55
25
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
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。 | |||
T27135 |
DDD85646
DDD 85646,DDD-85646 |
Parasite | Microbiology/Virology |
DDD85646 是 T. brucei N-myristoyltransferase 的抑制剂,Ki 为 1.44 nM,IC50 为 2 nM,EC50 为 2 nM。 hNMT 的 IC50 为 4 nM。 | |||
T125190 |
Bruceine C
|
||
Bruceine C 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 T125190。 | |||
T23973 |
DDD100097
DDD 100097,DDD-100097 |
Others | Others |
DDD100097 是一种有效的 N-肉豆蔻醇转移酶抑制剂,对布氏锥虫具有潜在的抑制作用,可用于研究神经系统疾病。 | |||
T10340 |
Antitrypanosomal agent 2
|
Parasite | Microbiology/Virology |
Antitrypanosomal agent 2 显示出针对布氏锥虫的有效且特异性的抗寄生虫活性。 | |||
T63059 |
CRK12-IN-1
|
Antibiotic | Microbiology/Virology |
CRK12-IN-1 是一种有效的CRK12抑制剂。CRK12-IN-1具有杀虫活性, 对布氏锥虫 (T.b. brucei) 和刚果锥虫 (T. congolense) 具有抑制作用EC50分别为1.3和18 nM。CRK12-IN-1能迅速杀死病原细胞。 | |||
T10339 |
Antitrypanosomal agent 1
|
Parasite | Microbiology/Virology |
Antitrypanosomal agent 1 是一种有效的选择性锥虫硫酮还原酶抑制剂,IC50为 3.3 μM。它抑制谷胱甘肽还原酶,IC50为 64.8 μM,抑制布氏锥虫,EC50为 1 μM。 | |||
T77551 |
6'-hydroxydihydrocinchonidine
|
Antibiotic; Drug Metabolite | Metabolism; Microbiology/Virology |
6'-hydroxydihydrocinchonidine 是奎宁的代谢产物,具有抗菌和抗肿瘤活性,对布氏锥虫和肺炎链球菌有抑制作用。 | |||
T77645 |
JC-229
|
TRP/TRPV Channel | Membrane transporter/Ion channel |
JC-229 是一种具有有效性和选择性的 TbRPA1 抑制剂,对布氏锥虫中的 RPA1 有抑制作用。 JC-229 可用于研究人类非洲锥虫病 (HAT) 。 | |||
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。 | |||
T23132 |
Pentamidine dihydrochloride
喷他脒二盐酸盐,MP-601205 dihydrochloride |
Phosphatase; Antibacterial; Antibiotic; Parasite; Antifungal | Metabolism; Microbiology/Virology |
Pentamidine dihydrochloride (MP-601205 dihydrochloride) 是一种抗微生物剂,会干扰 DNA 的生物合成。它是选择性蛋白酪氨酸磷酸酶和再生肝磷酸酶抑制剂。它可用于冈比亚锥虫病,抗锑利什曼病和卡氏肺孢子虫肺炎的研究,有抗肿瘤活性,抗菌活性。 | |||
T13223 |
Tuberculosis inhibitor 1
|
Others | Others |
Tuberculosis inhibitor 1 is a potent and non-cytotoxic inhibitor of trypanosoma brucei growth (EC50: 5 nM). | |||
T27456 |
GSK2188764
|
||
GSK2188764 is an inhibitor of T. brucei IPMK, partially inhibits rTbIPMK activity. | |||
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 = | |||
T6769 |
Elaiophylin
洋橄榄叶素,Efomycin E,Gopalamicin,Salbomycin,Azalomycin B |
Others; Autophagy | Autophagy; Others |
Elaiophylin (Salbomycin) 是一种自噬抑制剂,在卵巢癌细胞中有抗肿瘤活性。它对 Plasmodium falciparum K1a 和 Trypanosoma brucei brucei GUTat 3.1 菌株具有抗原生动物活性,IC50 分别为 0.36 μM 和 0.45 μM。 | |||
T11711 |
Jaspamycin
7-CN-7-C-Ino |
JAK | Angiogenesis; Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells |
Jaspamycin (7-CN-7-C-Ino) does not bind with purified human PKARIα. Anti-parasite activity. Jaspamycin (7-CN-7-C-Ino) is a potent activator of PKA, binding to the R site (PKAR), with an EC50 of 6.5 nM and Kd of 8 nM in Trypanosoma brucei. | |||
