GLPBio

MK-4827

Catalog No.: GC17802Purity:>98.00%
MK-4827 is an orally active PARP inhibitor that simultaneously inhibits both PARP1 (IC50=3.8nM) and PARP2 (IC50=2.1nM). MK-4827 blocks DNA repair by inhibiting PARP enzyme activity, thereby inducing cancer cell death.

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MK-4827
Cas No.: 1038915-60-4
10mM (in 1mL DMSO)In Stock
$48.00
1
5mgIn Stock
$43.00
1
10mgIn Stock
$74.00
1
25mgIn Stock
$95.00
1
50mgIn Stock
$133.00
1
100mgIn Stock
$217.00
1
500mgIn Stock
$407.00
1

Zitate (Citations)

2 publicationsPublikationen von Forschern, die dieses Produkt verwenden

Beschreibung (Description)

MK-4827 is an orally active PARP inhibitor that simultaneously inhibits both PARP1 (IC50=3.8nM) and PARP2 (IC50=2.1nM). MK-4827 blocks DNA repair by inhibiting PARP enzyme activity, thereby inducing cancer cell death[1-2]. MK-4827 is used in research for the treatment of various types of cancer[3-4].

In vitro, treatment of ovarian cancer OVCAR8 cells and pancreatic cancer MIA PaCa-2 cells with MK-4827 (10-20μM) for 48 to 72 hours, MK-4827 significantly suppressed STAT3 phosphorylation, induced apoptosis, downregulated the expression of the anti-apoptotic gene BCL2L1, and upregulated the expression of the pro-apoptotic genes CASP3, CASP8, and CASP9[5]. In esophageal squamous cell carcinoma KYSE-30 and KYSE-150 cells, treatment with MK-4827 (5μM) combined with radiotherapy (4Gy) for 24 hours, MK-4827 markedly enhanced radiation-induced DNA double-strand break damage (increased γ-H2AX expression) and promoted apoptosis, while also increasing radiosensitivity by inhibiting FANCG expression[6].

In vivo, in an ovarian cancer peritoneal metastasis model, oral administration of MK-4827 (50mg/kg) to tumor-bearing mice (inoculated with ID8 cells or patient-derived xenografts) three times per week for 3-8 weeks, starting from day 3 or 6 post-inoculation, MK-4827 significantly inhibited tumor growth, reduced the number of abdominal lesions and ascites volume, and induced ferroptosis in tumor cells[7]. In an atherosclerosis model, oral administration of MK-4827 (10mg/kg) to high-fat diet-fed ApoE⁻/⁻ or Ldlr⁻/⁻ mice three times per week for 8-12 weeks, starting from week 4 or 16 of dietary intervention, MK-4827 significantly reduced atherosclerotic plaque burden, decreased necrotic core area, increased fibrous cap thickness, and suppressed phenotypic switching of smooth muscle cells[8].

References:
[1] Jones P, Altamura S, Boueres J, et al. Discovery of 2-{4-[(3S)-piperidin-3-yl]phenyl}-2H-indazole-7-carboxamide (MK-4827): a novel oral poly(ADP-ribose)polymerase (PARP) inhibitor efficacious in BRCA-1 and -2 mutant tumors. J Med Chem. 2009 Nov 26;52(22):7170-85.
[2] Bridges KA, Toniatti C, Buser CA, et al. Niraparib (MK-4827), a novel poly(ADP-Ribose) polymerase inhibitor, radiosensitizes human lung and breast cancer cells. Oncotarget. 2014 Jul 15;5(13):5076-86.
[3] Wang L, Mason KA, Ang KK, et al. MK-4827, a PARP-1/-2 inhibitor, strongly enhances response of human lung and breast cancer xenografts to radiation. Invest New Drugs. 2012 Dec;30(6):2113-20.
[4] Mirza MR, Monk BJ, Herrstedt J, et al. Niraparib Maintenance Therapy in Platinum-Sensitive, Recurrent Ovarian Cancer. N Engl J Med. 2016 Dec 1;375(22):2154-2164.
[5] Zhao Q, Kohut A, Li YJ, et al. Niraparib-induced STAT3 inhibition increases its antitumor effects. Front Oncol. 2022 Oct 17;12:966492.
[6] Cui Y, Huang W, Du F, et al. Therapeutic benefits of niraparib tosylate as radio sensitizer in esophageal squamous cell carcinoma: an in vivo and in vitro preclinical study. Clin Transl Oncol. 2022 Aug;24(8):1643-1656.
[7] Jin N, Qian YY, Jiao XF, et al. Niraparib restricts intraperitoneal metastases of ovarian cancer by eliciting CD36-dependent ferroptosis. Redox Biol. 2025 Mar;80:103528.
[8] Pan H, Ho SE, Xue C, et al. Atherosclerosis Is a Smooth Muscle Cell-Driven Tumor-Like Disease. Circulation. 2024 Jun 11;149(24):1885-1898.

