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9
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T0786 |
Clidinium bromide
克利溴铵,Ro 2-3773 |
AChR | Neuroscience |
Clidinium bromide (Ro 2-3773) 是季胺抗毒蕈碱剂,可通过减少胃酸和减慢肠道速度,缓解痉挛和腹部疼痛的症状。 | |||
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。 | |||
T2455 |
PFK-015
PFK15,PFK 015 |
Glucokinase; Autophagy | Autophagy; Metabolism |
PFK-015 (PFK15) 是一种有效的 PFKFB3 抑制剂,对重组PFKFB3的IC50为110 nM。它能抑制 Y 细胞中的 PFKFB3 活性,IC50为20 nM。 | |||
T0424 |
Bismuth Subsalicylate
Bismuth subsalicylat,Bismuth(III) salicylate basic,Bismuth oxysalicylate,碱式水杨酸铋,次水杨酸铋 |
COX; PGE Synthase | Immunology/Inflammation; Neuroscience |
Bismuth Subsalicylate (Bismuth subsalicylat) 是口服抗酸和止泻试剂。它能够抑制体内前列腺素合成,抑制胃和肠道黏膜炎症反应。它广泛用于研究腹泻疾病,如恶心、消化不良、腹泻等。 | |||
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。 | |||
TP2030 |
Gastrin I, human
Gastrin I (human) |
cholecystokinin | GPCR/G Protein |
Gastrin I, human (Gastrin I (human)) 是胃中产生的内源性肽,通过 CCK2 受体增加大鼠的胃蛋白酶原和酸分泌。 | |||
T20914 |
Simethicone
Disflatyl,西甲硅油,Simeticone,Phazyme |
Others | Others |
Simethicone (Disflatyl) 是一种口服消泡剂,可用于减少因胃或肠道内过多气体引起的腹胀、疼痛和不适。 | |||
T0594 |
Diphenmanil methylsulfate
Diphemanil mesylate,Diphemanil Methylsulfate,甲硫二苯马尼 |
AChR | Neuroscience |
Diphenmanil methylsulfate (Diphemanil mesylate) 是一种抗胆碱能季铵盐,可与毒蕈碱乙酰胆碱受体结合,从而减少胃酸、汗液和唾液的分泌。 | |||
TP2030L1 |
Gastrin I (human) acetate
Gastrin I (human) acetate(10047-33-3 free base),Gastrin-17 acetate,Little gastrin I acetate,胃膜素醋酸盐 |
cholecystokinin | GPCR/G Protein |
Gastrin I (human) acetate (Gastrin-17 acetate) 是在胃中产生的内源性肽,通过胆囊收缩素 2 (CCK2) 受体增加胃酸分泌。 | |||
T6710 |
Troxipide
曲昔派特,曲昔匹特,Aplace |
Others | Others |
Troxipide (Aplace) 是非分泌型胃保护剂,是口服具有活力的胃炎和胃溃疡的防御因子的增强剂,具有抗溃疡、抗炎和粘液分泌作用。 | |||
T3937 |
Methyl L-histidinate dihydrochloride
L-Histidine methyl ester dihydrochloride,L-组氨酸甲酯二盐酸盐 |
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
Methyl L-histidinate dihydrochloride (L-Histidine methyl ester dihydrochloride) 在Sprague-Dawley 大鼠胃中组氨酸脱羧酶的抑制作用被评估为 14CO2 产生减少,活性值为 1.8 μM。 | |||
T72107 |
Werner syndrome RecQ helicase-IN-1
|
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Werner syndrome RecQ helicase-IN-1 是一种有效的 Werne r 综合征 RecQ DNA 解旋酶 (WRN) 抑制剂,可用研究像结肠癌和胃癌等癌症。 | |||
T0674 |
Lansoprazole
兰索拉唑,A-65006,AG-1749 |
Proton pump; Phospholipase; Antibacterial | Membrane transporter/Ion channel; Metabolism; Microbiology/Virology |
Lansoprazole (A-65006) 是一种可抑制胃酸生成的质子泵抑制剂。它是中性鞘磷脂酶的外泌体抑制剂。 | |||
T1651 |
Rabeprazole sodium
Dexrabeprazole Sodium,LY307640 sodium,Habeprazole Sodium,雷贝拉唑钠,Rebeprazole sodium,Aciphex Sodium |
Apoptosis; Proton pump | Apoptosis; Membrane transporter/Ion channel |
Rabeprazole sodium (Habeprazole Sodium) 是一种质子泵抑制剂,不可逆地抑制胃 H+/K+-ATPase,可研究胃溃疡和胃食管反流。它诱导细胞凋亡,也抑制尿苷核苷核糖水解酶 ,IC50为 0.3 μM。 | |||
T0992 |
Carbenoxolone disodium
Biogastrone,Duogastrone,甘珀酸钠,Bioral |
Gap Junction Protein | Cytoskeletal Signaling |
Carbenoxolone disodium (Duogastrone) 是甘草酸的活性代谢物和人11β-HSD 和细菌3α, 20β-HSD 的抑制剂。它是一种缝隙连接的解耦剂,可抑制牛痘病毒生长,用于消化性、食道和口腔溃疡和炎症的相关研究。 | |||
TP1325L |
Gastrin-Releasing Peptide, human(TFA)
|
Others | Others |
Gastrin-Releasing Peptide, human(TFA) (93755-85-2 free base) 是一种调节性人类肽,可引发胃泌素释放并调节胃酸分泌和肠道运动功能。支配胃G 细胞的迷走神经节后纤维释放GRP,刺激G 细胞释放胃泌素。 | |||
T4616 |
Metoclopramide
甲氧氯普胺,胃复安,5-Chloro-2-methoxyprocainamide |
Dopamine Receptor; 5-HT Receptor | GPCR/G Protein; Neuroscience |
Metoclopramide (5-Chloro-2-methoxyprocainamide) 是5-HT3和多巴胺D2受体拮抗剂,IC50值分别为 308 和 483 nM,可用于恶心呕吐、胃食管反流和胃轻瘫的研究。 | |||
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. | |||
