312
11
1
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15
Cat. No. | Product Name | ||
---|---|---|---|
L3300 | 组胺&褪黑色素化合物库 | 153 compounds | |
153 种生物活性小分子化合物,用于高通量、高内涵筛选; |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T38634 |
Histamine H4 receptor antagonist-1
Histamine H4 receptor antagonist-1 |
Others | Others |
Histamine H4 receptor antagonist-1 is a potent antagonist of the histamine H4 receptor. | |||
T22842 |
HTMT dimaleate
HTMT马来酸氢盐,Histamine Trifluoromethyl Toluidide Dimaleate |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
HTMT dimaleate (Histamine Trifluoromethyl Toluidide Dimaleate) 是一种 H1 和 H2 受体激动剂。在自然抑制细胞中,它在 H2 受体介导的效应中的活性是组胺的 4 x 104倍。 | |||
T9717 |
Chlorcyclizine
|
HCV Protease; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Microbiology/Virology; Neuroscience; Proteases/Proteasome |
Chlorcyclizine 是一种有效的组胺 H1拮抗剂。 | |||
T9353 |
OXOMEMAZINE
|
AChR; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Oxomemazine 是毒菌碱 M1 受体的选择性拮抗剂,具有明显的抗毒蕈碱活性。它是基于吩噻嗪的组胺 H1 受体阻滞剂,是抗组胺和抗胆碱能试剂,可用于咳嗽相关研究。 | |||
T10680 |
Carebastine
|
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Carebastine 是 Ebastine 的活性代谢产物,可抑制巨噬细胞移动抑制因子的表达。它是组胺 H1 受体拮抗剂,可抑制 VEGF 诱导的 HUVEC 和 HPAEC 增殖,迁移和血管生成。 | |||
T7477 |
Antazoline
|
Others | Others |
Antazoline 具有抗组胺和抗胆碱能作用。它用于治疗各种心律失常。 | |||
T22724 |
Dimaprit dihydrochloride
|
NOS; NO Synthase; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Dimaprit dihydrochloride 是组胺H2受体的一种选择性激动剂,可刺激胃酸的分泌。它还抑制nNOS,IC50值为 49 μM。 | |||
T8439 |
Clobenpropit dihydrobromide
|
Apoptosis; Histamine Receptor | Apoptosis; GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Clobenpropit dihydrobromide 是一种组胺H3R 拮抗剂/反向激动剂。它与 5-HT3 受体和 α2A/α2C 肾上腺素受体结合,对组胺H4受体起部分激动剂的作用,还能促进凋亡。 | |||
T5829 |
H4 Receptor antagonist 1
|
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
H4 Receptor antagonist 1 是选择性组胺 H4受体反向激动剂,其IC50值为19 nM。 | |||
T19680 |
Zotepine
|
Dopamine Receptor; 5-HT Receptor; Adrenergic Receptor; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Zotepine 是一种抗精神病剂,是有效的5-HT2A、5-HT2C、组胺H1、α1-肾上腺素能和多巴胺D2受体拮抗剂,Kd 值分别为 2.6、3.2、3.3、7.3 和 8 nM。它在体内表现出抗抑郁和抗焦虑作用。 | |||
T36949 |
Niaprazine
|
5-HT Receptor; Adrenergic Receptor; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Niaprazine 是有效的组胺 H1 受体拮抗剂,具有抗组胺和抗血清素活性。Niaprazine 在睡眠障碍方面有研究的价值。 | |||
T4563 |
Thonzylamine
neohetramine,松齐拉敏 |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Thonzylamine (neohetramine) 是可口服的H1组胺受体拮抗剂,具有抗组胺和抗过敏特性,可用于鼻充血、过敏性结膜炎和其他过敏性疾病的研究。 | |||
T4250 |
Bilastine
比拉斯汀,Bilaxten |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Bilastine (Bilaxten) 是新型抗组胺药,对H1组胺受体具有高度选择性,起效快,作用时间长的特性,可用于变应性鼻结膜炎和荨麻疹。 | |||
T11723L |
JNJ-39758979
|
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
JNJ-39758979是一种选择性的、高亲和力的、可口服的组胺 H4 受体拮抗剂,具有抗炎和止痒作用,对人、小鼠和猴子的组胺 H4 受体的 Ki 值分别为 12.5、5.3 和 25 nM。它对组胺诱导的 cAMP 抑制作用具有拮抗作用,pA2 为 7.9。 | |||
T12489 |
Pimethixene
Calmixen,匹美噻吨,Pimetixene |
Dopamine Receptor; 5-HT Receptor; AChR; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Pimethixene (Calmixen) 是抗组胺和抗血清素剂,用作抗偏头疼剂。它是高效多靶点拮抗剂。 | |||
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。 | |||
T7564 |
Chlorphenoxamine
