48
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Cat. No. | Product Name | Target | Signaling Pathways |
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T7478 |
2-Chloro-1-(4-fluorobenzyl)benzimidazole
|
Reductase | Endocrinology/Hormones; Metabolism |
2-Chloro-1-(4-fluorobenzyl)benzimidazole 是醛糖还原酶 (ALR2) 的抑制剂。 | |||
T9152 |
2-(2-Hydroxyphenyl)-1H-benzimidazole
|
Others | Others |
2-(2-Hydroxyphenyl)-1H-benzimidazole 已被用于合成聚合物和其他材料的催化剂。 | |||
Fr12535 |
2-(Trifluoromethyl)benzimidazole
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Compound Fr12535 是一种有用的有机化合物,可用于生命科学领域的相关研究。其产品编号为 Fr12535,CAS号为 312-73-2。 | |||
T28754 |
Sepin-1
Sepin 1,Sepin1,2H-Benzimidazole, 2,2-dimethyl-5-nitro-, 1,3-dioxide |
Others | Others |
Sepin-1 是一种分离酶的非竞争性抑制剂,IC50 为 14.8 µM。 Sepin-1可以通过抑制细胞增殖和诱导细胞凋亡来抑制小鼠和人类癌细胞系乳腺癌异种移植瘤的生长。 | |||
T4239 |
1,3-dimethyl-2-oxobenzimidazole-5-carbaldehyde
1,3-DIMETHYL-2-OXO-2,3-DIHYDRO-1H-BENZIMIDAZOLE-5-CARBALDEHYDE |
Others | Others |
1,3-dimethyl-2-oxobenzimidazole-5-carbaldehyde 是中间体。 | |||
T9016 |
AI-10-47
1H-Benzimidazole, 2-(2-pyridinyl)-6-(trifluoromethoxy)-AI-10-47 |
Others | Others |
AI-10-47 (1H-Benzimidazole, 2-(2-pyridinyl)-6-(trifluoromethoxy)-AI-10-47) 是 CBFβ-RUNX 结合的小分子抑制剂(IC50:3.2 μM)。 | |||
T77512 |
1H-Benzimidazole-6-carboxamide, N-[3-(aminocarbonyl)-4,5,6,7-tetrahydrobenzo[b]thien-2-yl]-
|
Others | Others |
1H-Benzimidazole-6-carboxamide, N-[3-(aminocarbonyl)-4,5,6,7-tetrahydrobenzo[b]thien-2-yl]-可能具有抗肿瘤活性。 | |||
T3979 |
Emedastine
LY188695,依美斯汀,Emadine |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Emedastine (LY188695) 是一种可口服的,选择性和高亲和力的组胺 H1受体拮抗剂,Ki 值为 1.3 nM。它是苯并咪唑衍生物,可用于过敏性鼻炎、过敏性皮肤疾病和过敏性结膜炎的研究。 | |||
T3124 |
Carbendazim
Bavistin,Carbendazole,多菌灵,Mercarzole |
Antifungal | Microbiology/Virology |
Carbendazim (Mercarzole) 是一种具有抗肿瘤活性的苯并咪唑衍生物,可用于癌症研究。它是一种口服广谱苯并咪唑杀菌剂,可作为真菌疾病研究的杀虫剂。 | |||
T9579 |
GLP-1 receptor agonist 9
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Glucagon Receptor | GPCR/G Protein |
1H-Benzimidazole-6-carboxylic acid 是GLP-1 receptor 激动剂。 | |||
T0662 |
2-Hydroxybenzimidazole
2-Benzimidazolinone,2-羟基苯并咪唑 |
Others | Others |
2-Hydroxybenzimidazole (2-Benzimidazolinone) 在工业上用作中间体。 | |||
T21642 |
4,5,6,7-Tetrabromobenzimidazole
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4,5,6,7-Tetrabromo-1H-benzimidazole 是一种酪蛋白激酶 2(CK2)的选择性和 ATP 竞争性抑制剂。 | |||
T67503 |
5-Methoxy-2-benzimidazolethiol
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5-Methoxy-2-benzimidazolethiol 是一种有用的有机化合物,可用于生命科学领域的相关研究。其产品编号为 T67503,CAS号为 37052-78-1。 | |||
T1141 |
Fenbendazole
Fenbendazol,苯硫咪唑,芬苯达唑,Phenbendasol,Panacur |
