NP-MRD: Showing NP-Card for methyl 2-[3,13,14-tris(acetyloxy)-6-(furan-3-yl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0²,¹¹.0⁵,¹⁰]heptadec-11-en-16-yl]acetate (NP0202751)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-04 22:01:53 UTC

Updated at

2022-09-04 22:01:53 UTC

NP-MRD ID

NP0202751

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 2-[3,13,14-tris(acetyloxy)-6-(furan-3-yl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0²,¹¹.0⁵,¹⁰]heptadec-11-en-16-yl]acetate

Description

Methyl 2-[3,13,14-tris(acetyloxy)-6-(furan-3-yl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0²,¹¹.0⁵,¹⁰]Heptadec-11-en-16-yl]acetate belongs to the class of organic compounds known as pentacarboxylic acids and derivatives. These are carboxylic acids containing exactly five carboxyl groups. methyl 2-[3,13,14-tris(acetyloxy)-6-(furan-3-yl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0²,¹¹.0⁵,¹⁰]heptadec-11-en-16-yl]acetate is found in Swietenia mahagoni. Based on a literature review very few articles have been published on methyl 2-[3,13,14-tris(acetyloxy)-6-(furan-3-yl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0²,¹¹.0⁵,¹⁰]Heptadec-11-en-16-yl]acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052200012D          

 45 49  0  0  0  0            999 V2000
   -0.4453    3.4161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6047    2.6067    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0166    2.0639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7973    2.3306    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1428    1.2545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4785    0.7117    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2148   -0.0700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4721    0.3870    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4045   -0.6152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5811   -0.8093    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0383   -1.4306    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3050   -2.2113    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1144   -2.3707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2378   -2.8326    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3628   -1.0730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4183   -1.8961    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1589   -2.2596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8440   -1.7999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2145   -3.0827    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1020   -0.7067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3657    0.0751    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1891    0.0227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5554   -0.7165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3787   -0.7689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7450   -1.5081    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8357   -0.0821    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4694    0.6571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9265    1.3440    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7508    1.3779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9732    2.1724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2863    2.6294    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6394    2.1174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6461    0.7095    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1031    1.3964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2798    1.4487    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4564    1.5011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0901    2.2404    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5472    2.9272    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1809    3.6664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3705    2.8748    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9994    0.8143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2177    1.0780    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1622    1.9011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0214   -0.0156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3228    0.4233    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  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  7 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  2  0  0  0  0
 10 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
 15 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 28 32  2  0  0  0  0
 27 33  1  0  0  0  0
 22 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
 35 36  1  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
 38 40  2  0  0  0  0
 36 41  1  0  0  0  0
 21 41  1  0  0  0  0
 41 42  1  0  0  0  0
  6 42  1  0  0  0  0
 42 43  1  0  0  0  0
 42 44  1  0  0  0  0
 15 44  1  0  0  0  0
 44 45  2  0  0  0  0
M  END

