ZK200775 (hydrate)

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ZK200775 (hydrate) Basic information
Product Name:ZK200775 (hydrate)
Synonyms:ZK200775 (hydrate);Fanapanel hydrate;MPQX hydrate
CAS:1255517-78-2
MF:C14H17F3N3O7P
MW:427.27
EINECS:
Product Categories:
Mol File:1255517-78-2.mol
ZK200775 (hydrate) Structure
ZK200775 (hydrate) Chemical Properties
storage temp. Store at -20°C
solubility DMSO: 5 mg/mL (11.70 mM)
form Solid
color Light yellow to yellow
InChI1S/C14H15F3N3O6P.H2O/c15-14(16,17)8-5-9-11(6-10(8)19-1-3-26-4-2-19)20(7-27(23,24)25)13(22)12(21)18-9;/h5-6H,1-4,7H2,(H,18,21)(H2,23,24,25);1H2
InChIKeyRYQLMFHPDNKPKY-UHFFFAOYSA-N
SMILESO.OP(O)(=O)CN1C(=O)C(=O)Nc2cc(c(cc12)N3CCOCC3)C(F)(F)F
Safety Information
WGK Germany WGK 3
Storage Class11 - Combustible Solids
MSDS Information
ZK200775 (hydrate) Usage And Synthesis
UsesFanapanel hydrate (ZK200775 hydrate) is a highly selective AMPA/kainate antagonist with little activity against NMDA; have Ki values of 3.2 nM, 100 nM, and 8.5 μM against quisqualate, kainate, and NMDA, respectively.
Biological ActivityFanapanel hydrate (ZK200775 hydrate) is a highly selective AMPA antagonist.
in vitro

In the cortical slice preparation assay, ZK200775 (hydrate) gave Ki values of 3.2 nM, 100 nM, and 8.5 μM against quisqualate, kainate, and NMDA, respectively. In the spreading depression assay, it gave IC50 values of 200 nM , 76 nM, 13 μM, and 18 μM against quisqualate, kainate, NMDA, and glycine [1].

in vivo

ZK200775 (hydrate) elevated the threshold for AMPA- and kainate-induced clonic seizures in mice with a THRD50 (threshold dose) of 2.9 (1.7–4.6) and 1.6 (1.3–2.0) mg/kg iv, whereas the threshold for NMDA-induced seizures was elevated only in doses, THRD50 of 24.1 (21.9–26.5) mg/kg iv, which affected motor coordination in the rotating rod, ED50 14.6 (12.1–17.6) mg/kg. It in doses of 10 and 30 mg/kg iv reduced muscle tone in genetically spastic rats [1]. It (3.0 but not 1.5 or 6.0 mg/kg) significantly decreased the nicotine-induced (0.6 mg/kg) DA release in the NAcc and nicotine-stimulated LMA . It (1.5, 3.0, 6.0 mg/kg) alone influenced neither DA release nor LMA. It showed 34-fold selectivity for AMPA receptors compared to NMDA receptors and no affinity to nicotine receptors [2].

target

AMPAR

References[1] Turski L, et al. ZK200775: a phosphonate quinoxalinedione AMPA antagonist for neuroprotection in stroke and trauma. Proc Natl Acad Sci U S A. 1998 Sep 1;95(18):10960-5. DOI:10.1073/pnas.95.18.10960
[2] Kosowski AR, et al. Nicotine-induced dopamine release in the nucleus accumbens is inhibited by the novel AMPA antagonist ZK200775 and the NMDA antagonist CGP39551. Psychopharmacology (Berl). 2004 Aug;175(1):114-23. DOI:10.1007/s00213-004-1797-7
ZK200775 (hydrate) Preparation Products And Raw materials
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