| S4067 |
Deferiprone
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Deferiprone (CP20) 是一种螯合剂,具有对铁离子的亲和性 (三价铁离子),与铁离子结合形成中性的3:1 (去铁铜:铁)复合物。 |
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Redox Biol, 2025, 85:103739
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bioRxiv, 2025, 2025.07.10.663832
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Cancer Lett, 2024, 592:216898
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| S2487 |
Mycophenolic Acid (Mycophenolate, MPA)
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Mycophenolic acid (Mycophenolate, RS-61443) 是一种有效的 IMPDH 抑制剂和免疫抑制药物的活性代谢物,可用于器官移植后的免疫排斥治疗。 |
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Cancers, October 21, 2025, 3389
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Antiviral Research, October 2017, 76-85
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Journal of Immunotoxicology, December 15, 2021, 154-162
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| S7828 |
Licochalcone A
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Licochalcone A 是一种提取自甘草的雌激素类黄酮,表现出抗疟疾,抗癌,抗菌和抗病毒的活性。Phase 3。
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European Journal of Pharmacology, October 15, 2023, 176031
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BioMed Research International, March 10, 2022, 5687832
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Oncology Reports, December 14, 2017, 1181-1190
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| S3608 |
Demethylzeylasteral (T-96)
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Demethylzeylasteral (T-96)是从Tripterygium wilfordii Hook F.中分离出的活性成分,能够抑制UDP-glucuronosyltransferase (UGT)的亚型UGT1A6和UGT2B7,具有免疫抑制活性。 |
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J Cancer, 2025, 16(1):227-240
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南京中医药大学学报, 2025, nan
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J Cancer, 2021, 12(13):3967-3975
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| S6828 |
Cremophor EL
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Cremophor EL是一种聚氧乙烯醚类的表面活性剂,可作为各种水溶性差的药物(包括抗癌药紫杉醇Taxol)的制剂载体。Cremophor EL 可应用于严重的类过敏反应,高血脂症,异常脂蛋白模式,红细胞聚集和周围神经病。 |
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Chinese Medicine, November 14 2025, 189
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Aging and disease, May 20 2024, 1120-1140
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Frontiers in Oncology, July 05 2022, 936145
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| S3018 |
Niflumic acid
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Niflumic acid(Nifluril)是环氧合酶-2 (COX-2)抑制剂,用于治疗关节和肌肉疼痛。 |
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Oncol Lett, 2020, 20(4):39
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Oncology Letters, 2020, 39
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| S0931 |
Jaceosidin
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Jaceosidin 是一种从Artemisia vestita中分离出来的类黄酮,在许多癌细胞中均具有抗肿瘤和抗增殖的活性。Jaceosidin 诱导凋亡,激活 Bax 并下调 Mcl-1 和 c-FLIP 表达。Jaceosidin 可抑制 COX-2 的表达和 NF-κB 的激活。 |
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| E2128 |
Corylifol A
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Corylifol A is a flavonoids islated from the seeds of Psoralea corylifolia L., which can inhibit IL-6-induced STAT3 activation and phosphorylation. |
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| E0766 |
Ophiopogonin D'
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Ophiopogonin D', isolated from the tubers of Ophiopogon japonicus, is a rare naturally occurring C29 steroidal glycoside, showing cytotoxic activity against two human tumor cell lines MG-63 and SNU387. |
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| E2797 |
Gitogenin
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Gitogenin, a natural steroid isolated from the whole plant of <i>Tribulus longipetalus</i>, is a selective inhibitor of UDP-glucuronosyltransferase 1A4 (UGT1A4) and enzyme α-glucosidase with IC50s of 0.69 μM (use trifluoperazine as a substrate) and 37.2 μM, respectively.
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|
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| S2487 |
Mycophenolic Acid (Mycophenolate, MPA)
|
Mycophenolic acid (Mycophenolate, RS-61443) 是一种有效的 IMPDH 抑制剂和免疫抑制药物的活性代谢物,可用于器官移植后的免疫排斥治疗。 |
- Cancers, October 21, 2025, 3389
- Antiviral Research, October 2017, 76-85
- Journal of Immunotoxicology, December 15, 2021, 154-162
|
|
| S3608 |
Demethylzeylasteral (T-96)
|
Demethylzeylasteral (T-96)是从Tripterygium wilfordii Hook F.中分离出的活性成分,能够抑制UDP-glucuronosyltransferase (UGT)的亚型UGT1A6和UGT2B7,具有免疫抑制活性。 |
- J Cancer, 2025, 16(1):227-240
- 南京中医药大学学报, 2025, nan
- J Cancer, 2021, 12(13):3967-3975
|
|
| S3018 |
Niflumic acid
|
Niflumic acid(Nifluril)是环氧合酶-2 (COX-2)抑制剂,用于治疗关节和肌肉疼痛。 |
- Oncol Lett, 2020, 20(4):39
- Oncology Letters, 2020, 39
|
|
| E2797 |
Gitogenin
|
Gitogenin, a natural steroid isolated from the whole plant of <i>Tribulus longipetalus</i>, is a selective inhibitor of UDP-glucuronosyltransferase 1A4 (UGT1A4) and enzyme α-glucosidase with IC50s of 0.69 μM (use trifluoperazine as a substrate) and 37.2 μM, respectively.
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