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Technical details about NCGC00024357-07, learn more about the structure, uses, toxicity, action, side effects and more

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2D Structure
Also known as: 114-49-8, Scopolamine hbr, Hyoscine hydrobromide, Scopos, (-)-scopolamine hydrobromide, Scopolamine (hydrobromide)
Molecular Formula
C17H22BrNO4
Molecular Weight
384.3  g/mol
InChI Key
WTGQALLALWYDJH-WYHSTMEOSA-N
FDA UNII
R3K67DRL3J

An alkaloid from SOLANACEAE, especially DATURA and SCOPOLIA. Scopolamine and its quaternary derivatives act as antimuscarinics like ATROPINE, but may have more central nervous system effects. Its many uses include an anesthetic premedication, the treatment of URINARY INCONTINENCE and MOTION SICKNESS, an antispasmodic, and a mydriatic and cycloplegic.
1 2D Structure

2D Structure

2 Identification
2.1 Computed Descriptors
2.1.1 IUPAC Name
[(1R,2R,4S,5S)-9-methyl-3-oxa-9-azatricyclo[3.3.1.02,4]nonan-7-yl] (2S)-3-hydroxy-2-phenylpropanoate;hydrobromide
2.1.2 InChI
InChI=1S/C17H21NO4.BrH/c1-18-13-7-11(8-14(18)16-15(13)22-16)21-17(20)12(9-19)10-5-3-2-4-6-10;/h2-6,11-16,19H,7-9H2,1H3;1H/t11?,12-,13-,14+,15-,16+;/m1./s1
2.1.3 InChI Key
WTGQALLALWYDJH-WYHSTMEOSA-N
2.1.4 Canonical SMILES
CN1C2CC(CC1C3C2O3)OC(=O)C(CO)C4=CC=CC=C4.Br
2.1.5 Isomeric SMILES
CN1[C@@H]2CC(C[C@H]1[C@H]3[C@@H]2O3)OC(=O)[C@H](CO)C4=CC=CC=C4.Br
2.2 Other Identifiers
2.2.1 UNII
R3K67DRL3J
2.3 Synonyms
2.3.1 MeSH Synonyms

1. Boro Scopol

2. Boro-scopol

3. Hyoscine

4. Isopto Hyoscine

5. Kwells

6. Scoburen

7. Scopace

8. Scopoderm Tts

9. Scopolamine

10. Scopolamine Cooper

11. Transderm Scop

12. Transderm V

13. Transderm-v

14. Travacalm Ho

15. Vorigeno

2.3.2 Depositor-Supplied Synonyms

1. 114-49-8

2. Scopolamine Hbr

3. Hyoscine Hydrobromide

4. Scopos

5. (-)-scopolamine Hydrobromide

6. Scopolamine (hydrobromide)

7. Beldavrin

8. Scopamin

9. Tranaxine

10. Hyosol

11. Hyoscine Bromide

12. (-)-hyoscine Hydrobromide

13. Scopolaminium Bromide

14. Scopolammonium Bromide

15. Scopine Hydrobromide

16. Euscopol

17. Isoscopil

18. Hysco

19. Kwells

20. (-)-scopolamine Bromide

21. Scopolamine Bromide

22. Scopolamine Hydrobromide Anhydrous

23. R3k67drl3j

24. L-hyoscine Hydrobromide

25. Sereen

26. Mls000069527

27. L-scopolamine-hydrobromide

28. Chebi:61271

29. Smr000058594

30. Dsstox_cid_12029

31. Dsstox_rid_78902

32. Dsstox_gsid_32029

33. Cas-114-49-8

34. Unii-r3k67drl3j

35. Einecs 204-050-6

36. Nsc 61806

37. Nsc-61806

38. Opera_id_496

39. Ec 204-050-6

40. Hyoscine Bromide (anhydrous)

41. Schembl40627

42. Scopolamine Bromide (anhydrous)

43. Chembl3185877

44. Dtxsid0032029

45. Hy-n0296a

46. Scopolaminium Bromide (anhydrous)

47. Regid_for_cid_6603108

48. Scopolammonium Bromide (anhydrous)

49. 672-21-9

50. Scopolamine Hydrobromide (anhydrous)

51. Tox21_110035

52. Tox21_302019

53. (-)-scopolamine Bromide (anhydrous)

54. S2508

55. Scopolamine Hydrobromide [mi]

56. (-)-hyoscine Hydrobromide (anhydrous)

57. Akos015965267

58. Hyoscine Hydrobromide [who-dd]

59. Tox21_110035_1

60. Ac-3389

61. Ccg-268451

62. Cs-2000

63. 1alphah,5alphah-tropan-3-alpha-ol, 5beta,7beta-epoxy-, (-)-tropate (ester), Hydrobromide

