49
22
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
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
|
||
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)。 | |||
T63420 |
Antimycobacterial agent-2
|
||
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)。 | |||
T79281 |
Antimycobacterial agent-6
|
||
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。 | |||
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]. | |||
T0891 |
Dapsone
DDS,4,4‘-Sulfonyldianiline,氨苯砜,Bis(4-aminophenyl) sulfone,Sulphadione,4,4'-Diaminodiphenylsulfone,4-Aminophenyl sulfone |
Reactive Oxygen Species; Antibacterial; Antibiotic; Parasite | Immunology/Inflammation; Metabolism; Microbiology/Virology; NF-κB |
Dapsone (Sulphadione) 是具有口服活性和血脑渗透通透性的磺酰类抗生素,具有抑菌、抗细菌和抗原虫活性。它有抗麻风活性,抑制麻风杆菌细胞提取物中叶酸的合成。它可研究皮肤病。 | |||
T6425 |
BTZ043 Racemate
BTZ044,BTZ10526038,Benzothiazinone 10526038 |
Antibacterial; DprE1 | Microbiology/Virology; Others |
BTZ043 Racemate (Benzothiazinone 10526038) 是一种癸二烯基磷酰-β-D-核糖 2'-差向异构酶(DprE1) 抑制剂,用作新的抗分枝杆菌剂。 | |||
T7342 |
BM212
|
Antibacterial | Microbiology/Virology |
BM212 是一种分枝杆菌膜蛋白 MmpL3抑制剂。它抑制结核分枝杆菌和部分非结核分枝杆菌,抗结核杆菌 H37Rv 菌株的 MIC 值为 5 µM。 | |||
T19794 |
Temafloxacin
替马沙星,Omniflox |
Antibiotic | Microbiology/Virology |
Temafloxacin (Omniflox) 是一种喹诺酮类广谱抗菌剂,对革兰氏阳性菌、革兰氏阴性菌和厌氧菌均有效。 | |||
T1501 |
Rifabutin
LM-427,Ansamycin,利福布汀,利福布丁 |
HSP; DNA/RNA Synthesis; Antibacterial; Antibiotic | Cell Cycle/Checkpoint; Cytoskeletal Signaling; DNA Damage/DNA Repair; Metabolism; Microbiology/Virology |
Rifabutin (LM-427) 是半合成的安莎霉素抗生素,抑制 DNA 依赖性 RNA 聚合酶,有抗分枝杆菌作用。 | |||
T11594 |
I2906
|
Others | Others |
I2906 showed antimycobacterial and cytotoxic activity against mycobacterium tuberculosis. | |||
T25462 |
Griselimycin
RP-11072-B,RP11072-B,RP 11072-B,Grisellimycin B |
||
Griselimycin is a natural antimycobacterial product that is currently being pursued as a therapy for 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。 | |||
T25565 | Kahalalide A | ||
Kahalalide A has antimycobacterial activity isolated from the mollusk Elysia rufescens. | |||
T35872 | BRD-8000.3 | ||
BRD-8000.3 is a narrow-spectrum, bactericidal antimycobacterial agent known for its specific inhibition of EfpA. It exhibits potent activity against wild-type strains and proves to be a valuable tool in tuberculosis research[1]. | |||
T80927 | Tuberculosis inhibitor 10 | ||
Tuberculosis inhibitor 10 对 MSMEG_6649 的酶活性呈现中等抑制效果,并增强了 PAS 对分枝杆菌的抑制作用。 | |||
T62087 | Tuberculosis inhibitor 4 | ||
Tuberculosis inhibitor 4 (compound 16) 是基于扁桃酸的螺噻唑烷酮,表现出有效的抗分枝杆菌 (antimycobacterial) 作用。Tuberculosis inhibitor 4 的浓度低于 6.25 μg/mL 时,能够抑制 98% 的结核分枝杆菌菌株 H37Rv。 | |||
