NP-MRD: Showing NP-Card for (1's,2r,4'r,5s,6r,7's,9's,10'e,12'e,14'r,16'e,19'r)-7',9'-dihydroxy-5,6,6',10',14',16'-hexamethyl-2',20'-dioxaspiro[oxane-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-5',10',12',16'-tetraen-3'-one (NP0305643)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-10 21:38:43 UTC

Updated at

2022-09-10 21:38:44 UTC

NP-MRD ID

NP0305643

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1's,2r,4'r,5s,6r,7's,9's,10'e,12'e,14'r,16'e,19'r)-7',9'-dihydroxy-5,6,6',10',14',16'-hexamethyl-2',20'-dioxaspiro[oxane-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-5',10',12',16'-tetraen-3'-one

Description

(1'S,2R,4'R,5S,6R,7'S,9'S,10'E,12'E,14'R,16'E,19'R)-7',9'-dihydroxy-5,6,6',10',14',16'-hexamethyl-2',20'-dioxaspiro[oxane-2,21'-tricyclo[17.3.1.0⁴,⁹]Tricosane]-5',10',12',16'-tetraen-3'-one belongs to the class of organic compounds known as milbemycins. These are a group of macrolides with a structure containing a 16-membered lactone ring fused to a 1,7-dioxaspiroundecane ring system and to either a benzofuran (or hydrogenated derivative thereof). In some cases (e.G. Milbemycin E), the tetrahydrofuranyl ring is missing. Milbemycins can be o-glycosylated at C13 to form Avermectins. Milbemycins are produced by Streptomyces species. (1's,2r,4'r,5s,6r,7's,9's,10'e,12'e,14'r,16'e,19'r)-7',9'-dihydroxy-5,6,6',10',14',16'-hexamethyl-2',20'-dioxaspiro[oxane-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-5',10',12',16'-tetraen-3'-one is found in Streptomyces hygroscopicus. Based on a literature review very few articles have been published on (1'S,2R,4'R,5S,6R,7'S,9'S,10'E,12'E,14'R,16'E,19'R)-7',9'-dihydroxy-5,6,6',10',14',16'-hexamethyl-2',20'-dioxaspiro[oxane-2,21'-tricyclo[17.3.1.0⁴,⁹]Tricosane]-5',10',12',16'-tetraen-3'-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102223382D          

 37 40  0  0  1  0            999 V2000
    7.2973   -5.3569    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2295   -4.5347    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4835   -4.1823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4157   -3.3601    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.6698   -3.0078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6020   -2.1855    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9916   -3.4776    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2457   -3.1252    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1779   -2.3030    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4319   -1.9506    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3641   -1.1284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0422   -0.6586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9744    0.1636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2284    0.5160    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6526    0.6335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3985    0.2811    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.0767    0.7509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4663   -0.5411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2123   -0.8935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2801   -1.7157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0261   -2.0681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7042   -1.5983    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0939   -2.8903    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.7720   -2.4205    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8398   -3.2427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9077   -4.0649    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.6536   -4.4172    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7537   -2.4205    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8216   -3.2427    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8894   -4.0649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2112   -4.5347    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4653   -4.1823    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7871   -4.6522    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3975   -3.3601    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6515   -3.0078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0756   -2.8903    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5675   -3.5950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  4  3  1  1  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
 10  9  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  1  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
  4 23  1  0  0  0  0
 23 24  1  1  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
  2 26  1  0  0  0  0
 26 27  1  6  0  0  0
 10 28  1  0  0  0  0
 29 28  1  6  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  6  0  0  0
 32 34  1  0  0  0  0
 34 35  1  1  0  0  0
 34 36  1  0  0  0  0
 29 36  1  0  0  0  0
 29 37  1  0  0  0  0
  8 37  1  0  0  0  0
M  END

