NP-MRD: Showing NP-Card for (+)-Anthothecol (NP0083000)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-04-29 04:03:34 UTC

Updated at

2022-04-29 04:03:34 UTC

NP-MRD ID

NP0083000

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-Anthothecol

Description

(1R,2R,4R,6R,7S,9R,10R,11S)-6-(furan-3-yl)-17-hydroxy-1,7,11,15,15-pentamethyl-14,18-dioxo-3-oxapentacyclo[8.8.0.0²,⁴.0²,⁷.0¹¹,¹⁶]Octadeca-12,16-dien-9-yl 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. (+)-Anthothecol is found in Khaya anthotheca. Based on a literature review very few articles have been published on (1R,2R,4R,6R,7S,9R,10R,11S)-6-(furan-3-yl)-17-hydroxy-1,7,11,15,15-pentamethyl-14,18-dioxo-3-oxapentacyclo[8.8.0.0²,⁴.0²,⁷.0¹¹,¹⁶]Octadeca-12,16-dien-9-yl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292206032D          

 35 40  0  0  1  0            999 V2000
    2.3055   -0.6539    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5858    0.1221    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0540    0.7528    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2419    0.6076    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9616   -0.1684    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4934   -0.7991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1370   -0.1416    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0923    0.6509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5906    1.1139    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3547    1.4248    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3693   -0.7929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1939   -0.7661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4742   -1.5420    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8229   -2.0484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1400   -1.5854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6017   -0.9107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3343    1.5287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8025    2.1594    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1464    1.6739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6782    1.0432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3979    0.2673    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9298   -0.3634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7419   -0.2182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0222    0.5577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8343    0.7029    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4904    1.1884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1021    1.7419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3736    2.0051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1176   -0.5086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4267    2.4498    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7431    1.5170    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8373   -1.2846    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5571   -2.0605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0889   -2.6912    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7449   -2.2057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  4  9  1  0  0  0  0
  9 10  1  1  0  0  0
  4 10  1  1  0  0  0
  7 11  1  6  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 11 15  1  0  0  0  0
  5 16  1  6  0  0  0
  3 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
  2 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  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
 20 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 21 29  1  6  0  0  0
 19 30  1  0  0  0  0
  3 31  1  1  0  0  0
  1 32  1  6  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 33 35  1  0  0  0  0
M  END

     RDKit          3D

 67 72  0  0  0  0  0  0  0  0999 V2000
    0.6393    3.9770    2.2044 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5276    2.5072    2.3941 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2709    1.9539    3.4793 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7225    1.7028    1.2880 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6611    0.3128    1.2583 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0234   -0.1685    0.8534 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1247   -0.3261   -0.6119 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0730    0.9500   -1.4048 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4153   -1.0458   -1.0480 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6283   -0.2907   -0.8126 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3377    0.5187   -1.6631 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4424    0.9742   -0.9374 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3752    0.4578    0.2620 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3228   -0.2938    0.3794 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0448   -1.2739   -2.4944 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6106   -1.8243   -2.2931 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6726   -2.7477   -1.2515 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1409   -1.3599   -1.1283 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1028   -1.4710   -0.2947 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1320   -2.4978    0.8251 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2120   -1.9120   -1.1756 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9629   -2.7010   -2.1205 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5634   -1.4247   -0.9303 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6533   -1.9852   -1.6393 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8270   -0.4786   -0.0714 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2674   -0.0859    0.0988 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.7563    0.8026   -0.9825 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1678   -1.3032    0.1401 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3411    0.5175    1.4796 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2055    1.3732    1.7326 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3555    0.0467    2.4861 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0878   -0.1310    2.1421 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7806    0.1789    0.7210 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9435    1.7115    0.6177 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4185   -0.1192    0.2728 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3714    4.3664    1.9149 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0032    4.4990    3.1136 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2887    4.1943    1.3196 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3895   -0.0631    2.2611 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8040    0.5888    1.1636 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3447   -1.1012    1.3441 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0357    1.2791   -1.8336 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4053    0.8435   -2.3130 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7509    1.8330   -0.7950 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4205   -2.0489   -0.5348 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1494    0.7854   -2.6888 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2033    1.6441   -1.3439 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0365   -0.8443    1.2914 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6820   -2.0339   -2.9721 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9222   -0.3558   -3.0641 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1098   -2.0649   -3.2310 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1920   -2.0415    1.8096 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6459   -3.3063    0.7615 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0955   -3.0200    0.6420 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5891   -2.2053   -2.6099 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1488    1.7861   -0.6523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6291    0.3529   -1.5507 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9742    0.8963   -1.7910 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6624   -2.2187    0.4523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9591   -1.0986    0.8914 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7489   -1.4186   -0.8217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7377   -0.1250    3.4705 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4374   -0.4708    2.8954 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1447    2.1895    0.0626 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1704    2.0806    1.6191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8802    1.9616    0.0312 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2531    0.5715   -0.6175 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  8  1  6
  7  9  1  0
  9 15  1  0
 15 16  1  0
 16 17  1  0
 18 17  1  1
 18 19  1  0
 19 20  1  1
 19 35  1  0
 35 33  1  0
 33 34  1  1
 33 32  1  0
 32 31  2  0
 31 29  1  0
 29 30  2  0
 29 26  1  0
 26 27  1  6
 26 28  1  0
 26 25  1  0
 25 23  2  0
 23 24  1  0
 23 21  1  0
 21 22  2  0
  9 10  1  0
 10 14  2  0
 14 13  1  0
 13 12  1  0
 12 11  2  0
 35  5  1  0
 25 33  1  0
 11 10  1  0
 18  7  1  0
 21 19  1  0
 18 16  1  0
  1 36  1  0
  1 37  1  0
  1 38  1  0
  5 39  1  1
  6 40  1  0
  6 41  1  0
  8 42  1  0
  8 43  1  0
  8 44  1  0
  9 45  1  1
 15 49  1  0
 15 50  1  0
 16 51  1  6
 20 52  1  0
 20 53  1  0
 20 54  1  0
 35 67  1  6
 34 64  1  0
 34 65  1  0
 34 66  1  0
 32 63  1  0
 31 62  1  0
 27 56  1  0
 27 57  1  0
 27 58  1  0
 28 59  1  0
 28 60  1  0
 28 61  1  0
 24 55  1  0
 14 48  1  0
 12 47  1  0
 11 46  1  0
M  END