T61192 | CBR-6672 | ||
CBR-6672, a type II NADH dehydrogenase inhibitor, demonstrates potent antimycobacterial activity against mycobacterium tuberculosis (Mtb) with a minimum inhibitory concentration (MIC) of 0.14 μM [1]. | |||
T60465 | Anti-infective agent 2 | ||
Anti-infective agent 2 (化合物 3k) 是一种抗原生动物和抗分枝杆菌剂。Anti-infective agent 2对P. falciparum 和T. brucei rhodesiense 显示出抗寄生虫活性,IC50值分别为 0.07 和 2.20 μM。Anti-infective agent 2 对耻垢分枝杆菌显示出抗分支杆菌活性,其MIC 为 32 μg/mL。 | |||
T80926 | Tuberculosis inhibitor 11 | ||
Tuberculosis inhibitor 11 (Compound 14) 是一种增强抗结核药物针对分枝杆菌活性的化学化合物。 | |||
T61984 | MtMetAP1-IN-1 | ||
MtMetAP1-IN-1 是一种蛋氨酸氨基肽酶1(MetAP1) 的抑制剂。MtMetAP1-IN-1 显示出抗分枝杆菌活性。 | |||
T7062 | Ethambutol | ||
Ethambutol 是一种抗分枝杆菌化合物,通过抑制阿拉伯糖基转移酶活性阻止细胞壁的形成。 | |||
T79029 |
IpOHA
|
||
IpOHA是一种高效的KARI抑制剂,同时具备抗结核分枝杆菌的药理活性,针对Mycobacterium tuberculosis (Mt)的Ki值达到97.7 nM。 | |||
T60468 | Anti-infective agent 3 | ||
Anti-infective agent 3 是一种抗原生动物和抗分枝杆菌剂。Anti-infective agent 3 (compound 3l) 对 P. falciparum 和 T. brucei rhodesiense 显示出抗寄生虫活性,IC50值分别为 0.47 和 0.13 μM。Anti-infective agent 3 对耻垢分枝杆菌显示出抗分支杆菌活性,MIC 值为 4 μg/mL。 | |||
T38355 |
Lariatin A
|
||
Lariatin A is an antimycobacterial lasso peptide originally isolated from R. jostii. It is active against M. tuberculosis and M. smegmatis in vitro (MICs = 0.39 and 0.1 μg/ml, respectively). Lariatin A increases survival in a silkworm model of M. smegmatis infection (ED50 = 0.5 μg/g). | |||
T37541 | Amycolatopsin C | ||
Amycolatopsin C is a polyketide macrolide originally isolated fromAmycolatopsisthat has antimycobacterial and anticancer activities.1It is active againstM. bovisandM. tuberculosis(IC50s = 2.7 and 5.7 μM, respectively) but notB. subtilis,S. aureus,E. coli, orP. aeruginosa(IC50s = >30 μM for all). Amycolatopsin C is cytotoxic to SW620 colorectal and NCI H460 lung cancer cells (IC50s = 10 and 5.9 μM, respectively). 1.Khalil, Z.G., Salim, A.A., Vuong, D., et al.Amycolatopsins A-C: Antimycobacterial ... | |||
T60315 | Anti-infective agent 1 | ||
Anti-infective agent 1 (化合物 3a) 是一种有效的、选择性的抗原生动物和抗结核分枝杆菌剂。Anti-infective agent 1 对P. falciparum 和T. brucei rhodesiense 具有抗寄生虫活性,IC50分别为 10.95 和 0.06 μM。Anti-infective agent 1 显示出对耻垢分枝杆菌的抗分支杆菌活性,MIC 为 8 μg/mL。 | |||
T60716 |
Antitubercular agent-28
|
||
Antitubercular agent-28 (compound 2) 对结核分枝杆菌 H37Rv 的耐药分离株具有抗分枝杆菌活性。Antitubercular agent-28 是有效的抗结核药剂,MICb 值为 4.5 μM,IC50值为 1.5 μM,IC90值为 2.5 μM。Antitubercular agent-28 显示出有效的细胞内抗分枝杆菌活性,并且细胞毒性低。 | |||
T63286 |
Antituberculosis agent-3
|
||
Antituberculosis agent-3 是一种具有抗霉菌作用的抗结核剂,对结核杆菌 H37Rv 株的生长具有抑制作用,其 MIC 值为 12.5 μg/mL。 | |||
T72262 | Antituberculosis agent-6 | ||
