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2-D08

Catalog No.GC10408

2-D08 es un inhibidor mecÁnicamente Único, permeable a las células, de la SUMOilaciÓn de proteÍnas. 2-D08 también inhibe Axl con un IC50 de 0,49 nM.

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2-D08 Chemical Structure

Cas No.: 144707-18-6

Tamaño Precio Disponibilidad Cantidad
10mM (in 1mL DMSO)
51,00 $
Disponible
1mg
21,00 $
Disponible
5mg
46,00 $
Disponible
10mg
70,00 $
Disponible
25mg
130,00 $
Disponible
50mg
210,00 $
Disponible
100mg
336,00 $
Disponible

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Sample solution is provided at 25 µL, 10mM.

Description of 2-D08

2-D08 is a synthetic flavonoid and cell-permeable small ubiquitin-like modifier (SUMO) inhibitor, which also inhibits the Axl target with an IC50 of 0.49nM[1]. Protein SUMOylation is a dynamic post-translational modification involved in various biological processes in cellular homeostasis and development. 2-D08 inhibits SUMOylation by preventing the transfer of SUMO from the UBC9-SUMO thioester to substrates[2]. 2-D08 is commonly used to investigate the role of SUMOylation in various biological pathways and diseases, such as acute myeloid leukemia and demyelinating disorders[3,4].

In vitro, incubation of C2C12 myoblasts with 2-D08 (50, 100μM) for 24h induced significant morphological changes and markedly inhibited cell viability, with the highest dose of 100µM reducing cell viability by up to 20%[5]. Treatment of human uterine leiomyosarcoma (Ut-LMS) SK-LMS-1 and SK-UT-1B cell lines with 2-D08 (10-100μM) for 7 days resulted in a dose-dependent decrease in cell survival fraction and inhibited the colony-forming ability of Ut-LMS cells[6]. Incubation of primary cultured oligodendrocyte precursor cells (OPCs) with 2-D08 (50μM) for 72h significantly increased the phosphorylation level of FYN tyrosine kinase and enhanced the expression of Kir4.1 and MBP proteins[4].

In vivo, administration of 2-D08 (1mg/kg; i.p.) daily, starting 48h after MOG35-55 immunization, significantly alleviated disease severity and promoted weight gain during the acute phase in experimental autoimmune encephalomyelitis (EAE) mice at 20 days post-immunization. 2-D08 (1mg/kg; i.v.) administered daily for 30 days, starting after symptom onset in EAE marmosets, promoted spinal cord myelin repair and improved motor coordination[4]. 2-D08 (10mg/kg; every three days) administered via intratumoral injection to C57BL/6J mice bearing RM-1 tumors for 2 weeks significantly suppressed tumor growth, reduced tumor mass, and increased tumor cell apoptosis[7].

References:
[1] FUJINO N, KUBO H, MACIEWICZ R A. Phenotypic screening identifies Axl kinase as a negative regulator of an alveolar epithelial cell phenotype[J]. Laboratory Investigation, 2017, 97(9): 1047-1062.
[2] KIM Y S, KEYSER S G L, SCHNEEKLOTH J S J. Synthesis of 2’, 3’, 4’-trihydroxyflavone (2-D08), an inhibitor of protein sumoylation[J]. Bioorganic & Medicinal Chemistry Letters, 2014, 24(4): 1094-1097.
[3] ZHOU P, CHEN X, LI M, et al. 2-D08 as a SUMOylation inhibitor induced ROS accumulation mediates apoptosis of acute myeloid leukemia cells possibly through the deSUMOylation of NOX2[J]. Biochemical and Biophysical Research Communications, 2019, 513(4): 1063-1069.
[4] LIU M, JIN S, FU X, et al. Activation of Kir4.1 Channels by 2-D08 Promotes Myelin Repair in Multiple Sclerosis[J]. Advanced Science, 2025: e02032.
[5] LIU H, LEE S M, JOUNG H. 2-D08 treatment regulates C2C12 myoblast proliferation and differentiation via the Erk1/2 and proteasome signaling pathways[J]. Journal of Muscle Research and Cell Motility, 2021, 42(2): 193-202.
[6] JOUNG H, LIU H. 2-D08 mediates notable anticancer effects through multiple cellular pathways in uterine leiomyosarcoma cells[J]. Oncology Reports, 2024, 52(1): 97.
[7] XIAO J, SUN F, WANG Y N, et al. UBC9 deficiency enhances immunostimulatory macrophage activation and subsequent antitumor T cell response in prostate cancer[J]. Journal of Clinical Investigation, 2023, 133(4): e158352.

Protocol of 2-D08

Cell experiment [1]:

Cell lines

C2C12 (Mouse myoblasts cells)

Preparation Method

C2C12 cells were plated in 96-well plates (5 × 103 cells/well) overnight under conducive growth conditions and treated with the indicated concentration of 2-D08 (0, 10, 20, 50, and 100μM) for 24h. To measure cell viability, the MTT assay was used to measure the cell proliferation rate.

Reaction Conditions

0, 10, 20, 50, and 100μM; 24h

Applications

Treatment of C2C12 cells with 2-D08 (50, 100μM) for 24h induced distinct morphological changes and significantly inhibited cell viability, with the maximum reduction of 20% observed at the highest dose of 100µM.

Animal experiment [2]:

Animal models

Adult male C57BL/6J mice model of EAE

Preparation Method

EAE mice were administered 1mg/kg of 2-D08 via daily intraperitoneal (i.p.) injection, starting 48h after immunization (prophylactic treatment).

Dosage form

1mg/kg; once daily; i.p.

Applications

2-D08 significantly alleviated disease severity and promoted weight gain during the acute phase of EAE in mice at 20 days post-immunization.

References:
[1] LIU H, LEE S M, JOUNG H. 2-D08 treatment regulates C2C12 myoblast proliferation and differentiation via the Erk1/2 and proteasome signaling pathways[J]. Journal of Muscle Research and Cell Motility, 2021, 42(2): 193-202.
[2] LIU M, JIN S, FU X, et al. Activation of Kir4.1 Channels by 2-D08 Promotes Myelin Repair in Multiple Sclerosis[J]. Advanced Science, 2025: e02032.

Chemical Properties of 2-D08

Cas No. 144707-18-6 SDF
Chemical Name 2-(2,3,4-trihydroxyphenyl)-4H-1-benzopyran-4-one
Canonical SMILES O=C1C2=CC=CC=C2OC(C3=CC=C(O)C(O)=C3O)=C1
Formula C15H10O5 M.Wt 270.2
Solubility ≤1mg/ml in ethanol;30mg/ml in DMSO;30mg/ml in dimethyl formamide Storage 4°C, protect from light
General tips Please select the appropriate solvent to prepare the stock solution according to the solubility of the product in different solvents; once the solution is prepared, please store it in separate packages to avoid product failure caused by repeated freezing and thawing.Storage method and period of the stock solution: When stored at -80°C, please use it within 6 months; when stored at -20°C, please use it within 1 month.
To increase solubility, heat the tube to 37°C and then oscillate in an ultrasonic bath for some time.
Shipping Condition Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request.

Complete Stock Solution Preparation Table of 2-D08

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1 mg 5 mg 10 mg
1 mM 3.701 mL 18.5048 mL 37.0096 mL
5 mM 740.2 μL 3.701 mL 7.4019 mL
10 mM 370.1 μL 1.8505 mL 3.701 mL
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Average Rating: 5 ★★★★★ (Based on Reviews and 27 reference(s) in Google Scholar.)

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