6
2
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T12630 |
(R)-(-)-α-Methylhistamine dihydrobromide
|
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
(R)-(-)-α-Methylhistamine dihydrobromide is a potent and selective agonist of H3 histamine receptor( Kd of 50.3 nM). | |||
T24698 |
(R)-(-)-α-Methylhistamine dihydrochloride
HISTAMINE DIHYDROCHLORIDE R(-)-A-METHYL |
||
R(-)-alpha-Methylhistamine 2HCl is an effective and selective agonist of the H3 histamine receptor. | |||
T23038 |
Nα-Methylhistamine dihydrochloride
|
Others | Others |
Nα-Methylhistamine dihydrochloride is a histamine H3 receptor agonist. | |||
T37279 |
1-Methyl-4-imidazoleacetic Acid (hydrochloride)
|
||
1-Methyl-4-imidazoleacetic acid (MIMA) is a stable metabolite of histamine that is produced by the oxidation of the primary metabolite, N-methylhistamine. Urinary levels of MIMA are commonly measured to evaluate histamine secretion, particularly in the context of systemic mastocytosis. | |||
T80645 | 4-Methylhistamine | Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
4-Methylhistamine 作为一种有效的组胺 4 受体 (H4R) 激动剂,显示出在研究免疫相关疾病,如癌症和自身免疫性疾病方面的应用潜力。 | |||
T28275 |
OUP-186
OUP186 |
||
OUP-186 is a high affinity and human/rat species-selective antagonist of histamine H3 receptor. OUP-186 suppressed the proliferation of breast cancer cells. The IC50 values at 48 hours for OUP-186 was approximately 50 μM. OUP-186 potently induced cell dea |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T4940 |
3-Methylhistamine dihydrochloride
|
Others; Endogenous Metabolite | Metabolism; Others |
3-Methylhistamine dihydrochloride 是一种组胺的降解产物,与免疫反应有关,并在接种过疫苗的小鼠中表现出上调作用。 | |||
T8790 |
1-Methylhistamine dihydrochloride
|
Endogenous Metabolite | Metabolism |
1-Methylhistamine dihydrochloride 是组胺代谢物。 |