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DPQ

CAT: 0013-GTR19187771-01Size: 25 mgDry Ice: NoHazardous: No
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CAT#:0013-GTR19187771-01Size:25 mg
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Description
DPQ is a potent and selective PARP-1 inhibitor used in neuroprotection research. It effectively reduces PARP activation and neuronal injury induced by NMDA exposure, helping to restore cellular ATP levels. This small molecule is a valuable tool for studying PARP-mediated cell death pathways in both in vitro and in vivo models of stroke and neurodegenerative diseases.
CAS Number
129075-73-6
Field of Research
Epigenetics & Chromatin, Molecular Biology
Smiles
O=C1NCCc2c (OCCCCN3CCCCC3) cccc12
Molecular Formula
C18H26N2O2
Molecular Weight
302.41
Storage Conditions
-20°C
Notes
For research use only.

Chemical Information

3,4-dihydro-5-(4-(1-piperidinyl)butoxy)-1(2H)-isoquinolinone
CAS Number129075-73-6
PubChem CID9948349
IUPAC Name5-(4-piperidin-1-ylbutoxy)-3,4-dihydro-2H-isoquinolin-1-one
Molecular FormulaC18H26N2O2
Molecular Weight302.4
XLogP2.8
Topological Polar Surface Area41.6
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count3
Rotatable Bond Count6
Heavy Atom Count22
Formal Charge0
Complexity355
SMILES
C1CCN(CC1)CCCCOC2=CC=CC3=C2CCNC3=O
InChI
InChI=1S/C18H26N2O2/c21-18-16-7-6-8-17(15(16)9-10-19-18)22-14-5-4-13-20-11-2-1-3-12-20/h6-8H,1-5,9-14H2,(H,19,21)
InChIKey
RVOUDNBEIXGHJY-UHFFFAOYSA-N
Chemical Structure
2D Structure
2D structure of 3,4-dihydro-5-(4-(1-piperidinyl)butoxy)-1(2H)-isoquinolinone
CAS: 129075-73-6
CID: 9948349
Formula: C18H26N2O2
MW: 302.4
Interactive 3D Structure
Loading 3D structure...
Computed Properties
PropertyValue
Molecular Weight302.4
XLogP32.8
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count3
Rotatable Bond Count6
Exact Mass302.199428076
Monoisotopic Mass302.199428076
Topological Polar Surface Area41.6 Ų
Heavy Atom Count22
Formal Charge0
Complexity355
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently-Bonded Unit Count1
Compound Is CanonicalizedYes

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