     RDKit          3D

 85 89  0  0  0  0  0  0  0  0999 V2000
   -3.1818    4.7105    2.2133 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8202    4.0256    1.0281 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2330    2.7434    1.0881 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0760    2.3009    2.2455 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8939    2.1195   -0.1858 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6731    0.6756   -0.2921 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8439   -0.1701   -0.0445 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9056   -0.0866   -1.1438 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6035    0.2098    1.2007 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4810   -1.6613    0.1655 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5920   -2.4740   -0.0308 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2771   -3.1932    0.8914 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4530   -4.0003    0.4291 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9023   -3.1520    2.0726 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2542   -2.0319   -0.5694 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1477   -3.3453   -1.0002 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1499   -4.4696   -0.2287 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0237   -5.7916   -0.8937 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2561   -4.3635    0.9970 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0265   -1.7756    0.2819 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7311   -0.7157    0.1735 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6763    0.1079   -1.0579 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4796    1.3165   -0.8702 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7270    2.0343   -2.0949 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5771    3.3795   -2.2381 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8518    4.0269   -3.5364 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2041    4.0810   -1.2681 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9129    0.9283   -0.4755 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0218   -0.1829    0.4956 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3048   -1.4995   -0.2402 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0987   -0.0311    1.5360 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2609    0.7717    1.0783 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4997    2.1308    1.1573 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7413    2.3232    0.5837 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2366    1.1784    0.1800 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3720    0.2360    0.4637 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6267    0.4079    2.7989 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5946   -0.2976    3.3839 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4498   -0.2696    4.6237 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7071   -1.0596    2.4647 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6811   -0.2575    1.2009 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7745    0.2643   -1.4410 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8941    1.0700   -2.6725 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1634   -1.1382   -1.7523 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3756   -1.4762   -2.8793 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0181    5.4203    1.9497 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6279    3.9722    2.8974 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3373    5.2811    2.6451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7648    2.4236   -0.8819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0734    2.7467   -0.6205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9829    0.4443    0.6164 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5100    0.8252   -0.9475 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5885   -0.9413   -0.9419 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5274   -0.0059   -2.1477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1039   -0.0464    2.1340 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5360   -0.5039    1.2288 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1208    1.1835    1.1446 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2537   -1.7250    1.2523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4305   -5.0015    0.9156 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4910   -4.0524   -0.6611 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3842   -3.4966    0.7590 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0043   -6.2143   -0.8101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2075   -5.7034   -2.0012 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8027   -6.4711   -0.5158 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2077   -2.5504    1.0250 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1299   -0.4581   -1.9333 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1285    2.0023   -0.0996 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8836    4.0635   -4.1119 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5871    3.4663   -4.1543 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1836    5.0815   -3.4349 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5164    0.6579   -1.3731 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3974    1.8335   -0.0569 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4044   -2.1449   -0.2694 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0943   -2.0894    0.2699 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6998   -1.2553   -1.2489 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5256   -1.0629    1.7618 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8186    2.8256    1.5881 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2230    3.2865    0.4884 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5779   -0.8157    0.2134 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1364   -2.0620    2.3487 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6854   -1.0962    2.8574 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4167    0.7799    1.4914 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0691    0.9206   -3.2526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6666    0.7399   -3.4006 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0154    2.1432   -2.5621 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  8  1  0
  7  9  1  0
  7 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  2  0
 10 15  1  0
 15 16  1  6
 16 17  1  0
 17 18  1  0
 17 19  2  0
 15 20  1  0
 20 21  2  0
 21 41  1  0
 41 40  1  0
 40 38  1  0
 38 39  2  0
 38 37  1  0
 37 31  1  0
 31 32  1  0
 32 36  2  0
 36 35  1  0
 35 34  1  0
 34 33  2  0
 31 29  1  0
 29 30  1  6
 29 28  1  0
 28 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 25 27  2  0
 23 22  1  0
 22 42  1  0
 42 43  1  6
 42 44  1  0
 44 45  2  0
 42  6  1  0
 44 15  1  0
 22 21  1  0
 29 41  1  0
 33 32  1  0
  1 46  1  0
  1 47  1  0
  1 48  1  0
  5 49  1  0
  5 50  1  0
  6 51  1  1
  8 52  1  0
  8 53  1  0
  8 54  1  0
  9 55  1  0
  9 56  1  0
  9 57  1  0
 10 58  1  1
 13 59  1  0
 13 60  1  0
 13 61  1  0
 18 62  1  0
 18 63  1  0
 18 64  1  0
 20 65  1  0
 41 82  1  1
 40 80  1  0
 40 81  1  0
 31 76  1  1
 36 79  1  0
 34 78  1  0
 33 77  1  0
 30 73  1  0
 30 74  1  0
 30 75  1  0
 28 71  1  0
 28 72  1  0
 23 67  1  1
 26 68  1  0
 26 69  1  0
 26 70  1  0
 22 66  1  6
 43 83  1  0
 43 84  1  0
 43 85  1  0
M  END


  Mrv1652309052200012D          

 45 49  0  0  0  0            999 V2000
   -0.4453    3.4161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6047    2.6067    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0166    2.0639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7973    2.3306    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1428    1.2545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4785    0.7117    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2148   -0.0700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4721    0.3870    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4045   -0.6152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5811   -0.8093    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0383   -1.4306    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3050   -2.2113    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1144   -2.3707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2378   -2.8326    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3628   -1.0730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4183   -1.8961    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1589   -2.2596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8440   -1.7999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2145   -3.0827    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1020   -0.7067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3657    0.0751    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1891    0.0227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5554   -0.7165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3787   -0.7689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7450   -1.5081    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8357   -0.0821    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4694    0.6571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9265    1.3440    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7508    1.3779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9732    2.1724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2863    2.6294    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6394    2.1174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6461    0.7095    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1031    1.3964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2798    1.4487    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4564    1.5011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0901    2.2404    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5472    2.9272    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1809    3.6664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3705    2.8748    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9994    0.8143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2177    1.0780    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1622    1.9011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0214   -0.0156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3228    0.4233    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  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  7 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  2  0  0  0  0
 10 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
 15 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 28 32  2  0  0  0  0
 27 33  1  0  0  0  0
 22 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
 35 36  1  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
 38 40  2  0  0  0  0
 36 41  1  0  0  0  0
 21 41  1  0  0  0  0
 41 42  1  0  0  0  0
  6 42  1  0  0  0  0
 42 43  1  0  0  0  0
 42 44  1  0  0  0  0
 15 44  1  0  0  0  0
 44 45  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0202751

