| S2541 |
Clomipramine HCl
|
Clomipramine HCl是一種三環(huán)抗抑郁藥,可有效抑制5-HT再攝取,IC50值為1.5 nM。鹽酸氯丙咪嗪用于抑郁癥、焦慮癥和強(qiáng)迫癥的研究。 |
-
Biomed Pharmacother, 2022, 153:113328
-
bioRxiv, 2020, 2020/9/20.4.7.30734
|
|
| S0970 |
Curzerene
|
Curzerene是從仙茅根莖中分離得到的具有抗癌活性的倍半萜類化合物,可抑制谷胱甘肽S-轉(zhuǎn)移酶A1(GSTA1)的mRNA和蛋白表達(dá),也可誘導(dǎo)細(xì)胞凋亡。 |
|
|
| S9698 |
Ezatiostat
|
Ezatiostat是一種谷胱甘肽的三肽類似物,是 Glutathione S-transferase P1-1 (GSTP1-1) 的擬肽抑制劑。Ezatiostat 可激活 c-Jun NH2 terminal kinase (JNK1) 和 ERK1/ERK2 并誘導(dǎo)凋亡。 |
|
|
| S5561 |
Ethacrynic Acid
|
Ethacrynic Acid is a loop or high ceiling diuretic used for the treatment of high blood pressure and edema caused by diseases like congestive heart failure, liver failure, and kidney failure. |
-
J Pharm Anal, 2024, 14(5):100923
-
Journal of Pharmaceutical Analysis, 2023, 10.1016/j.jpha.2023.12.013
|
|
| S4686 |
Vitamin E
|
Vitamin E (D-alpha-Tocopherol) 是一種脂溶性的維生素,具有有效的抗氧化特性。它是有效的過氧化氫自由基清除劑并在很多組織中,非競爭性地抑制環(huán)氧酶活性。同時(shí)通過抑制VEGF基因轉(zhuǎn)錄,抑制血管生成和腫瘤休眠。 |
-
Elife, 2025, 13RP94169
-
Cancer Drug Resist, 2025, 8:45
-
Signal Transduct Target Ther, 2024, 9(1):109
|
|
| S2541 |
Clomipramine HCl
|
Clomipramine HCl是一種三環(huán)抗抑郁藥,可有效抑制5-HT再攝取,IC50值為1.5 nM。鹽酸氯丙咪嗪用于抑郁癥、焦慮癥和強(qiáng)迫癥的研究。 |
- Biomed Pharmacother, 2022, 153:113328
- bioRxiv, 2020, 2020/9/20.4.7.30734
|
|
| S0970 |
Curzerene
|
Curzerene是從仙茅根莖中分離得到的具有抗癌活性的倍半萜類化合物,可抑制谷胱甘肽S-轉(zhuǎn)移酶A1(GSTA1)的mRNA和蛋白表達(dá),也可誘導(dǎo)細(xì)胞凋亡。 |
|
|
| S9698 |
Ezatiostat
|
Ezatiostat是一種谷胱甘肽的三肽類似物,是 Glutathione S-transferase P1-1 (GSTP1-1) 的擬肽抑制劑。Ezatiostat 可激活 c-Jun NH2 terminal kinase (JNK1) 和 ERK1/ERK2 并誘導(dǎo)凋亡。 |
|
|
| S5561 |
Ethacrynic Acid
|
Ethacrynic Acid is a loop or high ceiling diuretic used for the treatment of high blood pressure and edema caused by diseases like congestive heart failure, liver failure, and kidney failure. |
- J Pharm Anal, 2024, 14(5):100923
- Journal of Pharmaceutical Analysis, 2023, 10.1016/j.jpha.2023.12.013
|
|
| S4686 |
Vitamin E
|
Vitamin E (D-alpha-Tocopherol) 是一種脂溶性的維生素,具有有效的抗氧化特性。它是有效的過氧化氫自由基清除劑并在很多組織中,非競爭性地抑制環(huán)氧酶活性。同時(shí)通過抑制VEGF基因轉(zhuǎn)錄,抑制血管生成和腫瘤休眠。 |
- Elife, 2025, 13RP94169
- Cancer Drug Resist, 2025, 8:45
- Signal Transduct Target Ther, 2024, 9(1):109
|
|