6
6
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T0692 |
Allopurinol
Zyloric,别嘌醇,Zyloprim,Lopurin,别嘌呤醇 |
ROS; Xanthine Oxidase | Immunology/Inflammation; Metabolism |
Allopurinol (Zyloric) 是一种黄嘌呤氧化酶(XO)抑制剂,IC50=7.82±0.12 μM。 | |||
T6376 |
Allopurinol Sodium
1H-吡唑并[3,4-D]嘧啶-4-醇单钠盐,Allopurinol sodium salt,Sodium allopurinol |
ROS | Immunology/Inflammation |
Allopurinol Sodium 是黄嘌呤氧化酶抑制剂,其IC50= 0.2~50 μM。它能够抗利什曼原虫,也可用于研究痛风以及高尿酸血症。 | |||
T62574 |
Antileishmanial agent-6
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Antileishmanial agent-6 是一种有效的抗利什曼虫剂。Antileishmanial agent-6 对Leishmania donovani 和 L-6 具有抗利什曼虫活性 (IC50: 0.54 μM) 和细胞毒性 (IC50: 10.2 μM) 作用。 | |||
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。 | |||
T76070 |
Defensin HNP-1 human TFA
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Defensin HNP-1 human TFA,一种人中性粒细胞肽(HNPs),在早期动脉粥样硬化发展中涉及内皮细胞功能障碍。该化合物展现出广泛的抗菌及抗利什曼原虫活性。 | |||
T78973 |
DCN-83
|
Parasite | Microbiology/Virology |
DCN-83,作为一种抗利什曼虫试剂,在靶向无鞭毛体形式方面表现最佳,其半抑制浓度(IC50)为0.71 μM。该化合物显示出穿越血脑屏障并进入中枢神经系统的潜力。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN4660 |
Niranthin
|
Anti-infection; HBV; PAFR; Topoisomerase | DNA Damage/DNA Repair; GPCR/G Protein; Microbiology/Virology |
Niranthin 是一种木脂素,具有广泛的药理活性。它是L. donovaniIB 拓扑异构酶的非竞争性抑制剂,可用于研究耐药利什曼病的治疗。 | |||
TN1432 |
Bacopasaponin C
(-)-假马齿苋皂苷 C,假马齿苋皂苷C |
Anti-infection; GABA Receptor; NMDAR | Membrane transporter/Ion channel; Microbiology/Virology; Neuroscience |
Bacopasaponin C 是一种分离自Bacopa monniera 中的天然糖苷,具有抗肿瘤和抗利什曼原虫作用。 | |||
T2P2806 |
Hederacolchiside A1
黑海常春藤苷A1,革叶常春藤皂苷 A1,Raddeanoside R13 |
Apoptosis; ERK; MEK; Akt; PI3K; Parasite; mTOR | Apoptosis; Cytoskeletal Signaling; MAPK; Microbiology/Virology; PI3K/Akt/mTOR signaling |
Hederacolchiside A1 (Raddeanoside R13) 是从白头翁中分离的一种有抗利什曼原虫和抗肿瘤增殖活性的天然产物。 | |||
TN3729 |
Cuniloside B
|
Antifection | Microbiology/Virology |
Cuniloside B shows anti-leishmanial activity. | |||
TN4470 |
Lyoniside
|
Antifection | Microbiology/Virology |
Lyoniside and saracoside are cytotoxic to promastigotes and intracellular amastigotes, they demonstrate strong anti-leishmanial efficacies in BALB/c mice model of leishmaniasis, suggests that these two compounds potential anti-leishmanial candidates. The | |||
TN1409 |
Asimilobine
|
AChR; Antifection | Microbiology/Virology; Neuroscience |
(-)-Asimilobine shows antioxidative, anti-acetylcholinesterase (AChE), anti-α±-glucosidase, anti-leishmanial and anti-fungal activities; it displays weak inhibition against Streptococcus mutans (ATCC 25175), with a minimum inhibition concentration (MIC) o |