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cell cycle arrest

Cell cycle arrest was the first identified effect of HDAC inhibitors on cancer cells. HDAC inhibitors are capable of causing a cell cycle arrest in a broad range of cells, including numerous forms of cancer and both cancerous and noncancerous cells.
Cat. No. 製品名 CAS No. Purity Chemical Structure
T3774 Gracillin 19083-00-2 98%
Gracillin can induce cell cycle arrest, oxidative stress, and apoptosis in HL60 cells, and has the potential to be developed as an antitumor agent. Gracillin can...
T4189 4-Oxofenretinide 865536-65-8 96.89%
4-Oxofenretinide (3-Keto fenretinide) , a recently identified fenretinide metabolite, induces marked G2-M cell cycle arrest and apoptosis.
TN1174 Schinifoline 80554-58-1 99.34%
Schinifoline is a quinolone derivative extracted from Zanthoxylum schinifolium Sieb with cytotoxic activity that promotes radiosensitization of cancer cells, aff...
T3386 Kaempferitrin 482-38-2 99.51%
Kaempferitrin (Lespenephryl) has antidepressant-like effect related to the serotonergic system, principally 5-HT1A. Kaempferitrin exerts cytotoxic and antitumor ...
T3811 Ginsenoside C-K 39262-14-1 99.65%
Ginsenoside C-K (Ginsenoside K) is a bacterial metabolite of G-Rb1 exhibiting anti-inflammatory effects by reducing iNOS and COX-2.
Gracillin
T3774
Gracillin can induce cell cycle arrest, oxidative stress, and apoptosis in HL60 cells, and has the potential to be developed as an antitumor agent. Gracillin can...
4-Oxofenretinide
T4189
4-Oxofenretinide (3-Keto fenretinide) , a recently identified fenretinide metabolite, induces marked G2-M cell cycle arrest and apoptosis.
Schinifoline
TN1174
Schinifoline is a quinolone derivative extracted from Zanthoxylum schinifolium Sieb with cytotoxic activity that promotes radiosensitization of cancer cells, aff...
Kaempferitrin
T3386
Kaempferitrin (Lespenephryl) has antidepressant-like effect related to the serotonergic system, principally 5-HT1A. Kaempferitrin exerts cytotoxic and antitumor ...
Ginsenoside C-K
T3811
Ginsenoside C-K (Ginsenoside K) is a bacterial metabolite of G-Rb1 exhibiting anti-inflammatory effects by reducing iNOS and COX-2.