NP-MRD: Showing NP-Card for (1r,3r,4r,7r,9r,10r,12r,13r,19r,21r,23s)-23-{[(2r,3r,4r,5s,6s)-4,5-dihydroxy-3-methoxy-6-methyloxan-2-yl]oxy}-4,9-dihydroxy-12,19-dimethyl-5-oxo-6,25,26-trioxatetracyclo[19.3.1.1⁴,⁷.1¹⁰,¹³]heptacosa-15,17-dien-3-yl butanoate (NP0201996)

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Record Information

Version

2.0

Created at

2022-09-04 21:08:05 UTC

Updated at

2022-09-04 21:08:05 UTC

NP-MRD ID

NP0201996

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,3r,4r,7r,9r,10r,12r,13r,19r,21r,23s)-23-{[(2r,3r,4r,5s,6s)-4,5-dihydroxy-3-methoxy-6-methyloxan-2-yl]oxy}-4,9-dihydroxy-12,19-dimethyl-5-oxo-6,25,26-trioxatetracyclo[19.3.1.1⁴,⁷.1¹⁰,¹³]heptacosa-15,17-dien-3-yl butanoate

Description

(1R,3R,4R,7R,9R,10R,12R,13R,19R,21R,23S)-23-{[(2R,3R,4R,5S,6S)-4,5-dihydroxy-3-methoxy-6-methyloxan-2-yl]oxy}-4,9-dihydroxy-12,19-dimethyl-5-oxo-6,25,26-trioxatetracyclo[19.3.1.1⁴,⁷.1¹⁰,¹³]Heptacosa-15,17-dien-3-yl butanoate belongs to the class of organic compounds known as macrolides and analogues. These are organic compounds containing a lactone ring of at least twelve members. Based on a literature review very few articles have been published on (1R,3R,4R,7R,9R,10R,12R,13R,19R,21R,23S)-23-{[(2R,3R,4R,5S,6S)-4,5-dihydroxy-3-methoxy-6-methyloxan-2-yl]oxy}-4,9-dihydroxy-12,19-dimethyl-5-oxo-6,25,26-trioxatetracyclo[19.3.1.1⁴,⁷.1¹⁰,¹³]Heptacosa-15,17-dien-3-yl butanoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042223082D          

 50 54  0  0  1  0            999 V2000
   -1.8100   -1.2217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3316   -0.5495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5104   -0.6276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1674   -1.3779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6457   -2.0501    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6539   -1.4561    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1322   -0.7839    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5796   -0.1714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2433    0.5820    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0672    0.5396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5158    1.2320    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3397    1.1896    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7884    1.8820    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4131    2.6167    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8617    3.3090    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4864    4.0437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6856    3.2667    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1343    3.9590    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0609    2.5320    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8431    2.3807    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6123    1.8396    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9876    1.1049    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5389    0.4126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1405    1.9667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3166    2.0090    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7387    2.9244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3513    3.4770    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9012    4.1685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1046    3.8134    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9250    3.9004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7321    3.7297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4470    3.3179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9997    2.7054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3360    1.9520    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8174    1.3104    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2674    0.6189    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.0641    0.8332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1065    1.6571    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.7979    2.1072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8405   -0.3904    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.5127   -0.8687    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2280   -0.9430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4746   -1.2794    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8330   -0.7608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1415   -1.2108    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5195   -1.7528    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3558   -2.0075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8373   -2.6492    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1798   -2.0499    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1320    1.3167    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4  6  1  0  0  0  0
  7  6  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
 13 12  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  1  0  0  0
 15 17  1  0  0  0  0
 17 18  1  1  0  0  0
 17 19  1  0  0  0  0
 19 20  1  1  0  0  0
 19 21  1  0  0  0  0
 13 21  1  0  0  0  0
 21 22  1  1  0  0  0
 22 23  1  0  0  0  0
 11 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  1  0  0  0
 27 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  4  0  0  0
 31 32  2  0  0  0  0
 32 33  1  4  0  0  0
 33 34  1  0  0  0  0
 34 35  1  6  0  0  0
 36 35  1  6  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 34 38  1  0  0  0  0
 38 39  1  6  0  0  0
 36 40  1  0  0  0  0
 40 41  1  6  0  0  0
 40 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  1  0  0  0
 44 45  1  0  0  0  0
  7 45  1  0  0  0  0
 45 46  1  1  0  0  0
 45 47  1  0  0  0  0
 47 48  2  0  0  0  0
 47 49  1  0  0  0  0
 43 49  1  0  0  0  0
 25 50  1  6  0  0  0
  9 50  1  6  0  0  0
M  END

