GLPBio

SGC707

Catalog No.: GC12874Purity:>98.00%
SGC707 es un inhibidor potente, selectivo y no competitivo de PRMT3 (proteÍna arginina metiltransferasa 3) (IC50 = 31 nM, Kd = 53 nM).

Los productos son exclusivamente para uso en investigación. No aptos para uso humano. No vendemos a pacientes.


SGC707
Cas No.: 1687736-54-4
10mM (in 1mL DMSO)In Stock
$36.00
1
1mgIn Stock
$16.00
1
5mgIn Stock
$33.00
1
10mgIn Stock
$52.00
1
25mgIn Stock
$108.00
1
50mgIn Stock
$180.00
1
100mgIn Stock
$306.00
1

Citas (Citations)

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

Descripción (Description)

SGC707 is a selective allosteric inhibitor of protein arginine methyltransferase 3 (PRMT3) (IC50=31nM, Kd=53nM). SGC707 can be used in research related to cancers (such as glioblastoma, hepatocellular carcinoma), metabolic diseases (such as non-alcoholic fatty liver disease, atherosclerosis), and antiarrhythmic effects[1-4].

In vitro, SGC707 (10μM) was used to treat RS4;11 acute leukemia cells for 48 hours. SGC707 had no effect on cell growth and showed minimal downregulation of ADMA (asymmetric dimethylarginine) levels[5]. SGC707 (10μM) was used to treat glioblastoma cells (U251, U87, A172) for 48-96 hours. SGC707 impaired cell growth and abolished glycolysis in cancer cells[6].

In vivo, SGC707 (30mg/kg; once daily) was intraperitoneally injected into a mouse model of endometriosis for 5 consecutive days. SGC707 inhibited the occurrence of endometriosis, promoted deciduoma formation, and improved embryonic development[7]. SGC707 (10mg/kg; three times per week) was intraperitoneally injected into apoE knockout mice for 6 consecutive weeks. SGC707 alleviated hepatic steatosis, reduced weight gain, and altered white adipose tissue morphology[8].

References:
[1] Kaniskan HÜ, Szewczyk MM, Yu Z, et al. A potent, selective and cell-active allosteric inhibitor of protein arginine methyltransferase 3 (PRMT3). Angew Chem Int Ed Engl. 2015 Apr 20;54(17):5166-70.
[2] de Jong LM, Zhang Z, den Hartog Y, et al. PRMT3 inhibitor SGC707 reduces triglyceride levels and induces pruritus in Western-type diet-fed LDL receptor knockout mice. Sci Rep. 2022 Jan 10;12(1):483.
[3] Wang Y, Wang C, Guan X, et al. PRMT3-Mediated Arginine Methylation of METTL14 Promotes Malignant Progression and Treatment Resistance in Endometrial Carcinoma. Adv Sci (Weinh). 2023 Dec;10(36):e2303812.
[4] Zhang X, Hao Y, Han D, et al. PRMT3-Mediated Arginine Methylation Stabilizes PCSK9 to Promote Aortic Valve Calcification. Circulation. 2026 Mar 9.
[5] Zou W, Li M, Wan S, et al. Discovery of PRMT3 Degrader for the Treatment of Acute Leukemia. Adv Sci (Weinh). 2024 Oct;11(38):e2405963.
[6] Liao Y, Luo Z, Lin Y, et al. PRMT3 drives glioblastoma progression by enhancing HIF1A and glycolytic metabolism. Cell Death Dis. 2022 Nov 9;13(11):943.
[7] Sun F, Chen Y, Li Y, et al. PRMT3-mediated FOXO1 arginine methylation exacerbates oxidative stress-induced decidualization defects in the eutopic endometrium of endometriosis. Cell Mol Life Sci. 2025 Dec 27;83(1):45.
[8] Hoekstra M, Nahon JE, de Jong LM, et al. Inhibition of PRMT3 activity reduces hepatic steatosis without altering atherosclerosis susceptibility in apoE knockout mice. Biochim Biophys Acta Mol Basis Dis. 2019 Jun 1;1865(6):1402-1409.

Protocolo (Protocol)

Cell experiment [1]:

Cell lines

Glioblastoma cell line (U251, U87 and A172)

Preparation Method

The U251, U87 and A172 were cultured in DMEM medium with 10% fetal bovine serum (FBS) and 1% penicillin/streptomycin. The cells were treated with SGC707 (10μM) for 48-96 hours.

Reaction Conditions

10μM; 48-96 hours

Applications

Pharmacological inhibition of PRMT3 with SGC707 impaired the growth of GBM cells and abolished glycolysis.

Animal experiment [2]:

Animal models

C57BL/6 mice (six-week-old female and eight-week-old male)

Preparation Method

A mouse model of endometriosis was established. One month after establishing the endometriosis model, the mice with endometriosis were divided into an experimental group and a control group, and a decidualization model was established. The experimental group mice were intraperitoneally injected with SGC707 (30mg/kg) for 5 days.

Dosage form

30mg/kg; i.p.; five times

Applications

SGC707 inhibited the occurrence of endometriosis, promoted deciduoma formation, and improved embryonic development.

References:
[1] Liao Y, Luo Z, Lin Y, et al. PRMT3 drives glioblastoma progression by enhancing HIF1A and glycolytic metabolism. Cell Death Dis. 2022 Nov 9;13(11):943.
[2] Sun F, Chen Y, Li Y, et al. PRMT3-mediated FOXO1 arginine methylation exacerbates oxidative stress-induced decidualization defects in the eutopic endometrium of endometriosis. Cell Mol Life Sci. 2025 Dec 27;83(1):45.

Documentos del producto (Product Documents)

Purity:>98.00%Appearance:A solid

Propiedades químicas (Chemical Properties)

N.º CAS
1687736-54-4
Nombre químico
1-(isoquinolin-6-yl)-3-(2-oxo-2-(pyrrolidin-1-yl)ethyl)urea
SMILES
O=C(NCC(N1CCCC1)=O)NC2=CC3=CC=NC=C3C=C2
Fórmula molecular
C16H18N4O2
Peso molecular
298.34
Solubilidad
≥ 29.8mg/mL in DMSO
Almacenamiento
Store at -20°C
Consejos generales
Seleccione un disolvente adecuado según los datos de solubilidad del producto. Una vez preparada, divida la solución madre en alícuotas para evitar ciclos repetidos de congelación y descongelación.
Utilice las soluciones madre en un plazo de 6 meses si se conservan a -80°C, o de 1 mes si se conservan a -20°C.
Para mejorar la solubilidad, caliente el tubo a 37°C y soníquelo durante un periodo adecuado.
Condiciones de envío
Las muestras de evaluación se envían con acumuladores de frío. Los demás tamaños se envían a temperatura ambiente o, previa solicitud, con acumuladores de frío.

Calculadoras (Calculators)Molaridad / Dilución / Peso molecular / Conversión de unidades / Formulación in vivo / Solubilidad

g/mol

Reviews

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