Antituberculosis agent-6 是一种有效的抗结核分枝杆菌 (antimycobacterial) 剂。Antituberculosis agent-6 对M. tuberculosis 显示出显著的抑制活性,MIC 为 3.49 μM。Antituberculosis agent-6 还对A. niger 表现出良好的抗真菌 (antifungal) 活性,MIC 为 62.50 μM。 Antituberculosis agent-6 表现出高胃肠道吸收。 | |||
T37539 |
Amycolatopsin A
|
||
Amycolatopsin A is a macrolide polyketide originally isolated fromAmycolatopsisthat has antimycobacterial and anticancer activities.1It is active againstM. bovisandM. tuberculosis(IC50s = 0.4 and 4.4 μM, respectively) but notB. subtilis,S. aureus,E. coli, orP. aeruginosa(IC50s = >30 μM for all). Amycolatopsin A is cytotoxic to SW620 colorectal and NCI H460 lung cancer cells (IC50s = 0.08 and 1.2 μM, respectively). 1.Khalil, Z.G., Salim, A.A., Vuong, D., et al.Amycolatopsins A-C: Antimycobacteria... | |||
T37070 |
Pyridomycin
|
||
Pyridomycin is a structurally unusual antimycobacterial cyclodepsipeptide whose composition includes two rare moieties: 3-(3-pyridyl)-L-alanine and 2-hydroxy-3-methylpent-2-enoic acid. It inhibits NADH-dependent enoyl (Acyl-Carrier-Protein) reductase InhA, preventing mycolic acid synthesis in M. tuberculosis, including isoniazid-resistant strains (MICs = 0.31-0.63 μg/ml). | |||
T61665 | Antibacterial agent 118 | ||
Antibacterial agent 118 (also known as compound 20) is a potent antimycobacterial compound with activity against various mycobacterial strains, including Mtb H37Ra, M. aurum, M. smegmatis, Mtb H37Rv, and M. avium. The minimum inhibitory concentration (MIC) values for Antibacterial agent 118 against these strains are 40.7 μM, 10.2 μM, 163.0 μM, 62.5 μM, and 62.5 μM, respectively. This compound holds potential for tuberculosis research [1]. | |||
T78918 | Antitubercular agent-37 | ||
Antitubercular agent-37为具备显著抗分枝杆菌活性之抗菌剂,其最小抑菌浓度(MIC)为0.16 μg/mL,适用于结核病相关研究。 | |||
T78714 |
PptT-IN-4
|
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
PptT-IN-4 (Compound 3a) 为PptT抑制剂,IC50为0.71 μM。其对MtbH37Rv的MIC值为42 μM,并且还能抑制hERG、hCav1.2和hNav1.5通道,对应IC50s分别为11 μM、8.1 μM、6.9 μM。 | |||
T83222 |
AB131
|
||
AB131,作为MSMEG 6649和Rv2172c的抑制剂,显示出低微摩尔级别的抑制常数 (Ki值分别为0.16和0.02 μM)。该化合物能够提升抗结核药物对分枝杆菌属的抗菌效力。 | |||
T75019 | Antituberculosis agent-7 | ||
Antituberculosis agent-7 是一种氧杂环丁基喹啉衍生物,对P. mirabilis 具有良好的抗菌活性,MIC 为 31.25 μM。Antituberculosis agent-7 对A. niger 显示出良好的抗真菌活性,MIC 为 62.5 μM。Antituberculosis agent-7 显示出优异的抗分枝杆菌活性,对结核分枝杆菌 H37Rv 的 MIC 为 3.41 μM。 | |||
T79440 |
DprE1-IN-5
|
||
DprE1-IN-5(Compound 10)为一种DprE1抑制剂,对Mtb H37Rv菌株表现出抗结核活性(MIC: 4 μM),并对耐药菌株具有抗分枝杆菌效果,同时展现出较高的微粒体稳定性。 | |||
T61142 |
Antitubercular agent-17
|
||
