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Hyperforin (dicyclohexylammonium) salt_Molecular_structure_CAS_238074-03-8)
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Hyperforin (dicyclohexylammonium) salt

Catalog No. H1792 Name Sigma Aldrich
CAS Number 238074-03-8 Website http://www.sigmaaldrich.com
M. F. C47H75NO4 Telephone 1-800-521-8956
M. W. 718.1027 Fax
Purity ≥98% (HPLC) Email
Storage protect from light Chembase ID: 154772

SYNONYMS

IUPAC name
(1R,5S,6R,7S)-4-hydroxy-6-methyl-1,3,7-tris(3-methylbut-2-en-1-yl)-6-(4-methylpent-3-en-1-yl)-5-(2-methylpropanoyl)bicyclo[3.3.1]non-3-ene-2,9-dione; N-cyclohexylcyclohexanamine
IUPAC Traditional name
dicha; hyperforine
Synonyms
Hyperforin-DCHA
Hyp-DCHA

DATABASE IDS

CAS Number 238074-03-8
MDL Number MFCD04000098

PROPERTIES

Risk Statements 22-34-50/53
Safety Statements 26-36/37/39-45-60-61
Storage Condition protect from light
Storage Temperature -20°C
German water hazard class 3
GHS Pictograms GHS05
GHS Pictograms GHS07
GHS Pictograms GHS09
GHS Signal Word Danger
GHS Hazard statements H302-H314-H400
European Hazard Symbols Corrosive Corrosive (C)
European Hazard Symbols Nature polluting Nature polluting (N)
MSDS Link Download
GHS Precautionary statements P273-P280-P305 + P351 + P338-P310
Empirical Formula (Hill Notation) C35H52O4·C12H23N
Purity ≥98% (HPLC)
Apperance white to off-white powder
Solubility DMSO: ≥10 mg/mL

DETAILS

Description (English)
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.1
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.
Description (简体中文)
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.1
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.

REFERENCES