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Technical details about Biperiden Lactate, learn more about the structure, uses, toxicity, action, side effects and more

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$ API Ref.Price (USD/KG) : 22,993Xls
2D Structure
Also known as: Akineton, 09td6c5147, 1-piperidinepropanol, alpha-bicyclo(2.2.1)hept-5-en-2-yl-alpha-phenyl-, compd. with 2-hydroxypropanoic acid (1:1), Tasmolin (tn), Akineton lactate, Einecs 230-388-9
Molecular Formula
C24H35NO4
Molecular Weight
401.5  g/mol
InChI Key
GLPUBCPQWZZFNJ-UHFFFAOYSA-N
FDA UNII
09TD6C5147

1 2D Structure

2D Structure

2 Identification
2.1 Computed Descriptors
2.1.1 IUPAC Name
1-(2-bicyclo[2.2.1]hept-5-enyl)-1-phenyl-3-piperidin-1-ylpropan-1-ol;2-hydroxypropanoic acid
2.1.2 InChI
InChI=1S/C21H29NO.C3H6O3/c23-21(19-7-3-1-4-8-19,11-14-22-12-5-2-6-13-22)20-16-17-9-10-18(20)15-17;1-2(4)3(5)6/h1,3-4,7-10,17-18,20,23H,2,5-6,11-16H2;2,4H,1H3,(H,5,6)
2.1.3 InChI Key
GLPUBCPQWZZFNJ-UHFFFAOYSA-N
2.1.4 Canonical SMILES
CC(C(=O)O)O.C1CCN(CC1)CCC(C2CC3CC2C=C3)(C4=CC=CC=C4)O
2.2 Other Identifiers
2.2.1 UNII
09TD6C5147
2.3 Synonyms
2.3.1 MeSH Synonyms

1. Biperidene Lactate

2.3.2 Depositor-Supplied Synonyms

1. Akineton

2. 09td6c5147

3. 1-piperidinepropanol, Alpha-bicyclo(2.2.1)hept-5-en-2-yl-alpha-phenyl-, Compd. With 2-hydroxypropanoic Acid (1:1)

4. Tasmolin (tn)

5. Akineton Lactate

6. Einecs 230-388-9

7. Biperidenlactat

8. Unii-09td6c5147

9. Biperiden Lactate [usp:ban:jan]

10. Biperidenlactate

11. Alpha-5-norbornen-2-yl-alpha-phenyl-1-piperidinepropanol Lactate (salt)

12. Alpha-5-norbornen-2-yl-alpha-phenyl-1-piperidinepropanol Compd. With Lactic Acid (1:1)

13. Schembl41834

14. Biperiden Lactate (jan/usp)

15. Biperiden Lactate [jan]

16. Chembl1201067

17. Biperiden Lactate [vandf]

18. Dtxsid40991120

19. Biperiden Lactate [mart.]

20. Biperiden Lactate [who-dd]

21. Hy-13204b

22. Biperiden Lactate [orange Book]

23. Biperiden Lactate [usp Impurity]

24. Lactic Acid, Compd. With Alpha-5-norbornen-2-yl-alpha-phenyl-1-piperidinepropanol (1:1)

25. Lactic Acid, Compound With Alpha-bicyclo(2.2.1)hept-5-en-2-yl-alpha-phenylpiperidin-1-propanol (1:1)

26. Cs-0030940

27. D02247

28. Q27236503

29. .alpha.-5-norbornen-2-yl-.alpha.-phenyl-1-piperidinepropanol Lactate (salt)

30. 1-(2-bicyclo[2.2.1]hept-5-enyl)-1-phenyl-3-piperidin-1-ylpropan-1-ol;2-hydroxypropanoic Acid

31. 1-piperidinepropanol, .alpha.-bicyclo(2.2.1)hept-5-en-2-yl-.alpha.-phenyl-, Compd. With 2-hydroxypropanoic Acid (1:1)

2.4 Create Date
2005-06-24
3 Chemical and Physical Properties
Molecular Weight 401.5 g/mol
Molecular Formula C24H35NO4
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count5
Rotatable Bond Count6
Exact Mass401.25660860 g/mol
Monoisotopic Mass401.25660860 g/mol
Topological Polar Surface Area81 Ų
Heavy Atom Count29
Formal Charge0
Complexity481
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count5
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently Bonded Unit Count2
4 Pharmacology and Biochemistry
4.1 MeSH Pharmacological Classification

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.)


Antiparkinson Agents

Agents used in the treatment of Parkinson's disease. The most commonly used drugs act on the dopaminergic system in the striatum and basal ganglia or are centrally acting muscarinic antagonists. (See all compounds classified as Antiparkinson Agents.)


Parasympatholytics

Agents that inhibit the actions of the parasympathetic nervous system. The major group of drugs used therapeutically for this purpose is the MUSCARINIC ANTAGONISTS. (See all compounds classified as Parasympatholytics.)