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Cat. No.	Product Name	Field of Application
DC22038	BRD2879	BRD2879 (BRD-2879) is a potent, selective inhibitor of IDH1-R132H mutant with IC50 of 50 nM, inhibits cell-based production of R-2HG with EC50 of 0.3 uM.
DC20832	BRD3308 Featured	BRD3308 is a potent, selective HDAC3 inhibitor with IC50 of 54 nM, displays >20-fold selectivity over HDAC1 and HDAC2, >500-fold selectivity over other HDAC isoforms.
DC20839	BRD3731	BRD3731 is a potent, selective GSK3β inhibitor with IC50 of 15 nM, 14-fold selectivity for GSK3β over GSK3α (IC50=215 nM).
DC12426	BRD4 inhibitor Compound V	BRD4 inhibitor Compound V is a domain-selective inhibitor of BRD4 with IC50 of 1.8 uM for BRD4 BD1, displays 6- and 16-fold selectivity for BRD4 over BRD2 and BRD3, respectively.
DC23880	BRD50837	BRD50837 is a potent, selective, small-molecule inhibitor of the Sonic Hedgehog (Shh) pathway with EC50 of 90 nM, partially lowers Gli1 expression at concentrations of 2 uM, a useful probe of Shh signaling pathway. .
DC20833	BRD5459	BRD5459 is a nontoxic enhancer of reactive oxygen species (ROS) that strongly elevates markers of oxidative stress without causing cell death, ROS inducer..
DC20840	BRD5529	BRD5529 is a small-molecule inhibitor that disrupts the interaction of CARD9-E3 ubiquitin ligase TRIM62 with IC50 of 8.6 uM.
DC20834	BRD56491	BRD56491 is a nontoxic enhancer of reactive oxygen species (ROS) that strongly elevates markers of oxidative stress without causing cell death, ROS inducer..
DC22711	BRD5814 Featured	BRD5814 is a potent, selective, highly brain penetrant β-arrestin biased dopamine D2 receptor (D2R) antagonist with Ki of 0.27 uM.
DC23885	BRD6851	BRD6851 is a potent, cell-active Hedgehog (Hh) pathway inhibitor with IC50 of 0.4 uM against C3H10T1/2 cells undergoing Hh-induced activation acts predominantly as Smo antagonist.
DC8409	BRD7552 Featured	BRD7552 is an inducer of transcription factor PDX1, which increases insulin expression.
DC20836	BRD9092	BRD9092 is a nontoxic enhancer of reactive oxygen species (ROS) that strongly elevates markers of oxidative stress without causing cell death, ROS inducer..
DC23874	BRD9526	BRD9526 is a potent, small-molecule inhibitor of the Sonic Hedgehog (Shh) pathway with EC50 of 60 nM, partially lowers Gli1 expression at concentrations of 10 uM, a useful probe of Shh signaling pathway. .
DC20837	BRD9757	BRD9757 is a potent, selective HDAC6 inhibitor with IC50 of 8 nM, displays >20-fold selectivity over HDAC1/3 and other HDAC isoforms..
DC23373	BRD9-IN-28	BRD9-IN-28 is a highly potent and selective BRD7/9 bromodomain inhibitor with pIC50 of 6.9, Kd of 68 nM for BRD9.
DC23356	BRD-IN-17	BRD-IN-17 is a cell permeable, family VIII bromodomain tool compound with additional PB1(2) activity over and above that of PFI-3.
DC23367	BRD-IN-26	BRD-IN-26 is a potent bromodomain inhibitor that binds the fifth bromodomain of PB1 with a KD of 124 nM, SMARCA2B and SMARCA4 with KD values of 262 and 417 nM, respectively.
DC2091	Brefeldin A	Brefeldin A is a lactone antibiotic and ATPase inhibitor for protein transport with IC50 of 0.2 μM in HCT 116 cells.
DC20981	Brequinar sodium Featured	Brequinar sodium (DuP-785, Brequinar, NSC 368390) is a potent and selective inhibitor of DHODH with IC50 of 20 nM, triggers differentiation in the ER-HoxA9, U937, and THP1 cells with an ED50 of 1 uM.
DC8179	Briciclib(ON 013105,ON 014185) Featured	Briciclib is a small molecule that suppresses cyclin D1 accumulation in cancer cells.
DC23147	Brigatinib (AP-26113) Featured	Brigatinib (AP-26113, AP26113) is a potent, selective, second generation ALK inhibitor with IC50 of 0.62 nM, exhibits about fivefold greater potency in vitro compared with crizotinib.
DC4165	Brinzolamide	Brinzolamide is a potent carbonic anhydrase II inhibitor with IC50 of 3.19 nM.
DC9535	Brivaracetam Featured	Brivaracetam(UCB-34714) is a 4-substituted pyrrolidone butanamide as agent with significant antiepileptic activity; high affinity SV2A ligand and also shows an ability to inhibit Na+ channels.
DC10383	Brivudine	Brivudine is a thymidine analogue with antiviral activity, indicated for the early treatment of acute herpes zoster.
DC21871	BRK inhibitor P21d	BRK inhibitor P21d is a potent, selective, cell permeable inhibitor of breast tumor kinase (Brk, PTK6) with IC50 of 30 nM, shows no inhibitory activity against Aurora B and Lck (IC50>20 uM).
DC23461	BRL 37344 sodium	BRL 37344 is a potent and selective β3 adrenoceptor agonist with Ki of 287 nM.
DC7891	BRL 52537 HYDROCHLORIDE	BRL 52537 is a selective κ/μ opioid receptor agonist.
DC20180	BRL-50481 Featured	BRL-50481 is a novel and selective inhibitor of phosphodiesterase (PDE) 7 with a Ki value, derived from secondary (Dixon) plots, of 180±10 nM, being at least 200-fold selective for hrPDE7A1 over all other PDEs.
DC9124	Bromhexine HCl	Bromhexine Hydrochloride is a medication prescribed for coughs which works by dissolving hard phlegm.
DC22426	Bromocriptine	Bromocriptine (2-Bromoergocriptine.

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