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DSSTox_CID_3280
Also known as: Metharbitone, Methylbarbital, Gemonil, Metabarbital, N-methylbarbital, Endiemalum
Molecular Formula
C9H14N2O3
Molecular Weight
198.22  g/mol
InChI Key
FWJKNZONDWOGMI-UHFFFAOYSA-N
FDA UNII
02OS7K758T

Metharbital is a barbiturate anticonvulsant, similar to phenobarbital, marketed as Gemonil by Abbott Laboratories. It was patented in 1905 by Emil Fischer of Merck.
1 2D Structure

DSSTox_CID_3280

2 Identification
2.1 Computed Descriptors
2.1.1 IUPAC Name
5,5-diethyl-1-methyl-1,3-diazinane-2,4,6-trione
2.1.2 InChI
InChI=1S/C9H14N2O3/c1-4-9(5-2)6(12)10-8(14)11(3)7(9)13/h4-5H2,1-3H3,(H,10,12,14)
2.1.3 InChI Key
FWJKNZONDWOGMI-UHFFFAOYSA-N
2.1.4 Canonical SMILES
CCC1(C(=O)NC(=O)N(C1=O)C)CC
2.2 Other Identifiers
2.2.1 UNII
02OS7K758T
2.3 Synonyms
2.3.1 MeSH Synonyms

1. Endiemal

2. Metharbitone

3. Methobarbitone

2.3.2 Depositor-Supplied Synonyms

1. Metharbitone

2. Methylbarbital

3. Gemonil

4. Metabarbital

5. N-methylbarbital

6. Endiemalum

7. Metharbutal

8. 50-11-3

9. 1-methylbarbital

10. Endiemal

11. Gemonit

12. 5,5-diethyl-1-methylbarbituric Acid

13. 5,5-diethyl-1-methyl-1,3-diazinane-2,4,6-trione

14. Sch 412

15. An 23

16. Metharbital Ciii

17. Nsc 27156

18. 2,4,6(1h,3h,5h)-pyrimidinetrione, 5,5-diethyl-1-methyl-

19. Barbituric Acid, 5,5-diethyl-1-methyl-

20. Methabarbital

21. Nsc-27156

22. 5,5-diethyl-1-methylpyrimidine-2,4,6(1h,3h,5h)-trione

23. Methabarbitone

24. Metarbitale [dcit]

25. 02os7k758t

26. Metharbital Ciii (200 Mg)

27. Metarbital [inn-spanish]

28. Ncgc00181148-01

29. Metarbitale

30. Metharbitalum

31. Metarbital

32. Metharbitalum [inn-latin]

33. Gemonil (tn)

34. Metharbital (jan/inn)

35. Einecs 200-011-2

36. Brn 0184688

37. Unii-02os7k758t

38. 5,5-diethyl-1-methyl-2,4,6(1h,3h,5h)-pyrimidinetrione

39. Metharbital [usp:inn:ban:jan]

40. Metharbital [mi]

41. Metharbital [inn]

42. Metharbital [jan]

43. Dsstox_cid_3280

44. Chembl450

45. Metharbital [vandf]

46. Dsstox_rid_76955

47. Metharbital [mart.]

48. Dsstox_gsid_23280

49. Schembl78867

50. Metharbital [who-dd]

51. 5-24-09-00144 (beilstein Handbook Reference)

52. Gtpl7230

53. Dtxsid6023280

54. Schembl22556220

55. Chebi:31827

56. Metharbital [orange Book]

57. Metharbital 1.0 Mg/ml In Methanol

58. Nsc27156

59. Zinc5508997

60. Tox21_112752

61. Barbituric Acid,5-diethyl-1-methyl-

62. 1-methyl-5,5-diethyl Barbituric Acid

63. Akos006239548

64. Wln: T6vmvnv Fhj D1 F2 F2

65. Db00463

66. Cas-50-11-3

67. Ft-0692647

68. 5,5-diethyl-1-methyl-barbituric-acid

69. D01382

70. Q1176294

71. 5,5-diethyl-1-methyl-2,4,6-trioxo-hexahydropyrimidine

72. Z2205958937

73. 2,6(1h,3h,5h)-pyrimidinetrione, 5,5-diethyl-1-methyl-

74. 5,5-diethyl-1-methyl-2,4,6(1h,3h,5h)-pyrimidinetrione #

75. 5,5-diethyl-6-hydroxy-3-methyl-2,3,4,5-tetrahydropyrimidine-2,4-dione

76. Vok

2.4 Create Date
2005-03-25
3 Chemical and Physical Properties
Molecular Weight 198.22 g/mol
Molecular Formula C9H14N2O3
XLogP31.2
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count3
Rotatable Bond Count2
Exact Mass198.10044231 g/mol
Monoisotopic Mass198.10044231 g/mol
Topological Polar Surface Area66.5 Ų
Heavy Atom Count14
Formal Charge0
Complexity294
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently Bonded Unit Count1
4 Drug and Medication Information
4.1 Drug Indication

Metharbital is used for the treatment of epilepsy.


5 Pharmacology and Biochemistry
5.1 Pharmacology

Metharbital, a barbiturate, is used for the treatment of short term insomnia. It belongs to a group of medicines called central nervous system (CNS) depressants that induce drowsiness and relieve tension or nervousness. Little analgesia is conferred by barbiturates; their use in the presence of pain may result in excitation.


5.2 ATC Code

N - Nervous system

N03 - Antiepileptics

N03A - Antiepileptics

N03AA - Barbiturates and derivatives

N03AA30 - Metharbital


5.3 Mechanism of Action

Metharbital binds at a distinct binding site associated with a Cl- ionopore at the GABAA receptor, increasing the duration of time for which the Cl- ionopore is open. The post-synaptic inhibitory effect of GABA in the thalamus is, therefore, prolonged. All of these effects are associated with marked decreases in GABA-sensitive neuronal calcium conductance (gCa). The net result of barbiturate action is acute potentiation of inhibitory GABAergic tone. Barbiturates also act through potent (if less well characterized) and direct inhibition of excitatory AMPA-type glutamate receptors, resulting in a profound suppression of glutamatergic neurotransmission.


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