69
11
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T38359 |
Dup-721
|
Antibacterial | Microbiology/Virology |
DuP-721 是广谱的口服有效的抗菌剂,可以抑制多种临床敏感和耐药细菌,特别是结核杆菌M. tuberculosis。 | |||
T8694 |
ML406
|
Antibacterial; Antibiotic | Microbiology/Virology |
ML406 是一种小分子探针,通过抑制M.tuberculosisBioA(DAPA 合酶) 显示出抗结核活性,IC50为 30 nM。 | |||
T22365 |
Methyl α-D-mannopyranoside
甲基-D-丙噻,Methyl α-D-mannopyranoside |
Antibacterial | Microbiology/Virology |
Methyl α-D-mannopyranoside (Methyl α-D-mannopyranoside) 是一种化学合成的中间体,在抗结核吸入治疗中靶向巨噬细胞。 | |||
T3642 |
TBA-354
TBA 354 |
Antibacterial; Antibiotic | Microbiology/Virology |
TBA-354 有抗结核作用,对结核分枝杆菌 H37Rv 菌株具有活性。 | |||
T5400 |
Q203
IAP6,Telacebec |
Antibacterial; Antibiotic | Microbiology/Virology |
Q203 (Telacebec)是一种中氮杂吡啶酰胺。 在培养基中抑制结核分枝杆菌H37Rv 活性的MIC50值为2.7 nM。 | |||
T11497 |
Ganfeborole HCl
GSK3036656 HCl,GSK656 HCl |
Antibacterial | Microbiology/Virology |
Ganfeborole HCl (GSK3036656 HCl) 是一种具有抗结核活性的小分子化合物,是结核分枝杆菌(Mtb)亮氨酰-tRNA 合成酶(LeuRS;IC50:0.2 μM)的抑制剂。 | |||
T4531 |
GSK2200150A
|
Antibacterial | Microbiology/Virology |
GSK2200150A 是一种通过高通量筛选活动确定的抗结核剂,对 H37Rv 的 MIC 是 0.38 μM。 | |||
T10329 |
anti-TB agent 1
|
Antibiotic | Microbiology/Virology |
anti-TB agent 1是一种有效的口服活性抗结核化合物,对结核分枝杆菌H37Rv、rRMP 和rINH 的MICs<2nM。 | |||
T2585 |
Bedaquiline
R207910,TMC207,贝达喹啉 |
Antibacterial; Antibiotic | Microbiology/Virology |
Bedaquiline (R207910) 是一种二芳基喹啉药物,能同时靶向 c-亚基和 ε-亚基,抑制结核分枝杆菌 (Mtb) F1FO-ATP 合酶。它具有解偶联活性和有用于耐多药结核病的潜力。 | |||
T5997 |
TBAJ-587
|
Antibacterial; Antibiotic | Microbiology/Virology |
TBAJ-587 是一种抗结核药物,在 MABA 和 LORA 试验中抑制 M.tb 菌株 H37Rv 的生长,MIC90 分别为 0.006 和 <0.02 µg/mL。它对 M. tuberculosis 具有更有效的活性,并且在 TB 动物模型中具有更好的功效。 | |||
T6096 |
Pretomanid
(S)-PA 824,PA-824 |
Antibacterial; Antibiotic | Microbiology/Virology |
Pretomanid ((S)-PA 824) 是一种抗生素,可研究肺部多重耐药性结核病。它对结核病(MTB) 具有亚微摩尔作用活性。它对 MTB 泛敏感和抗 Rifampin 的临床分离株的 MIC 值为 0.015 至 0.25 μg/mL。 | |||
T12231 |
NITD-349
|
Others; Antibacterial | Microbiology/Virology; Others |
NITD-349 是MmpL3的抑制剂,它对毒性结核分枝杆菌 H37Rv 显示出高效的抗分枝杆菌活性,MIC50 为 23 nM。 | |||
T38345 |
SQ609
|
||
SQ609是从一个双哌啶衍生物库中选取的抗结核潜在药物。SQ609在体外小鼠巨噬细胞中具有显著的抗结核活性。 | |||
T4202 |
Delamanid
迪拉马尼,德拉马尼,OPC-67683 |
Anti-infection; Antibacterial; Antibiotic | Microbiology/Virology |
Delamanid (OPC-67683) 是一种新的分枝杆菌细胞壁合成抑制剂,可用于耐多药结核病。 | |||
T9085 |
JFD01307SC
[(1,1-DIOXIDOTETRAHYDROTHIEN-3-YL)AMINO] |
Antibacterial | Microbiology/Virology |
JFD01307SC ([(1,1-DIOXIDOTETRAHYDROTHIEN-3-YL)AMINO]) 是一种谷氨酰胺合成酶抑制剂。 它是抗结核剂,可作为 L-谷氨酸盐的模拟物,靶向参与谷氨酰胺生物合成的酶。 | |||
T11449L |
Golotimod
Gamma-D-glutamyl-L-tryptophan,SCV 07 |
Antibiotic | Microbiology/Virology |
Golotimod (SCV 07) 是一种具有抗菌活性的二肽,具有免疫调节活性,能显著提高抗结核治疗的疗效,诱导胸腺和脾脏细胞增殖,调节巨噬细胞功能,抑制 STAT3 信号传导。Golotimod 可用于研究复发性生殖器单纯疱疹病毒 2 (HSV-2)感染和口腔黏膜炎。 | |||
T11259 |
FadD32 Inhibitor-1
|
Others | Others |
FadD32 inhibitor -1 has anti-tuberculosis activity and is an effective FadD32 inhibitor. | |||
T33683 |
NITD-304
