Carothane complex ester , from plants of the Umbelliferae family.
Monomethyl Auristatin E (MMAE) is a synthetic analog of dolastatin 10 that similarly inhibits tubulin polymerization and exhibits potent cytotoxicity. It is com...
Mesaconitine has antinociceptive activity through cyclic AMP and stimulation of the central β-adrenergic system.
Ca2+-Activated K+ Channel Blocker
Seco-Duocarmycin DMG is a cytotoxic agent, used as the cytotoxic component in antibody-drug conjugates.
A methyl easter of Okadaic acid. Okadaic acid is a marine sponge toxin which potently inhibits certain serine/threonine protein phosphatases.
Fraxinellone is an insecticidal agent, inhibiting growth of larvae, used in the treatment and protection of crops and produce. Also, a naturally occurring compo...
A highly active peripheral M2-cholinoblocker alkaloid. Cervane alkaloid derivative of Imperialine from the plant Petilium eduardi.
Methimazole inhibits the enzyme thyroperoxidase, which normally acts in thyroid hormone synthesis by oxidizing the anion iodide (I−) to iodine (I2), hypoiodous ...
Synthetic, nicotinic AChR. Rigid bicyclic analog of TMA and TEA.
Non-selective K+ channel blocker.
Potent ganglioblocker, a neuronal nicotinic AChR antagonist. .
A muscarinic receptors antagonist.
Monomethyl auristatin D (MMAD), a potent tubulin inhibitor, is a toxin payload and antibody drug conjugate.
Seco-Duocarmycin DMA is a cytotoxic agent, used as the cytotoxic component in antibody-drug conjugates.
A terpenoid complex ester , from plants of the Umbelliferae family, a substance presenting an estrogenic activity.
A selective inhibitor of endoplasmic reticulum Ca2+-ATPase.
A natural compound extracted from Phellodendron chinense, exhibits a near planar framework
Microcystin-RR inhibits PP1C, PP1γ, and PP2A with Ki values of 0.15, 0.24, and 0.018 nM, respectively.
Synthetic, a potent inhibitor of high-affinity choline uptake (HAChU) in synaptosomes.