465
43
47
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T41244 |
Triticonazole
|
Antifungal | Microbiology/Virology |
Triticonazole 是一种三唑类农药。它具有杀菌和干扰内分泌作用。 | |||
T11991 |
Mefentrifluconazole
|
P450; Antifungal | Metabolism; Microbiology/Virology |
Mefentrifluconazole 是一种有效的、选择性的和具有口服活性的真菌 CYP51 (Kd= 0.5 nM) 抑制剂,但对人芳香酶的抑制活性较低,IC50值为0.92 μM。它是一种新型唑类衍生物,用作农用广谱抗真菌剂。 | |||
T0195 |
Secnidazole
RP-14539,PM-185184,塞克硝唑 |
Antibiotic; Parasite | Microbiology/Virology |
Secnidazole (PM-185184) 是一种具有口服活性唑类抗生素,半衰期比甲硝唑更长。它有潜力研究细菌性阴道病。 | |||
T22636 |
Phenyl-benzothiazole
2-(p-Aminophenyl)-6-methylbenzothiazole,4-(6-methyl-1,3-benzothiazol-2-yl)aniline,2-(4-Aminophenyl)-6-methylbenzothiazole,Dehydrothio-p-toluidine,2-(4-氨基苯基)-6-甲基苯并噻唑 |
Others | Others |
Phenyl-benzothiazole (2-(4-Aminophenyl)-6-methylbenzothiazole) 是一种用于蛋白质组学研究的唑类。 | |||
T6550 |
Isoconazole nitrate
硝酸异康唑,Travogyn,Fazol |
Antibacterial; Antibiotic; Antifungal | Microbiology/Virology |
Isoconazole nitrate (Fazol) 是一种唑类抗真菌试剂。它具有强效的抗真菌和革兰氏阳性菌的活性,以及快速吸收和系统性暴露低的特点。 | |||
T6499 |
Fenticonazole Nitrate
REC 15-1476,硝酸芬替康唑,Falvin,Lomexin |
Antibiotic; Antifungal | Microbiology/Virology |
Fenticonazole Nitrate (Lomexin) 是一种抗真菌的咪唑环衍生物。它阻止麦角固醇整合和依次破坏细胞质外膜起作用。它对革兰氏阳性菌,真菌病和阴道念珠菌病有效。 | |||
T2333 |
Efinaconazole
KP-103,艾氟康唑 |
Antifungal | Microbiology/Virology |
Efinaconazole (KP-103) 是一种三唑类抗真菌剂,抑制T. mentagrophytesSM-110和C. albicansATCC 10231菌株的MIC 值分别为 0.0039 μg/mL 和 0.00098 μg/mL | |||
T2411 |
Luliconazole
NND 502,卢立康唑 |
Antibiotic; Antifungal | Microbiology/Virology |
Luliconazole (NND 502) 是一种咪唑类抗生素,具有广谱抗真菌活性。它可研究皮肤感染。 | |||
T7824 |
Eberconazole Nitrate
硝酸依柏康唑,Ebernet |
Antifungal | Microbiology/Virology |
Eberconazole Nitrate (Ebernet) 是一种二氯咪唑衍生物,具有抗真菌活性,效果比Ketoconazole、Clotrimazole 和Miconazole 强。它通过局部给药对皮肤癣菌病具有潜在的研究价值。 | |||
T17022 |
Tebuconazole
|
P450; Antifungal | Metabolism; Microbiology/Virology |
Tebuconazole 是一种农用唑类杀菌剂,可抑制 CYP51,对白色念珠菌 CYP51 和truncated Homo sapiens CYP51 的IC50分别为 0.9 和 1.3 μM。 | |||
T2305 |
Isavuconazole
艾沙康唑,BAL-4815,RO-0094815 |
P450; Antibiotic; Antifungal | Metabolism; Microbiology/Virology |
Isavuconazole (RO-0094815) 是一种三唑类前药,对酵母、霉菌和二型真菌具有抗真菌活性。它抑制麦角固醇生物合成,导致真菌膜结构和功能的破坏。它是 CYP3A4抑制剂。 | |||
T1290 |
Oxiconazole nitrate
硝酸奥昔康唑,Ro 13-8996 |
Others; Antibiotic; Antifection; Antifungal | Microbiology/Virology; Others |
Oxiconazole nitrate (Ro 13-8996) 是广谱抗真菌药物,抑制T. tonsurans 和T.rubrum 的生长,MIC90值分别为 0.25 和 0.5 μg/mL。 | |||
T31362 |
Deferitazole
SPD602,FBS 0701,SPD-602,FBS0701,FBS-0701,SPD 602 |
Others | Others |
Deferitazole (FBS 0701) 是一种新型且具有口服活性、选择性和高亲和力的铁螯合剂。 | |||
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。 | |||
T0952 |
Carbimazole
卡比马唑,Athyromazole,卡比吗唑,Carbimazol,Neomercazole |
Thyroid hormone receptor(THR) | Endocrinology/Hormones |
Carbimazole (Athyromazole) 是咪唑类甲状腺拮抗试剂,在体内快速转化为 MMI 而发挥作用,在体外可转化为甲咪唑,可用于 Graves 病的研究。 | |||
T1187 |
Bifonazole
联苯苄唑,Bay H-4502 |
P450; Antibiotic; Antifungal | Metabolism; Microbiology/Virology |
Bifonazole (Bay H-4502) 是咪唑类抗真菌剂。 | |||
T2687 |
Omeprazole sulfide
Omeprazole metabolite Omeprazole sulfide,Ufiprazole,奥美拉唑硫醚 |
Proton pump; Drug Metabolite | Membrane transporter/Ion channel; Metabolism |
Omeprazole sulfide (Ufiprazole) 是 Omeprazole 的代谢物。 | |||
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。 | |||
T5328 |
Fosfluconazole
|
Antifungal | Microbiology/Virology |
Fosfluconazole 是 fluconazole 的水溶性磷酸盐前药。 它是一种抗真菌药物。 | |||
