NP-MRD: Showing NP-Card for (1s,2r,4s,7s,8s,11r,12s,18r,20r)-7-(furan-3-yl)-1,8,12,17,17-pentamethyl-5,10,15-trioxo-3,6,16-trioxapentacyclo[9.9.0.0²,⁴.0²,⁸.0¹²,¹⁸]icos-13-en-20-yl acetate (NP0156144)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-02 13:18:54 UTC

Updated at

2022-09-02 13:18:54 UTC

NP-MRD ID

NP0156144

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2r,4s,7s,8s,11r,12s,18r,20r)-7-(furan-3-yl)-1,8,12,17,17-pentamethyl-5,10,15-trioxo-3,6,16-trioxapentacyclo[9.9.0.0²,⁴.0²,⁸.0¹²,¹⁸]icos-13-en-20-yl acetate

Description

11-Oxo-7alpha-obacunyl acetate 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,7s,8s,11r,12s,18r,20r)-7-(furan-3-yl)-1,8,12,17,17-pentamethyl-5,10,15-trioxo-3,6,16-trioxapentacyclo[9.9.0.0²,⁴.0²,⁸.0¹²,¹⁸]icos-13-en-20-yl acetate is found in Toona sinensis. (1s,2r,4s,7s,8s,11r,12s,18r,20r)-7-(furan-3-yl)-1,8,12,17,17-pentamethyl-5,10,15-trioxo-3,6,16-trioxapentacyclo[9.9.0.0²,⁴.0²,⁸.0¹²,¹⁸]icos-13-en-20-yl acetate was first documented in 2004 (PMID: 15541734). Based on a literature review very few articles have been published on 11-Oxo-7alpha-obacunyl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022215182D          

 37 42  0  0  1  0            999 V2000
    3.1132    3.0917    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3050    2.9261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7575    3.5433    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0442    2.1434    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5917    1.5263    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3999    1.6918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9474    1.0746    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7219    1.3587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2964    1.9508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2725    2.0506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4270    0.9303    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5316    0.1120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3143   -0.1488    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9571   -0.4801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1360   -0.4000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6866    0.2919    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3681   -0.4691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8784    0.1264    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6176   -0.6563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1651   -1.2735    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8094   -0.8219    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2619   -0.2047    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0012   -0.9874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4537   -0.3702    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1929   -1.1529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6729   -1.8239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1830   -2.4878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5997   -2.2270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5936   -1.4020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0938    0.2470    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1670    1.0297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3804    1.6469    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9752    1.1952    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7835    1.3607    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5227    0.5780    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3309    0.7435    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2508    1.5646    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
  2  4  1  0  0  0  0
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  7  6  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
  8 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
  7 16  1  0  0  0  0
 16 17  1  1  0  0  0
 16 18  1  0  0  0  0
 18 19  1  1  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  6  0  0  0
 22 24  1  0  0  0  0
 24 25  1  6  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 25 29  2  0  0  0  0
 24 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
 33 34  1  1  0  0  0
 35 34  1  1  0  0  0
 33 35  1  0  0  0  0
 22 35  1  0  0  0  0
 35 36  1  0  0  0  0
  5 36  1  0  0  0  0
 18 36  1  0  0  0  0
 36 37  1  1  0  0  0
M  END