     RDKit          3D

108112  0  0  0  0  0  0  0  0999 V2000
    0.3981    7.5252    1.8786 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6373    6.8038    1.4468 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3500    5.6862    0.4807 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4605    4.6817    1.0747 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0662    4.8556    2.2600 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0259    3.5462    0.4047 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8198    2.6308    1.0273 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2289    1.2534    1.1551 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6666    0.8731    0.0261 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0375    0.4009    0.4838 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8618    0.1630   -0.7598 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6126   -1.0021   -0.6104 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9717   -0.7976   -0.5829 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.6674   -1.4141   -1.6047 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8968   -0.7462   -1.8113 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.6759    0.6259   -2.3852 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7032   -0.6929   -0.5441 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.8674    0.6157   -0.0802 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0417   -1.5724    0.4924 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.8071   -1.5273    1.6426 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5994   -1.2268    0.7289 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4992   -0.2688    1.7049 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7691   -0.7428    2.7780 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0322    0.1507   -2.0137 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6826   -0.4816   -1.8438 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7212   -1.9802   -2.0346 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6517   -2.5372   -1.6874 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1594   -3.4402   -2.7818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6288   -3.1782   -0.3458 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9824   -4.3766   -0.0071 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2651   -5.0315   -0.2333 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4570   -4.5353   -0.0750 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7915   -3.0902    0.0604 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.0739   -0.9887    1.3233 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.8531   -1.7107    0.2781 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3002   -3.1162    0.3728 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.3301   -3.8477   -0.9197 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8959    0.4800    1.0625 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.1684    1.0313    0.8781 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0596    0.7756   -0.1398 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5879    0.7409    0.2229 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1864    1.8946    1.1091 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1421    2.6327    0.2993 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5543    3.9608    0.1993 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1006    1.9940   -1.0072 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4867    2.3918   -2.0173 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8624    0.8407   -0.9809 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0985   -0.2277   -0.6167 O   0  0  0  0  0  0  0  0  0  0  0  0
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    0.6723    8.5714    2.1257 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3318    7.5615    1.0061 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0818    6.3370    2.3512 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2785    5.2711    0.0695 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7739    6.1557   -0.3705 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.0741    0.5482    1.3093 H   0  0  0  0  0  0  0  0  0  0  0  0
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    2.5320    1.1169    1.1594 H   0  0  0  0  0  0  0  0  0  0  0  0
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    7.3668    0.8080   -3.2219 H   0  0  0  0  0  0  0  0  0  0  0  0
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    7.9423    0.6270    0.9163 H   0  0  0  0  0  0  0  0  0  0  0  0
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    8.4434   -2.2806    1.6187 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0606   -2.1406    1.0669 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2455   -1.6515    3.2389 H   0  0  0  0  0  0  0  0  0  0  0  0
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    4.6560    0.0011    3.5869 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9376    1.1686   -2.4564 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.0004   -0.0801   -2.6215 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.9290   -2.2600   -3.0882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3564   -1.6853   -1.5964 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.9467   -1.7168    0.5041 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9636   -3.6556    1.0905 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2064   -3.4410   -1.5071 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4622   -3.7297   -1.5656 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6129   -4.9187   -0.7381 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5007    0.9314    1.9948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2472    1.4108   -0.0112 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1985    0.0217   -0.9336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2578    1.8000   -0.5320 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2844   -0.1833    0.7322 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0968    2.5096    1.2908 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8054    1.5789    2.0939 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1183    4.3617   -0.5999 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 27 29  1  0
 29 30  2  0
 30 31  1  0
 31 32  2  0
 32 33  1  0
 33 34  1  0
 34 35  1  0
 35 36  1  0
 36 37  1  0
 37 38  1  0
 38 39  1  0
 36 40  1  0
 40 41  1  0
 40 42  1  0
 42 43  1  0
 43 44  1  0
 44 45  1  0
 45 46  1  6
 45 47  1  0
 47 48  2  0
 47 49  1  0
 25 50  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 22 23  1  0
 45  7  1  0
 21 13  1  0
 50  9  1  0
 38 34  1  0
 49 43  1  0
  1 51  1  0
  1 52  1  0
  1 53  1  0
  2 54  1  0
  2 55  1  0
  3 56  1  0
  3 57  1  0
  7 58  1  1
  8 59  1  0
  8 60  1  0
  9 61  1  6
 10 62  1  0
 10 63  1  0
 11 64  1  6
 24 78  1  0
 24 79  1  0
 25 80  1  6
 26 81  1  0
 26 82  1  0
 27 83  1  1
 28 84  1  0
 28 85  1  0
 28 86  1  0
 29 87  1  0
 30 88  1  0
 31 89  1  0
 32 90  1  0
 33 91  1  0
 33 92  1  0
 34 93  1  1
 36 94  1  1
 37 95  1  0
 37 96  1  0
 38 97  1  1
 39 98  1  0
 39 99  1  0
 39100  1  0
 40101  1  1
 41102  1  0
 42103  1  0
 42104  1  0
 43105  1  1
 44106  1  0
 44107  1  0
 46108  1  0
 13 65  1  6
 15 66  1  6
 16 67  1  0
 16 68  1  0
 16 69  1  0
 17 70  1  6
 18 71  1  0
 19 72  1  6
 20 73  1  0
 21 74  1  1
 23 75  1  0
 23 76  1  0
 23 77  1  0
M  END


