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Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
10 Results for "
extrinsic apoptotic pathways
" in MedChemExpress (MCE) Product Catalog:
Products (10)
10 Results for "extrinsic apoptotic pathways" in MCE Product Catalog:
8
Cat. No.: HY-179124
Apoptosis inducer 52 is a derivative of flutamide that induces apoptosis in prostate cancer cells. Apoptosis inducer 52 promotes apoptosis by activating both intrinsic and extrinsic apoptotic pathways, without generating reactive oxygen species (ROS). Apoptosis inducer 52 triggers caspase 3/7 activity and the externalization of phosphatidylserine, leading to cell cycle arrest at the G0/G1 phase. Apoptosis inducer 52 can be used for the research of androgen receptor (AR)-dependent and -independent prostate cancers and leukemia .
Cat. No.: HY-P990901
CAS No.: 2796349-94-3
Synonyms: IGM-8444
Target:
Research Areas:
Cat. No.: HY-N10018
CAS No.: 154822-57-8
Synonyms: 25-Anhydrocimigenol xyloside
Target:
Cat. No.: HY-158210
CAS No.: 1809413-98-6
Wnt/β-catenin-IN-3 (compound 17) is a Wnt/β-catenin inhibitor with low micromolarGI50s against various cancer cells. Wnt/β-catenin-IN-3triggers G2/M cell cycle arrest though activation of p53-p21 pathway as well as intrinsic and extrinsic apoptotic death of colon cancer cells .
Cat. No.: HY-N0213R
CAS No.: 18059-10-4
Synonyms: Verticinone (Standard); Raddeanine (Standard)
Cat. No.: HY-W009929
CAS No.: 18979-55-0
Synonyms: 4-(Hexyloxy)phenol
AC-45594 (4-(Hexyloxy)phenol) is a UPR activator. AC-45594 induces endoplasmic reticulum stress, activates the unfolded protein response (UPR), and drives the transition from adaptive stress signaling to terminal stress signaling, ultimately leading to cell Apoptosis. AC-45594 activates Caspase-3, induces PARP cleavage, and increases the protein level of DR5. AC-45594 selectively inhibits the growth of Ewing sarcoma cells .
Cat. No.: HY-P11828
Cat. No.: HY-182031
Target:
Research Areas:
JS04 is a EGFR L858R/T790M kinase inhibitor. JS04 activates both endogenous and exogenous apoptosis (apoptosis) pathways and induces G2/M phase arrest of the cell cycle. JS04 is applicable to the research of drug-resistant non-small cell lung cancer .
Cat. No.: HY-N21972
CAS No.: 129587-09-3
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Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
