Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T3610 |
Ranitidine
雷尼替丁,HSDB 3925,Ranitidin |
P450; Antibacterial; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Metabolism; Microbiology/Virology; Neuroscience |
Ranitidine (HSDB 3925) 是一种选择性的,具有口服活性的组胺 H2 受体拮抗剂,IC50为 3.3 μM。它还一种是CYP2C19和CYP2C9的弱抑制剂,可抑制胃液分泌。 | |||
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。 | |||
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。 | |||
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。 | |||
T0157 |
Roxatidine Acetate hydrochloride
HOE 760,盐酸罗沙替丁醋酸酯,Roxatidine Acetate HCl |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Roxatidine Acetate hydrochloride (HOE 760) 是一种特异性和竞争性的组胺 H2 受体拮抗剂,能抑制胃酸分泌,可用于胃溃疡和十二指肠溃疡的研究。 | |||
T1575 |
Nizatidine
Axid,Acinon,尼扎替丁,Zanizal |
AChE; Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Nizatidine (Acinon) 是一种竞争性和可逆的组胺 H2 受体拮抗剂,具有抗酸活性,可用于胃溃疡的研究。 | |||
T31195 |
Dalcotidine
KU 1257,KU-1257 |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Dalcotidine (KU 1257) 是一种新型组胺H2受体拮抗剂,具有组胺H9受体拮抗活性和抗分泌作用,与豚鼠大脑皮层结合的Ki 值为0.040 对分离性豚鼠右心房组胺诱导的正变时反应的拮抗作用的KB 值为0.041。Dalcotidine 提高了溃疡愈合的质量,可能有助于降低溃疡的复发率和复发率。 | |||
T68146 |
Sufotidine
AH 25352X,AH25352X,AH-25352X |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Sufotidine (AH 25352X) 是一种具有高度选择性的竞争性 H2 受体拮抗剂。 | |||
T68122L |
Oxmetidine FA
Oxmetidine FA(72830-39-8 Free base) |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Oxmetidine FA 是一种可口服的特异性组胺 H2 受体拮抗剂,具有抗溃疡作用。 | |||
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。 | |||
T68056 |
Donetidine
|
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Donetidine 是一种组胺 H2 受体拮抗剂,可用于治疗消化系统疾病。 | |||
T8599 |
Betazole dihydrochloride
盐酸倍他唑,Betazole hydrochloride |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Betazole dihydrochloride (Betazole hydrochloride) 是吡唑类组胺,是一种口服活性 H2受体激动剂,能诱导胃酸分泌,导致胆总管压力立即显著升高。它作为一种诊断剂,用于研究胃酸分泌能力。 | |||
T68921 |
Impromidine hydrochloride
|
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Impromidine hydrochloride 是一种非常有效和特异性的组胺H2受体激动剂,可用于进行心血管研究。 | |||
T15005 |
CP-66948
|
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
CP-66948 是一种有效的 histamine H2 受体拮抗剂,对胃酸分泌有抑制作用,可用于保护胃黏膜和肠粘膜。 | |||
T68100 |
Mifentidine
DA 4577 |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Mifentidine (DA 4577) 是一种可口服的 H2 受体拮抗剂,可用于研究胃排空和实验性胃和十二指肠溃疡。 | |||
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。 | |||
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。 | |||
T11825 |
LCB-2853
|
PPAR | DNA Damage/DNA Repair; Metabolism |
LCB-2853 是一种有效的血栓素 A2/前列腺素 H2 (TXA2/PGH2) 受体拮抗剂,具有抗血小板聚集、抗血管痉挛和抗血栓作用。 | |||
T10000 |
(±)-Tazifylline
|
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
(±)-Tazifylline 是一种选择性的长效组胺 H1 受体拮抗剂。 Tazifylline 对 H2 受体、α- 和 β-肾上腺素能受体、5-羟色胺和毒蕈碱受体亚型的亲和力要低得多。 | |||
T68122 |
Oxmetidine
SKF 92994,Oxmetidina,Oxmetidinum |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Oxmetidine (SKF 92994) 是一种新型 H2 受体拮抗剂,具有细胞毒性。 Oxmetidine 抑制心脏和血管组织中跨膜钙通量,可用于治疗活动性十二指肠溃疡。 | |||
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。 | |||
T11324 |
FRG8701
|
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
FRG8701 is a new Histamine H2-receptor antagonist with an IC50 of ranging from 0.25 to 0.43 μM. | |||
T13163 |
Tiotidine
ICI 125211 |
Others | Others |
Tiotidine is a selective histamine H2-receptor antagonist (pA2=7.3-7.8 for guinea-pig right atrium). | |||
T23565 |
Zolantidine dimaleate
|
Others | Others |
H2 receptor antagonist | |||
T22848 | ICI 162,846 | Others | Others |
histamine H2 receptor antagonist | |||
T10575 |
BMY-25271
|
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
BMY-25271 is an antagonist of histamine H2 receptor. | |||