T28163 |
NEU-730
|
||
NEU-730, a novel inhibitor of TbrPDEB1, shows modest inhibition of T. brucei proliferation. | |||
T69765 | NPD-039 | ||
NPD-039 is an inhibitor of trypanosoma brucei phosphodiesterase B1 (TbrPDEB1). | |||
T69764 |
NPD-008
|
||
NPD-008 is an inhibitor of trypanosoma brucei phosphodiesterase B1 (TbrPDEB1). | |||
T28162 |
NEU-1923
|
||
NEU-1923 is a potent inhibitor of T. brucei proliferation (EC50= 0.37 μM). | |||
T70673 | NEU617 | ||
NEU617 is an inhibitor of the growth of protozoan parasites, against T. brucei bloodstream proliferation. | |||
T72267 | Antitrypanosomal agent 9 | ||
Antitrypanosomal agent 9 是一种有效的抗锥虫体剂。Antitrypanosomal agent 9 显示出对T. b. brucei 的抑制活性,其IC50为 1.15 μM。Antitrypanosomal agent 9 可用于人类非洲锥虫病 (HAT) 研究。 | |||
T78978 |
Antitrypanosomal agent 13
|
Parasite | Microbiology/Virology |
Antitrypanosomal agent 13 (compound 4b) 是一种高效的抗锥虫剂,具备显著的杀锥虫活性和细胞毒性。针对 T. brucei 和 HL-60,Antitrypanosomal agent 13 的 GI50 值分别为 0.18 μM 和 8.4 μM。 | |||
T63610 | SPR7 | ||
SPR7 是有效的、选择性的 rhodesain 抑制剂 (Ki: 0.51 nM)。SPR7 对 T. b. brucei 表现出抗寄生虫效果 (EC50: 1.65 μM)。 | |||
T79457 |
PEX5-PEX14 PPI-IN-1
|
||
PEX5-PEX14 PPI-IN-1(Compound 8)为PEX14-PEX5 PPI 抑制剂,其通过破坏PEX5-TbPEX14 PPI的作用并表现出53 μM的Ki值。该化合物还能抑制T. b. brucei的bloodstream形式,EC50为5 μM。 | |||
T61912 |
TbPTR1 inhibitor 1
|
||
TbPTR1 inhibitor 1 (compound 5d) 是有效的动基体蝶啶还原酶 1 (PTR1)抑制剂。TbPTR1 inhibitor 1抑制布氏锥虫 PTR1 (TbPTR1) 的 IC50<0.1 nM,抑制布氏锥虫 (Trypanosoma brucei) 活性的 EC50=0.66 μM。 | |||
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. | |||
T69313 |
Ascofuranone
|
||
Ascofuranone is an inhibitor of the ubiquinol oxidase activity of Trypanosoma brucei mitochondrial alternative oxidase (TAO), as well as an inhibitor of HsDHODH. | |||
T79254 |
Antitrypanosomal agent 14
|
Parasite | Microbiology/Virology |
Antitrypanosomal agent 14(Compound 1)是一种针对T. brucei的有效抑制剂,其EC50为0.47 μM。它对TbGSK3的抑制作用表现在IC50为12 μM。该化合物主要用于非洲人类锥虫病的研究。 | |||
T6642 |
Rimantadine
金刚乙胺,1-Rimantadine,盐酸左氧氟沙星 |
Influenza Virus | Microbiology/Virology |
Rimantadine (1-Rimantadine) 是一种抗流感病毒药物。 | |||
T74192 |
Z-Leu-Arg-AMC
|
||
Z-Leu-Arg-AMC为带有羧基苯甲酰(Z)的4-甲基香豆素基-7-酰胺(AMC)亮氨酸衍生物,是锥虫半胱氨酸蛋白酶Tb活性位点。 | |||
T68611 | GW837016X | ||
GW837016X, also known as NEU-391, is a potent inhibitor of protozoan parasite proliferation. GW837016X extended life of treated mice by 50%, compared to untreated controls. At the cellular level, GW837016X inhibited mitosis and cytokinesis in T. brucei. | |||
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。 | |||
T64035 | Antitrypanosomal agent 5 | ||
Antitrypanosal agent 5 是一种选择性的抗锥虫剂,能够作用于 T. brucei (IC50: 1 nM) 和 HEK293 细胞 (IC50: 483.3 μM)。 | |||
