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Cat. No. Product Name Field of Application Chemical Structure
DC90063 (-)-adenophorine
Moderate alpha-l-fucosidase inhibitor
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DC90062 (-)-5-hydroxy-equol
Natural microbial metabolite of isoflavone genistein, increasing the lifespan and improving the thermal and oxidative stress tolerance of C. elegans
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DC90061 Vx-445(r)
Less active enantiomer of Elexacaftor
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DC65217 BAY-805 Featured
BAY-805 is a potent and selective USP21 inhibitor. BAY-805 is a non-covalent inhibitor with low nanomolar affinity for USP21 and high selectivity over other DUB targets as well as kinases, proteases, and other common off-targets.
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DC90060 Vrt-18858
Metabolite of VX-740
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DC90059 Vmat2-in-i Hydrochloride
Vesicular monoamine transporter-2 (VMAT2) inhibitor, with 15-​fold greater affinity than GZ-​793A
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DC90058 Vinspinic
Inactive control for VinSpinIn
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DC90057 Unc5679
Negative control for EED inhibitor EED226
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DC90055 Unc4219
Negative control compound for UNC3866 which is a potent antagonist of the methyllysine (Kme) reading function of the Polycomb CBX and CDY families of chromodomains
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DC21015 FIT-039 Featured
FIT-039 is a potent, selective CDK9 inhibitor with IC50 of 5.8 uM for CKD9/cyclin T1, suppresses the replication of HSV-1 (IC50=0.69 uM).
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DC90054 Ucsf924nc
Negative control for UCSF924
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DC90053 Ucd74a Hydrochloride
Cell impermeant homolog of UCD38B, inhibitor of uPA (urokinase plasminogen activator)
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DC90052 Tpn-004
Negative control for TP-004
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DC90051 Tp-422
Negative control for TP-238
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DC90050 Tp-040n
Negative control for TP-040
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DC90049 Thpp-1-nc
Negative control for THPP-1
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DC90048 Th8321
Novel potent and selective NUDT15 inhibitor (MG IC50 = 35 nM), potentiating the anti-HCMV efficacy of ganciclovir
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DC90047 Th7285
Negative control for TH1760
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DC90046 Telmisartan Acyl-beta-d-glucuronide
Metabolite of Telmisartan
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DC90045 Tbaj-876
Novel novel anti-tuberculosis (TB) agent, possessing improved safety properties compared to bedaquiline
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DC90044 Tat-gap19(i130a)
Cell permeable Cx43 hemichannel blocker, being used a control peptide for TAT-Gap19
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DC90043 T3-clk-n
Negative control for T3-CLK
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DC90042 Sn-4(nps)2
Prodrug of ADAM17 inhibitor SN-4
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DC90041 Sgc-stk17b-1n
Negative control for SGC-STK17B-1, showing IC50 > 10,000 nM against STK17B
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DC90040 Sgc-clk-1n
Negative control for SGC-CLK-1
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DC90039 Sgc-ck2-1n
Negative control for SGC-CK2-1
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DC90038 Sgc-camkk2-1n
Negative control for SGC-CAMKK2-1
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DC90037 Sgc-brdviii-nc
Negative control for SGC-SMARCA-BRDVIII
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DC90036 Rwj-60475-(am)3
Novel cell permeable CD45 phosphatase inhibitor; Prodrug of RWJ-60475
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DC90035 Rp-101075
Metabolite of ozanimod, exhibiting a similar specificity profile as ozanimod at the S1P receptor family in vitro and pharmacodynamic profile in vivo
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