T12228 |
Niperotidine
|
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Niperotidine is an antagonist of histamine H2-receptor. | |||
T23811 |
BMY-25368
BMY25368 |
||
BMY-25368 is a long-acting antagonist of the H2-receptor. | |||
T68747 | Orf 17578 | ||
Orf 17578 is a histamine H2-receptor antagonist. | |||
T70297 |
IY-80843
|
||
IY-80843 is an H2-receptor antagonist. | |||
T26039 |
Ramixotidine
|
||
Ramixotidine is a competitive antagonist of histamine H2-receptor. | |||
T24162 |
Impromidine
Impromidina,Impromidinum |
||
Impromidine is a highly potent and specific agonist of the histamine H2 receptor. | |||
T13382 |
Zaltidine
CP-57361 |
Others | Others |
Zaltidine is an antagonist of H2-receptor, and has the antisecretory action. | |||
T70709 |
FCE-27262
|
||
FCE-27262 is a prostaglandin H2/thromboxane A2 receptor antagonist. | |||
T71086 |
IT-066 HCl
|
||
IT-066 HCl is a histamine H2 receptor antagonist. | |||
T23941 |
DA 4360
DA4360,DA-4360 |
||
DA 4360 is an H2-receptor antagonist. The compounds which were investigated in a wider concentration range, behaved as simple competitive antagonists, yielding apparent KB values comparable with those estimated in conventional H2-receptor assays. | |||
T23943 |
DA 4643
DA-4643,DA4643 |
||
DA 4643 is one of the histamine H2-receptor antagonists. Both mifentidine and DA 4643 interact with the histamine H2-receptor at the same site, utilizing in the binding process the same, or closely similar, receptor structural features. | |||
T68704 |
Orf 17583
|
||
Orf 17583 is a histamine H2-receptor antagonist. | |||
T68479 |
Orf 17910
|
||
Orf 17910 is a histamine H2-receptor antagonist. | |||
T28613 |
RP73870
RP 73870,RP-73870 |
||
RP73870 is a gastrin/cholecystokinin-B receptor antagonist and H2 receptor antagonist with potent anti-ulcer activity. | |||
T23942 |
DA 4626
DA4626,DA-4626 |
||
DA 4626 is H2-receptor antagonism. The compound which was investigated in a wider concentration range, behaved as simple competitive antagonists, yielding apparent KB values comparable with those estimated in conventional H2-receptor assays. | |||
T71529 |
NO 794
|
||
NO 794 is a histamine H2-receptor antagonist. | |||
T71390 | AY 29315 | ||
AY 29315 is a histamine H2-receptor antagonist with antisecretory and antiulcer activities. | |||
T15722 |
Lavoltidine
Loxtidine,AH-234844 |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Lavoltidine is an orally active and irreversible histamine H2-receptor antagonist. Lavoltidine strongly suppresses gastric acid secretion and also induces hypergastrinemia. | |||
T71928 | Nordimaprit dihydrochloride | ||
Nordimaprit dihydrochloride is a metabolite of Dimaprit -- a histamine analog and selective H2 histamine receptor agonist. | |||
T71470 | Famotidine hydrochloride | ||
Famotidine hydrochloride is a competitive histamine H2-receptor antagonist. Its main pharmacodynamic effect is the inhibition of gastric secretion. | |||
T70127 |
Famotine
|
||
Famotine is a histamine H2 receptor antagonist that inhibits stomach acid production. It is commonly used in the treatment of peptic ulcer disease and gastroesophageal reflux disease. | |||
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。 | |||
T31743 |
Famotine hydrochloride
Famotine HCl,UK-2054 |
||
Famotine Hydrochloride is a histamine H2 receptor antagonist that suppresses acid production in the stomach and commonly treats peptic ulcer disease and gastroesophageal reflux disease. | |||
T70090 |
Nizatidine amide
|
||
Nizatidine amide is a histamine H2 receptor antagonist that inhibits stomach acid production. It is commonly used in the treatment of peptic ulcer disease and gastroesophageal reflux disease. |