154
62
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T10336 |
Antimalarial agent 1
|
Parasite | Microbiology/Virology |
Antimalarial agent 1 是一种抗疟药。 | |||
T9984 |
Antimalarial agent 13
N2-(3-chlorophenyl)-N4-(furan-2-ylmethyl)quinazoline-2,4-diamine |
Parasite | Microbiology/Virology |
Antimalarial agent 13 (N2-(3-chlorophenyl)-N4-(furan-2-ylmethyl)quinazoline-2,4-diamine) 是一种有效的抗疟剂。 | |||
T22381 |
Antimalarial agent 14
4-hydroxy-3-phenyl-naphthalene-1,2-dione,2-Hydroxy-3-phenyl-1,4-naphthoquinone |
Others | Others |
Antimalarial agent 14 (NSC-102533) 是一种生物活性化学品。 | |||
T79535 |
Antimalarial agent 30
|
Parasite | Microbiology/Virology |
Antimalarial agent 30 具有抗伯氏疟原虫肝期寄生虫活性和抗疟活性,可用于研究疟感染。 | |||
T75067 | Antimalarial agent 19 | Parasite | Microbiology/Virology |
Antimalarial agent 19(compound 6e)是一种活性抗疟疾化合物,对K1型恶性疟原虫和伯氏疟原虫展现出较强的抑制效果,其EC50值分别为0.3 µM和15.3 µM。相较于γ-肝硫平,该化合物具有更好的水溶性、肠道渗透性以及微粒体稳定性。 | |||
T72416 | Antimalarial agent 18 | ||
Antimalarial agent 18 是一种有效抗疟剂,展现出电子、亲脂性和铁疏性特质。该化合物隶属于酰氧基甲基系列,可视为磷霉素的替代品,后者是针对非甲羟戊酸类异戊二烯生物合成途径的有效IspC抑制剂。Antimalarial agent 18 对恶性疟原虫和鲍曼疟原虫的生长抑制作用显著,其IC50值分别为50 nM和390 nM。 | |||
T63043 | Antimalarial agent 2 | ||
Antimalarial agent 2 是一种具有口服活性的、新型的抗疟药,在体外表现出快速的杀灭效果。 | |||
T62936 |
Antimalarial agent 8
|
||
Antimalarial agent 8 (Compound 7e) 是一种新型的、口服具有活力的抗疟药。Antimalarial agent 8 在体外能够有效作用于 P. falciparum,且在体内疟疾小鼠模型中口服有效 (40 mg/kg)。 | |||
T78952 | Antimalarial agent 26 | Parasite | Microbiology/Virology |
Antimalarial agent 26是一种1,4-萘醌衍生物,作为口服抗疟药物,对恶性疟原虫(P. falciparum)表现出细胞毒性,并具有优于哺乳动物细胞系的选择性。该化合物能够有效抑制体内P. berghei引起的寄生虫血症。 | |||
T79335 |
Antimalarial agent 31
|
Parasite | Microbiology/Virology |
Antimalarial agent 31 (compound 7k) 是抗恶性疟疾的口服活性抑制剂,针对恶性疟原虫天冬氨酸蛋白酶血浆蛋白酶 X (PMX)。 | |||
T61200 | Antimalarial agent 3 | ||
Antimalarial agent 3, an antimalarial agent, exhibits potent activity against Plasmodium with an IC50 of 0.035 μM. Furthermore, it demonstrates an exceptionally high selectivity index in relation to mammalian cells. | |||
T63052 |
Antimalarial agent 10
|
||
Antimalarial agent 10 (Compound 17b) 是一种氨基醇喹啉化合物。Antimalarial agent 10 也是一种抗疟药,能够作用于 Pf3D7 (IC50: 14.9 nM) 和 PfW2 (IC50: 11 nM),无论哪种细胞系,其选择性指数均大于 770。 | |||
T62537 | Antimalarial agent 7 | ||
Antimalarial agent 7 是一种有效的 PfATP4 的有效抑制剂。其中 PfATP4 是一种寄生虫表面必不可少的离子泵。Antimalarial agent 7 具有潜力进行人类疟原虫 Plasmodium falciparum 的研究。 | |||
T72396 |
Antimalarial agent 20
|
||
Antimalarial agent 20 是一种抗疟剂,在 NF54 蛋白测定中对P. falciparumNF54 寄生菌株的IC50为 0.6 nM。 | |||
T78936 |
Antimalarial agent 27
|
Parasite | Microbiology/Virology |
Antimalarial agent 27 (compound 11a) 是一款针对恶性疟原虫有效的抗疟疾化合物,展现出优异的抑制能力(IC50=0.37 μM)。其机制主要通过抑制目标疟原虫中的DXR (1-脱氧-D-木糖-5-磷酸还原酶),以达成较高抑制效果(IC50=0.11 μM)。 | |||
