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J & K SCIENTIFIC LTD.
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18210857532 |
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Product Name:3,4-Dihydro-5-[4-(1-piperidinyl)butoxy]-1(2H)-isoquinolinone CAS:129075-73-6 Package:2.5Mg,25Mg,5Mg
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DPQ manufacturers
- DPQ
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- $1230.00 / 50mg
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2025-04-30
- CAS:129075-73-6
- Min. Order:
- Purity:
- Supply Ability: 10g
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Product Name: | DPQ | Synonyms: | PARP Inhibitor III, DPQ;DPQ;3,4-DIHYDRO-5-[4-(1-PIPERIDINYL)BUTOXY]-1(2H)-ISOQUINOLINONE;3,4-DIHYDRO-5[4-(1-PIPERIDINYL)BUTOXYL]-1(2H)-ISOQUINOLINE;3,4-DIHYDRO-5-[4-(1-PIPERIDINYL)BUTOXYL]-1(2H)-ISOQUINOLINONE;3,4-DIHYDRO-5[4-(1-PIPERINDINYL)BUTOXY]-1(2H)-ISOQUINOLINE;5-[4-(1-PIPERIDINYL)-BUTYLOXY]-1,2,3,4-TETRAHYDROISOQUINOLIN-1-ONE;DMEM(Low Glucose) | CAS: | 129075-73-6 | MF: | C18H26N2O2 | MW: | 302.41 | EINECS: | | Product Categories: | | Mol File: | 129075-73-6.mol |  |
Melting point | 107-109° | Boiling point | 528.8±50.0 °C(Predicted) | density | 1.096±0.06 g/cm3(Predicted) | storage temp. | 2-8°C | solubility | DMSO: Soluble | form | solid | pka | 14.54±0.20(Predicted) | color | White to off-white | biological source | synthetic (organic) |
Hazard Codes | Xi | Risk Statements | 36/37/38 | Safety Statements | 26-36 | WGK Germany | 3 |
Description | The poly(ADP-ribose) polymerases (PARPs) form a family of enzymes with roles in DNA repair and apoptosis, particularly in response to reactive oxygen and nitrogen species. DPQ is a potent inhibitor of PARPs, inhibiting PARP1 with an IC50 value of 40 nM. It is approximately 10-fold less potent against PARP2. DPQ can be used in either cells or in animals. | Uses | DPQ has been used as a PARP1 (poly(ADP-ribose) polymerase 1) inhibitor in in vivo studies to determine the loss of γ-H2AX (H2A histone family member X) upon irradiation. | Uses | Reagent for inhibition of PARP. | Uses | 3,4-Dihydro-5-[4-(1-piperidinyl)butoxy]-1(2H)-isoquinolinone is a potent inhibitor of poly(ADP-ribose) polymerases, a family of enzymes that plays a crucial role in DNA repair and apoptosis in respons
e to reactive oxygen and nitrogen species. | Biochem/physiol Actions | 3,4-Dihydro-5-[4-(1-piperidinyl)butoxyl]-1(2H)-isoquinolinone (DPQ) is known to decrease the PARP 1 (poly(ADP-ribose) polymerase 1) mediated apoptosis under the influence of ischemia. It is considered as more effective inhibitor than the traditionally used PARP1 inhibitor 3-aminobenzamide. | in vivo | DPQ (10 mg/kg; intraperitoneal injection; single dose; 6 h) significantly attenuates lung inflammation, neutrophil infiltration, and vascular leakage in LPS-induced acute lung injury model of C57BL/6 mice, inhibiting NF-κB pathway activation[2].
DPQ (10 mg/kg; intraperitoneal injection; single dose; 4 weeks) improves cardiac function and reduced apoptosis and oxidative stress in myocardial infarction model of Wistar rats[3].
Animal Model: | LPS-Induced Acute Lung Injury Model in C57BL/6 mice (male, 8-10 weeks old) | Dosage: | 10 μg/kg (dissolved in 0.01% DMSO (PBS) | Administration: | Intraperitoneal injection, 30 min after LPS chanllenge (7.5 mg/kg; ip; single dose)
| Result: | Reduced neutrophil infiltration (50% decrease), MPO activity (40% decrease), and pro-inflammatory cytokines (TNF-α, IL-1β, IL-6) in lungs.
Restored vascular permeability (Evans blue extravasation reduced by 35%), and inhibited apoptotic cell death (TUNEL-positive cells decreased by 45%).
Suppressed NF-κB activation with reduced IkB-α degradation and p65 phosphorylation. |
Animal Model: |
Myocardial Infarction model in Wistar rats (male, 4 months old) via coronary artery ligation[3] | Dosage: | 10 mg/kg (dissolved in DMSO)
| Administration: | Intraperitoneal injection, single dose immediately after MI induction | Result: | Improved cardiac function (FS increased by 25%, EDD/ESD reduced by 15%), decreased apoptotic cardiomyocytes (TUNEL-positive cells reduced by 40%), and suppressed cleaved caspase-3 and PARP1 expression. Oxidative stress markers (O2-, nitrotyrosine) were reduced by 30-40% in infarcted myocardium. |
| IC 50 | PARP-1 | storage | +4°C |
| DPQ Preparation Products And Raw materials |
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