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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T10395L | ATM-3507 | Others | |
ATM-3507 is an inhibitor of tropomyosin. In human melanoma cell lines, the IC50s are from 3.83-6.84 μM. | |||
T62684 | ATM Inhibitor-5 | ||
ATM Inhibitor-5 [formula (1)] is a potent inhibitor of the serine/threonine protein kinase ATM. | |||
T2685 | KU-55933 | ATM Kinase Inhibitor | ATM/ATR , DNA-PK , PI3K , mTOR , Autophagy |
KU-55933 (ATM Kinase Inhibitor) is a potent and specific ATM inhibitor. | |||
T70113 | ATM-1001 | ||
ATM-1001 is an inhibitor of the cancer-associated tropomyosin 3.1 (Tpm3.1), suppressing glucose-stimulated insulin secretion (GSIS) from the pancreatic islets. | |||
T10395 | ATM-3507 trihydrochloride (1861449-70-8 free base) | ATM-3507 trihydrochloride | Others |
ATM-3507 trihydrochloride is a potent tropomyosin inhibitor (IC50s: 3.83-6.84 μM in human melanoma cell lines). | |||
T10396 | ATM Inhibitor-1 | ATM/ATR | |
ATM Inhibitor-1 is a highly potent, selective and orally active ATM inhibito (IC50: 0.7 nM) anti-tumor activity. It shows weak activity against mTOR (IC50, 21 μM), DNAPK (IC50, 2.8 μM), PI3Kα (IC50, 3.8 μM), PI3Kβ (IC50,... | |||
T63714 | ATM-IN-1 | ||
ATM-IN-1 is a potent inhibitor of ATM. ATM-IN-1 has shown research potential in cancer and neurological diseases. | |||
T79306 | ATM Inhibitor-9 | ATM/ATR | |
ATM Inhibitor-9 (Compd 7a) is a potent inhibitor of ATM kinase, exhibiting an IC50 value of 5 nM, and is utilized in cancer research [1]. | |||
T79305 | ATM Inhibitor-8 | ATM/ATR | |
ATM Inhibitor-8 (Compound 10r) is a potent, selective, and orally active inhibitor of ATM, exhibiting anti-tumor activity [1], characterized by an IC50 value of 1.15 nM. | |||
T63279 | ATM Inhibitor-2 | ||
ATM Inhibitor -2 is a potent and selective inhibitor of ATM (IC50<1 nM). | |||
T63317 | ATM Inhibitor-4 | ||
ATM Inhibitor -4 is a selective and potent ATM inhibitor (IC50: 0.32 nM) that strongly inhibits the activity of the PI3K kinase family and exhibits good metabolic stability. ATM Inhibitor -4 completely inhibits mTOR at 1... | |||
T63171 | ATM Inhibitor-3 | ||
ATM Inhibitor-3 is a potent and selective inhibitor of ATM (IC50: 0.71 nM). ATM Inhibitor-3 inhibits the PI3K kinase family and exhibits good metabolic stability. | |||
T72218 | ATM-3507 trihydrochloride | ||
ATM-3507 trihydrochloride, a potent inhibitor of tropomyosin, demonstrates inhibition concentration (IC50) values ranging from 3.83 to 6.84 μM across various human melanoma cell lines. | |||
T5175 | Azd1390 | ATM/ATR | |
AZD1390 is an exceptionally potent inhibitor of ATM in cells (IC50: 0.78 nM) with >10,000-fold selectivity over closely related members of the PIKK family of enzymes. | |||
T3338 | Ceralasertib | AZD6738 | ATM/ATR |
Ceralasertib (AZD6738) is an orally active, and selective ATR kinase inhibitor with IC50 of 1 nM. | |||
T4443 | AZ32 | ATM/ATR | |
AZ32 is an orally bioavailable and blood-brain barrier-penetrating ATM inhibitor with an IC50 of <6.2 nM for ATM enzyme, and an IC50 of 0.31 μM for ATM in cell. | |||
T1958 | AZ20 | ATM/ATR , mTOR | |
AZ20 is an effective and specific inhibitor of ATR kinase (IC50: 5 nM, in a cell-free assay), 8-fold selectivity over mTOR. | |||
T6770 | AZD0156 | Apoptosis , ATM/ATR | |
AZD0156 , an effective and specific inhibitors of ATM kinase, is potential antineoplastic activities and chemo-/radio-sensitizing. | |||
T1821 | CGK733 | CGK 733 | ATM/ATR |
CGK733 (CGK 733) is a potent and selective inhibitor of ATM/ATR. | |||
T3032 | VE-821 | ATR Inhibitor IV | ATM/ATR |
VE-821 (ATR Inhibitor IV) is a selective ATP competitive inhibitor of ATR( Ki/IC50: 13/26 nM in cell-free assays). |