Others; HIF/HIF Prolyl-Hydroxylase; Antibiotic; Parasite | Chromatin/Epigenetic; Metabolism; Microbiology/Virology; Others |
Fenbendazole (Fenbendazol) 是一种广谱苯并咪唑类驱虫剂,对胃肠寄生虫有效。 | |||
T6944 |
Thiophanate-Methyl
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Antifungal | Microbiology/Virology |
Thiophanate-Methyl 是一种甲基苯并咪唑氨基甲酸酯杀菌剂。 | |||
T0714 |
Oxfendazole
奥吩达唑,奥芬哒唑,RS-8858 |
Glucokinase; Microtubule Associated; Parasite | Cytoskeletal Signaling; Metabolism; Microbiology/Virology |
Oxfendazole (RS-8858) 是fenbendazole 的亚砜形式,是广谱苯并咪唑驱虫剂,可保护牲畜免受蛔虫、圆线虫和蛲虫的侵害。 | |||
T61107 |
Tilomisole
Wy 18251 |
Others | Others |
Tilomisole (Wy 18251) 是一种可口服的苯并咪唑噻唑,具有抗炎活性和免疫调节活性。Tilomisole 可用于研究癌症和炎症。 | |||
T4057 |
Hoechst 33258 trihydrochloride
Hoechst 33258,Pibenzimol,Bisbenzimide,H 33258 trihydrochloride,bisBenzimide H 33258 trihydrochloride,HOE 33258 |
Parasite | Microbiology/Virology |
Hoechst 33258 trihydrochloride (Bisbenzimide) 是一种能够用于 DNA 染色的荧光染料。 | |||
T6623 |
Oxibendazole
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Apoptosis; Parasite | Apoptosis; Microbiology/Virology |
Oxibendazole 是一种苯并咪唑驱虫药,用于防止马和一些家养宠物的蛔虫、圆线虫、线虫、蛲虫和肺虫感染。。它可诱导细胞凋亡,具有抗癌和抗炎活性。 | |||
T73577 |
TJ08
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Apoptosis | Apoptosis |
TJ08 是一种具有抗癌的1,2,5-三取代苯并咪唑衍生物,能够有效诱导G1/S期阻滞,同时促进多种癌细胞的凋亡作用。 | |||
T5840 |
Hoechst 33342
赫斯特荧光染料 33342,HOE 33342,bisBenzimide H 33342 |
Autophagy | Autophagy |
Hoechst 33342 (bisBenzimide H 33342) 是苯并咪唑荧光染料和细胞可渗透荧光 DNA 染料。 | |||
T2162 |
Maribavir
BW1263W94,GW257406X,Benzimidavir,马立巴韦,1263W94 |
Others; HCV Protease | Microbiology/Virology; Others; Proteases/Proteasome |
Maribavir (GW257406X) 是一种可口服的苯并咪唑核苷化合物,具有抗巨细胞病毒的活性。 | |||
T17006 |
TC-I 2014
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TRP/TRPV Channel | Membrane transporter/Ion channel |
TC-I 2014 是一种口服有效的、强效的、苯并咪唑类的、 TRPM8 的拮抗剂,其对犬类、人和大鼠通道的 IC50 值分别为 0.8 nM, 3.0 nM 和 4.4 nM。在疼痛动物模型中具有抗痛觉超敏作用。 | |||
T1021 |
(R)-Lansoprazole
Dexlansoprazole,右旋兰索拉唑,T 168390,TAK 390,R-(+)-Lansoprazole |
Proton pump | Membrane transporter/Ion channel |
(R)-Lansoprazole (T 168390) 是Lansoprazole 的R 型异构体。Lansoprazole 是口服有效的质子泵抑制剂,能抑制胃酸生成。Lansoprazole 是中性鞘磷脂酶(N-SMase)的抑制剂(外泌体抑制剂),能透过血脑屏障。 | |||
T6929 |
Pantoprazole sodium
Pantecta,泮托拉唑钠盐,SKF96022 sodium,SKF96022 (sodium),BY1023 (sodium),泮托拉唑钠,BY-1023 sodium,Pantoloc |
Apoptosis; Others; Proton pump; HIF; Autophagy | Angiogenesis; Apoptosis; Autophagy; Chromatin/Epigenetic; Membrane transporter/Ion channel; Others |
Pantoprazole sodium (Pantecta) 是一种具有口服活性的质子泵抑制剂,是一种取代的苯并咪唑,是H+/K+-ATPase 抑制剂,IC50为 6.8 μM。它可以改善 pH 值稳定性,具有抗分泌和抗溃疡的作用。它联合阿霉素可显著增加肿瘤生长延迟。 | |||
T1756 |
