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    Lasalocid A Sodium

    ACTIVE PHARMA INGREDIENTS

    FINISHED DOSAGE FORMULATIONS

    MARKET PLACE

    PharmaCompass
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    2D Structure
    Also known as: 25999-20-6, Bovatec, Avatec, Lasalocid a sodium salt, Lasalocid a sodium, Lasalocid sodium salt
    Molecular Formula
    C34H53NaO8
    Molecular Weight
    612.8  g/mol
    InChI Key
    RDHDUYAKDYQPEW-HWLWSTNVSA-M
    FDA UNII
    W2S5C71Y3G
    Cationic ionophore antibiotic obtained from Streptomyces lasaliensis that, among other effects, dissociates the calcium fluxes in muscle fibers. It is used as a coccidiostat, especially in poultry.
    1 2D Structure

    2D Structure

    2 Identification
    2.1 Computed Descriptors
    2.1.1 IUPAC Name
    sodium;6-[(3R,4S,5S,7R)-7-[(2S,3S,5S)-5-ethyl-5-[(2R,5R,6S)-5-ethyl-5-hydroxy-6-methyloxan-2-yl]-3-methyloxolan-2-yl]-4-hydroxy-3,5-dimethyl-6-oxononyl]-2-hydroxy-3-methylbenzoate
    2.1.2 InChI
    InChI=1S/C34H54O8.Na/c1-9-25(31-21(6)18-34(11-3,42-31)26-16-17-33(40,10-2)23(8)41-26)30(37)22(7)28(35)19(4)12-14-24-15-13-20(5)29(36)27(24)32(38)39;/h13,15,19,21-23,25-26,28,31,35-36,40H,9-12,14,16-18H2,1-8H3,(H,38,39);/q;+1/p-1/t19-,21+,22+,23+,25+,26-,28+,31+,33-,34+;/m1./s1
    2.1.3 InChI Key
    RDHDUYAKDYQPEW-HWLWSTNVSA-M
    2.1.4 Canonical SMILES
    CCC(C1C(CC(O1)(CC)C2CCC(C(O2)C)(CC)O)C)C(=O)C(C)C(C(C)CCC3=C(C(=C(C=C3)C)O)C(=O)[O-])O.[Na+]
    2.1.5 Isomeric SMILES
    CC[C@H]([C@@H]1[C@H](C[C@@](O1)(CC)[C@H]2CC[C@@]([C@@H](O2)C)(CC)O)C)C(=O)[C@@H](C)[C@H]([C@H](C)CCC3=C(C(=C(C=C3)C)O)C(=O)[O-])O.[Na+]
    2.2 Other Identifiers
    2.2.1 UNII
    W2S5C71Y3G
    2.3 Synonyms
    2.3.1 MeSH Synonyms

    1. Avatec

    2. Lasalocid

    3. Lasalocid A

    4. Ro 2 2985

    5. Ro 2-2985

    6. Ro 22985

    7. X-537a

    2.3.2 Depositor-Supplied Synonyms

    1. 25999-20-6

    2. Bovatec

    3. Avatec

    4. Lasalocid A Sodium Salt

    5. Lasalocid A Sodium

    6. Lasalocid Sodium Salt

    7. Sodium Lasalocid

    8. Sodium Lasalocid A

    9. Lasalocid (sodium)

    10. Bovatec 150fp

    11. Lasalocid A Monosodium Salt

    12. Mt 2007

    13. Lascaloid

    14. Mls001304052

    15. W2s5c71y3g

    16. Lasalocid A Sodium Salt Solution

    17. Smr000538906

    18. Mt2007

    19. Sodium;6-[(3r,4s,5s,7r)-7-[(2s,3s,5s)-5-ethyl-5-[(2r,5r,6s)-5-ethyl-5-hydroxy-6-methyloxan-2-yl]-3-methyloxolan-2-yl]-4-hydroxy-3,5-dimethyl-6-oxononyl]-2-hydroxy-3-methylbenzoate

    20. Bovate 20

    21. Nsc243046

    22. Nsc-243046

    23. Unii-w2s5c71y3g

    24. Lasalocid-na

    25. Lasalocid-a Sodium

    26. Ncgc00095029-01

    27. Einecs 247-400-3

    28. Cas-25999-20-6

    29. Nsc 243046

    30. Ro 2-2985 Sodium

    31. Ionophore X-537a Sodium

    32. Antibiotic X-537a Sodium

    33. Dsstox_cid_25895

    34. Dsstox_rid_81207

    35. Dsstox_gsid_45895

    36. Mls001173429

    37. Mls001334026

    38. Mls001334027

    39. Mls006011597

    40. Chembl1489769

    41. Dtxsid9045895

    42. Bdbm79589

    43. Chebi:91848

    44. Cid_6426773

    45. Hy-b1071a

    46. Lasalocid Sodium [mart.]

    47. Hms2097f17

    48. Hms2235p08

    49. Np167

    50. Sodium 6-[(3r,4s,5s,7r)-7-{(2s,3s,5s)-5-ethyl-5-[(2r,5r,6s)-5-ethyl-5-hydroxy-6-methyltetrahydro-2h-pyran-2-yl]-3-methyltetrahydrofuran-2-yl}-4-hydroxy-3,5-dimethyl-6-oxononyl]-2-hydroxy-3-methylbenzoate

