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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T6164 |
Ciproxifan
FUB-359,环丙基[4-[3-(1H-咪唑-4-基)丙氧基]苯基]甲酮马来酸盐 |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Ciproxifan (FUB-359) 是一种高效且特异性的组胺 H3 受体拮抗剂,IC50值为 9.2 nM,可用于研究衰老性疾病和阿尔兹海默症。 | |||
T41247 |
Thioperamide maleate
MR-12842 maleate,硫丙咪胺马来酸 |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Thioperamide maleate (MR-12842 maleate) 是一种有效且选择性的 H3 受体拮抗剂 (Ki = 4.3 nM),可抑制 [3H]histamine 的合成 (Ki = 31 nM)。 | |||
T23038L |
Nα-Methylhistamine FA
Nα-Methylhistamine FA(673-50-7 Free base) |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Nα-Methylhistamine FA 是一种组胺H3受体激动剂。 | |||
T27678 |
JNJ-39220675
JNJ 39220675,JNJ39220675 |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
JNJ-39220675 (JNJ 39220675) 是一种具有选择性和脑渗透性的组胺 H3 受体拮抗剂。 | |||
T12054 |
MK-0249
MK 0249,MK0249 |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
MK-0249 是一种具有口服活性、选择性和高效性的 histamine H3 受体拮抗剂(IC50:1.7 nM),可用于研究注意力缺陷和多动障碍。 | |||
T7413 |
JNJ-5207852
|
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
JNJ-5207852 是一种新型的非咪唑组胺 H3 受体拮抗剂,其对大鼠和人 H3 受体的 pKi 值分别为 8.9 和9.24。 | |||
T8822 |
JNJ-5207852 dihydrochloride
|
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
JNJ-5207852 dihydrochloride 是一种新型的非咪唑组胺 H3 受体拮抗剂,对大鼠和人类 H3受体的 pKi 值分别为 8.9 和 9.24。 | |||
TQ0066 |
GSK189254A
GSK189254 |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
GSK189254A (GSK189254) 是一种有效的特异性组胺 H3 受体拮抗剂,对人类和大鼠H3的pKi 值分别为9.59到9.90和8.51到9.17之间。 | |||
T67828 |
Enerisant
TS-091 |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Enerisant (TS-091) 是一种具有口服活性、选择性和高效性的组胺 H3 受体拮抗剂,在小鼠体内以剂量依赖的方式调节组胺H3受体。Enerisant 可促进促认知作,可逆转东莨菪碱诱导的认知障碍。 | |||
T79500L |
KSK94 FA
KSK94 FA(2566716-07-0 Free base) |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
KSK94 FA 是一种高效的组胺 H3 受体拮抗剂,抑制 H3 受体,可用于研究神经性疼痛和肥胖症。 | |||
T7176 |
Pitolisant hydrochloride
1-[3-[3-(4-氯丙基)丙氧基]丙基]-哌啶盐酸盐,BF 2649,Ciproxidine |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Pitolisant hydrochloride (Ciproxidine) 是一种有效的、选择性的组胺 H3 受体反向激动剂,Ki 为0.16 nM。 | |||
T14087 |
ABT-239
|
TRP/TRPV Channel | Membrane transporter/Ion channel |
ABT-239是一种新型、高效、非咪唑类H3R 拮抗剂,也是一种TRPV1拮抗剂。 | |||
T70489 |
Enerisant HCl
|
P450; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Metabolism; Neuroscience |
Enerisant HCl是一种新型强效选择性组胺H3受体拮抗剂,是P-gp的底物,由细胞色素P450(CYP)和转运蛋白介导。 | |||
T16476 |
PF-03654746
|
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
PF-03654746 是组胺 H3 受体的选择性拮抗剂。 PF-03654746 提高了阿尔茨海默病的认知功效和疾病改善作用。 PF-03654746 可用于治疗过敏性鼻炎的研究。 | |||
T60636 |
Pitolisant
Tiprolisant,BF-2.649,BF-2649 |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Pitolisant (Tiprolisant) 是一种具有选择性和高效性的非咪唑类重组人组胺 H3 受体拮抗剂,可用于研究发作性睡病患者白天过度嗜睡和猝倒。 | |||
T22864 |
Immethridine dihydrobromide
|
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Immethridine dihydrobromide 是一种新型高效且具有选择性的组胺 H3 受体 (H3R) 激动剂,抑制树突状细胞的功能,可缓解实验性自身免疫性脑脊髓炎。Immethridine dihydrobromide MesV 诱导神经元和MMN去极化,可防止心肾损伤。 | |||
T79499 |
KSK68
|
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
