103
37
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T12438 |
PfDHODH-IN-1
|
Dehydrogenase; Parasite | Metabolism; Microbiology/Virology |
PfDHODH-IN-1 是 Leflunomide 活性代谢物的类似物,具有抗疟疾活性。它是恶性疟原虫二氢乳清酸脱氢酶抑制剂。 | |||
T12909 |
SID 26681509
|
Cysteine Protease; Parasite | Microbiology/Virology; Proteases/Proteasome |
SID 26681509 是可逆的,竞争性的人组织蛋白酶 L 选择性抑制剂,IC50为 56 nM。它抑制Plasmodium falciparum 的体外繁殖,IC50为15.4 μM,抑制Leishmania major,IC5012.5 μM。 | |||
T8767 |
PfDHODH-IN-2
|
Dehydrogenase; Parasite | Metabolism; Microbiology/Virology |
PfDHODH-IN-2 是一种二氢噻吩酮衍生物,是一种有效的恶性疟原虫二氢乳清酸脱氢酶抑制剂,其IC50值为 1.11 µM。它具有抗疟作用,可研究疟疾。 | |||
T1491 |
Atovaquone
Atavaquone,阿托伐醌 |
Others; P450; Dehydrogenase; Antibiotic; Parasite | Metabolism; Microbiology/Virology; Others |
Atovaquone (Atavaquone) 是具有口服活性的选择性寄生虫线粒体细胞色素bc1复合物的抑制剂。它抑制人类和P. falciparum 细胞色素bc1活性,IC50值分别为 460 nM 和 2.0 nM。它有抗疟作用,有潜力用于疟疾、弓形体病、肺孢子虫肺炎和巴贝斯虫病的相关研究。 | |||
T5421 |
KDU691
|
Parasite; PI4K | Microbiology/Virology; PI3K/Akt/mTOR signaling |
KDU691 是一种咪唑吡嗪类药物,对血阶段的裂殖体、配子体和肝期具有较强的抗寄生虫活性,它是 PI4K 抑制剂,选择性抑制双氢青蒿素预处理的恶性疟原虫。 | |||
T16269 |
Nanaomycin A
|
DNA Methyltransferase; Dehydrogenase; Parasite | Chromatin/Epigenetic; Metabolism; Microbiology/Virology |
Nanaomycin A 是一种醌类抗生素,可重新激活人类癌细胞中沉默的肿瘤抑制基因。 Nanaomycin A 是 DNMT3B 的特异性抑制剂 (IC50 = 500 nM)。 | |||
T13246 |
UCT943
|
Parasite; PI4K | Microbiology/Virology; PI3K/Akt/mTOR signaling |
UCT943是恶性疟原虫PI4K 的抑制剂(IC50 = 23 nM)。 | |||
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. | |||
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。 | |||
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。 | |||
T67694 |
ZY-19489
|
Parasite | Microbiology/Virology |
ZY-19489是一种具有抗疟作用的化合物, 是一种潜在的单剂量根治性恶性疟原虫和间日疟原虫疟疾的药物,已获得美国 FDA 的孤儿药认定。 | |||
T14766 |
BPH-715
|
Others; Parasite | Microbiology/Virology; Others |
BPH-715 抑制恶性疟原虫的肝脏阶段生长,对 HepG2 细胞中的恶性疟原虫外红细胞的形成的 IC50 为 10 μM。 | |||
T3266 |
Lumefantrine
Benflumetol,dl-Benflumelol,苯芴醇 |
Others; Parasite; Autophagy | Autophagy; Microbiology/Virology; Others |
Lumefantrine (dl-Benflumelol) 是一种抗疟药,用于治疗急性单纯性疟疾。与Artemether 联用,可提高疗效。 | |||
T4220 |
BQR-695
BQR695,NVP-BQR695 |
PI3K; Parasite; PI4K | Microbiology/Virology; PI3K/Akt/mTOR signaling |
BQR-695 (NVP-BQR695) 是一种磷脂酰肌醇 4-激酶抑制剂,对于人类和疟原虫 PI4KIIIβ 的 IC50值分别为 80 和 3.5 nM。 | |||
T11027 |
DHODH-IN-4
|
Dehydrogenase | Metabolism |
DHODH-IN-4 是人和 Plasmodium falciparum 二氢乳清酸脱氢酶 (DHODH) 的抑制剂,其对 PfDHODH 和 HsDHODH 的IC50 值分别为 4 μM 和 0.18 μM。DHODH-IN-4 (compound 17) 具有抗疟疾活性。 | |||
T21022 |
Deacylketoconazole
Deacyl ketoconazole,脱乙酰酮康唑 |
Antifungal | Microbiology/Virology |
Deacylketoconazole (Deacyl ketoconazole) 是一种酮康唑衍生物,也是一种抗真菌剂。 脱酰基酮康唑对恶性疟原虫的活性是酮康唑的 15 至 50 倍。 | |||
T10903 |
CWHM-1552
|
Parasite | Microbiology/Virology |
CWHM-1552 是一种有效的恶性疟原虫抑制剂。 对于 3D7 和 Dd2 菌株,IC50 分别为 51 nM 和 53 nM。 | |||
T27400L |
Ganaplacide phosphate
Ganaplacide phosphate (1261113-96-5 Free base) |
