NP-MRD: Showing NP-Card for (1s,2r,4s,5r,9r,10r,13r,14s,15s,17r)-15-[(1s)-1-(acetyloxy)-2-methoxy-2-oxoethyl]-9-(furan-3-yl)-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.0²,⁴.0⁴,¹³.0⁵,¹⁰]octadecan-17-yl propanoate (NP0251709)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-07 14:58:47 UTC

Updated at

2022-09-07 14:58:48 UTC

NP-MRD ID

NP0251709

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2r,4s,5r,9r,10r,13r,14s,15s,17r)-15-[(1s)-1-(acetyloxy)-2-methoxy-2-oxoethyl]-9-(furan-3-yl)-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.0²,⁴.0⁴,¹³.0⁵,¹⁰]octadecan-17-yl propanoate

Description

(1S,2R,4S,5R,9R,10R,13R,14S,15S,17R)-15-[(1S)-1-(acetyloxy)-2-methoxy-2-oxoethyl]-9-(furan-3-yl)-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.0²,⁴.0⁴,¹³.0⁵,¹⁰]Octadecan-17-yl propanoate belongs to the class of organic compounds known as limonoids. These are highly oxygenated, modified terpenoids with a prototypical structure either containing or derived from a precursor with a 4,4,8-trimethyl-17-furanylsteroid skeleton. All naturally occurring citrus limonoids contain a furan ring attached to the D-ring, at C-17, as well as oxygen containing functional groups at C-3, C-4, C-7, C-16 and C-17. (1s,2r,4s,5r,9r,10r,13r,14s,15s,17r)-15-[(1s)-1-(acetyloxy)-2-methoxy-2-oxoethyl]-9-(furan-3-yl)-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.0²,⁴.0⁴,¹³.0⁵,¹⁰]octadecan-17-yl propanoate is found in Swietenia mahagoni. Based on a literature review very few articles have been published on (1S,2R,4S,5R,9R,10R,13R,14S,15S,17R)-15-[(1S)-1-(acetyloxy)-2-methoxy-2-oxoethyl]-9-(furan-3-yl)-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.0²,⁴.0⁴,¹³.0⁵,¹⁰]Octadecan-17-yl propanoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072216582D          

 43 48  0  0  1  0            999 V2000
    0.9777   -3.4344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5591   -2.7235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2659   -2.7305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6723   -3.4485    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6845   -2.0196    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2781   -1.3016    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5837   -1.3178    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6113   -0.5648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4361   -0.5859    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6217    0.1561    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6379    0.9809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2622    0.1443    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6601    0.8670    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4850    0.8837    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8829    1.6063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4560    2.3123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7077    1.6230    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2333    1.5730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5916    1.5563    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6312    2.2956    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2043    3.0016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7320   -0.5769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4528   -0.1755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4598   -0.9653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5175    0.1087    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9625    0.8296    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7922    0.8455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2082    0.1301    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6131    0.8489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0330    0.1450    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4325    0.8669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0833    1.6143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6863    2.1774    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4082    1.7779    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2513    0.9680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4584   -0.5618    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0589   -1.2837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4843   -1.9906    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2341   -1.2986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8087   -0.5918    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9614   -0.6609    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2659   -1.4595    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4540   -1.3582    0.0000 C   0  0  2  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  2  0  0  0  0
  3  5  1  0  0  0  0
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  6  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  6  0  0  0
 10 12  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 13 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 12 22  1  0  0  0  0
  6 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 10 25  1  0  0  0  0
 25 26  1  1  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  6  0  0  0
 28 30  1  0  0  0  0
 30 31  1  6  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 31 35  2  0  0  0  0
 30 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 37 39  1  0  0  0  0
 40 39  1  1  0  0  0
 28 40  1  0  0  0  0
 40 41  1  0  0  0  0
 25 41  1  0  0  0  0
 41 42  1  6  0  0  0
 43 42  1  6  0  0  0
  7 43  1  0  0  0  0
 41 43  1  0  0  0  0
M  END