Contristamine,氯苯沙明 |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Chlorphenoxamine (Contristamine) 是一种抗组胺药和抗胆碱能药,用作止痒药和抗帕金森病药。 | |||
T0081 |
Lafutidine
拉呋替丁,FRG-8813 |
5-HT Receptor; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Lafutidine (FRG-8813) 是一种组胺受体 H2RA 拮抗剂,可抑制胃酸分泌,具有胃粘膜保护作用,可用于研究胃食管反流疾病。 | |||
T7085 |
Mebhydrolin
Mebhydroline,美海屈林 |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Mebhydrolin (Mebhydroline) 是组胺H1受体的一种特异性拮抗剂。 | |||
T1278 |
Astemizole
Laridal,Histaminos,Paralergin,阿司咪唑 |
Potassium Channel; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Membrane transporter/Ion channel; Neuroscience |
Astemizole (Laridal) 是一种长效、非镇静抗组胺药,用于治疗季节性过敏性鼻炎、哮喘、过敏性结膜炎和慢性特发性荨麻疹。它是组胺 H1 受体的拮抗剂,IC50值为 4 nM,还阻断 hERG K+通道,IC50值为 0.9 nM,具有抗胆碱能和止痒作用。 | |||
T3963 |
VUF10460
|
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
VUF10460 是一种非咪唑组胺 H4 受体激动剂,与大鼠H4受体结合的pKi 值为7.46。 | |||
T4099 |
S 38093
S38093,S-38093 |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
S 38093 是一种可透过大脑的,可口服的组胺 H3 受体拮抗剂,对大小鼠和人的 H3 受体具有不同的亲和力,Ki 值分别为 8.8、1.44 和 1.2 µM。 | |||
T4196 |
Betahistine EP Impurity C
NSC19005 |
Others; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience; Others |
Betahistine EP Impurity C (NSC19005) 是 Betahistine 的杂质。 Betahistine 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。 | |||
T4566 |
Lodoxamide
Lodoxamidum,洛草氨酸 |
GPR; Histamine Receptor | Endocrinology/Hormones; GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Lodoxamide (Lodoxamidum) 是一种抗过敏药物,作为肥大细胞稳定剂,对治疗哮喘和过敏性结膜炎有效。 | |||
T16759 |
Ritanserin
利坦丝林,R 55667 |
Dopamine Receptor; 5-HT Receptor; Adrenergic Receptor; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Ritanserin (R 55667) 是一种长效、高效、相对选择性、可口服的5-HT2受体拮抗剂,IC50值为 0.9 nM。 | |||
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。 | |||
T22713 |
Decloxizine
|
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Decloxizine 是一种组胺受体H1拮抗剂。 | |||
T25180 |
Bromodiphenhydramine hydrochloride
|
Others | Others |
Bromodiphenhydramine hydrochloride 是一种控制皮肤的新型抗组胺药。 | |||
T0074 |
Chlorprothixene
Truxal,Clorprotixeno,Taractan,氯普噻吨 |
Dopamine Receptor; 5-HT Receptor; Antibacterial; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Microbiology/Virology; Neuroscience |
Chlorprothixene (Truxal) 是一种多巴胺和组胺受体拮抗剂,具有抗精神病作用。它高亲和力地结合人 D1,D2,D3,D5,H1 受体,Ki 分别为 18 nM,2.96 nM,4.56 nM,9 nM 和 3.75 nM。 | |||
T16280 |
Nedocromil
FPL 59002,尼多克罗 |
Leukotriene Receptor; Prostaglandin Receptor; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Nedocromil (FPL 59002) 对多种介质的作用或形成有抑制作用,包括组胺,前列腺素 D2和白三烯 C4。 | |||
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。 | |||
T4551 |
Acrivastine
Acrivastin,阿伐斯汀,BW825C,Semprex |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Acrivastine (Acrivastin) 是一种短效组胺 1 受体拮抗剂,可用于研究过敏性鼻炎。 | |||
T22746 |
Tesmilifene fumarate
DPPE fumarate |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Tesmilifene fumarate (DPPE fumarate) 是一种 H1C 受体拮抗剂,可增强化疗的细胞毒性且保护正常细胞。 | |||
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。 | |||
T1469 |
Levocetirizine
Levocetirizine HCl,左西替利嗪 |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Levocetirizine 是一种组胺 H1 受体拮抗剂,可用于研究变应性鼻炎和慢性特发性荨麻疹。它是一种抗组胺剂,是 Cetirizine 的 R 对映体,对组胺 H1 受体的亲和力高于 (S)-Cetirizine。 | |||
