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Stereochemistry of Solithromycin is wrong

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Hello,

I don't know how to exchange the picture, but I think the stereochemistry of solithromycin is wrong. Please check the methyl group opposite to the lactone. — Preceding unsigned comment added by 138.246.2.170 (talk) 14:12, 13 June 2018 (UTC)[reply]

I believe you are right. I have uploaded a corrected image. Please check to see if it looks correct to you now. Thanks for catching the problem and reporting it here. -- Ed (Edgar181) 15:21, 13 June 2018 (UTC)[reply]

structure

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The chemical formula shows a fluorine atom but there is no F in the structure. Sanity check! 96.88.198.77 (talk) 20:14, 23 August 2018 (UTC)[reply]

various problems

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Structure - Instead of the pyridine-imidazole group used on telthromycin - typo in telithromycin (and suggest "in" instead of "used on") Mechanism of action - Solithromycin inhibits bacterial translation by binding to the 23S ribosomal RNA to inhibit translation - redundant Preventing the offending bacteria from synthesizing proteins - sentence fragment - recommend combining into: Solithromycin inhibits bacterial translation (protein synthesis) by binding to the 23S ribosomal RNA. Development - In April 4, 2008 - recommend "On" instead of "In" as well the concentrations of the offending drugs - add "as" after "well" Commercial aspects - Cempra's general plan is to develop solithromycin develop products through late stage clinical trials and sell them to their hospital based sales force - delete "develop" after "solithromycin" and should that be "sell them through" instead of "sell them to"? References 18 & 19 are duplicates as are 21, 22, & 24 96.88.198.77 (talk) 06:25, 18 September 2018 (UTC)[reply]