GLPBio

Itareparib

Catalog No.: GC83292Purity:>99.00%Synonyms: NMS-03305293; NMS-293
Itareparib (NMS-03305293; NMS-293) is a selective, orally active, blood-brain barrier-permeable PARP1 inhibitor with an IC50 < 0.01 μM.

製品は研究用途にのみ使用できます。人体には使用できません。患者への販売は行っておりません。


Itareparib
Cas No.: 1606995-47-4
1mgIn Stock
$389.00
1

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    Nature
    641, 529–536 (2025)
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    Nature
    628, 630–638 (2024)
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    Nature
    632, 686–694 (2024)
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    Nature
    618, 1017–1023 (2023)
  • Nature cover
    Nature
    610, 366–372 (2022)
  • Cell cover
    Cell
    187(9):2288-2304 (2024)
  • Cell cover
    Cell
    183(7):1867-1883 (2020)
  • Science cover
    Science
    388(6745) (2025)
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    387(6739) (2025)
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    Science
    387(6734) (2025)
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    Cell Research
    35, 97–116 (2025)
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    34, 683–706 (2024)
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    33, 273–287 (2023)
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    33, 546–561 (2023)
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    33, 904–922 (2023)
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    Cell Research
    31, 1291–1307 (2021)

製品説明 (Description)

Itareparib (NMS-03305293; NMS-293) is a selective, orally active, blood-brain barrier-permeable PARP1 inhibitor with an IC50 < 0.01 μM. Itareparib does not form PARP1-DNA trapping complexes, avoids PARP-DNA "retention", reduces PAR levels and inhibits the growth of homologous recombination-deficient cells. Itareparib can be used in research on advanced solid tumors, recurrent gliomas and other conditions [1] [2].

In Vivo, Itareparib is active in breast cancer cells with BRCA mutations and in xenograft animal models derived from these cells[2].

In Vitro, Itareparib can selectively inhibit the growth of HR-deficient cells in vitro and reduce the PAR level of the cells[1]. Itareparib does not cause damage to normal myeloid cells, indicating that it has a lower risk of hematological toxicity compared to non-selective PARP inhibitors[2]. Itareparib shows effective anti-proliferative activity in breast cancer cell lines with BRCA mutations[2].

References:
[1]. Li Q, et al. A new wave of innovations within the DNA damage response. Signal transduction and targeted therapy. 2023 Sep 08;8(1):338.
[2]. Ray A, et al. Targeting PARP1: A Promising Approach for Next-Generation Poly (ADP-ribose) Polymerase Inhibitors. Current breast cancer reports. 2025;17(1):22.

製品資料 (Product Documents)

Purity:>99.00%Appearance:A solid

化学的性質 (Chemical Properties)

CAS番号
1606995-47-4
同義語
NMS-03305293; NMS-293
分子式
C20H26FN3O2
分子量
359.44
溶解性
DMSO: 4.17 mg/mL (11.60 mM; ultrasonic and warming and heat to 60°C)
保存条件
Store at 4°C, sealed storage, away from moisture
配送条件
評価用サンプルは保冷剤とともに発送します。その他の容量は室温で発送し、ご要望に応じて保冷剤を同梱します。

計算ツール (Calculators)モル濃度 / 希釈 / 分子量 / 単位変換 / in vivo製剤 / 溶解度

g/mol

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