38
20
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T4248 |
T.cruzi Inhibitor (1350920-22-7(free base))
|
Antibiotic | Microbiology/Virology |
T.cruzi Inhibitor (1350920-22-7(free base)) 是一种克氏锥虫抑制剂。 | |||
T4198 |
T.cruzi-IN-1
MDK1088,T.cruzi Inhibitor |
Antibiotic; Parasite | Microbiology/Virology |
T.cruzi-IN-1 (MDK1088) 是一种克氏锥虫抑制剂,IC50为 8 nM。它是一种 4-三氟甲基取代的类似物,有潜力治疗南美锥虫病的急性和慢性阶段。 | |||
T64320 |
ML251
|
Glucokinase; Parasite | Metabolism; Microbiology/Virology |
ML251 是一种有效的新型纳摩尔 T. brucei 和 T. cruzi 磷酸果糖激酶抑制剂,对 T. brucei PFK 和 T. cruzi PFK 的 IC50值为 0.37和 0.13 μM,可研究寄生虫。 | |||
T61114 | Anti-Trypanosoma cruzi agent-2 | ||
Anti-Trypanosoma cruzi agent-1 (Compd 3b) 对NINOA trypomastigote (IC50= 0.51 μM) 和 INC-5 epimastigote (IC50= 3.06 μM) 锥虫具有选择性,具有有效的抗弓形虫活性。 | |||
T63869 |
Anti-Trypanosoma cruzi agent-3
|
||
Anti-Trypanosoma cruzi agent-3 是一种抗原虫 (antiprotozoal) 剂。 | |||
T72134 | Anti-Trypanosoma cruzi agent-4 | ||
Anti-Trypanosoma cruzi agent-4是克氏锥虫抑制剂。Anti-Trypanosoma cruzi agent-4 可用于感染的研究。 | |||
T62333 | Anti-Trypanosoma cruzi agent-1 | ||
Anti-Trypanosoma cruzi agent-1 (Compd E5) 具有有效的抗弓形虫效果。 | |||
T5325 |
Nifurtimox
硝呋替莫,BAY-2502,BAY-A-2502 |
Dehydrogenase; Parasite | Metabolism; Microbiology/Virology |
Nifurtimox (BAY-A-2502) 是一种用于锥虫病的抗虫剂,可影响乳酸脱氢酶活性。它有潜力研究神经母细胞瘤细胞。 | |||
T2112 |
Fexinidazole
非昔硝唑,HOE 239 |
Others; Parasite | Microbiology/Virology; Others |
Fexinidazole (HOE 239) 是具有口服活性的硝基咪唑抗锥虫药物。它显示出对布鲁氏杆菌亚种和菌株的杀锥虫活性,IC50值为 0.7-3.3 μM (0.2-0.9 μg/ml)。它具有用于因感染布鲁氏菌引起的人类昏睡病的潜力。 | |||
T68109 |
Moxipraquine
|
Antibiotic | Microbiology/Virology |
Moxipraquine 是一种新型的8-氨基喹诺酮类化合物,对克氏锥虫具有抗感染活性。Moxipraquine 能有效抑制寄生虫血症,但不能根除小鼠或豚鼠的感染。Moxipraquine 对重度利什曼原虫、墨西哥乳杆菌和巴西乳杆菌的实验性感染有效,但对巴西乳杆菌无效。 | |||
T4982 |
Benznidazol
苄哒唑,苄硝唑,Radanil,Benznidazole,Ro 71051,Ro 07-1051 |
Antibiotic; Parasite | Microbiology/Virology |
Benznidazol (Benznidazole) 是一种抗寄生虫药物,对哥伦比亚 T. cruzi 菌株的 IC50值为 20.35 μM,有潜力研究美洲锥虫病。 | |||
T15641 |
K777
APC-3316 |
P450; Cysteine Protease; CCR | Immunology/Inflammation; Metabolism; Microbiology/Virology; Proteases/Proteasome |
K777 是有效的,具有口服活性的,不可逆的半胱氨酸蛋白酶 (cysteine protease) 抑制剂。K777是有效的 CYP3A4 抑制剂(IC50= 60 nM)。K777也是选择性的 CCR4 拮抗剂,显示出强的趋化性抑制作用。K777 对 Cruzain(克鲁斯锥虫的主要半胱氨酸蛋白酶)和组织蛋白酶 B 和 L 具有不可逆的抑制作用。K777 通过靶向组织蛋白酶介导的细胞进入,显示出广谱的抗病毒作用。K777 抑制 EBOV 和 SARS-CoV 病毒的进入,IC50 值分别为 0.87 nM 和 0.68 nM。 | |||
T25200 |
CA-IN-5g
CAIN5g |
||
CA-IN-5g is an effective carbonic anhydrase (CA) inhibitor. Carbonic anhydrase is isolated from Trypanosoma cruzi (TcCA). | |||
T27851 |
LP8
LP 8,LP-8 |
||
LP8 is a novel inhibitor of Trypanosoma cruzi CYP51. | |||
T27848 |
LP10
LP-10,LP 10 |
||
LP10 is a reverse type I inhibitor of Mycobacterium tuberculosis CYP125A1 and a Potent type II inhibitor of Trypanosoma cruzi CYP51. | |||
T25156 |
BiPNQ
|
||
BiPNQ is a Trypanosoma cruzi inhibitor. Trypanosoma cruzi is the etiological agent of Chagas disease (American trypanosomiasis). | |||