T0575 |
1-Methylimidazole
|
Others | Others |
1-Methylimidazole 是1-methyl-2-thioimidazole (methimazole)的代谢物,可抑制骨吸收。 | |||
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。 | |||
TQ0128 |
Furilazole
MON 13900,解草恶唑 |
Others | Others |
Furilazole (MON 13900) 是一种农药剂。 | |||
T19826 |
Rabeprazole
LY307640 |
Potassium Channel; STAT | JAK/STAT signaling; Membrane transporter/Ion channel; Stem Cells |
Rabeprazole (LY307640) 是一种 H+/K+-ATPase 抑制剂,通过靶向 STAT3 介导的糖酵解来抑制胃上皮细胞中的细胞增殖,可用于研究胃溃疡。 | |||
T61148 |
Flutrimazole
|
Antifungal | Microbiology/Virology |
Flutrimazole是一种具有双重作用的咪唑类抗真菌化合物,展现出抗炎和抗真菌的属性。值得注意的是,flutrimazole的经皮渗透性有限,这使其在治疗伴有炎症的真菌感染的局部应用中特别有优势。 | |||
T11013L2 |
Levorotation nimorazole phosphate ester TFA
|
Others | Others |
Levorotation nimorazole phosphate ester TFA 是一种抗厌氧菌和抗原虫感染的试剂。 | |||
T1647 |
Ronidazole
洛硝哒唑,Ronidazol,罗硝唑,Ridzol |
Antibacterial; Antibiotic; Parasite | Microbiology/Virology |
Ronidazole (Ronidazol) 是一种口服有效的抗原虫和抗菌试剂。它在猫模型中对胎儿三毛滴虫有效,还可研究组织口癣和猪痢疾。 | |||
T0644 |
3-Amino-5-methylisoxazole
|
Others | Others |
3-Amino-5-methylisoxazole 是医药中间体,用于生产磺胺类药物。 | |||
T14871 |
Carboxyamidotriazole Orotate
L-651582 Orotate,CAI Orotate |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Carboxyamidotriazole Orotate (L-651582 Orotate) 是一种可口服的信号转导抑制剂,是Carboxyamidotriazole (CAI) 的乳清酸盐形式。它是一种非电压性钙通道和钙通道介导的信号通路的细胞抑制剂,具有抗癌、抗炎活性和抗血管生成作用。 | |||
T4985 |
Neticonazole Hydrochloride
|
Antifungal | Microbiology/Virology |
Neticonazole hydrochloride 是一种咪唑衍生物,具有抗感染和抗癌作用。它也是一种长效抗真菌剂。 | |||
T5966 |
Hexaconazole
己唑醇,(-)-Hexaconazol |
Reactive Oxygen Species; Antifungal | Immunology/Inflammation; Metabolism; Microbiology/Virology; NF-κB |
Hexaconazole ((-)-Hexaconazol) 是一种广谱三唑类杀菌剂,通过抑制羊毛甾醇的细胞色素 P450 依赖性 14α-去甲基化来抑制麦角甾醇的生物合成,从而导致真菌细胞膜的破坏和细胞死亡。 | |||
T20714 |
Levolansoprazole
左旋兰索拉唑,(S)-Lansoprazole,(-)-Lansoprazole |
Proton pump | Membrane transporter/Ion channel |
Levolansoprazole ((S)-Lansoprazole) 是一种质子泵抑制剂,不可逆地抑制壁细胞中 H+/K+ 刺激的 ATPase 泵 (IC50: 5.2 µM)。它还抑制分离的犬壁细胞中的酸形成(IC50:82 µM)。 (R)-和 (S)-兰索拉唑均具有药理活性,具有相似的效力。 | |||
T1756L |
Ilaprazole
IY81149,艾普拉唑,IY 81149,IY-81149 |
Proton pump; TOPK | MAPK; Membrane transporter/Ion channel |
Ilaprazole (IY-81149) 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。 | |||
T15033 |
Cyproconazole
|
Antibacterial | Microbiology/Virology |
Cyproconazole 是一种三唑类杀菌剂,在农业上用于保护作物免受多种真菌病原体的侵害。 | |||
T2686 |
Esomeprazole Magnesium
(S)-Omeprazole magnesium,NEXIUM,埃索美拉唑镁,(-)-Omeprazole magnesium |
ATPase; Proton pump | Membrane transporter/Ion channel |
Esomeprazole Magnesium (NEXIUM) 是一种口服有效的 H+, K+-ATPase 抑制剂,在上消化道疾病和胃食管反流疾病中具有研究价值。Esomeprazole magnesium 是一种外泌体抑制剂,通过抑制 V-H+-ATPases 来阻断外泌体的释放。 | |||
T0444L |
Econazole nitrate
NSC 243115,硝酸益康唑 |
Antibacterial; Antibiotic; Antifection; Antifungal | Microbiology/Virology |
Econazole nitrate (NSC-243115) 是一种有抗菌活性的咪唑类抗真菌药物。 | |||
T1438 |
Butoconazole nitrate
RS 35887,硝酸布康唑 |
Estrogen/progestogen Receptor; Antifungal | Endocrinology/Hormones; Microbiology/Virology |
Butoconazole nitrate (RS 35887) 是一种咪唑类抗真菌药物,可治疗由白色念珠菌引起的阴道感染。它可通过抑制类固醇合成起到抗菌作用。 | |||
T12096L |
Morinidazole
|
Antibacterial | Microbiology/Virology |
Morinidazole 具有抗菌活性,可用于厌氧菌引起的阑尾炎、盆腔炎等细菌感染研究。 | |||
T19673 |
Fuberidazole
|
Antifungal | Microbiology/Virology |
Fuberidazole 是一种抗真菌剂。 | |||
T67498 |
3-Amino-1,2,4-triazole
Amitrole,3-AT,1H-1,2,4-Triazol-5-amine,Trapidil impurity B |
Reactive Oxygen Species | Immunology/Inflammation; Metabolism; NF-κB |