Others | Others |
Ganaplacide phosphate 对疟原虫症状性无性血期感染具有多阶段抗疟活性,并且能够在动物模型中预防传播和阻断感染。 | |||
T16125 |
MMV390048
|
Parasite; PI4K | Microbiology/Virology; PI3K/Akt/mTOR signaling |
MMV390048 是一种抗疟药,是一种新型化学疟原虫 PI4K 抑制剂。它与疟原虫 PI4K 的 ATP 结合位点结合,不与除人类 PIP4K2C 外的其他恶性疟原虫和人类激酶结合。 | |||
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。 | |||
T5420 |
Cycloguanil hydrochloride
Chloroguanide Triazine,环氯胍盐酸盐 |
Parasite; Drug Metabolite | Metabolism; Microbiology/Virology |
Cycloguanil hydrochloride (Chloroguanide Triazine) 是抗疟化合物氯胍的活性代谢物。 它作为二氢叶酸还原酶的抑制剂,对于疟原虫和人类形式的 Kis 值分别为 0.3 和 1.5 nM。 | |||
T15276 |
Ferroquine
SSR97193,Ferrochloroquine |
Others | Others |
Ferroquine (Ferrochloroquine) 是 Chloroquine 的二茂铁基类似物,具有抗疟疾活性。Ferroquine 具有杀疟原虫作用,机制是通过诱导氧化应激和随后的膜破坏。 | |||
T9858 |
5-(3-bromo-4,5-dihydroisoxazol-5-yl)-3-(4-(tert-butyl)phenyl)-1,2,4-oxadiazole
|
Parasite | Microbiology/Virology |
Antileishmanial agent-2 是一种基于 3-Br-isoxazoline 的疟原虫抑制剂恶性疟原虫(D10 和 W2 菌株)和利什曼原虫属。 (L. infantum 和 L.tropica) 前鞭毛体,IC50 为 0.035、0.058、3.5 和 7.5 μM。 | |||
T17257L |
WR99210 hydrochloride(47326-86-3 free base)
WR99210 hydrochloride(47326-86-3 free base),6,6-Dimethyl-1-[3-(2,4,5-trichlorophenoxy)propoxy]-1,6-dihydro-1,3,5-triazine-2,4-diamine |
Others | Others |
WR99210 hydrochloride 是恶性疟原虫二氢叶酸还原酶 (pfDHFR) 的有效抑制剂,pfDHFR 是主要的疟疾药物靶点。它对野生型、双突变体和四突变体二氢叶酸还原酶具有亚纳摩尔效力。 | |||
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。 | |||
T74696 |
SpdSyn binder-1
|
Parasite | Microbiology/Virology |
SpdSyn binder-1 是一种弱结合剂,结合在恶性疟原虫亚精胺合酶的活性位点,对疟疾有部分抑制作用,可用于研究疟疾。 | |||
T11030 |
DHODH-IN-8
|
Dehydrogenase | Metabolism |
DHODH-IN-8 是一种人和恶性疟原虫二氢乳清酸脱氢酶的抑制剂,IC50 分别为 0.13 μM 和 47.4 μM,Ki 分别为 0.016 μM 和 5.6 μM。DHODH-IN-8 具有抗疟疾能力。 | |||
T28824 |
SNX0723
SNX 0723,SNX- 0723 |
HSP | Cytoskeletal Signaling; Metabolism |
SNX0723 是一种 Hsp90 抑制剂,具有抗疟原虫活性。SNX0723 对 HsHsp90 和 PfHsp90 具有高结合亲和力,Ki 分别为 4.4 和 47 nM。SNX0723 抑制肝期伯氏疟原虫 ANKA 寄生虫,EC50 为 3.3 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。 | |||
T5493 |
Pyronaridine
|
Others | Others |
Pyronaridine 是一种具有口服活性的、含甘露醇的抗疟疾化合物,通过干扰红细胞内疟疾寄生虫(疟原虫)的复制而起作用。Pyronaridine 常与其他药联用来治疗疟疾,对对 P. falciparum 和 Echinococcus granulosus 具有抗感染活性。 | |||
T0049 |
Azlocillin sodium salt
Sodium azlocillin,Azlocillin sodium,阿洛西林钠 |
Antibacterial; Antibiotic; Parasite | Microbiology/Virology |
Azlocillin sodium salt 是一种半合成青霉素,是内酰胺类广谱抗生素。它具有抗假单胞杆菌的活性,并对抗寄生虫Plasmodium falciparum 有效。 | |||
T0850 |
Primaquine diphosphate
Primaquine phosphate,磷酸伯氨喹,Primaquine bisphosphate,磷酸伯安喹 |
Antibiotic; Parasite | Microbiology/Virology |
Primaquine diphosphate 是一种合成的 8-氨基喹啉衍生物,具有抗疟特性。它是一种能破坏间日疟原虫和卵形疟原虫肝脏晚期和潜在组织形态的化合物。 | |||
T30612 | Bulaquine | ||
Bulaquine is a derivative of 8-aminoquinoline and has effective activity against the liver stage of plasmodium falciparum and the dormant bodies of Plasmodium vivax and Plasmodium ovale. | |||
T33457 |
MMV007839
MMV-007839,MMV 007839 |
||
