Doxycycline

November 11, 2024
I鈥檓 an old-line antibiotic that is still used against many infections.
What molecule am I?
Image of Doxycycline 3D Image of Doxycycline

Doxycycline1 is a venerable antibiotic that was first described in 1958 by Charles R. Stephens and co-workers at Pfizer (Groton, CT). They used catalytic hydrogenolysis of a hydroxyl group in tetracycline2 to , one of which, 伪-6-deoxy-5-hydroxytetracycline (伪-6-DHT), later became known as doxycycline.

In the ensuing years, much more was discovered about 6-deoxytetracyclines.

  • 1960: J. R. D. McCormick and colleagues at American Cyanamid (Pearl River, NY) explored the in 6-deoxytetracyclines.
  • 1962: Stephens et al. at Pfizer studied how the configuration at C6 of 6-deoxytetracyclines affected antibiotic performance against the bacterium Klebsiella pneumoniae; .
  • 1963: The Stephens group expanded on the of 6-deoxytetracyclines, again including 伪-6-DHT.

Doxycycline was approved as a broad-range antibiotic by the US Food and Drug Administration in 1967. It is used ranging from acne to malaria to syphilis to tick-borne pathogens such as cause Lyme disease. It can be administered orally or intravenously. Doxycycline is commercially available as its monohydrate2 and its hyclate3, both of which release doxycycline in the body.

1. SciFindern name: 2-naphthacenecarboxamide, 4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,5,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-, (4S,4aR,5S,5aR,6R,12aS)-.
2.CAS Reg. No. 17086-28-1.
3.CAS Reg. No. 24390-14-5; 鈥渉yclate鈥� is a pharmaceutical term for hydrochloride hemiethanolate hemihydrate.

Doxycycline聽hazard information*

Hazard class**GHS code and hazard statement
Acute toxicity, oral, category 4H302鈥擧armful if swallowedChemical Safety Warning

*No safety data sheets for anhydrous doxycycline are available; data are for the monohydrate.
**Globally Harmonized System (GHS) of Classification and Labeling of Chemicals. .

Molecules from the Journals

Sodium nickelate1 (NaNiO2) is a salt with some unusual chemical and physical properties. It was first prepared in 1954, when Lawrence D. Dyer, Bernard S. Borie Jr., and G. Pedro Smith at Oak Ridge National Laboratory (TN) at 800 潞C. In 1994, Arabinda Ray and collaborators at Sardar Patel University (Vallabh Vidyanagar, India) and the University of Poona (India; now Savitribai Phule Pune University) described how from a solution of carbon in molten NaNiO2 at 鈮�850 潞C.

This past October Liam A. V. Nagle-Cocco and Si芒n E. Dutton at the University of Cambridge (UK) and 11 colleagues in the United Kingdom, the United States, and France described a . The authors believe that 鈥渢his study is the first to show a displacive Jahn鈥揟eller transition in any material using direct observations with local probe techniques.鈥�

Alectinib2 is an oral, highly potent anaplastic lymphoma kinase (ALK) inhibitor for treating ALK-positive non鈥搒mall-cell lung cancer (NSCLC). It was first described in 2010 by Kazutomo Kinoshita and co-inventors in to Chugai Pharmaceutical (Tokyo).

In October, Tomochiro Oki and a large team of co-workers at Chugai reported the development of a . The key to the process was forming the indole-containing tetracyclic core, which was accomplished through an intramolecular reductive cyclization and an intramolecular Friedel鈥揅rafts reaction.

1. CAS Reg. 12164-05-5.
2. CAS Reg. 1256580-46-7.

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Doxycycline聽fast facts

CAS Reg. No.564-25-0
Empirical
formula
C22H24N2O8
Molar mass444.44 g/mol
AppearanceYellow crystals or powder
Melting point201 掳C
Water
solubility
0.3 g/L (25 潞C)
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