3-Amino-1,2,4-triazole (Trapidil impurity B) 是一种过氧化氢酶抑制剂,能够诱导过氧化氢解毒的补偿机制。 该机制涉及增加谷胱甘肽过氧化物酶和谷胱甘肽还原酶的活性。 | |||
T21022 |
Deacylketoconazole
Deacyl ketoconazole,脱乙酰酮康唑 |
Antifungal | Microbiology/Virology |
Deacylketoconazole (Deacyl ketoconazole) 是一种酮康唑衍生物,也是一种抗真菌剂。 脱酰基酮康唑对恶性疟原虫的活性是酮康唑的 15 至 50 倍。 | |||
T25982 |
Pramiconazole
R-126638,R126638,R 126638,Azoline |
Antifungal | Microbiology/Virology |
Pramiconazole (R126638) 是一种可口服的抗真菌化合物。Pramiconazole 是治疗皮肤癣菌和皮肤酵母菌感染的候选化合物,可用于治疗脂溢性皮炎。 | |||
T10138 |
4-Desmethoxy Omeprazole
|
Drug Metabolite | Metabolism |
4-Desmethoxy Omeprazole 是 Omeprazole 的活性代谢物。Omeprazole 是质子泵抑制剂。Omeprazole 竞争性抑制 CYP2C19 活性,Ki=2 - 6 μM。Omeprazole 还抑制革兰氏阴性菌和革兰氏阳性菌生长。 | |||
T0874 |
Dimetridazole
1, 2-Dimethyl-5-nitroimidazole,1,2-Dimethyl-5-nitroimidazole,二甲硝咪唑 |
Antibiotic; Parasite | Microbiology/Virology |
Dimetridazole (1, 2-Dimethyl-5-nitroimidazole) 是一种对抗原生动物感染的硝基咪唑类药物。 | |||
T14319 |
Aripiprazole Lauroxil
|
Dopamine Receptor; 5-HT Receptor | GPCR/G Protein; Neuroscience |
Aripiprazole lauroxil 是一种长效注射剂 (LAI) 的抗精神病药物,是阿立哌唑的 N-酰氧基甲基前药形式。它能够被体内酯酶裂解为 N-羟甲基阿立哌唑(月桂酸),再裂解为阿立哌唑,无毒性。 | |||
T3445 |
Importazole
|
Apoptosis; Others | Apoptosis; Others |
Importazole 是一种核转运受体 importin-β 小分子抑制剂。 | |||
T7474 |
7-Nitroindazole
|
NOS | Immunology/Inflammation |
7-Nitroindazole 是一种具有抗损伤及心血管作用的选择性nNOS 抑制剂,也是评价一氧化氮在中枢神经系统中生物学效应的有效工具。 | |||
T28174 |
Niridazole
BA32644,BA-32644,Ambilhar,BA 32644 |
Others | Others |
Niridazole (Ambilhar) 是一种具有抗寄生虫活性的化合物,属于硝基咪唑类化合物。Niridazole 主要用于治疗血吸虫病,通过干扰寄生虫的新陈代谢,导致其死亡。Niridazole 在寄生虫体内迅速集中,抑制卵子和精子的发生,抑制磷酸果糖激酶活性。 | |||
T16536 |
Pimonidazole hydrochloride
|
Others | Others |
Pimonidazole hydrochloride 通过与大分子共价结合或在其硝基还原后形成还原性代谢物在缺氧细胞中积累。 可用于肿瘤缺氧的定性和定量评估。 它是一种新型的缺氧标志物,用于肿瘤缺氧和肿瘤细胞增殖的互补研究。 | |||
T50032 |
5-(2-furyl)-N-propylisoxazole-3-carboxamide
|
Others | Others |
5-(2-furyl)-N-propylisoxazole-3-carboxamide 是一种用作分子结构单元的化合物,被认为是 NMDA 受体的调节剂,已被证明对神经元细胞中谷氨酸诱导的兴奋性毒性和氧化应激具有保护作用。它也被发现具有抗炎活性,使其成为阿尔茨海默病和帕金森病等疾病的潜在治疗剂。 | |||
T1369 |
1-Methylindazole-3-carboxylic acid
|
Others | Others |
1-Methylindazole-3-carboxylic acid 是一种具有适当沸点的优良溶剂。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T21651 |
Lansoprazole sodium
兰索拉唑钠,Lansoprazole (sodium), AG-1749 sodium |
Proton pump; Phospholipase; Antibacterial | Membrane transporter/Ion channel; Metabolism; Microbiology/Virology |
Lansoprazole sodium (Lansoprazole (sodium)) 是一种质子泵抑制剂,是中性鞘磷脂酶的外泌体抑制剂,能抑制胃酸生成。 | |||
T19856 |
2-Mercaptobenzothiazole
Mercaptobenzothiazole,Dermacid,2-巯基苯并噻唑,Captax |
Others; Endogenous Metabolite | Metabolism; Others |
2-Mercaptobenzothiazole (Captax) 是内源性代谢产物的一种。 | |||
T0344L |
Miconazole nitrate
NSC 169434 Nitrate,硝酸咪康唑,R18134 nitrate |
Antibacterial; Antibiotic; Antifungal | Microbiology/Virology |
Miconazole nitrate (R18134 nitrate) 是咪唑类可抗菌的抗真菌剂。 | |||
T4842 |
1H-pyrazole
1,2-Diazole,Pyrazole,吡唑 |
Others; Endogenous Metabolite | Metabolism; Others |
1H-pyrazole (1,2-Diazole) 是内源性代谢产物的一种。 | |||
T7132 |
(Rac)-Brassinazole
BRASSINAZOLE,3-(4-氯苯基)-1-甲基-1-苯基-2-(1,2,4-三唑-1-基)-1-丙醇,(Rac)-芸苔素唑 |
P450 | Metabolism |
(Rac)-Brassinazole 是三唑型化合物,是油菜素甾醇 (BR) 生物合成抑制剂。它能够增强 CYP90B 在 BR 生物合成中的抑制作用。 | |||
T0444 |
Econazole
(±)-Econazol,益康唑 |
Antibiotic; Antifection; Antifungal | Microbiology/Virology |
Econazole ((±)-Econazol) 是一种咪唑衍生物,是一种抗真菌剂。 | |||
TN7167 |
2,4,5-Tribromoimidazole
2,4,5-三溴咪唑,2,4,5-Tribromo-1H-imidazole |
Others | Others |
