. Mamo; Ch. Owman; J. Seylaz 📂 Article 📅 1977 🏛 Springer 🌐 English ⚖ 314 KB

Time course of the pharmacological respo

Time course of the pharmacological response to beta-lactam antibiotics in vitro and in vivo

✍ Gerber, A. U. ;Feller, C. ;Brugger, H. P. 📂 Article 📅 1984 🏛 Springer-Verlag ⚖ 438 KB

The in vitro and in vivo pharmacology of

The in vitro and in vivo pharmacology of antisense oligonucleotides targeted to murine Stat6

✍ H. Danahay; S. Hill; F. Natt; C.E. Owen 📂 Article 📅 2000 🏛 SP Birkhäuser Verlag Basel 🌐 English ⚖ 209 KB

Preparation and properties in vitro and

Preparation and properties in vitro and in vivo of antitubercular pyrroles

✍ Michael J. Hearn; Michaeline F. Chen; Marianne S. Terrot; Eleanor R. Webster; Mi 📂 Article 📅 2010 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 123 KB

## Abstract magnified image 1‐Acylamino‐2,5‐dimethylpyrroles were prepared in the exploration of heterocyclic structures useful for their antitubercular activity. The pyrroles were conveniently formed from the reaction of aromatic acid hydrazides with hexane‐2,5‐dione in water or ethanol, without r