T24096 |
GNF7686
GNF-7686,GNF 7686 |
||
GNF7686 is a novel Trypanosoma cruzi inhibitor. | |||
T69249 |
AMXT1501
|
||
AMXT1501 is a polyamine uptake inhibitor, also inhibiting the putrescine transport in epimastigotes (the insect stage of t. cruzi) | |||
T61160 | Antiparasitic agent-2 | ||
Antiparasitic agent-2 (compound 8a) 对 L. infantum 和 T. cruzi 展示出较高的抗寄生效力,其 IC50 值分别为 7.28 μM 和 2.30 μM。同时,Antiparasitic agent-2 对 HepG2 癌细胞亦表现出一定的细胞毒性,CC50 值为 26.79 μM。 | |||
T60519 |
Antiparasitic agent-4
|
||
Antiparasitic agent-4 (compound 4q) 具有高抗寄生虫活性,其对于婴儿利什曼原虫 (L. infantum)的 IC50值为 8.51 μM,对克氏锥虫 (T. cruzi)的IC50值为2.20 μM。Antiparasitic agent-4 对癌细胞 HepG2 也具有细胞毒性,CC50值为 18.97 μM。 | |||
T28161 |
NEU-1045
NEU 1045,NEU1045 |
||
NEU-1045 is a T. brucei proliferation inhibitor, and is a promising lead with cross-pathogen activity. NEU-1045 inhibited T. brucei, T. cruzi, and L. major proliferation with good potency (T. brucei EC50 = 0.37 μM; T. cruzi EC50 = 2.8 μM; L. major EC50 = | |||
T63281 | Antileishmanial agent-11 | ||
Antileishmanial agent-11 是有效的抗利什曼原虫剂,能够作用于 Leishmania brazilensis (IC50: 28.3 μM)、Leishmania infantum (IC50: 24.8 μM) 和T. cruzi(IC50: 13.0 μM) 具有出抗原虫作用。 | |||
T72228 |
Antitrypanosomal agent 10
|
||
Antitrypanosomal agent 10,一种针对克氏锥虫 (Trypanosoma cruzi) 有抑制作用的抗锥虫药物,IC50 值达到 0.28 μM。 | |||
T72229 | Antitrypanosomal agent 11 | ||
Antitrypanosomal agent 11,抑制克氏锥虫(Trypanosoma cruzi),IC50值为0.23 μM,具有显著的抗锥虫活性。 | |||
T79316 |
Antitrypanosomal agent 15
|
Proteasome | Proteases/Proteasome; Ubiquitination |
Antitrypanosomal agent 15 (compound 26) 是一种具有口服活性、能穿透血脑屏障、对克氏锥虫蛋白酶体具有高选择性的抑制剂,其对克氏锥虫蛋白酶体的pIC50值为7.4,而对人蛋白酶体的pIC50值小于4。该化合物展现出良好的ADME性质,适合用于恰加斯病研究。 | |||
T75118 | AN15368 | ||
AN15368 是一种具有口服活性的小分子前药,可以被寄生虫羧肽酶激活,产生一种靶向 T. cruzi.中信使 RNA 加工途径的化合物 cruzi. AN15368 具有预防和研究南美锥虫病的潜力。 | |||
T62212 |
Antitrypanosomal agent 4
|
||
Antitrypanosomal agent 4 (compound 19) 是一种有效的、能够透过血脑屏障的抗锥体虫剂,对克氏锥 (T. cruzi) 和布氏锥虫 (T. b. brucei) 表现出良好的抗性,其 IC50 值分别为 1.2 μM 和 70 nM。 | |||
T28011 |
Megazol
CL 64855,CL-64855,CL64855 |
||
Megazol is a nitroimidazole based drug that cures some protozoan infections. A study of nitroimidazoles found the drug extremely effective against T. cruzi and T. brucei which cause Chagas disease and African sleeping sickness, respectively. | |||
T62401 | Anti-infective agent 4 | ||
Anti-infective agent 4 (compound 73) 是一种口服具有活力的 Trypanosoma cruzi 抑制剂 (IC50: 0.016 μM)。Anti-infective agent 4 能够有效降低体内寄生虫负担,能够用于研究感染。 | |||
T79415 | Antiparasitic agent-18 | Parasite | Microbiology/Virology |
Antiparasitic agent-18 (compound 3a) 对T. brucei (EC50=0.4 μM)、T. cruzi (EC50=0.21 μM) 和 L. donovani (EC50=0.26 μM) 表现出高度的活性和选择性,证明其为一种有效的抗原虫化合物。 | |||
T62330 | Antileishmanial agent-12 | ||
Antileishmanial agent-12 (compound 5a) 是一种有效的抗利什曼原虫剂,对 Leishmania brazilensis (IC50: 14.9 μM)、Leishmania infantum (IC50: 21.3 μM) 和 T. cruzi (IC50: 9.3 μM) 具有抗原虫作用。 | |||