NITD304 |
||
NITD-304 is an anti-tuberculosis drug candidate for the treatment of multidrug-resistant tuberculosis (MDR-TB), showing effective activity against both MTB drug-sensitive and multidrug-resistant clinical isolates. | |||
T27477 | GSK366A | ||
GSK366A is an anti-TB agent against Mycobacterium bovis BCG and Mycobacterium tuberculosis, targeting MmpL3 and inhibiting EchA6. | |||
T23621 |
Aconiazide
Aconiazida |
||
Aconiazide is a prodrug of anti-tuberculosis. | |||
T62086 | Tuberculosis inhibitor 5 | ||
Tuberculosis inhibitor 5 (Compound 11i) 是一种有效的抗结核剂,无明显细胞毒性。Tuberculosis inhibitor 5 是一种抗分枝杆菌 (antimycobacterial) 联苯类似物。 | |||
T28120 |
MTC420
MTC-420,MTC 420 |
||
MTC420 is a anti-tuberculosis agent with acceptable anti-tuberculosis activity (Mtb IC50 =525 nM, Mtb Wayne IC50 = 76 nM and MDR Mtb patient isolates IC50 = 140 nM). | |||
T27978 |
Maritinone
|
||
Maritinone is a novel anti-tuberculosis (anti-TB) agent. | |||
T10563 | BM635 | Others | Others |
BM635 is an MmpL3 inhibitor with outstanding anti-mycobacterial activity (MIC50: 0.12 μM against M. tuberculosis H37Rv). | |||
T10171 |
5-Hydroxypyrazine-2-Carboxylic Acid
|
Others | Others |
5-Hydroxypyrazine-2-Carboxylic Acid is a metabolite of anti-tuberculosis drug pyrazinamide. | |||
T30604 |
BTZ-N3
BTZ N3 |
||
BTZ-N3 is an effective and selective anti-tuberculosis drug candidate. | |||
T39091 |
Spectinamide 1599
|
||
Spectinamide-1599 is a combination partner for anti-tuberculosis therapy. | |||
T110951 |
Compound F0447-0245
|
||
Antitubercular agent-33 是一种 2-氨基噻唑衍生物,对于结核分枝杆菌 (Mycobacterium tuberculosis,Mtb)显示出有效的抗结核活性。 | |||
T63755 | Antitubercular agent-22 | ||
Antitubercular agent-22 (Compound 2) 是有效的抗念珠菌和抗结核剂,能够作用于 Candida albicansMTCC 3017 (MIC: 2.34 μg/ml) 和 M. tuberculosis(H37Rv) (MIC: 2 μg/ml)。 | |||
T16419 | Oxyphenbutazone | COX | Immunology/Inflammation; Neuroscience |
Oxyphenbutazone is a non-selective COX inhibitor. Oxyphenbutazone is a phenylbutazone derivative. It has an anti-inflammatory effect. Oxyphenbutazone selectively kills non-replicating Mycobaterium tuberculosis. | |||
T61303 |
MmpL3-IN-1
|
||
MmpL3-IN-1, also known as compound 32, is a highly effective inhibitor of Mycobacterial membrane protein large 3 (MmpL3). With an anti-tuberculosis activity exhibiting a minimum inhibitory concentration (MIC) of less than 0.016 μg/mL in M. tuberculosis, MmpL3-IN-1 is a valuable compound for research on drug-resistant tuberculosis [1]. | |||
T63525 | Antitubercular agent-23 | ||
Antitubercular agent-23 是有效的抗念珠菌及抗结核剂,能够作用于 Candida albicansMTCC 3017 (MIC: 1.1 μg/ml) 和 M. tuberculosis(H37Rv) (MIC: 1 μg/ml)。 | |||
T40520 |
Thiophene-2
Thiophene-2,TP2 |
||
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. | |||
T61676 |
4-Piperidinecarboxamide
|
||
4-Piperidinecarboxamide is a mycobacterial aspartyl-tRNA synthetase (AspS) inhibitor and a potential anti-tuberculosis (TB) agent [1]. | |||