     RDKit          3D

 83 88  0  0  0  0  0  0  0  0999 V2000
   -3.3964    6.3839   -0.2884 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6761    5.2609   -0.9781 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4892    4.1120   -0.0234 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9174    4.2123    1.1380 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8670    2.9518   -0.3688 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7033    1.8992    0.5288 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4335    1.3568    0.7691 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8396    0.2379    1.6867 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1801    0.2893    2.7921 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7016   -0.9994    0.8284 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1672   -2.1522    1.6592 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6688   -0.5641   -0.2352 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6161   -1.6329   -0.7105 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.4350   -2.2390    0.2070 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7907   -2.2799    0.0651 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6497   -2.9442    1.0773 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3659   -1.7600   -0.9230 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9633   -2.6812   -1.5499 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2311   -2.2887   -2.4914 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1057   -4.0330   -1.3675 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4532   -4.9426   -2.2071 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5208    0.6592    0.0264 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1054    1.0340   -1.3432 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6597    0.4691    0.9580 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7664   -0.9021    0.6010 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2906   -1.5618   -0.6358 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7454   -1.9762   -0.5312 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5845   -0.9928    0.2611 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8514   -1.5676    1.6326 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9005   -0.9028   -0.4630 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.8293    0.1321    0.0177 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0003    0.6602    1.2728 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0259    1.5747    1.1594 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4564    1.6107   -0.0651 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7674    0.7676   -0.7643 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5552   -0.5667   -1.8121 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8072    0.5771   -1.9735 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9591    1.2127   -3.0742 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8605    1.0900   -0.9584 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8984    0.3435    0.3285 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5702    0.2609    1.0343 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5222    0.8324    2.2753 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8826    1.6159    1.2042 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.1213    6.9026   -0.9490 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9245    6.0211    0.6326 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6672    7.1359    0.0631 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6855    5.6370   -1.3037 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2975    4.9362   -1.8364 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1723    2.2435    1.4909 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1892    1.0751   -0.3078 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4405   -3.0593    1.1003 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9187   -1.8823    2.4352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2641   -2.4658    2.2693 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0843   -0.3794   -1.2163 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3018   -1.1415   -1.4826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3944   -2.2023    1.4199 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0607   -3.3744    1.9093 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2128   -3.7908    0.6224 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8035   -5.9837   -2.0090 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6617   -4.7572   -3.2809 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3530   -4.9662   -2.0410 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1751    0.6854   -1.4250 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5456    0.6121   -2.1765 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1652    2.1215   -1.4952 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5805   -0.3334    1.6891 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6527    0.5253    0.4265 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7157    1.4076    1.6089 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1444   -1.6761    1.3823 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0443   -1.0833   -1.5733 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7659   -2.5709   -0.6683 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8896   -2.9738   -0.0718 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1059   -2.0684   -1.5874 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9193   -1.8152    1.8021 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3342   -2.5678    1.7545 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5312   -0.8730    2.4317 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3945   -1.9166   -0.4668 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4992    0.4599    2.2024 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4256    2.1882    1.9855 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8996    0.5786   -1.8168 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8796    1.1429   -1.4615 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1402    2.1824   -0.8369 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5848    0.9626    0.9874 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4928    2.5064    1.0341 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  1  0
  6  7  1  0
  7 43  1  0
 43 42  1  0
 41 42  1  1
 41 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  1
 28 40  1  0
 40 39  1  0
 39 37  1  0
 37 38  2  0
 37 36  1  0
 36 30  1  0
 30 31  1  0
 31 35  2  0
 35 34  1  0
 34 33  1  0
 33 32  2  0
 25 10  1  0
 10 11  1  1
 10 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  2  0
 13 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  0
 12 22  1  0
 22 23  1  0
 22 24  1  0
 10  8  1  0
  8  9  2  0
 22  6  1  0
  8  7  1  0
 41 43  1  0
 40 41  1  0
 32 31  1  0
 30 28  1  0
  1 44  1  0
  1 45  1  0
  1 46  1  0
  2 47  1  0
  2 48  1  0
  6 49  1  1
  7 50  1  6
 43 83  1  6
 25 68  1  1
 26 69  1  0
 26 70  1  0
 27 71  1  0
 27 72  1  0
 29 73  1  0
 29 74  1  0
 29 75  1  0
 40 82  1  1
 39 80  1  0
 39 81  1  0
 30 76  1  6
 35 79  1  0
 33 78  1  0
 32 77  1  0
 11 51  1  0
 11 52  1  0
 11 53  1  0
 12 54  1  6
 13 55  1  6
 16 56  1  0
 16 57  1  0
 16 58  1  0
 21 59  1  0
 21 60  1  0
 21 61  1  0
 23 62  1  0
 23 63  1  0
 23 64  1  0
 24 65  1  0
 24 66  1  0
 24 67  1  0
M  END


