84050-22-6

DPQ hydrochloride Chemical Structure
84050-22-6

Chemical Structure

DPQ hydrochloride

Synonym(s): 6,7-Dimethoxy-2-(1-piperazinyl)-4-quinazolinamine hydrochloride

  • CAS No.: 84050-22-6
  • Formula:C14H20ClN5O2
  • Molecular Weight:325.79

IUPAC Name: 6,7-dimethoxy-2-(piperazin-1-yl)quinazolin-4-amine hydrochloride

InChIKey: AUMKUQAWVQJGTR-UHFFFAOYSA-N

SMILES: NC1=C2C=C(OC)C(OC)=CC2=NC(N3CCNCC3)=N1.[H]Cl

Biological Activity: DPQ hydrochloride is a blood-brain barrier permeable and selective PARP-1 inhibitor that blocks PARP-1-mediated DNA damage repair and NAD+/ATP consumption, thereby inhibiting excessive inflammatory responses. DPQ hydrochloride inhibits NF-κB pathway activation, reduces the expression of pro-inflammatory factors (such as TNF-α, IL-6) and oxidative stress. DPQ hydrochloride can be used in inflammation-related studies of acute lung injury, myocardial infarction, and neurodegenerative diseases[1][2][3].

Cat. No. Product Name Purity Description Pricing
HY-W424851
DPQ hydrochloride 98.97% DPQ hydrochloride is a blood-brain barrier permeable and selective PARP-1 inhibitor that blocks PARP-1-mediated DNA damage repair and NAD+/ATP consumption, thereby inhibiting excessive inflammatory responses. DPQ hydrochloride inhibits NF-κB pathway activation, reduces the expression of pro-inflammatory factors (such as TNF-α, IL-6) and oxidative stress. DPQ hydrochloride can be used in inflammation-related studies of acute lung injury, myocardial infarction, and neurodegenerative diseases.
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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