     RDKit          3D

 83 86  0  0  0  0  0  0  0  0999 V2000
   -2.9454    4.2249   -1.4044 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9532    2.8828   -0.7154 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8849    2.3831   -0.1598 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7991    1.0822    0.5338 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9186    1.3612    1.7345 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3478    2.3617    2.4164 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1803    0.6805    2.0855 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4124    0.4654    1.4887 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6919   -0.9693    1.1761 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0508   -1.3085   -0.2077 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9106   -2.0905   -0.8907 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6113   -3.2527   -0.0159 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5888   -3.7522    0.2445 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8430   -4.2525    1.6258 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6951   -3.8560   -0.7433 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4144   -2.5691   -1.0136 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1936   -2.1842   -2.4853 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8950   -2.7016   -0.8969 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6310   -2.1009    0.0098 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2267   -1.5877    1.3048 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3159   -0.6583    1.5574 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3374   -0.9790    2.6645 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1563    0.6391    0.9104 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6880    1.6396    1.7638 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0316    0.7343   -0.3468 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2479    2.1799   -0.7148 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.7357    2.2874   -2.0402 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3694   -0.3032   -1.0722 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8966    0.8099   -0.4375 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2959    1.8684   -1.4422 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2425    2.8389   -0.8166 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4324    2.1935   -0.1834 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.6418    2.4530   -1.0556 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1827    0.7021   -0.0692 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.1827    0.1534    0.9329 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9123    0.4966    0.4443 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7162    1.4026    0.3445 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0948    4.1274   -2.4860 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0007    4.7732   -1.1894 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7554    4.8185   -0.9324 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9469    2.9892   -0.2128 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2695    0.4008   -0.1665 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1720    0.7666    2.2803 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7751   -1.5546    1.4592 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4835   -1.4057    1.8579 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9140   -2.0411   -0.2510 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3022   -2.3997   -1.8818 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1164   -1.3667   -0.9980 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5233   -3.7031    0.4286 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4323   -5.3030    1.6641 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9413   -4.3903    1.8105 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4676   -3.6281    2.4291 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3655   -4.2964   -1.7067 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4705   -4.5779   -0.3689 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1361   -1.7728   -0.3164 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2215   -2.6477   -2.7767 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9576   -2.6955   -3.1065 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2186   -1.1049   -2.6465 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3244   -3.3714   -1.6698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7016   -1.9725   -0.2328 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7159   -1.9876    2.2325 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1421   -0.1098    3.2887 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4915   -1.4768    2.2007 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7744   -1.7388    3.3812 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5235    1.4018    2.7166 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5453    0.2410   -1.1855 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0502    0.3274   -0.1068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0022    2.6702   -0.0615 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6896    2.5516   -2.0394 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3791    2.4349   -1.7412 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7552    1.4077   -2.3400 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5608    3.5545   -1.6303 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7063    3.4923   -0.0807 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5556    2.5833    0.8367 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4253    2.0520   -2.0611 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5564    1.9441   -0.6785 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7983    3.5485   -1.1230 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2891    0.1871   -1.0512 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9019   -0.8611    1.2880 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1885    0.1781    0.4688 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1364    0.8370    1.8129 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9450    2.4040    0.7326 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8741    1.4392   -0.3732 H   0  0  0  0  0  0  0  0  0  0  0  0
 33 32  1  0
 32 31  1  0
 31 30  1  0
 30 29  1  0
 29 37  1  0
 37  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 21 23  1  0
 23 24  1  1
 23 25  1  0
 25 26  1  0
 26 27  1  0
 26  2  1  0
  2  1  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  5  7  1  0
 10 28  1  0
 29 36  1  1
 36 34  1  0
 34 35  1  0
 34 32  1  0
 28 29  1  0
  7  8  1  0
  4 23  1  0
 33 75  1  0
 33 76  1  0
 33 77  1  0
 32 74  1  1
 31 72  1  0
 31 73  1  0
 30 70  1  0
 30 71  1  0
 37 82  1  0
 37 83  1  0
  8 43  1  1
  9 44  1  0
  9 45  1  0
 10 46  1  1
 11 47  1  0
 11 48  1  0
 12 49  1  0
 14 50  1  0
 14 51  1  0
 14 52  1  0
 15 53  1  0
 15 54  1  0
 16 55  1  1
 17 56  1  0
 17 57  1  0
 17 58  1  0
 18 59  1  0
 19 60  1  0
 20 61  1  0
 22 62  1  0
 22 63  1  0
 22 64  1  0
 24 65  1  0
 25 66  1  0
 25 67  1  0
 26 68  1  1
 27 69  1  0
  1 38  1  0
  1 39  1  0
  1 40  1  0
  3 41  1  0
  4 42  1  6
 34 78  1  6
 35 79  1  0
 35 80  1  0
 35 81  1  0
M  END