T62710 | Antitrypanosomal agent 6 | ||
Antitrypanosomal agent 6 (compound 18a) 是一种有效的抗锥体虫剂,表现出良好的 ADME 特性。Antitrypanosomal agent 6 抗布氏锥虫 (T. brucei) 的活性比 Nifurtimox 高两倍以上,IC50为 0.47 μM。Antitrypanosomal agent 6 与 DNA 具有很强的相互作用,可以选择性的结合富含 AT 碱基的 DNA。 | |||
T79253 |
HAT-IN-8
|
Parasite | Microbiology/Virology |
HAT-IN-8(Compound 38)是一款能穿透血脑屏障的T. brucei抑制剂(EC50:0.18 μM),适用于研究人类非洲锥虫病。 | |||
T62372 | Antitrypanosomal agent 8 | ||
Antitrypanosomal agent 8 (compound 3b) 对布氏锥虫 (Trypanosoma brucei) 表现出较强的抗锥虫体作用 (IC50: 0.79 μM)。Antitrypanosomal agent 8 对 L6 细胞具有一定的细胞毒性,其 IC50 值为 80.95 μM。 | |||
T14115 |
Acoziborole
SCYX-7158,AN5568 |
Others | Others |
Acoziborole (SCYX-7158) 是一种安全的、有效的、结构新颖的抗原虫剂,是一种 benzoxaborole 的衍生物,可用于人类非洲锥虫病 (HAT) 的研究。Acoziborole 对 T. b. brucei S427 菌株的MIC 值为 0.6 µg/mL。 | |||
T12250 | NPD-1335 | Others | Others |
NPD-1335 (Benzyl alkynamide 37) 一种有效的布氏锥虫磷酸二酯酶 B1 (TbrPDEB1) 抑制剂,具有针对布氏锥虫寄生虫的亚微摩尔活性。 NPD-1335 (Benzyl alkynamide 37) 显示出改善的细胞毒性谱。 NPD-1335 (Benzyl alkynamide 37) 会增加细胞内 cAMP 水平,导致细胞周期和细胞死亡的改变。 | |||
T79568 |
NPD-2975
|
Parasite | Microbiology/Virology |
NPD-2975(化合物30)是一款口服活性的抗锥虫药物,用于治疗非洲人类锥虫病(HAT)。在MRC-5人肺成纤维细胞及T. b. brucei感染的小鼠模型中,NPD-2975毒性低。此化合物展现了良好的代谢稳定性,在体外对T. b. brucei IC500抑制浓度为70 nM。NPD-2975还可抑制CYP450酶,对CYP1A2和CYP2C19的IC50分别为0.16 μM和0.42 μM。 | |||
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。 | |||
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。 | |||
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。 | |||
T81503 | PEX5-PEX14 PPI-IN-2 | ||
PEX5-PEX14 PPI-IN-2(化合物 12)是一种抑制PEX14-PEX5蛋白质-蛋白质相互作用(PPI)的化合物,其在T. b. brucei细胞和HepG2细胞中的EC50值分别为5 µM和17 µM。该化合物适用于研究与锥虫感染有关的疾病。 | |||
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。 | |||
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。 | |||
T63167 | Antitrypanosomal agent 7 | ||
Antitrypanosomal agent 7 (compound 18c) 是一种有效的抗锥体虫剂,显示出良好的 ADME 特性。Antitrypanosomal agent 7 的抗布氏锥虫 (T. brucei) 的活性 (IC50: 0.71 μM),比 Nifurtimox 高两倍以上。Antitrypanosomal agent 7 与 DNA 有很强的相互作用,且能够选择性结合富含 AT 碱基的 DNA。 | |||
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。 | |||
T23102 |
OBAA
|
Others | Others |
OBAA 是一种有效的磷脂酶 A2 (PLA2) 抑制剂(IC50= 70 nM),并且在布氏锥虫中阻断 Melittin 诱导的 Ca2+流入(IC50= 0.4 μM)。 | |||
T63737 | Purine phosphoribosyltransferase-IN-1 | ||
Purinephosphoribosyltransferase-IN-1 (Compound (S,R)-48) 是一种有效的恶性疟原虫 (Pf)、间日疟原虫 (Pv) 和布氏锥虫 (Tbr) 6-氧嘌呤磷酸核糖基转移酶 (PRT) 抑制剂,他们的 Ki 值分别为 50、20 和 2 nM。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T4S0590 |
Columbin
|
Phospholipase; COX; Parasite | Immunology/Inflammation; Metabolism; Microbiology/Virology; Neuroscience |
Columbin 是有口服活性的二萜呋喃内酯,选择性抑制COX-1和COX-2,EC50值为 327 μM 和 53.1 μM,具有抗炎和抗锥虫体作用。 | |||