T62300 | Antimalarial agent 11 | ||
Antimalarial agent 11 (compound 1) 一种有效的抗疟 (antimalarial) 剂,是一种螺环色烷。Antimalarial agent 11 具有良好的抗氯喹 Dd2 菌株的效果 (EC50: 350 nM)。Antimalarial agent 11 能够作用于 D6 (EC50: 1.48 μM) 和 ARC08-022 (EC50: 1.81 μM) 。 | |||
T63456 |
Antimalarial agent 12
|
||
Antimalarial agent 12 是有效的抗疟 (antimalarial) 药,能够抑制恶性疟原虫 Dd2 菌株、3D7 菌株生长,其 EC50值分别为155 nM、136 nM。Antimalarial agent 12 对大肠杆菌的 MIC>250,000 nM,也能够作用于 HEK-293 和 hPHep 细胞系,其 CC50值为 10,000-50,000 nM。 | |||
T63595 | Antimalarial agent 16 | ||
Antimalarial agent 16 是 parasite 抑制剂,表现出抗疟效果,对恶性疟原虫的生长具有抑制作用,其 IC50值为2.0 nM。 | |||
T74695 | Antimalarial agent 17 | ||
Antimalarial agent 17,一种兼具抗疟和除草功能的化合物,作为光系统 II 型抑制剂,在出苗后除草活性方面与市售除草剂表现出相当的效力。 | |||
T74845 | Antimalarial agent 23 | ||
Antimalarial agent 23,一种苯并咪唑抗疟药,对PfNF54和PfK1的IC50值均显示出良好的活性,分别为0.08 μM和0.10 μM。该化合物展现了有效的β-血红素抑制活性,但并不直接抑制血红素向疟原虫色素的转化。 | |||
T63655 | Antimalarial agent 9 | ||
Antimalarial agent 9 是有效的抗疟药,是一种喹啉-咪唑衍生物化合物。Antimalarial agent 9 在体外对 CQ 敏感株(IC50-0.14 μM)和 MDR 株(IC50-0.41 μM) 均显示出明显的抗疟效果,具有较小的细胞毒性和高度的选择性。 | |||
T63413 |
Antimalarial agent 15
|
||
Antimalarial agent 15 是 parasite 抑制剂,表现出抗疟作用,对恶性疟原虫 3D7 的生长具有抑制作用,其 IC50值为20 nM。 | |||
T78951 | Antimalarial agent 24 | Parasite | Microbiology/Virology |
Antimalarial agent 24(Compound 7)是一种抗疟化合物,具有显著的体外(in vitro)活性。针对P. falciparum W2菌株,其IC50值为0.81 μM。同时,Antimalarial agent 24展现在HepG2细胞上的CC50值高于200 μM,表明其对宿主细胞具有较高安全性。 | |||
T79534 | Antimalarial agent 29 | Parasite | Microbiology/Virology |
Antimalarial agent 29 (compound 16) 作为一种效力较高的抗疟化合物,其针对伯氏疟原虫肝期寄生虫的EC500值达到5.2 μM。 | |||
T83044 | Antimalarial agent 33 | Parasite | Microbiology/Virology |
Antimalarial agent 33 (compound 5g) 显示针对红细胞期和肝期疟原虫的抗活性,特别是对 K1 恶性疟原虫株,其EC50为1.1 μM。Antimalarial agent 33 还展示出提升的微粒体稳定性(T1/2=29分钟),并且对原代肝细胞未表现出明显的细胞毒效应。 | |||
T79460 |
Antimalarial agent 28
|
Parasite | Microbiology/Virology |
Antimalarial agent 28 (Compound 2i)为具有针对P. berghei三个发育阶段活性的化合物。该化合物的IC50s针对肝期P. berghei为0.561 μM,对早期配子体为0.14 μM,以及对环期P. berghei为4.34 μM,表明其具有抑制该寄生虫的潜力。 | |||
T9741 |
INE963
|
Others | Others |
INE963 是快速有效的血液阶段抗疟剂,EC50为 3-6 nM。INE963 有单纯性疟疾的研究潜力。 | |||
T5477 |
ELQ-300
|
Parasite | Microbiology/Virology |
ELQ-300 是一种有口服生物活性的抗疟疾剂,可作为细胞色素 bc1 复合物的还原位点的抑制剂 | |||
T8381 |
Amodiaquine
|
Others; Histone Methyltransferase; Parasite | Chromatin/Epigenetic; Microbiology/Virology; Others |
Amodiaquine 是一种合成的4-氨基喹啉类抗疟剂,是一种有口服活性的组胺 N-甲基转移酶抑制剂。它也是一种Nurr1激动剂,有抗炎活性,可特异性结合Nurr1的配体结合域,EC50约为20 μM。 | |||
T4382 |
Proguanil hydrochloride
Paludrine hydrochloride,盐酸氯胍,Chlorguanide hydrochloride,Chloroquanil |
Others; Dehydrogenase; DNA/RNA Synthesis; Antifolate; Parasite | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism; Microbiology/Virology; Others |
