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LDN193189 (Hydrochloride)

    99%

LDN193189 (Hydrochloride)

源葉(MedMol)
S80068
1062368-62-0
C25H26Cl4N6
552.3261
4-[6-(4-piperazin-1-ylphenyl)pyrazolo[1,5-a]pyrimidin-3-yl]quinoline hydrochloride; 3,5-Heptanedione,4-[6-(1,3-benzodioxol-5-yloxy)hexyl]; 4-[6-(3,4-Methylenedioxyphenoxy)hexyl]-3,5-heptanedione;
品牌 貨號 產(chǎn)品規(guī)格 價格(RMB) 庫存(上海) 北京 武漢 南京 購買數(shù)量
源葉(MedMol) S80068-1mg 99% ¥206.00元 7 - - -
源葉(MedMol) S80068-5mg 99% ¥465.00元 3 - - -
源葉(MedMol) S80068-10mg 99% ¥578.00元 5 - - -
源葉(MedMol) S80068-25mg 99% ¥935.00元 5 - - -
源葉(MedMol) S80068-50mg 99% ¥1700.00元 預(yù)計交期:2-3天 - - -
產(chǎn)品介紹 參考文獻(xiàn)(1篇) 質(zhì)檢證書(COA) 摩爾濃度計算器 相關(guān)產(chǎn)品

產(chǎn)品介紹

LDN193189 hydrochloride is a selective BMP type I receptor kinases inhibitor.
產(chǎn)品描述: LDN193189 hydrochloride is a selective BMP type I receptor kinases inhibitor.
靶點: ALK
體外研究: 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 ALK2R206H or ALK2Q207D mutant proteins.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
體內(nèi)研究: 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.LDN193189 dorsalizes zebrafish embryos by inhibiting signaling pathways induced by bone morphogenetic protein (BMP)6 without effect on vascular development.In PCa-118b tumor-bearing mice, LDN-193189 treatment attenuates tumor growth and reduces bone formation in the tumors.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.
細(xì)胞實驗: Concentrations: 3 μM
參考文獻(xiàn): 1. Derwall M, et al. Inhibition of bone morphogenetic protein signaling reduces vascular calcification and atherosclerosis. Arterioscler Thromb Vasc Biol, 2012, 32(3), 613-622. 2. Lee YC, et al. BMP4 promotes prostate tumor growth in bone through osteogenesis. Cancer Res, 2011, 71(15), 5194-5203. 3. Cannon JE, et al. Intersegmental vessel formation in zebrafish: requirement for VEGF but not BMP signalling revealed by selective and non-selective BMP antagonists. Br J Pharmacol, 2010, 161(1), 140-149. 4. Yu PB, et al. BMP type I receptor inhibition reduces heterotopic [corrected] ossification. Nat Med, 2008, 14(12), 1363-1369.
溶解性: soluble  in  DMSO
保存條件: -20℃
配置溶液濃度參考:
1mg 5mg 10mg
1 mM 1.811 ml 9.053 ml 18.105 ml
5 mM 0.362 ml 1.811 ml 3.621 ml
10 mM 0.181 ml 0.905 ml 1.811 ml
50 mM 0.036 ml 0.181 ml 0.362 ml
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