We have 2,268 products in: Biochemicals >> Chemical Type
Chemical Type beginning with J - M |
Code | Name | Details | Image Abreview Publication |
|---|---|---|---|
| Actin polymerization and stabilization inducer Purity: > 95% | | ||
| Mitochondrial membrane-potential dye Purity: > 98% | | ||
| Smoothened inhibitor Purity: > 98% | | ||
| Potent Hedgehog signaling inhibitor Purity: > 99% | | ||
| Selective H4 antagonist Purity: > 99% | | ||
| Potent, selective and reversible fatty acid amide hydrolase inhibitor Purity: > 99% | | ||
| Potent and selective α2C antagonist Purity: > 99% | | ||
| Potent, selective and cell-permeable BET bromodomain inhibitor. Purity: > 98% | | ||
| Potent, selective and irreversible inhibitor of monoacylglycerol lipase (MAGL) Purity: > 98% | | ||
| Highly potent inhibitor of protein and CAM kinases Purity: > 99% | | ||
| Potent, cell-permeable protein kinase C inhibitor and casein kinase II type ectokinase Purity: > 98% | | ||
| Potent, cell-permeable protein kinase C inhibitor Purity: > 98% | | ||
| Potent, highly selective CRF2 antagonist Purity: > 98% | | ||
| Dipeptidyl peptidase 4 (DPP4) inhibitor. Purity: > 98% | | ||
| Phytoestrogen. Proapoptotic agent. Purity: > 98% | | ||
| Prototypic kainate receptor agonist. Purity: > 99% | | ||
| Aminoglycoside antibiotic Purity: > 98% | | ||
| Promotes differentiation of human mesenchymal stems cells into chondrocytes Purity: > 98% | | ||
| A major component of kava kava extract, has antinociceptive activity. Purity: > 98% | | ||
| NCX inhibitor. TRPC blocker. Purity: > 99% | | ||
| Orally active atypical voltage-gated sodium channel blocker Purity: > 97% | | ||
| Synthetic peptide substrate for PKA Purity: > 95% | | ||
| Potent endothelin receptor antagonist. It is an antiosteoporotic with antibacterial and cytotoxic activity. Purity: > 98% | | ||
| CDK2, GSK3β and LCK inhibitor Purity: > 98% | | ||
| Selective 5-HT2 antagonist. Purity: > 98% | | ||
| Potent cytochrome P450 inhibitor. Anti-fungal agent. Purity: > 99% | | ||
| Oxoeicosanoid (OXE) receptor agonist. Chemoattractant for neutrophils and eosinophils. Purity: > 95% | | ||
| Highly potent COX1/2 inhibitor. Non-steroidal anti-inflammatory drug (NSAID). Purity: > 98% | | ||
| Active metabolite of prostacyclin (PGI2) Purity: > 99% | | ||
| Selective, H1 antagonist Purity: > 99% | | ||
| Highly selective c-Fms tyrosine kinase inhibitor Purity: > 95% | | ||
| AXOR12 agonist Purity: > 95% | | ||
| CaM kinase II inhibitor. P2X7 antagonist. Purity: > 98% | | ||
| Potent, specific CaMK II inhibitor Purity: > 99% | | ||
| Cell-permeable, selective inhibitor of cAMP-dependent protein kinase Purity: > 98% | | ||
| Potent, selective inhibitor of PKG Purity: > 95% | | ||
| Potent, selective, competitive ATM kinase inhibitor Purity: > 99% | | ||
| Endogenous ionotropic / nicotinic antagonist Purity: > 99% | | ||
| Endogenous ionotropic / nicotinic antagonist; water soluble Purity: > 99% | | ||
| An analgesic neuropeptide that inhibits peptide uptake. Purity: > 95% | | ||
| Dopamine ( Purity: > 99% | | ||
| Potent and selective EP4 receptor antagonist Purity: > 98% | | ||
| Voltage dependent L-type calcium channel blocker Purity: > 99% | | ||
| Potent thromboxane A2 receptor antagonist Purity: > 98% | | ||
| Potent and selective γ-secretase inhibitor Purity: > 98% | | ||
| Highly potent 5-HT1D/5-HT1B receptor agonist Purity: > 99% | | ||
| Potent and selective D2 antagonist Purity: > 99% | | ||
| Highly potent, selective brain penetrant D4 antagonist Purity: > 99% | | ||
| Phosphopeptide GSK-3 inhibitor Purity: > 99% | | ||
| Cell-permeable, potent and selective proteasome inhibitor Purity: > 95% | | ||
| Synthetic sugar with various pharmacological effects. Inhibits TNF expression. Purity: > 98% | | ||
| An anti-convulsant drug used to treat seizures, neuropathic pain and epilepsy. Purity: > 98% | | ||
| Somatostatin receptor analog Purity: > 98% | | ||
| Topoisomerase I inhibitor Purity: > 98% | | ||
| Potent ErbB-2 and EGFR dual tyrosine kinase inhibitor. Antitumor. Purity: > 99% | | ||
| Potent, selective tyrosine kinase inhibitor Purity: > 98% | | ||
| Tyrosine kinase inhibitor Purity: > 98% | | ||
| Potent EGF receptor tyrosine kinase inhibitor Purity: > 98% | | ||
| Potent, selective ALK2 and ALK3 inhibitor Purity: > 97% | | ||
| Reversible, competitive UCH-L1 inhibitor Purity: > 98% | | ||
| Pyruvate dehydrogenase kinase (PDK) inhibitor Purity: > 98% | | ||
| Immunomodulatory agent Purity: > 98% | | ||
| Thalidomide analog, TNF-α inhibitor Purity: > 98% | | ||
| Antibiotic, antifungal. Inhibitor of CRM-1 mediated nuclear export. Purity: > 98% | | ||
| Potent JAK2, FLT3 and TrkA receptor tyrosine kinase inhibitor Purity: > 98% | | ||
| Highly potent, reversible, selective aromatase inhibitor Purity: > 99% | | ||
| Calpain inhibitor Purity: > 98% | | ||
| Integrin CD11b/CD19 agonist Purity: > 97% | | ||
| Potent leukotriene A4 hydrolase suicide inhibitor Purity: > 95% | | ||
| Inhibitor of Leukotriene A4 hydrolase Purity: > 99% | | ||
| Potent chemoattractant. Leukotriene B4, BLT1 and BLT2 receptor agonist. Purity: > 99% | | ||
| Arachidonic acid metabolite. Cell-permeable immunomodulator. Purity: > 99% | | ||
| Potent leukotriene C4 receptor agonist Purity: > 98% | | ||
| Potent proinflammatory mediator Purity: > 98% | | ||
| Partial, selective CysLT1 and CysLT2 agonist Purity: > 98% | |