2451219-73-9

2451219-73-9 structure

Name: BRD4 Inhibitor-18
Chemical Name: BRD4 Inhibitor-18
CAS Number: 2451219-73-9
Molecular Formula: C₂₆H₂₆ClN₃O₃S
Molecular Weight: 496.02
Catalog: Signaling Pathways Apoptosis Apoptosis
Create Date: 2022-05-21 20:57:22
Modify Date: 2024-01-04 14:28:26
BRD4 Inhibitor-18 is a highly potent BRD4 inhibitor with IC50 value of 110 nM. BRD4 Inhibitor-18 has a hydrophobic acetylcyclopentanyl side chain. BRD4 Inhibitor-18 can significantly suppress the proliferation of MV-4-11 cells with high BRD4 level. BRD4 Inhibitor-18 has apoptosis-promoting and G0/G1 cycle-arresting activity[1].

Name	BRD4 Inhibitor-18

Description	BRD4 Inhibitor-18 is a highly potent BRD4 inhibitor with IC50 value of 110 nM. BRD4 Inhibitor-18 has a hydrophobic acetylcyclopentanyl side chain. BRD4 Inhibitor-18 can significantly suppress the proliferation of MV-4-11 cells with high BRD4 level. BRD4 Inhibitor-18 has apoptosis-promoting and G0/G1 cycle-arresting activity[1].
Related Catalog	Signaling Pathways >> Apoptosis >> Apoptosis Research Areas >> Cancer Signaling Pathways >> Apoptosis >> c-Myc Signaling Pathways >> Epigenetics >> Epigenetic Reader Domain
Target	IC50: 110 nM (BRD4)[1]
In Vitro	BRD4 Inhibitor-18 (compound 13f) (0-10 μM; 72 hours) can suppress the proliferation of HL-60 and MV-41 cells[1]. BRD4 Inhibitor-18 (0.5 and 5 μM; 12 hours) significantly arrests MV-4-11 cells in G1 phase in a dose-dependent manner[1]. BRD4 Inhibitor-18 (0.5 and 5 μM; 12 hours) effectively induces apoptosis of MV-4-11 cells in a dose-dependent manner[1]. BRD4 Inhibitor-18 (0.5 and 5 μM; 4 hours) inhibits the expression of c-Myc protein in a dose-dependent manner[1]. Cell Proliferation Assay Cell Line: HL-60 and MV-4-11[1] Concentration: 0-10 μM Incubation Time: 72 hours Result: Suppressed the proliferation of HL-60 and MV-41 cells with IC50s of 5.52 μM and 0.42 μM. Cell Cycle Analysis Cell Line: MV-4-11 cells[1] Concentration: 0.5 and 5 μM Incubation Time: 12 hours Result: Significantly arrested MV-4-11 cells in G1 phase in a dose-dependent manner. Apoptosis Analysis Cell Line: MV-4-11 cells[1] Concentration: 0.5 and 5 μM Incubation Time: 12 hours Result: Effectively induced apoptosis of MV-4-11 cells in a dose-dependent manner. Western Blot Analysis Cell Line: MV-4-11 cells[1] Concentration: 0.5 and 5 μM Incubation Time: 4 hours Result: Inhibited the expression of c-Myc protein in a dose-dependent manner.
References	[1]. Li Q, Li J, Cai Y, et al. Design, synthesis and biological evaluation of novel 6-phenyl-1,3a,4,10b-tetrahydro-2H-benzo[c]thiazolo[4,5-e]azepin-2-one derivatives as potential BRD4 inhibitors. Bioorg Med Chem. 2020;28(15):115601.

Molecular Formula	C₂₆H₂₆ClN₃O₃S
Molecular Weight	496.02

2451219-73-9	2490311-14-1
2761366-60-1	309951-18-6
2757865-63-5	2760307-53-5
2242582-40-5	2230873-66-0
1351978-48-7	2762382-51-2
1158522-08-7	940364-43-2
134104-43-1	131615-57-1
6906-52-1	2639448-54-5
930439-75-1	1018584-77-4
1375289-11-4	849349-65-1