NP-MRD: Showing NP-Card for 6-methyl-8-{22,25,26-trihydroxy-21,40-dimethyl-3-oxo-2,11,15,35,39-pentaoxapentacyclo[32.2.2.1¹²,¹⁶.1²⁰,²⁴.0¹⁰,¹⁴]tetraconta-4,6,8,17,27,31,37-heptaen-36-yl}non-7-enoic acid (NP0219124)

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Record Information

Version

1.0

Created at

2022-09-05 20:01:30 UTC

Updated at

2022-09-05 20:01:30 UTC

NP-MRD ID

NP0219124

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6-methyl-8-{22,25,26-trihydroxy-21,40-dimethyl-3-oxo-2,11,15,35,39-pentaoxapentacyclo[32.2.2.1¹²,¹⁶.1²⁰,²⁴.0¹⁰,¹⁴]tetraconta-4,6,8,17,27,31,37-heptaen-36-yl}non-7-enoic acid

Description

6-Methyl-8-{22,25,26-trihydroxy-21,40-dimethyl-3-oxo-2,11,15,35,39-pentaoxapentacyclo[32.2.2.1¹²,¹⁶.1²⁰,²⁴.0¹⁰,¹⁴]Tetraconta-4,6,8,17,27,31,37-heptaen-36-yl}non-7-enoic acid 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. 6-methyl-8-{22,25,26-trihydroxy-21,40-dimethyl-3-oxo-2,11,15,35,39-pentaoxapentacyclo[32.2.2.1¹²,¹⁶.1²⁰,²⁴.0¹⁰,¹⁴]tetraconta-4,6,8,17,27,31,37-heptaen-36-yl}non-7-enoic acid is found in Sorangium cellulosum. 6-Methyl-8-{22,25,26-trihydroxy-21,40-dimethyl-3-oxo-2,11,15,35,39-pentaoxapentacyclo[32.2.2.1¹²,¹⁶.1²⁰,²⁴.0¹⁰,¹⁴]Tetraconta-4,6,8,17,27,31,37-heptaen-36-yl}non-7-enoic acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171500512D          

 58 62  0  0  0  0            999 V2000
    2.2789   -0.9260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9934   -0.5135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9934    0.3115    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7079    0.7240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4223    0.3115    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1368    0.7240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8513    0.3115    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8513   -0.5135    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5657    0.7240    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7079   -0.9260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7079   -1.7510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4223   -2.1635    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9934   -2.1635    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2876   -1.7321    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5223   -2.0985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9049   -1.4714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4092   -0.7582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0615    0.0378    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0919    0.8741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0411    1.7371    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2077    2.5611    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6223    3.2977    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1937    3.9320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6581    4.5595    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9051    4.3936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5020    5.1134    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6769    4.7619    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6065    5.6006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2676    6.1053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1676    6.9242    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0315    5.7743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6771    6.2879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1854    4.9386    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0295    4.6954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8467    4.3725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6027    3.9148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3794    3.4580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2366    2.6128    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8654    2.0303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4011    2.5974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9247    2.9708    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1952    2.0867    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4956    1.4706    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0979    0.6320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7470   -0.2248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3979   -1.0622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9198   -1.7969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2848   -2.4017    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5333   -2.8440    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7223   -3.1174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8940   -3.9243    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8691   -3.1980    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0144   -3.0045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2612   -3.3846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5425   -2.9585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2745    3.6005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5228    4.3872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4726    4.4596    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  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
 10  2  1  4  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 17 16  1  4  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 21 20  1  4  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 33 34  1  0  0  0  0
 35 34  1  4  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 39 43  1  0  0  0  0
 44 43  1  4  0  0  0
 44 45  2  0  0  0  0
 46 45  1  4  0  0  0
 46 47  2  0  0  0  0
 48 47  1  4  0  0  0
 48 49  2  0  0  0  0
 49 50  1  0  0  0  0
 50 51  2  0  0  0  0
 50 52  1  0  0  0  0
 52 53  1  0  0  0  0
 13 53  1  0  0  0  0
 53 54  1  0  0  0  0
 54 55  2  0  0  0  0
 15 55  1  0  0  0  0
 41 56  1  0  0  0  0
 37 56  1  0  0  0  0
 56 57  1  0  0  0  0
 33 58  1  0  0  0  0
 27 58  1  0  0  0  0
M  END

