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(S)-Norcoclaurine

" in MedChemExpress (MCE) Product Catalog:

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Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-N2037C
    (S)-Higenamine hydrobromide
    1 Publications Verification

    (S)-Norcoclaurine hydrobromide

    		 Endogenous Metabolite Others
    (S)-Higenamine ((S)-Norcoclaurine) hydrobromide, a S-enantiomer of Higenamine, is the entry compound in benzylisoquinoline alkaloid biosynthesis. (S)-Higenamine hydrobromide is produced by the condensation of dopamine and 4-hydroxyphenylacetaldehyde (4-HPAA) by norcoclaurine synthase (NCS) .
    (S)-Higenamine hydrobromide
  • HY-N2037B
    (S)-Higenamine

    (S)-Norcoclaurine

    		 Endogenous Metabolite Others
    (S)-Higenamine ((S)-Norcoclaurine), a S-enantiomer of Higenamine, is the entry compound in benzylisoquinoline alkaloid biosynthesis. (S)-Higenamine is produced by the condensation of dopamine and 4-hydroxyphenylacetaldehyde (4-HPAA) by norcoclaurine synthase (NCS) .
    (S)-Higenamine
  • HY-E71129
    (S)-Norcoclaurine synthase

    		Biochemical Assay Reagents Others
    The reaction makes a six-membered ring by forming a bond between C-6 of the 3,4-dihydroxyphenyl group of the dopamine and C-1 of the aldehyde in the imine formed between the substrates. (S)-Norcoclaurine synthase (EC 3.5.99.14) , formerly known as (S)-norlaudanosoline synthase, will also catalyse the reaction of 4-(2-aminoethyl) benzene-1,2-diol + (3,4-dihydroxyphenyl) acetaldehyde to form (S)-norlaudanosoline.
    (S)-Norcoclaurine synthase

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