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Cat. No. Product Name Field of Application Chemical Structure
DCC4740 Sir-tz
Novel in situ tetrazine ligation reactive silicon-rhodamine dye
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DCC4739 Sirt3 Inhibitor P6
Novel selective SIRT3 inhibitor, exhibiting SIRT3 inhibitory selectivity with IC50 value of 7.2 µM over SIRT1 (32.6 µM) and SIRT2 (33.5 µM), showing potent inhibitory activity against a group of MLLr leukemic cell lines
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DCC4738 Sirt2-in-6f
Potent and selective inhibitor of SIRT2
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DCC4737 Sirt1-in-4bb
Novel SIRT1 inhibitor, inducing apoptosis in HCT116 human colon carcinoma cells partially by activating p53
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DCC4736 Sirt1-i5
Novel SIRT1 Inhibitor, showing potent effect on prostate cancer cell line
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DCC4735 Sirt1-enhancer-a03
First-in-class apolipoprotein E4 (ApoE4)-targeted sirtuin1 (SirT1) enhancer, normalizing sirtuin 1 levels and improving cognition in an Alzheimer's disease mouse model
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DCC4734 Sirt1-a2
Novel SIRT1 Activator
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DCC4733 Sipi-7623
Novel farnesoid X receptor antagonist
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DCC4732 Sipi-6360
Novel D2/5-HT2A Receptor Dual Antagonist
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DCC4731 Sinapine Sulfate
Antioxidant and antimicrobial agent, counteracting mitochondrial oxidative stress in cardiomyocytes
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DCC4730 Simfibrate
Peroxisome proliferator
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DCC4729 Sila-ibuprofen
Novel COX-I and COX-II inhibitor with four times higher solubility in physiological media and a lower melting enthalpy than ibuprofen
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DCC4728 Silagaba161
Silicon-Containing GABA Derivative, Treating Neuropathic Pain without Central-Nervous-System-Related Side Effects
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DCC4727 Silagaba132
Silicon-Containing GABA Derivative, Treating Neuropathic Pain without Central-Nervous-System-Related Side Effects
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DCC4726 Sid-7977382
Novel Complement Factor C1 Inhibitor
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DCC4725 Sid-24784551
Novel direct HIV-1 Nef antagonist with antiretroviral activity
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DCC4724 Sibopirdine
Novel cognitive enhancer; Nootropic agent
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DCC4723 Shr0687
Highly Potent and Peripheral Nervous System-Restricted KOR Agonist
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DCC4722 Shp2 Inhibitor C21
Inhibitor of shp2 protein tyrosine phosphatase (PTP)
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DCC4721 Showdomycin
Antineoplastic antibiotic
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DCC4720 Ship-2a
Cystathione gamma lyase (CSE) inhibitor, inhibiting H2S production and L-cysteine-induced relaxation of rat aortic rings ex vivo
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DCC4719 Shield-2
Novel potent stabilizing ligand for FKBP-derived destabilizing domains
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DCC4718 Sh-i-14
Novel Inhibitor of Phospho-STAT3 Through Induction of Protein Tyrosine Phosphatase PTPN6
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DCC4717 Sheta2
Selective inhibitor of cancer cell growth, exerting chemoprevention activity without evidence of toxicity
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DCC4716 Sherpa Bmi-135
Novel Selective Human ER Partial Agonist (ShERPA)
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DCC4715 She-196
First in Class Hypoglycemic Agent with Extra-Strong Action, increasing insulin sensitivity, improving glucose tolerance, reducing fasted insulin level and insulin sensitivity, decreasing total body and interscapular fat mass and also increasing the activi
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DCC4714 Sha 14-1
Stable and ROS-free antagonist against anti-apoptotic Bcl-2 proteins, bypassing drug resistances and synergizing cancer therapies in human leukemia cell
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DCC4713 Sh-2251
Novel selective inhibitor of the generation of IL-5-producing Th2 cells and induction of active histone modifications at the IL5 gene locus during Th2 cell differentiation
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DCC4712 Sh-11052
Novel inhibitor of endothelial cell growth
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DCC4711 Sh-11037
Novel potent sEH inhibitor, effectively blocking key angiogenic properties of human retinal endothelial cells (HRECs), inhibiting choroidal sprouting and significantly suppressing CNV lesion volume
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