     RDKit          3D

124128  0  0  0  0  0  0  0  0999 V2000
    6.7767    2.0997   -0.2935 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7940    1.0360   -0.1568 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7180   -0.1669   -0.6232 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5038   -1.0209   -1.4527 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.5494   -2.4497   -0.8751 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8269   -0.5783   -1.9157 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8743   -0.6302   -0.8283 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2142   -0.1288   -1.2911 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7103   -0.9602   -2.4279 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0636   -0.4500   -2.8597 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0968    0.5711   -3.5803 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.2189   -1.0951   -2.4669 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5757    1.4161    0.7428 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9537    0.3061    1.1374 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6128    0.2353    0.9427 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2460    0.7317   -0.4316 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6380    1.9755   -0.6698 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8232    2.5280    0.0925 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2492    3.3568    1.0888 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2275    4.7470    1.0640 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6685    5.3495    2.1142 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7349    5.5384   -0.0798 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5367    5.4566   -0.5978 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2567    5.5039    0.1175 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0233    4.8060    1.2127 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0263    3.3422    1.3134 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8233    2.5355    0.6342 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3068    2.5477    0.6665 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8657    3.6946    1.1579 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7073    4.2291    0.2143 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.1680    3.7395   -1.1413 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8971    2.2871   -0.7153 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.0807    1.6127   -0.6410 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0595    2.1245    0.1490 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.1474    1.4577    1.4938 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7612    0.2716    1.6649 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7438   -0.2602    0.6892 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0039   -1.7165    1.0377 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.8618   -2.4012    0.7431 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8939   -3.2405   -0.3308 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.9192   -4.3036   -0.0432 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2652   -3.6150   -0.0784 C   0  0  2  0  0  0  0  0  0  0  0  0
   -8.6794   -3.6647   -1.4312 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2669   -2.2278    0.4356 C   0  0  2  0  0  0  0  0  0  0  0  0
   -8.7879   -1.2943   -0.6672 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5194   -3.8049   -0.5715 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4934   -4.4342   -1.8352 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0319   -4.7013    0.5130 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2808   -5.7270   -0.1096 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1379   -3.9763    1.4610 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8290   -4.0419    1.4473 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9893   -4.1426    0.2314 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0158   -2.9824    0.1641 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2588   -1.9932    1.2424 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7049   -1.1364    1.6263 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0763   -1.1870    1.0758 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0791    3.6002    0.3313 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.7663    3.9648    1.6267 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7314    1.8488   -0.7070 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9921    2.4685    0.7684 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3448    3.0289   -0.7650 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7472   -0.7169   -0.2808 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8979   -1.2263   -2.4571 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6506   -2.2827    0.2382 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5625   -2.9102   -1.0211 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4048   -3.0255   -1.2589 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8262    0.3977   -2.4138 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2217   -1.3103   -2.7261 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0063   -1.7381   -0.6061 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5715   -0.1369    0.0892 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1059    0.9396   -1.6053 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.9005   -0.2165   -0.4193 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.0384   -0.8437   -3.3175 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.7420   -2.0098   -2.1030 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.4935   -1.0045   -1.4832 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1131    1.8700    1.6423 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1156    0.8594    1.7210 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7162    0.0930   -1.1146 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1567    2.5964   -1.3697 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3926    3.0909   -0.6510 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4928    6.2475   -0.4889 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4622    5.3379   -1.6935 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5792    6.1609   -0.2359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2789    5.3562    2.1492 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7089    2.8934    2.0280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3794    1.7801   -0.0142 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5835    1.6328    1.2561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7900    5.3239    0.2497 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9465    3.7352   -1.9121 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2520    4.2696   -1.3989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2151    1.7843   -1.3940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0409    1.8440   -0.3433 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1533004171500512D          

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M  END
> <DATABASE_ID>
NP0219124

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(CCCCC(O)=O)C=C(C)C1OC2CC=CCCC=CC(O)C(O)C3CC(O)C(C)C(CC=CC4OC5CC(OC5C=CC=CC=CC(=O)OC1C=C2)C4C)O3

