35
10
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T1154 |
Rifaximin
|
DNA/RNA Synthesis; Antibacterial; Antibiotic | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology |
Rifaximin 是一种胃肠道选择性抗生素,与细菌 DNA 依赖性 RNA 聚合酶的 β 亚基结合,抑制细菌 RNA 合成。与革兰氏阴性菌(MIC:8-50 毫克/毫升)相比,它对革兰氏阳性菌株(MIC:0.03-5 毫克/毫升)的敏感性更高。 | |||
T9103 |
BVDV-IN-1
|
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
BVDV-IN-1 是一种牛病毒性腹泻病毒 (BVDV) 的非核苷抑制剂 (NNI),EC50 为 1.8 μM。它直接与 BVDV RdRp 的疏水口袋结合,对耐 NNI 氨基硫脲 (TSC) 的 BVDV 具有抗病毒活性。 | |||
T7603 |
Pinaverium bromide
|
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Pinaverium bromide 是一种具有解痉作用的钙通道阻滞剂,可有效缓解疼痛、腹泻和肠道不适。 | |||
T2486 |
IOWH-032
IOWH032,IOWH 032 |
CFTR; Autophagy | Autophagy; Membrane transporter/Ion channel |
IOWH-032 (IOWH032) 是一种合成 CFTR 抑制剂,可用于研究治疗霍乱、腹泻和分泌性腹泻,在T84和CHO-CFTR 细胞实验中IC50为1.01 uM。 | |||
T1176 |
Racecadotril
Acetorphan,消旋卡多曲 |
Neprilysin; Proteasome | Metabolism; Proteases/Proteasome; Ubiquitination |
Racecadotril (Acetorphan) 是一种中性内肽酶 (NEP) 抑制剂,具有止泻作用。Racecadotril 及其活性代谢物 Thiorphan 抑制小鼠脑中纯化的NEP 活性,Ki 分别为 4500 和 6.1 nM。 | |||
T26630 |
Ani9
Ani 9,Ani-9,Apelin-12 acetate (229961-08-4 Free base) |
Chloride channel | Membrane transporter/Ion channel |
Ani9 是 Anoctamin1 (ANO1)/跨膜蛋白 16A (TMEM16A) 的高选择性阻断剂,IC50 为 77 nM,可用于关于 ANO1 和治疗癌症、高血压、疼痛、腹泻和哮喘的研究。 | |||
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。 | |||
T4562L |
Ramosetron hydrochloride
盐酸雷莫司琼,YM 060,YM-060,YM060 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Ramosetron hydrochloride (YM-060) 是一种 5-HT3 受体拮抗剂,用于治疗以腹泻为主的肠易激综合征和恶心。 | |||
T36619 |
Aligeron
|
Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation |
Aligeron 是一种非选择性的prostaglandin (PG)拮抗剂,对PGF2α和PGE2诱导的猫血压下降有抑制作用,可用于抑制PGF2α诱导的小鼠腹泻和PGE2诱导的大鼠爪水肿。Aligeron 对血管并发症具有抗氧化保护作用。 | |||
T72054 |
SLC26A3-IN-1
|
transporter | Metabolism |
SLC26A3-IN-1 是一种阴离子交换蛋白 SLC26A3 的抑制剂 ,IC50值为340 nM。SLC26A3 属于溶质载体 (SLC) 蛋白,是 SLC26 家族成员之一。SLC26 家族对氯化物、碳酸氢盐、硫酸盐和草酸盐具有广泛的阴离子特异性。SLC26A3 在腺瘤 (DRA) 中下调,参与氯化物和草酸盐的肠道吸收且与氯离子丢失性腹泻有关。 | |||
T67801 |
GS-6620 PM
|
||
GS-6620 PM 是GS-6620的衍生物。GS-6620是一种口服的抗丙型肝炎病毒聚合酶抑制剂,是一种新型强效的C-核苷腺嘌呤类似物单磷酸酯原药。GS-6620对其他病毒的活性有限,对密切相关的牛病毒性腹泻病毒仅保持部分活性(EC50,1.5μM)。 | |||
T4562 |
Ramosetron
|
5-HT Receptor | GPCR/G Protein; Neuroscience |
Ramosetron 是一种血清素 5-HT3 受体拮抗剂,用于治疗恶心和呕吐。它被认为比其他一代 5-HT3 拮抗剂如昂丹司琼具有更高的效力和更长的止吐作用。它还适用于治疗“男性以腹泻为主的肠易激综合征”。它仅获准在日本和选定的东南亚国家使用。 | |||
T29868 |
Alkofanone
|
||
Alkofanone is a biochemical used in the treatment of primary diarrhea. | |||
T71145 |
Racecadotril-d5
|
||
Racecadotril-d5 is intended for use as an internal standard for the quantification of racecadotril by GC- or LC-MS. Racecadotril is a prodrug form of the neprilysin (NEP) inhibitor thiorphan. In vivo, racecadotril reduces or prevents castor oil-induced diarrhea without delaying intestinal transit in rats when administered at doses of 80 or 100 mg/kg, respectively. It also decreases the duration of diarrhea and increases body weight gain in a neonatal gnotobiotic pig model of human rotavirus-indu... | |||
