About 7 results found for searched term "C75" (0.077 seconds)
Cat.No. | Name | Target |
---|---|---|
M1812 | GANT58 | Gli |
NSC75503 | ||
GANT58 (NSC75503) is a potent GLI antagonist that inhibits GLI1-induced transcription with an IC50 of 5 μM. | ||
M2076 | SP600125 | JNK |
JNK Inhibitor II; 1PMV; NSC75890; Pyrazolanthrone | ||
SP600125 is a novel and selective inhibitor of c-Jun N-terminal kinase (JNK), inhibited phosphorylation of c-Jun with an IC50 of 5-10 microM. | ||
M2604 | C75 | FAS |
C75 is a novel, potent synthetic inhibitor of fatty acid synthase (FAS). C75 inhibits prostate cancer cells PC3 with an IC50 of 35 μM. C75 is a potent CPT1A activator. | ||
M4940 | SC75741 | NF-κB |
SC-75741 | ||
SC75741 is a broad and potent INHIBITOR of NF-κB with an IC50 of 200 nM against P65. SC75741 blocks replication of influenza viruses. SC75741 leads to decreased expression of cytokines, chemokines, and pro-apoptotic factors by impairing DNA binding of NF-κB subunit P65. Inhibit caspase activation and block caspase-mediated nuclear output of viralribonucleoproteins. | ||
M8493 | NSC756093 | Others |
NSC756093, a podophyllotoxin analog, is a potent and specific inhibitor of GBP1:PIM1 interaction that inhibits proliferation of paclitaxel resistant cancer cells. | ||
M9508 | C75 trans | FAS |
(±)-C75 | ||
C75 trans is an enantiomer of C75, which is a synthetic fatty-acid synthase (FASN) inhibitor. | ||
M13554 | LDC7559 | Pyroptosis |
LDC7559 is a gasdermin D (GSDMD) inhibitor via blocking neutrophil extracellular trap (NET) in the late stages . |
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