|Product Name||Nitrarine 2HCl|
|Description||Nitrarine 2HCl is a hypotensive, spasmolytic, coronary dilator, sedative in experimental arrhythmias.|
Alkaloid , from plants of the Ungernia genus, Amaryllidaceae.
Na+,K+-ATPase inhibiting activity of cardiac glycosides from Erysimum cheiranthoides
DM4 is a cytotoxic agent. It is used as the cytotoxic component in antibody-drug conjugates.
Potent antagonist for α7-containing neuronal nicotinic receptors (Ki = 1.4 nM). Interacts with α4β2 and α6β2 receptors at concentrations > 40 nM. Attenuates MET...
Synthetic., a GABA-gated chloride channel blocker, non-competitive GABA antagonist in mammals.
Fraxinellone is an insecticidal agent, inhibiting growth of larvae, used in the treatment and protection of crops and produce. Also, a naturally occurring compo...
Nitrodienamine, an inhibitor of Ca2+/Mg2+ ATPase.
Ca2+-Activated K+ Channel Blocker
A reversible myorelaxant and ganglioblocker Diterpenoid alkaloid Semi-Synthetic, from Methyllicoctonine isolated from Delphinium rotundifolium Afan. (Ranunculac...
omega conotoxin MVIIA
ω conotoxin MVIIA (omega conotoxin MVIIA) has been isolated from the venom of the cone Conus magus. Omega-conotoxins act at presynaptic membranes, they bind and...
Paclitaxel is a microtubule polymer stabilizer with IC50 of 0.1 pM in human endothelial cells.
DM3 is a cytotoxic agent. It is used as the cytotoxic component in antibody-drug conjugates.
Synthetic, a selective irreversible inhibitor of carboxylesterases
Microcystin-LR is a selective inhibitor of protein phosphatase 2A (PP2A) (IC50= 0.04 nM) and will completely inhibit this enzyme without affecting PP1 when used...
A muscarinic receptors antagonist.
Seco-Duocarmycin CN is a cytotoxic agent, used as the cytotoxic component in antibody-drug conjugates.
Potent blocker of voltage-sensitive K+ channels (IC50 values are 0.1, 1.1 and 25 nM for KV1.3, KV1.1 and KV1.2 channels) respectively). Also inhibits Ca2+-activ...
Synthetic, GABAA-gated Cl- channels blocker; non-competitive GABAA antagonist.
Seco-Duocarmycin TM is a cytotoxic agent, used as the cytotoxic component in antibody-drug conjugates.
Methimazole inhibits the enzyme thyroperoxidase, which normally acts in thyroid hormone synthesis by oxidizing the anion iodide (I−) to iodine (I2), hypoiodous ...