KSK68 是一种高效的 sigma-1 和 组胺 H3 受体双重拮抗剂,具有潜在的镇痛活性,对 H3 受体、sigma-1、sigma-2 受体有很高的亲和力。KSK68 可用于研究与疼痛相关的疾病。 | |||
T0246 |
Betahistine dihydrochloride
PT-9,Betahistine 2HCl,盐酸倍他司汀 |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Betahistine dihydrochloride (Betahistine 2HCl) 是可口服的组胺 H1 受体激动剂和 H3 受体的拮抗剂,可用作血管扩张剂,用于类风湿性关节炎的研究。 | |||
T32191 |
Irdabisant
CEP-26401,CEP 26401,CEP26401 |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Irdabisant (CEP-26401) 是选择性、口服活性和血脑屏障渗透性的组胺 H3 受体 (histamine H3 receptor, H3R) 拮抗剂/逆激动剂。Irdabisant 显示人 H3R 和大鼠 H3R 的 Ki 分别为 2.0 nM 和 7.2 nM。Irdabisant 抑制 hERG 电流的活性相对较低 (IC50= 13.8 μM)。在大鼠社会认知模型中,Irdabisant 具有认知增强和唤醒作用。Irdabisant 可用于研究精神分裂症或认知障碍。 | |||
T0246L |
Betahistine mesylate
Extovyl,甲磺酸倍他司汀,Melopat,Meginalisk |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Betahistine mesylate (Extovyl) 是可口服的组胺 H1 受体激动剂和 H3 受体的拮抗剂,可用作血管扩张剂,用于类风湿性关节炎的研究。 | |||
T8514 |
LML134
LML-134 |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
LML134 (LML-134) 是一种可口服的高选择性组胺 H3 受体反向激动剂,有用于过度睡眠障碍的潜力,对 hH3R 的 cAMP 和 bdg 的Kis 分别为 0.3 和 12 nM。 | |||
T4195 |
Betahistine
PT 9 base,倍他司汀,Vasomotal,Serc base |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Betahistine (Vasomotal) 是可口服的组胺 H1 受体激动剂和 H3 受体的拮抗剂,可用作血管扩张剂,用于类风湿性关节炎的研究。 | |||
T14970 |
Cipralisant
GT-2331 |
Others | Others |
Cipralisant is a selective histamine H3 receptor antagonist in vivo, and an agonist in vitro (pKi: 9.9 for histamine H3 receptor; Ki: 0.47 nM for rat histamine H3 receptor). It has the potential for the treatment of attention-deficit hyperactivity disorde | |||
T27473 |
GSK334429
GSK-334429,GSK 334429 |
Others | Others |
GSK334429 is an antagonist of histamine H3 receptor. | |||
T23519 |
VUF 5681 dihydrobromide
|
Others | Others |
histamine H3 receptor silent antagonist | |||
T22878 |
JNJ 10181457 dihydrochloride
|
Others | Others |
JNJ 10181457 dihydrochloride is a Histamine H3 receptor antagonist. | |||
T23038 |
Nα-Methylhistamine dihydrochloride
|
Others | Others |
Nα-Methylhistamine dihydrochloride is a histamine H3 receptor agonist. | |||
T23190 |
Proxyfan oxalate
|
Others | Others |
histamine H3 receptor ligand | |||
T70111 |
GT-2394
|
Others | Others |
GT-2394 is a histamine H3 receptor agonist. | |||
T70112 |
GT-2227
|
Others | Others |
GT-2227 is a histamine H3 receptor antagonist. | |||
T29043 |
UCL-1972
UCL 1972 |
Others | Others |
UCL-1972, a Histamine H3 Receptor Antagonist, used to treat cognitive disorders. | |||
T69756 |
GT-2331
|
Others | Others |
GT-2331 is a histamine H3 receptor antagonist. | |||
T22866 |
Impentamine dihydrobromide
|
Others | Others |
Impentamine dihydrobromide is a histamine H3 receptor antagonist. | |||
T71270 |
ZEL-H16
|
Others | Others |
ZEL-H16 is an agonist of the histamine H3 receptor. | |||
T12416 |
PF-03654746 Tosylate
|
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
PF-03654746 Tosylate is selective antagonist of histamine H3 receptor with high brain penetration. | |||
T22863 |
Immepip dihydrobromide
|
Others | Others |
Immepip dihydrobromide is a histamine H3 receptor agonist. | |||
T24698 |
