Chemical Structure : JNJ-7777120
CAS No.: 459168-41-3
Catalog No.: PC-23473Not For Human Use, Lab Use Only.
JNJ-7777120 (JNJ 7777120) is potent and selective histamine H4 receptor (H4R) antagonist with Ki of 4.5 nM (hH4R), >1000-fold selectivity over H1, H2, or H3 receptors.
Packing | Price | Stock | Quantity |
---|---|---|---|
5 mg | $58 | In stock | |
10 mg | $88 | In stock | |
25 mg | $138 | In stock | |
50 mg | $218 | In stock | |
100 mg | Get quote |
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JNJ-7777120 (JNJ 7777120) is potent and selective histamine H4 receptor (H4R) antagonist with Ki of 4.5 nM (hH4R), >1000-fold selectivity over H1, H2, or H3 receptors.
JNJ-7777120 (JNJ 7777120) is equipotent against the human, mouse, and rat receptors.
JNJ 7777120 blocks histamine-induced chemotaxis and calcium influx in mouse bone marrow-derived mast cells.
JNJ 7777120 blocks the histamine-induced migration of tracheal mast cells from the connective tissue toward the epithelium in mice.
JNJ 7777120 significantly blocks neutrophil infiltration in a mouse zymosan-induced peritonitis model.
M.Wt | 277.75 | |
Formula | C14H16ClN3O | |
Appearance | Solid | |
Storage |
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Solubility |
10 mM in DMSO |
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Chemical Name/SMILES |
1-[(5-chloro-1H-indol-2-yl)carbonyl]-4-methylpiperazine |
1. Thurmond RL, et al. J Pharmacol Exp Ther. 2004 Apr;309(1):404-13.
2. Lim HD, et al. J Pharmacol Exp Ther. 2005 Sep;314(3):1310-21.
3. Ling P, et al. Br J Pharmacol. 2004 May;142(1):161-71.
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