Cat. No. | Product Name | CAS No. | Purity | Chemical Structure |
---|---|---|---|---|
T16112 | ML67-33
化合物 T16112
|
1443290-89-8 | 98% |
|
ML67-33 rapidly and reversibly affects K2P2.1 (TREK-1) (EC50s: 36.3 μM and 9.7 μM in cell-free and HEK293 cells, respectively). ML67-33 is a selective activator ... | ||||
TN1670 | Ganodermanondiol
灵芝酮二醇
|
107900-76-5 | 98% |
|
Ganodermanondiol exhibits potent cytoprotective effects on t-BHP-induced hepatotoxicity in human liver-derived HepG2 cells, presumably through Nrf2-mediated anti... | ||||
T12420 | Pentosan Polysulfate
化合物 T12420
|
37300-21-3 | 98% |
|
Pentosan Polysulfate is a potent and selective anti-HIV agent.with anti-inflammatory and pro-chondrogenic properties,and used for treatment of interstitial cysti... | ||||
TN4911 | Rhuscholide A
化合物 TN4911
|
944804-58-4 | 98% |
|
Rhuscholide A possesses significant anti-HIV-1 activity with an EC50 value of 1.62 microM and a therapeutic index (TI) of 42.40. | ||||
TN5012 | Shizukaol C
化合物 TN5012
|
142279-41-2 | 98% |
|
1. Shizukaol C shows anti-HIV-1 replication activities in both wild-type HIV-1 and two NNRTIs-resistant strains. 2. Shizukaol C has significant cytotoxicit... |
||||
T16555 | PNU-103017
化合物 T16555
|
166335-18-8 | 98% |
|
PNU-103017 is an inhibitor of HIV protease. | ||||
TN1302 | 6,8-Diprenylorobol
化合物6,8-Diprenylorobol
|
66777-70-6 | 98% |
|
6,8-Diprenylorobol possesses weaker anti-H. pylori activity, it may be a useful chemopreventive agent for peptic ulcer or gastric cancer in H. pylori-infected in... | ||||
TN4264 | Isoapetalic acid
化合物 TN4264
|
34366-34-2 | 98% |
|
Isoapetalic acid and apetalic acid exhibit cytotoxic activities towards both cancer cell lines(human breast cancer (MCF-7) and human lung carcinoma (A-549) cell ... | ||||
T39264L | Cyclotriazadisulfonamide hydrochloride
化合物 Cyclotriazadisulfonamide hydrochloride
|
392287-03-5 | 98% |
|
Cyclotriazadisulfonamide hydrochloride 是 CD4 靶向 HIV 进入的选择性抑制剂,并以信号肽依赖性方式抑制人 CD4 共翻译易位进入 ER 腔。 | ||||
TN1852 | Lancifodilactone F
化合物 TN1852
|
850878-47-6 | 98% |
|
Lancifodilactone F exerts minimal cytotoxicity against C8166 cells (CC50 > 200 microg/mL) and shows anti-HIV activity with EC50 = 20.69 +/- 3.31 microg/mL and a ... | ||||
TN4835 | Przewalskin
化合物 TN4835
|
119400-87-2 | 98% |
|
Przewalskin A and Przewalskin B showed modest anti-HIV-1 activity with EC50 = 41 and 30 microg/mL, respectively. | ||||
TN1660 | Ganoderic acid C1
灵芝酸C1
|
95311-97-0 | 98% |
|
Ganoderic acid C1 是分离自 G. lucidum 中的天然产物,能够抑制小鼠巨噬细胞TNF-α 的生成。 | ||||
T10714 | CCR5 antagonist 1
化合物 T10714
|
716354-86-8 | 98% |
|
CCR5 antagonist 1 is a CCR5 antagonist extracted from WO 2004054974 A2. It can inhibit HIV replication. | ||||
T30791 | Censavudine
化合物Censavudine
|
634907-30-5 | 98% |
|
Censavudine (OBP-601) 是一种核苷类似物,是一种核苷逆转录酶 (nucleoside reverse transcriptase) 抑制剂,可用于预防和治疗人类免疫缺陷病毒 1 (HIV-1)。Censavudine 对 HIV-2 和 HIV-1 具有抑制作用, EC50 范围分别为 30-81 n... | ||||
TMA1012 | Ganoderiol F
化合物 TMA1012
|
114567-47-4 | 98% |
|
Ganoderiol F has anti-inflammatory, cytotoxic and anti-HIV activity, it inhibits activity of topoisomerases in vitro, and it inhibits human immunodeficiency viru... | ||||
T12420L | Pentosan Polysulfate Sodium (W/W 43%)
化合物 T12420L
|
140207-93-8 | 98% |
|
Pentosan Polysulfate Sodium is a potent and selective anti-HIV agent.with anti-inflammatory and pro-chondrogenic properties,and used for treatment of interstitia... | ||||
TN4934 | Salaspermic acid
化合物 TN4934
|
71247-78-4 | 98% |
|
Salaspermic acid is an inhibitor of HIV reverse transcriptase and HIV replication in H9 lymphocyte cells. | ||||
T13796 | Nigranoic acid
化合物 T13796
|
39111-07-4 | 98% |
|
Nigranoic acid is a natural product,and inhibits HIV-1 reverse transcriptase. | ||||
TQ0073 | Andropanolide
穿心莲内酯
|
869807-57-8 | 98% |
|
Andropanolide 是一种来自穿心莲的二帖类化合物,具有抗HIV、抗疟和抗癌活性,对 Lipopolysaccharides (LPS) 刺激的 RAW264.7 巨噬细胞中一氧化氮 (NO) 的过量产生有抑制作用。 | ||||
TN3444 | Aristolactam BII
化合物 TN3444
|
53948-09-7 | 98% |
|
Aristolactam BII exhibits antimicrobial and antiinflammatory activity, it shows significant activity towards DPPH radical scavenging and potent inhibitory effect... |