2,4,5-Tribromoimidazole (2,4,5-Tribromo-1H-imidazole) 是一种海洋来源的天然产物,存在于 Hexaplex trunculus。 | |||
TN7165 |
3,6-Dibromocarbazole
3,6-Dibromo-9H-carbazole,3,6二溴咔唑 |
Others | Others |
3,6-Dibromocarbazole (3,6-Dibromo-9H-carbazole) 是一种海洋来源的天然产物,存在于Kyrtuthrix maculans。 | |||
T40807 |
1,3-Dimethylpyrazole
1,3-Dimethyl-1H-pyrazole,2,5-Dimethylpyrazole |
Others | Others |
1,3-Dimethylpyrazole (2,5-Dimethylpyrazole) 是一种存在于毛竹根的生物活性物质。 | |||
TN7176 |
1,3,5-Trimethyl-1H-Pyrazole-4-Carboxylic Acid
MFCD00159648,1,3,5-trimethylpyrazole-4-carboxylic acid,trimethyl-1H-pyrazole-4-carboxylic acid,1,3,5-三甲基-1H-吡唑-4-甲酸 |
Others | Others |
1,3,5-Trimethyl-1H-Pyrazole-4-Carboxylic Acid (1,3,5-trimethylpyrazole-4-carboxylic acid) 是一种海洋来源的天然产物,存在于Cinachyrella sp.。 | |||
T64343 |
3-Methylcarbazole
NSC 10154 |
Others | Others |
3-Methylcarbazole (NSC-10154) 是具有抗癌作用的咔唑生物碱化合物。3-Methylcarbazole 对人纤维肉瘤 HT-1080 细胞具有生长抑制活性 (IC50 为 25 μg/mL)。 | |||
T1079 |
Metronidazole
Flagyl,Metronidazol,甲硝唑,Anagiardil |
Apoptosis; NADPH; Hydrogenase; Antibacterial; Antibiotic; Parasite; Antifection | Apoptosis; Metabolism; Microbiology/Virology |
Metronidazole (Metronidazol) 是一种合成的硝基咪唑衍生物,一种抗生素和抗原虫剂,具有口服活性和血脑屏障渗透性。Metronidazole 可用于治疗或预防厌氧菌引起的系统或局部感染。 | |||
T1155 |
Mebendazole
甲苯达唑,甲苯咪唑,Telmin,Mebenvet,Vermox,Pantelmin |
Apoptosis; Microtubule Associated; Parasite | Apoptosis; Cytoskeletal Signaling; Microbiology/Virology |
Mebendazole (Mebenvet) 是一种 hedgehog 抑制剂,用作驱虫药。 | |||
TN7164 |
2,7-Dibromo-9H-Carbazole
2,7-Dibromocarbazole,2,7-二溴咔唑 |
Others | Others |
2,7-Dibromo-9H-Carbazole (2,7-Dibromocarbazole) 是一种海洋来源的天然产物,存在于Kyrtuthrix maculans。 | |||
T1152 |
Albendazole
SKF-62979,阿苯达唑 |
HIF/HIF Prolyl-Hydroxylase; Microtubule Associated; Antibiotic; Parasite | Chromatin/Epigenetic; Cytoskeletal Signaling; Metabolism; Microbiology/Virology |
Albendazole (SKF-62979) 是一种广谱抗寄生虫剂,具有高效,低宿主毒性的特点。 它用于研究人类和动物的胃肠道寄生虫。 | |||
T1705 |
5-Amino-3H-imidazole-4-Carboxamide
4-Amino-5-imidazolecarboxamide,AICA,4-氨基-5-咪唑甲酰胺,5-Aminoimidazole-4-carboxamide |
Endogenous Metabolite | Metabolism |
5-Amino-3H-imidazole-4-Carboxamide (AICA) 是一种合成嘌呤(尤其是核碱基腺嘌呤和鸟嘌呤)的重要前体。 | |||
TN7203 |
9H-Carbazole, 1-methyl-
1-甲基咔唑,1-Methyl-carbazole,1-Methyl-9H-carbazole,1-methyl carbazole |
Others | Others |
9H-Carbazole, 1-methyl- (1-methyl carbazole)是一种海洋来源的天然产物,存在于Tedania (Tedania) ignis。 | |||
T1011 |
Itraconazole
伊曲康唑,R51211 |
P450; Hedgehog/Smoothened; Antibiotic; Autophagy; Antifungal | Autophagy; GPCR/G Protein; Metabolism; Microbiology/Virology; Stem Cells |
Itraconazole (R51211) 属于三唑类天然产物,是一种抗真菌剂,具有口服活性。Itraconazole 是一种 Hedgehog 信号通路拮抗剂,一种 oxysterol-binding protein (OSBP) 抑制剂,也是一种细胞色素 P-450 依赖性酶的抑制剂。 | |||
T0146 |
Tioconazole
UK-20349,Vagistat,噻康唑 |
Antibiotic; Antifection; Antifungal | Microbiology/Virology |
Tioconazole (Vagistat) 是一种广谱性的抗真菌咪唑衍生物。它抑制几种皮肤真菌和几种酵母菌的 MIC50分别小于 3.12 mg/L 和 9 mg/L。 | |||
T1556 |
Ornidazole
Tiberal,Ornidazolum,NSC 95075,Ro 7-0207,奥硝唑 |
Antibacterial; Antibiotic; Parasite | Microbiology/Virology |
Ornidazole (Tiberal) 是一种5-硝基咪唑衍生物,能抗原生动物和厌氧菌。 | |||
T1388 |
Fluconazole
氟康唑,UK-49858 |
Antibiotic; Antifection; Antifungal | Microbiology/Virology |
Fluconazole (UK-49858) 是一种对多种真菌具有活性的三唑类抗真菌剂,抑制 C. albicans 和 Candida kefyr 的 IC99为 0.20 μg/mL 至 0.39 μg/mL。 | |||
TN7175 |
9H-Carbazole, 3,6-diiodo-
3,6-Diiodo-9H-carbazole,3,6-diiodocarbazole,3,6-二碘-9H-咔唑 |
Others | Others |
9H-Carbazole, 3,6-diiodo- (3,6-diiodocarbazole)是一种海洋来源的天然产物,存在于Kyrtuthrix maculans。 | |||