> <INCHI_IDENTIFIER>
InChI=1S/C47H66O11/c1-30(17-14-15-23-44(50)51)27-31(2)47-40-26-25-34(54-47)18-10-6-5-7-11-19-35(48)46(53)43-28-36(49)32(3)37(56-43)21-16-22-38-33(4)41-29-42(55-38)39(57-41)20-12-8-9-13-24-45(52)58-40/h6,8-13,16,19-20,22,24-27,30,32-43,46-49,53H,5,7,14-15,17-18,21,23,28-29H2,1-4H3,(H,50,51)

> <INCHI_KEY>
OTABDKFPJQZJRD-UHFFFAOYSA-N

> <FORMULA>
C47H66O11

> <MOLECULAR_WEIGHT>
807.034

> <EXACT_MASS>
806.460512945

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
124

> <JCHEM_AVERAGE_POLARIZABILITY>
88.3810244322398

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
6-methyl-8-{22,25,26-trihydroxy-21,40-dimethyl-3-oxo-2,11,15,35,39-pentaoxapentacyclo[32.2.2.1¹²,¹⁶.1²⁰,²⁴.0¹⁰,¹⁴]tetraconta-4,6,8,17,27,31,37-heptaen-36-yl}non-7-enoic acid

> <ALOGPS_LOGP>
5.77

> <JCHEM_LOGP>
6.688619186666666

> <ALOGPS_LOGS>
-5.58

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
13.05676356262757

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.694376052686352

> <JCHEM_PKA_STRONGEST_BASIC>
-2.891445432832752

> <JCHEM_POLAR_SURFACE_AREA>
161.21

> <JCHEM_REFRACTIVITY>
229.71990000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.10e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6-methyl-8-{22,25,26-trihydroxy-21,40-dimethyl-3-oxo-2,11,15,35,39-pentaoxapentacyclo[32.2.2.1¹²,¹⁶.1²⁰,²⁴.0¹⁰,¹⁴]tetraconta-4,6,8,17,27,31,37-heptaen-36-yl}non-7-enoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0       4.254  -1.728   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.588  -0.958   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.588   0.582   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.921   1.352   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.255   0.582   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.589   1.352   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.922   0.582   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      10.922  -0.958   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0      12.256   1.352   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       6.921  -1.728   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.921  -3.268   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.255  -4.038   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.588  -4.038   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       4.270  -3.233   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       2.842  -3.917   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.689  -2.747   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.764  -1.415   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.115   0.070   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.171   1.632   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.077   3.243   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.388   4.781   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.162   6.156   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.228   7.340   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       1.228   8.511   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       3.556   8.201   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       2.804   9.545   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       4.997   8.889   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.865  10.455   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.100  11.397   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       5.913  12.925   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       7.525  10.779   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       8.731  11.738   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       7.813   9.219   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       9.388   8.765   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      10.914   8.162   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      12.325   7.308   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      13.775   6.455   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      13.508   4.877   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0      14.682   3.790   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      15.682   4.849   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      16.659   5.545   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0      17.164   3.895   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0      15.858   2.745   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      15.116   1.180   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      14.461  -0.420   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      13.809  -1.983   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      12.917  -3.354   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      11.732  -4.483   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      10.329  -5.309   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0       8.815  -5.819   0.000  0.00  0.00           C+0
HETATM   51  O   UNK     0       9.136  -7.325   0.000  0.00  0.00           O+0
HETATM   52  O   UNK     0       7.222  -5.970   0.000  0.00  0.00           O+0
HETATM   53  C   UNK     0       5.627  -5.608   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0       4.221  -6.318   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0       2.879  -5.523   0.000  0.00  0.00           C+0
HETATM   56  C   UNK     0      15.446   6.721   0.000  0.00  0.00           C+0
HETATM   57  C   UNK     0      15.909   8.189   0.000  0.00  0.00           C+0
HETATM   58  O   UNK     0       6.482   8.325   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   10                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    2   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   53                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   55                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   58                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34   58                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38   56                                                  
CONECT   38   37   39                                                       
CONECT   39   38   40   43                                                  
CONECT   40   39   41                                                       
CONECT   41   40   42   56                                                  
CONECT   42   41   43                                                       
CONECT   43   42   39   44                                                  
CONECT   44   43   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45   47                                                       
CONECT   47   46   48                                                       
CONECT   48   47   49                                                       
CONECT   49   48   50                                                       
CONECT   50   49   51   52                                                  
CONECT   51   50                                                            
CONECT   52   50   53                                                       
CONECT   53   52   13   54                                                  
CONECT   54   53   55                                                       
CONECT   55   54   15                                                       
CONECT   56   41   37   57                                                  
CONECT   57   56                                                            
CONECT   58   33   27                                                       
MASTER        0    0    0    0    0    0    0    0   58    0  124    0
END

