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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T2649 | Menin-MLL inhibitor MI-2 | Menin-MLL Inhibitor,MI2,MI-2,Menin-MLL inhibitor 2,MI 2 | Apoptosis , Epigenetic Reader Domain , Histone Methyltransferase |
Menin-MLL inhibitor MI-2 (MI2) is a potent menin-MLL interaction inhibitor with IC50 of 446 nM. | |||
T9399 | Menin-MLL inhibitor 20 | Epigenetic Reader Domain , Histone Methyltransferase | |
Menin-MLL inhibitor 20 is an irreversible inhibitor of menin-MLL interaction with antitumor activities. | |||
T2643 | MI-3 | Menin-MLL Inhibitor,Menin-MLL inhibitor 3,MI 3 | Apoptosis , Epigenetic Reader Domain , Histone Methyltransferase |
MI-3 (Menin-MLL Inhibitor) (Menin-MLL Inhibitor) is an effective inhibitor of Menin-MLL interaction (IC50: 648 nM). | |||
T12002 | Menin-MLL inhibitor 4 | Others | |
Menin-MLL inhibitor 4 has antitumor activity.Menin-MLL inhibitor 4 is an inhibitor of Menin- MLL (mixed-lineage leukemia protein) interaction . | |||
T79737 | Menin-MLL inhibitor 29 | Epigenetic Reader Domain | |
Menin-MLL Inhibitor 29 (Compound C1) is a Menin-MLL protein-protein interaction (PPI) inhibitor that demonstrates high affinity to Menin with a dissociation constant (K D) of 138 nM and impedes Menin's interaction with M... | |||
T78151 | Bleximenib oxalate | Menin-MLL inhibitor 24 oxalate | Epigenetic Reader Domain |
Menin-MLL Inhibitor 24 (compound A) oxalate, a menin-mixed-lineage leukemia 1 (menin-MLL) inhibitor, is utilized in cancer research [1]. | |||
T72360 | Menin-MLL inhibitor 26 | ||
Menin-MLL inhibitor 26 is a Menin-MLL inhibitor. Menin-MLL inhibitor 26 also is an active reference. Menin-MLL inhibitor 26 can inhibits cell growth. Menin-MLL inhibitor 26 can be used for the research of leukemia . | |||
T79117 | Menin-MLL inhibitor 27 | Epigenetic Reader Domain | |
Menin-MLL inhibitor 27 effectively inhibits the interaction between Menin and MLL, serving as a potential tool in cancer research, particularly for acute myeloid leukemia (AML) [1]. | |||
T72135 | (1s,4s)-Menin-MLL inhibitor-23 | ||
(1s,4s)-Menin-MLL Inhibitor-23, an enantiomer of Menin-MLL Inhibitor-23 (Example 99A), functions as an inhibitor of the menin-MLL interaction [1]. | |||
T12943 | SNDX-5613 | Epigenetic Reader Domain , Histone Methyltransferase | |
SNDX-5613 is a potent and specific inhibitor of Menin-MLL(Ki of 0.149 nM and a cell based IC50 of 10-20 nM). SNDX-5613 can be used for the research of MLL-rearranged (MLL-r) acute leukemias. | |||
T13336 | VTP50469 | Apoptosis , Epigenetic Reader Domain , Histone Methyltransferase | |
VTP50469 is a highly selective and orally active inhibitor of Menin-MLL interaction( Ki: 104 pM) and has potently anti-leukemia activity. | |||
T28036 | MI-2-2 | MI22,MI 2 2 | Histone Methyltransferase |
MI-2-2 is an inhibitor of bivalent protein-protein interaction between menin and MLL with an IC50 of 46 nM. MI-2-2 binds to menin with Kd of 22 nM. | |||
T69628 | Iptacopan hydrochloride hydrate | ||
Iptacopan hydrochloride hydrate is a highly potent and highly selective factor B inhibitor. | |||
TN7068 | Sinomenine N-oxide | Others | |
Sinomenine N-oxide is one of the major metabolites of the cyclic metabolic mechanism of Sinomenine. | |||
T2921 | Sinomenine hydrochloride | Sabianine A hydrochloride,Cucoline hydrochloride,Kukoline hydrochloride | Apoptosis , NF-κB , Opioid Receptor , Autophagy |
Sinomenine hydrochloride (Kukoline hydrochloride) is extracted from Sinomenium Acutum Rehderett Wilson. | |||
TN3628 | Chamaejasmenin B | Others | |
Chamaejasmenin B is a compound isolated from Stellera chamaejasme L. Chamaejasmenin B has anticancer and antitumor activity, inhibiting cancer cell migration and invasion, and inhibiting tumor metastasis.Chamaejasmenin B... | |||
T2726 | Sinomenine | Cucoline,Kukoline | Apoptosis , Others , NF-κB , Opioid Receptor , Autophagy |
Sinomenine (Kukoline) is a pure alkaloid isolated from the Sinomenium acutum, is utilized in the treatment of rheumatism and arthritis. | |||
TN4651 | Neuchromenin | Others | |
(-)-Neuchromenin is an inducer of neurite outgrowth of PC12 cells at concentration of 2.5-10 ug/ml. | |||
T20705 | Desmeninol | ||
Desmeninol is an active endogenous metabolite, detected mainly in urine, and in cells located mainly in the cytoplasm and fat bodies. It is used as a catalyst, chlorinating agent, curing agent and stabilizer in organic s... | |||
TN4802 | Plathymenin | Others | |
Plathymenin is a natural product isolated from Spatholobus suberectus. |