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描述 | Palovarotene is a selective retinoic acid receptor gamma (RAR-γ) agonist for the treatment of emphysema. |
体内研究 | Palovarotene effectively inhibits post-traumatic chondrogenesis and osteogenesis, along with mitigating trauma-induced ectopic bone formation. Administered orally at 1 mg/kg/day for 14 days, starting either on post-operative day (POD) 1 or POD-5, palovarotene significantly inhibits subcutaneous and intramuscular heterotopic ossification (HO) in mice. Assessment for up to 84 days post-injury demonstrates a 50 to 60% reduction in HO regardless of treatment initiation time or the presence of infection, compared to vehicle-control animals [1]. In Acvr1cR206H/+ mice, palovarotene treatment for 14 days via daily gavage starting from day 1 of injury significantly diminishes HO formation by over 80% based on bone volume/total volume quantification, compared to mice receiving vehicle as control [2]. |
计算器 | ||||
存储液制备 | ![]() |
1mg | 5mg | 10mg |
1 mM 5 mM 10 mM |
2.41mL 0.48mL 0.24mL |
12.06mL 2.41mL 1.21mL |
24.12mL 4.82mL 2.41mL |
CAS号 | 410528-02-8 |
分子式 | C27H30N2O2 |
分子量 | 414.54 |
SMILES Code | O=C(O)C1=CC=C(/C=C/C2=C(CN3N=CC=C3)C=C4C(C)(C)CCC(C)(C)C4=C2)C=C1 |
MDL No. | MFCD10565968 |
别名 | R 667; Ro 3300074 |
运输 | 蓝冰 |
InChI Key | YTFHCXIPDIHOIA-DHZHZOJOSA-N |
Pubchem ID | 10295295 |
存储条件 |
In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Sealed in dry, store in freezer, under -20°C |
溶解方案 |
DMSO: 25 mg/mL(60.31 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO 以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
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