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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T8438 | 4i | CHEMBL1269981,5-HT3 antagonist-4i | 5-HT Receptor |
4i (CHEMBL1269981) is a 5-HT3 receptor antagonist,It modulates the serotonergic system. | |||
T2437 | O4I2 | O-4I2,O4I2 | OCT |
O4I2 is an effective Oct3/4 inducer in various human cell lines including human fibroblasts. | |||
T2439 | O4I1 | OCT | |
O4I1 is an effective Oct3/4 inducer. | |||
T74186 | PROTAC-O4I2 | Apoptosis , PROTACs | |
PROTAC-O4I2, a PROTAC ligand targeting splicing factor 3B1 (SF3B1), induced FLAG-SF3B1 degradation in K562 cells with an IC50 value of 0.244 μM. PROTAC-O4I2 induced apoptosis in K562 WT cells. | |||
T39335 | Anti-virus agent 1 | Anti-virus agent 1,Remdesivir isopropyl ester analog | |
Anti-virus agent 1 (compound 4i), a phosphoramidate prodrug of GS-5734, exhibits potent antiviral efficacy. It is primarily utilized in the study of coronavirus and Ebola virus (EBOV). | |||
T61255 | SDH-IN-1 | ||
SDH-IN-1 (compound 4i) is a potent succinate dehydrogenase (SDH) inhibitor, exhibiting an IC 50 value of 4.53 μM. This compound displays strong antifungal properties, particularly against S. sclerotiorum, with an EC 50 v... | |||
T78862 | EGFR-IN-86 | EGFR | |
EGFR-IN-86 (compound 4i), an EGFR inhibitor (IC50: 1.5 nM), demonstrates potent activity against glioblastoma by inducing apoptosis and causing G2/M phase cell cycle arrest in U87 cells [1]. | |||
T61426 | NOS-IN-2 | ||
NOS-IN-2 (Compound 4i), an imidamide-derived NOS inhibitor, exhibits high potency and selectivity, specifically inhibiting iNOS with an IC50 of 20 μM while sparing eNOS. Demonstrating minimal toxicity, it is suitable for... | |||
T79694 | EGFR-IN-88 | EGFR | |
EGFR-IN-88 (Compound 4i), an EGFR inhibitor with an IC50 of 87 nM, exhibits cytotoxic effects on A549 cells at an IC50 of 3.902 μM and can induce cell apoptosis [1]. | |||
T79686 | FGFR1 inhibitor-10 | FGFR | |
FGFR1 inhibitor-10 (Compound 4i), with an IC50 of 28 nM, effectively inhibits FGFR1 phosphorylation. This compound demonstrates anti-angiogenic and anti-invasion properties, as well as a significant anti-tumor effect [1]... | |||
T60714 | Gp120-IN-2 | ||
gp120-IN-2 (compound 4i) exhibits anti-HIV-1 activity which is a potent inhibitor of HIV-1 gp120 with an IC 50 of 7.5 μM and CC 50 of 112.93 μM. gp120-IN-2 dose-dependently shows cytotoxicity in SUP-T1 cells [1]. | |||
T79714 | HDAC3-IN-2 | HDAC | |
HDAC3-IN-2 (compound 4i), a pyrazinyl hydrazide-based HDAC3 inhibitor with an IC50 of 14 nM, effectively targets triple-negative breast cancer cells. Demonstrating cytotoxic activity, HDAC3-IN-2 exhibits an IC50 of 0.55 ... |