GLPBio

SJB3-019A

Catalog No.: GC13401Purity:>97.00%
SJB3-019A is a novel and potent USP1 inhibitor, exhibiting an IC₅₀ value of 0.0781μM in K562 cells.

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SJB3-019A
Cas No.: 2070015-29-9
10mM (in 1mL DMSO)In Stock
$97.00
1
1mgIn Stock
$42.00
1
2mgIn Stock
$64.00
1
5mgIn Stock
$84.00
1
10mgIn Stock
$151.00
1
25mgIn Stock
$257.00
1
50mgIn Stock
$386.00
1

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Description

SJB3-019A is a novel and potent USP1 inhibitor, exhibiting an IC₅₀ value of 0.0781μM in K562 cells[1-2]. SJB-019A can be used in the study of leukemia and related diseases[3-4].

In vitro, MM.1S multiple myeloma cells were treated with SJB3-019A (0.1–1μM) for 24 hours. SJB3-019A significantly induced the activation of caspase-3/8/9 and the cleavage of PARP, inhibited the DNA repair pathway by increasing the ubiquitination levels of FANCD2/FANCI/PCNA, and simultaneously downregulated the expression of the ID protein family to promote cell differentiation[5]. B-cell acute lymphoblastic leukemia cells (CCRF-SB, Sup-B15, and KOPN-8) were treated with SJB3-019A (0.2–0.6μM) for 24 hours. SJB3-019A significantly induced G2/M phase arrest and apoptosis via the mitochondrial pathway, and reduced AKT phosphorylation levels by inhibiting the USP1-ID1 axis[6].

In vivo, nude mice and C57BL/6 mice bearing MHCC-97H cell xenografts or orthotopic liver tumors were administered daily intraperitoneal injections of SJB3-019A (0.5mg/kg) in combination with Doxorubicin (1mg/kg) for 2 weeks. SJB3-019A significantly enhanced the tumor suppression induced by Doxorubicin[7].

References:
[1] Tan L, Shan H, Han C, et al. Discovery of Potent OTUB1/USP8 Dual Inhibitors Targeting Proteostasis in Non-Small-Cell Lung Cancer. J Med Chem. 2022 Oct 27;65(20):13645-13659.
[2] Kong T, Laranjeira ABA, Letson CT, et al. RSK1 dependency in FLT3-ITD acute myeloid leukemia. Blood Cancer J. 2024 Nov 26;14(1):207.
[3] Ishikawa C, Mori N. Role of Ubiquitin-specific Protease 1 in the Pathogenesis and Treatment of Adult T-Cell Leukemia. Anticancer Res. 2025 Nov;45(11):4827-4840.
[4] Takahashi H, Yamanaka S, Kuwada S, et al. A Human DUB Protein Array for Clarification of Linkage Specificity of Polyubiquitin Chain and Application to Evaluation of Its Inhibitors. Biomedicines. 2020 Jun 4;8(6):152.
[5] Das DS, Das A, Ray A, et al. Blockade of Deubiquitylating Enzyme USP1 Inhibits DNA Repair and Triggers Apoptosis in Multiple Myeloma Cells. Clin Cancer Res. 2017 Aug 1;23(15):4280-4289.
[6] Kuang X, Xiong J, Lu T, et al. Inhibition of USP1 induces apoptosis via ID1/AKT pathway in B-cell acute lymphoblastic leukemia cells. Int J Med Sci. 2021 Jan 1;18(1):245-255.
[7] Lu Z, Zhang Z, Yang M, et al. Ubiquitin-specific protease 1 inhibition sensitizes hepatocellular carcinoma cells to doxorubicin by ubiquitinated proliferating cell nuclear antigen-mediated attenuation of stemness. Anticancer Drugs. 2022 Aug 1;33(7):622-631.

Protocol

Cell experiment [1]:

Cell lines

CCRF-SB, Sup-B15, and KOPN-8 cells (human B-cell acute lymphoblastic leukemia lines)

Preparation Method

Cells were cultured in complete medium with 10% fetal bovine serum at 37°C, 5% CO₂. Cells were treated with SJB3-019A at concentrations of 0.2–0.6μM for 24 hours.

Reaction Conditions

0.2–0.6μM; 24h.

Applications

SJB3-019A significantly suppressed cell viability in a dose-dependent manner and induced apoptosis. SJB3-019A triggered G2/M phase cell cycle arrest. Mechanistically, SJB3-019A downregulated USP1 expression, leading to reduced ID1 protein levels and inhibition of AKT phosphorylation (p-AKT), thereby activating the ID1/AKT apoptotic pathway.

Animal experiment [2]:

Animal models

6-week-old male nude mice with MHCC-97H cell-derived subcutaneous xenografts and C57BL/6 mice with orthotopic liver tumors

Preparation Method

Mice were intraperitoneally injected with SJB3-019A (0.5mg/kg/day) alone or in combination with Doxorubicin (1mg/kg/day) for 2 weeks.

Dosage form

0.5mg/kg/day; 14-day treatment.

Applications

SJB3-019A significantly enhanced Dox-induced tumor growth inhibition in both subcutaneous xenograft and orthotopic liver tumor models, with combined treatment showing superior efficacy compared to monotherapy.

References:
[1] Kuang X, Xiong J, Lu T, et al. Inhibition of USP1 induces apoptosis via ID1/AKT pathway in B-cell acute lymphoblastic leukemia cells. Int J Med Sci. 2021 Jan 1;18(1):245-255.
[2] Lu Z, Zhang Z, Yang M, et al. Ubiquitin-specific protease 1 inhibition sensitizes hepatocellular carcinoma cells to doxorubicin by ubiquitinated proliferating cell nuclear antigen-mediated attenuation of stemness. Anticancer Drugs. 2022 Aug 1;33(7):622-631.

Product Documents

Purity:>97.00%Appearance:A solid

Chemical Properties

CAS No.
2070015-29-9
Chemical Name
2-(pyridin-3-yl)naphtho[2,3-d]oxazole-4,9-dione
SMILES
O=C(C1=C2OC(C3=CN=CC=C3)=N1)C4=CC=CC=C4C2=O
Molecular Formula
C16H8N2O3
Molecular Weight
276.25
Solubility
≥ 10.85mg/mL in DMSO with gentle warming
Storage
Store at -20°C
General tips
Select a suitable solvent according to the product solubility data. Once prepared, aliquot the stock solution to avoid repeated freeze-thaw cycles.
Use stock solutions within 6 months when stored at -80°C or within 1 month when stored at -20°C.
To improve solubility, warm the tube to 37°C and sonicate it for an appropriate period.
Shipping Condition
Evaluation samples are shipped with blue ice. Other available sizes are shipped at room temperature or with blue ice upon request.

CalculatorsMolarity / Dilution / Molecular Weight / Unit Conversion / In Vivo Formulation / Solubility

g/mol

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