Proguanil hydrochloride (Chloroquanil) 是一种双胍类抗疟疾剂,在体内代谢形成环胍。它还是一种二氢叶酸还原酶抑制剂。 | |||
T6992 |
Sulfadiazine sodium
Sulfadiazin-natrium,磺胺嘧啶钠,Sodium sulfadiazine |
Others; Antibacterial; Antibiotic; Parasite | Microbiology/Virology; Others |
Sulfadiazine sodium (Sulfadiazin-natrium) 是一种磺胺类抗生素具有抗疟活性,可研究弓形虫病。 | |||
T40417 |
Ethylhydrocupreine hydrochloride
Optochin hydrochloride,乙氢去甲奎宁盐酸盐;奥普托欣盐酸盐 |
Antibacterial; Parasite | Microbiology/Virology |
Ethylhydrocupreine hydrochloride (Optochin hydrochloride) 是奎宁的一种衍生物,具有抗菌作用,可抑制肺炎链球菌的活性。Ethylhydrocupreine hydrochloride 具有抗疟活性,对 Plasmodium falciparum 的IC50为 25.75 nM。Ethylhydrocupreine hydrochloride 是Gallus gallus2 受体 (ggTas2r1,ggTas2r2和ggTas2r7) 激动剂。 | |||
T0849 |
Pyrimethamine
Pirimecidan,RP 4753,Pirimetamin,乙胺嘧啶 |
DHFR; Antifolate; Parasite | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Metabolism; Microbiology/Virology |
Pyrimethamine (Pirimecidan) 是一种二氢叶酸还原酶的竞争性抑制剂,用作抗疟药。 | |||
T11558 |
Hexyl gallate
没食子酸己酯,Gallic acid hexyl ester,Hexyl 3,4,5-trihydroxybenzoate |
Antibacterial | Microbiology/Virology |
Hexyl gallate (Gallic acid hexyl ester) 是没食子酸的烷基酯衍生物,对恶性疟原虫具有很强的抗疟活性,IC50为 0.11 mM。它具有抗菌活性,通过抑制 RhlR 抑制鼠李糖脂和绿脓杆菌素的产生。 | |||
T0860 |
Mefloquine hydrochloride
Mefloquin hydrochloride,Mefloquine HCl,盐酸甲氟喹 |
Potassium Channel; SARS-CoV; Reactive Oxygen Species; Parasite; Autophagy | Autophagy; Immunology/Inflammation; Membrane transporter/Ion channel; Metabolism; Microbiology/Virology; NF-κB |
Mefloquine hydrochloride (Mefloquin hydrochloride) 是喹啉抗疟药,是抗 SARS-CoV-2进入抑制剂,可研究疟疾、系统性红斑狼疮和癌症。它也是 K+通道(KvQT1/minK) 拮抗剂,IC50约为 1 μM。 | |||
T7744 |
Piperaquine tetraphosphate tetrahydrate
4,4'-(1,3-丙烷双-4,1-哌嗪基)双(7-氯喹啉)磷酸盐水合物,四磷酸哌喹四水合物 |
Parasite | Microbiology/Virology |
Piperaquine tetraphosphate tetrahydrate 是一种双喹啉抗寄生虫剂,可与青蒿素联用研究抗疟。 | |||
T0381 |
Amodiaquine dihydrochloride dihydrate
Amodiaquine hydrochloride,阿莫地喹盐酸盐,Amodiaquin dihydrochloride dihydrate |
Histone Methyltransferase; Parasite; Histamine Receptor | Chromatin/Epigenetic; GPCR/G Protein; Immunology/Inflammation; Microbiology/Virology; Neuroscience |
Amodiaquine dihydrochloride dihydrate (Amodiaquine hydrochloride) 是一种具有口服活性的组胺 N-甲基转移酶抑制剂,也是一种Nurr1激动剂,可特异性结合Nurr1的配体结合域,EC50约为20 μM。它是 4-氨基喹啉衍生物,具有抗疟和抗炎特性。 | |||
T0860L |
Mefloquine
Ro215998,WR 142490,Ro-215998,氟甲喹羟哌啶,Lariam,Ro 215998 |
Others | Others |
Mefloquine (Ro 215998) 是一种喹啉抗疟药,是一种抗 SARS-CoV-2 进入抑制剂。 Mefloquine 也是一种 K+ 通道 (KvQT1/minK) 拮抗剂,IC50 为 ~1 μM。它可用于疟疾、系统性红斑狼疮和癌症研究。 | |||
T7532 |
Piperaquine
|
Parasite | Microbiology/Virology |
Piperaquine 是一种双喹啉化合物,可抑制来自疟疾感染患者的恶性疟原虫分离株的离体生长,IC50 范围为 11.8-217.3 nM。 | |||
T6888 |
Methylene Blue