T3S0153 |
Xanthatin
苍耳亭,叶黄制菌素 |
Apoptosis; VEGFR; Lipoxygenase; Wnt/beta-catenin; Antibacterial | Angiogenesis; Apoptosis; Cytoskeletal Signaling; Metabolism; Microbiology/Virology; Stem Cells; Tyrosine Kinase/Adaptors |
Xanthatin 是一种从Xanthium strumarium 叶子中提取的天然产物,可诱导细胞凋亡。它抑制布鲁氏菌的IC50值为 2.63 μg/ mL,对寄生虫特异性锥虫硫磷还原酶具有不可逆的弱抑制作用。它通过抑制PGE2的合成和 5-脂氧合酶的活性而显示出抗炎活性。 | |||
T2S2046 |
Bruceine A
Dihydrobrusatol,鸦胆子素 A,NSC31616 |
Antibiotic; Parasite | Microbiology/Virology |
Bruceine A (NSC-31616) 是一种从鸦胆子 (L.) 的干果中提取的天然类苦素化合物,有治疗犬巴贝斯虫病的潜力。 | |||
TWS2045 |
Bruceine D
鸦胆子素D,鸦胆子苦素D |
Apoptosis; Antiviral; Gamma-secretase; Parasite | Apoptosis; Immunology/Inflammation; Microbiology/Virology; Neuroscience; Proteases/Proteasome; Stem Cells |
Bruceine D 是Notch 抑制剂,有抗癌活性,诱导几种人癌细胞调亡。它是一种有效的植物性昆虫拒食剂,有显著的系统特性和抑制害虫生长的作用。它具有较强的驱虫活性,抑制D. intermedius 的 EC50值为 0.57 mg/L。 | |||
TN1128 |
Bruceine E
|
Others | Others |
Bruceine E 是从 B. javanica 种子中分离得到的,具有降血糖作用。 Bruceine E 可用于作为胰岛素促分泌剂的研究。 | |||
T75485 | Dehydrobruceine B | ||
Dehydrobruceine B 是一种苦木素,可从鸦胆子 (Brucea javanica) 中分离得到。Dehydrobruceine B 与 Cisplatin 通过线粒体途径,协同诱导细胞凋亡 (apoptosis)。Dehydrobruceine B 还增加凋亡诱导因子 (AIF) 和 Bax 表达,抑制 Keap1-Nrf2。 | |||
T5768 | bruceine B | TNF; Parasite | Apoptosis; Microbiology/Virology |
Bruceine B 是一种有效的白细胞-内皮细胞粘附抑制剂,可抑制蛋白质和核酸合成。 | |||
T75558 | Bruceine J | ||
Bruceine J 是一种类黄酮,是一种天然产物,可以从Br. jaVanica 的果实中分离得到。Bruceine J 具有抗巴贝斯活性。 | |||
TN3797 | Dehydrobruceine A | Antifection | Microbiology/Virology |
Dehydrobruceine A shows strong antitrypanosomal activities with IC(50) values in the range of 2.9-17.8nM. | |||
T3792 |
Ajugol
益母草苷,益母草苷A,Leonuride |
Parasite | Microbiology/Virology |
Ajugol (Leonuride) 是从Sideritis germanicopolitana 分离得到的一种环烯醚糖苷。它有抗原生动物活性,对Trypanosoma b. rhodesiense 锥虫的 IC50为 31.8 μg/mL。 | |||
TN1030 |
N-p-trans-Coumaroyltyramine
N-反式对香豆酰基酪胺,N-反式-对香豆酰酪胺 |
AChE; Parasite | Microbiology/Virology; Neuroscience |
N-p-trans-Coumaroyltyramine 是从蓼属植物中分离出的肉桂酰苯乙酰胺,是一种乙酰胆碱酯酶抑制剂,IC50 为 122 μM。它具有抗锥虫活性,对T. brucei rhodesiense 作用的 IC50值为 13.3 µM。 | |||
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。 | |||
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。 | |||
T12286 |
Obtusifoliol
|
Others | Others |
Obtusifoliol is a specific inhibitor of CYP51(Trypanosoma brucei (TB) and human CYP51 with Kd values of 1.2 µM and 1.4 µM, respectively). | |||
TN3220 |
7',8'-Dihydroobolactone
|
Antifection | Microbiology/Virology |
7',8'-Dihydroobolactone can inhibit Trypanosoma brucei brucei with an IC(50) of 2.8 microM. | |||
TN2485 |
1,2-Dihydrotanshinone
1,2-Dihydrotanshinquinone |
Antifection | Microbiology/Virology |