T5202 |
Imidazole
Glyoxaline,1,3-Diaza-2,4-cyclopentadiene,1,3-diazole,咪唑 |
Others | Others |
Imidazole 是一种高极性化合物,是一种平面五元环,已被广泛用作腐蚀抑制剂。 | |||
T8042 |
2-Acetylthiazole
2-Acetylthiazole;2 Acetylthiazole,2-Acetylthiazole,2-Thiazolyl methyl ketone,2 Acetylthiazole,1-(2-Thiazolyl)ethanone |
Others | Others |
2-Acetylthiazole (2-Acetylthiazole;2 Acetylthiazole) 用于制备手性醇、三唑并噻唑,也用于羟醛缩合反应。 | |||
T4753 |
Imidazoleacetic acid hydrochloride
I4AA,(4-Imidazolyl)acetic acid hydrochloride,4-咪唑乙酸盐酸盐,4-Imidazoleacetic acid hydrochloride |
Endogenous Metabolite; Antibiotic | Metabolism; Microbiology/Virology |
Imidazoleacetic acid hydrochloride (I4AA) 是咪唑衍生物,具有潜在的抗结核性能。它还用于制备β-分泌酶的酰基胍抑制剂。 | |||
T4824 |
5,6-Dimethyl-1H-benzo[d]imidazole
5,6-Dimethylbenzimidazole,5,6-二甲基苯并咪唑 |
Others; Endogenous Metabolite | Metabolism; Others |
5,6-Dimethyl-1H-benzo[d]imidazole (5,6-Dimethylbenzimidazole) 是内源性代谢产物的一种。 | |||
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。 | |||
TN6217 |
3-Formylcarbazole
|
||
3-Formylcarbazole 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN6217,CAS号为 51761-07-0。 | |||
TN6253 |
7-Hydroxy-1-methoxy-3-methylcarbazole
|
||
7-Hydroxy-1-methoxy-3-methylcarbazole 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN6253,CAS号为 107672-54-8。 | |||
T66965 |
4-Hydroxymethylpyrazole
|
Others | Others |
4-Hydroxymethylpyrazole 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 T66965,CAS号为 25222-43-9。 | |||
TN4529 |
Methyl 3-carbazolecarboxylate
|
||
Methyl 3-carbazolecarboxylate is a natural product from Micromelum sp. | |||
TN6210 |
N-Methoxy-3-formylcarbazole
|
||
N-Methoxy-3-formylcarbazole 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN6210,CAS号为 117592-01-5。 | |||
TN6194 |
1-Prenyl-2-methoxy-6-formyl-8-hydroxy-9H-carbazole
|
||
1-Prenyl-2-methoxy-6-formyl-8-hydroxy-9H-carbazole 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN6194,CAS号为 484678-79-7。 | |||
T38241 |
2-Aminoimidazole
|
Others | Others |
2-Aminoimidazole is a potent antibiofilm agent and adjuvant to antimicrobial treatments, which effectively disrupts bacterial self-protection mechanisms by inhibiting biofilm formation and genetically-encoded antibiotic resistance traits. Additionally, 2-Aminoimidazole acts as a weak noncompetitive inhibitor of human arginase I, with a Ki value of 3.6 mM[1][2][3]. | |||
T13464L |
(-)-Ketoconazole
(-)-R 41400,(-)-Ketoconazol |
Others | Others |
(-)-Ketoconazole is one of the enantiomer of Ketoconazole. Ketoconazole is a racemic mixture of two enantiomers. | |||
TN6190 |
N-Methoxy-3-hydroxymethylcarbazole
N-Methoxy-3-hydroxymethyl-9H-carbazole |
||
N-Methoxy-3-hydroxymethylcarbazole 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN6190,CAS号为 142768-49-8。 | |||
T81660 |
Nocarimidazole A
|
Others | Others |
Nocarimidazole A,一种来源于海洋放线菌Nocardiopsis的白色无定形固体生物碱,具紫外线活性。 | |||
TN5611 | Aflavazole | ||
Aflavazole displays significant antifeedant activity against the fungivorous beetle Carpophilus hemipterus. | |||
T13735 |
Imidazoleacetic acid
Imidazolyl-4-acetic acid |
Others | Others |
Imidazoleacetic acid, an endogenous ligand, stimulates imidazole receptors. | |||
T35949 |
4-Carboxypyrazole
|
Others | Others |
4-Carboxypyrazole is an endogenous metabolite. | |||
T13820 | Pi-Methylimidazoleacetic acid | Others | Others |
Pi-Methylimidazoleacetic acid is a potential neurotoxin. | |||
T7910 |
4-Methoxybenzaldehyde