Antitubercular agent-17 (Compound 8a) 是一种抗结核剂,对 M. tuberculosisH37Rv、Spec. 192、Spec 210 和 Spec. 800 的 MIC 值分别为 2、2、2 和 128 μg/ml。Antitubercular agent-17 表现出高选择性的抗分支杆菌效果。 | |||
T61141 | Antitubercular agent-27 | ||
Antitubercular agent-27 (compound 1) 是一种有效的抗结核药剂,IC50值为 3.2 μM,MICb> 值为 7.8 μM,IC90值为 7.0 μM。Antitubercular agent-27 对结核分枝杆菌 H37Rv 的耐药分离株显示出抗分枝杆菌活性。Antitubercular agent-27 显示出有效的细胞内抗分枝杆菌活性和低细胞毒性。 | |||
T61143 |
Antitubercular agent-18
|
||
Antitubercular agent-18 (Compound 9a) 为抗结核剂,对M. tuberculosisH37Rv、Spec. 192、Spec 210 及 Spec. 800 的最小抑制浓度(MIC)值依次为2、2、2 及128 μg/ml,展现出对分支杆菌的高选择性抗菌活性。 | |||
T78746 |
Mtb-IN-3
|
||
Mtb-IN-3(化合物10c)是针对结核分枝杆菌(Mtb)的选择性抑制剂。该化合物具有有效的体外抗Mtb活性,并且不表现出细胞毒性。在小鼠结核病模型中,Mtb-IN-3可抑制脾脏的集落形成。 | |||
T79442 |
DprE1-IN-7
|
||
DprE1-IN-7 (Compound 64) 是一款具有抗结核活性的DprE1抑制剂,对Mtb H37Rv菌株表现出明显的功效(MIC: 4 μM),并对耐药分枝杆菌株也显示出活性。此化合物在微粒体中稳定性强,并具有中等的清除速率。 | |||
T78883 |
DprE1-IN-9
|
||
DprE1-IN-9(compound B18)是一款高效的可逆DprE1抑制剂,能够结合至DprE1的受体腔。该化合物对分枝杆菌表现出显著的抗菌活性,作用于非致病性菌株H37Ra(MIC=0.18 µg/mL)及致病性H37Rv菌株,并对多重耐药(MDR)和极度耐药(XDR)的临床分离株同样有效。 | |||
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... | |||
T60570 |
Anti-inflammatory agent 11
|
||
Anti-inflammatory agent 11 (化合物 16) 是有效的抗结核分枝杆菌剂,可用于结核病(TB)的研究。Anti-inflammatory agent 11 抑制Mtb H37Rv 和M299的生长,MIC50分别为 1.3 和 6.9 μM。Anti-inflammatory agent 11 也是一种抗炎剂,通过抑制 iNOS 的表达抑制NO,同时抑制 TNF-α 和 IL-1β 的产生。 | |||
T60560 | Anti-inflammatory agent 15 | ||
Anti-inflammatory agent 15 (化合物 29) 是有效的抗结核分枝杆菌剂,可用于结核病(TB)的研究。Anti-inflammatory agent 15 抑制 Mtb H37Rv 和 M299生长,MIC50分别为 2.3 和 7.8 μM。Anti-inflammatory agent 15也是一种抗炎剂, 通过抑制 iNOS 的表达来抑制 NO,同时也抑制 TNF-α 和 IL-1β 的产生。 | |||
T35706 |
25-Desacetyl Rifampicin
|
||
25-Desacetyl rifampicin is a major active metabolite of the rifamycin antibiotic rifampicin .125-Desacetyl rifampicin is active againstM. smegmatis(MIC99= 2.66 μM). 1.Kigondu, E.M., Njoroge, M., Singh, K., et al.Synthesis and synergistic antimycobacterial screening of chlorpromazine and its metabolitesMed. Chem. Commun.5502-506(2014) | |||
T37540 | Amycolatopsin B | ||
Amycolatopsin B is a bacterial metabolite originally isolated fromAmycolatopsisthat has anticancer activity.1It is cytotoxic to NCI H460 lung and SW620 colon cancer cells (IC50s = 0.28 and 0.14 μM, respectively). 1.Khalil, Z.G., Salim, A.A., Vuong, D., et al.Amycolatopsins A-C: Antimycobacterial glycosylated polyketide macrolides from the Australian soil Amycolatopsis sp. MST-108494J. Antibiot. (Tokyo)70(12)1097-1103(2017) |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN1121 |
Evocarpine
|
Apoptosis; cAMP; Anti-infection; Calcium Channel; Antibacterial | Apoptosis; GPCR/G Protein; Membrane transporter/Ion channel; Metabolism; Microbiology/Virology |
