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Cat. No. Product Name Information
PC-63413

JNJ-28610244

Histamine H4 agonist

JNJ-28610244 is a potent, selective agonist of histamine H4 receptor (H4R) with pKi of 7.3 and pEC50 of 7.0 respectively,
PC-63410

JNJ-28307474

Histamine H4 antagonist

JNJ-28307474 is a potent, selective antagonist of the histamine H4 receptor (H4R), inhibits LPS-induced TNF production.
PC-63399

Toreforant

Histamine H4 antagonist

Toreforant (JNJ-38518168) is a potent, selective histamine H4 receptor (H4R) antagonist with Ki of 8.4 nM, shows excellent selectivity over other receptors including the other histamine receptors.
PC-63035

MK-0249

Histamine H3 antagonist

MK-0249 is a potent, selective and orally active histamine H3 receptor antagonist, with an IC50 of 1.7 nM for human H3.
PC-63034

PF-03654746

Histamine H3 antagonist

PF-03654746 (PF-3654746) is a potent, selective, orally bioactive antagonist of H3 receptor with Ki of 2.3 nM.
PC-63033

PF-03654764

Histamine H3 antagonist

PF-03654764 (PF-3654764) is a potent, selective, orally bioactive antagonist of H3 receptor with Ki of 1.4 nM.
PC-63032

ABT-288

Histamine H3 antagonist

ABT-288 is a potent, selective and competitive antagonist of H3 receptor with Ki of 1.9/8.2 nM for human/rat H3 respectively.
PC-61996

LY2624803

H1R/5-HT2A modulator

LY2624803 is a novel potent histamine H1 and 5-HT2A receptor modulator in the pipeline for treating insomnia.
PC-61663

JNJ-10181457 dihydrochloride

Histamine H3 antagonist

JNJ-10181457 dihydrochloride is a neutral, potent and selective, brain penetrant H3 antagonist with pKi of 8.93, pA2 of 9.22 for hH3.
PC-61662

JNJ-10181457

Histamine H3 antagonist

JNJ-10181457 is a neutral, potent and selective, brain penetrant H3 antagonist with pKi of 8.93, pA2 of 9.22 for hH3.
PC-61661

JNJ-39220675

Histamine H3 antagonist

JNJ-39220675 is potent and selective, brain penetrant H3 antagonist with Ki of 1.4 nM, pA2 of 9.42 for hH3.
PC-61616

Irdabisant hydrochloride

H3 receptor antagonist

Irdabisant (CEP-26401) hydrochloride is a potent, selective, orally active histamine H3 receptor antagonist with Ki of 2 nM and 7 nM for human and rat H3Rs, respectivity.

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