30479-81-3

JPC0661 Chemical Structure
30479-81-3

Chemical Structure

JPC0661

Synonym(s): JFD 00458

  • CAS No.: 30479-81-3
  • Formula:C15H13N3O5S
  • Molecular Weight:347.35

IUPAC Name: 4-(1-methyl-1H-imidazol-2-yl)azepan-4-ol

InChIKey: ZZSAILZSWKPTCT-UHFFFAOYSA-N

SMILES: O=C1N(C2=CC(S(=O)(O)=O)=C(OC3=CC=CC=C3)C=C2)N=C(N)C1

Biological Activity: JPC0661 is a direct and allosteric ΔFOSB inhibitor. JPC0661 inhibits the binding of ΔFOSB/JUND and ΔFOsB to DNA with IC50 values in the micromolar range (9-52 uM), directly inhibits ΔFOSB-mediated transcription with IC50 of 0.82 μM in vitro. JPC0661 significantly reduces ΔFOSB occupancy at genomic AP1 sites in vivo. JPC0661 binds to a novel groove outside the DNA-binding cleft of ΔFOSB and disrupt the formation of the ΔFOSB/JUND-DNA complex. JPC0661 can be used for Alzheimer's disease research[1].

Cat. No. 상품명 Purity 제품 설명 Pricing
HY-W471288
JPC0661 JPC0661 is a direct and allosteric ΔFOSB inhibitor. JPC0661 inhibits the binding of ΔFOSB/JUND and ΔFOsB to DNA with IC50 values in the micromolar range (9-52 uM), directly inhibits ΔFOSB-mediated transcription with IC50 of 0.82 μM in vitro. JPC0661 significantly reduces ΔFOSB occupancy at genomic AP1 sites in vivo. JPC0661 binds to a novel groove outside the DNA-binding cleft of ΔFOSB and disrupt the formation of the ΔFOSB/JUND-DNA complex. JPC0661 can be used for Alzheimer's disease research.
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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