T30936 |
Cilansetron Hydrochloride
KC-9946,KC9946,KC 9946 |
||
Cilansetron Hydrochloride can be used for irritable Bowel Syndrome (IBS) with Diarrhea Predominance. | |||
T11867 |
Loperamide-d6 hydrochloride
R-18553 D6 hydrochloride |
Others | Others |
Loperamide D6 hydrochloride, a deuterium-labeled variant of Loperamide hydrochloride, acts as an opioid receptor agonist utilized for diarrhea treatment. | |||
T21235 |
Alosetron
Lotronex,GR68755,GR-68755,GR 68755,阿洛司琼 |
||
Alosetron, a 5-HT3 antagonist, is used for the management of severe diarrhea-predominant irritable bowel syndrome (IBS) in women only. | |||
T40949 |
5'-O-TBDMS-N2-ibu-dG
5'-O-TBDMS-N2-ibu-dG |
||
5'-O-TBDMS-N2-ibu-dG is a nucleoside derivative that possesses potent anti-bovine viral diarrhea virus activity. It serves as a valuable compound for the synthesis of lead compounds with such activity. | |||
T24563 |
Nummularine B
N-Demethylamphibine H,Daechuine S27 |
||
Nummularine B is a cyclopeptide alkaloid. It has antiviral activity against the porcine epidemic diarrhea virus. It also has potent inhibitory effects on PEDV replication. | |||
T15651 | KDU731 | Others | Others |
KDU731 is a promising drug candidate for the treatment of diarrhea caused by Cryptosporidium and meets a broad range of safety. KDU731is an orally active C. parvum inhibitor of PI4K (IC50: 25 nM). KDU731 blocks Cryptosporidium infection in vitro and in vi | |||
T80150 |
Guanylin (mouse, rat)
|
Guanylate cyclase | GPCR/G Protein |
Guanylin (mouse, rat) 是一种由15个氨基酸组成的多肽,并作为肠道鸟苷酸环化酶的激活剂。它可用于腹泻研究。 | |||
T26828 |
BIT225
BIT 225,BIT-225 |
||
BIT-225 is a NCp7 zinc finger inhibitor. BIT225 inhibits HIV-1 replication in myeloid dendritic cells. BIT225 inhibits HIV-1 release from human macrophages. BIT225 inhibits bovine viral diarrhea virus in vitro and shows synergism with recombinant interfer | |||
T63412 | DB772 hydrate | ||
DB772 hydrate 是一种牛病毒性腹泻病毒 (BVDV) 抑制剂,同时表现出抗朊病毒作用。 | |||
T81924 | LK-44 | ||
hCES2A-IN-2 (Compound 44) 为口服活性人羧酸酯酶 2 (hCES2A) 抑制剂,IC50 值为5.02 μM,能够有效改善Irinotecan 引起的迟发性腹泻。 | |||
T21423 |
Methysergide maleate
Deseril, Sansert,UML 491,UML491,Methysergide,UML-491 |
||
Methysergide is used for prophylaxis of migraine headaches/cluster headaches but is no longer recommended due to retropulmonary/retroperitoneal fibrosis. It may also be used in the treatment of serotonin syndrome. It is also used in carcinoid syndrome to | |||
T16948 |
Suclofenide
PB385,Neosulfalepsine,琥氯非尼 |
Others | Others |
Suclofenide 是一种苯磺酰胺衍生物,可作为抗惊厥和抗癫痫剂。在临床前模型中,它对小鼠电击和戊四唑诱导的惊厥表现出强大的抗惊厥活性。亚致死毒性表现为嗜睡、肌阵挛抽搐和腹泻。 | |||
T82231 | hCES2-IN-1 | ||
hCES2-IN-1(Compound 24)是一种选择性的hCES2可逆抑制剂,其IC50值为6.72 μM。该化合物能够减少活细胞中hCES2的表达量,并且能有效抵抗由Irinotecan引起的迟发性腹泻以及DSS诱发的溃疡性结肠炎。 | |||
