1393102-59-4

HUHS2002 Chemical Structure
1393102-59-4

Chemical Structure

HUHS2002

  • CAS No.: 1393102-59-4
  • Formula:C17H24O3
  • Molecular Weight:276.37

IUPAC Name: (E)-4-(4-(hept-1-en-1-yl)phenoxy)butanoic acid

InChIKey: UISWKZAGZZSFDP-SOFGYWHQSA-N

SMILES: O=C(CCCOC1=CC=C(C=C1)/C=C/CCCCC)O

Biological Activity: HUHS2002 is a free fatty acid derivative with the ability to enhance α7 cholinergic receptor activity. HUHS2002 enhances whole-cell membrane currents of α7 ACh receptors expressed in Xenopus oocytes in a concentration-dependent manner. The effects of HUHS2002 were blocked in the presence of the Ca2 /calmodulin-dependent protein kinase II (CaMKII) inhibitor KN-93. HUHS2002 activated CaMKII in cultured rodent hippocampal neurons, and this activation was abolished by KN-93. HUHS2002 also partially inhibited the activity of protein phosphatase 1 (PP1) in a cell-free PP1 activity assay[1].

Cat. No. Product Name Purity Description Pricing
HY-116153
HUHS2002 HUHS2002 is a free fatty acid derivative with the ability to enhance α7 cholinergic receptor activity. HUHS2002 enhances whole-cell membrane currents of α7 ACh receptors expressed in Xenopus oocytes in a concentration-dependent manner. The effects of HUHS2002 were blocked in the presence of the Ca2 /calmodulin-dependent protein kinase II (CaMKII) inhibitor KN-93. HUHS2002 activated CaMKII in cultured rodent hippocampal neurons, and this activation was abolished by KN-93. HUHS2002 also partially inhibited the activity of protein phosphatase 1 (PP1) in a cell-free PP1 activity assay.
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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