  Mrv1652309042223082D          

 50 54  0  0  1  0            999 V2000
   -1.8100   -1.2217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3316   -0.5495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5104   -0.6276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1674   -1.3779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6457   -2.0501    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6539   -1.4561    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1322   -0.7839    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5796   -0.1714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2433    0.5820    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0672    0.5396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5158    1.2320    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3397    1.1896    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7884    1.8820    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4131    2.6167    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8617    3.3090    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4864    4.0437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6856    3.2667    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1343    3.9590    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0609    2.5320    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8431    2.3807    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6123    1.8396    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9876    1.1049    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5389    0.4126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1405    1.9667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3166    2.0090    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7387    2.9244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3513    3.4770    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9012    4.1685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1046    3.8134    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9250    3.9004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7321    3.7297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4470    3.3179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9997    2.7054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3360    1.9520    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8174    1.3104    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2674    0.6189    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.0641    0.8332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1065    1.6571    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.7979    2.1072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8405   -0.3904    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.5127   -0.8687    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2280   -0.9430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4746   -1.2794    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8330   -0.7608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1415   -1.2108    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5195   -1.7528    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3558   -2.0075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8373   -2.6492    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1798   -2.0499    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1320    1.3167    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4  6  1  0  0  0  0
  7  6  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
 13 12  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  1  0  0  0
 15 17  1  0  0  0  0
 17 18  1  1  0  0  0
 17 19  1  0  0  0  0
 19 20  1  1  0  0  0
 19 21  1  0  0  0  0
 13 21  1  0  0  0  0
 21 22  1  1  0  0  0
 22 23  1  0  0  0  0
 11 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  1  0  0  0
 27 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  4  0  0  0
 31 32  2  0  0  0  0
 32 33  1  4  0  0  0
 33 34  1  0  0  0  0
 34 35  1  6  0  0  0
 36 35  1  6  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 34 38  1  0  0  0  0
 38 39  1  6  0  0  0
 36 40  1  0  0  0  0
 40 41  1  6  0  0  0
 40 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  1  0  0  0
 44 45  1  0  0  0  0
  7 45  1  0  0  0  0
 45 46  1  1  0  0  0
 45 47  1  0  0  0  0
 47 48  2  0  0  0  0
 47 49  1  0  0  0  0
 43 49  1  0  0  0  0
 25 50  1  6  0  0  0
  9 50  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0201996

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCC(=O)O[C@@H]1C[C@H]2C[C@H](C[C@@H](C[C@@H](C)C=CC=CC[C@H]3O[C@H](C[C@H]3C)[C@H](O)C[C@@H]3C[C@]1(O)C(=O)O3)O2)O[C@@H]1O[C@@H](C)[C@@H](O)[C@@H](O)[C@H]1OC

