Catalog |
name |
Description |
price |
R-R-2484 |
BAY1238097 CAS No.1564268-08-1 |
BAY1238097/CAS No.1564268-08-1 is a potent and selective inhibitor of BET binding to histones and has strong anti-proliferative activity in different AML (acute myeloid leukemia) and MM (multiple myeloma) models through down-regulation of c-Myc levels and its downstream transcriptome (IC50 <100 nM). |
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R-R-2485 |
(S)-JQ-35 CAS No.1349719-98-7 |
(S)-JQ-35 (TEN-010)/CAS No.1349719-98-7 is an inhibitor of the Bromodomain and Extra-Terminal (BET) family bromodomain-containing proteins with potential antineoplastic activity. |
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R-R-2486 |
ACBI2 CAS No.2913161-19-8 |
ACBI2/CAS No.2913161-19-8 is a highly potent and orally active VHL PROTAC SMARCA2 degrader (EC50: 7 nM), which selectively degrades SMARCA2 with a DC50 value of 1 nM in RKO cells. ACBI2 can be used in the research of lung cancer. |
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R-R-2487 |
GSK620 CAS No.2088410-46-0 |
GSK620/CAS No.2088410-46-0 is a potent and orally active pan-BD2 inhibitor with excellent broad selectivity, developability and in vivo oral pharmacokinetics. GSK620 is highly selective for the BET-BD2 family of proteins, with >200-fold selectivity over all other bromodomains. GSK620 shows an anti-inflammatory phenotype in human whole blood. |
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R-R-2488 |
MI-538 CAS No.1857417-10-7 |
MI-538/CAS No.1857417-10-7 is an inhibitor of the interaction between menin and MLL fusion proteins with an IC50 of 21 nM. |
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R-R-2489 |
CFT8634 CAS No.2704617-96-7 |
CFT8634/CAS No.2704617-96-7 is an oral activity degrader targeting BRD9 extracted from patent WO2021178920A1 compound 174. CFT8634 can be used for the research of synovial sarcoma and SMARCB1-deleted solid tumors. |
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R-R-2490 |
INCB-057643 CAS No.1820889-23-3 |
INCB-057643/CAS No.1820889-23-3 is a novel, orally bioavailable BET inhibitor. |
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R-R-2491 |
ZL0454 CAS No.2229042-77-5 |
ZL0454/CAS No.2229042-77-5 is a potent and selective Bromodomain-containing protein 4 (BRD4) inhibitor with an IC50 of 49 and 32 nM for BD1 and BD2. |
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R-R-2492 |
MI-136 CAS No.1628316-74-4 |
MI-136/CAS No.1628316-74-4 is an inhibitor of the menin-MLL protein-protein interaction (PPI), with an IC50 of 31 nM and a Kd of 23.6 nM. MI-136 shows to block AR signaling and has the potential for the study in castration-resistant tumors. |
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R-R-2493 |
SIM1 CAS No.2719051-84-8 |
SIM1/CAS No.2719051-84-8 is a potent von Hippel-Lindau (VHL)-based trivalent PROTAC capable of degradation for all BET family members, with preference for BRD2 degradation (IC50=1.1 nM; Kd=186 nM). SIM1 shows sustained anti-cancer activity. |
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