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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC0562 | Alrestatin Sodium |
Specific inhibitor of aldose reductase
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| DCC0561 | Alpha-tocopherol Phosphate |
Prodrug of Vitamin E, modulating atherosclerotic and inflammatory events more efficiently than the unphosphorylated alpha-tocopherol
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| DCC0560 | Alpha-ra-f |
Novel modulator of collagen synthesis and matrix metalloproteinases (MMPs) expression levels, boosting collagen synthesis and reducing MMPs expression levels in human fibroblasts without cytotoxicity
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| DCC0559 | Alpha-methylserotonin Creatinine Sulfate |
Neurotransmitter; stimulating nicotinic receptors
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| DCC0558 | Alpha-lipoic Acid |
One of the most effective antioxidants, being involved in the cellular antioxidant system
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| DCC0557 | Alpha-ketoamide-13b |
Novel potent inhibitor of the SARS-CoV-2 Mpro, revealing a pronounced lung tropism and suitability for administration by the inhalative route
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| DCC0556 | Alpha-ethylmescaline |
Psychedelic, an analog of mescaline
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| DCC0555 | Alpha-cf3-tmc |
Novel inhibitor of JAK2 and STAT5 phosphorylation in response to interleukin-3 without altering STAT5 mobility in SDS-PAGE
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| DCC0554 | Alpha-br-tmc |
Novel JAK2/STAT5 inhibitor
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| DCC0553 | Alpha-amplexichromanol |
Highly potent, orally effective, and metabolically stable allosteric 5-LOX Inhibitor
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| DCC0552 | Alpha7-pam-3ea |
Novel potent type I positive allosteric modulator (PAM) of human α7 nAChR
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| DCC0551 | Allylpyrocatechol |
Antioxidant, attenuating collagen-induced arthritis via attenuation of oxidative stress secondary to modulation of the MAPK, JAK/STAT, and Nrf2/HO-1 pathways
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| DCC0550 | Alloxan Hydrate [3237-50-1] |
Natural chemical suppressor of mlo-mediated resistance in monocotyledonous barley (Hordeum vulgare) and dicotyledonous Arabidopsis thaliana
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| DCC0549 | Alloswitch-1 |
Novel allosteric modulator to control endogenous G protein-coupled receptors with light
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| DCC0548 | Allo-ile-isoindoline Hcl |
Irreversible and selective dipeptidyl peptidase 8 and 9 (DPP-8/9) inhibitor
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| DCC0547 | Allo-i1e-isoindoline |
Irreversible and selective dipeptidyl peptidase 8 and 9 (DPP-8/9) inhibitor
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| DCC0544 | Alk-gw9662 |
Clickable PPARγ inhibitor
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| DCC0542 | Alk/ros1-in-7d |
Potent and selective L1196M ALK and ROS1 dual inhibitor
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| DCC0541 | Aldoxorubicin |
Prodrug of the anthracycline antibiotic doxorubicin, binding selectively to the cysteine-34 position of albumin via its maleimide moiety, inhibiting DNA synthesis, and inducing apoptosis
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| DCC0540 | Aldi-6 Hydrochloride |
Novel ALDH inhibitor, inhibiting ALDH3A1 activity in SCC4 HNSCC xenografts
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| DCC0539 | Aldi-2 |
Potent and specific covalent inhibitor of aldehyde dehydrogenases
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| DCC0538 | Alda-89 |
Novel activator of ALDH3A1
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| DCC0537 | Alcuronium Chloride |
Neuromuscular blocking (NMB) agent
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| DCC0536 | Albucidin |
Novel nucleoside phytotoxin
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| DCC0535 | Albiziabioside A |
Natural antitumor agent, inducing caspase-dependent apoptosis and ferroptosis as a p53 activator through the mitochondrial pathway
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| DCC0534 | Albicidin |
Potent DNA gyrase inhibitor
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| DCC0533 | Alazocine |
Potent analgesic, psychotomimetic or hallucinogen, and morphine or opioid antagonist
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| DCC0532 | Ala-vpa Conjugate-1 |
α-Linolenic acid-Valproic acid conjugate, not only modulating microglia polarization, but also counteracting neurodegeneration and demyelination and induce oligodendrocyte precursor cell differentiation, by acting on multiple biochemical and epigenetic pa
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| DCC0531 | Alalevonadifloxacin Mesylate |
Novel anti-MRSA antibacterial agent, targeting infections caused by Gram-positive bacteria
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| DCC0530 | Al-661 |
Novel HCV NS5B Polymerase Inhibitor for the Treatment of Chronic Hepatitis C
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