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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DC47111 | Ecubectedin |
Ecubectedin is a derivative. Ecteinascidins is a family of tetrahydroisoquinoline alkaloids with wide range of antitumor and antimicrobial activities.
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| DC47110 | Deudomperidone |
Domperidone-d4 is a deuterium labeled Domperidone (R33812).Domperidone is a selective dopamine-2 receptor antagonist. Domperidone acts as an antiemetic and a prokinetic agent through its effects on the chemoreceptor trigger zone and motor function of the stomach and small intestine.
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| DC47109 | Cimpuciclib |
Cimpuciclib is a cyclin-dependent kinase(CDK) inhibitor and antineoplastic.
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| DC47107 | 14-Deoxy-11-oxoandrographolide |
14-Deoxy-11-oxoandrographolide is an antileishmanial agent. 14-Deoxy-11-oxoandrographolide inhibits the replication of heal chikungunya virus (CHIKV) and can be used for CHIKV infection research.
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| DC47106 | [18F]-Labeled L-dopa precursor |
[18F]-Labeled L-dopa precursor is a precursor for synthesis of 18F-labeled L-dopa extracted from patent WO2014095739A1, example 8.
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| DC47105 | Complanatoside B |
Complanatoside B is a P. chinense Fisch flavonoid with potential anti-inflammatory effects.
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| DC47104 | 1,2-Dilauroyl-sn-glycero-3-phosphocholine |
1,2-Dilauroyl-sn-glycero-3-phosphocholine (DLPC) is an LRH-1 agonist ligand.
1,2-Dilauroyl-sn-glycero-3-phosphocholine is a phospholipid for biological study.
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| DC47103 | SB 202474 |
SB 202474, a negative analog of SB203580. SB 202474, which has no ability to inhibit p38 MAPK activity and is widely used as a negative control compound in p38 MAPK studies, also suppressed melanin synthesis induction.
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| DC47102 | SSAO inhibitor-1 |
SSAO inhibitor-1 is a semicarbazide-sensitive amine oxidase (SSAO) inhibitor. SSAO inhibitor-1 has anti-inflammatory activity and can be used for liver diseases research.
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| DC47101 | γ-Linolenic acid ethyl ester |
γ-Linolenic acid ethyl ester (Ethyl γ-linolenate) is a leukotriene B4 receptor 4 (LTB4) antagonist.
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| DC47100 | MARK-IN-4 |
MARK-IN-4 is a potent microtubule affinity regulating kinase (MARK) inhibitor with an IC50 of 1 nM. Inhibition of microtubule affinity regulating kinase (MARK) represents a potentially attractive means of arresting neurofibrillary tangle pathology in Alzheimer's disease.
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| DC47099 | (Rac)-Golgicide A |
(Rac)-Golgicide A ((Rac)-GCA) is a racemate of Golgicide A. Golgicide A (GCA) is a potent, highly specific, and reversible inhibitor of the cis-Golgi ADP-ribosylation factor guanine nucleotide exchange factors (ArfGEF) GBF1.Golgicide A drastically reduced replication of coxsackievirus B3 (CVB3) and other human enterovirus species.
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| DC47098 | KDM2B-IN-1 |
KDM2B-IN-1 is a histone demethylase (kdm2b) inhibitor and can be used for hyperproliferative diseases research.
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| DC47097 | Navafenterol saccharinate |
Navafenterol (AZD-8871) saccharinate is an inhaled, long-acting bronchodilator, which is a muscarinic antagonist and β2 agonist.
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| DC47096 | Umckalin |
Umckalin is a oxygenated coumarin from Pelargonium sidoides.
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| DC47095 | Larsucosterol sodium |
Larsucosterol sodium is a cholesterol metabolite from the nuclei of normal human liver tissues, epigenetically regulates the transcription of proteins and enzymes involved in lipid synthesis, inflammation, and apoptosis.
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| DC47092 | Lazuvapagon |
Lazuvapagon is a vasopressin V2 receptor agonist for the research of nocturia.
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| DC47091 | Guretolimod |
Guretolimod is a Toll-like receptor 7 (TLR7) agonist.
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| DC47089 | Treprostinil palmitil |
Treprostinil palmitil (TP) is the prodrug of DP1 and EP2 agonist, Treprostinil (UT-15), whose EC50 values were 0.6 and 6.2 nM, respectively. Treprostinil palmitil is a pure prodrug and possesses no inherent binding to G-protein coupled receptors including prostanoid receptors.
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| DC47088 | Amdizalisib |
Amdizalisib is a PI3K inhibitor and used for the research of inflammatory disease, autoimmune disease or cancer.
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| DC47087 | Orismilast |
Orismilast (LEO-32731) is a PDE4 inhibitor used for the research of inflammatory diseases.
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| DC47086 | 7,3′,4′-Tri-O-methyleriodictyol |
7,3′,4′-Tri-O-methyleriodictyol is a flavonoid with an antimutagenic activity. 7,3′,4′-Tri-O-methyleriodictyol inhibits the furylfuramide-induced SOS response and has potency as bioantimutagens.
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| DC47085 | AZD-CO-Ph-PEG4-Ph-CO-AZD |
AZD-CO-Ph-PEG4-Ph-CO-AZD is a bis-β-lactam linker can be used for antibody-siRNA conjugate synthesis.
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| DC47083 | Exaluren |
Exaluren (ELX-02) is an synthetic eukaryotic ribosome-selective glycoside that induces read through of nonsense mutations, resulting in normally localized full-length functional proteins. Exaluren is used for the research of cystic fibrosis caused by nonsense mutations.
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| DC47082 | Zelquistinel |
Zelquistinel is a N-methyl-D-aspartate (NMDA) receptor partial agonist used for the research of depression, anxiety and other related psychiatric disorders.
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| DC47081 | Zavacorilant |
Zavacorilant is capable of modulating glucocorticoid receptor (GR).
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| DC47079 | Valiloxibic acid |
Valiloxibic acid is a prodrug of γ-Hydroxybutyric acid (GHB).GHB is a naturally occurring neurotransmitter and a psychoactive drug, it acts on the GHB receptor and is a weak agonist at the GABAB receptor.
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| DC47078 | Umifoxolaner |
Umifoxolaner is an anti-parasitic agent (veterinary).
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| DC47076 | Udonitrectag |
Udonitrectag (REC 0559), a low molecular weight compound that mimics NGF, aims to address the issue of NGF stability.
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| DC47075 | Syringetin |
Syringetin, a flavonoid derivative, is associated with increased BMP-2 production. Syringetin stimulates osteoblast differentiation at various stages, from maturation to terminally differentiated osteoblasts.
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