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Other Targets

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Cat. No. Product Name Field of Application Chemical Structure
DC23520 VU 6001966
A potent and selective, CNS penetrant mGlu2 negative allosteric modulator with IC50 of 78 nM.
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DC22885 TAN-67 dihydrobromide
A potent and selective δ-opioid receptor agonist that has high affinity and selectivity for the δ1 subtype with Ki of 1.12 nM.
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DC20627 ABT 089 dihydrochloride
A potent and selective α4β2 nAChR agonist with Ki of 16 nM.
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DC25087 Vandetanib trifluoroacetate
A potent and selective VEGFR2 (KDR) inhibitor with IC50 of 40 nM.
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DC23839 IN-1233 phosphate
A potent and selective TGF-βRI (ALK5) inhibitor with IC50 of 34 nM, prevents tissue hyperplasia in the rat urethra or common iliac artery..
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DC23840 IN-1233
A potent and selective TGF-βRI (ALK5) inhibitor with IC50 of 34 nM, prevents tissue hyperplasia in the rat urethra or common iliac artery..
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DC22715 RP-67580
A potent and selective tachykinin NK1 receptor antagonist with Ki of 2.9 nM.
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DC24175 A-770041
A potent and selective small-molecule inhibitor of Lck with IC50 of 147 nM.
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DC22341 H-1152
A potent and selective ROCK inhibitor with Ki of 1.6 nM.
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DC26074 CD 1530
A potent and selective RARγ receptor agonist with Ki of 150 nM.
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DC22968 TC-E 5005
A potent and selective PDE10A inhibitor with IC50 of 7.28 nM.
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DC22970 BMS 843496
A potent and selective PDE10A inhibitor with binding affinity (Kd) of 0.15 nM, IC50 of 2.11 nM.
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DC22671 Saredutant
A potent and selective non-peptide antagonist of the neurokinin A (NK2) receptor.
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DC20474 Nek2 inhibitor (R)-21
A potent and selective NIMA-related Kinase 2 (NEK2) inhibitor with IC50 of 22 nM, >200-fold selectivity over Plk1, Mps1, Aurora A and CDK2.
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DC23966 mTOR-IN-1
A potent and selective mTOR inhibitor with Ki of 1.5 nM.
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DC22887 THIQ
A potent and selective melanocortin 4 receptor (MC4R) agonist with EC50 of 2.1 nM.
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DC23410 BI 186908
A potent and selective MCH-R1 antagonist with IC50 of 22 nM, Ki of 14 nM.
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DC22707 Ibodutant
A potent and selective linear tachykinin NK2 receptor antagonist with pKb of 9.3.
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DC26102 TK05
A potent and selective inhibitors of leukotriene C4 synthase (LTC4S) with IC50 of 95 nM, Ki of 6 nM.
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DC23278 AM-7209
A potent and selective inhibitor of the MDM2-p53 interaction with Kd of 38 pM, and IC50 of 1.6 nM.
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DC22973 UK-414495
A potent and selective inhibitor of neutral endopeptidase (NEP) with IC50 of 18.9 nM for hNEP.
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DC24124 TH-588 hydrochloride
A potent and selective inhibitor of MTH1 protein with IC50 of 5 nM.
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DC20590 Cortistatin A
A potent and selective inhibitor of mediator-associated kinase CDK8 (IC50=12 nM) and its paralogue CDK19.
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DC22992 NSC95682
A potent and selective inhibitor of IRE1 endoribonuclease with IC50 of 0.41 uM.
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DC22509 DPC-681
A potent and selective inhibitor of HIV-1 protease with IC90 of 4-40 nM.
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DC22813 OXA-11
A potent and selective inhibitor of FAK phosphorylation with biochemical IC50 of 1.2 pM (pFAK Y397), cellular IC50 of 1 nM.
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DC22770 NK150460
A potent and selective inhibitor of breast cancer cells via activation the aryl hydrocarbon receptor (AhR) pathway.
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DC22381 BMS-345541 free base
A potent and selective IKK-2 inhibitor with IC50 of 0.3 uM.
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DC23428 TAK-259
A potent and selective human α1D adrenoceptor (α1D-AR) antagonist with Ki of 1.1 nM.
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DC23452 TAK-259 hydrochloride
A potent and selective human α1D adrenoceptor (α1D-AR) antagonist with Ki of 1.1 nM.
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