T2004 |
Ciproxifan maleate
FUB 359 maleate,FUB 359 |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Ciproxifan maleate (FUB 359) 是一种选择性的,可口服和竞争性的组胺H3受体拮抗剂,IC50值为 9.2 nM。它对其他受体亚型的表观亲和力低,可用于研究衰老性疾病和阿尔兹海默症。 | |||
T1822 |
Clemizole
克立咪唑,吡咯咪唑 |
HCV Protease; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Microbiology/Virology; Neuroscience; Proteases/Proteasome |
Clemizole 是一种 H1 组胺受体拮抗剂,可抑制 NS4B 的 RNA 结合和丙型肝炎病毒复制。它也是TRP5通道抑制剂。 | |||
T1336 |
Benztropine mesylate
Benzotropine mesylate,苯扎托品,Benzatropine mesylate,Benztropine methanesulfonate,甲磺酸苯扎托品 |
Dopamine Receptor; AChR; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Benztropine mesylate (Benztropine methanesulfonate) 是一种可口服的中枢性抗胆碱能剂,用于帕金森氏病的研究。它是抗组胺剂,抑制多巴胺的吸收。它也是人 D2多巴胺受体的变构拮抗剂,具有抗癌症干细胞的作用。 | |||
T6562 |
Latrepirdine dihydrochloride
Dimebolin dihydrochloride,Latrepirdine,Latrepirdine 2HCl,Dimebolin |
Beta Amyloid; 5-HT Receptor; Adrenergic Receptor; GluR; Autophagy; Histamine Receptor | Autophagy; GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Latrepirdine dihydrochloride (Dimebolin dihydrochloride) 是一种具有口服活性和神经活性的多种药物靶点的拮抗剂,可刺激淀粉样前体蛋白分解代谢和 β-淀粉样蛋白分泌。 | |||
T15195 |
Ebrotidine
FI3542,乙溴替丁 |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Ebrotidine (FI3542) 是有效的、竞争性的H2受体的拮抗剂,Ki 为127.5nM。Ebrotidine 具有抗分泌活性,可用于胃保护。 | |||
T2533 |
Alcaftadine
R89674,Lastacaft,阿卡他定 |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Alcaftadine (Lastacaft) 是一种 H1 组胺受体拮抗剂,用于预防与过敏性结膜炎相关的瘙痒。它是一种广谱抗组胺剂,对组胺H1和H2受体具有高亲和力,对H4受体的亲和力较低,还具有调节免疫细胞募集和肥大细胞稳定的作用。 | |||
T1090 |
Perphenazine
Perphenazin,Etaperazine,Trilafon,奋乃静 |
CaMK; Dopamine Receptor; 5-HT Receptor; Adrenergic Receptor; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Perphenazine (Trilafon) 是吩噻嗪衍生物和多巴胺拮抗剂,具有止吐和抗精神病特性。它能够抑制5-HT2A 受体,α1A 肾上腺素能受体,多巴胺D2、D3、D2L 受体,以及组胺H1受体,对应的Ki 值分别为5.6、10、0.765、0.13、3.4 和 8 nM。 | |||
T1627 |
Famotidine
MK-208,法莫替丁 |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Famotidine (MK-208) 是一种具有抗酸活性的丙脒和组胺 H2 受体拮抗剂。 | |||
T0137 |
Mirtazapine
米氮平,6-Azamianserin,Org3770 |
Dopamine Receptor; 5-HT Receptor; Opioid Receptor; Adrenergic Receptor; Histamine Receptor | Endocrinology/Hormones; GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Mirtazapine (6-Azamianserin) 是一种有效的具有口服活性的去甲肾上腺素能和特异性血清素能抗抑郁剂 (NaSSA)。它也是一种5-HT2、5-HT3、组胺 H1 受体和 α2-肾上腺素受体拮抗剂,pKi 值分别为 8.05、8.1、9.3 和 6.95。 | |||
T7524 |
Metiamide
甲硫米特,SK&F 92058 |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Metiamide (SK&F 92058) 是一种组胺H2受体拮抗剂。 | |||
T0865 |
Ranitidine Hydrochloride
AH19065,盐酸雷尼替丁 |
P450; Antibacterial; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Metabolism; Microbiology/Virology; Neuroscience |
Ranitidine Hydrochloride (AH19065) 是一种具有口服活性的组胺 H2 受体选择性拮抗剂,IC50为 3.3 μM。它还是一种CYP2C19和CYP2C9的弱抑制剂,可抑制胃液分泌。 | |||
T0445L |
Promethazine hydrochloride
盐酸异丙嗪,Promethazine HCl,Phenergan |
Adrenergic Receptor; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Promethazine hydrochloride (Promethazine HCl) 是抗组胺药物,是 H1 受体的强拮抗剂和 mACh 受体的中度拮抗剂,对 5-HT2A、5-HT2C、D2 和 α1-肾上腺素能受体具有中等亲和力。 | |||
T0298 |
Dimenhydrinate