T18310 |
AZ1508
MC-Lys-MMETA |
Others | Others |
AZ1508, a tubulin inhibitor[1], serves as a drug-linker conjugate for antibody-drug conjugates (ADC) targeting breast and stomach cancer treatment. | |||
T32599 |
Lauroylglycyrrhetinic acid
BX 24,BX24,BX-24 |
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Lauroylglycyrrhetinic acid, an analog of carbenoxolone, can be used in the treatment of stomach ulcer. | |||
T34566 |
Sch 12223
Sch12223,Sch-12223 |
||
SCH 12223 is a unique drug that protects the stomach and intestinal epithelium from harmful irritation. | |||
T20775 |
Ranitidine-N-oxide
|
||
Ranitidine-N-oxide is a metabolite of Ranitidine. Ranitidine is a antagonist of histamine H2-receptor, it inhibits the normal and meal-stimulated secretion of stomach acid. Ranitidine is a medication decreaseing stomach acid production. | |||
T28331 |
PD 136450
Cam1189,PD136450,Cam-1189,PD-136450,Cam 1189 |
||
Cholecystokinin type B receptor antagonist PD-136,450 is a partial secretory agonist in the stomach and a full agonist in the pancreas of the rat. Gastrin (cholecystokinin type B (CCK-B)) receptor antagonists may help to elucidate the physiological role o | |||
T61453 |
Propantheline
|
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Propantheline is an orally active antagonist of muscarinic acetylcholine receptors (mAChRs), commonly employed to investigate smooth muscle dysfunction, hyperhidrosis, smooth muscle spasms or cramps in the stomach, intestines, or bladder, as well as involuntary urination [1] [2] [3]. | |||
T11816 |
Lansoprazole-d4
AG-1749 D4,Lansoprazole D4 |
Proton pump | Membrane transporter/Ion channel |
Lansoprazole D4 (AG-1749 D4) is a deuterium labeled Lansoprazole. Lansoprazole is an inhibitor of proton pump which prevents the stomach from producing acid. | |||
T70127 |
Famotine
|
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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. | |||
T68725 |
Famotidine propanamide
|
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Famotidine propanamide 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. | |||
T71509 |
Famotidine sulfamoyl propanamide
|
||
Famotidine sulfamoyl propanamide 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. | |||
T71049 | Famotidine disulfide | ||
Famotidine disulfide 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. | |||
T70090 |
Nizatidine amide
|
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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. | |||
T71485 |
Famotidine propionic acid
|
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Famotidine propionic acid 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. | |||
T37588 |
GIP (1-30) amide, porcine
|
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This GIP fragment has potent insulinotropic activity in the isolated, perfused rat pancreas but greatly reduced somatostatinotropic activity in the isolated perfused rat stomach. The site responsible for insulinotropic activity apparently lies between residues 19 and 30 of GIP. | |||
T37642 |
Pravastatin lactone
|
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Pravastatin lactone is a metabolite of pravastatin , a hydroxymethylglutaryl-coenzyme A (HMG-CoA) reductase inhibitor that is a ring-hydroxylated metabolite of mevastatin . Pravastatin lactone is formed when pravastatin undergoes acid-catalyzed non-enzymatic lactonization in the stomach following oral administration. | |||
T28612 |
RP-72540
RPR 102681,RPR-102681,RPR102681 |
