1809058-37-4

Hypercohin K Chemical Structure
1809058-37-4

Chemical Structure

Hypercohin K

  • CAS No.: 1809058-37-4
  • Formula:C33H40O4
  • Molecular Weight:500.68

IUPAC Name: (1aR,6S,7aR)-4-benzoyl-6-((E)-3,7-dimethylocta-2,6-dien-1-yl)-2,2-dimethyl-6-(3-methylbut-2-en-1-yl)-1a,2-dihydro-1H,5H-cyclopropa[c]benzofuran-5,7(6H)-dione

InChIKey: UKPXQYJEQKDSRD-OGZJLKFCSA-N

SMILES: O=C1[C@@]23[C@@](C2)(C(C)(C)OC3=C(C(=O)C4=CC=CC=C4)C(=O)[C@]1(C/C=C(/CCC=C(C)C)\C)CC=C(C)C)[H]

Biological Activity: Hypercohin K is a polycyclic polyprenylated acylphloroglucinol isolated from Hypericum henryi, containing a rare spiro-fused cyclopropane ring in its structure. Hypercohin K exhibits anti-inflammatory, antitumor, and AChE-enhancing activities. Hypercohin K reduces intracellular lipid accumulation by regulating lipid metabolism genes, and can inhibit NO production to exert anti-inflammatory effects. Hypercohin K can be used in research on non-alcoholic steatohepatitis and tumors[1][2][3][4].

Cat. No. Product Name Purity Description Pricing
HY-N21706
Hypercohin K Hypercohin K is a polycyclic polyprenylated acylphloroglucinol isolated from Hypericum henryi, containing a rare spiro-fused cyclopropane ring in its structure. Hypercohin K exhibits anti-inflammatory, antitumor, and AChE-enhancing activities. Hypercohin K reduces intracellular lipid accumulation by regulating lipid metabolism genes, and can inhibit NO production to exert anti-inflammatory effects. Hypercohin K can be used in research on non-alcoholic steatohepatitis and tumors.
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This product is a controlled substance and not for sale in your territory.

This product is not for sale in your territory.

This compound is listed in the SVHC (Substances of Very High Concern) candidate list of ECHA (European Chemicals Agency).

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References