1,2 Dihydrotanshinquinone is active against both Trypanosoma brucei rhodesiense and Plasmodium falciparum. | |||
TN4041 |
Eupatoriopicrin
|
Others | Others |
Eupatoriopicrin shows anti-trypanosomal activity and cytotoxicity against Trypanosoma brucei rhodesiense. Eupatoriopicrin-induced DNA damage may play a role in the observed cytotoxicity, it shows a weak sensitizing capacity in guinea pigs. | |||
TN4933 |
Sahandol
|
Antifection | Microbiology/Virology |
Sahandol shows antiprotozoal activity against P. falciparum and T. brucei rhodesiense. | |||
TN1930 | Methylenetanshinquinone | Antifection | Microbiology/Virology |
Methylenetanshinquinone shows antiplasmodial and antitrypanosomal activity, it is active against both Trypanosoma brucei rhodesiense and Plasmodium falciparum. | |||
TN5588 |
Kolavenol
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Kolavenol shows a trypanocidal activity with an IC50 value of 2.5 microg/ml (8.6 microM) against Trypanosoma brucei rhodesiense, the causing agent of the acute form of human African trypanosomiasis. | |||
TN4578 |
Monomethyl kolavate
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Antifection | Microbiology/Virology |
Monomethyl kolavate is a power Trypanosoma brucei glyceraldehyde-3-phosphate dehydrogenase (TbGAPDH) inhibitor, with an IC50 value of 12uM. | |||
T75617 | Salviandulin E | ||
Salviandulin E 是一种二萜类化合物,可从墨西哥鼠尾草中分离。Salviandulin E 显示出对 T. b. bruceiGUTat 3.1寄生虫 (parasites) 的抗锥虫体活性,IC50值为 0.72 µg/mL。 | |||
T35761 |
Carviolin
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Carviolin is an anthraquinone fungal metabolite that has been found inZ. longicaudatawith immunosuppressive and antitrypanosomal activities.1,2It inhibits LPS- or concanavalin A-induced proliferation of mouse splenocytes (IC50s = 4 and 4.5 μg/ml, respectively).1Carviolin is active againstT. b. brucei(MIC = 41.66 μM).2 1.Fujimoto, H., Nakamura, E., Okuyama, E., et al.Six immunosuppressive features from an ascomycete, Zopfiella longicaudata, found in a screening study monitored by immunomodulatory... | |||
T35741 |
Gliovirin
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Gliovirin is a fungal metabolite that has been found inT. harzianumand has fungicidal, antimicrobial and anti-inflammatory activities.1It is active against the plant pathogenic fungusP. ultimum(MIC = 60 ng/ml) and the parasiteT. brucei brucei(IC50= 90 ng/ml), but has no effect on the plant pathogenic fungiR. solani,P. omnivorum,T. basicola,R. arrhizus, andV. dahliaeor the bacteriaB. thuringiensis,P. fluorescens, andX. malvacearumwhen used at concentrations up to 1,000 ng/ml.2,3Gliovirin decrease... | |||
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... |