     RDKit          3D

 69 74  0  0  0  0  0  0  0  0999 V2000
   -1.0386    4.9980    0.0641 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3540    3.6856   -0.5742 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8978    3.5624   -1.6877 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0142    2.5522    0.1292 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2325    1.2219   -0.3098 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1682    0.5898    0.6714 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3989   -0.8849    0.4894 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8523   -1.0982    0.2557 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5422   -0.5275    1.5168 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4503   -0.3462   -0.8992 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2990   -2.4146    0.1658 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6571   -3.5695    0.5781 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3629   -4.4972    1.0801 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2288   -3.8403    0.4958 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2778   -2.9984    0.0760 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4365   -1.5720   -0.4137 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8428   -1.6712   -1.8307 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0892   -0.9745   -0.1560 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0329   -1.6326   -0.8336 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0363   -2.5764   -1.5645 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3765   -1.0142   -0.5565 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3480    0.0709    0.4513 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4571   -0.5589    1.8357 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5890    0.9237    0.2499 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7791    0.1685   -0.1538 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2784    0.0629   -1.4603 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3871   -0.7325   -1.3725 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5522   -1.0825   -0.1254 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6283   -0.5756    0.6330 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7601    1.6579    1.4557 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5476    2.0272    2.0761 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6604    2.3946    3.2899 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2410    1.9883    1.3621 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4434    2.3854   -0.0017 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1747    1.0191    0.3748 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0508    0.4959   -0.4543 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5027    0.6600   -1.9168 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8546    5.2830    0.7600 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1211    4.8995    0.7025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8868    5.7833   -0.6960 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7241    1.3597   -1.3200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1283    1.1845    0.6105 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7723    0.8557    1.6962 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2090   -1.3356    1.5172 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4295   -1.1178    1.7934 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9149    0.5060    1.3169 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8658   -0.5162    2.3757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5217   -0.0879   -0.6368 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5815   -1.0276   -1.7921 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9783    0.6016   -1.1463 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8877   -4.8370    0.8084 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3109   -3.4367    0.1131 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2550   -0.7650   -2.2889 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0399   -2.0322   -2.4676 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6564   -2.4532   -1.8954 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0761   -1.0932    0.9370 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9860   -1.8642   -0.1266 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9050   -0.7506   -1.4965 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3806   -0.2601    2.3725 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4704   -1.6676    1.7876 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6330   -0.2248    2.5036 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3513    1.6565   -0.5630 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8109    0.5500   -2.3067 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0034   -1.0065   -2.2198 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5860   -0.7493    1.7205 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4501    2.5160    1.9305 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3698    1.3183   -2.0143 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7226   -0.3058   -2.3794 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3101    1.1200   -2.5364 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7 16  1  0
 16 17  1  6
 16 15  1  0
 15 14  2  0
 14 12  1  0
 12 13  2  0
 12 11  1  0
 11  8  1  0
  8  9  1  0
  8 10  1  0
 16 18  1  0
 18 19  1  0
 19 20  2  0
 19 21  1  0
 21 22  1  0
 22 23  1  1
 22 24  1  0
 24 30  1  0
 30 31  1  0
 31 32  2  0
 31 33  1  0
 33 34  1  0
 35 34  1  6
 35 36  1  0
 36 37  1  6
 24 25  1  0
 25 29  2  0
 29 28  1  0
 28 27  1  0
 27 26  2  0
 36  5  1  0
 26 25  1  0
  8  7  1  0
 36 18  1  0
 35 22  1  0
 35 33  1  0
  1 38  1  0
  1 39  1  0
  1 40  1  0
  5 41  1  6
  6 42  1  0
  6 43  1  0
  7 44  1  1
 17 53  1  0
 17 54  1  0
 17 55  1  0
 15 52  1  0
 14 51  1  0
  9 45  1  0
  9 46  1  0
  9 47  1  0
 10 48  1  0
 10 49  1  0
 10 50  1  0
 18 56  1  1
 21 57  1  0
 21 58  1  0
 23 59  1  0
 23 60  1  0
 23 61  1  0
 24 62  1  6
 33 66  1  1
 37 67  1  0
 37 68  1  0
 37 69  1  0
 29 65  1  0
 27 64  1  0
 26 63  1  0
M  END