> <INCHI_IDENTIFIER>
InChI=1S/C37H58O13/c1-6-10-31(39)50-30-18-25-16-24(47-35-34(44-5)33(41)32(40)22(4)45-35)15-23(46-25)13-20(2)11-8-7-9-12-28-21(3)14-29(49-28)27(38)17-26-19-37(30,43)36(42)48-26/h7-9,11,20-30,32-35,38,40-41,43H,6,10,12-19H2,1-5H3/t20-,21+,22-,23+,24-,25+,26+,27+,28+,29+,30+,32+,33+,34+,35-,37+/m0/s1

> <INCHI_KEY>
XPUZQNDQEJOFMQ-HMLQMNEESA-N

> <FORMULA>
C37H58O13

> <MOLECULAR_WEIGHT>
710.858

> <EXACT_MASS>
710.387741928

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
108

> <JCHEM_AVERAGE_POLARIZABILITY>
76.78069398152323

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,3R,4R,7R,9R,10R,12R,13R,19R,21R,23S)-23-{[(2R,3R,4R,5S,6S)-4,5-dihydroxy-3-methoxy-6-methyloxan-2-yl]oxy}-4,9-dihydroxy-12,19-dimethyl-5-oxo-6,25,26-trioxatetracyclo[19.3.1.1^{4,7}.1^{10,13}]heptacosa-15,17-dien-3-yl butanoate

> <JCHEM_LOGP>
2.1318604449999987

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.751991890655876

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.33596250412479

> <JCHEM_PKA_STRONGEST_BASIC>
-3.1863040201798167

> <JCHEM_POLAR_SURFACE_AREA>
179.67

> <JCHEM_REFRACTIVITY>
180.8801

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,3R,4R,7R,9R,10R,12R,13R,19R,21R,23S)-23-{[(2R,3R,4R,5S,6S)-4,5-dihydroxy-3-methoxy-6-methyloxan-2-yl]oxy}-4,9-dihydroxy-12,19-dimethyl-5-oxo-6,25,26-trioxatetracyclo[19.3.1.1^{4,7}.1^{10,13}]heptacosa-15,17-dien-3-yl butanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0      -3.379  -2.280   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.486  -1.026   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.953  -1.172   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.312  -2.572   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -1.205  -3.827   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0       1.221  -2.718   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       2.113  -1.463   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.082  -0.320   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.454   1.086   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.992   1.007   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.830   2.300   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       4.367   2.221   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       5.205   3.513   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       4.504   4.884   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       5.342   6.177   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.641   7.548   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.880   6.098   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       7.717   7.390   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       7.580   4.726   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       9.040   4.444   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       6.743   3.434   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       7.443   2.063   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       6.606   0.770   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.129   3.671   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.591   3.750   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.379   5.459   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.522   6.490   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       1.682   7.781   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.929   7.118   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.460   7.281   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       6.967   6.962   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       8.301   6.193   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       9.333   5.050   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       9.960   3.644   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       8.993   2.446   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       9.833   1.155   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      11.320   1.555   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      11.399   3.093   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      12.689   3.933   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       9.036  -0.729   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      10.290  -1.622   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       7.892  -1.760   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       6.486  -2.388   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       5.288  -1.420   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       3.998  -2.260   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0       2.836  -3.272   0.000  0.00  0.00           O+0
HETATM   47  C   UNK     0       4.398  -3.747   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0       3.430  -4.945   0.000  0.00  0.00           O+0
HETATM   49  O   UNK     0       5.936  -3.826   0.000  0.00  0.00           O+0
HETATM   50  O   UNK     0      -0.246   2.458   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8   45                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   50                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   24                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   21                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   13   22                                                  
CONECT   22   21   23                                                       
CONECT   23   22                                                            
CONECT   24   11   25                                                       
CONECT   25   24   26   50                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35   38                                                  
CONECT   35   34   36                                                       
CONECT   36   35   37   40                                                  
CONECT   37   36   38                                                       
CONECT   38   37   34   39                                                  
CONECT   39   38                                                            
CONECT   40   36   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40   43                                                       
CONECT   43   42   44   49                                                  
CONECT   44   43   45                                                       
CONECT   45   44    7   46   47                                             
CONECT   46   45                                                            
CONECT   47   45   48   49                                                  
CONECT   48   47                                                            
CONECT   49   47   43                                                       
CONECT   50   25    9                                                       
MASTER        0    0    0    0    0    0    0    0   50    0  108    0
END