  Mrv1652309102223382D          

 37 40  0  0  1  0            999 V2000
    7.2973   -5.3569    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2295   -4.5347    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4835   -4.1823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4157   -3.3601    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.6698   -3.0078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6020   -2.1855    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9916   -3.4776    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2457   -3.1252    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1779   -2.3030    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4319   -1.9506    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3641   -1.1284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0422   -0.6586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9744    0.1636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2284    0.5160    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6526    0.6335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3985    0.2811    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.0767    0.7509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4663   -0.5411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2123   -0.8935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2801   -1.7157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0261   -2.0681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7042   -1.5983    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0939   -2.8903    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.7720   -2.4205    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8398   -3.2427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9077   -4.0649    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.6536   -4.4172    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7537   -2.4205    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8216   -3.2427    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8894   -4.0649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2112   -4.5347    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4653   -4.1823    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7871   -4.6522    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3975   -3.3601    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6515   -3.0078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0756   -2.8903    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5675   -3.5950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  4  3  1  1  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
 10  9  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  1  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
  4 23  1  0  0  0  0
 23 24  1  1  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
  2 26  1  0  0  0  0
 26 27  1  6  0  0  0
 10 28  1  0  0  0  0
 29 28  1  6  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  6  0  0  0
 32 34  1  0  0  0  0
 34 35  1  1  0  0  0
 34 36  1  0  0  0  0
 29 36  1  0  0  0  0
 29 37  1  0  0  0  0
  8 37  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0305643

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1CC[C@]2(C[C@@H]3C[C@@H](C\C=C(C)\C[C@@H](C)\C=C\C=C(C)\[C@]4(O)C[C@H](O)C(C)=C[C@H]4C(=O)O3)O2)O[C@@H]1C

> <INCHI_IDENTIFIER>
InChI=1S/C31H46O6/c1-19-8-7-9-23(5)31(34)18-28(32)22(4)15-27(31)29(33)35-26-16-25(11-10-20(2)14-19)37-30(17-26)13-12-21(3)24(6)36-30/h7-10,15,19,21,24-28,32,34H,11-14,16-18H2,1-6H3/b8-7+,20-10+,23-9+/t19-,21-,24+,25+,26-,27-,28-,30-,31+/m0/s1

> <INCHI_KEY>
LJOBOTWVBIZFLJ-NTGTVSSRSA-N

> <FORMULA>
C31H46O6

> <MOLECULAR_WEIGHT>
514.703

> <EXACT_MASS>
514.329439201

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
83

> <JCHEM_AVERAGE_POLARIZABILITY>
58.6948319226452

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1'S,2R,4'R,5S,6R,7'S,9'S,10'E,12'E,14'R,16'E,19'R)-7',9'-dihydroxy-5,6,6',10',14',16'-hexamethyl-2',20'-dioxaspiro[oxane-2,21'-tricyclo[17.3.1.0^{4,9}]tricosane]-5',10',12',16'-tetraen-3'-one

> <JCHEM_LOGP>
4.816223596333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.665198239447122

