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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DC9798 | Leteprinim Featured |
Leteprinim (Neotrofin, AIT-082) is a hypoxanthine derivative drug with neuroprotective and nootropic effects.
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| DC8314 | Leuprolide Acetate Featured |
Leuprolide acetate (Leuprorelin) is a GnRH analog; leuprolide acetate acts as an agonist at pituitary GnRH receptors.
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| DC10147 | LH-21 Featured |
LH 21 is a 1,2,4-triazole that acts as a cannabimimetic.
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| DC23065 | Ligustilide Featured |
Ligustilide possesses neuroprotective, vasorelaxation, antinociceptive and anti-inflammatory activities, it blocked the activation of MAPKs/IKK and the downstream transcription factors AP-1 and NF-κB.
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| DC23026 | Linderane Featured |
Linderane is a mechanism-based inactivator of CYP2C9.
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| DC10820 | Roquinimex(Linomide) Featured |
Linomide is an Immunomodulator; anti-angiogenic.
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| DC11011 | Lipofermata Featured |
Lipofermata (CB16.2 aka) is a specific fatty acid transport (FATP) inhibitor, blocks human FATP2-mediated fatty acid uptake (IC50=4.84 uM in Caco-2 cells) without impacting other cellular functions.
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| DC33476 | Antihelmycin |
Hygromycin B is a protein translocation inhibitor that suppresses protein and RNA synthesis of bacteria. and viruses by inducing misreadings during translation.
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| DC11640 | PK-11195 Featured |
PK 11195 is a ligand of translocator protein. It targets Leishmania chemotherapy (IC50s of 14.2 μM, 8.2 μM, 3.5 μM for L. amazonensis, L. major and L. braziliensis, respectively).
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| DC12068 | Fosmidomycin sodium salt Featured |
Fosmidomycin sodium salt is a phosphonic acid antibiotic and a antimalarial drug, which is active against both Gram-negative and Gram-positive bacteria.
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| DC12086 | AC-55649 Featured |
AC-55649 is a potent, highly isoform-selective agonist of human RARβ2 receptor, with a pEC50 of 6.9.
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| DC12216 | Dodecanoylcarnitine Featured |
Dodecanoylcarnitine is present in fatty acid oxidation disorders such as long-chain acyl CoA dehydrogenase deficiency, carnitine palmitoyltransferase I/II deficiency, and is also associated with celiac disease.
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| DC12233 | Eicosadienoic acid Featured |
Eicosadienoic acid is a rare, naturally occurring n-6 polyunsaturated fatty acid found mainly in animal tissues.
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| DC12247 | Fluspirilene (R 6218; Redeptin) Featured |
Fluspirilene is a non-competitive antagonist of L-type calcium channels with an IC50 of 0.03 μM. Fluspirileneis a long-acting injectable depot antipsychotic drug used for schizophrenia.
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| DC12602 | LMT-28 Featured |
LMT-28 (LMT28) is a specific blocker of IL-6 signaling via inhibits IL-6Rβ (gp130) with IC50 of 5.9 uM (IL-6–induced luciferase activity), selectively inhibits IL-6–induced phosphorylation of STAT3, JAK2, and gp130.
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| DC20009 | KH7 Featured |
KH7 is a soluble adenylyl cyclase (sAC)-specific inhibitor, with IC50s of 3-10 μM toward both recombinant purified human sACt protein and heterologously expressed sACt in cellular assays.
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| DC20021 | Calmidazolium chloride (R 24571) Featured |
Calmidazolium chloride (R 24571) is a calmodulin (CaMK) antagonist, antagonizing CaM-dependent phosphodiesterase and calmodulin-induced activation of erythrocyte Ca2+-transporting ATPase with IC50s of 0.15 and 0.35 μM, respectively. Also in anti-cancer re
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| DC20139 | SPD304 Featured |
SPD304 is a selective inhibitor of tumor necrosis factor α (TNFα) and promotes dissociation of TNF trimers and therefore blocks the interaction of TNF and its receptor, with an IC50 of 22 µM for inhibiting in vitro TNF receptor 1 (TNFR1) binding to TNF-α.
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| DC20027 | PF 750 Featured |
PF 750 is a selective and covalent fatty acid amide hydrolase (FAAH) inhibitor, with IC50s varied from 16.2-595 nM in different pre-incubation times. Covalently modifies the enzyme’s active site serine nucleophile.
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| DC22415 | SB-612111 Featured |
SB-612111 is a potent, selective nociceptin/orphanin FQ receptor (NOP receptor) antagonist with Ki of 0.33 nM.
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| DC22443 | Paxilline Featured |
A potent blocker of high-conductance Ca2+-activated K+ (BKCa, KCa1.1) channels that binds to the α-subunit of BKCa with Ki of 1.9 nM.
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| DC22737 | CP-346086 Featured |
A potent, orally active microsomal triglyceride transfer protein (MTP) inhibitor that inhibits both human and rodent MTP with IC50 of 2 nM.
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| DC10892 | LMI070 (NVS-SM1) Featured |
LMI070 (NVS-SM1) is a highly potent, selective and orally active small molecule SMN2 splicing modulator.
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| DC25003 | LOC14 Featured |
LOC-14 is a small molecule reversible Protein disulfide isomerase (PDI) inhibitor with Kd of 62 nM.
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| DC10694 | Loflucarban Featured |
Loflucarban is an antiinfective drug
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| DC10867 | LP-211 Featured |
LP-211 is a selective and blood−brain barrier penetrant 5-HT7 receptor agonist, with a Ki of 0.58 nM, with high selectivity over 5-HT1A receptor (Ki, 188 nM) and D2 receptor (Ki, 142 nM).
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| DC48082 | CCK Octapeptide (Sincalide) |
CCK Octapeptide (Sincalide, Cholecystokinin Octapeptide, CCK-OP, CCK-8, SQ 19,844) is a endogenous peptide hormone found in the intestine and brain that stimulates digestion.
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| DC48079 | DL-α-tocopherol acetate |
DL-α-Tocopherol acetate (DL-Alpha-tocopherol acetate , Vitamin E acetate), a vitamin E derivative, is used as a vitamin E supplement in poultry feeds.
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| DC48078 | Heptamidine Dimethanesulfonate |
Heptamidine (SBi4211) Dimethanesulfonate is a novel and potent Pentamidine-related inhibitor of the calcium-binding protein S100B with a Kd of 6.9 μM.
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| DC48076 | MSDC-0602K Potassium |
MSDC-0602K is a insulin sensitizer that modulates the mitochondrial pyruvate carrier (MPC).
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