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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DCC3358 | Miglustat |
Product Description:
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| DCC3357 | Mig-7 Inhibitor D-39 |
Novel inhibitor of Migration-Inducting Gene 7 (MIG-7) expression, suppressing EOC cell growth and VEGFA expression
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| DCC3356 | Mifamurtide |
Immunomodulator, regulating the activation of monocytes and macrophages, upregulating the secretion of pro-inflammatory cytokines such as TNF-alpha, IL-1, IL-8, nitric oxide and prostaglandins E2 and D2
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| DCC3355 | Mif Degrader Md13 |
Novel Potent MIF Degrader
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| DCC3354 | Microtubule Inhibitor 185322 |
Novel inhibitor of microtubule assembly, inducung mitotic arrest and apoptosis of MM cells
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| DCC3353 | mi-888 Tfa Salt |
Highly Potent and Efficacious MDM2 Inhibitor
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| DCC3352 | Mi-432 |
Novel matriptase-1/matriptase-2 (MT-1/2) inhibitor, also inhibiting TMPRSS2, proteolytic activation and multiplication of influenza A virus in Calu-3 cells
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| DCC3351 | Mi-319 |
Novel MDM2 antagonist, restoring p53 functions and increases the life span of orally treated follicular lymphoma bearing animals
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| DCC3350 | Mi-1900 |
Novel inhibitor of TMPRSS2, also strongly preventing SARS-CoV-2 multiplication and CPE in Calu-3 cells in a dose-dependent manner. causing strong inhibition of SARS-CoV-2 replication
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| DCC3349 | Mi-1061 |
Novel Chemically Stable, Potent, and Efficacious MDM2 Inhibitor
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| DCC3348 | Mhy884 |
Novel tyrosinase inhibitor, suppressing UVB-induced activation of NF-κB signaling pathway through the downregulation of oxidative stress
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| DCC3347 | mhy-794 |
Novel tyrosinase inhibitor, directly inhibiting mushroom tyrosinase
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| DCC3346 | mhy498 |
Novel inhibitor of nitric oxide-induced melanogenesis, targeting the NO-induced cGMP signaling pathway
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| DCC3345 | Mhy-449 |
Novel inducer of G2/M phase arrest in the cell cycle progression, resulting in growth inhibition and induction of apoptosis in a concentration-dependent manner, and inhibition of proliferation in a time-dependent manner
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| DCC3344 | mhy407 |
Novel sensitizer of cancer cells, significantly increasing DNA damage as determined by DNA breakage, levels of damage-responsive proteins, and DNA foci
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| DCC3343 | mhy384 |
Novel tyrosinase inhibitor, down-regulating of MITF and tyrosinase through direct tyrosinase inhibition
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| DCC3342 | mhy336 |
Novel topoisomerase II inhibitor, markedly inducing apoptotic cell death via the mitochondria-mediated intrinsic pathway in LNCaP cells
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| DCC3341 | Mhy219 |
Novel potent histone deacetylase (HDAC) inhibitor, inducing apoptosis via up-regulation of androgen receptor expression in human prostate cancer cells
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| DCC3340 | mhy218 |
Novel potent HDAC inhibitor, possessing potent anticancer activities
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| DCC3339 | mhy1556 |
Novel tyrosinase inhibitor, showing concentration-dependent inhibitory effects with no significant cytotoxicity in cell viability assay
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| DCC3338 | Mhi-i2 |
Novel photodynamic antitumor agent
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| DCC3337 | Mhi-148 |
Near-infrared cyanine dye, acting as an optical imaging agent
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| DCC3336 | Mgs-0039 |
Potent and orally active group II mGluR antagonist with antidepressant-like potential
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| DCC3335 | Mgs-0028 |
Selective metabotropic glutamate 2/3 receptor agonist
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| DCC3334 | Mgcd516 |
Novel, multi-targeted kinase inhibitor, demonstrating potent inhibition of Trk, RET and DDR, in addition to Met, Axl and VEGFRs
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| DCC3331 | Mg2-1812 |
Novel potent negative allosteric modulator (NAM) of mGlu2
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| DCC3330 | Mfn103 |
Novel Dual Fluorescent and Magnetic Resonance False Neurotransmitter
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| DCC3329 | Metrizoate Calcium |
Radiographic Contrast Agent
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| DCC3328 | Metocurine |
Non-depolarizing muscle relaxant
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| DCC3327 | Metoclopramide Hydrochloride |
Dopamine D2 antagonist, antiemetic
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