View in JSmol

Synonyms

Value	Source
(1R,3R,4R,7R,9R,10R,12R,13R,19R,21R,23S)-23-{[(2R,3R,4R,5S,6S)-4,5-dihydroxy-3-methoxy-6-methyloxan-2-yl]oxy}-4,9-dihydroxy-12,19-dimethyl-5-oxo-6,25,26-trioxatetracyclo[19.3.1.1,.1,]heptacosa-15,17-dien-3-yl butanoic acid	Generator

Chemical Formula

C₃₇H₅₈O₁₃

Average Mass

710.8580 Da

Monoisotopic Mass

710.38774 Da

IUPAC Name

Traditional Name

CAS Registry Number

Not Available

SMILES

CCCC(=O)O[C@@H]1C[C@H]2C[C@H](C[C@@H](C[C@@H](C)C=CC=CC[C@H]3O[C@H](C[C@H]3C)[C@H](O)C[C@@H]3C[C@]1(O)C(=O)O3)O2)O[C@@H]1O[C@@H](C)[C@@H](O)[C@@H](O)[C@H]1OC

InChI Identifier

InChI=1S/C37H58O13/c1-6-10-31(39)50-30-18-25-16-24(47-35-34(44-5)33(41)32(40)22(4)45-35)15-23(46-25)13-20(2)11-8-7-9-12-28-21(3)14-29(49-28)27(38)17-26-19-37(30,43)36(42)48-26/h7-9,11,20-30,32-35,38,40-41,43H,6,10,12-19H2,1-5H3/t20-,21+,22-,23+,24-,25+,26+,27+,28+,29+,30+,32+,33+,34+,35-,37+/m0/s1

InChI Key

XPUZQNDQEJOFMQ-HMLQMNEESA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as macrolides and analogues. These are organic compounds containing a lactone ring of at least twelve members.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Macrolides and analogues

Sub Class

Not Available

Direct Parent

Macrolides and analogues

Alternative Parents

Substituents

Macrolide
Hexose monosaccharide
O-glycosyl compound
Glycosyl compound
Fatty acid ester
Fatty acyl
Oxane
Monosaccharide
Gamma butyrolactone
Dicarboxylic acid or derivatives
Tetrahydrofuran
Tertiary alcohol
Secondary alcohol
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Ether
Dialkyl ether
Carboxylic acid derivative
Acetal
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	2.13	ChemAxon
pKa (Strongest Acidic)	11.34	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	179.67 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	180.88 m³·mol⁻¹	ChemAxon
Polarizability	76.78 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

162855402

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,3r,4r,7r,9r,10r,12r,13r,19r,21r,23s)-23-{[(2r,3r,4r,5s,6s)-4,5-dihydroxy-3-methoxy-6-methyloxan-2-yl]oxy}-4,9-dihydroxy-12,19-dimethyl-5-oxo-6,25,26-trioxatetracyclo[19.3.1.1⁴,⁷.1¹⁰,¹³]heptacosa-15,17-dien-3-yl butanoate (NP0201996)

MOL for NP0201996 ((1r,3r,4r,7r,9r,10r,12r,13r,19r,21r,23s)-23-{[(2r,3r,4r,5s,6s)-4,5-dihydroxy-3-methoxy-6-methyloxan-2-yl]oxy}-4,9-dihydroxy-12,19-dimethyl-5-oxo-6,25,26-trioxatetracyclo[19.3.1.1⁴,⁷.1¹⁰,¹³]heptacosa-15,17-dien-3-yl butanoate)

3D MOL for NP0201996 ((1r,3r,4r,7r,9r,10r,12r,13r,19r,21r,23s)-23-{[(2r,3r,4r,5s,6s)-4,5-dihydroxy-3-methoxy-6-methyloxan-2-yl]oxy}-4,9-dihydroxy-12,19-dimethyl-5-oxo-6,25,26-trioxatetracyclo[19.3.1.1⁴,⁷.1¹⁰,¹³]heptacosa-15,17-dien-3-yl butanoate)