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)CC1C(C)(C)C(OC(C)=O)C2(OC(C)=O)C=C3C4CC(=O)OC(C5=COC=C5)C4(C)CC(OC(C)=O)C3C1(C)C2=O

> <INCHI_IDENTIFIER>
InChI=1S/C33H40O12/c1-16(34)42-22-14-31(6)21(11-25(38)44-27(31)19-9-10-41-15-19)20-13-33(45-18(3)36)28(39)32(7,26(20)22)23(12-24(37)40-8)30(4,5)29(33)43-17(2)35/h9-10,13,15,21-23,26-27,29H,11-12,14H2,1-8H3

> <INCHI_KEY>
KWDDOLPNMJRDQX-UHFFFAOYSA-N

> <FORMULA>
C33H40O12

> <MOLECULAR_WEIGHT>
628.671

> <EXACT_MASS>
628.251976728

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
85

> <JCHEM_AVERAGE_POLARIZABILITY>
63.659180489135565

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl 2-[3,13,14-tris(acetyloxy)-6-(furan-3-yl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0^{2,11}.0^{5,10}]heptadec-11-en-16-yl]acetate

> <JCHEM_LOGP>
2.503988345333334

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-2.888670957974239

> <JCHEM_POLAR_SURFACE_AREA>
161.71

> <JCHEM_REFRACTIVITY>
153.2229

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
methyl [3,13,14-tris(acetyloxy)-6-(furan-3-yl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0^{2,11}.0^{5,10}]heptadec-11-en-16-yl]acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0      -0.831   6.377   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -1.129   4.866   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       0.031   3.853   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       1.488   4.350   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -0.267   2.342   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.893   1.328   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.401  -0.131   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.881   0.722   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.755  -1.148   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.085  -1.511   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       0.071  -2.670   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       0.569  -4.128   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.080  -4.425   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -0.444  -5.287   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       2.544  -2.003   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       2.648  -3.539   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       4.030  -4.218   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.309  -3.360   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       4.134  -5.754   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       3.924  -1.319   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.416   0.140   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.953   0.042   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.637  -1.338   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       8.174  -1.435   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       8.857  -2.815   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       9.027  -0.153   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       8.343   1.227   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       9.196   2.509   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      10.735   2.572   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      11.150   4.055   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       9.868   4.908   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       8.660   3.953   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       6.806   1.324   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       7.659   2.607   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       6.122   2.704   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       4.585   2.802   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       3.902   4.182   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       4.755   5.464   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       4.071   6.844   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       6.292   5.366   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       3.732   1.520   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       2.273   2.012   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       2.169   3.549   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       1.907  -0.029   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0       0.603   0.790   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7   42                                                  
CONECT    7    6    8    9   10                                             
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    7   11   15                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15   10   16   20   44                                             
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   15   21                                                       
CONECT   21   20   22   41                                                  
CONECT   22   21   23   33                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   28   33                                                  
CONECT   28   27   29   32                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   28                                                       
CONECT   33   27   22   34   35                                             
CONECT   34   33                                                            
CONECT   35   33   36                                                       
CONECT   36   35   37   41                                                  
CONECT   37   36   38                                                       
CONECT   38   37   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38                                                            
CONECT   41   36   21   42                                                  
CONECT   42   41    6   43   44                                             
CONECT   43   42                                                            
CONECT   44   42   15   45                                                  
CONECT   45   44                                                            
MASTER        0    0    0    0    0    0    0    0   45    0   98    0
END

View in JSmol

Synonyms

Value	Source
Methyl 2-[3,13,14-tris(acetyloxy)-6-(furan-3-yl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0,.0,]heptadec-11-en-16-yl]acetic acid	Generator