亚甲蓝,methylthioninium chloride,CI-52015,Tetramethylthionine chloride,亚甲兰,Basic Blue 9 |
Guanylate cyclase; Microtubule Associated; NO Synthase; Parasite; Monoamine Oxidase | Cytoskeletal Signaling; GPCR/G Protein; Immunology/Inflammation; Microbiology/Virology; Neuroscience |
Methylene Blue (Tetramethylthionine chloride) 是鸟苷酸环化酶,是单胺氧化酶 A 和 NO 合酶抑制剂。它有抗伤害感受、抗疟疾、抗抑郁和抗焦虑作用,可研究高铁血红蛋白血症、神经退行性疾病和异环磷酰胺引起的脑病。它是血管加压剂,用作色素内窥镜检查中的染料。 | |||
T0006 |
Methylene Blue trihydrate
碱性亚甲蓝三水合物,Methylthionine chloride,Basic blue 9,亚甲蓝三水合物,Methylene Blue |
Guanylate cyclase; Microtubule Associated; NO Synthase; Parasite; Monoamine Oxidase | Cytoskeletal Signaling; GPCR/G Protein; Immunology/Inflammation; Microbiology/Virology; Neuroscience |
Methylene Blue trihydrate (Basic blue 9) 是鸟苷酸环化酶,单胺氧化酶 A 和 NO 合酶抑制剂。它是血管加压药,在医疗中通常用作染料。它具有抗伤害感受,抗疟疾,抗抑郁和抗焦虑作用,可用于高铁血红蛋白血症,神经退行性疾病和异环磷酰胺引起的脑病的研究。 | |||
T20102 |
8-Azahypoxanthine
NSC 22709,NSC-22709,阿扎次黄嘌呤,NSC22709 |
Nucleoside Antimetabolite/Analog | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
8-Azahypoxanthine (NSC-22709) 抑制次黄嘌呤-鸟嘌呤-黄嘌呤磷酸核糖基转移酶并具有抗疟特性。 | |||
T10378 |
Artelinic acid
|
Others | Others |
Artelinic acid, a derivative of Artemisinin, is an antimalarial drug for the treatment of multidrug-resistant strains of Plasmodium falciparum. | |||
T67695 |
MMV688533
|
Parasite | Microbiology/Virology |
MMV688533具有抗疟活性。 | |||
T17313 |
(+)-SJ733
SJ000557733 |
ATPase; Parasite | Membrane transporter/Ion channel; Microbiology/Virology |
(+)-SJ733 (SJ000557733) 是一种有效的 Na+-ATPase PfATP4 抑制剂,具有抗疟活性,可用于研究疟疾。 | |||
T0519 |
Euquinine
Quinine ethylcarbonate,无味奎宁 |
Others | Others |
Euquinine (Quinine ethylcarbonate) 通常用作退热药、抗疟药和补品。 | |||
T9591 |
YCN47284
|
Parasite | Microbiology/Virology |
YCN47284 是一种抗疟化合物,对恶性疟原虫的 IC50 为 1 μM。 | |||
T10356 |
AQ-13 dihydrochloride
|
Parasite | Microbiology/Virology |
AQ-13 dihydrochloride 是一种氨基喹啉类抗疟药,对耐药型菌株 Plasmodium falciparum 有抑制作用。 | |||
T67880 |
NITD-609 Enantiomer
|
Others | Others |
NITD-609 Enantiomer 是 NITD-609 的对映体,NITD-609 是一种具有抗疟活性的螺酮类药物。 | |||
T16326 |
Cipargamin
KAE609,NITD609 |
Parasite | Microbiology/Virology |
Cipargamin (NITD609) 是一种有效的抗疟药物,对恶性疟原虫的IC50值约为 1 nM。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T6S0084 |
Tuberostemonine
对叶百部碱,Tuberstemonine |
Parasite | Microbiology/Virology |
Tuberostemonine (Tuberstemonine) 是一种生物碱,可作为抗疟疾剂,有较高的肠道通透性。 | |||
T10835 |
Cletoquine
Desethylhydroxychloroquine |
Parasite; Antifection | Microbiology/Virology |
Cletoquine 是 Hydroxychloroquine 的主要活性代谢物。 Cletoquine 具有对抗基孔肯雅病毒 (CHIKV) 的能力。 Cletoquine 具有抗疟作用,并具有治疗自身免疫性疾病的潜力。 | |||
TN2027 |
Oxysanguinarine
8-Oxosanguinarine,氧化血根碱,Hydroxysanguinarine |
Parasite | Microbiology/Virology |
