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SR1078 (Synonyms: SR 1078;SR-1078)

رقم الكتالوجGC16392

SR1078 is an agonist of the retinoic acid receptor-related orphan receptors (RORs) RORα and RORγ, with IC50 values of 1-3µM.

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SR1078 التركيب الكيميائي

Cas No.: 1246525-60-9

الحجم السعر المخزون الكميّة
1mg
30٫00
متوفر
5mg
69٫00
متوفر
10mg
89٫00
متوفر
50mg
336٫00
متوفر
200mg
1153٫00
متوفر

Tel:(909) 407-4943 Email: sales@glpbio.com


مراجعات العميل

بناء على آراء العملاء.

Sample solution is provided at 25 µL, 10mM.

Product has been cited by 1 publications

Description of SR1078

SR1078 is an agonist of the retinoic acid receptor-related orphan receptors (RORs) RORα and RORγ, with IC50 values of 1-3µM[1]. SR1078 can directly bind to the ligand binding domains of RORα and RORγ, increasing the transcriptional activity of these receptors, thereby stimulating the transcription of RORα/γ target genes[2, 3]. SR1078 can regulate osteoblast metabolism through anti-inflammatory effects[4].

In vitro, SR1078 (2-10µM) treatment of human neuroblastoma SH-SY5Y cells for 24h increased the expression of A2BP1, CYP19A1, NLGN1 and IPTR1 genes in the cells in a dose-dependent manner, with an EC50 range of 3-5μM[5]. SR1078 (1, 5µM) treatment of HepG2 cells increased the expression of p53 protein and induced cell apoptosis[6].

In vivo, SR1078 (20mg/kg) was intraperitoneally injected into mice bearing colorectal cancer cell xenografts, significantly inhibiting the growth of subcutaneous tumors and the metastasis of tumor cells[7].

References:
[1] Wang Y, Kumar N, Nuhant P, et al. Identification of SR1078, a synthetic agonist for the orphan nuclear receptors RORα and RORγ[J]. ACS chemical biology, 2010, 5(11): 1029-1034.
[2] Kamenecka T M, Lyda B, Chang M R, et al. Synthetic modulators of the retinoic acid receptor-related orphan receptors[J]. MedChemComm, 2013, 4(5): 764-776.
[3] Nematisouldaragh D, Kirshenbaum E, Uzonna M, et al. The Role of Retinoic-Acid-Related Orphan Receptor (RORs) in Cellular Homeostasis[J]. International Journal of Molecular Sciences, 2024, 25(21): 11340.
[4] Fernandes J, Benderdor M, Shi Q. SR1078, A synthetic ligand of nuclear receptor ror alpha, modulates osteoblast metabolism with anti-inflammatory effects[J]. Osteoarthritis and Cartilage, 2012, 20: S115-S116.
[5] Wang Y, Billon C, Walker J K, et al. Therapeutic effect of a synthetic RORα/γ agonist in an animal model of autism[J]. ACS Chemical Neuroscience, 2016, 7(2): 143-148.
[6] Wang Y, Solt L A, Kojetin D J, et al. Regulation of p53 stability and apoptosis by a ROR agonist[J]. PloS one, 2012, 7(4): e34921.
[7] Wang Y N, Ruan D Y, Wang Z X, et al. Targeting the cholesterol-RORα/γ axis inhibits colorectal cancer progression through degrading c-myc[J]. Oncogene, 2022, 41(49): 5266-5278.

Protocol of SR1078

Cell experiment [1]:

Cell lines

SH-SY5Y cells

Preparation Method

SH-SY5Y were treated with SR1078 (2-10µM), and after 24h cells were harvested and cDNA prepared to assess the expression of autism spectrum disorder (ASD)-associated genes by quantitative PCR.

Reaction Conditions

2-10µM; 24h

Applications

SR1078 increases the expression of ASD-associated genes in SH-SY5Y cells. SR1078 treatment increased the expression of A2BP1, CYP19A1, NLGN1, and IPTR1 in a dose-dependent manner with EC50 ranging from 3-5μM.

Animal experiment [2]:

Animal models

Female BALB/c athymic nude mice

Preparation Method

To establish the subcutaneous tumour model, 2×106 CRC cells were suspended in 100μL PBS and then injected subcutaneously. Tumour volumes were measured every 3 or 4 days with a caliper and were calculated. For the drug treatment studies, daily doses of 20mg/kg atorvastatin, 20mg/kg SR1078 or the combination were administered via intraperitoneal (i.p.) injection. After the mice were euthanized, the tumours were excised and weighed.

Dosage form

20mg/kg; i.p.

Applications

SR1078 significantly inhibited tumour growth in nude mice subcutaneously.

References:
[1] Wang Y, Billon C, Walker J K, et al. Therapeutic effect of a synthetic RORα/γ agonist in an animal model of autism[J]. ACS Chemical Neuroscience, 2016, 7(2): 143-148.
[2]Wang Y N, Ruan D Y, Wang Z X, et al. Targeting the cholesterol-RORα/γ axis inhibits colorectal cancer progression through degrading c-myc[J]. Oncogene, 2022, 41(49): 5266-5278.

Chemical Properties of SR1078

Cas No. 1246525-60-9 SDF
المرادفات SR 1078;SR-1078
Chemical Name N-[4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)phenyl]-4-(trifluoromethyl)benzamide
Canonical SMILES C1=CC(=CC=C1C(=O)NC2=CC=C(C=C2)C(C(F)(F)F)(C(F)(F)F)O)C(F)(F)F
Formula C17H10F9NO2 M.Wt 431.25
الذوبان ≥ 43.2 mg/mL in DMSO, ≥ 43.4 mg/mL in EtOH Storage Store at -20°C
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 SR1078

Prepare stock solution
1 mg 5 mg 10 mg
1 mM 2.3188 mL 11.5942 mL 23.1884 mL
5 mM 463.8 μL 2.3188 mL 4.6377 mL
10 mM 231.9 μL 1.1594 mL 2.3188 mL
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