  Mrv1652304292206032D          

 35 40  0  0  1  0            999 V2000
    2.3055   -0.6539    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5858    0.1221    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0540    0.7528    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2419    0.6076    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9616   -0.1684    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4934   -0.7991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1370   -0.1416    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0923    0.6509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5906    1.1139    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3547    1.4248    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3693   -0.7929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1939   -0.7661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4742   -1.5420    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8229   -2.0484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1400   -1.5854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6017   -0.9107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3343    1.5287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8025    2.1594    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1464    1.6739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6782    1.0432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3979    0.2673    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9298   -0.3634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7419   -0.2182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0222    0.5577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8343    0.7029    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4904    1.1884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1021    1.7419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3736    2.0051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1176   -0.5086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4267    2.4498    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7431    1.5170    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8373   -1.2846    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5571   -2.0605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0889   -2.6912    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7449   -2.2057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  4  9  1  0  0  0  0
  9 10  1  1  0  0  0
  4 10  1  1  0  0  0
  7 11  1  6  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 11 15  1  0  0  0  0
  5 16  1  6  0  0  0
  3 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
  2 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  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
 20 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 21 29  1  6  0  0  0
 19 30  1  0  0  0  0
  3 31  1  1  0  0  0
  1 32  1  6  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 33 35  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0083000

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)O[C@@H]1C[C@@]2(C)[C@@H](C[C@H]3O[C@@]23[C@@]2(C)[C@H]1[C@]1(C)C=CC(=O)C(C)(C)C1=C(O)C2=O)C1=COC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C28H32O7/c1-14(29)34-17-12-26(5)16(15-8-10-33-13-15)11-19-28(26,35-19)27(6)21(17)25(4)9-7-18(30)24(2,3)22(25)20(31)23(27)32/h7-10,13,16-17,19,21,31H,11-12H2,1-6H3/t16-,17+,19+,21+,25-,26-,27-,28+/m0/s1

> <INCHI_KEY>
AJTULIWKBMDPCJ-UHEFJMSXSA-N

> <FORMULA>
C28H32O7

> <MOLECULAR_WEIGHT>
480.557

> <EXACT_MASS>
480.21480337

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
67

> <JCHEM_AVERAGE_POLARIZABILITY>
50.261778056767724

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2R,4R,6R,7S,9R,10R,11S)-6-(furan-3-yl)-17-hydroxy-1,7,11,15,15-pentamethyl-14,18-dioxo-3-oxapentacyclo[8.8.0.0^{2,4}.0^{2,7}.0^{11,16}]octadeca-12,16-dien-9-yl acetate

