We have 2,268 products in: Biochemicals >> Chemical Type
Chemical Type beginning with A |
Code | Name | Details | Image Abreview Publication |
|---|---|---|---|
| Potent ALK4, 5 and 7 kinase inhibitor Purity: > 98% | | ||
| Ca2+ ionophore Purity: > 99% | | ||
| A halogenated analogue of A23187. It is a nonfluorescent Ca2+ ionophore used in calibration for determining cytoplasmic Ca2+ by fluorescent probes. Purity: > 98% | | ||
| Highly selective D4 agonist Purity: > 98% | | ||
| Potent, competitive P2X7 receptor antagonist Purity: > 98% | | ||
| AMP-activated protein kinase activator Purity: > 99% | | ||
| Active metabolite of leflunomide. Dihydroorotate dehydrogenase inhibitor. Purity: > 98% | | ||
| Potent and selective antagonist for the heptapeptide angiotensin-(1-7). Prevents ANG-(1-7)-induced inhibition of angiogenesis. Purity: > 95% | | ||
| Selective NaV1.8 channel blocker Purity: > 98% | | ||
| Phospholipase-A2 inhibitor Purity: > 98% | | ||
| Potent, selective and cell-permeable VEGFR inhibitor Purity: > 98% | | ||
| Phytohormone; produced by a variety of cells in humans and animals Purity: > 99% | | ||
| Novel and potent pan Bcl-2 inhibitor Purity: > 95% | | ||
| Peroxidase substrate | | ||
| Reversible granzyme B and caspase-8 inhibitor Purity: > 95% | | ||
| Potent, selective amylin receptor antagonist Purity: > 98% | | ||
| Potent α-glucosidase inhibitor Purity: > 98% | | ||
| Potent, selective ACC2 (Acetyl-CoA Carboxylase) inhibitor Purity: > 98% | | ||
| Potent, selective CB1 agonist Purity: > 98% | | ||
| Potent, selective CB1 agonist Purity: > 98% | | ||
| Derivative of indomethacin, as potent as indomethacin as an inhibitor of COX 2, but less active on COX1. Purity: > 98% | | ||
| Selective COX-3 inhibitor Purity: > 98% | | ||
| NF-κB inhibitor Purity: > 98% | | ||
| Specific S-farnesylcysteine methyl transferase inhibitor Purity: > 98% | | ||
| Cell-permeable biologically inactive analog of AFC and AGGC Purity: > 98% | | ||
| Synthetic substrate of isoprenylated protein methyltransferase Purity: > 98% | | ||
| A cysteine conjugate of benzyl isothiocyanate. Purity: > 98% | | ||
| Important mediator in lipid metabolism Purity: > 98% | | ||
| Endogenous neurotransmitter active at acetylcholine receptors | | ||
| A cysteine conjugate of methyl isothiocyanate. Purity: > 98% | | ||
| A cysteine conjugate of phenylhexyl isothiocyanate. Purity: > 98% | | ||
| A cysteine conjugate of phenyl isothiocyanate. Purity: > 98% | | ||
| Intermediate for the semi-synthesis of various taxanes. Purity: > 98% | | ||
| Inhibits lipolysis in peripheral tissues and induces large reduction in circulating serum-free fatty acids. The mechanism of triglyceride lowering appears to be an increase of VLDL-Tg clearance. Purity: > 98% | | ||
| γ-glutamyl transpeptidase inhibitor Purity: > 98% | | ||
| Topoisomerase I and II inhibitor Purity: > 95% | | ||
| CB1 agonist Purity: > 98% | | ||
| Adrenocorticotropin, stimulates adrenal glands to release cortisol Purity: > 95% | | ||
| Adrenocorticotropin, stimulates androgen production Purity: > 95% | | ||
| Adrenocorticotropin, increases production and release of corticosteroids Purity: > 95% | | ||
| Potent ACTH/MC2 receptor agonist Purity: > 95% | | ||
| Potent melanocortin 2 (MC2) receptor agonist Purity: > 95% | | ||
| Truncated adrenocorticotropic hormone peptide Purity: > 95% | | ||
| Potent melanocortin receptor agonist and endogenous adrenocorticotropic hormone (ACTH) fragment Purity: > 95% | | ||
| Potent, endogenous melanocortin receptor 2 (MC2) agonist Purity: > 98% | | ||
| Purity: > 98% | | ||
| Leucine aminopeptidase inhibitor. Purity: > 98% | | ||
| Inhibits viral DNA polymerase. Antiherpetic agent Purity: > 99% | | ||
| Selective RARβ and RARγ agonist Purity: > 98% | | ||
| Endogenous P1 receptor agonist Purity: > 99% | | ||
| Second messenger. PKA activator. Purity: > 98% | | ||
| Methyl donor and cofactor for enzyme-catalyzed methylations Purity: > 95% | | ||
| Energy metabolism regulator. Insect neuropeptide. Purity: > 98% | | ||
| Energy metabolism regulator. Insect neuropeptide. Purity: > 95% | | ||
| Potent vasodilating peptide found in human pheochromocytoma from the adrenal medulla. | | ||
| Potent vasodilating peptide found in human pheochromocytoma from the adrenal medulla. | | ||
| Potent vasodilating peptide found in human pheochromocytoma from the adrenal medulla. | | ||
| Balanced μ- and κ-opioid receptor agonist while having no effects on δ-opioid receptors. | | ||
| Adriamycin Pig ELISA Kit | sELISA | | |
| Dopamine agonist Purity: > 99% | | ||
| Peroxidase substrate | | ||
| Interferes with key events in angiogenesis, and displays a strong anti-tumor effect on epidermal growth factor dependent tumor lines. It has also shown antileukemic activity. Purity: > 96% | | ||
| M2/M4 antagonist Purity: > 99% | | ||
| M2 antagonist Purity: > 99% | | ||
| A potent hepatoxin and hepatocarcinogen found in poorly stored grains and nuts. Chronic exposure is shown to produce mutagenesis, necrosis and liver carcinogenesis. Purity: > 98% | | ||
| A mycotyxin produced by aspergillus parasiticus. A toxic and carcinogenic mycotoxin that induces mutation of human chromosomes. Purity: > 98% | | ||
| A mycotyxin produced by aspergillus parasiticus. Binds to DNAse II, exhibits inhibition effects. Purity: > 98% | | ||
| A potent hepatoxic mycotoxin metabolite of Aflatoxin B1. Often found in milk of cattle fed on AfB1 contaminated feed. Exhibits cytotoxic activities. Purity: > 98% | | ||
| Tyrosine kinase inhibitor Purity: > 98% | | ||
| Non-selective tyrosine kinase inhibitor Purity: > 98% | | ||
| Selective PDGFR tyrosine kinase inhibitor Purity: > 99% | | ||
| Potent, selective EGF receptor tyrosine kinase Purity: > 99% | | ||
| Potent specific PDGF receptor tyrosine kinase inhibitor Purity: > 99% | | ||
| Selective EGF receptor tyrosine kinase inhibitor Purity: > 98% | | ||
| JAK2/3 inhibitor Purity: > 99% | |