  Mrv1652309022215182D          

 37 42  0  0  1  0            999 V2000
    3.1132    3.0917    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3050    2.9261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7575    3.5433    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0442    2.1434    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5917    1.5263    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3999    1.6918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9474    1.0746    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7219    1.3587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2964    1.9508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2725    2.0506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4270    0.9303    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5316    0.1120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3143   -0.1488    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9571   -0.4801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1360   -0.4000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6866    0.2919    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3681   -0.4691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8784    0.1264    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6176   -0.6563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1651   -1.2735    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8094   -0.8219    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2619   -0.2047    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0012   -0.9874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4537   -0.3702    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1929   -1.1529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6729   -1.8239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1830   -2.4878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5997   -2.2270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5936   -1.4020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0938    0.2470    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1670    1.0297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3804    1.6469    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9752    1.1952    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7835    1.3607    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5227    0.5780    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3309    0.7435    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2508    1.5646    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
  2  4  1  0  0  0  0
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  7  6  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
  8 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
  7 16  1  0  0  0  0
 16 17  1  1  0  0  0
 16 18  1  0  0  0  0
 18 19  1  1  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  6  0  0  0
 22 24  1  0  0  0  0
 24 25  1  6  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 25 29  2  0  0  0  0
 24 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
 33 34  1  1  0  0  0
 35 34  1  1  0  0  0
 33 35  1  0  0  0  0
 22 35  1  0  0  0  0
 35 36  1  0  0  0  0
  5 36  1  0  0  0  0
 18 36  1  0  0  0  0
 36 37  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0156144

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)O[C@@H]1C[C@@H]2[C@](C)(C=CC(=O)OC2(C)C)[C@H]2C(=O)C[C@@]3(C)[C@@H](OC(=O)[C@H]4O[C@@]34[C@]12C)C1=COC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C28H32O9/c1-14(29)34-18-11-17-24(2,3)36-19(31)7-9-25(17,4)20-16(30)12-26(5)21(15-8-10-33-13-15)35-23(32)22-28(26,37-22)27(18,20)6/h7-10,13,17-18,20-22H,11-12H2,1-6H3/t17-,18+,20+,21-,22+,25-,26-,27+,28+/m0/s1

> <INCHI_KEY>
UYUWMYJJTNAZHW-VKCGEEOUSA-N

> <FORMULA>
C28H32O9

> <MOLECULAR_WEIGHT>
512.555

> <EXACT_MASS>
512.20463261

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
69

> <JCHEM_AVERAGE_POLARIZABILITY>
51.5033421742648

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2R,4S,7R,8S,11R,12S,18R,20R)-7-(furan-3-yl)-1,8,12,17,17-pentamethyl-5,10,15-trioxo-3,6,16-trioxapentacyclo[9.9.0.0^{2,4}.0^{2,8}.0^{12,18}]icos-13-en-20-yl acetate

> <ALOGPS_LOGP>
3.49

> <JCHEM_LOGP>
2.8366663166666672

> <ALOGPS_LOGS>
-4.16

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
16.663076440844446

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8726338008331718

> <JCHEM_POLAR_SURFACE_AREA>
121.64000000000001

> <JCHEM_REFRACTIVITY>
126.82749999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.54e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,4S,7R,8S,11R,12S,18R,20R)-7-(furan-3-yl)-1,8,12,17,17-pentamethyl-5,10,15-trioxo-3,6,16-trioxapentacyclo[9.9.0.0^{2,4}.0^{2,8}.0^{12,18}]icos-13-en-20-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0       5.811   5.771   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.303   5.462   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       3.281   6.614   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       3.816   4.001   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       4.838   2.849   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.346   3.158   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.368   2.006   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.814   2.536   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.887   3.641   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.975   3.828   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      10.130   1.737   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      10.326   0.209   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      11.787  -0.278   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       9.253  -0.896   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.720  -0.747   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.882   0.545   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.287  -0.876   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.373   0.236   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.886  -1.225   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       5.908  -2.377   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       3.378  -1.534   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.356  -0.382   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.869  -1.843   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.847  -0.691   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.360  -2.152   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.256  -3.405   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.342  -4.644   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -1.119  -4.157   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -1.108  -2.617   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -0.175   0.461   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       0.312   1.922   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      -0.710   3.074   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       1.820   2.231   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       3.329   2.540   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       2.842   1.079   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       4.351   1.388   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       4.201   2.921   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   36                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   16                                                  
CONECT    8    7    9   10   11                                             
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    8   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15    7   17   18                                             
CONECT   17   16                                                            
CONECT   18   16   19   36                                                  
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23   24   35                                             
CONECT   23   22                                                            
CONECT   24   22   25   30                                                  
CONECT   25   24   26   29                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   25                                                       
CONECT   30   24   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34   35                                                  
CONECT   34   33   35                                                       
CONECT   35   34   33   22   36                                             
CONECT   36   35    5   18   37                                             
CONECT   37   36                                                            
MASTER        0    0    0    0    0    0    0    0   37    0   84    0
END

