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The term "biguanidine" often refers specifically to a class of drugs that function as oral antihyperglycemic drugs used for diabetes mellitus or prediabetes treatment. [4] Examples include: Metformin - widely used in treatment of diabetes mellitus type 2; Phenformin - withdrawn from the market in most countries due to toxic effects
In 1990, Bangladesh Association for Plant Tissue Culture (BAPTC) was formed which has been organising several international conferences since its inception. In September 1993, the government of Bangladesh formed a National Committee on Biotechnology Product Development to select potential biotechnological projects which could be leased out for ...
The pharmaceutical industry in Bangladesh is one of the most developed industrial sectors within the country. Manufacturers produce insulin, hormones, and cancer drugs. This sector provides 98% [1] of the total domestic demand for medicine requirement in the country. This makes Bangladesh almost self sufficient in the pharmaceutical sector.
This page was last edited on 14 May 2014, at 13:04 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply ...
After the independence of Bangladesh in 1971, BCSIR was established by a resolution of the Government of the People's Republic of Bangladesh which subsequently was reconstituted as the Bangladesh Council of Scientific and Industrial Research through a Presidential Ordinance namely Ordinance No. (V) of 1978. [2]
This is a list of notable pharmaceutical companies of Bangladesh This is a dynamic list and may never be able to satisfy particular standards for completeness. You can help by adding missing items with reliable sources .
People gather to celebrate the fall of Bangladesh Prime Minister Sheikh Hasina in Dhaka on Aug. 5, 2024. Anik Rahman—Middle East Images/AFP/Getty Images
The Staudinger synthesis, also called the Staudinger ketene-imine cycloaddition, is a chemical synthesis in which an imine 1 reacts with a ketene 2 through a non-photochemical 2+2 cycloaddition to produce a β-lactam 3. [1] The reaction carries particular importance in the synthesis of β-lactam antibiotics. [2]