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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DC22802 | MK2-IN-28 |
A potent and selective, non-ATP competitive, allosteric MAPKAPK2/3 (MK2/3) inhibitor with IC50 of 8 nM for MK2, hTNFα EC50 of 0.31 uM.
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| DC22978 | PF-04471141 hydrochloride |
A potent and selective, CNS-penetrant PDE1 inhibitor with IC50 of 35 nM for PDE1B..
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| DC22979 | PF-04822163 |
A potent and selective, CNS-penetrant PDE1 inhibitor with IC50 of 2.4 nM for PDE1B..
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| DC23521 | VU 6010572 |
A potent and selective, CNS penetrant mGlu3 negative allosteric modulator with IC50 of 245 nM.
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| 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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