> <ALOGPS_LOGP>
3.98

> <JCHEM_LOGP>
3.584001375000001

> <ALOGPS_LOGS>
-4.37

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.34949625175758

> <JCHEM_PKA_STRONGEST_BASIC>
-2.786218523458466

> <JCHEM_POLAR_SURFACE_AREA>
106.34

> <JCHEM_REFRACTIVITY>
127.34529999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.03e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,4R,6R,7S,9R,10R,11S)-6-(furan-3-yl)-17-hydroxy-1,7,11,15,15-pentamethyl-14,18-dioxo-3-oxapentacyclo[8.8.0.0^{2,4}.0^{2,7}.0^{11,16}]octadeca-12,16-dien-9-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0       4.304  -1.221   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.827   0.228   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.834   1.405   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.318   1.134   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.795  -0.314   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.788  -1.492   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.256  -0.264   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.172   1.215   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.102   2.079   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       2.529   2.660   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -0.689  -1.480   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.229  -1.430   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -2.752  -2.878   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -1.536  -3.824   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.261  -2.959   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.123  -1.700   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.357   2.854   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       3.365   4.031   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       5.873   3.125   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.866   1.947   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.343   0.499   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.336  -0.678   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.852  -0.407   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.375   1.041   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      10.891   1.312   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       8.382   2.218   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       9.524   3.252   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       8.164   3.743   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       5.820  -0.949   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       6.397   4.573   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       3.254   2.832   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       5.296  -2.398   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       4.773  -3.846   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       5.766  -5.024   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       3.257  -4.117   0.000  0.00  0.00           C+0
CONECT    1    2    6   32                                                  
CONECT    2    1    3   21                                                  
CONECT    3    2    4   17   31                                             
CONECT    4    3    5    9   10                                             
CONECT    5    4    6    7   16                                             
CONECT    6    5    1                                                       
CONECT    7    5    8   11                                                  
CONECT    8    7    9                                                       
CONECT    9    8    4   10                                                  
CONECT   10    9    4                                                       
CONECT   11    7   12   15                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   11                                                       
CONECT   16    5                                                            
CONECT   17    3   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   30                                                  
CONECT   20   19   21   26                                                  
CONECT   21   20    2   22   29                                             
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   20   27   28                                             
CONECT   27   26                                                            
CONECT   28   26                                                            
CONECT   29   21                                                            
CONECT   30   19                                                            
CONECT   31    3                                                            
CONECT   32    1   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33                                                            
MASTER        0    0    0    0    0    0    0    0   35    0   80    0
END

View in JSmol

Synonyms

Value	Source
(1R,2R,4R,6R,7S,9R,10R,11S)-6-(Furan-3-yl)-17-hydroxy-1,7,11,15,15-pentamethyl-14,18-dioxo-3-oxapentacyclo[8.8.0.0,.0,.0,]octadeca-12,16-dien-9-yl acetic acid	Generator

Chemical Formula

C₂₈H₃₂O₇

Average Mass

480.5570 Da

Monoisotopic Mass

480.21480 Da

IUPAC Name

(1R,2R,4R,6R,7S,9R,10R,11S)-6-(furan-3-yl)-17-hydroxy-1,7,11,15,15-pentamethyl-14,18-dioxo-3-oxapentacyclo[8.8.0.0^{2,4}.0^{2,7}.0^{11,16}]octadeca-12,16-dien-9-yl acetate

Traditional Name

(1R,2R,4R,6R,7S,9R,10R,11S)-6-(furan-3-yl)-17-hydroxy-1,7,11,15,15-pentamethyl-14,18-dioxo-3-oxapentacyclo[8.8.0.0^{2,4}.0^{2,7}.0^{11,16}]octadeca-12,16-dien-9-yl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)O[C@@H]1C[C@@]2(C)[C@@H](C[C@H]3O[C@@]23[C@@]2(C)[C@H]1[C@]1(C)C=CC(=O)C(C)(C)C1=C(O)C2=O)C1=COC=C1

InChI Identifier

InChI=1S/C28H32O7/c1-14(29)34-17-12-26(5)16(15-8-10-33-13-15)11-19-28(26,35-19)27(6)21(17)25(4)9-7-18(30)24(2,3)22(25)20(31)23(27)32/h7-10,13,16-17,19,21,31H,11-12H2,1-6H3/t16-,17+,19+,21+,25-,26-,27-,28+/m0/s1

InChI Key

AJTULIWKBMDPCJ-UHEFJMSXSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Khaya anthotheca	Plant	KNApSAcK

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
17-furanylsteroid skeleton
Steroid ester
7-oxosteroid
Oxosteroid
3-oxo-delta-1-steroid
Steroid
Delta-1-steroid
Naphthopyran
Naphthalene
Cyclohexenone
Pyran
Oxane
Heteroaromatic compound
Furan
Cyclic ketone
Ketone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Ether
Oxirane
Enol
Dialkyl ether
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
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	3.98	ALOGPS
logP	3.58	ChemAxon
logS	-4.4	ALOGPS
pKa (Strongest Acidic)	8.35	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	106.34 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	127.35 m³·mol⁻¹	ChemAxon
Polarizability	50.26 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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

162858826

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (+)-Anthothecol (NP0083000)

MOL for NP0083000 ((+)-Anthothecol)

3D MOL for NP0083000 ((+)-Anthothecol)

3D SDF for NP0083000 ((+)-Anthothecol)

3D-SDF for NP0083000 ((+)-Anthothecol)

PDB for NP0083000 ((+)-Anthothecol)

3D PDB for NP0083000 ((+)-Anthothecol)

SMILES for NP0083000 ((+)-Anthothecol)

INCHI for NP0083000 ((+)-Anthothecol)

Structure for NP0083000 ((+)-Anthothecol)

3D Structure for NP0083000 ((+)-Anthothecol)