Hyperforin (dicyclohexylammonium) salt
SIGMA/H1792
Synonym: Hyp-DCHA; Hyperforin-DCHA
CAS Number: 238074-03-8
Empirical Formula (Hill Notation): C35H52O4·C12H23N
Molecular Weight: 718.10
MDL Number: MFCD04000098
Linear Formula: C35H52O4·C12H23N
Product Type: Chemical
| assay | ≥98% (HPLC) |
| color | white to off-white |
| form | powder |
| InChI | 1S/C35H52O4.C12H23N/c1-22 |
| InChI key | ZUYCAROZOLUHJY-DNSWOBEMSA |
| Quality Level | 100 ![]() |
| SMILES string | C1CCC(CC1)NC2CCCCC2.CC(C) |
| solubility | DMSO: ≥10 mg/mL |
| storage condition | protect from light |
| storage temp. | −20°C |
| Biochem/physiol Actions: | Hyperforin is believed to be the primary active constituent responsible for the antidepressant and anxiolytic properties of the extracts of St. John′s wort. |
| Biochem/physiol Actions: | Hyperforin is believed to be the primary active constituent responsible for the antidepressant and anxiolytic properties of the extracts of St. John′s wort. It acts as a reuptake inhibitor of monoamines, including serotonin, norepinephrine, dopamine, and of GABA and glutamate by activating the transient receptor potential ion channel TRPC6. It also is an activator of the pregnane X receptor (PXR), which serves as a key regulator of CYP3A4 transcription, a member of the cytochrome (CYP) P450 enzyme system. Recent studies have found it to have neuroprotective effects against Alzheimer′s disease (AD) neuropathology, including the ability to disassemble amyloid-β aggregates in vitro and improve spatial memory in vivo. |
| Biochem/physiol Actions: | Stable salt of hyperforin. |
| Biochem/physiol Actions: | Stable salt of hyperforin. Hyperforin is believed to be the primary active constituent responsible for the antidepressant and anxiolytic properties of the extracts of St. John′s wort. It acts as a reuptake inhibitor of monoamines, including serotonin, norepinephrine, dopamine, and of GABA and glutamate by activating the transient receptor potential ion channel TRPC6. Activation of TRPC6 induces the entry of sodium and calcium into the cell which causes inhibition of monoamine reuptake. It also is an activator of the pregnane X receptor (PXR), which serves as a key regulator of CYP3A4 transcription, a member of the cytochrome (CYP) P450 enzyme system. Recent studies have found other neurological effects, effects on inflammation, as well as antibacterial, antitumoral and antiangiogenic effects. |
| Packaging: | 1 mg in glass bottle |
| Symbol | ![]() ![]() GHS05,GHS07,GHS09 |
| Signal word | Danger |
| Hazard statements | H302 - H314 - H400 |
| Precautionary statements | P273 - P280 - P305 + P351 + P338 - P310 |
| Hazard Codes | C,N |
| Risk Statements | 22-34-50/53 |
| Safety Statements | 26-36/37/39-45-60-61 |
| RIDADR | UN 1759 8 / PGIII |
| WGK Germany | WGK 3 |
| Flash Point(F) | Not applicable |
| Flash Point(C) | Not applicable |
| Purity | ≥98% (HPLC) |
| Storage Temp. | −20°C |
| UNSPSC | 12352200 |




