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Cat. No. Product Name Field of Application Chemical Structure
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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DCC4710 Sh-053-s-ch3-2'f
Potent and selective agonist of GABAA receptors α5 subunit
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DCC4709 Sh-053-r-ch3-2’f
Selective agonist of GABA A receptors α5 subunit
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DCC4708 Sgx393
Novel inhibitor of the CML mutant Bcr-AblT315I, preempting in vitro resistance when combined with nilotinib or dasatinib.
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DCC4707 Sglt1/2-in-8
Novel Potent SGLT1/2 Dual Inhibitor
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DCC4706 Sgk1 Inhibitor 17a
Novel highly selective SGK1 inhibitor with a highly optimized profile suitable for oral dosing as a potentially disease-modifying agent for osteoarthritis
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DCC4705 Sgi-9380
PKM2 activator, potently inhibiting proliferation of cancer cells in media lacking serine
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DCC4704 Sgi-10067
PKM2 activator, potently inhibiting proliferation of cancer cells in media lacking serine
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DCC4703 Sge201
Novel potent allosteric modulator of N-methyl-D-aspartate receptors (NMDAR)
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DCC4702 Sgc-gak-1n
Negative control for SGC-GAK-1 (GLXC-31266)
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DCC4701 Sgc-clk-1
Novel probe for CLK1, CLK2, and CLK4
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DCC4700 Sgc-camkk2-1
Novel probe for CAMKK2/CAMKK1
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DCC4699 Sfti-1
Highly Potent and Selective Plasmin Inhibitor, Attenuating Fibrinolysis in Plasma
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