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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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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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| DC90034 | Rl2578 |
Negative control for Borussertib, being >1000 fold less potent in vitro than Borussertib
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| DC90032 | Remodelin-yne |
Clickable Remodelin analog
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| DC90031 | Rac-ac-ro5203548 |
Prodrug of RO5203548, a selective agonist of the trace amine-associated receptor 1 (TAAR1)
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| DC90030 | Qpx7831 Sodium |
Novel Orally Bioavailable Prodrug of Boronic Acid β-Lactamase Inhibitor QPX7728
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| DC90029 | Pu-h54-iso |
An isomer of PU-H54, a novel Grp94- and Hsp90-selective inhibitor
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| DC90028 | Pro-dmocptl-13 |
Prodrug of DMOCPTL
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| DC90027 | Primordazine Nc-6364997 |
Negative control for Primordazine A and Primordazine B
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| DC90026 | Pptn-nc |
Negative control for PPTN
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| DC90025 | Pim-in-72 |
Less active enantiomer of LGH447, acting as a selective weak pan-PIM inhibitor (IC 50 (µM): PIM1 0.095; PIM2 0.522; PIM3 0.369) in comparision with LGH447 (IC 50 (µM): PIM1 0.001; PIM2 0.002; PIM3 0.002)
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| DC90024 | Phip-d |
Deuterated internal standard for PhIP
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| DC90023 | Pfi-6n |
Negative control for PFI-6
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| DC90022 | Pfi-653-n |
Negative control for PFI-653
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| DC90021 | Pf-06465603 |
Metabolite of PF-04691502, a highly potent and selective ATP competitive kinase inhibitor of class 1 PI3Ks and mTOR
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| DC90020 | Pafuramidine Maleate |
Pro-drug of furamidine, acting as antiprotozoal/antifungal agent
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| DC90019 | Pa-9-3d |
Novel PA-9 analog, acting as an antagonist of the PAC1 receptor, showing improved antagonistic activities than PA-9
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| DC90018 | Oncrasin-266 |
Prodrug of antitumor agent oncrasin-72, with improved stability, pharmacokinetics, and safety
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| DC90017 | Og-881 |
Novel potent and highly selective KDM1A chemoprobe, exhibiting a selectivity profile similar to the parent compound ORY-1001
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