T83024 | Antiparasitic agent-20 | Parasite | Microbiology/Virology |
Antiparasitic agent-20 (Compound 1p) 是一种抗寄生虫剂,对T. brucei和T. cruzi展现出显著效力,其EC50值分别为0.09 μM和14.1 μM,表现出其广泛的抗寄生虫活性。 | |||
T37255 |
12-methyl Myristic Acid methyl ester
|
||
12-methyl Myristic acid methyl ester is a methylated fatty acid methyl ester that has been found in vermicomposts of cattle manure, carica papaya leaves, and cuticular wax of K. africana. It is a volatile compound in lipid-lowering granulated tea. Levels of 12-methyl myristic acid methyl ester are decreased in T. cruzi treated with nifurtimox compared to non-treated controls. | |||
T83025 | Antiparasitic agent-19 | ||
Antiparasitic agent-19 (compound 40) 是一种化合物,具备广泛的抗寄生虫活性,且对布氏锥虫、婴儿利什曼原虫和克氏锥虫具有较低的毒性。 | |||
T35760 |
Carnaubadiol
|
||
Carnaubadiol is a triterpene that has been found in E. corollata and has antiprotozoal activities.1,2 It is active against L. infantum promastigotes and amastigotes, as well as T. cruzi trypomastigotes (IC50s = 46.2, 7.8, and 14.9 μM, respectively).2 |1. Piatak, D.M., and Reimann, K.A. Plant investigations IV. Corollatadiol A new triterpene from euphorbia corollata. Tetrahedron Lett. 13(44), 4525-4528 (1972).|2. de Almeida, B.C., Araújo, B.Q., Carvalho, A.A., et al. Antiprotozoal activity of ext... | |||
T79390 |
Antileishmanial agent-23
|
Parasite | Microbiology/Virology |
Antileishmanial agent-23 (compound G1/9) 作为一种选择性trypanothione reductase (TR)抑制剂效力显著,展现了2.24 ± 0.52 μM的IC50值。该化合物有效抑制了利什曼原虫、克氏锥虫和布氏锥虫的生长。 | |||
T61158 | Anti-infective agent 5 | ||
Anti-infective agent 5 (compound 74) is an orally active inhibitor of Trypanosoma cruzi exhibiting an IC50 value of 0.10 μM. In addition to its potent inhibitory effect, anti-infective agent 5 demonstrates efficacy in reducing parasite burden in vivo. Consequently, this compound holds promising potential for research pertaining to infection. [1] | |||
T37062 |
L-Leucine-7-amido-4-methylcoumarin hydrochloride
|
||
L-Leu-AMC is a fluorogenic substrate for leucine aminopeptidase.1Upon enzymatic cleavage by leucine aminopeptidase, AMC is released and its fluorescence can be used to quantify leucine aminopeptidase activity. AMC displays excitation/emission maxima of 340-360/440-460 nm, respectively. 1.Izquierdo, M., Lin, D., O’Neill, S., et al.Development of a high-throughput screening assay to identify inhibitors of the major M17-leucyl aminopeptidase from Trypanosoma cruzi using rapidfire mass spectrometryS... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN7074 |
(2E)-3-(1,3-Benzodioxol-5-yl)-2-propenoic acid
|
Antibiotic | Microbiology/Virology |
(2E)-3-(1,3-Benzodioxol-5-yl)-2-propenoic acid 对克氏锥虫的 EC50 值为 73.5 μM。 | |||
TN1375 |
α-Lapachone
ALPHA-拉杷醌,alpha-Lapachone |
Topoisomerase; Antifection | DNA Damage/DNA Repair; Microbiology/Virology |
α-Lapachone 具有杀锥虫作用。 | |||
TN6930 |