View in JSmol

Synonyms

Value	Source
11-oxo-7a-Obacunyl acetate	Generator
11-oxo-7a-Obacunyl acetic acid	Generator
11-oxo-7alpha-Obacunyl acetic acid	Generator
11-oxo-7Α-obacunyl acetate	Generator
11-oxo-7Α-obacunyl acetic acid	Generator

Chemical Formula

C₂₈H₃₂O₉

Average Mass

512.5550 Da

Monoisotopic Mass

512.20463 Da

IUPAC Name

(1S,2R,4S,7R,8S,11R,12S,18R,20R)-7-(furan-3-yl)-1,8,12,17,17-pentamethyl-5,10,15-trioxo-3,6,16-trioxapentacyclo[9.9.0.0^{2,4}.0^{2,8}.0^{12,18}]icos-13-en-20-yl acetate

Traditional Name

(1S,2R,4S,7R,8S,11R,12S,18R,20R)-7-(furan-3-yl)-1,8,12,17,17-pentamethyl-5,10,15-trioxo-3,6,16-trioxapentacyclo[9.9.0.0^{2,4}.0^{2,8}.0^{12,18}]icos-13-en-20-yl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)O[C@@H]1C[C@@H]2[C@](C)(C=CC(=O)OC2(C)C)[C@H]2C(=O)C[C@@]3(C)[C@@H](OC(=O)[C@H]4O[C@@]34[C@]12C)C1=COC=C1

InChI Identifier

InChI=1S/C28H32O9/c1-14(29)34-18-11-17-24(2,3)36-19(31)7-9-25(17,4)20-16(30)12-26(5)21(15-8-10-33-13-15)35-23(32)22-28(26,37-22)27(18,20)6/h7-10,13,17-18,20-22H,11-12H2,1-6H3/t17-,18+,20+,21-,22+,25-,26-,27+,28+/m0/s1

InChI Key

UYUWMYJJTNAZHW-VKCGEEOUSA-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
Toona sinensis	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
Naphthopyran
Naphthalene
Tricarboxylic acid or derivatives
1,4-dioxepane
Delta valerolactone
Dioxepane
Delta_valerolactone
Pyran
Oxane
Heteroaromatic compound
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Furan
Lactone
Ketone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Ether
Oxirane
Dialkyl ether
Organooxygen compound
Carbonyl group
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
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	3.49	ALOGPS
logP	2.84	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Acidic)	16.66	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	121.64 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	126.83 m³·mol⁻¹	ChemAxon
Polarizability	51.5 Å³	ChemAxon
Number of Rings	6	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

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

101366552

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Mitsui K, Maejima M, Fukaya H, Hitotsuyanagi Y, Takeya K: Limonoids from Cedrela sinensis. Phytochemistry. 2004 Dec;65(23):3075-81. doi: 10.1016/j.phytochem.2004.08.041. [PubMed:15541734 ]
LOTUS database [Link]

