(+)-ZK 216348

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(+)-ZK 216348 Basic information
Product Name:(+)-ZK 216348
Synonyms:(+)-ZK 216348;7-Benzofuranbutanamide, 2,3-dihydro-α-hydroxy-γ,γ-dimethyl-N-(4-methyl-1-oxo-1H-2,3-benzoxazin-6-yl)-α-(trifluoromethyl)-, (+)-;ZK 216348
CAS:669073-68-1
MF:C24H23F3N2O5
MW:476.45
EINECS:
Product Categories:
Mol File:669073-68-1.mol
(+)-ZK 216348 Structure
(+)-ZK 216348 Chemical Properties
density 1.39±0.1 g/cm3(Predicted)
pka10.33±0.29(Predicted)
form Solid
color White to off-white
Safety Information
MSDS Information
(+)-ZK 216348 Usage And Synthesis
UsesZK 216348 ((+)-ZK 216348) is a nonsteroidal selective glucocorticoid receptor agonist with an IC50 of 20.3 nM. ZK 216348 also binds to Progesterone and mineralocorticoid receptors with IC50s of 20.4 nM and 79.9 nM, respectively. ZK 216348 has antiinflammatory activity similar to Prednisolone and induces less transactivation-mediated side effects[1][2].
in vivo

ZK 216348 (1-30 mg/kg; subcutaneous injection; for 24 hours; NMRI mice and Wistar rats) treatment inhibits ear edema in both mice and rats. A markedly superior side-effect profile is found in ZK 216348 with regard to increases in blood glucose, spleen involution, and, to a lesser extent, skin atrophy[1].

Animal Model:NMRI mice (26-28 g) and Wistar rats (140-160 g) injection with Croton oil[1]
Dosage:1 mg/kg, 3 mg/kg, 10 mg/kg and 30 mg/kg
Administration:Subcutaneous injection; for 24 hours
Result:Inhibited ear edema in mice and rats.
References[1] Schcke H, et al. Dissociation of transactivation from transrepression by a selective glucocorticoid receptor agonist leads to separation of therapeutic effects from side effects. Proc Natl Acad Sci U S A. 2004 Jan 6;101(1):227-32. DOI:10.1073/pnas.0300372101
[2] Reuter KC, et al. Selective glucocorticoid receptor agonists for the treatment of inflammatory bowel disease: studies in mice with acute trinitrobenzene sulfonic acid colitis. J Pharmacol Exp Ther. 2012 Apr;341(1):68-80. DOI:10.1124/jpet.111.183947
(+)-ZK 216348 Preparation Products And Raw materials
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