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About This Item
Empirical Formula (Hill Notation):
C30H16O8
CAS Number:
Molecular Weight:
504.44
NACRES:
NA.77
PubChem Substance ID:
EC Number:
208-941-0
Beilstein/REAXYS Number:
1917913
MDL number:
UNSPSC Code:
51101500
assay
~95% (HPLC)
solubility
1 M NaOH: 10 mg/mL, turbid, dark green
SMILES string
Cc1cc(O)c2C(=O)c3c(O)cc(O)c4c5c(O)cc(O)c6C(=O)c7c(O)cc(C)c8c1c2c(c34)c(c78)c56
InChI
1S/C30H16O8/c1-7-3-9(31)19-23-15(7)16-8(2)4-10(32)20-24(16)28-26-18(12(34)6-14(36)22(26)30(20)38)17-11(33)5-13(35)21(29(19)37)25(17)27(23)28/h3-6,31-36H,1-2H3
InChI key
BTXNYTINYBABQR-UHFFFAOYSA-N
General description
Application
Hypericin from Hypericum perforatum has been used:
- in the broth macrodilution test and antibacterial assay against bacterial strains
- as a medium supplement for human malignant melanoma cells for irradiation and localization studies
- as a ligand for pregnane X receptor (PXR) and as defatting medium supplement for primary human hepatocytes culture
Biochem/physiol Actions
Hypericin is a potent inhibitor of protein kinase C (PKC), telomerase, cytochrome P450 and reverse transcriptase. It is exploited for its photosensitizing functionality in photodynamic therapy (PDT) and photodynamic diagnosis (PDD) in cancer cells.
Anthraquinone-derivative within St. John′s wort. Antibacterial effective against Gram-positive and Gram-negative bacteria.
Packaging
Bottomless glass bottle. Contents are inside inserted fused cone.
Signal Word
Warning
Hazard Codes
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral
Storage Class
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
PPE (personal protective equipment)
dust mask type N95 (US), Eyeshields, Gloves
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