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.52559863281817

> <JCHEM_PKA_STRONGEST_BASIC>
-3.011034249743396

> <JCHEM_POLAR_SURFACE_AREA>
85.22000000000001

> <JCHEM_REFRACTIVITY>
147.71060000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1'S,2R,4'R,5S,6R,7'S,9'S,10'E,12'E,14'R,16'E,19'R)-7',9'-dihydroxy-5,6,6',10',14',16'-hexamethyl-2',20'-dioxaspiro[oxane-2,21'-tricyclo[17.3.1.0^{4,9}]tricosane]-5',10',12',16'-tetraen-3'-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0      13.622 -10.000   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.495  -8.465   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      12.103  -7.807   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.976  -6.272   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.584  -5.614   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      10.457  -4.080   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       9.318  -6.491   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       7.925  -5.834   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.799  -4.299   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.406  -3.641   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.280  -2.106   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.545  -1.229   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.419   0.305   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.026   0.963   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.685   1.182   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.077   0.525   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      11.343   1.402   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      10.204  -1.010   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      11.596  -1.668   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      11.723  -3.203   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      13.115  -3.860   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      14.381  -2.983   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      13.242  -5.395   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      14.508  -4.518   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      14.634  -6.053   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      14.761  -7.588   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      16.153  -8.246   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       5.140  -4.518   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       5.267  -6.053   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.393  -7.588   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.128  -8.465   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       2.735  -7.807   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       1.469  -8.684   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       2.609  -6.272   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       1.216  -5.614   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       3.874  -5.395   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       6.659  -6.711   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   26                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   23                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   37                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   28                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21    4   24   25                                             
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25    2   27                                                  
CONECT   27   26                                                            
CONECT   28   10   29                                                       
CONECT   29   28   30   36   37                                             
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   29                                                       
CONECT   37   29    8                                                       
MASTER        0    0    0    0    0    0    0    0   37    0   80    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₁H₄₆O₆

Average Mass

514.7030 Da

Monoisotopic Mass

514.32944 Da

IUPAC Name

(1'S,2R,4'R,5S,6R,7'S,9'S,10'E,12'E,14'R,16'E,19'R)-7',9'-dihydroxy-5,6,6',10',14',16'-hexamethyl-2',20'-dioxaspiro[oxane-2,21'-tricyclo[17.3.1.0^{4,9}]tricosane]-5',10',12',16'-tetraen-3'-one

Traditional Name

(1'S,2R,4'R,5S,6R,7'S,9'S,10'E,12'E,14'R,16'E,19'R)-7',9'-dihydroxy-5,6,6',10',14',16'-hexamethyl-2',20'-dioxaspiro[oxane-2,21'-tricyclo[17.3.1.0^{4,9}]tricosane]-5',10',12',16'-tetraen-3'-one

CAS Registry Number

Not Available

SMILES

C[C@H]1CC[C@]2(C[C@@H]3C[C@@H](C\C=C(C)\C[C@@H](C)\C=C\C=C(C)\[C@]4(O)C[C@H](O)C(C)=C[C@H]4C(=O)O3)O2)O[C@@H]1C

InChI Identifier

InChI=1S/C31H46O6/c1-19-8-7-9-23(5)31(34)18-28(32)22(4)15-27(31)29(33)35-26-16-25(11-10-20(2)14-19)37-30(17-26)13-12-21(3)24(6)36-30/h7-10,15,19,21,24-28,32,34H,11-14,16-18H2,1-6H3/b8-7+,20-10+,23-9+/t19-,21-,24+,25+,26-,27-,28-,30-,31+/m0/s1

InChI Key

LJOBOTWVBIZFLJ-NTGTVSSRSA-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
Streptomyces hygroscopicus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as milbemycins. These are a group of macrolides with a structure containing a 16-membered lactone ring fused to a 1,7-dioxaspiroundecane ring system and to either a benzofuran (or hydrogenated derivative thereof). In some cases (e.G. Milbemycin E), the tetrahydrofuranyl ring is missing. Milbemycins can be o-glycosylated at C13 to form Avermectins. Milbemycins are produced by Streptomyces species.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Macrolides and analogues

