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Pimaricin, Streptomyces sp. |产品详情|进口榴莲视频免费观看采购网





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    上海榴莲视频下载地址入口生物科技公司
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    Pimaricin, Streptomyces sp.
    品牌:AG Scientific
    货号:
    规格:100 mg
    货期:

    CAS:7681-93-8Formula:C33H47NO13MW:665.733Appearance:lightyellowSolidPurity:95%byHPLC

    商品详情 参考文献 相关资料

    Pimaricin is a macrocyclic tetraene originally isolated from Streptomyces natalensis in 1957. Pimaricin exhibits broad spectrum antifungal activity against yeast and filamentous fungi by binding specifically to ergoesterol to block fungal growth. Unlike the related polyenes, nystatin and filipin, pimaricin does not change the permeability of the plasma membrane. Pimaricin is used in the food industry for surface treatment of cheeses as mold inhibitor.

    Additional Information

    SynonymsNatamycin, Antibiotic A 5283, Delvolan, Delvocid, Delvopos, Mychophyt, Myprozine, Natacyn, Natafucin, Pimafucin, Pimafugin, Synogil, Tennecetin, Tymasil, A5263, CL 12625, E23
    Product #P-1637
    CAS #7681-93-8
    Chemical Name(1R,3S,5R,7R,8E,12R,14E,16E,18E,20E,22R,24S,25R,26S)-22-(((3S,4S,5S,6R)-4-AMINO-3,5-DIHYDROXY-6-METHYLTETRAHYDRO-2H-PYRAN-2-YL)OXY)-1,3,26-TRIHYDROXY-12-METHYL-10-OXO-6,11,28-TRIOXATRICYCLO[22.3.1.0(5,7)]OCTACOSA-8,14,16,18,20-PENTAENE-25-CARBOXYLIC ACID
    FormulaC33H47NO13
    MW665.733
    Appearancelight yellow Solid
    Purity95% by HPLC
    SolubilitySoluble in ethanol, methanol, DMF or DMSO. Limited water solubility.
    Melting Point280 °C
    Storage Temp-20°C
    Therapeutic AreaInfectious Diseases
    UseAn antifungal polyene macrolide is used to treat fungal infections

    Additional Information

    MDL NumberMFCD00135085
    ChemACXX1005609-4
    InChIInChI=1S/C33H47NO13/c1-18-10-8-6-4-3-5-7-9-11-21(45-32-30(39)28(34)29(38)19(2)44-32)15-25-27(31(40)41)22(36)17-33(42,47-25)16-20(35)14-24-23(46-24)12-13-26(37)43-18/h3-9,11-13,18-25,27-30,32,35-36,38-39,42H,10,14-17,34H2,1-2H3,(H,40,41)/b4-3+,7-5+,8-6+,11-9+,13-12+/t18-,19-,20+,21+,22+,23-,24-,25+,27-,28+,29-,30+,32+,33-/m1/s1
    SMILESC[C@@H]1C/C=C/C=C/C=C/C=C/[C@@H](C[C@H]2[C@@H]([C@H](C[C@](O2)(C[C@H](C[C@@H]3[C@H](O3)/C=C/C(=O)O1)O)O)O)C(=O)O)O[C@H]4[C@H]([C@H]([C@@H]([C@H](O4)C)O)N)O
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