Ilaprazole sodium
IY-81149 sodium,艾普拉唑钠 |
Proton pump; TOPK | MAPK; Membrane transporter/Ion channel |
Ilaprazole sodium (IY-81149 sodium) 是一种具有口服活性质子泵抑制剂,以剂量依赖性方式不可逆地抑制 H+/K+-ATPase,在兔壁细胞制剂中的 IC50为 6 μM。它也是一种有效的 T 细胞起源蛋白激酶(TOPK)抑制剂,用于胃溃疡的研究。 | |||
T38361 |
GSK717
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IL Receptor; NOD | Immunology/Inflammation; NF-κB |
GSK717 是 NOD2(核苷酸结合寡聚结构域 2) 的选择性抑制剂。它抑制壁酰二肽 (MDP) 诱导的 NOD2 介导的信号转导,抑制 MDP 刺激的 HEK293/hNOD2 细胞分泌 IL-8 (IC50为 400 nM)。 | |||
T27484 |
GSK579289A
GSK-579289A,GSK 579289A |
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GSK579289A is an inhibitor of benzimidazole thiophene. | |||
T26813 |
BI-L 45XX
BI-L-45 XX,BI L 45 XX,BIL45XX |
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BI-L 45XX, an anti-inflammatory benzimidazole derivative, has inhibitory effects on neutrophil function. | |||
T3124L |
Carbendazim HCl
Lignasan,Carbendazim hydrochloride,Sandomil P |
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Carbendazim HCl is a widely used, broad-spectrum benzimidazole fungicide and a metabolite of benomyl. | |||
T60448 | Diethofencarb | ||
Diethofencarb 是对 Botrytis cinerea 和耐 Benzimidazole 的 Botryis spp 具有高度活性的杀菌剂,用作抗真菌作用。 | |||
T20960 |
Luxabendazole
HOE 216V |
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Luxabendazole is a benzimidazole carbamate broad-spectrum anthelmintic agent. It has proved to be effective against immature and adult stages of the major gastrointestinal nematodes, cestodes, and trematodes. | |||
T26957 |
CAY10575
CAY-10575,CAY 10575 |
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CAY10575, a benzimidazole analog IKK-ε inhibitor, inhibits IKK-ε with an IC50 value of ~15.8 µM. | |||
T30538 |
BMS-695735
CHEMBL459729,DNC008930,BMS 695735,BMS695735,BDBM27888 |
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BMS-695735, a benzimidazole inhibitor of insulin-like growth factor-1 receptor, has broad-spectrum antitumor activity in vivo. It was found that BMS-695735 had strong inhibition of CYP3A4, induction of CYP3A4 mediated by PXR transactivation, poor water so | |||
T25716L |
Liarozole HCl
R75251,Liarozole hydrochloride,R 75251,R-75251 |
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Liarozole HCl is a benzimidazole derivative with antineoplastic activity. As a retinoic acid metabolism blocking agent, liarozole inhibits CYP450-dependent all-trans-retinoic acid (ATRA)-4-hydroxylase, leading to an increase in endogenous ATRA production, | |||
T62967 | Anti-inflammatory agent 10 | ||
Anti-inflammatory agent 10 是一种基于 tilomisole 的苯并咪唑噻唑衍生物,口服具有活性。Anti-inflammatory agent 10 对 COX-2 酶的活性比 COX-1 高。 | |||
