Fig. 1 · Structure
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(S)-Higenamine hydrobromide
S-enantiomer of Higenamine
(S)-Higenamine hydrobromide is the S-enantiomer of Higenamine, primarily involved in benzylisoquinoline alkaloid biosynthesis. This compound is synthesized through the enzymatic condensation of dopamine and 4-hydroxyphenylacetaldehyde (4-HPAA) by norcoclaurine synthase (NCS). (S)-Higenamine hydrobromide exhibits bioactive properties relevant for research in the fields of neurobiology and plant biochemistry. Its ability to influence specific biochemical pathways makes it a valuable tool for investigating alkaloid metabolism and its potential implications in pharmacological studies.
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Specifications
| Manufacturer | Adooq Bioscience |
|---|---|
| CAS Number | 105990-27-0 |
| Applications | S-enantiomer of Higenamine |
| Formula | C16H18BrNO3 |
| Molecular Weight | 352.22 |
| Synonyms | (S)-Norcoclaurine hydrobromide |
| SMILES | OC1=CC2=C([C@H](CC3=CC=C(O)C=C3)NCC2)C=C1O.[H]Br |
Storage & Solubility
In Vitro Solubility
Reported Solubility
No reported solubility data are available for this product.
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| Concentration | |
|---|---|
Values use four significant digits. Prepare to the final solution volume; this is not the volume of solvent to add.
Stock preparation is unavailable for this product molecular weight.
Calculated stock concentrations do not establish solvent solubility. Refer to the reported solubility data for experimental guidance.
Storage
Store powder at -20°C, keep desiccated.
In powder form, the chemical is stable for 36 months.
In solution, store at -20°C and use within 1 month to prevent loss of potency. Aliquot to avoid multiple freeze/thaw cycles.