Normustine

Nitrogen mustard used as a chemotherapy agent
Normustine
Clinical data
Other namesBis(2-chloroethyl)carbamic acid
Identifiers
  • Bis(2-chloroethyl)carbamic acid
CAS Number
  • 78619-95-1
PubChem CID
  • 18377863
UNII
  • Q2KPX8TH4K
CompTox Dashboard (EPA)
  • DTXSID701337180 Edit this at Wikidata
Chemical and physical data
FormulaC5H9Cl2NO2
Molar mass186.03 g·mol−1
3D model (JSmol)
  • Interactive image
  • C(CCl)N(CCCl)C(=O)O
InChI
  • InChI=1S/C5H9Cl2NO2/c6-1-3-8(4-2-7)5(9)10/h1-4H2,(H,9,10)
  • Key:TTYAKTJQJVVKED-UHFFFAOYSA-N

Normustine, also known as bis(2-chloroethyl)carbamic acid, is a nitrogen mustard and alkylating antineoplastic agent (i.e., chemotherapy agent).[1][2][3] It is a metabolite of a number of antineoplastic agents that have been developed for the treatment of tumors, including estramustine phosphate, alestramustine, cytestrol acetate, and ICI-85966 (stilbostat), but only the former of which has actually been marketed.[1][2][3]

References

  1. ^ a b Brunton L, Chabner B, Knollman B (14 January 2011). Goodman and Gilman's The Pharmacological Basis of Therapeutics, Twelfth Edition. McGraw Hill Professional. p. 1709. ISBN 978-0-07-176939-6.
  2. ^ a b Fox BW, Fox M (6 December 2012). Antitumor Drug Resistance. Springer Science & Business Media. pp. 199–. ISBN 978-3-642-69490-5.
  3. ^ a b Decker M (5 April 2017). Design of Hybrid Molecules for Drug Development. Elsevier Science. pp. 201–. ISBN 978-0-08-101118-8.


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SPs/MIs
(M phase)
Block microtubule assembly
Block microtubule disassembly
DNA replication
inhibitor
DNA precursors/
antimetabolites
(S phase)
Folic acid
Purine
Pyrimidine
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Topoisomerase inhibitors
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I
II
II+Intercalation
Crosslinking of DNA
(CCNS)
Alkylating
Platinum-based
Nonclassical
Intercalation
Photosensitizers/PDTOther
Enzyme inhibitors
Receptor antagonists
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