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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DC43240 | Cannabichromene |
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| DC43239 | Coniferaldehyde |
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| DC43238 | Encecalin |
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| DC43237 | CL-214828 |
Strong neuroleptic agent, showing no cataleptic effect and antagonism against apomorphine
More description
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| DC43236 | Faradiol |
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| DC43235 | Lansiumarin C |
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| DC43233 | Curzerenone |
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| DC43232 | Epitaraxerol |
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| DC43230 | (-)-Maackiain |
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| DC43229 | Saponarin |
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| DC43228 | Calyxin H |
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| DC43227 | CPI203-rac |
A novel potent, selective and cell permeable inhibitor of BET bromodomain
More description
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| DC43226 | 1,3,7-Trihydroxy-2-prenylxanthone |
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| DC43225 | Epicatechin pentaacetate |
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| DC43224 | Isodiospyrin |
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| DC43223 | Liquiritin apioside |
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| DC43222 | SJ572403 |
Novel Inhibitor of the Disordered Protein, p27(Kip1)
More description
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| DC43221 | CP-465022 Maleate |
Novel class of noncompetitive NR2C/D subunit-selective N-methyl-D-aspartate(NMDA) receptor antagonist
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| DC43220 | Methyllucidone |
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| DC43219 | Lucidone |
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| DC43218 | CMF-019 Potassium |
The first potent biased small molecule agonist at the apelin receptor, increasing cardiac contractility in vivo
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| DC43217 | Humulene epoxide II |
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| DC43216 | Cabralealactone |
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| DC43215 | Alisol A 23-acetate |
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| DC43214 | Erythrodiol 3-palmitate |
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| DC43213 | SGC A-196 |
Potent inhibitor of SUV420H1 (IC50 = 25 nM) and SUV420H2 (IC50 = 144 nM), a closely related pair of proteins which catalyze the di- and tri-methylation of H4K20
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| DC43212 | CRT0273750 |
Novel potent inhibitor of the lysophospholipase autotaxin
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| DC43211 | Pseudopalmatine |
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| DC43210 | Stigmasterol glucoside |
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| DC43209 | Murrayone |
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