64
3
8
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T1371 |
1H-1,2,4-Triazole-3-carboxylic acid
|
Others | Others |
1H-1,2,4-Triazole-3-carboxylic acid,具有 isoprenyl transferases 抑制蛋白质的特性。 | |||
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。 | |||
T77765 |
FSEN1
3-(4-bromophenyl)-6-((4-(4-methoxyphenyl)piperazin-1-yl)methyl)thiazolo[2,3-c][1,2,4]triazole |
Ferroptosis | Apoptosis |
FSEN1 是一种新型高效的非竞争性 FSP1 抑制剂,IC50 值为 313 nM。 FSEN1 通过抑制 FSP1 诱导癌细胞中的铁死亡。FSEN1 可用于预防和治疗癌症。 | |||
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。 | |||
T7867 |
Flutriafol
|
NMDAR; Antifungal | Microbiology/Virology; Neuroscience |
Flutriafol 是一种三唑类广谱杀菌试剂。 | |||
T17676 |
Boc-NH-PEG3-C2-triazole-DBCO-PEG4-VC-PAB-DMEA
|
Others; ADC Linker | Antibody-drug Conjugate/ADC Related; Others |
Boc-NH-PEG3-C2-triazole-DBCO-PEG4-VC-PAB-DMEA is a double claevable 3-unit and 4-unit PEG linker for antibody-drug-conjugation (ADC). | |||
T67137 |
1-Methyl-1,2,4-triazole
|
Others | Others |
1-Methyl-1,2,4-triazole 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 T67137,CAS号为 6086-21-1。 | |||
T12103 |
MR-L2
|
PDE | Metabolism |
MR-L2 是可逆的、非竞争性的长型异构体磷酸二酯酶 -4激活剂,可以激活代表性的 PDE4 长型异构体 (PDE4A4、PDE4B1、PDE4C3、PDE4D5)。它可抑制 PGE2- 诱导的 MDCK 细胞囊肿形成,其EC50=1.2 µM。 | |||
T78235 |
4-Phenyl-1H-1,2,3-triazole
|
Indoleamine 2,3-Dioxygenase (IDO) | Metabolism |
4-Phenyl-1H-1,2,3-triazole,一种IDO1抑制剂(IC50:60 μM),可应用于癌症研究。 | |||
T9998 |
MIND4-19
|
Sirtuin | Chromatin/Epigenetic; DNA Damage/DNA Repair |
MIND4-19 是一种具有抗肿瘤活性的 SIRT2 抑制剂。 | |||
T0120 |
Voriconazole
UK-109496,伏立康唑 |
Antifection; Antifungal | Microbiology/Virology |
Voriconazole (UK-109496) 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 | |||
T67127 |
1H-1,2,4-Triazole-1-carboximidamide hydrochloride
|
Others | Others |
1H-1,2,4-Triazole-1-carboximidamide hydrochloride 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 T67127,CAS号为 19503-26-5。 | |||
T66475 |
Methyl 1-(2,6-difluorobenzyl)-1H-1,2,3-triazole-4-carboxylate
|
Others | Others |
Methyl 1-(2,6-difluorobenzyl)-1H-1,2,3-triazole-4-carboxylate 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 T66475,CAS号为 217448-86-7。 | |||
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。 | |||
T67440 |
Ethyl 1-(4-bromophenyl)-5-methyl-1H-1,2,3-triazole-4-carboxylate
|
Others | Others |
Ethyl 1-(4-bromophenyl)-5-methyl-1H-1,2,3-triazole-4-carboxylate 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 T67440,CAS号为 361990-21-8。 | |||
T67318 |
1-((2-(2,4-Difluorophenyl)oxiran-2-yl)methyl)-1H-1,2,4-triazole methanesulfonate
|
Others | Others |
1-((2-(2,4-Difluorophenyl)oxiran-2-yl)methyl)-1H-1,2,4-triazole methanesulfonate 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 T67318,CAS号为 86386-77-8。 | |||
TNU0339 |
Ribavirin carboxylic acid
|
Others | Others |
Nucleoside Derivatives - Other modified nucleosides; Drugs and Inhibitors; Ribavirin related compound A; metabolite of Ribavirin | |||
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。 | |||
T5953 |
1-Aminobenzotriazole
3-Aminobenzotriazole,1-氨基苯并三唑,ABT |
P450 | Metabolism |
1-Aminobenzotriazole (ABT) 是一种不可逆的细胞色素 P450 非特异性抑制剂。 | |||
T25403 |
Farnesylthiotriazole
|
Others | Others |
