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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T9575 | MRTX9768 | Histone Methyltransferase | |
MRTX-9768 is a synthetic lethal-based inhibitor designed to bind the PRMT5-MTA complex and selectively target MTAP/CDKN2A-deleted tumors. | |||
T60152 | AZ5576 | CDK | |
AZ5576 is a potent and highly selective CDK9 inhibitor. AZ5576 can be used for the research of Hematological Malignancy [1]. | |||
T13044 | Mevociclib | SY-1365 | CDK |
Mevociclib (SY-1365) is a highly selective covalent inhibitor of CDK7. SY-1365 possesses therapeutic potential in both hematological and solid tumors. | |||
T0783 | Mianserin hydrochloride | Mianserin HCl,Org GB 94,ORG GB-94 HCl | Dopamine Receptor , 5-HT Receptor , Opioid Receptor , Adrenergic Receptor , Histamine Receptor |
Mianserin hydrochloride (Org GB 94) is a tetracyclic compound with antidepressant effects. it apparently blocks alpha-adrenergic, histamine H1, and some types of serotonin receptors. It may cause drowsiness and hematolog... | |||
T1890 | Pracinostat | SB939 | Apoptosis , HDAC |
Pracinostat (SB939) is a novel HDAC inhibitor with improved in vivo properties compared to other HDAC inhibitors currently in Clinicalal trials, allowing oral dosing. Data demonstrate that Pracinostat is a potent and eff... | |||
T13058 | T025 | CDK | |
T025 is a pan CLK inhibitor with Kds of 4.8, 0.096, 6.5, 0.61, and 0.074 nM for CLK1-4, respectively. T025 displays anti-proliferative activities with IC50s of 30-300 nM in hematological and solid cancer cell lines. T025... | |||
TQ0236 | Tirabrutinib | ONO-4059,GS-4059,Velexbru | BTK |
Tirabrutinib (GS-4059) (ONO-4059) is an orally active Bruton’s Tyrosine Kinase (Btk) inhibitor (can cross the blood-brain barrier (BBB)), with an IC50 of 6.8 nM. Tirabrutinib irreversibly and covalently binds to Btk and ... | |||
T38951 | Isatuximab | SAR-650984,hu38SB19,Isatuximab-irfc | Apoptosis , CD38 |
Isatuximab is a monoclonal antibody targeting the transmembrane receptor and extracellular enzyme CD38 in malignant cells of the hematological system and is a highly expressed protein in multiple myeloma. Isatuximab has ... | |||
T19661 | 8-Chloroadenosine | NSC 354258,8-Cl-Ado,NSC354258,NSC-354258 | AMPK |
8-Chloroadenosine (NSC-354258) is a 5' AMP-activated protein kinase agonist potentially for the treatment of chronic lymphocytic leukemia. 8-chloroadenosine activity is associated with inhibition of the mTOR pathway.8-Ch... | |||
T35000 | Uproleselan sodium | GMI 1271,GMI1271,GMI-1271 | |
Uproleselan sodium (GGI-1271) is a small molecule E-selector antagonist originally targeted at AML as an adjuvant to standard chemotherapy for hematological malignancies. | |||
T11603 | Ibrutinib-MPEA | Others | |
Ibrutinib-MPEA is ibrutinib derivative. Ibrutinib is a covalent and irreversible BTK inhibitor that has been used to treat hematological malignancies. | |||
T15111 | Diacetoxyscirpenol | Others | |
Diacetoxyscirpenol, a trichothecene mycotoxin, is a secondary metabolite product of fungi. Diacetoxyscirpenol consumption induces hematological disorders in humans and animals. | |||
T37077 | Syk-IN-4 | ||
Syk-IN-4 is a potent, selective, and orally bioavailable inhibitor of SYK, demonstrating an IC50 of 0.31 nM. It targets SYK, which has been identified as a potential therapeutic target for autoimmunity and hematological ... | |||
T21329 | Gemcitabine monophosphate disodium salt | Gemcitabine monophosphate disodium salt monohydrate,Gemcitabine monophosphate disodium,GemMP | |
R306465 is a novel HDAC inhibitor with broad-spectrum antitumor activity against solid (IC50: 30 to 300 nM) and hematological malignancies. R306465 was found to be a potent inhibitor of HDAC1 and -8 (class I) in vitro. | |||
T61337 | PTG-0861 | ||
PTG-0861 is a highly specific inhibitor of histone deacetylase 6 (HDAC6), demonstrating an impressive IC50 value of 5.92 nm. This compound effectively triggers apoptosis and holds potential for research pertaining to acu... | |||
T63955 | MU1656 | ||
MU1656, a potent and selective histone methyltransferase DOT1L inhibitor, demonstrates an IC50 of 2 nM. It is applicable in the research of hematological malignancies [1]. | |||
T77183 | Ripertamab | ||
Ripertamab (SCT400), a recombinant human-mouse chimeric anti-CD20 IgG1κ monoclonal antibody (mAb), has applications in the research of hematological malignancies, particularly non-Hodgkin’s lymphoma (NHL) [1]. | |||
T76929 | Betifisolimab | ||
Betifisolimab (MSB-2311), a humanized monoclonal antibody targeting the immunosuppressive ligand PD-L1, shows promise for research in advanced solid tumors and hematological malignancies [1]. | |||
T79840 | Bocodepsin hydrochloride | OKI-179 hydrochloride | HDAC |
Bocodepsin hydrochloride (OKI-179) is a selective HDAC inhibitor with antitumor properties, efficacious via oral administration. It is employed in the suppression of both solid tumors and hematological malignancies [1]. | |||
T78516 | NUC-7738 | Others | |
NUC-7738, a 5′-aryloxy phosphoramidate prodrug of 3′-deoxyadenosine (3′-dA), exhibits potent cytotoxic activity against various hematological cancer cell lines and is utilized in cancer research [1]. |