|Description||A natural compound extracted from Phellodendron chinense, exhibits a near planar framework|
|Solubility||Soluble in ether, bensol, chloroform|
|Storage||Store at +4 °C, in dark place.|
|Melting Point||141°C (acetone)|
A methyl easter of Okadaic acid. Okadaic acid is a marine sponge toxin which potently inhibits certain serine/threonine protein phosphatases.
Seco-Duocarmycin DME is a cytotoxic agent, used as the cytotoxic component in antibody-drug conjugates.
A selective blocker of the delayed rectifier K+ channel found in virtual screening
Cynaroside is a flavone, a flavonoid-like chemical compound. It is a 7-O-glucoside of luteolin.
A cytostatic substance Isotryptamine.
Is any neutral chemical compound with a positively charged cationic functional group such as a quaternary ammonium or phosphonium cation which bears no hydrogen...
a nicotinic cholinoreceptor antagonist at the neuromuscular junction; curare-like ganglioblocker. Bis-quaternary quinuclidine derivative, , synthetic.
Synthetic, a neuronal nicotinic AChR antagonist.
Tubulysin M is a Tubulysin D analog with potential anti-cancer properties, used as the cytotoxic component in antibody-drug conjugates.
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 ...
Ryanodine High Purity
Potent inhibitor of Ca2+ release from sarcoplasmic reticulum
Noscapine is often used as an antitussive medication.
A non-toxic, complement-activating component of cobra venom Three polypeptide chains with molecular masses of about 70, 50, and 30 kDa, the two large subunits b...
A potent antiarrhytmic and local anesthetic. Alkaloid , from plants of the Ranunculaceae family. Inhibitorand Enhancers of Uridine Diphosphate-Glucuronosyltrans...
A muscarinic receptors antagonist.
Extracted from Korolkowia sewrtzowii. Potent antiarrhythmic (class I) belonging to a novel structural class.
DM 4 is an intermediate used to prepare semisynthetic maytansine analogs which can be conjugated with antibodies for the targeted treatment of cancer.
Bicyclic diterpenoid of the clerodane series
Synthetic, a weak AChR antagonist.
Cloflubicyne is a potent non-competitive GABA antagonist, convulsant, laboratory insecticide.