大茴香醛,Anisaldehyde,p-Anisaldehyde,Anisic aldehyde,4-Anisaldehyde,4-甲氧基苯甲醛,P-Methoxybenzaldehyde |
Others; Endogenous Metabolite | Metabolism; Others |
4-Methoxybenzaldehyde (p-Anisaldehyde) 是一种天然存在的芳香酚类化合物,存在于许多植物物种中,包括辣根,茴香,八角茴香等。它是一种能够能的神经毒物,已经表现出致死亡率,吸引力和干扰宿主寻求的影响。 | |||
TN7560 |
PF-1163A
|
Others | Others |
PF-1163A, a depsipeptide antifungal compound isolated from Penicillium, blocks ergosterol synthesis with an IC50 of 12 ng/ml. This compound specifically inhibits the enzyme ERG25p, a C-4 methyl oxidase in the ergosterol biosynthetic pathway, leading to its antifungal activity. Notably, in Saccharomyces cerevisiae modified to express ERG biosynthesis genes, PF-1163A exhibits an inhibition concentration (MIC value) of 12.5 µg/ml against ERG25p, though strains overexpressing ERG25p show resistance.... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T11817 |
Lansoprazole Sulfide D4
|
Proton pump | Membrane transporter/Ion channel |
Lansoprazole Sulfide D4 is a deuterium labeled Lansoprazole Sulfide. Lansoprazole Sulfide is an orally active anti-TB (Mycobacterium tuberculosis) agent with IC50 values of 0.59 μM intracellularly and 0.46 μM in broth.Lansoprazole Sulfide is an active metabolite of the proton pump inhibitor Lansoprazole. | |||
T13031 |
Sulfamethoxazole-d4
Ro 4-2130 D4,磺胺甲恶唑 D4 |
Others | Others |
Sulfamethoxazole D4 is a deuterium labeled Sulfamethoxazole (Ro 4-2130). Sulfamethoxazole is a sulfonamide bacteriostatic antibiotic. | |||
T12523 |
Posaconazole-D5
SCH 56592-D5 |
Others | Others |
Posaconazole-D5, a deuterium-labeled variant of Posaconazole, is a second-generation, broad-spectrum triazole compound with antifungal activity. | |||
TMIH-0604 |
Voriconazole-d3
|
||
Voriconazole-d3 是 Voriconazole 的氘代化合物。Voriconazole 的 CAS 号为 137234-62-9。Voriconazole 是一种三唑类抗真菌剂,可抑制真菌麦角甾醇的生物合成。它特异性抑制由真菌细胞色素 P450 酶介导的 14-α-羊毛甾醇去甲基化作用 | |||
T11585 |
Hydroxy Itraconazole D8
R-63373 D8 |
Others | Others |
Hydroxy Itraconazole D8 is the deuterium-labeled Hydroxy Itraconazole. Hydroxy Itraconazole is an active metabolite of Itraconazole, which is a triazole antifungal agent. | |||
TMIH-0301 |
Levolansoprazole-d4
|
||
Levolansoprazole-d4 是 Levolansoprazole 的氘代化合物。Levolansoprazole 的 CAS 号为 138530-95-7。Levolansoprazole 是一种质子泵抑制剂,不可逆地抑制壁细胞中 H+/K+ 刺激的 ATPase 泵 (IC50: 5.2 µM)。它还抑制分离的犬壁细胞中的酸形成(IC50:82 µM)。 (R)-和 (S)-兰索拉唑均具有药理活性,具有相似的效力。 | |||
T12308 |
Omeprazole-d3
奥美拉挫 D3,H 16868 D3 |
Others | Others |
Omeprazole D3 is deuterium labeled Omeprazole. Omeprazole is a proton pump inhibitor (PPI) | |||
TMIJ-0020 |
Hydroxy Metronidazole-d4
|
||
Hydroxy Metronidazole-d4 是 Hydroxy Metronidazole 的氘代化合物。Hydroxy Metronidazole 的 CAS 号为 4812-40-2。Hydroxymetronidazole (Metronidazole OH) 是一种硝基咪唑化合物,作为甲硝唑的代谢产物。Hydroxymetronidazole 通常用于家禽研究,以研究细菌和原生动物疾病,以及研究猪痢疾和牛生殖器滴虫病。 | |||
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. | |||
TMIJ-0214 |
Itraconazole-d5
|
||
Itraconazole-d5 是 Itraconazole 的氘代化合物。Itraconazole 的 CAS 号为 84625-61-6。Itraconazole是三唑类抗真菌药,也是口服活性的Hedgehog信号通路拮抗剂,IC50约为 800 nM。它也是 oxysterol-binding protein抑制剂。它抑制羊毛甾醇 14α-脱甲基酶,从而抑制羊毛甾醇向麦角固醇的氧化转化。它有抗癌和抗血管作用。 | |||
TMIJ-0192 |
Pantoprazole-d6
|
||
Pantoprazole-d6 是 Pantoprazole 的氘代化合物。Pantoprazole 的 CAS 号为 102625-70-7。Pantoprazole 是一种质子泵抑制剂,用于短期治疗由胃食管反流病引起的食管糜烂和溃疡。它联合阿霉素可显著增加肿瘤生长延迟。它是一种取代的苯并咪唑,是H+/K+-ATPase抑制剂,可改善 pH 值稳定性,具有抗分泌和抗溃疡的作用。 | |||
TMIJ-0299 |
Metronidazole-hydroxy-d2
|
||