64. Ncgc00013722-01

65. Ncgc00024357-07

66. Ncgc00255166-01

67. (-)-scopolamine Hydrobromide (anhydrous)

68. As-35324

69. N2570

70. Sw199343-2

71. 114s498

72. A935283

73. Sr-01000597758

74. Sr-01000597758-1

75. W-108599

76. Q27130957

77. (-)-scopolamine Hydrobromide;hyoscine Hydrobromide;scopine Hydrobromide

78. 1alphah,5alphah-tropan-3alpha-ol, 6beta,7beta-epoxy-, (-)-tropate (ester), Hydrobromide

79. (?,s)-?-(hydroxymethyl)benzeneacetic Acid (1?,2?,4?,5?,7?)-9-methyl-3-oxa-9-azatricyclo[3.3.1.02,4]non-7-yl Ester Hydrobromide

80. (1r,2r,4s,5s,7s)-9-methyl-3-oxa-9-azatricyclo[3.3.1.0(2,4)]non-7-yl (2s)-3-hydroxy-2-phenylpropanoate Hydrobromide

81. (1r,2r,4s,5s,7s,9s)-7-{[(2s)-3-hydroxy-2-phenylpropanoyl]oxy}-9-methyl-3-oxa-9-azoniatricyclo[3.3.1.0(2,4)]nonane Bromide

82. 1-alpha-h,5-alpha-h-tropan-3-alpha-ol, 6-beta,7-beta-epoxy-, (-)-tropate (ester), Hydrobromide

83. 6.beta.,7.beta.-epoxy-1.alpha.h,5.alpha.h-tropan-3.alpha.-ol (-)-tropate (ester) Hydrobromide

84. Benzeneacetic Acid, .alpha.-(hydroxymethyl)-, (1.alpha.,2.beta.,4.beta.,5.alpha.,7.beta.)-9-methyl-3-oxa-9-azatricyclo3.3.1.02,4non-7-yl Ester, (.alpha.s)- Hydrobromide

85. Benzeneacetic Acid, Alpha-(hydroxymethyl)-, (1alpha,2beta,4beta,5alpha,7beta)-9-methyl-3-oxa-9-azatricyclo(3.3.1.02,4)non-7-yl Ester, Hydrobromide (1:1), (alphas)-

86. Benzeneacetic Acid, Alpha-(hydroxymethyl)-, (1alpha,2beta,4beta,5alpha,7beta)-9-methyl-3-oxa-9-azatricyclo(3.3.1.02,4)non-7-yl Ester, Hydrobromide, (alphas)-

87. Benzeneacetic Acid, Alpha-(hydroxymethyl)-, 9-methyl-3-oxa-9-azatricyclo(3.3.1.02,4)non-7-yl Ester, Hydrobromide, (7(s)-(1alpha,2beta,4beta,5alpha,7beta))-

2.4 Create Date
2006-05-25
3 Chemical and Physical Properties
Molecular Weight 384.3 g/mol
Molecular Formula C17H22BrNO4
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count5
Rotatable Bond Count5
Exact Mass383.07322 g/mol
Monoisotopic Mass383.07322 g/mol
Topological Polar Surface Area62.3 Ų
Heavy Atom Count23
Formal Charge0
Complexity418
Isotope Atom Count0
Defined Atom Stereocenter Count5
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently Bonded Unit Count2
4 Pharmacology and Biochemistry
4.1 MeSH Pharmacological Classification

Adjuvants, Anesthesia

Agents that are administered in association with anesthetics to increase effectiveness, improve delivery, or decrease required dosage. (See all compounds classified as Adjuvants, Anesthesia.)


Antiemetics

Drugs used to prevent NAUSEA or VOMITING. (See all compounds classified as Antiemetics.)


Cholinergic Antagonists

Drugs that bind to but do not activate CHOLINERGIC RECEPTORS, thereby blocking the actions of ACETYLCHOLINE or cholinergic agonists. (See all compounds classified as Cholinergic Antagonists.)


Muscarinic Antagonists

Drugs that bind to but do not activate MUSCARINIC RECEPTORS, thereby blocking the actions of endogenous ACETYLCHOLINE or exogenous agonists. Muscarinic antagonists have widespread effects including actions on the iris and ciliary muscle of the eye, the heart and blood vessels, secretions of the respiratory tract, GI system, and salivary glands, GI motility, urinary bladder tone, and the central nervous system. (See all compounds classified as Muscarinic Antagonists.)


Mydriatics

Agents that dilate the pupil. They may be either sympathomimetics or parasympatholytics. (See all compounds classified as Mydriatics.)


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