|Description||a CNS stimulant. Alkaloid, , purified from plants of Coffea genus, Rubiaceae.|
Harmine is a fluorescent harmala alkaloid belonging to the beta-carboline family of compounds. It occurs in a number of different plants, most notably the Middl...
An antimitotic agent that disrupts microtubles by binding to tubulin and preventing its polymerization. Stimulates the intrinsic GTPase activity of tubulin.
Monomethyl auristatin D Hcl (MMAD Hcl), a potent tubulin inhibitor, is a toxin payload in antibody drug conjugate.
M2 muscarinic receptor antagonist; myorelaxant. Steroid alkaloid derivative of Imperialine from the plant Petilium eduardi, and P. raddeanae.
Potent ganglioblocker, a neuronal nicotinic AChR antagonist. .
Duocarmycin B1 is a cytotoxic agent, used as the cytotoxic component in antibody-drug conjugates.
Synthetic, a selective irreversible inhibitor of carboxylesterases
Triterpene glycoside Extracted from Dipsacus azureas
Quinoline Alkaloid Extracted from Haplophyllum bucharicum
Tubulysin B is a cytotoxic agent, used as the cytotoxic component in antibody-drug conjugates.
Alkaloid extracted from Haplophyllum perforatum, a sedative and analgesic compound Tetrahydroquinoline
A muscarinic receptors antagonist.
Sanguinarine is a toxic quaternary ammonium salt from the group of benzophenanthridine alkaloids. It is extracted from some plants, including bloodroot (Sanguin...
Quinoline alkaloid, extracted from Haplophyllum bucharicum (Rutacae)
Idarubicin is an anthracycline antibiotic and a DNA topoisomerase II (topo II) inhibitor for MCF-7 cells with IC50 of 3.3 ng/mL.
Is any neutral chemical compound with a positively charged cationic functional group such as a quaternary ammonium or phosphonium cation which bears no hydrogen...
Synthetic, nicotinic AChR. Rigid bicyclic analog of TMA and TEA.
Kaliotoxin (1-37)NH2 is a selective voltage-dependent K+ channels blocker, a blocker of Ca2+-activated K+ channels of high conductance and some voltage-dependen...
A Na+ channel blocker; potent antiarrhythmic, inhibits voltage-gated Na+ channels in rat brain synaptosomes.
Nitrodienamine, an inhibitor of Ca2+/Mg2+ ATPase.