Thioacetazone

Chemical compound
  • J04AM04 (WHO)
Identifiers
  • N-{4-[(Ethanethioamidoimino)methyl]phenyl}acetamide
CAS Number
  • 104-06-3 ☒N
PubChem CID
  • 9568512
ChemSpider
  • 7843221 checkY
UNII
  • MMG78X7SSR
KEGG
  • D08584 checkY
ChEMBL
  • ChEMBL375492 checkY
CompTox Dashboard (EPA)
  • DTXSID2022593 Edit this at Wikidata
ECHA InfoCard100.002.882 Edit this at WikidataChemical and physical dataFormulaC10H12N4OSMolar mass236.29 g·mol−13D model (JSmol)
  • Interactive image
  • O=C(Nc1ccc(cc1)\C=N\NC(=S)N)C
InChI
  • InChI=1S/C10H12N4OS/c1-7(15)13-9-4-2-8(3-5-9)6-12-14-10(11)16/h2-6H,1H3,(H,13,15)(H3,11,14,16)/b12-6+ checkY
  • Key:SRVJKTDHMYAMHA-WUXMJOGZSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Thioacetazone (INN, BAN), also known as amithiozone (USAN), is an oral antibiotic which is used in the treatment of tuberculosis.[1][2][3][4] It has fallen into almost complete disuse due to toxicity and the introduction of improved anti-tuberculosis drugs like isoniazid.[5] The drug has only weak activity against Mycobacterium tuberculosis and is only useful in preventing resistance to more powerful drugs such as isoniazid and rifampicin. It is never used on its own to treat tuberculosis; it is used in a similar way to ethambutol.

There is no advantage to using thioacetazone if the regimen used already contains ethambutol, but many countries in sub-Saharan Africa still use thioacetazone because it is extremely cheap. Use of thioacetazone is declining because it can cause severe (sometimes fatal) skin reactions in HIV positive patients.[6][7]

The biological target of thioacetazone has proven elusive and its mechanism of action remains unknown, although it is thought to interfere with mycolic acid synthesis.[4]

Adverse effects

One of the documented adverse effects of thioacetazone is the excessive accumulation of serum (or blood plasma) in the brain. Another is weakening of the thyroid glands. These were found in a treatment combining conteben with PAS acid p-amino-salicylic acid.[8]

See also

References

  1. ^ Buckingham J (2 December 1993). Dictionary of Natural Products. CRC Press. pp. 208–. ISBN 978-0-412-46620-5.
  2. ^ Martindale: The Extra Pharmacopoeia (30th ed.). London: The Pharmaceutical Press. 1993. p. 217. ISBN 978-0-85369-300-0.
  3. ^ "List of Antituberculosis agents - Generics Only". Drugs.com.
  4. ^ a b Grayson ML, Crowe SM, McCarthy JS, Mills J, Mouton JW, Norrby SR, Paterson DL, Pfaller MA (29 October 2010). "Thioacetazone". Kucers' The Use of Antibiotics: A Clinical Review of Antibacterial, Antifungal and Antiviral Drugs (Sixth ed.). CRC Press. pp. 1673–. ISBN 978-1-4441-4752-0.
  5. ^ Schaaf HS, Seddon JA, Caminero JA (2011). "Second-line Antituberculosis Drugs: Current Knowledge, Recent Research Findings and Controversies". In Donald PR, Van Helden PD (eds.). Antituberculosis Chemotherapy. Karger Medical and Scientific Publishers. pp. 92–. ISBN 978-3-8055-9627-5.
  6. ^ Rieder HL, Arnadottir T, Trébucq A, Enarson DA (January 2001). "Tuberculosis treatment: dangerous regimens?". The International Journal of Tuberculosis and Lung Disease. 5 (1): 1–3. PMID 11263509.
  7. ^ Nunn P, Porter J, Winstanley P (1993). "Thiacetazone--avoid like poison or use with care?". Transactions of the Royal Society of Tropical Medicine and Hygiene. 87 (5): 578–582. doi:10.1016/0035-9203(93)90096-9. PMID 7505496.
  8. ^ Bergqvist N, De Mare O (August 1952). "Hypothyroidism and cerebral edema following combined treatment of tuberculosis with conteben (TB I 698) and p-amino-salicylic acid". Acta Medica Scandinavica. 143 (5): 323–335. doi:10.1111/j.0954-6820.1952.tb14267.x. PMID 12976024.

External links

  • "Conteben". Chemindustry. Archived from the original on 23 February 2012.
  • "Wie einst Robert Koch". Der Spiegel Wissenschaft. 25 December 1951. Im November 1947 macht der für alles Neue aufgeschlossene Freiburger Internist Professor Dr. Ludwig Heilmeyer, ein Mitschüler des Atomphysikers Heisenberg, die erste schwache Andeutung, daß sich Domagks Präparat in seiner Klinik zu bewähren scheine. Genaue Zahlen gibt aber erst drei Monate später ein bis dahin unbekannter Arzt, Dr. Berthold Mikat, der nur in Vertretung seines Chefs, Dr. Fritz Kuhlmann aus Mölln, spricht: Im Krankenhaus der Landesversicherungsanstalt Schleswig-Holstein ist nach Tb I-Behandlung bei 49 von 66 Patienten mit Lungentuberkulose eindeutige Besserung nachgewiesen worden. Das ist der Start für die Einführung des Tb I, das später den Namen Conteben bekommt.
30S
Aminoglycosides
(initiation inhibitors)
-mycin (Streptomyces)
-micin (Micromonospora)
other
Tetracycline antibiotics
(tRNA binding)
Tetracyclines
Glycylcyclines
50S
Oxazolidinone
(initiation inhibitors)
Peptidyl transferase
Amphenicols
Pleuromutilins
MLS (transpeptidation/translocation)
Macrolides
Ketolides
Lincosamides
Streptogramins
EF-G
Steroid antibacterials
  • v
  • t
  • e
Beta-lactams
(inhibit synthesis
of peptidoglycan
layer of bacterial
cell wall by binding
to and inhibiting
PBPs, a group of
D-alanyl-D-alanine
transpeptidases)
Penicillins (Penams)
Narrow
spectrum
β-lactamase sensitive
(1st generation)
β-lactamase resistant
(2nd generation)
Extended
spectrum
Aminopenicillins (3rd generation)
Carboxypenicillins (4th generation)
Ureidopenicillins (4th generation)
Other
Carbapenems / Penems
Cephems
Cephalosporins
Cephamycins
Carbacephems
1st generation
2nd generation
3rd generation
4th generation
5th generation
Siderophore
Veterinary
Monobactams
β-lactamase inhibitors
Combinations
Polypeptides
Glycopeptides
Lipoglycopeptides
Lipopeptides
Polymyxins
Other
  • Inhibits PG elongation and crosslinking: Ramoplanin§
Intracellular
Other
  • v
  • t
  • e
Antifolates
(inhibit bacterial
purine metabolism,
thereby inhibiting
DNA and RNA
synthesis)
DHFR inhibitor
Sulfonamides
(DHPS inhibitor)
Short-acting
Intermediate-acting
Long-acting
Other/ungrouped
Combinations
Other DHPS inhibitors
Quinolones
(inhibit bacterial
topoisomerase
and/or DNA gyrase,
thereby inhibiting
DNA replication)
1st generation
Fluoroquinolones
2nd generation
3rd generation
4th generation
Veterinary
Newer non-fluorinated
Related (DG)
Anaerobic DNA
inhibitors
Nitroimidazole derivatives
Nitrofuran derivatives
RNA synthesis
Rifamycins/
RNA polymerase
Lipiarmycins