MMV007839 is a potent Plasmodium lactate transporter PfFNT. | |||
T25448 | Genz-669178 | ||
Genz-669178 is a wild-type inhibitor of Plasmodium falciparum dihydroorotate dehydrogenase (PfDHODH). | |||
T20910 |
Dibemethine
Dibemetina,DBMA,AI3-26795,Dibemethinum |
||
Dibemethine is active against chloroquinone-resistant Plasmodium falciparum by the inhibition of P. falciparum chloroquine-resistance transporter (PfCRT). | |||
T23935 |
D44
D 44,D-44 |
||
D44 is a Plasmodium FKBPs inhibitor. | |||
T71061 | DSM267 | ||
DSM267 is a novel Plasmodium falciparum Dihydroorotate Dehydrogenase (PfDHODH) Inhibitor. | |||
T11331L |
FTI 276
|
Others | Others |
FTI-276 is an inhibitor of protein farnesyltransferase (PFT) (IC50s: 0.9 and 0.5 nM for Plasmodium falciparum and human). | |||
T40291 |
DSM705
DSM705 |
||
DSM705 is a pyrrole-based inhibitor of Dihydroorotate Dehydrogenase (DHODH). It demonstrates high potency in the nanomolar range against Plasmodium DHODH and Plasmodium parasites, while not interfering with mammalian DHODHs. DSM705 shows significant efficacy as an antimalarial compound. | |||
T40087 |
DSM502
|
||
DSM502, a pyrrole-based Dihydroorotate Dehydrogenase (DHODH) inhibitor, demonstrates potent nanomolar activity against Plasmodium DHODH and Plasmodium parasites, while not inhibiting mammalian DHODHs. | |||
T120656 | N004-0015 | ||
Plasmodium falciparum, EC50: 7.21 nM | |||
T68421 |
MMV019662
|
||
MMV019662 is a novel inhibitor of Plasmodium falciparum. | |||
T24490 |
MMV666693
MMV-666693,MMV 666693 |
||
MMV666693 is a selective allosteric Plasmodium Kinesin-5 inhibitor. | |||
T25815 |
Mirincamycin HCl
U24,729A,U-24,729A,U-24729 A,U 24729 A,U 24,729A,Mirincamycin hydrochloride |
||
Mirincamycin HCl is a close analog of the drug clindamycin used for the treatment of Plasmodium falciparum blood stages. | |||
T23625 |
ACT-451840
ACT451840 |
||
ACT-451840 is a drug of antimalarial activity. It has effective activity against sensitive and resistant Plasmodium falciparum strains. | |||
T11331 |
FTI 276 TFA
|
Others | Others |
FTI 276 TFA is effective against plasmodium falciparum and humans.It is a protein-based nikyltransferase (PFT) inhibitor with an IC50s of 0.9 nM and 0.5 nM, respectively. | |||
T25524 | IDI-3783 | ||
IDI-3783 is a mutant-selective inhibitor of Plasmodium falciparum dihydroorotate dehydrogenase (PfDHODH). | |||
T10902 | CWHM-1008 | Others | Others |
CWHM-1008 is an effective oral antimalarial drug. The EC50 values of the drug-sensitive Plasmodium falciparum 3D7 and drug-resistant Dd2 strains are 46 and 21 nM, respectively. | |||
T61651 |
Quinoprazine
|
||
Quinoprazine, a powerful inhibitor of Vaccinia virus DNA synthesis (IC50 = 10 μM), exhibits notable antimalarial activity against Plasmodium berghei. Additionally, it demonstrates significant antiprion potency, effectively reducing levels of PrPSc [1]-[5]. |