Evocarpine 是从 Evodiae fructus 分离得到的一种喹诺酮类生物碱,有抗细菌活性。它可通过电压依赖性钙通道抑制 Ca2+内流。 | |||
TN6729 |
Azadiradione
AZD |
Others | Others |
Azadiradione (AZD) 是 HSF1的一种,是由印楝树中提取得到,具有一定生物活性的柠檬苦素。 | |||
TN1926 |
Methyl caffeate
Methyl caffeate acid,金银花,咖啡酸甲酯 |
Others; Antibacterial | Microbiology/Virology; Others |
Methyl caffeate (Methyl caffeate acid) acid 是一种抗微生物剂,有抗菌和抗分枝杆菌活性。它还抑制 α-葡萄糖苷酶,有氧化应激抑制活性,抗血小板活性,子宫颈癌的抗增殖活性以及肺和白细胞的抗癌活性。 | |||
TN2101 |
Primin
|
Antifection | Microbiology/Virology |
Primin 是存在于 Primula obconica 叶和茎毛状体中的天然产物,显示出抗菌和抗癌活性。 | |||
T0810 |
Ethambutol dihydrochloride
Ethambutol 2HCl,盐酸乙胺丁醇,Emb dihydrochloride,CL40881 |
Antibacterial; Antibiotic; Antifungal | Microbiology/Virology |
Ethambutol dihydrochloride (CL40881) 能抗分枝杆菌,可抑制阿拉伯糖基转移酶活性来阻止细胞壁形成。 | |||
T1426 |
Pyrazinamide
Pyrazinoic acid amide,Pyrazinecarboxamide,吡嗪酰胺 |
Antibacterial; Antibiotic; Autophagy; Fatty Acid Synthase | Autophagy; Metabolism; Microbiology/Virology |
Pyrazinamide (Pyrazinecarboxamide) 是一种口服抗结核类抗生素。它是一种前药,通过结核分枝杆菌pncA 基因编码的 PZase/烟酰胺酶转化为活性吡嗪酸形式。 | |||
TN5503 |
Linaroside
|
Antibacterial | Microbiology/Virology |
Linaroside 在 6.25 microg mL(-1) 浓度下对结核分枝杆菌、菌株 H(37)Rv 的抗分枝杆菌活性表现出 30%的抑制作用。 | |||
T5747 |
ISOBERGAPTEN
|
Others | Others |
Isobergapten 是一种化感抑制剂,分离自Hevacleum laciniatum 种子。 | |||
TN2755 |
2-Desoxy-4-epi-pulchellin
|
Anti-infection | Microbiology/Virology |
2-Desoxy-4-epi-pulchellin 是分离自 Polygonum hydropiper 的二氯甲烷可溶部分的一种化合物。 | |||
TN1019 |
Beta-mangostin
β-Mangostin,beta-倒捻子素 |
Apoptosis; Antibacterial; Parasite | Apoptosis; Microbiology/Virology |
Beta-mangostin (β-Mangostin) 是存在 Cratoxylum arborescens 中的一种氧杂蒽酮类天然产物,有抗癌和抗菌活性,对结核分枝杆菌的 MIC 值为 6.25 μg/mL。它在体外有抗疟活性,对恶性疟原虫的 IC50值为 3.00 μg/mL。 | |||
T6S1684 |
8-Gingerol
|
Antioxidant; Antibacterial; TRP/TRPV Channel | Membrane transporter/Ion channel; Microbiology/Virology; oxidation-reduction |
8-Gingerol 分离自姜的根状茎,是口服有效的 TRPV1激活剂,EC50值为5.0 µM。8-Gingerol 抑制 COX-2,还能抑制体外 H. pylori 的生长。 | |||
TN5684 |
5,6-Desmethylenedioxy-5-methoxyaglalactone
|
||
5,6-Desmethylenedioxy-5-methoxyaglalactone is cytotoxic to small cell lung cancer (NCI-H187) cell line. It has antimycobacterial activity against Mycobacterium tuberculosis H(37)Ra. | |||
TN5657 | Goniotriol | ||
Goniotriol shows antimycobacterial activity against Mycobacterium tuberculosis (MIC =100 microg/mL). It exhibits antiplasmodial activity against Plasmodium falciparum (IC50=2.6 microg/mL). Goniotriol shows cytotoxicity against cancer cells, KB, BC1, NCI-H | |||
T11274 |
Ferulenol
|
Others | Others |
