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    Olodaterol Hydrochloride

    ACTIVE PHARMA INGREDIENTS

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    2D Structure
    Also known as: 869477-96-3, Olodaterol hcl, Striverdi respimat, Bi 1744 cl, Bi-1744-cl, Bi 1744 hydrochloride
    Molecular Formula
    C21H27ClN2O5
    Molecular Weight
    422.9  g/mol
    InChI Key
    KCEHVJZZIGJAAW-FERBBOLQSA-N
    FDA UNII
    65R445W3V9
    1 2D Structure

    2D Structure

    2 Identification
    2.1 Computed Descriptors
    2.1.1 IUPAC Name
    6-hydroxy-8-[(1R)-1-hydroxy-2-[[1-(4-methoxyphenyl)-2-methylpropan-2-yl]amino]ethyl]-4H-1,4-benzoxazin-3-one;hydrochloride
    2.1.2 InChI
    InChI=1S/C21H26N2O5.ClH/c1-21(2,10-13-4-6-15(27-3)7-5-13)22-11-18(25)16-8-14(24)9-17-20(16)28-12-19(26)23-17;/h4-9,18,22,24-25H,10-12H2,1-3H3,(H,23,26);1H/t18-;/m0./s1
    2.1.3 InChI Key
    KCEHVJZZIGJAAW-FERBBOLQSA-N
    2.1.4 Canonical SMILES
    CC(C)(CC1=CC=C(C=C1)OC)NCC(C2=C3C(=CC(=C2)O)NC(=O)CO3)O.Cl
    2.1.5 Isomeric SMILES
    CC(C)(CC1=CC=C(C=C1)OC)NC[C@@H](C2=C3C(=CC(=C2)O)NC(=O)CO3)O.Cl
    2.2 Other Identifiers
    2.2.1 UNII
    65R445W3V9
    2.3 Synonyms
    2.3.1 MeSH Synonyms

    1. 6-hydroxy-8-(1-hydroxy-2-((2-(4-methoxyphenyl)-1,1-dimethylethyl)amino)ethyl)-2h-1,4-benzoxazin-3(4h)-one

    2. Bi 1744 Cl

    3. Bi-1744 Cl

    4. Olodaterol

    5. Striverdi Respimat

    2.3.2 Depositor-Supplied Synonyms

    1. 869477-96-3

    2. Olodaterol Hcl

    3. Striverdi Respimat

    4. Bi 1744 Cl

    5. Bi-1744-cl

    6. Bi 1744 Hydrochloride

    7. Bi-1744 Cl

    8. Olodaterol Hydrochloride [usan]

    9. Chebi:83309

    10. Olodaterol (hydrochloride)

    11. 65r445w3v9

    12. 2h-1,4-benzoxazin-3(4h)-one, 6-hydroxy-8-((1r)-1-hydroxy-2-((2-(4-methoxyphenyl)- 1,1-dimethylethyl)amino)ethyl)-, Hydrochloride (1:1)

    13. 6-hydroxy-8-((1r)-1-hydroxy-2-((2-(4-methoxyphenyl)-1,1-dimethylethyl)amino)ethyl)- 2h-1,4-benzoxazin-3(4h)-one Hydrochloride

    14. Striverdi Respimat (tn)

    15. 6-hydroxy-8-[(1r)-1-hydroxy-2-[[1-(4-methoxyphenyl)-2-methylpropan-2-yl]amino]ethyl]-4h-1,4-benzoxazin-3-one;hydrochloride

    16. Unii-65r445w3v9

    17. (r)-6-hydroxy-8-(1-hydroxy-2-((1-(4-methoxyphenyl)-2-methylpropan-2-yl)amino)ethyl)-2h-benzo[b][1,4]oxazin-3(4h)-one Hydrochloride

    18. 869477-96-3 (hcl)

    19. Schembl560669

    20. Bi-1744 Hcl

    21. Chembl2105743

    22. Dtxsid901027733

    23. Amy16778

    24. Bcp16765

    25. Ex-a2815

    26. Olodaterol(bi-1744) Hydrochloride

    27. Bdbm50538807

    28. Hy-14301a

    29. Olodaterol Hydrochloride (jan/usan)

    30. Olodaterol Hydrochloride [mi]

    31. S5925

    32. Akos030524628

    33. Olodaterol Hydrochloride [vandf]

    34. Olodaterol Hydrochloride [who-dd]

    35. Ac-29884

    36. As-58291

    37. Cs-0021887

    38. Olodaterol Hydrochloride [orange Book]

    39. D10020

    40. A862976

    41. Q27156746

    42. 2h-1,4-benzoxazin-3(4h)-one, 6-hydroxy-8-[(1r)-1-hydroxy-2-[[2-(4-methoxyphenyl)-1,1-dimethylethyl]amino]ethyl]-, Hydrochloride (1:1)

    43. 6-hydroxy-8-[(1r)-1-hydroxy-2-{[1-(4-methoxyphenyl)-2-methylpropan-2-yl]amino}ethyl]-2h-1,4-benzoxazin-3(4h)-one Hydrochloride

    44. N-[(2r)-2-hydroxy-2-(6-hydroxy-3-oxo-3,4-dihydro-2h-1,4-benzoxazin-8-yl)ethyl]-1-(4-methoxyphenyl)-2-methylpropan-2-aminium Chloride

    2.4 Create Date
    2006-10-26
    3 Chemical and Physical Properties
    Molecular Weight 422.9 g/mol
    Molecular Formula C21H27ClN2O5
    Hydrogen Bond Donor Count5
    Hydrogen Bond Acceptor Count6
    Rotatable Bond Count7
    Exact Mass422.1608497 g/mol
    Monoisotopic Mass422.1608497 g/mol
    Topological Polar Surface Area100 Ų
    Heavy Atom Count29
    Formal Charge0
    Complexity521
    Isotope Atom Count0
    Defined Atom Stereocenter Count1
    Undefined Atom Stereocenter Count0
    Defined Bond Stereocenter Count0
    Undefined Bond Stereocenter Count0
    Covalently Bonded Unit Count2
    4 Drug and Medication Information
    4.1 Drug Indication

    Treatment of cystic fibrosis

    5 Pharmacology and Biochemistry
    5.1 MeSH Pharmacological Classification

    Bronchodilator Agents

    Agents that cause an increase in the expansion of a bronchus or bronchial tubes. (See all compounds classified as Bronchodilator Agents.)