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。 | |||
TN7103 |
13,21-Dihydroeurycomanone
Pasakbumin C |
Anti-infection; Parasite | Microbiology/Virology |
13,21-Dihydroeurycomanone (Pasakbumin C) 是从 Eurycoma longifolia 根部分离得到的一种天然产物,有抗寄生虫活性。 | |||
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。 | |||
T3682 |
(-)-Catechin gallate
(-)-Catechin 3-O-gallate,儿茶素没食子酸酯,几茶素没食子酸酯,(-)-Catechin 3-gallate |
Others; COX | Immunology/Inflammation; Neuroscience; Others |
(-)-Catechin gallate ((-)-Catechin 3-O-gallate) 是绿茶儿茶素中的微量组分,可抑制COX-1和COX-2活性。它抑制人 Beta-secretase,对氯喹敏感的恶性疟原虫 NF54 和耐氯喹的恶性疟原虫 K1 具有抗疟原虫活性。 | |||
TN1190 |
14,15 β-Dihydroxyklaineanone
14,15beta-Dihydroxyklaineanone |
Parasite | Microbiology/Virology |
14,15 β-Dihydroxyklaineanone(14,15beta-Dihydroxyklaineanone)从 Eurycoma longifolia 中分离得到的苦味素类化合物,具有抗肿瘤促进、抗血吸虫和杀疟原虫活性。 | |||
TN3790 |
Dehydroabietinol
Pomiferin A,Dehydroabietyl alcohol |
Antifection | Microbiology/Virology |
Dehydroabietinol (Pomiferin A) 在体外抑制红细胞中的氯喹敏感及氯喹抵抗型疟原虫,IC50为26-27 μM. | |||
T0392 |
Artemisinin
Qinghaosu,Artemisinine,Qinghaosu,NSC 369397,青蒿素,Artemisinine |
HCV Protease; Ferroptosis; Akt; Parasite | Apoptosis; Cytoskeletal Signaling; Microbiology/Virology; PI3K/Akt/mTOR signaling; Proteases/Proteasome |
Artemisinin (Qinghaosu) 是一种倍半萜烯内酯,是从青蒿植物的地上部分分离的一种抗疟疾药物。它有神经保护和抗癌作用。 | |||
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。 | |||
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。 | |||
T35749 |
Thymohydroquinone
Thymoquinol |
Antioxidant; Reactive Oxygen Species | Immunology/Inflammation; Metabolism; NF-κB; oxidation-reduction |
Thymohydroquinone (Thymoquinol) 是中药材百里香、牛至和其他唇形科植物中含有的单萜酚类化合物。 Thymohydroquinone 抑制癌细胞生长、减少氧化应激和调节炎症反应,在无细胞实验中清除2,2-二苯基-1-picrylhydrazyl 自由基(IC50 = 2.4 μg/ml),在浓度为1.6至6.4 μg/ml 的氧自由基吸收能力(ORAC)实验中,它的Trolox 当量值为2.6胸腺对苯二酚对A2780、OVCAR-8和CIS-A2780卵巢癌细胞(IC50分别为3.1、8.9和9.8 μM)和人卵巢永生化上皮细胞(IC50 = 14 μM)的生长有抑制作用,体外对恶性疟原虫也有抑制作用(IC50 = 15.9 μM)。 | |||
TN3466 |
Atherosperminine
|
cAMP; Calcium Channel; AChR; Parasite | GPCR/G Protein; Membrane transporter/Ion channel; Metabolism; Microbiology/Virology; Neuroscience |
Atherosperminine 是一种天然生物碱,在体外表现出抗疟原虫活性,IC50为 5.80 μM。它具有DPPH 自由基清除活性,其IC50值为 29.56 µg/mL。它对气管有非特异性的弛缓作用。它是一种良好的还原剂,具有螯合金属的能力。 | |||
T11681 |
Isochondrodendrine
Isochondrodendrin |
Others | Others |
Isochondodendrine has strong antiplasmodial activity against Plasmodium falciparum. Isochondrodendrine is a class of bisbenzylisoquinoline alkaloid isolated from Isolona ghesquiereina. | |||
TN4314 |
Isonardoperoxide
|
Antifection | Microbiology/Virology |
Isonardoperoxide shows strong antimalarial activity against Plasmodium falciparum malaria (6.0 × 10-7 M). | |||
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. | |||
TN2485 |
1,2-Dihydrotanshinone
1,2-Dihydrotanshinquinone |
Antifection | Microbiology/Virology |
1,2 Dihydrotanshinquinone is active against both Trypanosoma brucei rhodesiense and Plasmodium falciparum. | |||