  Mrv1652309072216582D          

 43 48  0  0  1  0            999 V2000
    0.9777   -3.4344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5591   -2.7235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2659   -2.7305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6723   -3.4485    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6845   -2.0196    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2781   -1.3016    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5837   -1.3178    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6113   -0.5648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4361   -0.5859    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6217    0.1561    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6379    0.9809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2622    0.1443    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6601    0.8670    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4850    0.8837    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8829    1.6063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4560    2.3123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7077    1.6230    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2333    1.5730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5916    1.5563    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6312    2.2956    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2043    3.0016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7320   -0.5769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4528   -0.1755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4598   -0.9653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5175    0.1087    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9625    0.8296    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7922    0.8455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2082    0.1301    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6131    0.8489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0330    0.1450    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4325    0.8669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0833    1.6143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6863    2.1774    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4082    1.7779    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2513    0.9680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4584   -0.5618    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0589   -1.2837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4843   -1.9906    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2341   -1.2986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8087   -0.5918    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9614   -0.6609    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2659   -1.4595    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4540   -1.3582    0.0000 C   0  0  2  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  2  0  0  0  0
  3  5  1  0  0  0  0
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  6  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  6  0  0  0
 10 12  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  1  6  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 13 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 12 22  1  0  0  0  0
  6 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 10 25  1  0  0  0  0
 25 26  1  1  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  6  0  0  0
 28 30  1  0  0  0  0
 30 31  1  6  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 31 35  2  0  0  0  0
 30 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 37 39  1  0  0  0  0
 40 39  1  1  0  0  0
 28 40  1  0  0  0  0
 40 41  1  0  0  0  0
 25 41  1  0  0  0  0
 41 42  1  6  0  0  0
 43 42  1  6  0  0  0
  7 43  1  0  0  0  0
 41 43  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0251709

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC(=O)O[C@@H]1[C@H]2[C@H]3O[C@@]33[C@H](CC[C@]4(C)[C@H]3CC(=O)O[C@H]4C3=COC=C3)[C@](C)([C@@H]([C@H](OC(C)=O)C(=O)OC)C1(C)C)C2=O

> <INCHI_IDENTIFIER>
InChI=1S/C32H40O11/c1-8-19(34)41-26-21-24(36)31(6,23(29(26,3)4)22(28(37)38-7)40-15(2)33)17-9-11-30(5)18(32(17)27(21)43-32)13-20(35)42-25(30)16-10-12-39-14-16/h10,12,14,17-18,21-23,25-27H,8-9,11,13H2,1-7H3/t17-,18-,21+,22+,23+,25+,26-,27-,30-,31-,32-/m1/s1