T10294 | AM9405 | 5-HT Receptor | GPCR/G Protein; Neuroscience |
AM9405是一种新型的外周活性大麻素1型 (CB1)和5-羟色胺3型受体激动剂。 AM9405抑制回肠和结肠的抽搐收缩,IC50分别为45.71 和 0.076 nM。AM9405 在生理条件下显着减缓小鼠肠道蠕动. | |||
T70267 |
ADL 08-0011 HCl
|
||
ADL 08-0011 is an active metabolite of the μ-opioid receptor antagonist alvimopan. It is produced from alvimopan via amide hydrolysis by gut microbiota. ADL 08-0011 is a μ-opioid receptor antagonist (Ki = 0.25 nM). It is selective for μ-opioid receptors over κ- and δ-opioid receptors (Kis = 15.8 and 31.6 nM, respectively). ADL 08-0011 inhibits endomorphin 1-induced inhibition of electrically induced contraction of isolated guinea pig ileum (pA2 = 9.4). In vivo, ADL 08-0011 (0.03-1 mg/kg) reverse... | |||
T74815 | SLC26A3-IN-2 | ||
SLC26A3-IN-2 是一种口服有效的阴离子交换蛋白 SLC26A3的抑制剂 (IC50=360 nM)。SLC26A3 属于溶质载体 (SLC) 蛋白,属于 SLC26 家族。SLC26 家族对氯化物、碳酸氢盐、硫酸盐和草酸盐具有广泛的阴离子特异性。SLC26A3 在腺瘤 (DRA) 中下调,参与氯化物和草酸盐的肠道吸收。SLC26A3 功能突变的丧失与氯离子丢失性腹泻有关。 | |||
T71293 |
Nifuroxazide-d4
|
||
Nifuroxazide-d4 is intended for use as an internal standard for the quantification of nifuroxazide by GC- or LC-MS. Nifuroxazide is a nitrofuran antibiotic. It is active against strains of the enteropathogenic bacteria C. jejuni, Salmonella, Y. enterocolitica, Shigella, and E. coli. It inhibits quorum sensing and virulence factor production in P. aeruginosa. Nifuroxazide inhibits STAT3 activity in a reporter assay and decreases viability of U266 and INA-6 myeloma cells, which have constitutive S... | |||
T70070 |
Cisapride tartrate
|
||
Cisapride tartrate is chemically related to metoclopramide, but unlike metoclopramide, it does not cross the blood-brain barrier or have antidopaminergic effects. Cisapride is a serotonin-4 (5-HT4) receptor agonist. Cisapride was indicated for the symptomatic treatment of adult patients with nocturnal heartburn due to gastroesophageal reflux disease. The Food and Drug Administration (FDA) in America stopped the marketing of cisapride as of 14th July 2000. They had received at least 341 reports o... | |||
T31194 |
Dalapon
Basfapon B,Dowpon M,Dawpon-Rae |
||
Dalapon is a selective herbicide used to control perennial grasses. The major use of dalapon is on food crops including sugarcane and sugar beets. Its use is no longer authorized in France. The National Institute for Occupational Safety and Health in the | |||
T37582 |
Ganglioside GM1 Mixture (ovine) (ammonium salt)
|
||
Ganglioside GM1is a monosialylated ganglioside and the prototypic ganglioside for those containing one sialic acid residue.1,2It is found in a large variety of cells, including immune cells and neurons, and is enriched in lipid rafts in the cell membrane.3It associates with growth factor receptors, including TrkA, TrkB, and the GDNF receptor complex containing Ret and GFRα, and is required for TrkA expression on the cell surface. Ganglioside GM1interacts with other proteins to increase calcium i... | |||
