Product Information
- (1aR,1bS,4aR,7aS,7bS,8R,9R,9aS)-9a-(acetyloxy)-4a,7b-dihydroxy-3-(hydroxymethyl)-1,1,6,8-tetramethyl-5-oxo-1a,1b,4,4a,5,7a,7b,8,9,9a-decahydro-1H-cyclopropa[3,4]benzo[1,2-e]azulen-9-yl 2-(methylamino)benzoate
- 12-O-(N-Methylanthranilate) phorbol-13-acetate
- 1H-Cyclopropa[3,4]benz[1,2-e]azulene, benzoic acid deriv.
- Benzoic acid, 2-(methylamino)-, (1aR,1bS,4aR,7aS,7bS,8R,9R,9aS)-9a-(acetyloxy)-1a,1b,4,4a,5,7a,7b,8,9,9a-decahydro-4a,7b-dihydroxy-3-(hydroxymethyl)-1,1,6,8-tetramethyl-5-oxo-1H-cyclopropa(3,4)benz(1,2-e)azulen-9-yl ester
- Benzoic acid, 2-(methylamino)-, 9a-(acetyloxy)-1a,1b,4,4a,5,7a,7b,8,9,9a-decahydro-4a,7b-dihydroxy-3-(hydroxymethyl)-1,1,6,8-tetramethyl-5-oxo-1H-cyclopropa(3,4)benz(1,2-e)azulen-9-yl ester, (1aR-(1a-alpha,1b-beta,4a-beta,7a-alpha,7b-alpha,8-alpha,9-beta,9a-alpha))-
- Benzoic acid, 2-(methylamino)-, 9a-(acetyloxy)-1a,1b,4,4a,5,7a,7b,8,9,9a-decahydro-4a,7b-dihydroxy-3-(hydroxymethyl)-1,1,6,8-tetramethyl-5-oxo-1H-cyclopropa[3,4]benz[1,2-e]azulen-9-yl ester, [1aR-(1aα,1bβ,4aβ,7aα,7bα,8α,9β,9aα)]-
- Ccris 7233
Sapintoxin D is a cytotoxic agent that has been shown to inhibit the growth of prostate cancer cells. It is a basic protein with a molecular weight of approximately 10kDa, and it binds to the regulatory domain of epidermal growth factor (EGF) and epidermal growth factor (EGF-R). This binding results in an inhibition of EGF-induced cell proliferation. The mechanism by which sapintoxin D exerts its cytotoxic effect on prostate cancer cells is synergistic interaction with phorbol ester. Sapintoxin D acts as an agonist for the receptor tyrosine kinase, leading to phosphorylation of its downstream signaling molecules, such as cd-1 mice, which activates ferroptosis. Ferroptosis is a form of regulated necrosis that occurs by the accumulation of reactive oxygen species (ROS) and iron ions in the cells. This process leads to oxidative stress and necrotic cell death.
Chemical properties
Technical inquiry about: 3D-FDA99807 Sapintoxin D
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