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RP-72540 is a cholecystokinin B receptor antagonist. RP 72540 showed selectivity factors in express of 200 for CCKA versus CCKB receptors and also had high affinity for gastrin binding sites in the stomach. Administration of RP-72540 resulted in a dose-de | |||
T33314 |
Methantheline Bromide
Frenogastrico,Dixamone bromide,Banthine,Asabaine,Methanthelinium bromide |
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Methantheline Bromide is a synthetic spasmolytic used to relieve cramps or spasms of the stomach, bowel, and bladder. It is also useful for intestinal or gastric ulcers (peptic ulcer disease), intestinal problems, pancreatitis, gastritis, biliary dysmotil | |||
T6415 |
Bismuth Subcitrate Potassium
|
Others; Antibacterial; Antibiotic | Microbiology/Virology; Others |
Bismuth subcitrate potassium 是针对 12 种幽门螺杆菌菌株的抗生素,MIC50为 8 μg/ml。它用于幽门螺杆菌感染的上胃肠道疾病的研究。 | |||
T81224 |
SALMF amide 2
|
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SALMF amide 2为源自海星Asterias rubens的神经肽S2,涉及海星心脏胃外翻调控机制。 | |||
T40850 |
[D-Trp11]-Neurotensin
[D-Trp11]-Neurotensin |
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[D-Trp11]-Neurotensin is a compound that functions as a selective antagonist of Neurotensin (NT) in perfused rat hearts, while exhibiting full agonist properties in guinea pig atria and rat stomach strips. Additionally, this compound can inhibit hypotension induced by NT. | |||
TP1976 |
Oxyntomodulin
胃泌酸调节素,Oxyntomodulin (porcine, bovine) |
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GLP-1 receptor agonist. Endogenous preproglucagon-derived neuropeptide that modulates feeding and metabolism. Also secreted by intestinal L-cells. Increases cAMP production and inhibits gastric acid secretion in rat stomach. Also weak glucagon receptor ag | |||
TP1325 |
Gastrin-Releasing Peptide, human
|
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Gastrin-Releasing Peptide, human is a regulatory human peptide that elicits gastrin release and regulates gastric acid secretion and enteric motor function. The post-ganglionic fibers of the vagus nerve that innervate the G cells of the stomach release GRP, which stimulates the G cells to release gastrin. | |||
TP1232 |
Amylin, amide, rat
Amylin (rat) |
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Amylin is a peptide that displays 50% homology with calcitonin gene-related peptide (CGRP), Amylin is colocalized with somatostatin in endocrine cells of the gastric fundus. In isolated mouse stomach, amylin caused a concentration-dependent decrease in ac | |||
T36148 |
13,14-dihydro-15-keto Prostaglandin F1α
13,14-dihydro-15-keto Prostaglandin F1α |
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13,14-dihydro-15-keto Prostaglandin F1α (13,14-dihydro-15-keto PGF1α) is a metabolite of PGF1α that has been reported in the rat stomach. The measurement of 13,14-dihydro-15-keto PGF1α can be used as a marker of the in vivo production of PGF1α. | |||
T71980 |
Omeprazole acid
|
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Omeprazole acid is a medication used in the treatment of gastroesophageal reflux disease, peptic ulcer disease, and Zollinger–Ellison syndrome. It is also used to prevent upper gastrointestinal bleeding in people who are at high risk. Omeprazole is a proton pump inhibitor and as such blocks the release of stomach acid. | |||
T63819 | Domperidone monomaleate | ||
Domperidone (R33812) monomaleate 是选择性的、口服具有活力的多巴胺-2 受体 (dopamine-2 receptor) 拮抗剂。Domperidone monomaleate 能够影响胃和小肠的化学感受器触发区和运动功能,具有止吐和促动力剂作用。 | |||