Sub Class

Milbemycins

Direct Parent

Milbemycins

Alternative Parents

Substituents

Milbemycin
Ketal
Oxane
Tertiary alcohol
Carboxylic acid ester
Lactone
Secondary alcohol
Acetal
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Oxacycle
Organoheterocyclic compound
Organic oxide
Organic oxygen compound
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	4.82	ChemAxon
pKa (Strongest Acidic)	13.53	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	85.22 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	147.71 m³·mol⁻¹	ChemAxon
Polarizability	58.69 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	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

8729259

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10553868

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1's,2r,4'r,5s,6r,7's,9's,10'e,12'e,14'r,16'e,19'r)-7',9'-dihydroxy-5,6,6',10',14',16'-hexamethyl-2',20'-dioxaspiro[oxane-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-5',10',12',16'-tetraen-3'-one (NP0305643)

MOL for NP0305643 ((1's,2r,4'r,5s,6r,7's,9's,10'e,12'e,14'r,16'e,19'r)-7',9'-dihydroxy-5,6,6',10',14',16'-hexamethyl-2',20'-dioxaspiro[oxane-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-5',10',12',16'-tetraen-3'-one)

3D MOL for NP0305643 ((1's,2r,4'r,5s,6r,7's,9's,10'e,12'e,14'r,16'e,19'r)-7',9'-dihydroxy-5,6,6',10',14',16'-hexamethyl-2',20'-dioxaspiro[oxane-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-5',10',12',16'-tetraen-3'-one)

3D SDF for NP0305643 ((1's,2r,4'r,5s,6r,7's,9's,10'e,12'e,14'r,16'e,19'r)-7',9'-dihydroxy-5,6,6',10',14',16'-hexamethyl-2',20'-dioxaspiro[oxane-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-5',10',12',16'-tetraen-3'-one)

3D-SDF for NP0305643 ((1's,2r,4'r,5s,6r,7's,9's,10'e,12'e,14'r,16'e,19'r)-7',9'-dihydroxy-5,6,6',10',14',16'-hexamethyl-2',20'-dioxaspiro[oxane-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-5',10',12',16'-tetraen-3'-one)

PDB for NP0305643 ((1's,2r,4'r,5s,6r,7's,9's,10'e,12'e,14'r,16'e,19'r)-7',9'-dihydroxy-5,6,6',10',14',16'-hexamethyl-2',20'-dioxaspiro[oxane-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-5',10',12',16'-tetraen-3'-one)

3D PDB for NP0305643 ((1's,2r,4'r,5s,6r,7's,9's,10'e,12'e,14'r,16'e,19'r)-7',9'-dihydroxy-5,6,6',10',14',16'-hexamethyl-2',20'-dioxaspiro[oxane-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-5',10',12',16'-tetraen-3'-one)

SMILES for NP0305643 ((1's,2r,4'r,5s,6r,7's,9's,10'e,12'e,14'r,16'e,19'r)-7',9'-dihydroxy-5,6,6',10',14',16'-hexamethyl-2',20'-dioxaspiro[oxane-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-5',10',12',16'-tetraen-3'-one)

INCHI for NP0305643 ((1's,2r,4'r,5s,6r,7's,9's,10'e,12'e,14'r,16'e,19'r)-7',9'-dihydroxy-5,6,6',10',14',16'-hexamethyl-2',20'-dioxaspiro[oxane-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-5',10',12',16'-tetraen-3'-one)

Structure for NP0305643 ((1's,2r,4'r,5s,6r,7's,9's,10'e,12'e,14'r,16'e,19'r)-7',9'-dihydroxy-5,6,6',10',14',16'-hexamethyl-2',20'-dioxaspiro[oxane-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-5',10',12',16'-tetraen-3'-one)

3D Structure for NP0305643 ((1's,2r,4'r,5s,6r,7's,9's,10'e,12'e,14'r,16'e,19'r)-7',9'-dihydroxy-5,6,6',10',14',16'-hexamethyl-2',20'-dioxaspiro[oxane-2,21'-tricyclo[17.3.1.0⁴,⁹]tricosane]-5',10',12',16'-tetraen-3'-one)