Oxysanguinarine (Hydroxysanguinarine) 是一种来自Meconopsis simplicifolia 的小檗生物碱,具有抗疟和抗血小板聚集活性,对登革热病毒具有潜在的抑制作用。 | |||
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。 | |||
TN1012 |
Febrifugine
|
IL Receptor; Anti-infection; Parasite | Immunology/Inflammation; Microbiology/Virology |
Febrifugine 是存在于常山的根和叶中的一种喹唑啉酮类生物碱,有抗疟活性。它是一种有效的抗球虫药,具有杀灭裂殖体的作用。 | |||
TN1012L |
Febrifugine dihydrochloride
ISF-2123,Propyldazine hydrochloride,Atensil,(+)-Febrifugine dihydrochloride,常山乙素二盐酸盐,Pildralazine dihydrochloride |
Parasite | Microbiology/Virology |
Febrifugine dihydrochloride (Propyldazine hydrochloride) 是存在于常山的根和叶中的一种喹唑啉酮类生物碱,具有治疗疟疾、癌症、纤维化和炎症性疾病的活性。 | |||
T3324 |
Lycorine
Galanthidine,Narcissine,石蒜碱,Amarylline,Belamarine,Licorine,番石榴碱 |
Apoptosis; Virus Protease; Antibacterial; AChR; Fatty Acid Synthase | Apoptosis; Metabolism; Microbiology/Virology; Neuroscience |
Lycorine (Narcissine) 是从金眼科植物科中提取的一种天然生物碱。它是一种具有口服活性的SCAP 抑制剂,Kd 值 15.24 nM。它也是黑色素瘤血管生成抑制剂,有用于前列腺癌和代谢疾病的研究潜力。 | |||
T7059 |
α-Dihydroartemisinin
α-Artenimol,α-Dihydroqinghaosu |
Parasite | Microbiology/Virology |
α-Dihydroartemisinin (α-Dihydroqinghaosu) 是青蒿素类抗疟化合物的中间体,具有良好的抗疟抗癌活性,可用于研究红斑狼疮。 | |||
TN1145 |
Isofebrifugine
|
Parasite | Microbiology/Virology |
Isofebrifugine 是一种来自虎耳草科植物常山的生物碱,具有抗疟抗感染活性。 | |||
T3S1447 |
Arteannuin B
|
SARS-CoV; Ferroptosis | Apoptosis; Microbiology/Virology |
Arteannuin B 与青蒿素共同存在,有强效抗疟活性,具有抗 SARS-CoV-2 的活性,EC50为 10.28 μM。 | |||
T1323 |
Artemether
SM224,蒿甲醚,Dihydroartemisinin methyl ether,Dihydroqinghaosu methyl ether,CGP 56696 |
Antibiotic; Parasite | Microbiology/Virology |
Artemether (CGP 56696) 是一种用于治疗急性单纯性疟疾的抗疟药。 | |||
T25114 |
Ascaridole
NSC-406266,NSC 406266,NSC406266 |
Parasite | Microbiology/Virology |
Ascaridole (NSC-406266) 可作为驱虫化合物,能驱除人体和植物中的寄生蠕虫(蠕虫),具有较弱的抗疟活性。 | |||
T3327 |
Artemotil
SM-227,β-Arteether,Beta-Arteether,蒿乙醚,Arteether,(+)-Arteether |
CXCR; CCR; Parasite | Autophagy; GPCR/G Protein; Immunology/Inflammation; Microbiology/Virology |
Artemotil (SM-227) 是一种新型的速效抗疟药,可研究耐Plasmodium falciparum 的恶性疟原虫疟疾,IC50值为 1.61 nM。 | |||
T4333 |
Quinine dihydrochloride
盐酸奎宁,Quinine bimuriate |
Others | Others |
Quinine dihydrochloride (Quinine bimuriate) 是Cinchona(Rubiaceae) 各种物种的主要生物碱。它也是一种抗疟药和肌肉松弛剂(骨骼)。 | |||
T7938 |
Quinidine
奎尼丁,奎宁树 |
Parasite | Microbiology/Virology |
Quinidine 是一种抗心律失常剂,也是 K+通道的有效阻断剂,其 IC50值为 19.9 μM。它是一种选择性细胞色素 P450db 的有效抑制剂,也可研究疟疾。 | |||
T8859 |
NITIDINE
|
Others | Others |
NITIDINE 是一种从花椒根中分离出来的具有生物活性的植物苯并菲啶生物碱。它具有抗癌、神经保护、抗疟疾、抗 HIV、镇痛、抗炎和抗真菌活性。 | |||
T3819 |
Ursolic acid acetate
熊果酸乙酸酯,Acetylursolic acid,3-Acetylursolic Acid |
AChE | Neuroscience |
Ursolic acid acetate (Acetylursolic acid) 分离于 Ficus microcarpa 的气根中,对 KB 细胞显示细胞毒性(IC50:8.4 μM)。 | |||
T0194 |
Chloroquine phosphate