Farnesylthiotriazole is a persistent PKC activator agent. | |||
T14872 |
Carboxyamidotriazole
CAI,L-651582 |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Carboxyamidotriazole is a cytostatic inhibitor of non-voltage-operated calcium channels and calcium channel-mediated signaling pathways. It shows anti-inflammatory, anti-tumor, and antiangiogenic effects. | |||
T20058 |
Prothioconazole
HSDB7893,HSDB-7893,Proline 480 SC Fungicide,JAU 6476,丙硫菌唑,HSDB 7893 |
Antifungal | Microbiology/Virology |
Prothioconazole (Proline 480 SC Fungicide) 是一种手性三唑类杀菌剂,用于植物病原控制。 | |||
T7152 |
Ravuconazole
立福康唑,雷夫康唑,BMS-207147,ER-30346 |
Antifungal | Microbiology/Virology |
Ravuconazole (ER-30346) 是一种口服的三唑广谱抗真菌剂。 | |||
T2523 |
Rufinamide
CGP 33101,E 2080,卢非酰胺,RUF 331 |
Sodium Channel | Membrane transporter/Ion channel |
Rufinamide (E 2080) 是一种新型镇痫化合物,可用于研究 Lennox-Gastaut 综合症。 | |||
T26829 |
Bitertanol
KWG-0599,联苯三唑醇,KWG0599,Baycor,Biloxazol,KWG 0599,Sibutol |
Antifungal | Microbiology/Virology |
Bitertanol (KWG 0599) 是一种三唑类杀菌剂。 Bitertanol 抑制去甲基化,破坏膜功能,并阻止甾醇合成。 | |||
T67766 |
HHS-0701
|
Others | Others |
HHS-0701,一种硫-三唑交换 (SuTEx) 配体,是酪氨酸反应性前列腺素还原酶 2 (PTGR2) 的有效抑制剂。HHS-0701 可以抑制脂质底物 15-Keto-PGE2 的 PTGR2 代谢。 | |||
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。 | |||
T2199 |
Myclobutanil
Systhane,腈菌唑 |
Antifungal | Microbiology/Virology |
Myclobutanil (Systhane) 是康唑类抗真菌剂,可用作农药。 | |||
T11070 |
DO34 analog
|
Others | Others |
DO34 analog 是二酰基甘油脂肪酶 α (DAGLα) 的抑制剂,DO34 analog 也是 DO34 的一个类似物。 | |||
T67988 |
Embeconazole
R 120758,CS 758 |
Antifungal | Microbiology/Virology |
Embeconazole (R 120758) 是一种三唑类抗真菌剂。Embeconazole 对念珠菌、曲霉菌、新型隐球菌等临床重要真菌具有较强的体外活性。 | |||
T7086 |
Tris(benzyltriazolylmethyl)amine
三[(1-苄基-1H-1,2,3-三唑-4-基)甲基]胺,TBTA |
Others | Others |
Tris(benzyltriazolylmethyl)amine (TBTA) 是一种能作为生化工具的配体,可用于标记蛋白质和酶。 | |||
T60929 |
Brassinazole
(2S,3R)-Brassinazole |
Others | Others |
Brassinazole 是一种选择性的三唑型类固醇 (BR)生物合成抑制剂。Brassinazole 可用于调节油芸素类固醇 (BR) 信号转导通路,用于调节植物木质部的生长和发育。 | |||
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。 | |||
T27617 |
Inz-1
|
P450 | Metabolism |
Inz-1 是一种有效的真菌特异性线粒体细胞色素 bc1 抑制剂,对酵母和人类的 IC50 分别为 8.092 和 45.320 μM。 Inz-1 可逆转氟康唑或其他三唑类抗真菌药对致病性真菌白色念珠菌的耐药性。 | |||
T2213 |
Terconazole
Gyno-Terazol,Terazol 3,Terazol 7,Triaconazole,特康唑,曲康唑,R42470 |
Antifection; Antifungal | Microbiology/Virology |
Terconazole (Terazol 7) 是一种广谱抗真菌药物,用于研究阴道酵母菌感染。 | |||
T7866 |
Difenoconazole
|
Others; Antifungal | Microbiology/Virology; Others |
Difenoconazole 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。 | |||
T38273 |
Paclobutrazol
(2R,3R)-Paclobutrazol,多效唑,(R,R)-paclobutrazol,2R,3R-Paclobutrazol |
Antifungal | Microbiology/Virology |
Paclobutrazol ((R,R)-paclobutrazol) 是一种含有三唑的植物生长延缓剂,能抑制赤霉素的生物合成。Paclobutrazol 还具有抗真菌 (antifungal) 活性。Paclobutrazol 能抑制脱落酸的合成,诱导植物的耐冷性植物。Paclobutrazol 通常用于赤霉素在植物生物学中作用的研究。 | |||
T3934 |
Isavuconazonium sulfate
|
Antifungal | Microbiology/Virology |
Isavuconazonium sulfate 是一种口服活性抗真菌药,是活性三唑类抗真菌药物 Isavuconazole 的前药,可用于侵袭性曲霉菌病和毛霉菌病。 | |||
T17731L |
CL2A-SN-38 DCA 1279680-68-0(free base)
|
Others | Others |