Protokoll (Protocol)

Cell experiment [1]:

Cell lines

OVCAR8 (human ovarian cancer cell line), MIA PaCa-2 (human pancreatic ductal adenocarcinoma cell line), PANC-1 (human pancreatic ductal adenocarcinoma cell line), PEO1 (human ovarian cancer cell line)

Preparation Method

Cells were maintained in DMEM or RPMI-1640 medium supplemented with 10% fetal bovine serum (FBS) at 37°C, 5% CO₂. Cells were treated with MK-4827 at concentrations of 10µM or 20µM for 24 to 72 hours.

Reaction Conditions

10–20μM; 24–72 hours

Applications

MK-4827 significantly inhibited STAT3 phosphorylation (pSTAT3-Y705) in ovarian and pancreatic cancer cell lines, regardless of BRCA mutation status. MK-4827 downregulated the expression of the anti-apoptotic gene BCL2L1 and upregulated pro-apoptotic genes CASP3, CASP8, and CASP9. MK-4827 treatment for 72 hours induced significant apoptosis. The pro-apoptotic effects were mediated through inhibition of the SRC/STAT3 signaling pathway.

Animal experiment [2]:

Animal models

BALB/c nude mice, C57BL/6 mice

Preparation Method

ID8 ovarian cancer cells were injected intraperitoneally into mice. Mice were treated with MK-4827 at 50mg/kg via oral gavage three times per week for 3-8 weeks, either starting from day 6 post-inoculation (prevention) or after 16 weeks of tumor establishment (therapy).

Dosage form

50mg/kg; p.o.; Three times per week for 3-8 weeks.

Applications

MK-4827 significantly inhibited ovarian cancer progression and induced regression of established metastases in mouse models. MK-4827 reduced tumor burden, decreased ascites volume, and diminished the number of abdominal lesions.

References:
[1] Zhao Q, Kohut A, Li YJ, et al. Niraparib-induced STAT3 inhibition increases its antitumor effects. Front Oncol. 2022 Oct 17;12:966492.
[2] Jin N, Qian YY, Jiao XF, et al. Niraparib restricts intraperitoneal metastases of ovarian cancer by eliciting CD36-dependent ferroptosis. Redox Biol. 2025 Mar;80:103528.

Produktdokumente (Product Documents)

Purity:>98.00%Appearance:A solid

Chemische Eigenschaften (Chemical Properties)

CAS-Nr.
1038915-60-4
Chemischer Name
2-[4-[(3S)-piperidin-3-yl]phenyl]indazole-7-carboxamide
SMILES
C1CC(CNC1)C2=CC=C(C=C2)N3C=C4C=CC=C(C4=N3)C(=O)N
Summenformel
C19H20N4O
Molekulargewicht
320.39
Löslichkeit
≥ 32 mg/mL in DMSO, ≥ 50.9 mg/mL in EtOH with gentle warming
Lagerung
Store at -20°C
Allgemeine Hinweise
Wählen Sie anhand der Löslichkeitsdaten des Produkts ein geeignetes Lösungsmittel. Aliquotieren Sie die Stammlösung nach der Herstellung, um wiederholte Gefrier-Auftau-Zyklen zu vermeiden.
Verwenden Sie Stammlösungen bei Lagerung bei -80°C innerhalb von 6 Monaten bzw. bei -20°C innerhalb von 1 Monat.
Zur Verbesserung der Löslichkeit das Röhrchen auf 37°C erwärmen und für eine angemessene Dauer beschallen.
Versandbedingungen
Evaluierungsmuster werden mit Kühlakkus versandt. Andere verfügbare Größen werden bei Raumtemperatur oder auf Anfrage mit Kühlakkus versandt.

Rechner (Calculators)Molarität / Verdünnung / Molekulargewicht / Einheitenumrechnung / In-vivo-Formulierung / Löslichkeit

g/mol

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