General steroid structure

  • Keep the tablets in a safe place, out of the reach of children.
  • If your doctor decides to stop the treatment, return any remaining tablets to the pharmacist. Do not flush them down the toilet or throw them away.
  • Tell your doctor if you are sick just after taking a tablet, as you may need to take another one.
  • If you forget to take your tablet, do not take a double dose. Ask your doctor or nurse for advice.
  • If you're having a short course of steroids as part of your treatment, do not get more from your GP.

Dr. Baggish received his medical degree from the University of Connecticut School of Medicine and then completed internal medicine training and cardiovascular fellowship at the Massachusetts General Hospital. His on-going research focuses on heart function and heart disease in athletic individuals. He is the Director of the Cardiovascular Performance Program , a Massachusetts General Hospital Heart Center program that provides clinical care and exercise testing for active individuals. Dr. Baggish is medical director for the Boston Marathon and serves as team cardiologist for the New England Patriots, the Boston Bruins, the New England Revolution, US Men's and Women's Soccer, and US Rowing.

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If you compare this to testosterone, you will notice that the methyl group on C10 has been removed and the oxygen on C3 has been reduced to a hydroxyl (-OH) group. These two changes reduce the number of bonds on all the carbons, so aromatization occurs, and alternating double bonds form. In order for aromatase to function and aromatize a steroid, the steroid must have a methyl group attached to the C10. This is another example of the lock and key model. For this reason, Nandrolone does not aromatize and is not converted to an estrogen. It does not have the methyl group.

General steroid structure

general steroid structure

If you compare this to testosterone, you will notice that the methyl group on C10 has been removed and the oxygen on C3 has been reduced to a hydroxyl (-OH) group. These two changes reduce the number of bonds on all the carbons, so aromatization occurs, and alternating double bonds form. In order for aromatase to function and aromatize a steroid, the steroid must have a methyl group attached to the C10. This is another example of the lock and key model. For this reason, Nandrolone does not aromatize and is not converted to an estrogen. It does not have the methyl group.

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