    51. Tox21_111396

    52. Mfcd00078065

    53. Lasalocid Sodium [green Book]

    54. Akos025311506

    55. Cs-5930

    56. 6-(7-(5-ethyl-5-(5-ethyltetrahydro-5-hydroxy-6-methyl-2h-pyran-2-yl)tetrahydro-3-methyl-2-furanyl)-4-hydroxy-3,5-dimethyl-6-oxononyl)-2-hydroxy-3-methylbenzoic Acid Monosodium Salt, (2r-(2alpha(2s*(3r*,4s*,5s*,7r*),3s*,5s*),5alpha,6beta))-

    57. Antibiotic X-537a Sodiumlasalocid-a Sodium

    58. Lasalocid A Sodium 100 Microg/ml In Methanol

    59. Lasalocid A Sodium 100 Microg/ml In Acetonitrile

    60. J-016217

    61. Q27292230

    62. Lasalocid A Sodium Salt (solution In Acetonitrile 0.2mg/2ml)

    63. Lasalocid A Sodium Salt Solution, ~100 Microg/ml In Acetonitrile

    64. Lasalocid-a Sodium; Ionophore X-537a Sodium; Antibiotic X-537a

    65. 2,3-cresotic Acid, 6-(7-(5-ethyl-5-(5-ethyltetrahydro-5-hydroxy-6-methyl-2h-pyran-2-yl)tetrahydro-3-methyl-2-furyl)-4-hydroxy-3,5-dimethyl-6-oxononyl)-, Monosodium Salt. (-)-

    66. Benzoic Acid, 6-((3r,4s,5s,7r)-7-((2s,3s,5s)-5-ethyl-5-((2r,5r,6s)-5-ethyltetrahydro-5-hydroxy-6-methyl-2h-pyran-2-yl)tetrahydro-3-furanyl)-4-hydroxy-3,5-dimethyl-6-oxononyl)-2-hydroxy-3-methyl-, Monosodium Salt

    67. Benzoic Acid, 6-((3r,4s,5s,7r)-7-((2s,3s,5s)-5-ethyl-5-((2r,5r,6s)-5-ethyltetrahydro-5-hydroxy-6-methyl-2h-pyran-2-yl)tetrahydro-3-methyl-2-furanyl)-4-hydroxy-3,5-dimethyl-6-oxononyl)-2-hydroxy-3-methyl-, Sodium Salt (1:1)

    68. Benzoic Acid, 6-(7-(5-ethyl-5-(5-ethyltetrahydro-5-hydroxy-6-methyl-2h-pyran-2-yl)tetrahydro-3-methyl-2-furanyl)-4-hydroxy-3,5-dimethyl-6-oxononyl)-2-hydroxy-3-methyl-, Monosodium Salt, (2r-(2alpha(2s*(3r*,4s*,5s*,7r*),3s*,5s*),5alpha,6beta))-

    69. Benzoic Acid,6-[(3r,4s,5s,7r)-7-[(2s,3s,5s)-5-ethyl-5-[(2r,5r,6s)-5-ethyltetrahydro-5-hydroxy-6-methyl-2h-pyran-2-yl]tetrahydro-3-methyl-2-furanyl]-4-hydroxy-3,5-dimethyl-6-oxononyl]-2-hydroxy-3-methy

    70. Lasalocid A Sodium Salt Solution, 100 Mug/ml In Acetonitrile, Vetranal(tm), Analytical Standard

    71. Sodium (1s,9s)-1,5:6,9-dianhydro-9-[(3r,5s,6s,7r)-9-(2-carboxylato-3-hydroxy-4-methylphenyl)-6-hydroxy-5,7-dimethyl-4-oxononan-3-yl]-3,4,7,8-tetradeoxy-6-ethyl-2-c-ethyl-1,8-dimethyl-d-galacto-nonitol

    2.4 Create Date
    2006-04-28
    3 Chemical and Physical Properties
    Molecular Weight 612.8 g/mol
    Molecular Formula C34H53NaO8
    Hydrogen Bond Donor Count3
    Hydrogen Bond Acceptor Count8
    Rotatable Bond Count13
    Exact Mass612.36381293 g/mol
    Monoisotopic Mass612.36381293 g/mol
    Topological Polar Surface Area136 Ų
    Heavy Atom Count43
    Formal Charge0
    Complexity917
    Isotope Atom Count0
    Defined Atom Stereocenter Count10
    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

    Anti-Bacterial Agents

    Substances that inhibit the growth or reproduction of BACTERIA. (See all compounds classified as Anti-Bacterial Agents.)

    Ionophores

    Chemical agents that increase the permeability of biological or artificial lipid membranes to specific ions. Most ionophores are relatively small organic molecules that act as mobile carriers within membranes or coalesce to form ion permeable channels across membranes. Many are antibiotics, and many act as uncoupling agents by short-circuiting the proton gradient across mitochondrial membranes. (See all compounds classified as Ionophores.)

    Coccidiostats

    Agents useful in the treatment or prevention of COCCIDIOSIS in man or animals. (See all compounds classified as Coccidiostats.)