Metisazone

From Infogalactic: the planetary knowledge core
(Redirected from Methisazone)
Jump to: navigation, search
Metisazone
Skeletal formula of methisazone
Space-filling model of the methisazone molecule
Names
IUPAC name
[(1-Methyl-2-oxoindol-3-ylidene)amino]thiourea
Other names
Metisazone
Identifiers
1910-68-5 YesY
ChEMBL ChEMBL1512080 N
ChemSpider 5259074
EC Number 217-616-2
Jmol 3D model Interactive image
KEGG D02496
MeSH D008720
PubChem 6861563
UNII K3QML4J07E N
  • InChI=1S/C10H10N4OS/c1-14-7-5-3-2-4-6(7)8(9(14)15)12-13-10(11)16/h2-5H,1H3,(H3,11,13,16)/b12-8-
    Key: DLGSOJOOYHWROO-WQLSENKSSA-N
  • InChI=1/C10H10N4OS/c1-14-7-5-3-2-4-6(7)8(9(14)15)12-13-10(11)16/h2-5H,1H3,(H3,11,13,16)/b12-8-
    Key: DLGSOJOOYHWROO-WQLSENKSBL
  • CN1C2=CC=CC=C2C(=NNC(=S)N)C1=O
Properties
C10H10N4OS
Molar mass 234.28 g/mol
Pharmacology
ATC code J05AA01
Vapor pressure {{{value}}}
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

Methisazone (USAN) or metisazone (INN) is an antiviral drug that works by inhibiting mRNA and protein synthesis, especially in pox viruses. It has been used in the past to treat smallpox.[1]

Methisazone has been described as being used in prophylaxis since at least 1965.[2][3]

Synthesis

Methisazone synthesis: Bauer, Sadler, Br. J. Pharmacol. 15, 101 (1960); GB 975357  (1964 to Wellcome Foundation).

When isatin is treated with NaH and MeI, the acidic hydrogen is alkylated to product 2. Then, reaction of the ketone carbonyl with thiosemicarbazine (3) leads to methisazone (4).

References

  1. Methisazone, Merriam-Webster's Medical Dictionary
  2. Lua error in package.lua at line 80: module 'strict' not found.
  3. Lua error in package.lua at line 80: module 'strict' not found.


<templatestyles src="Asbox/styles.css"></templatestyles>