茶苯海明,Dramamine,Chloranautine,乘晕宁,Vomex A |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Dimenhydrinate (Vomex A) 是一种乙醇胺和组胺拮抗剂,具有抗过敏活性,可作为抗催吐剂。 | |||
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。 | |||
T0053 |
Hydroxyzine Pamoate
Hydroxyzine embonate,双羟萘酸羟嗪,Bobsule,Equipose |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Hydroxyzine Pamoate (Bobsule) 是一种组胺 H1 受体拮抗剂,可有效治疗慢性荨麻疹、皮炎和组胺介导的瘙痒。它可作为止吐剂和镇静剂,缓解焦虑和紧张。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T0965 |
Histamine
Ergamine,组胺 |
5-HT Receptor; Endogenous Metabolite; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Metabolism; Neuroscience |
Histamine (Ergamine) 是通过组胺的酶促脱羧衍生的胺。它是一种强大的胃分泌兴奋剂、支气管平滑肌的收缩剂、血管扩张剂以及中枢作用的神经递质。 | |||
T6535 |
Histamine Phosphate
组胺磷酸盐,Histamine diphosphate,二磷酸组胺,Histamine acid phosphate |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Histamine Phosphate (Histamine acid phosphate) 是组胺受体的强激活剂和血管扩张神经剂,可激活一氧化氮合成酶。 | |||
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。 | |||
T20884 |
Hydroxyzine
Hydroxyzine free base,羟嗪 |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Hydroxyzine (Hydroxyzine free base) 是一种组胺 H1 受体拮抗剂,可有效治疗慢性荨麻疹、皮炎和组胺介导的瘙痒。它可作为止吐剂和镇静剂,缓解焦虑和紧张。 | |||
T0330 |
Diphenhydramine hydrochloride
盐酸苯海拉明,Diphenhydramine HCl,DPH |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Diphenhydramine hydrochloride (DPH) 是一种组胺 H1 拮抗剂,用作镇咳药和止吐药。它还用于治疗瘙痒和皮肤病、过敏反应、抗帕金森病、催眠药和普通感冒制剂的成分。 | |||
T2520 |
Desloratadine
Sch34117,地氯雷他定,NSC 675447 |
Endogenous Metabolite; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Metabolism; Neuroscience |
Desloratadine (Sch34117) 是非镇静H1抗组胺药 Loratadine 的主要口服代谢物,可减少对支气管平滑肌、毛细血管和胃肠道平滑肌中 H1 受体的典型组胺能作用,包括血管舒张、支气管收缩、血管通透性增加、疼痛、瘙痒和胃肠道平滑肌的痉挛性收缩。它是一种选择性H1受体拮抗剂,具有抗过敏和抗炎活性。 | |||
TN1008 |
Psoralenoside
|
CaMK; Calcium Channel; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism; Neuroscience |
Psoralenoside 是源于补骨脂中的苯并呋喃苷,具有抗肿瘤、抗菌、促进成骨细胞增殖和雌激素样活性。它对组胺 H1、钙调素和电压门控 l 型钙通道具有较高的亲和力。 | |||
T2848 |
Osthole
Osthol,NSC 31868,蛇床子素,Ostol |
Apoptosis; HBV; Parasite; Histamine Receptor | Apoptosis; GPCR/G Protein; Immunology/Inflammation; Microbiology/Virology; Neuroscience |
Osthole (Osthol) 是一种天然抗组胺药替代试剂,可刺激成骨细胞增殖和分化。它可抑制组胺 H1受体活性,还可抑制细胞培养物中 HBV 的分泌。 | |||
T19443 |
N-Acetylhistamine
N-Omega-acetylhistamine,N-乙酰组胺 |
Endogenous Metabolite; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Metabolism; Neuroscience |
N-Acetylhistamine (N-Omega-acetylhistamine) 是组胺的代谢物。 | |||
T0783 |
Mianserin hydrochloride
Mianserin HCl,Org GB 94,盐酸米安色林,ORG GB-94 HCl |
Dopamine Receptor; 5-HT Receptor; Opioid Receptor; Adrenergic Receptor; Histamine Receptor | Endocrinology/Hormones; GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Mianserin hydrochloride (Org GB 94) 是一种有抗抑郁活性的 H1 受体反向激动剂。 | |||
T20597 |
Alginic acid
Protanal LF,褐藻酸,Snow acid algin G,Kelacid,Sazzio,Norgine |
Apoptosis; Autophagy; Histamine Receptor | Apoptosis; Autophagy; GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Alginic acid (Snow acid algin G) 是一种从褐海藻中提取的天然多糖,具有抗过敏和抗炎活性。 Alginic acid 抑制组胺释放,可用于食品工业。 |
Cat. No. | Product Name | Species | Expression System |
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TMPH-01469 |
HRH1 Protein, Human, Recombinant (His)
Histamine H1 receptor,HRH1 |