T63601 | PAD2-IN-1 hydrochloride | ||
PAD2-IN-1 hydrochloride 是有效的、选择性的蛋白精氨酸脱亚氨酶 2 (PAD2) 抑制剂,且对 PAD2 的选择性优于 PAD4 (95 倍) 和 PAD3 (79 倍),是一种基于苯并咪唑的衍生物。 | |||
T39515 |
PAD2-IN-1
PAD2-IN-1 |
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PAD2-IN-1, a benzimidazole-based derivative, is an efficacious and specific inhibitor of protein arginine deiminase 2 (PAD2). Demonstrating remarkable selectivity, PAD2-IN-1 exhibits a 95-fold higher affinity for PAD2 in comparison to PAD4 and a 79-fold higher affinity than PAD3. | |||
T72812 |
(R)-Tegoprazan
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(R)-Tegoprazan (example 3) 是一种苯并咪唑衍生物,是一种有效的胃H+/K+-ATP 酶抑制剂,对犬肾 Na+/K+-ATPase 的IC50为 98 nM。(R)-Tegoprazan 具有胃肠道疾病研究的潜力。 | |||
T79858 |
TIE-2/VEGFR-2 kinase-IN-3
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TIE-2/VEGFR-2 kinase-IN-3,为苯并咪唑衍生物,具备高效的抑制作用于TIE-2与VEGFR-2受体酪氨酸激酶,其IC50值分别达到6.9 nM和3.5 nM。本化合物主要用于血管生成相关研究。 | |||
T63023 | PTP1B-IN-19 | ||
PTP1B-IN-19 (Compound 43) 是一种有潜力的选择性苯并咪唑衍生物,能够作为蛋白质酪氨酸磷酸酶 1B (PTP1B) 抑制剂 (Ki: 23.3 μM)。PTP1B-IN-17 能够用于研究 2 型糖尿病。 | |||
T79859 |
TIE-2/VEGFR-2 kinase-IN-4
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TIE-2/VEGFR-2 kinase-IN-4,一种苯并咪唑衍生物,作为有效的TIE-2和VEGFR-2酪氨酸激酶受体抑制剂,其IC50值分别为5.2 nM和5.1 nM,适用于血管生成相关研究。 | |||
T63435 | PTP1B-IN-16 | ||
PTP1B-IN-16 是有潜力的、选择性的苯并咪唑衍生物,也是一种蛋白质酪氨酸磷酸酶 1B (PTP1B) 抑制剂 (Ki: 12.6 μM)。PTP1B-IN-16 能够用于研究 2 型糖尿病。 | |||
T63021 |
PTP1B-IN-17
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PTP1B-IN-17 (Compound 45) 是一种有潜力的选择性苯并咪唑衍生物,能够作为蛋白质酪氨酸磷酸酶 1B (PTP1B) 抑制剂 (Ki: 30.2 μM)。PTP1B-IN-17 能够用于研究 2 型糖尿病。 | |||
T74845 | Antimalarial agent 23 | ||
Antimalarial agent 23,一种苯并咪唑抗疟药,对PfNF54和PfK1的IC50值均显示出良好的活性,分别为0.08 μM和0.10 μM。该化合物展现了有效的β-血红素抑制活性,但并不直接抑制血红素向疟原虫色素的转化。 | |||
T68225 |
Fc 11a-2
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Fc 11a-2 是一种苯并咪唑化合物,一种具有口服活性且有效的NLRP3炎症小体 (NLRP3inflammasome) 抑制剂。Fc 11a-2 通过抑制caspase-1的激活进而抑制 IL-1b/IL-18 的激活来抑制NLRP3炎性体的形成。Fc 11a-2 可防止Dextran sulfate sodium(DSS) 诱导的小鼠实验性结肠炎。 | |||
T79088 | Chlamydia pneumoniae-IN-1 | ||
Chlamydia pneumoniae-IN-1 (compound 55),一种抗衣原体的苯并咪唑类化合物,对肺炎衣原体具有高度抑制作用,在10 μM 浓度下能够抑制99%的肺炎衣原体生长,并对宿主细胞的活力产生95%的抑制效果。此外,Chlamydia pneumoniae-IN-1 对CV-6菌株亦显示出明显的抗菌活性,其最小抑菌浓度(MIC)为12.6 μM。 | |||
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 |
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T0938 |
Thiabendazole
2-(4-Thiazolyl)benzimidazole,噻菌灵 |
Microtubule Associated; Mitochondrial Metabolism; Parasite | Cytoskeletal Signaling; Metabolism; Microbiology/Virology |
Thiabendazole (2-(4-Thiazolyl)benzimidazole) 是具有驱虫特性的苯并咪唑衍生物。 |