(R)-(-)-α-Methylhistamine dihydrochloride
HISTAMINE DIHYDROCHLORIDE R(-)-A-METHYL |
Others | Others |
R(-)-alpha-Methylhistamine 2HCl is an effective and selective agonist of the H3 histamine receptor. | |||
T26480 |
A331440
A-331440,A331440 free base,A 331440 |
Others | Others |
A331440 is an modulator of L-histidine and histamine H3 receptor. | |||
T10911 |
H3 receptor antagonist 1
|
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
H3 receptor antagonist 1 is used in the study of neurological diseases, histamine H3 receptor antagonist. | |||
T26643 |
Aplysamine-1
Aplysamine |
Others | Others |
Aplysamine-1 is an antagonist of histamine H3 receptor. | |||
T10499 |
H3 receptor-MO-1
|
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
H3 receptor-MO-1 是一种有效的组胺 H3 受体 (histamine H3 receptor) 调节剂,可用于研究神经分裂和认知障碍。 | |||
T27022 |
Cipralisant maleate
GT-2331,Cipralisant maleate. trade name Perceptin,GT 2331,GT2331 |
Others | Others |
Cipralisant maleate is a potent, selective Histamine H3 receptor antagonist. | |||
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). | |||
T71605 |
APD-916 dicitrate
|
Others | Others |
APD-916 dicitrate is a potent and selective inverse agonist of the histamine H3 receptor. | |||
T19628 |
GSK 189254 HCl
GSK-189254A,GSK 189254A,GSK 189254 hydrochloride,GSK189254A |
Others | Others |
GSK 189254A is a histamine H3 receptor antagonist for the treatment of narcolepsy. Histamine H3 receptor antagonists have been shown to increase the release of neurotransmitters in the brain and to enhance cognition in vivo. The compound may also be usefu | |||
T68521 |
MK-3134
|
Others | Others |
MK-3134 is a novel histamine H3 receptor inverse agonist. | |||
T69654 |
VUF16839
|
Others | Others |
VUF16839 is a high-affinity non-imidazole histamine H3 receptor agonist. | |||
T12491 |
Pitolisant oxalate
Tiprolisant oxalate |
Others | Others |
Pitolisant oxalate is a potent and selective inverse agonist of nonimidazole at the recombinant human histamine H3 receptor with Ki of 0.16 nM. | |||
T19762 |
Clobenpropit 2HBr
VUF-9153,VUF 9153,Clobenpropit Dihydrobromide,VUF9153 |
Others | Others |
Clobenpropit 2HBr is a histamine H3 receptor antagonist. It has neuroprotective effects via stimulation of GABA release in the brain. | |||
T15590 |
Iodophenpropit dihydrobromide
|
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Iodophenpropit dihydrobromide is an effective and selective antagonist of the histamine H3 receptor. The binding of [125I]Iodophenpropit is readily reversible, selective, and of high affinity (KD: 0.32 nM). |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T20712 |
Conessine
Conessinum,Wrightine,地麻素,Roquessine,Neriine,Konessin |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Conessine (Conessinum) 是一种具有抗疟活性的甾体生物碱,是高效选择性H3 受体拮抗剂,对于人、狗、豚鼠和大鼠 H3受体的Ki 分别为 5.4、6.0、5.7 和 25 nM。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TMIJ-0338 |
Pitolisant-d6 HCl
|
||
Pitolisant-d6 HCl 是 Pitolisant HCl 的氘代化合物。Pitolisant HCl 的 CAS 号为 903576-44-3。Pitolisant hydrochloride 是一种有效的、选择性的组胺 H3 受体反向激动剂,Ki为0.16 nM。 |