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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC4581 | Sap2-in-23h |
Novel Potent Non-peptidic Inhibitor of Secreted Aspartic Protease 2 (SAP2) for the Treatment of Resistant Fungal Infections
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| DCC4580 | Sant-2 |
Novel potent inhibitor of Shh signaling pathway
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| DCC4579 | Sansanmycin |
Uridyl peptide antibiotic, exhibiting antibacterial activity against Mycobacterium tuberculosis H(37)Ra and Pseudomonas aeruginosa with MIC values of 10 and 12.5 mug/ml, respectively
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| DCC4578 | Sampatrilat |
Vasopeptidase or dual inhibitor of ACE and neutral endopeptidase with potential application in the treatment of hypertension and congestive heart failure
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| DCC4577 | Sampangine |
Natural antimicrobial and antitumor agent, inducing reactive oxygen species (ROS), and alterating heme biosynthesis
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| DCC4576 | Samidorphan L-malate |
Opioid receptor antagonist for the treatment of alcoholism and cocaine addiction
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| DCC4575 | Saliphe |
Novel potent V-ATPase inhibitor, blocking viral entry
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| DCC4574 | Salinomycin Sodium |
Antibiotic, Inhibiting CD44 expression in breast cancer cells and mammary tumor growth
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| DCC4573 | Salbutamol |
ß2-adrenoceptor agonist
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| DCC4572 | Salazinic Acid |
Natural α-glucosidase inhibitor, potently modulating Nrf 2 , NF-κB and STAT3 pathways
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| DCC4571 | Salacinol |
Natural α-glucosidase inhibitor
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| DCC4570 | Saha-obp |
Novel Endogenous Reactive oxygen species (ROS)-activated HDAC inhibitor prodrug, demonstrating selective activity against multiple cancer cell lines such as HeLa, MCF-7, MDA-MB-231 and B16-F10, while remaining benign to non-cancer cells
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| DCC4569 | Saha-bpyne |
Novel clickable HDAC inhibitor, selectively labeling HDAC complex proteins
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| DCC4568 | Sag1.5 |
Novel Smoothened receptor agonist
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| DCC4567 | Safrazine Hydrochloride |
Irreversible and nonselective Monoamine_oxidase_inhibitor>monoamine oxidase inhibitor (MAOI)
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| DCC4566 | Sab378 |
Peripherally restricted cannabinoid CB1/CB2 receptor agonist, inhibiting gastrointestinal motility with no effect on experimental colitis in mice
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| DCC4565 | S-8921 |
Novel ileal Na /bile acid cotransporter inhibitor
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| DCC4564 | S-8510 Phosphate |
Partial benzodiazepine inverse agonist, showing antidepressant-like pharmacological activity and acting as a cognitive enhancer
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| DCC4563 | S8155-7 |
Novel Analogue of SUN-B8155, acting as a cell active and functionally-relevant agonist of calcitonin receptor (CTR), inducing different Gs or arrestin activities through CTR
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| DCC4562 | S-73362 |
Dual PPARα/γ agonist
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| DCC4561 | S-50612 |
Novel glucokinase (GK) activator
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| DCC4560 | S-49164 |
Novel glucokinase (GK) activator
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| DCC4559 | S-4048 |
Potent inhibitor of glucose-6-phosphate translocase (G6P T1)
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| DCC4558 | S3qel-1 |
Novel modulator of the retrograde signaling including cellular responses to hypoxic and oxidative stress, selectively eliminating superoxide production by complex III without altering oxidative phosphorylation
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| DCC4557 | s3i-201.1066 |
Potent and selective inhibitor of constitutive Stat3 DNA-binding and transcriptional activities
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| DCC4556 | S-34324 |
alpha2-Adrenoceptor Antagonist, Norepinephrine Transporter (NET) Inhibitor, Serotonine Transporter (SERT) Inhibitor
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| DCC4555 | S32797 |
Potent quinone reductase 2 (QR2) inhibitor
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| DCC4554 | S27847 |
Potent activator of the AMP-activated protein kinase (AMPK)
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| DCC4553 | S23757 |
Potent and selective ligand of imidazoline 1 receptor (I1R)
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| DCC4552 | S23515 Hydrochloride |
Potent and selective ligand of imidazoline 1 receptor (I1R)
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