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Other Targets

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Cat. No. Product Name Field of Application Chemical Structure
DC34154 Citiolone Citiolone is a mucolytic agent for the treatment of certain hepatic disorders.
DC34155 Sodium D-Pantothenate Sodium D-Pantothenate is a vitamin that performs an important role in the oxidation of fats and carbohydrates and certain amino acids. It is also a precursor in the biosynthesis of coenzyme A.
DC34156 3,3',5'-Triiodo-L-thyronine 3,3',5'-Triiodo-L-thyronine, also known as rT3, inhibits the increase of sodium current generated by other thyroid hormone analogs in neonatal rat myocytes. The ratio of triiodothryonine (T3) to rT3 has been investigated as in indicator of insulin resistance.
DC34157 Ioxitalamic Acid Ioxitalamic Acid, also known as Telebrix or Vasobrix, is a medical contrast medium. It enhances the contrast of structures or fluids within the body in medical imaging.
DC34158 Isosorbide Isosorbide is a precursor of Isosorbide mononitrate or dinitrate, which relax vascular smooth muscle by formation of the free radical nitric oxide (NO).
DC34159 Gefarnate Gefarnate is an antiulcer agent that stimulates in-vitro secretion of mucin-like glycoprotein in conjunctival tissue. It also ameliorates corneal epithelial damage in animal dry-eye models.
DC34160 Lithocolic acid Lithocolic acid is a bile acid formed from chenodeoxycholate by bacterial action. It acts as a detergent to solubilize fats for absorption and is itself absorbed.
DC34161 Pamoic acid Pamoic acid is an agonist of the orphan G protein-coupled receptor GPR35. It activates ERK and beta-arrestin2 and causes antinociceptive activity.
DC34162 Bronidox Bronidox is an antimicrobial agent. It works by inhibiting enzyme activity in bacteria.
DC34163 Diatrizoic Acid Dihydrate Diatrizoic Acid Dihydrate is used as a radiocontrast agent for imaging the gastrointestinal tract in patients allergic to barium.
DC34164 Hyodeoxycholic acid sodium salt Hyodeoxycholic acid sodium salt is a natural secondary bile acid. It improves high-density lipoprotein (HDL) function, reduces farnesoid X receptor antagonist bile acids and the gene expression levels of sterol regulatory element binding protein 1c, acetyl-CoA carboxylase, fatty acid synthase, and stearoyl-CoA desaturase-1, and induces strong cytotoxicity, apoptosis and IL-8 synthesis.
DC34165 Ritanserin Ritanserin is a selective and potent serotonin-2 antagonist. Ritanserin acts as a selective 5-HT2A (Ki = 0.45 nM) and 5-HT2C receptor (Ki = 0.71 nM) antagonist.
DC34166 Quinine sulfate dihydrate Quinine sulfate dihydrate is an antimalarial agent. It works by reducing oxygen intake and carbohydrate metabolism, disrupting DNA replication and transcription via DNA intercalation, and reducing excitability of muscle fibers via alteration of calcium distribution. It is also an inhibitor of P-glycoprotein.
DC34167 Eprosartan Eprosartan is a competitive and reversible angiotensin II receptor antagonist used for the treatment of high blood pressure. The drug acts on the renin-angiotensin system to decrease total peripheral resistance in two ways. First, it blocks the binding of angiotensin II to AT1 receptors in vascular smooth muscle, causing vascular dilatation. Second, it inhibits sympathetic norepinephrine production, further reducing blood pressure.
DC34168 17A-Hydroxyprogesterone 17A-Hydroxyprogesterone is a metabolite of progesterone. It serves as an intermediate in the biosynthesis of hydrocortisone and gonadal steroid hormones.
DC34169 Propentofylline Propentofylline is a phosphodiesterase inhibitor with neuroprotective effect. It was studied for the treatment of Alzheimer's disease and multi-infarct dementia, as well as its action as an adenosine reuptake inhibitor.
DC34170 5-Methyltryptamine hydrochloride 5-Methyltryptamine hydrochloride acts as a 5-HT receptor agonist.
DC34171 CP-380736 CP-380736 is an inhibitor of the epidermal growth factor receptor (EGFR). EGFR is a tyrosine kinase that activates MAPK, JNK, and Akt pathways, and is an important mediator of several types of cancer, including lung cancer and glioblastoma multiforme.
DC34172 DL-Adrenaline DL-Adrenaline is a non-selective adrenoceptor agonist. It induces lipolysis and systemic muscle contraction, and shows systemic vasoconstrictive, bronchodilatory, positive chronotropic and gastrointestinal relaxant effects in vivo.
DC34173 CCT036477 CCT036477 is a selective inhibitor of wingless-type MMTV integration site family (WNT)-dependent transcription. It reduces the transcriptional activity of the T-cell factor/lymphoid enhancer factor transcription factor family at the ?-catenin level.
DC34174 DS2 DS2 is a selective positive allosteric modulator of d-GABAA receptors.
DC34175 CAPE CAPE is an inhibitor of BAF. It works by activating latent HIV-1, inhibiting PDGF-induced proliferation of vascular smooth muscle cells through the activation of p38 mitogen-activated protein kinase (MAPK), hypoxia-inducible factor (HIF)-1alpha and subsequent induction of heme oxygenase-1 (HO-1).
DC34176 SW203668 Featured SW203668 is a potent, tumor-specific inhibitor of stearoyl CoA desaturase (SCD) with better bioavailability than SW208108.
DC34177 Glaucine Glaucine is an inhibitor of TNF-alpha and IL-6 production induced by Toll-like receptor (TLR) ligands.
DC34178 CBIO CBIO is a potent, cell-permeable, D-amino acid oxidase (DAO) reversible inhibitor. In rat models, CBIO prevents formalin-induced tonic pain but not acute nociception.
DC34179 Acyclovir sodium Acyclovir sodium is an antimetabolite. It inhibits HSV-specified DNA polymerases and prevents further viral DNA synthesis without affecting the normal cellular processes.
DC34180 Calcein Featured Calcein is a fluorescent dye that is useful for testing cell viability and for short-term labeling of cells.
DC34181 Y198561 Barnidipine Hydrochloride is a long-acting calcium channel blocker.
DC34182 (R)-Citalopram oxalate (R)-Citalopram oxalate is a less active enantiomer of Escitalopram Oxalate, a potent and selective inhibitor of serotonin reuptake.
DC34183 L-Dehydroascorbic acid L-Dehydroascorbic acid is the oxidized form of L-Ascorbic acid. It selectively induces cell death in KRAS and BRAF mutant cells in vitro.

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