Showing NP-Card for (1s,2r,4s,7s,8s,11r,12s,18r,20r)-7-(furan-3-yl)-1,8,12,17,17-pentamethyl-5,10,15-trioxo-3,6,16-trioxapentacyclo[9.9.0.0²,⁴.0²,⁸.0¹²,¹⁸]icos-13-en-20-yl acetate (NP0156144)

MOL for NP0156144 ((1s,2r,4s,7s,8s,11r,12s,18r,20r)-7-(furan-3-yl)-1,8,12,17,17-pentamethyl-5,10,15-trioxo-3,6,16-trioxapentacyclo[9.9.0.0²,⁴.0²,⁸.0¹²,¹⁸]icos-13-en-20-yl acetate)

3D MOL for NP0156144 ((1s,2r,4s,7s,8s,11r,12s,18r,20r)-7-(furan-3-yl)-1,8,12,17,17-pentamethyl-5,10,15-trioxo-3,6,16-trioxapentacyclo[9.9.0.0²,⁴.0²,⁸.0¹²,¹⁸]icos-13-en-20-yl acetate)

3D SDF for NP0156144 ((1s,2r,4s,7s,8s,11r,12s,18r,20r)-7-(furan-3-yl)-1,8,12,17,17-pentamethyl-5,10,15-trioxo-3,6,16-trioxapentacyclo[9.9.0.0²,⁴.0²,⁸.0¹²,¹⁸]icos-13-en-20-yl acetate)

3D-SDF for NP0156144 ((1s,2r,4s,7s,8s,11r,12s,18r,20r)-7-(furan-3-yl)-1,8,12,17,17-pentamethyl-5,10,15-trioxo-3,6,16-trioxapentacyclo[9.9.0.0²,⁴.0²,⁸.0¹²,¹⁸]icos-13-en-20-yl acetate)

PDB for NP0156144 ((1s,2r,4s,7s,8s,11r,12s,18r,20r)-7-(furan-3-yl)-1,8,12,17,17-pentamethyl-5,10,15-trioxo-3,6,16-trioxapentacyclo[9.9.0.0²,⁴.0²,⁸.0¹²,¹⁸]icos-13-en-20-yl acetate)

3D PDB for NP0156144 ((1s,2r,4s,7s,8s,11r,12s,18r,20r)-7-(furan-3-yl)-1,8,12,17,17-pentamethyl-5,10,15-trioxo-3,6,16-trioxapentacyclo[9.9.0.0²,⁴.0²,⁸.0¹²,¹⁸]icos-13-en-20-yl acetate)

SMILES for NP0156144 ((1s,2r,4s,7s,8s,11r,12s,18r,20r)-7-(furan-3-yl)-1,8,12,17,17-pentamethyl-5,10,15-trioxo-3,6,16-trioxapentacyclo[9.9.0.0²,⁴.0²,⁸.0¹²,¹⁸]icos-13-en-20-yl acetate)

INCHI for NP0156144 ((1s,2r,4s,7s,8s,11r,12s,18r,20r)-7-(furan-3-yl)-1,8,12,17,17-pentamethyl-5,10,15-trioxo-3,6,16-trioxapentacyclo[9.9.0.0²,⁴.0²,⁸.0¹²,¹⁸]icos-13-en-20-yl acetate)

Structure for NP0156144 ((1s,2r,4s,7s,8s,11r,12s,18r,20r)-7-(furan-3-yl)-1,8,12,17,17-pentamethyl-5,10,15-trioxo-3,6,16-trioxapentacyclo[9.9.0.0²,⁴.0²,⁸.0¹²,¹⁸]icos-13-en-20-yl acetate)

3D Structure for NP0156144 ((1s,2r,4s,7s,8s,11r,12s,18r,20r)-7-(furan-3-yl)-1,8,12,17,17-pentamethyl-5,10,15-trioxo-3,6,16-trioxapentacyclo[9.9.0.0²,⁴.0²,⁸.0¹²,¹⁸]icos-13-en-20-yl acetate)