Palovarotene (R-667)|RAR-γ inhibitor|DC Chemicals

Cas No.:	410528-02-8
Chemical Name:	R667,R 667,R667,RO-3300074,RO 3300074,RO3300074
Synonyms:	R667,R 667,R667,RO-3300074,RO 3300074,RO3300074
SMILES:	OC(C1=CC=C(/C=C/C2C(CN3N=CC=C3)=CC3C(CCC(C)(C)C=3C=2)(C)C)C=C1)=O
Formula:	C₂₇H₃₀N₂O₂
M.Wt:	414.54
Sotrage:	2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO

Description:

Palovarotene is a nuclear retinoic acid receptor γ (RAR-γ) agonist.

In Vivo:

Palovarotene suppresses post-traumatic chondrogenesis and osteogenesis and mitigated trauma-induced ectopic bone formation. Palovarotene inhibits subcutaneous and intramuscular heterotopic ossification (HO) in mice. Palovarotene is given orally for 14 days at 1 mg/kg/day starting on post-operative day (POD) 1 or POD-5, and HO amount, wound dehiscence and related processes are monitored for up to 84 days post injury. Compared to vehicle-control animals, Palovarotene significantly decreases HO by 50 to 60% regardless of when the treatment started and if infection is present[1]. Starting from day 1 of injury, half of the Acvr1cR206H/+ mice are treated with Palovarotene by daily gavage for 14 days and the other half received vehicle as control. Analysis by mCT and 3D image reconstruction at day 14 shows that large HO tissue masses have formed in the targeted leg of Acvr1cR206H/+ mutant mice receiving vehicle, but HO formation is greatly diminished in Palovarotene-treated companions by more than 80% based on bone volume/total volume quantification[2].

MSDS

COA

LOT NO.	DOWNLOAD

2018-0101
2018-0101

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Palovarotene(R 667)