T61520 |
Antitubercular agent-24
|
||
Antitubercular agent-24 (Compound 1) exhibits anti-tubercular properties against M. tuberculosis H37Rv. It demonstrates an extracellular IC50 of 0.83 μM and an intracellular IC50 of 0.17 μM [1]. | |||
T38298 |
Tuberculosis inhibitor 3
|
||
Tuberculosis inhibitor 3 (compound 2i) displays potent anti-TB activity (MIC < 0.016 μg/mL) against drug-sensitive/resistant MTB strains. Tuberculosis inhibitor 3 (compound 2i) shows acceptable PK profiles with oral bioavailability[1]. | |||
T73329 |
MMV676584
|
||
MMV676584 具有抗结核活性。MMV676584是一种新的真霉菌瘤候选药物。 | |||
T10887 |
CRS400393
|
Antibacterial | Microbiology/Virology |
CRS400393 is an effective anti-mycobacterial drug , with MIC of 0.03, 2, and ≤ 0.12 µg/mL against M. abs., M. avium, M. intracellulare, and M. tuberculosis, respectively. | |||
T10513 |
Benzothiohydrazide
|
Antibacterial | Microbiology/Virology |
Benzothiohydrazide 是异烟肼的类似物,具有抗结核活性,可用于分离真菌和细菌。 | |||
T61149 | Antibacterial agent 121 | ||
Antibacterial agent 121 (Compound 10) demonstrates antibacterial properties and exhibits efficacy against mycobacterial strains while also possessing anti-inflammatory activity. This compound finds potential applications in Tuberculosis (TB) research [1]. | |||
T63786 |
WX-081
|
||
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)。 | |||
T72177 |
Oxyphenbutazone monohydrate
羟布宗一水合物 |
||
Oxyphenbutazone monohydrate 是一种保泰松 (Phenylbutazone) 代谢物,具有抗炎作用。Oxyphenbutazone monohydrate 是一种具有口服活性的非选择性 COX 抑制剂。Oxyphenbutazone monohydrate 能选择性地杀死不复制的结核分枝杆菌 (Mycobaterium tuberculosis)。 | |||
T10563L2 |
BM635 mesylate (1493762-74-5 free base)
BM635 mesylate |
Others | Others |
BM635 mesylate is an MmpL3 inhibitor with outstanding anti-mycobacterial activity (MIC50: 0.12 μM against M. tuberculosis H37Rv). | |||
T10563L |
BM635 hydrochloride (1493762-74-5 free base)
BM635 hydrochloride |
Others | Others |
BM635 hydrochloride is an MmpL3 inhibitor with outstanding anti-mycobacterial activity (MIC50: 0.12 μM against M. tuberculosis H37Rv). | |||
T62910 | Antibacterial agent 62 | ||
Antibacterial agent 62 是一种新型氧化还原循环抗结核化合物,对生长和营养缺乏的表型耐药非生长细菌表现出显著的杀菌作用。 | |||
T38073 |
Thiocarlide
Isoxyl |
||
Thiocarlide (isoxyl) is a thiourea derivative that was used in the 1960s to successfully treat tuberculosis (TB). It has considerable antimycobacterial activity in vitro and is effective against multi-drug resistant strains of Mycobacterium tuberculosis in the range of 1-10 µg/ml. [1] [2] At concentrations of 10 µM, isoxyl inhibits the synthesis of M. bovis during six hours of exposure which is similar to isoniazid (INH) and ethionamide (ETH), two other predominant anti-tuberculosis drug... | |||
T61772 | PknB-IN-1 | ||
PknB-IN-1 (Compound 2) is an inhibitor of protein kinase B (PknB) with a concentration causing 50% inhibition (IC50) of 14.4 μM. This compound demonstrates anti-mycobacterial activity by effectively suppressing the growth of M. tuberculosis H37Rv strain, with a minimum inhibitory concentration (MIC) of 6.2 μg/mL [1]. | |||
