GLPBio

JAK1/2 ligand 1

Catalog No.: GC80947Purity:>99.50%
JAK1/2 ligand 1 is a ligand for the PROTAC target protein of JAK1/2, which can be used to synthesize PROTAC JAK1/2 degrader-1.

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。


JAK1/2 ligand 1
Cas No.: 1026028-96-5
10mM (in 1mL DMSO)In Stock
$190.00
1
5mgIn Stock
$173.00
1
10mgIn Stock
$281.00
1

引用文献 (Citations)

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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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    Science
    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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    Cell Research
    34, 683–706 (2024)
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    33, 273–287 (2023)
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    Cell Research
    33, 546–561 (2023)
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    Cell Research
    33, 904–922 (2023)
  • Cell Research cover
    Cell Research
    31, 1291–1307 (2021)

製品説明 (Description)

JAK1/2 ligand 1 is a ligand for the PROTAC target protein of JAK1/2, which can be used to synthesize PROTAC JAK1/2 degrader-1. JAK1/2 ligand 1 is applicable to the research of colitis [1].

In Vivo, JAK1/2 ligand 1 (compound 8b) (40 mg/kg; p.o.; daily; 7 days) provides mild protective effects against DSS-induced colitis in C57BL/6 mice[1].

In Vitro, JAK1/2 ligand 1 (compound 8b) (1.5 μM) does not induce JAK1 degradation in LPS-stimulated Raw 264.7 cells, either alone or in combination with Pomalidomide [1]. JAK1/2 ligand 1 (0.469-60 μM; 24 h) exhibits a favorable cellular safety profile in LPS-stimulated Raw 264.7 cells, showing no significant cytotoxicity within the tested concentration range[1]. JAK1/2 ligand 1 (0.469-60 μM; 24 h) exhibits only weak inhibitory activity against LPS-induced NO production[1]. AK1/2 ligand 1 (0.94-60 μM; 24 h) promotes JAK2 degradation in LPS-stimulated RAW 264.7 cells[1]. JAK1/2 ligand 1 (0.05-60 μM; 24 h) shows weaker inhibitory activity against LPS-induced TNF-α and IL-6 secretion[1]. JAK1/2 ligand 1 (0.029-3.75 μM; 24 h) suppresses LPS-induced NO, IL-6, and TNF-α production in a dose-dependent manner in Raw 264.7 cells and is non-cytotoxic at concentrations up to 3.75 μM[1].

References:
[1]. Li G, et al. Development of potent JAK1/2 PROTAC degraders for the treatment of inflammatory bowel diseases. European journal of medicinal chemistry. 2026 Jan 15;302(Pt 3):118374.

製品資料 (Product Documents)

Purity:>99.50%Appearance:A solid

化学的性質 (Chemical Properties)

CAS番号
1026028-96-5
分子式
C17H13N3O2
分子量
291.3
溶解性
DMSO: 25.75 mg/mL (88.40 mM; Need warming)
保存条件
Store at 4°C, stored under nitrogen
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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