Human | E. coli |
HRH1 Protein, Human, Recombinant (His) is expressed in E. coli. | |||
TMPH-03107 |
Complement C5a Protein, Pig, Recombinant (His)
Complement C5a anaphylatoxin,C5 |
Sus scrofa (Pig) | P. pastoris (Yeast) |
Derived from proteolytic degradation of complement C5, C5a anaphylatoxin is a mediator of local inflammatory process. Binding to the receptor C5AR1 induces a variety of responses including intracellular calcium release, contraction of smooth muscle, increased vascular permeability, and histamine release from mast cells and basophilic leukocytes. C5a is also a potent chemokine which stimulates the locomotion of polymorphonuclear leukocytes and directs their migration toward sites of inflammation.... | |||
TMPH-01640 |
MRGPRX2 Protein, Human, Recombinant (His)
Mas-related G-protein coupled receptor member X2,MR... |
Human | E. coli |
Mast cell-specific receptor for basic secretagogues, i.e. cationic amphiphilic drugs, as well as endo- or exogenous peptides, consisting of a basic head group and a hydrophobic core. Recognizes and binds small molecules containing a cyclized tetrahydroisoquinoline (THIQ), such as non-steroidal neuromuscular blocking drugs (NMBDs), including tubocurarine and atracurium. In response to these compounds, mediates pseudo-allergic reactions characterized by histamine release, inflammation and airway c... | |||
TMPJ-00028 |
CCL2 Protein, Mouse, Recombinant
Ccl2,Je,Mcp1,C-C motif chemokine 2,Platelet-derived growth f... |
Mouse | E. coli |
C-C motif chemokine 2 (CCL2) is a member of the C-C or β chemokine family. Mouse CCL2 shares 82% amino acid (aa) identity with rat CCL2 over the entire sequence, and 58%, 56%, 55%, 53% and 53% aa identity with human, equine, porcine, bovine and canine CCL2, respectively. Fibroblasts, glioma cells, smooth muscle cells, endothelial cells, lymphocytes and mononuclear phagocytes can produce CCL2 either constitutively or upon mitogenic stimulation, but monocytes and macrophages appear to be the major... |
Cat. No. | Product Name | Target | Signaling Pathways |
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T10241 |
Acrivastine D7
BW825C D7 |
Others | Others |
Acrivastine D7 is a deuterium labeled Acrivastine. Acrivastine is a short acting antagonist of histamine 1 receptor. | |||
T11592 |
Hydroxyzine D8
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Others | Others |
Hydroxyzine D8, a deuterium-labeled version of Hydroxyzine, acts as a histamine H1-receptor antagonist. | |||
T19234 |
Cetirizine D8 dihydrochloride
盐酸西替利嗪 D8 |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Cetirizine D8 dihydrochloride is a deuterium-labeled Cetirizine. Cetirizine is a second-generation antihistamine and a long-acting histamine H1-receptor antagonist. | |||
T11591 |
Hydroxyzine D4
羟嗪 D4 |
Others | Others |
Hydroxyzine D4 is a deuterium-labeled variation of Hydroxyzine, a chemical compound known for its anticholinergic, anxiolytic, and analgesic properties. It is classified as a heterocyclic histamine H1-receptor antagonist. | |||
T19233 |
Cetirizine D4 dihydrochloride
Cetirizine D4 dihydrochloride (1219803-84-5 free base) |
Others | Others |