5-Desmethylsinensetin
|
Others | Others |
5-desmethylsinensetin 是分离自Stevia satureiifoliavar.satureiifolia 的天然产物,显示出抗原生动物的活性,抑制T. cruzi epimastigotes 和trypomastigotes 的IC50分别为 0.4 μg/mL 和75.1 μg/mL。 | |||
T2S1792 |
Lycobetaine
石蒜内胺,Ungeremine,石蒜醋胺,石蒜碱内铵盐 |
Antibacterial | Microbiology/Virology |
Lycobetaine (Ungeremine) 是一种潜在的抗罗克福尔青霉和黑曲霉的生物杀菌剂。它对柱状黄杆菌有很强的抗菌活性。它有效地靶向哺乳动物以及细菌I 型和II 型拓扑异构酶。它显示出强烈的乙酰胆碱酯酶抑制活性(IC(50) 值为 0.35 microM)。 它具有抗原生动物活性,在体外试验中对Trypanosoma brucei rhodesiense、T. cruzi 表现出良好的活性。 | |||
T3794 |
Pentagalloylglucose
Penta-O-galloyl-β-D-glucose,1,2,3,4,6-O-Pentagalloylglucose,1,2,3,4,6-Penta-O-galloyl-beta-D-glucopyranose,1,2,3,4,6-五没食子酰葡萄糖 |
Influenza Virus | Microbiology/Virology |
1,2,3,4,6-O-Pentagalloylglucose (Penta-O-galloyl-β-D-glucose) 存在于多种植物中,具有重要的药理作用。Pentagalloylglucose 表现出显著的抗狂犬病病毒 (RABV) 活性。 | |||
TN2931 |
3-Epikatonic acid
|
Antifection | Microbiology/Virology |
Epikatonic acid shows less active against T. (S.) cruzi trypanosome. | |||
TN4227 |
Horminone
|
NADPH-oxidase; DNA/RNA Synthesis; Antifection | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Immunology/Inflammation; Microbiology/Virology |
Horminone has antimicrobial activity, it can inhibit the protein synthesis in several types of bacteria; it can inhibit the in vitro growth of Trypanosoma cruzi, 30 microM drug concentration producing total inhibition of growth. After administration of plant extracts containing Horminone has possibility of toxic effect. | |||
T82716 |
cis-Melilotoside
|
||
cis-Melilotoside, 一种 o-Coumaric acid 衍生物,显示出强大的抗氧化活性。该化合物针对T. cruzi表现出适度抗原生动物活性,IC50值为78.2 ug/mL。 | |||
T73068 | Mammea A/BA | ||
Mammea A/BA 对克氏锥虫 (T. cruzi) 显示出有效抗性。通过诱导线粒体功能障碍、产生活性氧 (ROS)、DNA 片段化以及增加酸性液泡数量,Mammea A/BA 触发细胞死亡机制,包括细胞凋亡 (apoptosis)、细胞自噬 (autophagy) 和细胞坏死,对于南美锥虫病的研究具有潜在应用价值。 | |||
T72234 |
3β-Hydroxy-hop-22(29)-ene
|
||
3β-Hydroxy-hop-22(29)-ene 是一种有效的抗寄生虫剂 (antiparasiticagent)。3β-Hydroxy-hop-22(29)-ene 对克氏锥虫和墨西哥利什曼原虫具有一定的抑制活性。 | |||
TN6501 | Isololiolide | ||
Isololiolide has phytotoxicity, it inhibited seedling growth of cress and barnyard grass. It also showed in vitro activity against both trypomastigote and intracellular amastigotes of Trypanosoma cruzi, with IC50 values of 32 μM and 40 μM, respectively. I | |||
TN3549 | Burchellin | Antifection | Microbiology/Virology |
Burchellin has larvicidal activity, it can interfer with the development cycle of the mosquito, where its strongest toxic effect is 100% mortality in larvae (L3) at concentrations ¥ 30 ppm. Burchellin and licarin A have activity against Trypanosoma cruzi | |||
TN3721 |
Cryptofolione
|
Antifection | Microbiology/Virology |
Z-Cryptofolione and Cryptomoscatone D2 as highly efficacious inhibitors of the G(2) checkpoint, G(2) checkpoint inhibitors can force cells arrested in G(2) phase by DNA damage to enter mitosis. Cryptofolione shows moderate cytotoxicity in both macrophages and T. cruzi amastigotes, it also displays a mild inhibitory effect on the promastigote form of Leishmania spp. | |||