Chloroquine diphosphate,Aralen phosphate,磷酸氯喹,Chingamin phosphate |
SARS-CoV; TLR; HIV Protease; Antibiotic; Parasite; Autophagy | Autophagy; Immunology/Inflammation; Microbiology/Virology; Proteases/Proteasome |
Chloroquine phosphate (Aralen phosphate) 是广泛用于疟疾和类风湿性关节炎的抗疟疾和抗炎剂。它是autophagy 和toll-like receptors 抑制剂,有效抑制SARS-CoV-2(COVID-19) 感染 (EC50=1.13 μM)。 | |||
T21065 |
Artemisitene
|
Others | Others |
Artemisitene 是青蒿素的氧化形式,是一种抗疟药。青蒿素前体是青蒿素生物合成的重要基础物质,包括青蒿素 B、青蒿素、青蒿酸等。 | |||
TN1100 |
Nepodin
|
transporter; COX; AMPK; Parasite | Chromatin/Epigenetic; Immunology/Inflammation; Metabolism; Microbiology/Virology; Neuroscience; PI3K/Akt/mTOR signaling |
Nepodin 是从Rumex crispus 中分离的一种醌氧化还原酶抑制剂,具有抗糖尿病和抗疟疾的作用。。它通过激活 AMPK 刺激 GLUT4 向质膜的转运。 | |||
T2830 |
Betulinic acid
白桦脂酸,桦木酸,ALS-357,Lupatic acid,Betulic acid |
Apoptosis; Mitophagy; NF-κB; HIV Protease; Topoisomerase; Endogenous Metabolite; Aminopeptidase; Autophagy | Apoptosis; Autophagy; DNA Damage/DNA Repair; Metabolism; Microbiology/Virology; NF-κB; Proteases/Proteasome |
Betulinic acid (ALS-357) 是从白桦树皮中分离出来的一种五环三萜类天然产物,是真核细胞拓扑异构酶 I 的抑制剂,IC50值为 5 μM,具有抗逆转录病毒、抗疟疾、抗癌和抗炎特性。 | |||
TN1393 |
(-)-Anonaine
番荔枝碱 |
Apoptosis; Antioxidant; Parasite; Antifungal | Apoptosis; Microbiology/Virology; oxidation-reduction |
(-)-Anonaine 可从木兰科和安妮科的几个物种中提取出来,具有抗疟、抗菌、抗真菌、抗氧化、抗癌、抗抑郁和血管舒张的活性。(-)-Anonaine 通过 Bax 和 caspase 依赖性途径诱导人类宫颈癌(HeLa)细胞的凋亡,诱导 DNA 损伤并抑制人类肺癌 h1299细胞的生长和迁移。 | |||
TN4883 |
Quinine sulfate dihydrate
奎宁树 |
Others | Others |
Quinine sulfate dihydrate 在钾通道阻滞剂中起主要作用。它也被用作抗疟疾、抗胆碱能、抗高血压和降糖药。它抑制线粒体atp 调节的钾通道。它也被用来研究生物结晶血红素,血红素,在疟疾寄生虫的代谢和研究血红素(FP)复合物的毒性。 | |||
T3417 |
Amentoflavone
Didemethyl-ginkgetin,穗花杉双黄酮,Amenthoflavone,3',8''-Biapigenin |
Apoptosis; P450; Phospholipase; Reactive Oxygen Species; Opioid Receptor; COX; Antibacterial; RSV; Antifungal | Apoptosis; Endocrinology/Hormones; GPCR/G Protein; Immunology/Inflammation; Metabolism; Microbiology/Virology; Neuroscience; NF-κB |
Amentoflavone (3',8''-Biapigenin) 是一种具有很多生物活性的双黄酮类天然产物,有抗炎、抗氧化和神经保护等作用。 | |||
TN2254 |
Taccalonolide A
根薯酮内酯A,根薯酮内酯 A |
Apoptosis; Microtubule Associated | Apoptosis; Cytoskeletal Signaling |
Taccalonolide A 是从水田七根茎中分离得到的一种类固醇,具有细胞毒性和抗疟活性。它在体外对过表达 p 糖蛋白、多药耐药蛋白 7 细胞系有抑制作用,抑制 SK-OV-3 细胞生长的 IC50值为 622 nM。它是微管稳定剂,能引起 G2-M 期滞留、Bcl-2 磷酸化,并引发细胞凋亡。 | |||
TN4276 |
Isocudraniaxanthone B
|
Sodium Channel; Antifection | Membrane transporter/Ion channel; Microbiology/Virology |
Isocudraniaxanthone B may have antimalarial activity. | |||
TN5937 |
Walsuronoid B
|
||
Walsuronoid B shows weak antimalarial activity. | |||
TN4314 |
Isonardoperoxide
|
Antifection | Microbiology/Virology |
Isonardoperoxide shows strong antimalarial activity against Plasmodium falciparum malaria (6.0 × 10-7 M). | |||
