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Merck
CN

5.04277

CB2 Inverse Agonist, SR 144528 - CAS 192703-06-3 - Calbiochem

别名:

CB2 Inverse Agonist, SR 144528 - CAS 192703-06-3 - Calbiochem, 5-​(4-​chloro-​3-​methylphenyl)-​1-​[(4-​methylphenyl)methyl]-​N-​[(1S,​2S,​4R)-​1,​3,​3-​trimethylbicyclo[2.2.1]hept-​2-​yl]-​1H-​pyrazole-, 5-​(4-​chloro-​3-​methylphenyl)-​1-​[(4-​methylphenyl)methyl]-​N-​[(1S,​2S,​4R)-​1,​3,​3-​trimethylbicyclo[2.2.1]hept-​2-​yl]-​1H-​pyrazole-3

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关于此项目

经验公式(希尔记法):
C29H34ClN3O
化学文摘社编号:
分子量:
476.05
UNSPSC Code:
12352200
MDL number:
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InChI

1S/C29H34ClN3O/c1-18-6-8-20(9-7-18)17-33-25(21-10-11-23(30)19(2)14-21)15-24(32-33)26(34)31-27-28(3,4)22-12-13-29(27,5)16-22/h6-11,14-15,22,27H,12-13,16-17H2,1-5H3,(H,31,34)/t22-,27-,29+/m1/s1

InChI key

SUGVYNSRNKFXQM-XRHWURSXSA-N

assay

≥98% (HPLC)

form

solid

manufacturer/tradename

Calbiochem®

storage condition

OK to freeze, protect from light

color

off-white

solubility

DMSO: 20 mg/mL

storage temp.

−20°C

General description

A selective inverse agonist for peripheral cannabinoid (CB2) receptors (Ki = 0.6 nM and 400 nM for CB2 and CB1 receptors, respectively). Has been used in studies related to control of pain initiation, suppression of inflammation, and immune activation.

Biochem/physiol Actions

Primary Target
CB₂ Receptor
Target Ki: 0.6 nM and 400 nM for CB₂ and CB₁ receptors, respectively.

Preparation Note

Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.

Other Notes

Barth, F., et al. 1999. Curr. Med. Chem.6, 745.
Iwamura, H., et al. 2001. J. Pharmacol. Exp. Ther.296, 420.

Wright, K., et al. 2008. Br. J. Pharmacol.153, 263.
Di Marzo, V. 2008. Nat. Rev. Drug Discov.7, 438.

Rinaldi-Carmona, M., et al. 1998. J. Pharmacol. Exp. Ther.284, 644.
Portier, M., et al. 1999. J. Pharmacol. Exp. Ther.288, 582.

Legal Information

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

Disclaimer

Toxicity: Standard Handling (A)

法规信息

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