Sch412348

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Products Intro: Product Name:Sch412348
CAS:377727-26-9
Purity:98.00% Package:100 mg;500 mg Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: TargetMol Chemicals Inc.
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Products Intro: Product Name:Sch412348
CAS:377727-26-9
Package:50mg;1980USD|25mg;1520USD|100mg;2500USD
Company Name: TargetMol Chemicals Inc.
Tel: +17819995354
Email: marketing@targetmol.com
Products Intro: Product Name:Sch412348
CAS:377727-26-9
Package:50mg;1980USD|25mg;1520USD|100mg;2500USD
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Products Intro: Product Name:Sch412348
CAS:377727-26-9
Purity:580RMB/1mg Package:>98%
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Products Intro: Product Name:Sch 412348
CAS:377727-26-9
Purity:98% Package:5mg;10mg;20mg;50mg;100mg;200mg

Sch412348 manufacturers

  • Sch412348
  • Sch412348 pictures
  • $1980.00 / 50mg
  • 2024-10-28
  • CAS:377727-26-9
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Sch412348 Basic information
Product Name:Sch412348
Synonyms:Sch412348;7H-Pyrazolo[4,3-e][1,2,4]triazolo[1,5-c]pyrimidin-5-amine, 7-[2-[4-(2,4-difluorophenyl)-1-piperazinyl]ethyl]-2-(2-furanyl)-;Sch412348,Sch-412348
CAS:377727-26-9
MF:C22H21F2N9O
MW:465.46
EINECS:
Product Categories:
Mol File:377727-26-9.mol
Sch412348 Structure
Sch412348 Chemical Properties
density 1.62±0.1 g/cm3(Predicted)
storage temp. Store at -20°C
solubility Soluble in DMSO
pka5.88±0.10(Predicted)
Safety Information
MSDS Information
Sch412348 Usage And Synthesis
UsesSch412348 is a potent competitive antagonist of the human adenosine A2A receptor (Ki=0.6 nM) and has >1000-fold selectivity over all other adenosine receptors.
in vivo

Oral administration of Sch412348 (0.1-1 mg/kg) to rats potentiates 3,4-dihydroxy-L-phenylalanine (L-Dopa)-induced contralateral rotations after 6-hydroxydopamine lesions in the medial forebrain bundle and potently attenuates the cataleptic effects of haloperidol. Sch412348 (1 and 3 mg/kg) dose-dependently attenuates haloperidol-induced catalepsy 1 h [F(3,20)=3.9, p<0.05] and 4 h [F(3,20)=7.5, p<0.01] after dosing. Sch412348 [F(2,51) =10.6, p<0.01] (0.1-1 mg/kg) reduces immobility time in the mouse tail suspension test (TST) at 1 mg/kg. Sch412348 (SCH 412348) significantly increases activity levels in the mouse [F(4,27)=2.9, p<0.05]. Both the 0.3 and 3 mg/kg treatment groups are significantly more active than vehicle-treated mice. The 1 mg/kg group approached significance (p=0.052)[1].

References[1] Hodgson RA, et al. Characterization of the potent and highly selective A2A receptor antagonists preladenant and SCH 412348 [7-[2-[4-2,4-difluorophenyl]-1-piperazinyl]ethyl]-2-(2-furanyl)-7H-pyrazolo[4,3-e][1,2,4]triazolo[1,5-c]pyrimidin-5-amine] in rodent models of movement disorders and depression. J Pharmacol Exp Ther. 2009 Jul;330(1):294-303. DOI:10.1124/jpet.108.149617
Sch412348 Preparation Products And Raw materials
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