> <INCHI_KEY>
RZHCWHKYSBLXTK-HVBDNANNSA-N

> <FORMULA>
C32H40O11

> <MOLECULAR_WEIGHT>
600.661

> <EXACT_MASS>
600.257062108

> <ALOGPS_LOGP>
3.56

> <ALOGPS_LOGS>
-4.18

> <ALOGPS_SOLUBILITY>
3.97e-02 g/l

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0       1.825  -6.411   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.044  -5.084   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.496  -5.097   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -1.255  -6.437   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0      -1.278  -3.770   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -0.519  -2.430   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.090  -2.460   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.141  -1.054   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       2.681  -1.094   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       1.160   0.291   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.191   1.831   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.489   0.269   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.232   1.618   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -2.772   1.650   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -3.515   2.999   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.718   4.316   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -5.054   3.030   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -0.435   2.936   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       1.104   2.905   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      -1.178   4.285   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -0.381   5.603   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.366  -1.077   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -2.712  -0.328   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -2.725  -1.802   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.833   0.203   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.663   1.549   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.212   1.578   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       5.989   0.243   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.744   1.585   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       7.528   0.271   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       8.274   1.618   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       7.622   3.013   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       8.748   4.064   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      10.095   3.319   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       9.802   1.807   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       8.322  -1.049   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       7.577  -2.396   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       8.371  -3.716   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       6.037  -2.424   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       5.243  -1.105   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       3.661  -1.234   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       4.230  -2.724   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0       2.714  -2.535   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7   22                                                  
CONECT    7    6    8   43                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   12   25                                             
CONECT   11   10                                                            
CONECT   12   10   13   22                                                  
CONECT   13   12   14   18                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18   13   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20                                                            
CONECT   22   12    6   23   24                                             
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25   10   26   41                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   30   40                                             
CONECT   29   28                                                            
CONECT   30   28   31   36                                                  
CONECT   31   30   32   35                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   31                                                       
CONECT   36   30   37                                                       
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40                                                       
CONECT   40   39   28   41                                                  
CONECT   41   40   25   42   43                                             
CONECT   42   41   43                                                       
CONECT   43   42    7   41                                                  
MASTER        0    0    0    0    0    0    0    0   43    0   96    0
END

View in JSmol

Synonyms

Value	Source
(1S,2R,4S,5R,9R,10R,13R,14S,15S,17R)-15-[(1S)-1-(Acetyloxy)-2-methoxy-2-oxoethyl]-9-(furan-3-yl)-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.0,.0,.0,]octadecan-17-yl propanoic acid	Generator

Chemical Formula

C₃₂H₄₀O₁₁

Average Mass

600.6610 Da

Monoisotopic Mass

600.25706 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CCC(=O)O[C@@H]1[C@H]2[C@H]3O[C@@]33[C@H](CC[C@]4(C)[C@H]3CC(=O)O[C@H]4C3=COC=C3)[C@](C)([C@@H]([C@H](OC(C)=O)C(=O)OC)C1(C)C)C2=O

InChI Identifier

InChI=1S/C32H40O11/c1-8-19(34)41-26-21-24(36)31(6,23(29(26,3)4)22(28(37)38-7)40-15(2)33)17-9-11-30(5)18(32(17)27(21)43-32)13-20(35)42-25(30)16-10-12-39-14-16/h10,12,14,17-18,21-23,25-27H,8-9,11,13H2,1-7H3/t17-,18-,21+,22+,23+,25+,26-,27-,30-,31-,32-/m1/s1

InChI Key

RZHCWHKYSBLXTK-HVBDNANNSA-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
Swietenia mahagoni	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as limonoids. These are highly oxygenated, modified terpenoids with a prototypical structure either containing or derived from a precursor with a 4,4,8-trimethyl-17-furanylsteroid skeleton. All naturally occurring citrus limonoids contain a furan ring attached to the D-ring, at C-17, as well as oxygen containing functional groups at C-3, C-4, C-7, C-16 and C-17.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Limonoids

Alternative Parents

Substituents

Limonoid skeleton
Mexicanolide
Naphthopyran
Tetracarboxylic acid or derivatives
Naphthalene
Delta valerolactone
Delta_valerolactone
Oxepane
Oxane
Pyran
Furan
Heteroaromatic compound
Methyl ester
Lactone
Ketone
Carboxylic acid ester
Oxacycle
Ether
Oxirane
Dialkyl ether
Organoheterocyclic compound
Carboxylic acid derivative
Carbonyl group
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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

