What are organic drugs?

 

Organic drugs are natural substances extracted from plants and animals.

 Examples of them include marijuana, heroin, opium, cocaine and hallucinogenic mushrooms.

Currently, manufacturers of synthetic prescription drugs are held accountable when they produce their products, but even drug manufacturers find it in their best interest to alter drugs’ chemical compositions to make a cheaper product or to produce drugs faster. Many synthetic drugs can be used without causing serious harm. If a drug is taken as prescribed, the effects will be minimal, and generally outweighed by the benefits they provide for a medical condition.

However all drugs cause a chemical reaction in the brain, so the longer someone uses any chemical, organic or synthetic, the more change it will cause

For more details: Drug Discovery 2023

Comments

Post a Comment

Popular posts from this blog

Why is drug discovery important?

Image
  The goal of a preclinical drug discovery program is to deliver one or more clinical candidate molecules, each of which has sufficient evidence of biologic activity at a target relevant to a disease as well as sufficient safety and drug-like properties so that it can be entered into human testing. Most discovery programs seek to produce more than one candidate molecule because, as is shown in, many molecules do not move through the entire process because of problems with safety, kinetics, potency, intellectual property protection, or other factors. There is no simple formula for producing a viable clinical candidate molecule, although extensive collaboration of chemistry, biology, toxicology, and pharmacokinetics is almost universally the norm in modern drug discovery programs small molecule drug discovery programs typically produce massive amounts of data using high-throughput screening techniques that evaluate many compounds at many doses against many assays For more deatails :  Dru
Read more

What is meant by drug development?

Image
    Drug development is a term used to define the entire process of bringing a new drug or device to market. It is an integrated, multidisciplinary endeavor that includes drug discovery, chemistry and pharmacology, nonclinical safety testing, manufacturing, clinical trials, and regulatory submissions. This report summarizes presentations of a workshop entitled "Drug Development 101," held at the 39th Annual Meeting of the American College of Toxicology in West Palm Beach, Florida. The workshop was designed to provide an introductory overview of drug development. Experienced scientists from industry and government provided overviews of each area, with a focus on safety assessment, and described some of the challenges that can arise. The role of chemistry and manufacturing was discussed in the context of early- and late-stage product development and approaches to assess, control, and limit impurities. The toxicologic assessment was emphasized in early-phase development, from th
Read more