CL2A-SN-38 DCA 1279680-68-0(free base) 是一种药物-接头偶联物,由有效的 DNA 拓扑异构酶 I 抑制剂 SN-38 和接头 CL2A 组成,用于制造抗体药物偶联物 (ADC)。CL2A-SN-38 由有效的 DNA 拓扑异构酶组成I 抑制剂 SN-38 和接头 CL2A 以制造抗体药物偶联物 (ADC)。 CL2A-SN-38 对一系列人类实体瘤类型提供显着和特异性的抗肿瘤作用。 CL2A 是一种不可切割的复杂 PEG8 和含有三唑的 PABC-肽-mc 接头。 CL2A 可通过 pH 敏感性裂解,产生旁观者效应,并通过二硫键在半胱氨酸残基处结合抗体。 | |||
T21276 |
Amisulbrom
|
Others | Others |
Amisulbrom is classified under the triazole group of fungicides. | |||
T28717 |
Sch 39304
Sch-39304,Sch39304 |
Others | Others |
Sch 39304 is an oral triazole antifungal. | |||
T16714 |
Saperconazole
沙康唑,R66905 |
Others | Others |
Saperconazole is a broad-spectrum antifungal triazole (MIC90: 0.19 mg/L). | |||
T37796 |
Voriconazole N-oxide
|
Others | Others |
Voriconazole N-oxide is a major metabolite of the triazole antifungal voriconazole . It is formed via oxidation of voriconazole by the cytochrome P450 (CYP) isoforms CYP3A4 and CYP2C19. | |||
T62763 |
VEGFR-2-IN-12
|
Others | Others |
VEGFR-2-IN-12 (compound 6g) 是一种 2-oxoquinoxalinyl-1,2,4-triazole,是一种 VEGFR-2 的有效抑制剂 (IC50: 0.037 μM)。VEGFR-2-IN-12 能够高度抑制 MCF-7 细胞的生长 (GI50: 1.6 μM)。VEGFR-2-IN-12 具有抗肿瘤作用。 | |||
T23174 |
Posaconazole hydrate
|
Others | Others |
Posaconazole is a broad-spectrum, second generation, triazole compound with antifungal activity. Posaconazole is a sterol C14ɑ demethylase inhibitor (IC50: 0.25 nM). Posaconazole strongly inhibits 14-alpha demethylase, a cytochrome P450-dependent enzyme. | |||
T19974 |
Propargyl-PEG3-azide
Propargyl-PEG3-amine |
Others | Others |
Propargyl-PEG3-amine is a PEG derivative containing a propargyl group and an amino group. The propargyl group can be reacted with azide-bearing compounds or biomolecules via copper-catalyzed azide-alkyne Click Chemistry to yield a stable triazole linkage. | |||
T60939 |
Neuraminidase-IN-6
|
Others | Others |
Neuraminidase-IN-6 (Compound 5c) 是1,3,4-triazole-3-acetamide 的衍生物。Neuraminidase-IN-6 是神经氨酸酶的有效抑制剂,IC50值为 0.11 μM。神经氨酸酶 (NA) 是抗流感药物开发的理想靶点。 | |||
T17732 |
CL2A
|
Others; ADC Linker | Antibody-drug Conjugate/ADC Related; Others |
CL2A is a pH-sensitive, cleavable PEG8- and triazole-containing PABC-peptide-mc linker, characterized by its ability to induce a bystander effect. It forms a disulfide bond with an antibody at a cysteine residue. Labetuzumab govitecan utilizes this linker for its drug conjugation[1]. | |||
T80982 |
TIS108
|
Others | Others |
TIS108为一种抑制三唑型独脚金内酯生物合成的化合物。它抑制拟南芥的胚胎发生并降低水稻中2′-epi-5-deoxystrigol (epi-5DS)的含量。 | |||
T61960 |
Fluconazole mesylate
|
Others | Others |
Fluconazole 甲磺酸盐是一种具有抗真菌活性的化合物,可用于抗表面和全身性真菌感染的研究。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
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。 | |||
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。 | |||
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。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
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. | |||
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. | |||
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. | |||
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. | |||
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。 | |||
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 | |||
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。 | |||
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... |