3D SDF for NP0201996 ((1r,3r,4r,7r,9r,10r,12r,13r,19r,21r,23s)-23-{[(2r,3r,4r,5s,6s)-4,5-dihydroxy-3-methoxy-6-methyloxan-2-yl]oxy}-4,9-dihydroxy-12,19-dimethyl-5-oxo-6,25,26-trioxatetracyclo[19.3.1.1⁴,⁷.1¹⁰,¹³]heptacosa-15,17-dien-3-yl butanoate)

3D-SDF for NP0201996 ((1r,3r,4r,7r,9r,10r,12r,13r,19r,21r,23s)-23-{[(2r,3r,4r,5s,6s)-4,5-dihydroxy-3-methoxy-6-methyloxan-2-yl]oxy}-4,9-dihydroxy-12,19-dimethyl-5-oxo-6,25,26-trioxatetracyclo[19.3.1.1⁴,⁷.1¹⁰,¹³]heptacosa-15,17-dien-3-yl butanoate)

PDB for NP0201996 ((1r,3r,4r,7r,9r,10r,12r,13r,19r,21r,23s)-23-{[(2r,3r,4r,5s,6s)-4,5-dihydroxy-3-methoxy-6-methyloxan-2-yl]oxy}-4,9-dihydroxy-12,19-dimethyl-5-oxo-6,25,26-trioxatetracyclo[19.3.1.1⁴,⁷.1¹⁰,¹³]heptacosa-15,17-dien-3-yl butanoate)

3D PDB for NP0201996 ((1r,3r,4r,7r,9r,10r,12r,13r,19r,21r,23s)-23-{[(2r,3r,4r,5s,6s)-4,5-dihydroxy-3-methoxy-6-methyloxan-2-yl]oxy}-4,9-dihydroxy-12,19-dimethyl-5-oxo-6,25,26-trioxatetracyclo[19.3.1.1⁴,⁷.1¹⁰,¹³]heptacosa-15,17-dien-3-yl butanoate)

SMILES for NP0201996 ((1r,3r,4r,7r,9r,10r,12r,13r,19r,21r,23s)-23-{[(2r,3r,4r,5s,6s)-4,5-dihydroxy-3-methoxy-6-methyloxan-2-yl]oxy}-4,9-dihydroxy-12,19-dimethyl-5-oxo-6,25,26-trioxatetracyclo[19.3.1.1⁴,⁷.1¹⁰,¹³]heptacosa-15,17-dien-3-yl butanoate)

INCHI for NP0201996 ((1r,3r,4r,7r,9r,10r,12r,13r,19r,21r,23s)-23-{[(2r,3r,4r,5s,6s)-4,5-dihydroxy-3-methoxy-6-methyloxan-2-yl]oxy}-4,9-dihydroxy-12,19-dimethyl-5-oxo-6,25,26-trioxatetracyclo[19.3.1.1⁴,⁷.1¹⁰,¹³]heptacosa-15,17-dien-3-yl butanoate)

Structure for NP0201996 ((1r,3r,4r,7r,9r,10r,12r,13r,19r,21r,23s)-23-{[(2r,3r,4r,5s,6s)-4,5-dihydroxy-3-methoxy-6-methyloxan-2-yl]oxy}-4,9-dihydroxy-12,19-dimethyl-5-oxo-6,25,26-trioxatetracyclo[19.3.1.1⁴,⁷.1¹⁰,¹³]heptacosa-15,17-dien-3-yl butanoate)

3D Structure for NP0201996 ((1r,3r,4r,7r,9r,10r,12r,13r,19r,21r,23s)-23-{[(2r,3r,4r,5s,6s)-4,5-dihydroxy-3-methoxy-6-methyloxan-2-yl]oxy}-4,9-dihydroxy-12,19-dimethyl-5-oxo-6,25,26-trioxatetracyclo[19.3.1.1⁴,⁷.1¹⁰,¹³]heptacosa-15,17-dien-3-yl butanoate)