Chemical Formula

C₃₃H₄₀O₁₂

Average Mass

628.6710 Da

Monoisotopic Mass

628.25198 Da

IUPAC Name

methyl 2-[3,13,14-tris(acetyloxy)-6-(furan-3-yl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0^{2,11}.0^{5,10}]heptadec-11-en-16-yl]acetate

Traditional Name

methyl [3,13,14-tris(acetyloxy)-6-(furan-3-yl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0^{2,11}.0^{5,10}]heptadec-11-en-16-yl]acetate

CAS Registry Number

Not Available

SMILES

COC(=O)CC1C(C)(C)C(OC(C)=O)C2(OC(C)=O)C=C3C4CC(=O)OC(C5=COC=C5)C4(C)CC(OC(C)=O)C3C1(C)C2=O

InChI Identifier

InChI=1S/C33H40O12/c1-16(34)42-22-14-31(6)21(11-25(38)44-27(31)19-9-10-41-15-19)20-13-33(45-18(3)36)28(39)32(7,26(20)22)23(12-24(37)40-8)30(4,5)29(33)43-17(2)35/h9-10,13,15,21-23,26-27,29H,11-12,14H2,1-8H3

InChI Key

KWDDOLPNMJRDQX-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
Swietenia mahagoni	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pentacarboxylic acids and derivatives. These are carboxylic acids containing exactly five carboxyl groups.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Pentacarboxylic acids and derivatives

Direct Parent

Pentacarboxylic acids and derivatives

Alternative Parents

Substituents

Pentacarboxylic acid or derivatives
Naphthopyran
Naphthalene
Delta valerolactone
Cyclohexenone
Delta_valerolactone
Alpha-acyloxy ketone
Pyran
Oxane
Furan
Heteroaromatic compound
Methyl ester
Carboxylic acid ester
Ketone
Lactone
Oxacycle
Organoheterocyclic compound
Hydrocarbon derivative
Carbonyl group
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
logP	2.5	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	161.71 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	153.22 m³·mol⁻¹	ChemAxon
Polarizability	63.66 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	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

75082497

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 2-[3,13,14-tris(acetyloxy)-6-(furan-3-yl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0²,¹¹.0⁵,¹⁰]heptadec-11-en-16-yl]acetate (NP0202751)

MOL for NP0202751 (methyl 2-[3,13,14-tris(acetyloxy)-6-(furan-3-yl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0²,¹¹.0⁵,¹⁰]heptadec-11-en-16-yl]acetate)

3D MOL for NP0202751 (methyl 2-[3,13,14-tris(acetyloxy)-6-(furan-3-yl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0²,¹¹.0⁵,¹⁰]heptadec-11-en-16-yl]acetate)

3D SDF for NP0202751 (methyl 2-[3,13,14-tris(acetyloxy)-6-(furan-3-yl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0²,¹¹.0⁵,¹⁰]heptadec-11-en-16-yl]acetate)

3D-SDF for NP0202751 (methyl 2-[3,13,14-tris(acetyloxy)-6-(furan-3-yl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0²,¹¹.0⁵,¹⁰]heptadec-11-en-16-yl]acetate)

PDB for NP0202751 (methyl 2-[3,13,14-tris(acetyloxy)-6-(furan-3-yl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0²,¹¹.0⁵,¹⁰]heptadec-11-en-16-yl]acetate)

3D PDB for NP0202751 (methyl 2-[3,13,14-tris(acetyloxy)-6-(furan-3-yl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0²,¹¹.0⁵,¹⁰]heptadec-11-en-16-yl]acetate)

SMILES for NP0202751 (methyl 2-[3,13,14-tris(acetyloxy)-6-(furan-3-yl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0²,¹¹.0⁵,¹⁰]heptadec-11-en-16-yl]acetate)

INCHI for NP0202751 (methyl 2-[3,13,14-tris(acetyloxy)-6-(furan-3-yl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0²,¹¹.0⁵,¹⁰]heptadec-11-en-16-yl]acetate)

Structure for NP0202751 (methyl 2-[3,13,14-tris(acetyloxy)-6-(furan-3-yl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0²,¹¹.0⁵,¹⁰]heptadec-11-en-16-yl]acetate)

3D Structure for NP0202751 (methyl 2-[3,13,14-tris(acetyloxy)-6-(furan-3-yl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0²,¹¹.0⁵,¹⁰]heptadec-11-en-16-yl]acetate)