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JNJ-7777120

Chemical Structure : JNJ-7777120

CAS No.: 459168-41-3

JNJ-7777120 (JNJ7777120)

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.

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

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.

Physicochemical Properties

M.Wt 277.75
Formula C14H16ClN3O
Appearance Solid
CAS No.
Storage
Solide Powder
-20°C 12 Months; 4°C 6 Months
In Solvent
-80°C 6 Months; -20°C 6 Months
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

1-[(5-chloro-1H-indol-2-yl)carbonyl]-4-methylpiperazine

References

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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