|Molecular Formula||C11H12N2.HCl .2H2O|
|Description||A substance which inhibits cholinesterases reversibly. Alkaloid , from plants of the Zygophyllaceae family|
|Solubility||dissolves in water, in alcohol; slightly in chloroform; not in acetone.|
|Storage||stable in dry state; store at +4 °C, in dark place.|
|Melting Point||255-256 °C.|
Seco-Duocarmycin MA is a cytotoxic agent, used as the cytotoxic component in antibody-drug conjugates.
Used as an antihypertensive and antianginal. A dihydorpyridine calcium channel blocker.
Rebaudioside A is a glycoside from the stevia plant. Rebaudioside A is used as a sweetener with sweetness about 300 times that of sugar with negligible effect o...
β-Bungarotoxin is a form of bungarotoxin that is fairly common in Krait (Bungaros multicinctus) venoms. A pre-synaptic toxin with enzymatic activity.
Diterpenoid alkaloids from the roots of Delphinium scabriflorum.
Alkaloid , from plants of the Ungernia genus, Amaryllidaceae.
Polyprenols are natural long-chain isoprenoid alcohols of the general formula H-(C5H8)n-OH where n is the number of isoprene units. Any prenol with more than 4 ...
Ricinine is an alkaloid extract from the seeds of the castor-oil plant (Ricinus communalis). Ricinine is a central nervous system stimulant that could potential...
Camptothecin (CPT) is a potent DNA enzyme topoisomerase I (topo I) inhibitor with an IC50 and IC70 of 50 nM and 0.225 μM for breast cancer cell line MDA-MB-231.
Duocarmycin SA is a cytotoxic agent, used as the cytotoxic component in antibody-drug conjugates.
Laticauda semifasciata III
Polypetide, an antagonist of the nicotinic acetylcholine receptor at the neuromuscular junction with a weaker affinity to the receptor than Erabutoxins a and b.
Synthetic, a neuronal nicotinic AChR antagonist.
A selective blocker of the delayed rectifier K+ channel found in virtual screening
Ryanodine High Purity
Potent inhibitor of Ca2+ release from sarcoplasmic reticulum
A nicotinic antagonist.
DM3 is a cytotoxic agent. It is used as the cytotoxic component in antibody-drug conjugates.
Extract from plants of the Leguminosae family, an antiatherosclerotic and angioprotective, reduces platelet aggregation.
Maitansine, a cytotoxic agent, inhibits the assembly of microtubules by binding to tubulin at the rhizoxin binding site.
Dihydropyridine calcium channel blocker. Antianginal; antihypertensive.
Synthetic, nicotinic AChR. Rigid bicyclic analog of TMA and TEA.