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Cat. No. | Product Name | Target | Signaling Pathways |
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T14830 |
Bromperidol
溴哌利多,R-11333 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Bromperidol (R-11333) 是一种苯丁酮衍生物,是一种强效长效精神安定药。它被用作治疗精神分裂症的抗精神病药。 | |||
T0972 |
Isoniazid
INH,异烟肼,Isonicotinic acid hydrazide,Isonicotinic hydrazide |
Mitophagy; Dehydrogenase; CAT; Antibacterial; Autophagy | Autophagy; Metabolism; Microbiology/Virology; oxidation-reduction |
Isoniazid (Isonicotinic hydrazide) 是一种必须被细菌过氧化氢酶 KatG 激活的前药,具有抗菌活性。它对快速分裂的分枝杆菌具有杀菌作用。 | |||
T60073 |
Antimycobacterial agent-4
4-nitro-N-[4-(2-pyridyl)thiazol-2-yl]benzamide |
Antibacterial | Microbiology/Virology |
Antimycobacterial agent-4 (4-nitro-N-[4-(2-pyridyl)thiazol-2-yl]benzamide) 对结核分枝杆菌具有抗菌活性。 | |||
T63865 |
Antimycobacterial agent-3
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Antimycobacterial agent-3 是一种抗分枝杆菌 (antimycobacterial) 剂,细胞毒性较低。Antimycobacterial agent-3 能够有效作用于药敏的 MTB 菌株 H37Rv 和耐药的临床分离株 (MIC< 0.029-0.110 μM)。 | |||
T61853 | Antimycobacterial agent-1 | ||
Antimycobacterial agent-1 (compound 33) demonstrates potent antimycobacterial activity against Mycobacterium tuberculosis H37Ra, with a minimal inhibitory concentration (MIC) value of 1 μg/ml. Notably, antimycobacterial agent-1 exhibits low cytotoxicity in normal cells, as evidenced by an IC50 value of 143.2 μg/ml in Vero cells [1]. | |||
T72306 | Mycobacterial Zmp1-IN-1 | ||
Mycobacterial Zmp1-IN-1 是一种分枝杆菌锌金属蛋白酶-1(Zmp1)抑制剂。Mycobacterial Zmp1-IN-1 对 MtbH37Ra 具有剂量依赖性抑制的抗分枝杆菌活性。Mycobacterial Zmp1-IN-1 可用于结核病 (TB) 的研究。 | |||
T79281 |
Antimycobacterial agent-6
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Antimycobacterial agent-6 (compound 25) 是抗结核药物,针对野生型及氟喹诺酮耐药的结核分枝杆菌 (Mtb) 株有效。此化合物对 Mtb DprE1-C387S 突变具有抑制作用,其最小抑菌浓度(MIC90)对 H37Rv 和 MoxR 株均为 0.9 μM,对 DprE1-P116S 株为 0.5 μM。 | |||
T63420 |
Antimycobacterial agent-2
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Antimycobacterial agent-2 是有效的抗分枝杆菌剂,对结核分枝杆菌 (M.tb) H37Rv 的MIC99为 0.8 μM。Antimycobacterial agent-2 具有出细胞毒作用,能够作用于 CHO 细胞 (IC50: 48.1 μM)。 | |||
T0377 |
Clofazimine
NSC-141046,氯法齐明,氯苯吩嗪 |
DNA; Antibacterial; Antibiotic | DNA Damage/DNA Repair; Microbiology/Virology |
Clofazimine (NSC-141046) 是一种具有显著的抗炎效果的亚氨基酚嗪类染料,与其它抗分支杆菌药物联用来治疗AIDS 和克罗恩病。 | |||
T21023 |
Bedaquiline fumarate
TMC 207,R403323,TMC-207,TMC207,R-403323,贝达喹啉富马酸盐,R 403323 |
Antibacterial; Antibiotic | Microbiology/Virology |
Bedaquiline fumarate (TMC207) 是二芳基喹啉抗生素,作用于 ATP 合成酶,常用于结核杆菌感染的研究。 | |||
T7518 |
Deoxycytidine triphosphate trisodium salt
2'-脱氧胞苷-5'-三磷酸三钠盐,2'-DEOXYCYTIDINE-5'-TRIPHOSPHATE TRISODI |
Nucleoside Antimetabolite/Analog; DNA/RNA Synthesis; Endogenous Metabolite; Antibiotic | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism; Microbiology/Virology |
Deoxycytidine triphosphate trisodium salt (2'-DEOXYCYTIDINE-5'-TRIPHOSPHATE TRISODI) 是可用于 DNA 合成的核苷三磷酸,可用于实时荧光定量 PCR、cDNA 合成和 DNA 测序。 | |||
T23979 |
Deoxypheganomycin D
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Deoxypheganomycin D is a specific mycobacteria inhibitor. | |||
T26189 |
Setomimycin
AM 2947,Antibiotic A 39183B,AM2947,AM-2947 |
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Setomimycin is an antibiotic against Gram positive bacteria, including mycobacteria. | |||
T60486 | Mycobactin-IN-1 | ||
Mycobactin-IN-1 (compound 44) 是一种吡唑啉类似物。Mycobactin-IN-1 与分支菌素生物合成途径中的关键酶,水杨酸-AMP 连接酶 (MbtA) 结合。Mycobactin-IN-1 是分支菌素生物合成的抑制剂,具有抗分枝杆菌的作用。 | |||