View in JSmol

Synonyms

Value	Source
6-Methyl-8-{22,25,26-trihydroxy-21,40-dimethyl-3-oxo-2,11,15,35,39-pentaoxapentacyclo[32.2.2.1,.1,.0,]tetraconta-4,6,8,17,27,31,37-heptaen-36-yl}non-7-enoate	Generator
6-Methyl-8-{22,25,26-trihydroxy-21,40-dimethyl-3-oxo-2,11,15,35,39-pentaoxapentacyclo[32.2.2.1¹²,¹⁶.1²⁰,²⁴.0¹⁰,¹⁴]tetraconta-4,6,8,17,27,31,37-heptaen-36-yl}non-7-enoate	Generator

Chemical Formula

C₄₇H₆₆O₁₁

Average Mass

807.0340 Da

Monoisotopic Mass

806.46051 Da

IUPAC Name

6-methyl-8-{22,25,26-trihydroxy-21,40-dimethyl-3-oxo-2,11,15,35,39-pentaoxapentacyclo[32.2.2.1¹²,¹⁶.1²⁰,²⁴.0¹⁰,¹⁴]tetraconta-4,6,8,17,27,31,37-heptaen-36-yl}non-7-enoic acid

Traditional Name

6-methyl-8-{22,25,26-trihydroxy-21,40-dimethyl-3-oxo-2,11,15,35,39-pentaoxapentacyclo[32.2.2.1¹²,¹⁶.1²⁰,²⁴.0¹⁰,¹⁴]tetraconta-4,6,8,17,27,31,37-heptaen-36-yl}non-7-enoic acid

CAS Registry Number

Not Available

SMILES

CC(CCCCC(O)=O)C=C(C)C1OC2CC=CCCC=CC(O)C(O)C3CC(O)C(C)C(CC=CC4OC5CC(OC5C=CC=CC=CC(=O)OC1C=C2)C4C)O3

InChI Identifier

InChI=1S/C47H66O11/c1-30(17-14-15-23-44(50)51)27-31(2)47-40-26-25-34(54-47)18-10-6-5-7-11-19-35(48)46(53)43-28-36(49)32(3)37(56-43)21-16-22-38-33(4)41-29-42(55-38)39(57-41)20-12-8-9-13-24-45(52)58-40/h6,8-13,16,19-20,22,24-27,30,32-43,46-49,53H,5,7,14-15,17-18,21,23,28-29H2,1-4H3,(H,50,51)

InChI Key

OTABDKFPJQZJRD-UHFFFAOYSA-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

Species Name	Source	Reference
Sorangium cellulosum	LOTUS Database	35616633

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
Medium-chain fatty acid
1,4-dioxepane
Branched fatty acid
Dioxepane
Heterocyclic fatty acid
Hydroxy fatty acid
Methyl-branched fatty acid
Dicarboxylic acid or derivatives
Fatty acyl
Fatty acid
Unsaturated fatty acid
Oxane
Pyran
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Oxolane
Secondary alcohol
Carboxylic acid ester
Lactone
Polyol
Carboxylic acid derivative
Carboxylic acid
Dialkyl ether
Oxacycle
Ether
Organoheterocyclic compound
Organooxygen compound
Organic oxide
Hydrocarbon derivative
Carbonyl group
Alcohol
Organic oxygen compound
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	5.77	ALOGPS
logP	6.69	ChemAxon
logS	-5.6	ALOGPS
pKa (Strongest Acidic)	4.69	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	161.21 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	229.72 m³·mol⁻¹	ChemAxon
Polarizability	88.38 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