TN1930 | Methylenetanshinquinone | Antifection | Microbiology/Virology |
Methylenetanshinquinone shows antiplasmodial and antitrypanosomal activity, it is active against both Trypanosoma brucei rhodesiense and Plasmodium falciparum. | |||
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. | |||
TN4717 | Oplopanone | Antifection | Microbiology/Virology |
Oplopanone exhibits noteworthy anti-plasmodial activity against Plasmodium falciparum strain. | |||
T11509 |
Guanfu base H
Atisinium chloride |
Others | Others |
Guanfu base H is a diterpenoid alkaloid isolated from Aconitum coreanum. It has antiplasmodial activity against the malarial Plasmodium falciparum strains TM4/8.2 (wild type) and K1CB1 (IC50s: 4 μM and 3.6 μM). | |||
TN3563 | Caesalmin B | Antifection | Microbiology/Virology |
Caesalmin B shows significant dose-dependent inhibitory effects on Plasmodium falciparum FCR-3/A2 growth in vitro. | |||
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 | |||
T79984 |
Chaparrinone
|
Parasite | Microbiology/Virology |
Chaparrinone为苦木素类化合物,源自Eurycoma Harmandiana根部提取。该物质对Plasmodium falciparum和P-388细胞展示出抗疟及细胞毒效应,IC50值分别为0.037 μg/mL和0.34 μg/mL。 | |||
T75568 | Z-Antiepilepsirine | ||
Z-Antiepilepsirine 是一种酰胺生物碱,存在于 Piper capense L.f 中。Z-Antiepilepsirine 显示抗疟原虫活性,对 PlasmodiumfalciparumW2 菌株的 IC50值为 27 µM。 | |||
TN2747 | 2-Acetoxy-3-deacetoxycaesaldekarin E | Antifection | Microbiology/Virology |
2-Acetoxy-3-deacetoxycaesaldekarin E shows significant dose-dependent inhibitory effects on Plasmodium falciparum FCR-3/A2 growth in vitro. | |||
TN1442 | Betulinic acid methyl ester | Antifection | Microbiology/Virology |
Betulinic acid methyl ester showed antiplasmodial activity against chloroquine-resistant Plasmodium falciparum parasites in vitro.It also inhibited B16 2F2 cell proliferation by induction of apoptosis. | |||
TN4202 |
(-)-Heraclenol
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Antifection | Microbiology/Virology |
(-)-Heraclenol shows in vitro anti-plasmodial activity against chloroquine-sensitive and chloroquine-resistant strains of Plasmodium falciparum.(-)-Heraclenol has moderate antibacterial and antifungal activities. | |||
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. | |||
TN4716 |
Oplodiol
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Influenza Virus | Microbiology/Virology |
Oplodiol exhibits noteworthy anti-plasmodial activity against Plasmodium falciparum strains. Oplodiol has a stimulative effect on significantly proliferation and differentiation of culture osteoblasts; it also shows moderate cytotoxic effects on the human | |||
TN3124 |
5-Hydroxysophoranone
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Antibacterial; Parasite; Antifection | Microbiology/Virology |
5-Hydroxysophoranone 从 Erythrina subumbrans 茎中提取,对恶性疟原虫具有高抗疟原虫活性 (IC50 = 2.5 μg/mL)。 | |||