T60493 |
Guaiacol Carbonate
|
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Guaiacol Carbonate 是一种祛痰剂,其作用是通过胃的反射作用,通过胃神经到达延髓中枢,然后再通过外周进入呼吸道,从而起到祛痰作用。 | |||
T75993 | Pepsin A | ||
Pepsin A 是人和猪胃中的主要蛋白酶,是一种类似胃蛋白酶的胃小蛋白水解酶。Pepsin A 有助于脊椎动物胃中食物蛋白质的蛋白质水解。 | |||
T36208 |
15(R)-Pinane Thromboxane A2
15(R)-Pinane Thromboxane A2 |
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15(R)-Pinane thromboxane A2 is the (R)-epimer of pinane thromboxane A2 . 15(R)-PTA2 does not inhibit collagen-induced platelet aggregation (IC50s = 120-130 μM). It does not affect gastric tone in isolated rat gastric fundus when used at concentrations of 0.5 or 1.5 μg/ml and is less effective than PTA2 at inhibiting prostaglandin-induced contraction of isolated rat stomach muscle. | |||
T75992 |
Buforin II
|
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Buforin II,来源于 buforin I,从亚洲蟾蜍 Bufo bufo gargarizans 胃中分离得到的蛋白,是一种高效的抗菌 (antimicrobial) 肽。Buforin II 对广谱的革兰氏阳性和革兰氏阴性细菌具有抗菌活性。 | |||
T76107 | Urease | ||
Urease 由多种类型细菌产生,是一些致病菌的有效毒力因子。Urease 还是幽门螺杆菌代谢和毒力的中心,帮助其在胃粘膜中定植。 | |||
T71055 |
Albendazole-d7
|
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Albendazole-d7 is intended for use as an internal standard for the quantification of albendazole by GC- or LC-MS. Albendazole is an orally bioavailable benzimidazole anthelmintic that is active against a variety of helminths, including liver flukes, tapeworms, and roundworms. It eliminates Trichostrongylus in the fourth stomach of cattle and sheep when orally administered at doses ranging from 2.5 to 10 mg/kg as well as other species in the fourth stomach and the small and large intestine. Alben... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T5S0384 |
Rhapontin
Ponticin,土大黄苷,Rhaponiticin,Rhaponticin,Rhapontigenin glucoside |
Apoptosis; Others | Apoptosis; Others |
Rhapontin (Ponticin) 是药用大黄的一种成分,可减轻KK/Ay 糖尿病小鼠肝脏脂肪变性,改善血糖和血脂,表明其具有显着的降糖作用,有望成为治疗2型糖尿病及其并发症的新药。 | |||
T2S1840 |
Rebaudioside D
莱苞迪苷D,瑞鲍迪甙D |
Others | Others |
Rebaudioside D 是一种苷类化合物,存在于甜菊叶中,可用作甜味剂。 | |||
TJS0928 |
Calenduloside E
去葡萄糖竹节参皂苷,Silphioside F |
Others | Others |
Calenduloside E (Silphioside F) 是从辽东楤木中提取的一种五环三萜皂苷。它靶向热休克蛋白90 (Hsp90) ,具有抗凋亡作用。 | |||
T3S0509 |
Gaultherin
|
COX | Immunology/Inflammation; Neuroscience |
Gaultherin 是一种分离自 Gaultheria yunnanensis 中的天然水杨酸酯衍生物。它是一种非甾体类抗炎药,具有止痛和抗炎作用,与 Aspirin 相比没有胃溃疡作用。 | |||
T5803 |
D(-)-Tartaric acid
|
Others | Others |
D(-)-Tartaric acid 存在于许多植物中,特别是罗望子和葡萄,口服后通过与碳酸氢钠相互作用产生二氧化碳。二氧化碳会延伸胃部并在双造影射线照相期间提供负造影剂。 | |||
TN5952 |
2,3-Dihydro-3α-methoxynimbolide
|
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2,3-Dihydro-3α-methoxynimbolide induces apoptosis via both mitochondrial and death receptor pathways in stomach (AZ521) cancer cell line. | |||
TMA1841 | Dihydrodaidzin | Others | Others |
Dihydrodaidzin shows cytotoxic activities against human stomach carcinoma (Hs 740.T, Hs 756 T), breast adenocarcinoma (Hs 578 T, Hs 742.T), and prostate carcinoma (DU 145, LNCaP-FGC) cell lines. | |||
T82463 | Entadamide A 2'-O-(6''-O-β-D-glucopyranosyl)-β-D-glucopyranoside | ||
Entadamide A 2'-O-(6''-O-β-D-glucopyranosyl)-β-D-glucopyranoside (MFLNH I) (compound 5) 是一种从泰国药用植物 Entada rheedei 的种子仁中提取的化合物,具有抑制胃痛的功效。 | |||
TN4937 |
Sambutoxin
|
Others | Others |
Sambutoxin, a new mycotoxin produced by toxic Fusarium isolates obtained from rotted potato tubers, it can cause toxic effects in rats, including body weight loss, feed refusal, hemorrhage in the stomach and intestines, and, finally, death when rats were |