163697

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 6-methyl-8-{22,25,26-trihydroxy-21,40-dimethyl-3-oxo-2,11,15,35,39-pentaoxapentacyclo[32.2.2.1¹²,¹⁶.1²⁰,²⁴.0¹⁰,¹⁴]tetraconta-4,6,8,17,27,31,37-heptaen-36-yl}non-7-enoic acid (NP0219124)

MOL for NP0219124 (6-methyl-8-{22,25,26-trihydroxy-21,40-dimethyl-3-oxo-2,11,15,35,39-pentaoxapentacyclo[32.2.2.1¹²,¹⁶.1²⁰,²⁴.0¹⁰,¹⁴]tetraconta-4,6,8,17,27,31,37-heptaen-36-yl}non-7-enoic acid)

3D MOL for NP0219124 (6-methyl-8-{22,25,26-trihydroxy-21,40-dimethyl-3-oxo-2,11,15,35,39-pentaoxapentacyclo[32.2.2.1¹²,¹⁶.1²⁰,²⁴.0¹⁰,¹⁴]tetraconta-4,6,8,17,27,31,37-heptaen-36-yl}non-7-enoic acid)

3D SDF for NP0219124 (6-methyl-8-{22,25,26-trihydroxy-21,40-dimethyl-3-oxo-2,11,15,35,39-pentaoxapentacyclo[32.2.2.1¹²,¹⁶.1²⁰,²⁴.0¹⁰,¹⁴]tetraconta-4,6,8,17,27,31,37-heptaen-36-yl}non-7-enoic acid)

3D-SDF for NP0219124 (6-methyl-8-{22,25,26-trihydroxy-21,40-dimethyl-3-oxo-2,11,15,35,39-pentaoxapentacyclo[32.2.2.1¹²,¹⁶.1²⁰,²⁴.0¹⁰,¹⁴]tetraconta-4,6,8,17,27,31,37-heptaen-36-yl}non-7-enoic acid)

PDB for NP0219124 (6-methyl-8-{22,25,26-trihydroxy-21,40-dimethyl-3-oxo-2,11,15,35,39-pentaoxapentacyclo[32.2.2.1¹²,¹⁶.1²⁰,²⁴.0¹⁰,¹⁴]tetraconta-4,6,8,17,27,31,37-heptaen-36-yl}non-7-enoic acid)

3D PDB for NP0219124 (6-methyl-8-{22,25,26-trihydroxy-21,40-dimethyl-3-oxo-2,11,15,35,39-pentaoxapentacyclo[32.2.2.1¹²,¹⁶.1²⁰,²⁴.0¹⁰,¹⁴]tetraconta-4,6,8,17,27,31,37-heptaen-36-yl}non-7-enoic acid)

SMILES for NP0219124 (6-methyl-8-{22,25,26-trihydroxy-21,40-dimethyl-3-oxo-2,11,15,35,39-pentaoxapentacyclo[32.2.2.1¹²,¹⁶.1²⁰,²⁴.0¹⁰,¹⁴]tetraconta-4,6,8,17,27,31,37-heptaen-36-yl}non-7-enoic acid)

INCHI for NP0219124 (6-methyl-8-{22,25,26-trihydroxy-21,40-dimethyl-3-oxo-2,11,15,35,39-pentaoxapentacyclo[32.2.2.1¹²,¹⁶.1²⁰,²⁴.0¹⁰,¹⁴]tetraconta-4,6,8,17,27,31,37-heptaen-36-yl}non-7-enoic acid)

Structure for NP0219124 (6-methyl-8-{22,25,26-trihydroxy-21,40-dimethyl-3-oxo-2,11,15,35,39-pentaoxapentacyclo[32.2.2.1¹²,¹⁶.1²⁰,²⁴.0¹⁰,¹⁴]tetraconta-4,6,8,17,27,31,37-heptaen-36-yl}non-7-enoic acid)

3D Structure for NP0219124 (6-methyl-8-{22,25,26-trihydroxy-21,40-dimethyl-3-oxo-2,11,15,35,39-pentaoxapentacyclo[32.2.2.1¹²,¹⁶.1²⁰,²⁴.0¹⁰,¹⁴]tetraconta-4,6,8,17,27,31,37-heptaen-36-yl}non-7-enoic acid)