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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DCC3380 | mitopy1 |
Novel selective fluorescent H2O2 probe, tracking the mitochondria of live biological specimens and responds to local fluxes of hydrogen peroxide (H2O2) by a turn-on fluorescence enhancement
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| DCC3379 | Mito-peg5-ato |
Novel potent antiproliferative mitochondria-targeted OXPHOS inhibitor (IC50=38 nM) in MiaPaCa-2 cells, being more effective than other inhibitors of OXPHOS in MiaPaCa-2 and U87MG cells
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| DCC3378 | Mitofp |
Novel mitochondrial-targeted pan-APT inhibitor
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| DCC3377 | Mitoebselen-2 |
Radiation Mitigator, reducing lipid hydroperoxides and preventing apoptotic cell death
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| DCC3376 | Mitodpp-2 |
Fluorescent probe for measuring the activity levels of erasers of S-palmitoylation, acyl-protein thioesterases (APTs), within mitochondria of live cells
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| DCC3375 | Mitobady |
Sensitive and specific Raman probe for live cell imaging of mitochondria
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| DCC3374 | mitf-in-17 |
The first small molecule inhibitor of Mitf-E-box DNA binding with depigmenting activity
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| DCC3373 | miroistonil |
Novel inhibitor of AMA1-RON2 interaction, blocking merozoite invasion from schizont-infected RBCs; Antidepressant; Acetylcholinesterase inhibitor
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| DCC3372 | Miro1 Reducer 3 |
Novel degrader of Miro1 (mitochondrial Rho GTPase 1), reducing Miro1 levels in fibroblasts and stress-induced degeneration of dopaminergic neurons derived from Parkinson's disease (PD) patients, as well as age-dependent neuronal loss and prolongs lifespan
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| DCC3371 | Miro1 Reducer |
Novel Miro1 degrader, rescuing dopaminergic neurodegeneration and promoting Miro1 degradation in Parkinson’s Disease fibroblasts
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| DCC3370 | Mir-21 Inhibitor-1 |
Novel inhibitor of microRNA-21 (miR-21)
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| DCC3369 | Mir-21 Inhibitor |
Novel specific and efficient inhibitor of miR-21 expression, inducing a 485% increase in the luciferase reporter signal at 10 μM
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| DCC3368 | Mipsagargin |
Novel thapsigargin-based PSMA-activated prodrug, inhibiting the sarcoplasmic/endoplasmic reticulum calcium adenosine triphosphatase (SERCA) pump protein
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| DCC3367 | Mips1780 |
Novel selective positive allosteric modulator (PAM) at the M1 muscarinic acetylcholine receptor
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| DCC3366 | Mips1455 |
Novel photoactivatable allosteric ligand for the M1 muscarinic acetylcholine receptor
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| DCC3365 | Mipe-1686 |
Novel long-lasting myostatin inhibitor, significantly increasing muscle mass and hindlimb grip strength in Duchenne muscular dystrophic model mice
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| DCC3364 | Mip-1095 |
Novel inhibitor of the prostate-specific membrane antigen (PSMA)
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| DCC3363 | Mip-1072 |
Novel inhibitor of the prostate-specific membrane antigen (PSMA)
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| DCC3362 | Minigastrin I (human) |
Inhibitor of cholecystokinin B receptors (CCK2)
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| DCC3361 | Mina53-in-10 |
First-in-class inhibitor of MYC-induced nuclear antigen (MINA53) with selectivity over NO66 and other JmjC oxygenases
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| DCC3360 | Miliusol |
Natural anti-tumor agent, demonstrating with tumor inhibitory efficacy comparable or even superior to the mainstay chemotherapeutics paclitaxel or fluorouracil
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| DCC3359 | Milacemide Hydrochloride |
MAO-B inhibitor and glycine prodrug, being studied for treatment for the symptoms of Alzheimer's disease
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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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