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(S)-Higenamine hydrobromide

(S)-Higenamine hydrobromide
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(S)-Higenamine hydrobromide

Catalog No. T38132Cas No. 105990-27-0
(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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Product Introduction

Bioactivity
Description
(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].
In vitro
The biosynthetic pathway for benzylisoquinoline alkaloids begins with the enzyme-catalyzed condensation of dopamine and 4-hydrophenylacetaldehyde, producing (S)-norcoclaurine. These substrates are secondary metabolites stemming from the decarboxylation, hydroxylation, and deamination of tyrosine[1].
Chemical Properties
Molecular Weight352.228
FormulaC16H18BrNO3
Cas No.105990-27-0
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year

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