TN3452 | Arteannuin M | TNF; Antifection | Apoptosis; Microbiology/Virology |
Arteannuin has antimalarial activity. It can degrade the level of TNF-α in rats with ostarthritis,and effectively inhibit the inflammation. | |||
TN4229 | Humulene epoxide II | Antifection | Microbiology/Virology |
Humulene epoxide II has antimalarial activity. | |||
TN3583 | Canophyllal | Antifection | Microbiology/Virology |
Canophyllal shows antiplasmodial activity against the W2 strain of Plasmodium falciparum which is resistant to chloroquine and other antimalarial drugs. | |||
T12517 |
Polyketomycin
|
Others | Others |
Polyketomycin is a tetracyclic quinone glycoside antibiotic isolated from Streptomyces sp. or Streptomyces diastatochromogenes, has antibacterial, anticancer, antimalarial activities. | |||
TN4535 |
Methyl 6-acetoxyangolensate
|
Antifection | Microbiology/Virology |
Methyl-6-acetoxy angolensate may have antimalarial activity. | |||
T11534 |
Haemanthamine
|
Others | Others |
Haemanthamine is an alkaloid isolated from the Amaryllidaceae plants with potent anticancer activity. It inhibits protein biosynthesis during the elongation stage of translation. It has antimalarial, pro-apoptotic, antiviral, antioxidant, and anticonvulsa | |||
TN4275 |
Isocudraniaxanthone A
|
Antifection | Microbiology/Virology |
Isocudraniaxanthone A may have antimalarial activity. | |||
TN3453 | Arteannuin N | TNF; Antifection | Apoptosis; Microbiology/Virology |
Arteannuin has antimalarial activity. It can degrade the level of TNF-α in rats with ostarthritis,and effectively inhibit the inflammation. | |||
TN4666 |
Norcaesalpinin E
|
Antifection | Microbiology/Virology |
Norcaesalpinin E shows antimalarial activity against the malaria parasite Plasmodium falciparum FCR-3/A2 clone in vitro, with an IC50 value of 0.090 microM. | |||
TN3427 |
Aphadilactone B
|
Antifection | Microbiology/Virology |
Aphadilactone B shows significant antimalarial activity with the IC50 value of 1350 ± 150 nM. | |||
T79997 |
(±)-Emodin bianthrone
|
Parasite | Microbiology/Virology |
(±)-Emodin bianthrone (compound 10) 是具抗疟、抗结核及抗真菌作用的天然化合物。 | |||
TN4733 |
Pancixanthone A
胡桐,海棠木 |
Antifection | Microbiology/Virology |
Pancixanthone A may have antimalarial activity, it also shows a significant antileishmanial activity against the promastigote forms of Leishmania mexicana and L. infantum and against the amastigote forms of L. infantum. | |||
TN1349 | 9-Hydroxycalabaxanthone | Antifection | Microbiology/Virology |
9-Hydroxycalabaxanthone exhibits cytotoxicity against the HT-29 cell line with ED50 values of 9.1 microM. The combination of 9-hydroxycalabaxanthone with α±-mangostin shows the synergistic antimalarial interaction in both clones. | |||
