What molecule am I?


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 4 | H302鈥擧armful if swallowed | ![]() |
*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.
Molecules from the Journals
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Doxycycline聽fast facts
CAS Reg. No. | 564-25-0 |
Empirical formula | C22H24N2O8 |
Molar mass | 444.44 g/mol |
Appearance | Yellow crystals or powder |
Melting point | 201 掳C |
Water solubility | 0.3 g/L (25 潞C) |

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