Ferulenol, a sesquiterpene prenylated coumarin derivative, exhibits potent antimycobacterial activity and haemorrhagic action. This compound selectively targets succinate ubiquinone reductase within the ubiquinone cycle as its specific mode of inhibition. | |||
TN5581 |
Rediocide C
|
||
Rediocide C exhibits antimycobacterial activity, with the MIC value of 3.84 uM; it also exhibits potent activity against D. pteronyssinus with respective LC50 values of 5.59 microg/cm2. | |||
T38295 |
Calpinactam
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Calpinactam is a fungal metabolite originally isolated from M. alpina that has antimycobacterial activity. It is active against M. smegmatis (MIC = 0.78 μg/ml) but not a panel of 13 other bacteria and fungi. Calpinactam increases survival in a silkworm model of M. smegmatis infection (ED50 = 5 μg/larva). | |||
TN5134 |
Tetrahydroxysqualene
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Antifection | Microbiology/Virology |
Tetrahdroxysqualene shows antimycobacterial activity with an MIC of 10.0 microg/mL, while showing only modest cytotoxicity. | |||
TN3560 |
Cabralealactone
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Antifection | Microbiology/Virology |
Cabralealactone displays antimycobacterial activity against Mycobacterium tuberculosis, it is weakly cytotoxic to a breast cancer (BC) cell line, it is moderately active against a small-cell lung cancer (NCI-H187) cell line. | |||
TN3559 |
Cabraleahydroxylactone
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HSV | Microbiology/Virology |
Cabraleahydroxylactone displays antimycobacterial activity against Mycobacterium tuberculosis, it is weakly cytotoxic to a breast cancer (BC) cell line.It shows antiviral activity against herpes simplex virus type-1 with an IC50 value of 3.20 ug/mL, in comparison with the standard acyclovir (IC50=1.90ug/mL). | |||
TN3557 |
Cabraleadiol
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ATPase; Antifection | Membrane transporter/Ion channel; Microbiology/Virology |
Cabraleadiol displays antimycobacterial activity against Mycobacterium tuberculosis, it also is weakly cytotoxic to a breast cancer (BC) cell line. Cabraleadiol inhibits photosystem II (PS II) and induces the appearance of small G band which is related wi | |||
TN3924 | Eichlerialactone | Others | Others |
Eichlerialactone and ethyl eichlerianoate show antimycobacterial activity against mycobacterium tuberculosis H37Ra, with minimum inhibitory concentration in the range of 25-50ug/mL; eichlerialactone exhibits good antibacterial activity against both the Gr | |||
T75631 | Ganorbiformin B | ||
Ganorbiformin B是一种具有与灵芝酸相同羊毛甾烷骨架的羊毛甾烷三萜类化合物。其C-3差向异构体灵芝酸T对结核分枝杆菌H37Ra显示出强抗分枝杆菌活性。 |