Metronidazole-hydroxy-d2 是 Metronidazole-hydroxy 的氘代化合物。Metronidazole-hydroxy 的 CAS 号为 4812-40-2。 | |||
TMIJ-0484 |
Thiabendazole NH-d6
|
||
Thiabendazole NH-d6 是 Thiabendazole NH 的氘代化合物。Thiabendazole NH 的 CAS 号为 148-79-8。Thiabendazole 是具有驱虫特性的苯并咪唑衍生物。 | |||
TMIJ-0423 |
4-Methylimidazole-d6
|
||
4-Methylimidazole-d6 是 4-Methylimidazole 的氘代化合物。4-Methylimidazole 的 CAS 号为 822-36-6。 | |||
TMIJ-0031 |
Sulfamethoxazole-13C6
|
||
Sulfamethoxazole-13C6 是 Sulfamethoxazole 的 13C 的标记化合物。Sulfamethoxazole 的 CAS 号为 723-46-6。Sulfamethoxazole是磺胺类抗菌素,用于细菌感染。Sulfonamides是对氨基苯甲酸的竞争性拮抗剂。 | |||
TMIH-0287 |
Itraconazole-d3
|
||
Itraconazole-d3 是 Itraconazole 的氘代化合物。 | |||
TMIJ-0033 |
4-Methylimidazole-d3
|
||
4-Methylimidazole-d3 是 4-Methylimidazole 的氘代化合物。4-Methylimidazole 的 CAS 号为 822-36-6。 | |||
TMIJ-0297 |
Acetylsulfamethoxazole-d4
|
||
Acetylsulfamethoxazole-d4 是 Acetylsulfamethoxazole 的氘代化合物。Acetylsulfamethoxazole 的 CAS 号为 21312-10-7。N4-Acetylsulfamethoxazole 是磺胺甲恶唑的一种代谢物。Sulfamethoxazole 属于磺胺类抗菌素,可用于细菌感染。 | |||
TMIJ-0449 |
Dimetridazole-d3
|
||
Dimetridazole-d3 是 Dimetridazole 的氘代化合物。Dimetridazole 的 CAS 号为 551-92-8。Dmetridazole 是一种对抗原生动物感染的硝基咪唑类药物。 | |||
TMID-0039 |
Hydroxy Dimetridazole-d3
|
||
Hydroxy Dimetridazole-d3 是 Hydroxy Dimetridazole 的氘代化合物。Hydroxy Dimetridazole 的 CAS 号为 936-05-0。Hydroxy Dimetridazole 是Dimetridazol的羟基化代谢产物。Dimetridazol 是一种硝基咪唑类药物,可用于对抗原生动物感染。 | |||
TMIH-0077 |
Albendazole sulfone-d3
|
||
Albendazole sulfone-d3 是 Albendazole sulfone 的氘代化合物。 | |||
TMIJ-0188 |
(±)-Voriconazole-d3 (Mixture of Enantiomers)
|
||
(±)-Voriconazole-d3 (Mixture of Enantiomers) 是 (±)-Voriconazole 的氘代化合物。(±)-Voriconazole 的 CAS 号为 188416-29-7。 | |||
TMID-0081 |
Fluconazole-d4
|
||
Fluconazole-d4 是 Fluconazole 的氘代化合物。Fluconazole 的 CAS 号为 86386-73-4。Fluconazole是一种对多种真菌具有活性的三唑类抗真菌剂,抑制C. albicans和Candida kefyr的 IC99为 0.20 μg/mL 至 0.39 μg/mL。 | |||
TMIJ-0301 |
Esomeprazole-d3 Sodium Salt
|
||
Esomeprazole-d3 Sodium Salt 是 Esomeprazole Sodium Salt 的氘代化合物。 | |||
TMIJ-0394 |
Hydroxy Ipronidazole-d3
|
||
Hydroxy Ipronidazole-d3 是 Hydroxy Ipronidazole 的氘代化合物。Hydroxy Ipronidazole 的 CAS 号为 35175-14-5。 | |||
T71055 |
Albendazole-d7
|
||
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... | |||
T13035 |
Sulfathiazole-d4
|
Others | Others |
Sulfathiazole D4 is a deuterium labeled Sulfathiazole. Sulfathiazole used as a short-acting sulfonamide antibiotic. | |||
T12522 |
Posaconazole-D4
SCH 56592-D4 |
Others | Others |
Posaconazole-D4, a deuterium-labeled variant of Posaconazole, is a broad-spectrum, second-generation triazole with antifungal activity. | |||
T12011 |
Methimazole D3
|
Others | Others |
Methimazole D3, a deuterium-labeled version of Methimazole, serves as an antithyroid medication for treating hyperthyroidism in both humans and animals. | |||
T19184 |
Albendazole sulfoxide D3
Albendazole oxide D3,Ricobendazole D3 |
Others | Others |
Albendazole sulfoxide D3 is deuterium-labeled Albendazole sulfoxide. Albendazole sulfoxide is a broad-spectrum anthelmintic. | |||
TMIH-0344 |
Metronidazole-d3
|
||
Metronidazole-d3 是 Metronidazole 的氘代化合物。 | |||
TMIH-0570 |
Thiabendazole-d4
|
||
Thiabendazole-d4 是 Thiabendazole 的氘代化合物。 | |||
TMIJ-0302 |
Esomeprazole-d3
|
||
Esomeprazole-d3 是 Esomeprazole 的氘代化合物。Esomeprazole 的 CAS 号为 119141-88-7。Esomeprazole 是奥美拉唑(omeprazole) 的S-异构体,抑制溶酶体半胱氨酸蛋白酶legumain,防止癌症转移。它是一种质子泵抑制剂(PPI)。 | |||
TMIJ-0295 |
Flubendazole-d3 (methyl-d3)
|
||
