The chemical reactions and pathways resulting in the formation of chanoclavine-I aldehyde. Chanoclavine-I aldehyde is at a branching point in the biosynthetic pathways of fumigaclavine C and ergotamine.
cinnamic acid biosynthetic process
cinnamic acid ester biosynthetic process +
cortisol biosynthetic process +
eugenol biosynthetic process
ferulate biosynthetic process
formaldehyde biosynthetic process
fumigaclavine C biosynthetic process +
funalenone biosynthetic process
geraniol biosynthetic process
glyceraldehyde-3-phosphate biosynthetic process
glyoxal biosynthetic process
helvolic acid biosynthetic process +
hexadecanal biosynthetic process +
isopentenol biosynthetic process
kojic acid biosynthetic process +
methylglyoxal biosynthetic process
negative regulation of ergot alkaloid biosynthetic process +
neoxanthin biosynthetic process
olefin biosynthetic process +
paxilline biosynthetic process
positive regulation of ergot alkaloid biosynthetic process +
prenol biosynthetic process
progesterone biosynthetic process +
pyridoxal biosynthetic process
pyridoxal phosphate biosynthetic process +
regulation of ergot alkaloid biosynthetic process +