T33537 |
Mycobactin P
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Mycobactin P is one of iron(III) chelating compounds produced by most species of Mycobacteria which act as growth factors. | |||
T25955 |
Picromycin
Antibiotic B 62169A,Amaromycin,Albomycetin,Pikromycin |
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Picromycin is a 14-membered macrolide antibiotic and Prolyl endopeptidase (PREP) inhibitor. Pikromycin shows activity against gram-positive bacteria including mycobacteria. | |||
T62840 |
Bromperidol hydrochloride
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Bromperidol hydrochloride (R-11333 hydrochloride) 具有抗精神病作用,能够较好的亲和中枢多巴胺受体 D2 (dopamine receptors D2)。Bromperidol hydrochloride 与 Spectinomycin 能够协同杀灭分枝杆菌 (mycobacteria)。 | |||
T16749 |
Rifalazil
利福拉齐,KRM-1648,ABI-1648 |
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Rifalazil is a rifamycin derivative, inhibits the bacterial DNA-dependent RNA polymerase and kills bacterial cells by blocking off the β-subunit in RNA polymerase. Rifalazil is an antibiotic, exhibits high potency against mycobacteria, gram-positive bacteria, Helicobacter pylori, C. pneumoniae and C. trachomatis (MIC: 0.00025 to 0.0025 μg/ml). | |||
T40520 |
Thiophene-2
Thiophene-2,TP2 |
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Thiophene-2 (TP2) is a targeted inhibitor of polyketide synthase 13 (Pks13), specifically designed to disrupt mycolic acid biosynthesis. By doing so, it effectively induces rapid cell death in mycobacteria. Thiophene-2 demonstrates notable anti-tuberculosis activity and exhibits a minimum inhibitory concentration (MIC) value of 1 μM against Mycobacterium tuberculosis. | |||
T73271 |
MMV688845
(R)-GSK1729177A |
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MMV688845 是一种作用于非结核分枝杆菌的 RNA 聚合酶抑制剂,可有效杀灭脓肿分枝杆菌,并展现出对结核病的治疗潜力。 | |||
T75313 | Methdilazine | ||
Methdilazine hydrochloride,一种口服活性抗生素(组胺拮抗剂),在体外和体内均能有效抑制多种分枝杆菌的活性。其最小抑菌浓度(MIC)值介于5-15 μg/mL之间,适用于传染病相关研究。 | |||
T63786 |
WX-081
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WX-081 是抗结核剂 (anti-tuberculosis),对 M. tuberculosisH37Rv 表现出明显的抗分枝杆菌效果,并能够作用于药物敏感结核病 (DS-TB) 杆菌 (MIC: 0.083 μg/ml) 和耐多药结核病 (MDR-TB) 菌株 (MIC: 0.11 μg/ml),对 hERG 通道表现出抑制作用 (IC50: 1.89 μM)。 | |||
T83940 |
sCy5DL-amide
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sCy5DL-amide是一种荧光D-氨基酸,适用于标记多种细菌的肽聚糖,包括革兰氏阳性菌、革兰氏阴性菌和分枝杆菌。特别适合于革兰氏阳性的B.subtilis的标记。使用sCy5DL-amide标记的细菌可通过单分子定位显微镜技术(SMLM;也称为PALM或STORM)进行成像。激发/发射最大值为646/666 nm。 | |||
T83939 |
sCy5DA
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sCy5DA是一种荧光D-氨基酸,适用于标记活细菌中的肽聚糖。它能高效地整合进各种细菌的肽聚糖中,包括革兰氏阳性菌、革兰氏阴性菌和分枝杆菌,尤其在革兰氏阴性的C. crescentus中整合效果显著。使用sCy5DA标记的细菌可以通过单分子定位显微镜(SMLM;也称为PALM或STORM)进行成像。激发/发射峰值=646/665 nm。 |
Cat. No. | Product Name | Target | Signaling Pathways |
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T0793 |
Kanamycin sulfate
硫酸卡那霉素,Kanamycin monosulfate,Kanamycin A monosulfate,Ophtalmokalixan |
ribosome; Antibacterial; Antibiotic | Microbiology/Virology |
Kanamycin sulfate (Kanamycin monosulfate) 是氨基糖苷类杀菌抗生素,它通过与细菌30S 核糖体结合起作用。 | |||
TN6057 |
1-Methyl-2-[(Z)-6-undecenyl]-4(1H)-quinolone
(Z)-1-Methyl-2-(undec-6-enyl)quinolin-4(1H)-one |
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(Z)-1-Methyl-2-(undec-6-enyl)quinolin-4(1H)-one shows strong inhibitory activity on leukotriene biosynthesis in human polymorphonuclear granulocytes, and it is very effective against mycobacteria. |