4-{6-[4-(piperazin-1-yl)phenyl]pyrazolo[1,5-a]pyrimidin-3-yl}quinoline

• ChemBase编号: 73113
• 分子式: C25H22N6
• 平均质量: 406.48238
• 单一同位素质量: 406.19059473
• SMILES: c1(ccc(cc1)c1cnc2n(c1)ncc2c1ccnc2c1cccc2)N1CCNCC1
• Canonical SMILES: N1CCN(CC1)c1ccc(cc1)c1cnc2n(c1)ncc2c1ccnc2c1cccc2
• InChI: InChI=1S/C25H22N6/c1-2-4-24-22(3-1)21(9-10-27-24)23-16-29-31-17-19(15-28-25(23)31)18-5-7-20(8-6-18)30-13-11-26-12-14-30/h1-10,15-17,26H,11-14H2
• InChIKey: CDOVNWNANFFLFJ-UHFFFAOYSA-N

名称和登记号

名称

• IUPAC标准名: 4-{6-[4-(piperazin-1-yl)phenyl]pyrazolo[1,5-a]pyrimidin-3-yl}quinoline
• IUPAC传统名: 4-{6-[4-(piperazin-1-yl)phenyl]pyrazolo[1,5-a]pyrimidin-3-yl}quinoline
• 别名: LDN 193189; LDN193189

登记号

• CAS号: 1062368-24-4
• PubChem SID: 162038033
• PubChem CID: 25195294

理论计算性质

• 质子受体: 5
• 质子供体: 1
• LogD (pH = 5.5): 0.67203116
• LogD (pH = 7.4): 2.1977062
• Log P: 3.6771934
• 摩尔折射率: 133.1513 cm^3
• 极化性: 50.401436 Å^3
• 极化表面积: 58.35 Å^2
• 可自由旋转的化学键: 3
• 里宾斯基五规则: true

分子性质

安全信息

• 保存条件: -20°C

药理学性质

• 作用靶点: ALK

产品相关信息

• 成盐信息: Free Base

详细说明

Selleck Chemicals - S2618

Research Area

• Description: Cancer

Biological Activity

• Description: LDN193189 is a selective inhibitor of ALK2 and ALK3 with IC50 of 5 nM and 30 nM, respectively.
• Targets: ALK2; ALK3
• IC50: 5 nM ^[1]; 30 nM ^[1]
• In Vitro: LDN193189 potently inhibits BMP4-mediated Smad1, Smad5 and Smad8 activation with IC50 of 5 nM, and efficiently inhibits transcriptional activity of the BMP type I receptors ALK2 and ALK3 with IC50 of 5 nM and 30 nM, respectively. Furthermore, LDN193189 also shows the inhibitory effect on the transcriptional activity induced by either constitutively active ALK2^R206H or ALK2^Q207D mutant proteins. ^[1] A recent study shows that LDN-193189 blocks the production of reactive oxygen species induced by oxidized LDL during atherogenesis in human aortic endothelial cells. ^[4]
• In Vivo: In conditional caALK2-transgenic mice with Ad.Cre on on postnatal day 7 (P7), LDN-193189 (3 mg/kg i.p) leads to mild calcifications surrounding the left tibia and fibula first visible at P13, and prevents radiographic lesions at P15 without causing weight loss or growth retardation, spontaneous fractures, decreased bone density or behavioral abnormalities. ^[1] LDN193189 dorsalizes zebrafish embryos by inhibiting signaling pathways induced by bone morphogenetic protein (BMP)6 without effect on vascular development. ^[2] In PCa-118b tumor-bearing mice, LDN-193189 treatment attenuates tumor growth and reduces bone formation in the tumors. ^[3] In LDL receptor-deficient (LDLR-/-) mice, LDN-193189 potently inhibits development of atheroma. Moreover, LDN-193189 also exhibits the inhibitory effects on associated vascular inflammation, osteogenic activity, and calcification. ^[4]

Protocol

• Protocol: Kinase Assay ^[1]
• Alkaline phosphatase activity: C2C12 cells are seeded into 96-well plates at 2,000 cells per well in DMEM supplemented with 2% FBS. The wells are treated in quadruplicate with BMP ligands and LDN-193189 or vehicle. The cells are collected after 6 days in culture in 50 μL Tris-buffered saline and 1% Triton X-100. The lysates are added to p-nitro-phenylphosphate reagent in 96-well plates for 1 hours and then evaluated alkaline phosphatase activity (absorbance at 405 nm). Cell viability and quantity are measured by Cell Titer Aqueous One (absorbance at 490 nm), using replicate wells treated identically to those used for alkaline phosphatase measurements.
• Protocol: Animal Study ^[1]
• Animal Models: Ad.Cre on P7 is injected into conditional caALK2–transgenic and wild-type mice.
• Formulation: LDN193189 is dissolved in DMSO and then diluted in water.
• Doses: ≤3 mg/kg
• Administration: Administered via i.p.

References

• References: [1] Yu PB, et al. Nat Med, 2008, 14(12), 1363-1369.
• References: [2] Cannon JE, et al. Br J Pharmacol, 2010, 161(1), 140-149.
• References: [3] Lee YC, et al. Cancer Res, 2011, 71(15), 5194-5203.
• References: [4] Derwall M, et al. Arterioscler Thromb Vasc Biol, 2012, 32(3), 613-622.

参考文献

• Yu PB, et al. Nat Med, 2008, 14(12), 1363-1369.
• Cannon JE, et al. Br J Pharmacol, 2010, 161(1), 140-149.
• Lee YC, et al. Cancer Res, 2011, 71(15), 5194-5203.
• Derwall M, et al. Arterioscler Thromb Vasc Biol, 2012, 32(3), 613-622.