T36881 | NHC-diphosphate triammonium | ||
NHC-triphosphate triammonium is an active phosphorylated intracellular metabolite of β-d-N4-Hydroxycytidine (NHC) as a triphosphate form[1]. NHC-triphosphate triammonium is a weak alternative substrate for the viral polymerase and can be incorporated into HCV replicon RNA[1][2]. In an intracellular metabolism assay, HCV replicon cells are treated with 10 μM 3H-labeled NHC, and intracellular nucleotide levels are determined after 1, 2 and 8 hours incubations. NHC is rapidly convered into the mono... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T4S0999 |
(2S)-Isoxanthohumol
Isoxanthohumol,(2S)-异黄腐酚,异黄腐醇 |
Virus Protease; HSV | Microbiology/Virology |
(2S)-Isoxanthohumol 是一种由啤酒花原异戊烯基二氢黄酮 Isoxanthohumol 的微生物转化代谢物。 | |||
T1273 |
Diacerein
双醋瑞因,Diacerhein,Fisiodar,Diacetylrhein |
IL Receptor; Interleukin | Immunology/Inflammation |
Diacerein (Fisiodar) 是一种慢效具有白介素-1β 抑制效果的蒽醌类化合物。 | |||
T6194 |
Fidaxomicin
非达米星,Tiacumicin B,OPT-80,Clostomicin B1,PAR-101 |
Apoptosis; DNA/RNA Synthesis; Antibacterial; Antibiotic | Apoptosis; Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Microbiology/Virology |
Fidaxomicin (Tiacumicin B) 是一种大环RNA 聚合酶抑制剂,具有窄谱活性。它选择性地根除致病性艰难梭菌,对构成正常健康肠道菌群的多种细菌影响很小。 | |||
T3332 |
Isosteviol
异甜菊醇,(-)-Isosteviol |
IL Receptor; Potassium Channel; TNF; NF-κB; Reactive Oxygen Species; COX; Topoisomerase | Apoptosis; DNA Damage/DNA Repair; Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism; Neuroscience; NF-κB |
Isosteviol ((-)-Isosteviol) 是一种常见的天然甜味剂,属于四环二萜糖苷,是甜菊糖苷通过酸催化水解产生的。它抑制 DNA 聚合酶和 DNA 拓扑异构酶,具有抗菌、抗癌和抗结核作用。 | |||
T5231 |
2-Methylsuccinic acid
Pyrotartaric Acid,Methylbutanedioic acid,甲基丁二酸 |
Others; Endogenous Metabolite | Metabolism; Others |
2-Methylsuccinic acid (Pyrotartaric Acid) 是乙基丙二酸脑病的主要生化指标,是人体液中的正常代谢物。 | |||
T6S0071 |
Fraxinellone
|
HIF/HIF Prolyl-Hydroxylase; STAT; PD-1/PD-L1 | Apoptosis; Cell Cycle/Checkpoint; Chromatin/Epigenetic; Immunology/Inflammation; JAK/STAT signaling; Metabolism; Stem Cells |
Fraxinellone 是从白鲜的根皮中分离出来的一种天然产物,是PD-L1抑制剂,可抑制HIF-1α蛋白质合成。它通过靶向 PD-L1,有用于癌症免疫的潜力。 | |||
T75643 |
Isoxanthohumol
|
HSV | Microbiology/Virology |
Isoxanthohumol 是一种从啤酒花和啤酒中提取的一种前黄酮类化合物,对几种人类癌细胞株具有抗增殖活性。Isoxanthohumol对肿瘤细胞肺转移灶的转移或侵袭有抑制作用。Isoxanthohumol具有抗病毒活性,对疱疹病毒(HSV1和HSV2)和牛病毒性腹泻病毒(BVDV)具有抑制作用。 | |||
T81080 | Strictinin | ||
Strictinin 是从普洱茶 (Pu'er teas) 分离得到的酚类化合物,展现出潜在的抗病毒、抗菌和通便活性。这些活性是由于它加速小肠转运所致,并非因增强胃排空、增加食物摄入或诱导大鼠腹泻而发挥作用。 | |||
T15097 |
Deoxynivalenol
Vomitoxin,4-Deoxynivalenol |
||
Deoxynivalenol (Vomitoxin) 是一种单端孢菌素家族镰刀菌属产生的霉菌毒素,常见于受到污染的食物和饲料中。Deoxynivalenol 通过紧密连接处的细胞旁路来穿过肠粘膜。Deoxynivalenol 转运不受P-糖蛋白 (PgP) 或多药耐药相关蛋白 (MRP) 抑制剂的影响。Deoxynivalenol 通常会导致人类和动物腹泻、呕吐和胃肠道炎症。 | |||
TN1783 |
Isolicoflavonol
异甘草黄酮醇 |
Lipid | Metabolism |
Isolicoflavonol 以可逆和混合的方式抑制人羧酸酯酶2介导的荧光素二乙酸酯水解, Ki 小于1.0 μM。 |