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    Ifenprodil Tartrate

    ACTIVE PHARMA INGREDIENTS

    DEVELOPMENTS

    DIGITAL CONTENT

    PharmaCompass
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    2D Structure
    Also known as: Ifenprodil tartrate salt, 23210-58-4, Ifenprodil hemitartrate, Prestwick_623, 2-(4-benzylpiperidino)-1-(4-hydroxyphenyl)-1-propanol hemitartrate, Prestwick0_000311
    Molecular Formula
    C25H33NO8
    Molecular Weight
    475.5  g/mol
    InChI Key
    FFYMSFGBEJMSFP-UHFFFAOYSA-N
    1 2D Structure

    2D Structure

    2 Identification
    2.1 Computed Descriptors
    2.1.1 IUPAC Name
    4-[2-(4-benzylpiperidin-1-yl)-1-hydroxypropyl]phenol;2,3-dihydroxybutanedioic acid
    2.1.2 InChI
    InChI=1S/C21H27NO2.C4H6O6/c1-16(21(24)19-7-9-20(23)10-8-19)22-13-11-18(12-14-22)15-17-5-3-2-4-6-17;5-1(3(7)8)2(6)4(9)10/h2-10,16,18,21,23-24H,11-15H2,1H3;1-2,5-6H,(H,7,8)(H,9,10)
    2.1.3 InChI Key
    FFYMSFGBEJMSFP-UHFFFAOYSA-N
    2.1.4 Canonical SMILES
    CC(C(C1=CC=C(C=C1)O)O)N2CCC(CC2)CC3=CC=CC=C3.C(C(C(=O)O)O)(C(=O)O)O
    2.2 Synonyms
    2.2.1 MeSH Synonyms

    1. 2-(4-benzylpiperidino)-1-(4-hydroxyphenyl)-2-methyl-1-ethanol

    2. 4-benzyl-alpha-(p-hydroxyphenyl)-beta-methyl-1-piperidineethanol

    3. 61 91 Rc

    4. Alpha-(4-hydroxyphenyl)-beta-methyl-4-(phenylmethyl)-1-piperidine Ethanol

    5. Ifenprodil

    6. Ifenprodil Hydrochloride

    7. Ifenprodil Hydrochloride, (+-)-isomer

    8. Ifenprodil Tartrate (1:1), (r*,s*)-(+-)-(r-(r*,r*))-isomer

    9. Ifenprodil Tartrate (1:1), (r-(r*,r*))-isomer

    10. Ifenprodil Tartrate (2:1), (r-(r*,r*))-isomer

    11. Ifenprodil, (r*,s*)-(+-)-isomer

    12. Ifenprodil, Tartrate(r-(r*,r*))-isomer

    13. Vadilex

    2.2.2 Depositor-Supplied Synonyms

    1. Ifenprodil Tartrate Salt

    2. 23210-58-4

    3. Ifenprodil Hemitartrate

    4. Prestwick_623

    5. 2-(4-benzylpiperidino)-1-(4-hydroxyphenyl)-1-propanol Hemitartrate

    6. Prestwick0_000311

    7. Prestwick1_000311

    8. Prestwick2_000311

    9. Prestwick3_000311

    10. Lopac0_000661

    11. Bspbio_000302

    12. Mls000069744

    13. Schembl364019

    14. Spbio_002521

    15. Bpbio1_000334

    16. Chembl1256662

    17. Hms1568p04

    18. Hms2095p04

    19. Hms2231m13

    20. Hms3369e02

    21. Hms3712p04

    22. Ccg-220311

    23. Ac-33093

    24. Smr000058797

    25. 210i584

    26. Http://www.dcchemicals.com/product_show-dc23902.html

    27. Sr-01000075169-10

    28. 4-[(1r*,2s*)-2-(4-benzyl-piperidin-1-yl)-1-hydroxy-propyl]-pheno

    29. 4-(2-(4-benzylpiperidin-1-yl)-1-hydroxypropyl)phenol 2,3-dihydroxysuccinate

    30. 4-[2-(4-benzyl-1-piperidyl)-1-hydroxy-propyl]phenol; 2,3-dihydroxybutanedioic Acid

    31. 1-piperidineethanol, .alpha.-(4-hydroxyphenyl)-.beta.-methyl-4-(phenylmethyl)-, 2,3-dihydroxybutanedioate (1:1) (salt)

    2.3 Create Date
    2006-04-14
    3 Chemical and Physical Properties
    Molecular Weight 475.5 g/mol
    Molecular Formula C25H33NO8
    Hydrogen Bond Donor Count6
    Hydrogen Bond Acceptor Count9
    Rotatable Bond Count8
    Exact Mass475.22061701 g/mol
    Monoisotopic Mass475.22061701 g/mol
    Topological Polar Surface Area159 Ų
    Heavy Atom Count34
    Formal Charge0
    Complexity487
    Isotope Atom Count0
    Defined Atom Stereocenter Count0
    Undefined Atom Stereocenter Count4
    Defined Bond Stereocenter Count0
    Undefined Bond Stereocenter Count0
    Covalently Bonded Unit Count2
    4 Pharmacology and Biochemistry
    4.1 MeSH Pharmacological Classification

    Excitatory Amino Acid Antagonists

    Drugs that bind to but do not activate excitatory amino acid receptors, thereby blocking the actions of agonists. (See all compounds classified as Excitatory Amino Acid Antagonists.)

    Vasodilator Agents

    Drugs used to cause dilation of the blood vessels. (See all compounds classified as Vasodilator Agents.)

    Adrenergic alpha-Antagonists

    Drugs that bind to but do not activate alpha-adrenergic receptors thereby blocking the actions of endogenous or exogenous adrenergic agonists. Adrenergic alpha-antagonists are used in the treatment of hypertension, vasospasm, peripheral vascular disease, shock, and pheochromocytoma. (See all compounds classified as Adrenergic alpha-Antagonists.)