| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DC22515 | Trans-ACPD Featured | trans-ACPD is a selective agonist for metabotropic glutamate receptors, acting at both group I and group II mGlu receptors. |
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| DC24194 | Tripelennamine hydrochloride | A first-generation antihistamine that acts primarily as H1 receptor antagonist. |
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| DC20738 | Livoletide Featured | A first-in-class analogue of unacylated ghrelin, and unacylated ghrelin receptor agonist. |
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| DC12001 | AG311 | A first-in-class antitumor and antimetastatic agent that induces necrosis in breast cancer tumors, inhibits inhibit mitochondria complex I activity and reduces HIF-1α stabilization. |
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| DC11813 | CM-414 | A first-in-class, dual inhibitor of PDE5 and HDAC that inhibits HDAC1/2/3/6 (IC50=310/490/322/91 nM, respectively) and PDE5 (IC50=60 nM). |
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| DC11815 | trans CM-414 | A first-in-class, dual inhibitor of PDE5 and HDAC that inhibits HDAC1/2/3/6 (IC50=310/490/322/91 nM, respectively) and PDE5 (IC50=60 nM). |
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| DC11814 | cis CM-414 | A first-in-class, dual inhibitor of PDE5 and HDAC that inhibits HDAC1/2/3/6 (IC50=310/490/322/91 nM, respectively) and PDE5 (IC50=60 nM). |
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| DC11707 | MDVN-1003 | A first-in-class, selective, orally bioavailable, dual inhibitor of BTK and PI3Kδ kinases with IC50 of 32.3 nM and 16.9 nM, respectively. |
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| DC11531 | Teslexivir | A first-in-class, small molecule protein-protein inhibitor of the interaction between the E1 and E2 proteins of HPV types 6 and 11. |
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| DC22520 | Porcine dynorphin A(1-13) | A form of dynorphin and an endogenous opioid peptide with the amino acid sequence: Tyr-Gly-Gly-Phe-Leu-Arg-Arg-Ile-Arg-Pro-Lys-Leu-Lys.. |
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| DC22352 | Gatifloxacin hydrochloride | A fourth-generation fluoroquinolone antibiotic that inhibits the bacterial DNA gyrase and topoisomerase IV. |
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| DC22351 | Gatifloxacin mesylate | A fourth-generation fluoroquinolone antibiotic that inhibits the bacterial DNA gyrase and topoisomerase IV. |
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| DC22353 | Gatifloxacin | A fourth-generation fluoroquinolone antibiotic that inhibits the bacterial DNA gyrase and topoisomerase IV. |
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| DC24178 | Moxifloxacin Featured | A fourth-generation synthetic fluoroquinolone, broad-spectrum antibacterial agent that is active against both Gram-positive and Gram-negative bacteria. |
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| DC11489 | 6-alkynyl Fucose | A fucose analog that inhibits Dll-induced Notch signaling by reducing Notch ligand Dll1-Notch1 binding, but not Jag1. |
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| DC23737 | Azaphilone-9 | A fungal natural product that binds to HuR and inhibits HuR-RNA interaction in vitro with IC50 of 1.2 uM. |
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| DC24161 | Acamprosate calcium | A GABA receptor agonist and modulator of glutamatergic systems. |
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| DC21669 | SNAP 5114 | A GABA transport inhibitor with IC50 of 5, 21, 388 and 140 uM for hGAT-3, rGAT-2, hGAT-1 and BGT-1, respectively. |
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| DC20497 | PGRMC2-IN-25 | A gain-of-function ligand for PGRMC2 (progesterone receptor membrane component 2) to promote adipogenesis. |
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| DC21363 | Lucerastat | A galactose analogue that is an UDP-glucose ceramide glucosyltransferase (UGCG/GCS) inhibitor (IC50=41.4 uM). |
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| DC22490 | 3-Bromopyruvic acid Featured | A glycolytic inhibitor that inhibits hexokinase II activity, suppresses ATP production, and induces endoplasmic reticulum (ER) stress. |
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| DC21844 | Carbenoxolone | A glycyrrhetinic acid derivative that inhibits 11β-hydroxysteroid dehydrogenase (11β-HSD), a gap junction blocker and mineralocorticoid agonist.. |
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| DC21845 | Carbenoxolone disodium | A glycyrrhetinic acid derivative that inhibits 11β-hydroxysteroid dehydrogenase (11β-HSD), a gap junction blocker and mineralocorticoid agonist.. |
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| DC22527 | Cyclic somatostatin Featured | A growth hormone-release inhibiting factor used in the treatment of severe, acute hemorrhages of gastroduodenal ulcers. |
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| DC22347 | Penciclovir Featured | A guanosine analogue antiviral agent used for the treatment of various herpesvirus (HSV) infections. |
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| DC22358 | Valproic acid sodium salt | A HDAC inhibitor that selectively inhibits the catalytic activity of class I HDACs, and induces proteasomal degradation of HDAC2. |
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| DC22359 | Valproic acid | A HDAC inhibitor that selectively inhibits the catalytic activity of class I HDACs, and induces proteasomal degradation of HDAC2. |
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| DC23983 | Pyraclonil | A herbicide agent. . |
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| DC24171 | Furilazole | A herbicide safener for gramineous crops.. |
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| DC22635 | SPDP Featured | SPDP (SPDP Crosslinker) is a short-chain crosslinker for amine-to-sulfhydryl conjugation via NHS-ester and pyridyldithiol reactive groups that form cleavable (reducible) disulfide bonds with cysteine sulfhydryls. It is a glutathione cleavable ADC linker u |
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