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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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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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| 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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