T78602 | Chaetoglobosin C | ||
Chaetoglobosin C (Compound 4),源自真菌Chaetomium globosum KMITL-N0802,为一种蒽醌-色酮类化合物,具备抗结核分枝杆菌的活性。 | |||
T73271 |
MMV688845
(R)-GSK1729177A |
||
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。 | |||
T73441 |
TBI-166
|
||
TBI-166,一种利米吩嗪类似物,是一种具有口服活性的抗结核药物,不良反应比 riminophenazine 化合物 Clofazimine 小。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
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。 | |||
T8298 |
Vasicine hydrochloride
鸭嘴花碱盐酸盐,Peganine hydrochloride |
Antibacterial; Antibiotic | Microbiology/Virology |
Vasicine hydrochloride (Peganine hydrochloride) 是从Justicia adhatoda 中分离得到的一种喹唑啉类生物碱,有抗结核活性。 | |||
T67136 |
1-Hydroxy-2-butanone
|
Endogenous Metabolite; Antibiotic | Metabolism; Microbiology/Virology |
1-Hydroxy-2-butanone 是可从竹子汁和番茄叶中提取得到的天然产物,具有抗结核活性。 | |||
TN1622 |
Ermanin
堪非醇3,4'-二-O-甲醚 |
NOS; Influenza Virus; COX; HIV Protease; Antibacterial; Antibiotic | Immunology/Inflammation; Microbiology/Virology; Neuroscience; Proteases/Proteasome |
Ermanin 是一种从 Tanacetum microphyllum 中分离出来的类黄酮。Ermanin抑制血小板聚集,具有抗结核和抗病毒/细菌特性。Ermanin 可抑制 iNOS 和 COX-2 的表达,从而具有抗炎活性。Ermanin 可能具有抗 HIV-1 活性。Ermanin 在较低浓度下可有效地抑制 Dione juno 幼虫。 | |||
T3S1612 |
kuwanon G
桑黄酮G,Moracenin B,桑黄酮 G,Kuwanone G |
Phosphatase; Antibacterial; Bombesin Receptor; AChR; AChE; Glucosidase | GPCR/G Protein; Metabolism; Microbiology/Virology; Neuroscience |
Kuwanon G (Moracenin B) 是一种从桑树中得到的黄酮类蛙皮素受体拮抗剂,具有杀菌作用。 | |||
TN5614 |
Dehydrobruceantin
|
||
Dehydrobruceantin has anti-tuberculosis activity. | |||
TN3674 |
Clauszoline M
|
Antifection | Microbiology/Virology |
Clauszoline M shows a significant anti-tuberculosis activity. | |||
TN5648 | Porson | ||
Porson exhibited anti-tubercular activity against Mycobacterium tuberculosis H37Rv in vitro and MICs values of 40.0 μg/mL. | |||
TN1378 |
α-Viniferin
ALPHA-VINIFERIN,Alpha-葡萄素 |
P450; NO Synthase; Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation; Metabolism |
α-Viniferin 也称为2-芳基苯并呋喃类黄酮,是前列腺素H2合成酶抑制剂。具有抗阿尔茨海默病、抗结核、抗肿瘤、抗炎、抗糖尿病等多种药理活性 | |||
T72742 |
(-)-Pinocembrin
(-)-乔松素 |
||
(-)-Pinocembrin 对 H37Ra 结核分枝杆菌展示了抗菌活性,无论是休眠还是活跃期,其 IC50 值分别为1.11 mg/mL 和 1.21 mg/mL。作为一种抗增殖剂,(-)-Pinocembrin 对于 THP-1、A549、Panc-1、HeLa 和 MCF7 细胞系,IC50 值范围为 1.88 至 11.00 mg/mL。 | |||
T38330 |
Collinin
|
||
Collinin is a coumarin that has been found in Z. schinifolium and has diverse biological activities.1,2,3,4 It is active against drug-susceptible and -resistant strains of M. tuberculosis (MIC50s = 3.13-6.25 μg/ml).1 Collinin inhibits LPS-induced nitric oxide (NO) production (IC50 = 5.9 μM) and reduces COX-2 protein levels in RAW 264.7 cells.2 It completely inhibits aggregation of isolated rabbit platelets induced by arachidonic acid , collagen, or platelet activating factor (PAF) when used at a... |