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

163045541

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,2r,4s,5r,9r,10r,13r,14s,15s,17r)-15-[(1s)-1-(acetyloxy)-2-methoxy-2-oxoethyl]-9-(furan-3-yl)-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.0²,⁴.0⁴,¹³.0⁵,¹⁰]octadecan-17-yl propanoate (NP0251709)

MOL for NP0251709 ((1s,2r,4s,5r,9r,10r,13r,14s,15s,17r)-15-[(1s)-1-(acetyloxy)-2-methoxy-2-oxoethyl]-9-(furan-3-yl)-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.0²,⁴.0⁴,¹³.0⁵,¹⁰]octadecan-17-yl propanoate)

3D MOL for NP0251709 ((1s,2r,4s,5r,9r,10r,13r,14s,15s,17r)-15-[(1s)-1-(acetyloxy)-2-methoxy-2-oxoethyl]-9-(furan-3-yl)-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.0²,⁴.0⁴,¹³.0⁵,¹⁰]octadecan-17-yl propanoate)

3D SDF for NP0251709 ((1s,2r,4s,5r,9r,10r,13r,14s,15s,17r)-15-[(1s)-1-(acetyloxy)-2-methoxy-2-oxoethyl]-9-(furan-3-yl)-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.0²,⁴.0⁴,¹³.0⁵,¹⁰]octadecan-17-yl propanoate)

3D-SDF for NP0251709 ((1s,2r,4s,5r,9r,10r,13r,14s,15s,17r)-15-[(1s)-1-(acetyloxy)-2-methoxy-2-oxoethyl]-9-(furan-3-yl)-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.0²,⁴.0⁴,¹³.0⁵,¹⁰]octadecan-17-yl propanoate)

PDB for NP0251709 ((1s,2r,4s,5r,9r,10r,13r,14s,15s,17r)-15-[(1s)-1-(acetyloxy)-2-methoxy-2-oxoethyl]-9-(furan-3-yl)-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.0²,⁴.0⁴,¹³.0⁵,¹⁰]octadecan-17-yl propanoate)

3D PDB for NP0251709 ((1s,2r,4s,5r,9r,10r,13r,14s,15s,17r)-15-[(1s)-1-(acetyloxy)-2-methoxy-2-oxoethyl]-9-(furan-3-yl)-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.0²,⁴.0⁴,¹³.0⁵,¹⁰]octadecan-17-yl propanoate)

SMILES for NP0251709 ((1s,2r,4s,5r,9r,10r,13r,14s,15s,17r)-15-[(1s)-1-(acetyloxy)-2-methoxy-2-oxoethyl]-9-(furan-3-yl)-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.0²,⁴.0⁴,¹³.0⁵,¹⁰]octadecan-17-yl propanoate)

INCHI for NP0251709 ((1s,2r,4s,5r,9r,10r,13r,14s,15s,17r)-15-[(1s)-1-(acetyloxy)-2-methoxy-2-oxoethyl]-9-(furan-3-yl)-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.0²,⁴.0⁴,¹³.0⁵,¹⁰]octadecan-17-yl propanoate)

Structure for NP0251709 ((1s,2r,4s,5r,9r,10r,13r,14s,15s,17r)-15-[(1s)-1-(acetyloxy)-2-methoxy-2-oxoethyl]-9-(furan-3-yl)-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.0²,⁴.0⁴,¹³.0⁵,¹⁰]octadecan-17-yl propanoate)

3D Structure for NP0251709 ((1s,2r,4s,5r,9r,10r,13r,14s,15s,17r)-15-[(1s)-1-(acetyloxy)-2-methoxy-2-oxoethyl]-9-(furan-3-yl)-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.0²,⁴.0⁴,¹³.0⁵,¹⁰]octadecan-17-yl propanoate)