T1235L |
Lincomycin
U 10149,U10149,U-10149 |
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Lincomycin is a lincosamide antibiotic that comes from the actinomycete Streptomyces lincolnensis. Although similar in structure, antibacterial spectrum, and mechanism of action to macrolides, lincomycin is also effective against other organisms including | |||
T11802 |
L-Canaline
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Others | Others |
L-Canaline, a nonprotein amino acid found in many leguminous plants, exhibits potent anticancer and antiproliferative effects. It effectively inhibits the growth of the malaria parasite Plasmodium falciparum with an IC50 of 297 nM. Additionally, L-Canaline acts as a cytotoxic metabolite produced from L-canavanine through arginase catalysis and serves as a potent and irreversible inhibitor of ornithine aminotransferase. | |||
T75450 | P-orlandin | ||
P-orlandin,一种真菌代谢产物,具有阻止FREP1与其配子体或[卵动细胞]结合的功能。该化合物能有效抑制蚊子体内的恶性疟原虫感染。 | |||
T75447 | Asperaculane B | ||
Asperaculane B,一种真菌代谢产物,以IC50 7.89 µM抗恶性疟原虫传播,同时以IC50 3 µM抑制无性恶性疟原虫的发育,对人类细胞无毒。 | |||
TN4113 |
Garcinone E
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Antifection | Microbiology/Virology |
Garcinone E is active constituents in the anticomplement assay used. Garcinone E exhibits potent activity in vitro against Plasmodium falciparum chloroquine-resistant strain W2, with IC50 values below 3 µM. It has potent cytotoxic effect on all hepatocellular carcinomas cell lines as well as on the other gastric and lung cancer cell lines included in the screen, may be potentially useful for the treatment of certain types of cancer. | |||
TN5474 |
Bonducellin
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Bonducellin has anti-inflammatory activities, it can significantly and dose-dependently inhibit the inflammatory mediators; nitric oxide (NO), and cytokines [tumor necrosis factor (TNF)-alpha and interleukin (IL)-12. Bonducellin shows weak antimalarial ac | |||
TN4449 |
Longistylin C
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Antifection | Microbiology/Virology |
Longistylin A and longistylin C show some cytotoxic effects, with IC(50) values of 0.7-14.7 microM against the range of cancer cell lines. Longistylin A and longistylin C, and betulinic acid show a moderately high in vitro activity against the chloroquine | |||
TN4683 |
Nyasol
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ERK; IL Receptor; IκB/IKK; NOS; NF-κB; Akt; Antifection | Cytoskeletal Signaling; Immunology/Inflammation; MAPK; Microbiology/Virology; NF-κB; PI3K/Akt/mTOR signaling |
Nyasol may have potential to be developed as medicines for the treatment of allergies by inhibiting the activation of mast cells. Nyasol shows anti-inflammatory properties by inhibiting iNOS expression; it also has antifungal activity, it is significantly |