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(S)-Higenamine

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(S)-Higenamine
T7564122672-77-1
(S)-Higenamine ((S)-Norcoclaurine), the S-enantiomer instrumental in benzylisoquinoline alkaloid biosynthesis, results from the condensation of dopamine with 4-hydroxyphenylacetaldehyde (4-HPAA) catalyzed by norcoclaurine synthase (NCS) [1].
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(S)-Higenamine hydrobromide
T38132105990-27-0
(S)-Higenamine hydrobromide, an S-enantiomer of Higenamine, serves as the preliminary compound in benzylisoquinoline alkaloid biosynthesis. It is formed through the condensation of dopamine and 4-hydroxyphenylacetaldehyde (4-HPAA) via norcoclaurine synthase (NCS)[1].
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