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213250-70-5

213250-70-5 structure
213250-70-5 structure
  • Name: 2MD
  • Chemical Name: 2MD
  • CAS Number: 213250-70-5
  • Molecular Formula: C27H44O3
  • Molecular Weight: 416.64
  • Catalog: Signaling Pathways Vitamin D Related VD/VDR
  • Create Date: 2023-04-14 10:45:45
  • Modify Date: 2025-08-27 19:11:34
  • 2MD is an orally active vitamin D analog. 2MD stimulates periosteal bone formation and decreases trabecular bone resorption. Thus 2MD restores trabecular and cortical bone mass and strength. 2MD also regulates intraocular pressure (IOP)-relative genes and reduces IOP in non-human primates[1][2].

Name 2MD
Description 2MD is an orally active vitamin D analog. 2MD stimulates periosteal bone formation and decreases trabecular bone resorption. Thus 2MD restores trabecular and cortical bone mass and strength. 2MD also regulates intraocular pressure (IOP)-relative genes and reduces IOP in non-human primates[1][2].
Related Catalog
In Vivo 2MD (5 μg/eye; 滴注; 单次剂量) 处理 7-8 小时后,可使食蟹猴同侧眼眼压逐渐降低 20%,对侧眼眼压逐渐降低至 15% 或更低[1]。 2MD (0.5-10 ng/kg, 0,1 mL/day; 口服给药; 每天 1 次, 共 16 周) 不仅可以恢复骨小梁和皮质骨质量,还可以通过刺激骨膜表面骨形成和减少骨小梁表面骨吸收,增加大鼠的骨质量和强度[2]。 Animal Model: Ovariectomized (OVX) rats model (Sprague-Dawley female rats; 4-month-old)[2] Dosage: 0.5, 1, 2.5, 5, and 10 ng/kg, 0,1 mL/day Administration: Oral gavage; once daily for 16 weeks Result: Significantly increased serum calcium at 2.5, 5, or 10 ng/kg/day. Dose-dependent reduction in osteoclast number and trabecular osteoclast surface, and dose-dependent increased in periosteal bone formation.
References

[1]. Kutuzova GD, et al. 1α,25-Dihydroxyvitamin D(3) and its analog, 2-methylene-19-nor-(20S)-1α,25-dihydroxyvitamin D(3) (2MD), suppress intraocular pressure in non-human primates. Arch Biochem Biophys. 2012 Feb 1;518(1):53-60.  

[2]. Ke HZ, et al. A new vitamin D analog, 2MD, restores trabecular and cortical bone mass and strength in ovariectomized rats with established osteopenia. J Bone Miner Res. 2005 Oct;20(10):1742-55.  

Molecular Formula C27H44O3
Molecular Weight 416.64
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