Flubendazole-d3 (methyl-d3) 是 Flubendazole 的氘代化合物。Flubendazole 的 CAS 号为 31430-15-6。Flubendazole 是用于治疗人类蠕虫感染的驱虫药。它通过抑制微管功能等机制发挥抗癌作用。它诱导p53介导的细胞凋亡,抑制 G2/M 细胞周期。 | |||
T71142 |
Tebuconazole-d9
|
||
Tebuconazole-d9 is intended for use as an internal standard for the quantification of tebuconazole by GC- or LC-MS. Tebuconazole is a triazole fungicide that is active against both seed and foliar fungi. It inhibits 14α-demethylase isolated from U. maydis and S. bicolor with IC50 values of 0.05 and 0.16 nM, respectively. It inhibits the androgenic effect of the androgen receptor agonist DHT (IC20 = 2.89 µM) and is cytotoxic (EC20 = 38.9 µM) in an MDA-kb2 assay. Tebuconazole (50 and 100 mg/kg per... | |||
T10611 |
Brexpiprazole S-oxide D8
DM-3411 D8 |
Dopamine Receptor; 5-HT Receptor | GPCR/G Protein; Neuroscience |
Brexpiprazole S-oxide D8 (DM-3411 D8) is a deuterium labeled Brexpiprazole S-oxide. Brexpiprazole S-oxide is a main metabolite of Brexpiprazole. Brexpiprazole is a partial agonist of human 5-HT1A and dopamine receptors (Kis: 0.12 nM and 0.3 nM). | |||
T11679 |
Isavuconazole-d4
BAL-4815 D4,RO-0094815 D4,Isavuconazole D4 |
Others | Others |
Isavuconazole D4 is a deuterium labeled Isavuconazole. Isavuconazole is a triazole prodrug with antifungal activity against yeasts, molds, and dimorphic fungi. | |||
TMIH-0187 |
Dexlansoprazole-d4
(R)-Lansoprazole-d4 |
||
Dexlansoprazole-d4 是 Dexlansoprazole 的氘代化合物。Dexlansoprazole 的 CAS 号为 138530-94-6。(R)-Lansoprazole 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。 | |||
T19183 |
Albendazole-d3
Albendazole D3 |
Others | Others |
Albendazole D3 is the deuterium-labeled Albendazole. Albendazole is used as a drug indicated for the treatment of a variety of worm infestations. | |||
T10368 |
Aripiprazole (D8)
OPC-14597 D8 |
Others | Others |
Aripiprazole D8 (OPC-14597 D8) is the deuterium-labeled Aripiprazole. Aripiprazole is a human 5-HT1A receptor partial agonist (Ki: 4.2 nM). | |||
TMIH-0222 |
Esomeprazole sodium-d6
|
||
Esomeprazole sodium-d6 是 Esomeprazole sodium 的氘代化合物。Esomeprazole sodium 的 CAS 号为 161796-78-7。Esomeprazole sodium 是一种口服有效的活性质子泵抑制剂。Esomeprazole sodium通过抑制胃壁细胞中的H+, K+-ATPase来降低酸分泌,在胃食管反流疾病中有研究价值。Esomeprazole 是一种外泌体抑制剂,通过抑制 V-H+-ATPases 来阻断外泌体的释放。 | |||
TMIH-0343 |
Metronidazole-d4
|
||
Metronidazole-d4 是 Metronidazole 的氘代化合物。 | |||
T10610 |
Brexpiprazole-d8
OPC-34712 D8 |
Others | Others |
Brexpiprazole D8 (OPC-34712 D8) is a deuterium-labeled Brexpiprazole. Brexpiprazole is a partial agonist of human 5-HT1A and dopamine receptors (Ki: 0.12 nM and 0.3 nM). | |||
TMIJ-0112 |
Aripiprazole-d8
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Aripiprazole-d8 是 Aripiprazole 的氘代化合物。Aripiprazole 的 CAS 号为 129722-12-9。Aripiprazole 是血清素受体 5-HT1A 和多巴胺 D2 受体的部分激动剂,还用作突触后拮抗剂和血清素受体 5-HT2A 的拮抗剂。 | |||
TMIJ-0471 |
Mebendazole-d3
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Mebendazole-d3 是 Mebendazole 的氘代化合物。Mebendazole 的 CAS 号为 31431-39-7。Mebendazole是一种hedgehog抑制剂,用作驱虫药。 | |||
TMIJ-0335 |
Dehydro aripiprazole-d8
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Dehydro aripiprazole-d8 是 Dehydro aripiprazole 的氘代化合物。Dehydro aripiprazole 的 CAS 号为 129722-25-4。Dehydroaripiprazole 是 Aripiprazole 的活性代谢产物,具有抗精神病活性。Aripiprazole 是也一种抗精神病药。 | |||
TMIJ-0307 |
Fenbendazole-d3
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Fenbendazole-d3 是 Fenbendazole 的氘代化合物。Fenbendazole 的 CAS 号为 43210-67-9。Fenbendazole是一种广谱苯并咪唑类驱虫剂,对胃肠寄生虫有效。 |