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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DC42856 | ML-095 (hydrochloride) Featured |
Inhibitor of placental alkaline phosphatase (PLAP)
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| DC32615 | Talinolol Featured |
Talinolol is a beta(1)-adrenergic receptor antagonist and a probe drug for P-glycoprotein (P-gp) activity in humans.
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| DC23978 | hPGDS-IN-1 Featured |
hPGDS-IN-1 is a potent, selective hPGDS inhibitor with IC50 of 12 nM in FP or EIA assays..
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| DC43721 | Phentolamine HCl |
α-Adrenergic blocker
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| DC43709 | Methylecgonine |
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| DC43663 | Benzquinamide |
A discontinued antiemetic drug used in post-operative care
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| DC43657 | 1-Hydroxy-2-methylanthraquinone |
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| DC43655 | 2-Hydroxy-1-methoxyanthraquinone |
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| DC43638 | beta-Amyrin palmitate |
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| DC43394 | 5-Methoxy-7-hydroxycoumarin |
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| DC43297 | Epifriedelanol acetate |
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| DC43279 | Eichlerialactone |
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| DC42672 | Delucemine Hydrochloride |
Novel NMDA receptor antagonist
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| DC43939 | PT-Yellow (BDNCA3-D2) |
Novel non-toxic fluorescent probe to label the renal proximal tubules in zebrafishReference1) The small molecule probe PT-Yellow labels the renal proximal tubules in zebrafish; Chem Commun (Camb). 2015;51(2):395-8. doi: 10.1039/c4cc08075k. Epub 2014 Nov 1
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| DC43937 | UNC2170 maleate |
Novel ligand for the Methyl-lysine Binding Protein, 53BP1.
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| DC43936 | MT1 (Bis-CPI203)-PEG7) |
Novel highly potent BET bromodomain inhibitor with more than 100-fold higher cellular potency than the corresponding monovalent antagonist JQ1
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| DC43935 | Anavenol |
Anti-inflammatory drug
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| DC43933 | CBHcy |
Novel inhibitor of human betaine-homocysteine S-methyltransferase (BHMT)References: 1) Strakova J, Gupta S, Kruger WD, Dilger RN, Tryon K, Li L, Garrow TA. Inhibition of betaine-homocysteine S-methyltransferase in rats causes hyperhomocysteinemia and redu
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| DC43931 | DMHCA |
Gene-selective LXR modulator that mediates potent transcriptional activation of ABCA1 gene expression while exhibiting minimal effects on SREBP-1c
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| DC43930 | R(+)-8-Hydroxy DPAT HBr |
Full 5-HT1A serotonin receptor agonist; more active enantiomer.
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| DC43929 | CGS-9895 |
A GABA antagonist that acts via the benzodiazepine binding site of ag containing GABA receptors
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| DC43928 | SF-22 (TRPML3 activator) |
Novel activator of the transient receptor potential channel ML3 (TRPML3)
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| DC43927 | Modafinil |
Psychostimulant that displays neuroprotective and antiparkinsonian activity in a primate model of Parkinson's disease
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| DC43926 | Fenoldopam hydrobromide |
Selective dopamine agonist
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| DC43925 | Germanicol |
Apoptosis inducer with selective antiproliferative activity.
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| DC43924 | RBC6 |
Novel inhibitor of Ral binding to its effector RALBP1 and inhibiting Ral-mediated cell spreading of murine embryonic fibroblasts and anchorage-independent growth of human cancer cell lines
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| DC43922 | AA43279 |
Novel selective Nav1.1 activator, increasing the firing activity of parvalbumin-expressing, fast-spiking GABAergic interneurons and increasing the spontaneous inhibitory post-synaptic currents (sIPSCs) recorded from pyramidal neurons
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| DC43921 | HPCG |
Novel HIF-1α prolyl hydroxylase inhibitor
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| DC43919 | SB 271046 hydrochloride |
Selective, orally active 5-HT6 antagonist
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| DC43918 | ML233 |
Functional Agonist of the Apelin (APJ) Receptor
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