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SCH-58261

SKU: orb1226068

Description

SCH-58261 is a potent and selective, competitive A2A adenosine receptor antagonist with Ki of 2.3 nM and 2.0 nM in rat and bovine brain, respectively; displays 323-, 53- and 100-fold selectivity over A1, A2B and A3 receptors, respectively; reverses reperfusion injury (IR) increased hippocampal Glu, GABA, glycine and aspartate, MPO, TNF-α, nitric oxide, and PGE in Male Wistar rats.

Images & Validation

Key Properties

CAS Number160098-96-4
MW345.358
Purity>98% (HPLC)
FormulaC18H15N7O
SMILESNC1=NC(N(CCC2=CC=CC=C2)N=C3)=C3C4=NC(C5=CC=CO5)=NN14
TargetAdenosine Receptor
SolubilityDMSO: ≥ 34 mg/mL

Bioactivity

In Vivo
Animal model: 4 6 weeks old athymic nude mice (NCI) with PC9 cells xenograft. Dosage: 2 mg/kg. Administration: Intraperitoneal injection; daily; for 20 days. Result: Decreased tumor growth.
In Vitro
Cell Viability Assay Cell line: H1975 cells. Concentration: 10 nM-10 μM. Incubation time: 7 days. Result: Produced a concentration-dependent decrease in H1975 cell growth. Cell Proliferation Assay Cell line: CAF cells. Concentration: 25 μM. Incubation time: 72 hours. Result: Inhibit the growth of CAF1 and CAF2 cells.

Storage & Handling

StorageStorage temperature: -20°C. Stability: ≥ 2 years
Expiration Date12 months from date of receipt.
DisclaimerFor research use only

Alternative Names

SCH 58261 | SCH58261

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    160098-96-4

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    2 mg, 5 mg, 10 mg, 25 mg, 50 mg, 1 mg, 100 mg, 1 ml x 10 mM (in DMSO)
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SCH-58261 (orb1226068)

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Available Sizes

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200 mg
500 mg
2 mg
$ 90.00
5 mg
$ 130.00
10 mg
$ 210.00
25 mg
$ 390.00
50 mg
$ 720.00
100 mg
$ 1,040.00