Active Pharmaceutical Ingredients (API), popularly speaking, are the raw materials of medicines, only pharmaceutical raw materials are processed into pharmaceutical preparations , can they become medicines available for clinical use, so drugs we usually eat are the finished drugs through processing. Active Pharmaceutical Ingredients based on its sources can be divided into two major categories ,including chemical synthetic drugs and natural chemical drugs. Chemical synthetic drugs can be divided into organic synthetic drugs and inorganic synthetic drugs. Inorganic synthetic drugs are inorganic compounds ( very few is element), such as aluminum hydroxide, magnesium trisilicate which are used for the treatment of gastric and duodenal ulcers ; organic synthetic drugs are mainly composed of drugs made by basic organic chemical raw materials, through a series of organic chemical reactions (such as aspirin, chloramphenicol, caffeine, etc.). Natural chemical drugs ,based on its sources,can be divided into two categories including biochemical drugs and plant chemical drugs. Antibiotics are generally made by the microbial fermentation, which belongs to the biochemistry category. A variety of semi-synthetic antibiotics occurs in recent years,which are biosynthesis and chemical synthesis combining products.Among active Pharmaceutical Ingredients, the organic synthetic drugs varieties, yields and values have the largest proportion,which are the main pillars of the chemical and pharmaceutical industries. The quality of active Pharmaceutical Ingredients decides whether the formulation is good or bad , so its quality standards are very strict ,countries in the world have developed national pharmacopoeia standards and strict quality control methods for its widely used active Pharmaceutical ingredients.
Side effects of Sparfloxacin
Sparfloxacin (AT-4140, CI-978, PD 131501) is a newer-generation aminodifluoroquinolone with broad spectrum antibacterial activity. It has the chemical formula 5-amino-1-cyclopropyl-7-(cis-3,5-dimethyl
Mar 25,2022 APIAztreonam: Antimicrobial Activity, Susceptibility, Administration and Dosage, Clinical Uses etc.
Aztreonam belongs to the class of beta-lactam antibiotics known as monobactams. Unlike penicillins and cephalosporins the monobactams have only the beta-lactam ring.
Mar 25,2022 APICeftobiprole: Antimicrobial Activity, Susceptibility, Administration and Dosage, Clinical Uses etc.
Ceftobiprole, formerly BAL9141 or Ro 63-9141, is a novel pyrrolidinone-3-ylidene-methyl cephalosporin with clinically demonstrable activity against methicillin-resistant Staphylococcus aureus (MRSA).
Mar 25,2022 APICeftaroline: Antimicrobial Activity, Susceptibility, Administration and Dosage, Clinical Uses etc.
Ceftaroline, also referred to as PPI-0903M or T-91825, is one of the anti-methicillin-resistant Staphylococcus aureus (MRSA) cephalosporins currently under development.
Mar 25,2022 APICefepime: Antimicrobial Activity, Susceptibility, Administration and Dosage, Clinical Uses etc.
Cefepime is an oxymino b-lactam with an amino thiazolyn side chain classified as a fourth-generation cephalosporin. In general, it has a wider spectrum and greater potency than the third-generation ce
Mar 25,2022 APISynthetic method of sulfanilic acid
Sulfanilic acid, also known as p-aminobenzenesulfonamide, with the molecular formula C6H8N2O2S, is an organic compound with medicinal value.
Mar 25,2022 APICefpirome: Antimicrobial Activity, Susceptibility, Administration and Dosage, Clinical Uses etc.
Cefpirome is a parenteral fourth-generation cephalosporin antibiotic (aminothiazolemethoxyimine cephalosporin). Like cefepime, it shows broad-spectrum activity against many Gram-positive and Gramnega
Mar 25,2022 APIThe reactions of 2,5,6-tetrachloropyridine
It has been reported that on treatment with lithium aluminium hydride pentafluoropyridine gives 2,5,6-tetrafluoropyridine and that further reduction occurs at the 2-position
Mar 25,2022 APICeftazidime: Antimicrobial Activity, Susceptibility, Administration and Dosage, Clinical Uses etc.
Ceftazidime is a semisynthetic third-generation cephalosporin with notable activity against Pseudomonas aeruginosa (O’Callaghan et al., 1980; Verbist and Verhaegen, 1981).
Mar 24,2022 APICefixime: Antimicrobial Activity, Susceptibility, Administration and Dosage, Clinical Uses etc.
Cefixime is an orally administered cephalosporin with a broader antimicrobial spectrum than those of earlier oral cephalosporins, such as cephalexin and cefaclor.
Mar 24,2022 API












