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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DCC0286 | 5-mca-nat |
Melatonin analogue, selectively binding on MT3 subsites
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| DCC0285 | 5-hydroxydiclofenac |
Active metabolite of diclofenac, targeting COX and CaMKIIα hub domain
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| DCC0284 | 5'-hydroxydatiscetin |
Morin isomer, antioxidant
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| DCC0283 | 5-hydroxydantrolene |
Metabolite of dantrolene
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| DCC0282 | 5-ht7r Antagonist 2c |
Novel potent and selective G protein-biased 5-HT 7 R Antagonist, significantly reducing self-grooming duration time to the level of wild-type mice
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| DCC0280 | 5-ht2c Agonist 58 |
Novel selective 5-HT 2C agonist with >300-fold functional selectivity over 5-HT 2B and >70-fold functional selectivity over 5-HT 2A , reducing food intake in an acute rat feeding model
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| DCC0279 | 5-hiaa |
Serotonin metabolite, systemically inhibiting RAS/MAPK signaling in different organs of C. elegans
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| DCC0278 | 5-fu Prodrug 4 |
Novel palladium-activated 5-FU prodrug, being completely innocuous to cells and highly resistant to metabolization by primary hepatocytes and liver S9 fractions (the main metabolic route for 5-FU degradation), and rapidly converted into 5-FU in the presen
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| DCC0277 | 5-formylcytosine |
Rare base found in mammalian DNA, having functional roles in DNA that go beyond being a demethylation intermediate
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| DCC0276 | 5-cltep |
HIV-1 integrase inhibitor
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| DCC0275 | 5-citep |
Novel HIV-1 integrase inhibitor
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| DCC0274 | 5-chloro-ds2 |
Novel potent δ-selective allosteric modulator, Ki(α4β1δ) 0.14 µM
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| DCC0273 | 5-bromo-ds2 |
Novel potent δ-selective allosteric modulator, Ki(α4β1δ) 0.06 µM
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| DCC0272 | 5'-brluc |
Brominated luciferin, being more cell permeant than luciferin
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| DCC0271 | 5'-amino-5'-deoxyadenosine |
Adenosine kinase inhibitor
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| DCC0269 | 5-actmf |
Novel Inducer of G2/M arrest, Apoptosis and Autophagy in Cancer Cells
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| DCC0268 | 5172-mcp1p3 |
Novel inhibitor of HCV NS3-NS4A Serine Proteinase
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| DCC0267 | 5,6-eet |
Inhibitor of T-type voltage-gated calcium channels (Cav3), inhibiting isoforms Cav3.1, Cav3.2, and Cav3.3, decreasing nifedipine-resistant phenylephrine-induced vasoconstriction via Cav3.2 blockade
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| DCC0266 | 4-quinolineacetonitrile |
Bulding Block
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| DCC0265 | 4-quinolin-4-yl-2h-pyrazol-3-ylamine |
Useful pharmaceutical building block
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| DCC0264 | 4-pridin-4-yl-2h-pyrazol-3-ylamine |
Useful pharmaceutical building block
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| DCC0263 | 4'-o-methylresveratrol |
Inhibitor of Androgen_receptor>androgen receptor (AR) transcriptional activity, more effective than resveratrol in inhibiting AKT>Akt phosphorylation
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| DCC0262 | 4'-o-methylgrynullarin |
Novel anti-austerity agent, inducing PANC-1 human pancreatic cancer cell death under nutrition starvation via inhibition of Akt/mTOR pathway
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| DCC0261 | 4-ome-arm1 |
Novel ligand for LTA4H, dose responsively reducing LTB4 production in human neutrophils
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| DCC0260 | 4-me-pdtic |
Novel Potent and Selective Kappa Opioid Receptor Antagonist
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| DCC0259 | 4-fluoroamphetamine Hydrochloride |
Dopamine reuptake inhibitor
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| DCC0258 | 4'-dma-7,8-dhf |
Potent agonist of tropomyosin-receptor-kinase B (TrkB) receptor, possessing robust anti-apoptotic activity, promoting neurogenesis, and exhibiting potent antidepressant effect
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| DCC0257 | 4-cyclopentene-1,3-dione |
Potent Antifungal Inhibitor of Chitin Synthesis
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| DCC0256 | 4-cl-imt |
Novel selective ligand of the Transport Inhibitor Resistant 1 (TIR1)
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| DCC0255 | 4-chlorokynurenine |
Prodrug of 7-Cl-kynurenic acid (7-Cl-KYNA), a potent, selective antagonist of the NMDA/glycine receptor
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