الصفحة الرئيسية>>Signaling Pathways>> GPCR/G protein>> LPL Receptor>>ONO-7300243

ONO-7300243

رقم الكتالوجGC12362

ONO-7300243 هو مضاد جديد وقوي لمستقبل حمض الليزوفوسفاتيدك 1 (LPA1) مع IC50 من 0.16 ميكرومتر

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ONO-7300243 التركيب الكيميائي

Cas No.: 638132-34-0

الحجم السعر المخزون الكميّة
5mg
71٫00
متوفر
25mg
263٫00
متوفر
500mg
1542٫00
متوفر

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Sample solution is provided at 25 µL, 10mM.

Description of ONO-7300243

IC50: 160 nM

ONO-7300243 is a LPA1 antagonist.

Lysophosphatidic acids (LPAs), a bioactive class of phospholipids, are produced by autotaxin from lysophosphatidylcholine in blood. LPAs have a wide range of cellular responses, such as cell proliferation, intracellular Ca2+ mobilization, cell survival, and cell motility. Based on their specific properties, LPAs have been involved in various complex physiological responses, such as the contraction of smooth muscle, wound healing, coagulation, demyelization, as well as immunological competence.

In vitro: ONO-7300243 was identified as a novel and potent LPA1 antagonist. Importantly, it was found that ONO-7300243 showed equal potency to the α1 adrenoceptor antagonist tamsulosin that is clinically used for the treatment of dysuria with benign prostatic hyperplasia (BPH) [1].

In vivo: Animal study reported that although ONO-7300243 showed only modest in vitro activity (IC50 = 0.16 μM), the oral dosing of ONO-7300243 to rats resulted in much stronger effects on reducing intraurethral pressure (88% inhibition at 10 mg/kg i.d., 62% inhibition at 3 mg/kg i.d.). When compared with tamsulosin, ONO-7300243 had no effect on the mean blood pressure at this dose, which suggested that LPA1 antagonists could be used to treat BPH without affecting the blood pressure [1].

Clinical trial: Up to now, ONO-7300243 is still in the preclinical development stage.

Reference:
[1] Terakado M et al.  Discovery of ONO-7300243 from a Novel Class of Lysophosphatidic Acid Receptor 1 Antagonists: From Hit to Lead. ACS Med Chem Lett. 2016 Aug 19;7(10):913-918. eCollection 2016.

Protocol of ONO-7300243

Animal experiment:

Rats[1] The oral administration of ONO-7300243 (30 mg/kg, p.o.) is investigated to determine its effect on rat IUP. ONO-7300243 is studied in an LPA-induced rat intraurethral pressure (IUP) model.

References:

[1]. Terakado M, et al. Discovery of ONO-7300243 from a Novel Class of Lysophosphatidic Acid Receptor 1 Antagonists: From Hit to Lead. ACS Med Chem Lett. 2016 Aug 19;7(10):913-918.

Chemical Properties of ONO-7300243

Cas No. 638132-34-0 SDF
Chemical Name 2-(4-((3,5-dimethoxy-4-methyl-N-(3-phenylpropyl)benzamido)methyl)phenyl)acetic acid
Canonical SMILES O=C(O)CC1=CC=C(CN(C(C2=CC(OC)=C(C)C(OC)=C2)=O)CCCC3=CC=CC=C3)C=C1
Formula C28H31NO5 M.Wt 461.22
الذوبان ≥ 46.1mg/mL in DMSO 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 ONO-7300243

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1 mg 5 mg 10 mg
1 mM 2.1682 mL 10.8408 mL 21.6816 mL
5 mM 0.4336 mL 2.1682 mL 4.3363 mL
10 mM 0.2168 mL 1.0841 mL 2.1682 mL
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Average Rating: 5 ★★★★★ (Based on Reviews and 13 reference(s) in Google Scholar.)

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