T40643 |
Prodigiosin hydrochloride
盐酸灵菌红素,Prodigiosine hydrochloride |
||
Prodigiosin hydrochloride, a red pigment, is a bioactive secondary metabolite produced by bacteria. It exhibits potent proapoptotic activity and functions as an inhibitor of the Wnt/β-catenin pathway. Additionally, this compound possesses antibacterial, antifungal, antiprotozoal, antimalarial, immunosuppressive, and anticancer properties. | |||
TN2738 | 2,6-Dimethoxy-1-acetonylquinol | Antifection | Microbiology/Virology |
2,6-Dimethoxy-1-acetonylquinol shows varying degrees of in vitro antimalarial activity against Plasmodium falciparum. It is devoid of significant cytotoxicity to the human oral epidermoid KB cancer cell line. | |||
TN3799 |
Dehydrocrebanine
|
Antifection | Microbiology/Virology |
Dehydrocrebanine has strong activity against promyelocytic leukemia cells (HL-60) with an IC50 of 2.14 ug/mL. It also shows potent antimalarial activity with an IC50 value of 70 ng/ml. | |||
TN2567 |
10-Hydroxycanthin-6-one
|
Antifection | Microbiology/Virology |
10-Hydroxycanthin-6-one has potential to be an antimicrobial agent. 10-Hydroxycanthin-6-one has in vitro antimalarial activity; it also has cytotoxic activity, it could be a plant anticancer agent. | |||
TN3422 |
Anisofolin A
|
Antifection | Microbiology/Virology |
Anisofolin A has promising antimalarial activity (IC50 4.39 ± 0.25 uM). It has promising antimycobacterium activity [IC50 4.50 ± 0.75 uM (3.31 ug/mL)] against M. tuberculosis H37Ra and at 100 ug/mL, shows 55.6 % inhibition of M. bovis. | |||
TN3428 |
Aphadilactone C
|
Others | Others |
Aphadilactone C shows significant antimalarial activity with the IC50 value of 170 ± 10 nM. It shows potent and selective inhibition against the diacylglycerol O-acyltransferase-1 (DGAT-1) enzyme (IC50 = 0.46 ± 0.09 uM, selectivity index > 217). | |||
TN4776 | Physalin D | TNF; Antifection | Apoptosis; Microbiology/Virology |
Physalin D shows antimalarial activity; it also exhibits a minimum inhibitory concentration value (MIC) against Mycobacterium tuberculosis H(37)Rv strain of 32 microg/mL. Physalin D displays considerable cytotoxicity against several cancer cell lines. It | |||
T75663 | 7-Methoxy-β-carboline-1-propionic acid | ||
7-Methoxy-β-carboline-1-propionic acid (compound 46) 是一种从东革阿里根中提取的化合物,具有细胞毒性和抗疟疾功能。 | |||
T64246 | Cinchonine monohydrochloride hydrate | ||
Cinchonine ((8R,9S)-Cinchonine) monohydrochloride hydrate 是一种天然的、有效的抗疟剂,也是一种人血小板聚集的抑制剂。Cinchonine monohydrochloride hydrate 能够激活内质网应激,诱导的人肝癌细胞凋亡,并可抑制脂肪的生成。 | |||
------------------------ 更多 ------------------------ |