TN4664 |
Norarmepavine
|
Others | Others |
N-norarmepavine shows significant cytotoxic activities against HL-60 carcinoma cell line with inhibitory ratios of 51.43% at concentration of 1 x 10(-5) M. Norarmepavine shows inhibition against Trypanosoma cruzi. D-(+)- N-norarmepavine exhibits significa | |||
TN5404 |
(+)-Conocarpan
|
||
Conocarpan has antinociceptive effects. Conocarpan is quite active against S. aureus and B. subtilis with MIC of 6.25 micrograms/ml, it also shows activity against M. tuberculosis (MIC=15.6 ug/ml). Conocarpan shows considerable activity against epimastigo | |||
T72459 | 3-Oxo-hop-22(29)-ene | ||
3-Oxo-hop-22(29)-ene 是一种yeast α-glucosidase 抑制剂。3-Oxo-hop-22(29)-ene 具有中等的抗克氏锥虫和抗墨西哥利什曼原虫活性。3-Oxo-hop-22(29)-ene 具有微弱的抗炎活性。 | |||
T38243 | Hygrolidin | ||
Hygrolidin is a macrocyclic lactone originally isolated from S. hygroscopicus. It inhibits proliferation of a variety of cancer cell lines, including DLD-1 colon cancer, LNCaP prostate cancer, and K562 leukemia cells (IC50s = 2.9, 5.2, and 33 ng/ml, respectively). Hygrolidin induces the expression and levels of p21 in DLD-1 cells, but not WI-38 fibroblasts, and leads to cell accumulation in the G1 and S phases without inducing apoptosis. It has antiparasitic activity against T. cruzi, L. donovan... | |||
TN5243 |
Vitexilactone
|
NADPH-oxidase; HIV Protease; Antifection | Immunology/Inflammation; Microbiology/Virology; Proteases/Proteasome |
Vitexilactone is a HIV-1 reverse transcriptase inhibitor in virtual screening against Indonesian Herbal Database using AutoDock4 performed on HIV-1 reverse transcriptase. It has trypanocidal activity, the minimum lethal concentration against epimastigotes | |||
T35750 |
Trypacidin
|
||
Trypacidin is a fungal metabolite originally isolated fromA. fumigatus.1It is active againstB. subtilisandM. bovis(MICs = 12.5 and 1.25 μg/ml, respectively), as well asT. cruziandT. gondii(MICs = 5-10 and 10-20 μg/ml, respectively).1,2It reduces viability and induces lysis of A549 human lung cancer cells (IC50s = 7.4 μM for both).3Trypacidin increases survival in a mouse model ofT. gondiiinfection when administered in six doses of 12.5 mg/kg each.1 1.Balan, J., Ebringer, L., Nemec, P., et al.Ant... | |||
T36448 |
(E)-Ajoene
|
||
(E)-Ajoene is a disulfide that has been found inA. sativumand has diverse biological activities.1,2,3,4It is active against Gram-positive and Gram-negative bacteria (MICs = 10-250 and 150->500 μg/ml, respectively) and fungi (MICs = 15-50 μg/ml).1(E)-Ajoene inhibits proliferation of a variety of cancer cells, including MDA-MB-231 breast, HeLa cervical, and WHCO1 esophageal cancer cells (IC50s = 18.6, 61, and 39.2 μM, respectively).2It also inhibits human glutathione reductase andT. cruzitrypanoth... |