Cetirizine D4 dihydrochloride is a deuterium-labeled Cetirizine. Cetirizine is a second-generation antihistamine and a long-acting histamine H1-receptor antagonist. | |||
T10770 |
Cetirizine D8
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Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Cetirizine D8 is a deuterium-labeled Cetirizine. Cetirizine is a second-generation antihistamine and a long-acting histamine H1-receptor antagonist. | |||
T10769 |
Cetirizine D4
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Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Cetirizine D4 is a deuterium-labeled Cetirizine. Cetirizine is a second-generation antihistamine and a long-acting histamine H1-receptor antagonist. | |||
TMIJ-0189 |
Ranitidine-d6 HCl
|
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Ranitidine-d6 HCl 是 Ranitidine HCl 的氘代化合物。Ranitidine HCl 的 CAS 号为 66357-59-3。Ranitidine hydrochloride 是一种具有口服活性的组胺 H2 受体选择性拮抗剂,IC50为 3.3 μM。它还是一种CYP2C19和CYP2C9的弱抑制剂,可抑制胃液分泌。 | |||
TMIJ-0200 |
Loratadine-d5
|
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Loratadine-d5 是 Loratadine 的氘代化合物。Loratadine 的 CAS 号为 79794-75-5。Loratadine是一种组胺 H1受体反向激动剂,IC50>32 μM。它抑制炎症介质的免疫释放,具有抗登革热病毒的活性。 | |||
TMIJ-0338 |
Pitolisant-d6 HCl
|
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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。 | |||
TMIH-0271 |
Hydroxyzine dihydrochloride-d4
(R)-2-(2-(4-((4-chlorophenyl)(phenyl)methyl)piperazin-1-yl)ethoxy-1,1,2,2-d4)ethan-1-ol dihydrochloride |
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Hydroxyzine dihydrochloride-d4 是 Hydroxyzine dihydrochloride 的氘代化合物。Hydroxyzine dihydrochloride 的 CAS 号为 2192-20-3。Hydroxyzine dihydrochloride是一种苯二氮卓抗组胺剂,是可口服的组胺 H1 受体和血清素拮抗剂,可有效治疗慢性荨麻疹、皮炎和组胺介导的瘙痒。它还可以作为止吐剂和镇静剂,有缓解焦虑和紧张的作用。 | |||
TMIJ-0260 |
Bilastine-d4
|
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Bilastine-d4 是 Bilastine 的氘代化合物。Bilastine 的 CAS 号为 202189-78-4。Bilastine是新型抗组胺药,对H1组胺受体具有高度选择性,起效快,作用时间长的特性,可用于变应性鼻结膜炎和荨麻疹。 | |||
TMIJ-0259 |
Bilastine-d6
|
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Bilastine-d6 是 Bilastine 的氘代化合物。Bilastine 的 CAS 号为 202189-78-4。Bilastine是新型抗组胺药,对H1组胺受体具有高度选择性,起效快,作用时间长的特性,可用于变应性鼻结膜炎和荨麻疹。 | |||
T11088 |
Doxepin D3 Hydrochloride
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Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Doxepin D3 Hydrochloride is a deuterium-labeled doxepin hydrochloride.Doxepin hydrochloride is an oral active tricyclic antidepressant used as a sedative.Doxepin hydrochloride is also an effective CYP450 inhibitor, significantly inhibiting CYP450 2C19 and | |||
T70960 |
Maprotiline-d3 hydrochloride
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Maprotiline-d3 is intended for use as an internal standard for the quantification of maprotiline by GC- or LC-MS. Maprotiline is a tricyclic antidepressant. It binds to the norepinephrine transporter (NET) and is selective for NET over the serotonin and dopamine transporters. Maprotiline also binds to the serotonin (5-HT) receptor subtype 5-HT2A, as well as histamine H1, muscarinic acetylcholine, α1-adrenergic, and dopamine D2 receptors. In vivo, maprotiline inhibits norepinephrine reuptake in r... |