NP-MRD: Showing NP-Card for 13-[(1e)-2,6-dimethylhepta-1,5-dien-1-yl]-8,10,14-trihydroxy-2,2-dimethyl-13h-1,6,12-trioxapentaphen-11-one (NP0272536)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-08 19:11:40 UTC

Updated at

2022-09-08 19:11:40 UTC

NP-MRD ID

NP0272536

Secondary Accession Numbers

None

Natural Product Identification

Common Name

13-[(1e)-2,6-dimethylhepta-1,5-dien-1-yl]-8,10,14-trihydroxy-2,2-dimethyl-13h-1,6,12-trioxapentaphen-11-one

Description

Macaranone D belongs to the class of organic compounds known as pyranoflavonoids. Pyranoflavonoids are compounds containing a pyran ring fused to a 2-phenyl-1,4-benzopyran skeleton. 13-[(1e)-2,6-dimethylhepta-1,5-dien-1-yl]-8,10,14-trihydroxy-2,2-dimethyl-13h-1,6,12-trioxapentaphen-11-one is found in Macaranga sampsonii. Based on a literature review very few articles have been published on Macaranone D.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082221112D          

 37 41  0  0  0  0            999 V2000
   -0.1105   -5.3033    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -4.5888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105   -3.8743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -4.5888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -3.8743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -3.8743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -3.1599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -3.1599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -1.7309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4895    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4895    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4895   -1.0164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520   -1.7309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -1.7309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -0.3020    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7425   -0.1178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7425    0.9428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 C   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
  2  4  2  0  0  0  0
  4  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  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  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
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  2  0  0  0  0
 15 22  1  0  0  0  0
 22 23  1  0  0  0  0
 12 23  1  0  0  0  0
 23 24  2  0  0  0  0
 13 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  2  0  0  0  0
 25 31  1  0  0  0  0
 10 31  1  0  0  0  0
 28 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
 33 36  1  0  0  0  0
 36 37  2  0  0  0  0
 27 37  1  0  0  0  0
M  END

     RDKit          3D

 67 71  0  0  0  0  0  0  0  0999 V2000
    6.3739    0.3161    1.6809 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4534   -0.6437    0.5914 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7809   -1.3939    0.4795 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5396   -0.9279   -0.2781 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1839   -0.4334   -0.4816 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5979    0.5437    0.4442 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1794    0.9205    0.0198 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4022    1.8997    0.8205 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6158    0.3935   -1.0508 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2381    0.7236   -1.5115 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1133    2.0387   -1.3544 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2743    2.5192   -0.8620 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2452    1.6694   -0.4033 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3880    2.0454    0.0860 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7110    3.3134    0.1810 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9379    3.6592    0.7084 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2846    5.0002    0.8112 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5140    5.3077    1.3411 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3821    5.9487    0.3785 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1585    5.5935   -0.1470 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2455    6.5384   -0.5842 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7880    4.2485   -0.2601 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5660    3.8895   -0.7847 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7403    4.7280   -1.1794 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9411    0.2324   -0.4847 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8882   -0.6837   -0.0106 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6916   -2.0449   -0.0267 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4796   -2.5010   -0.5468 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5354   -1.6047   -1.0189 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6530   -2.0948   -1.5266 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7581   -0.2451   -0.9914 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2980   -3.8577   -0.5560 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1839   -4.8190   -0.1081 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5185   -5.5763    1.0453 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5155   -5.8015   -1.2329 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4346   -4.2802    0.4251 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6781   -2.9980    0.4667 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2731    1.3489    1.2417 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3596    0.4008    2.2432 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5708    0.1703    2.4176 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6261   -2.3495   -0.0404 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4197   -0.7429   -0.1493 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2451   -1.4982    1.4647 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8218   -1.7312   -1.0694 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1549    0.0388   -1.5255 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5267   -1.3679   -0.5416 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1157    1.5098    0.4904 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5233    0.1021    1.4650 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3169    2.8873    0.3567 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9956    2.0817    1.7659 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4504    1.4677    1.1975 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1900   -0.3394   -1.6457 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2438    0.5234   -2.6367 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6232    2.8912    1.0387 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1586    4.6160    1.6506 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6476    6.9806    0.4571 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4985    7.5160   -0.5091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8123   -0.2806    0.3830 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8655   -3.0760   -1.5698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7829   -4.9153    1.5470 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0109   -6.4859    0.6911 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2639   -5.8588    1.8226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0579   -5.2298   -2.0097 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1876   -6.5697   -0.8472 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5791   -6.1634   -1.6612 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2125   -4.9681    0.8109 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6108   -2.5814    0.8636 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 17 19  2  0
 19 20  1  0
 20 21  1  0
 20 22  2  0
 22 23  1  0
 23 24  2  0
 13 25  1  0
 25 26  2  0
 26 27  1  0
 27 28  2  0
 28 32  1  0
 32 33  1  0
 33 34  1  0
 33 35  1  0
 33 36  1  0
 36 37  2  0
 28 29  1  0
 29 30  1  0
 29 31  2  0
 31 10  1  0
 23 12  1  0
 31 25  1  0
 22 15  1  0
 37 27  1  0
  1 38  1  0
  1 39  1  0
  1 40  1  0
  3 41  1  0
  3 42  1  0
  3 43  1  0
  4 44  1  0
  5 45  1  0
  5 46  1  0
  6 47  1  0
  6 48  1  0
  8 49  1  0
  8 50  1  0
  8 51  1  0
  9 52  1  0
 10 53  1  6
 16 54  1  0
 18 55  1  0
 19 56  1  0
 21 57  1  0
 26 58  1  0
 34 60  1  0
 34 61  1  0
 34 62  1  0
 35 63  1  0
 35 64  1  0
 35 65  1  0
 36 66  1  0
 37 67  1  0
 30 59  1  0
M  END


  Mrv1652309082221112D          

 37 41  0  0  0  0            999 V2000
   -0.1105   -5.3033    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -4.5888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105   -3.8743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -4.5888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -3.8743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -3.8743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -3.1599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -3.1599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -1.7309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4895    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4895    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4895   -1.0164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520   -1.7309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -1.7309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -0.3020    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7425   -0.1178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7425    0.9428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 C   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
  2  4  2  0  0  0  0
  4  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  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  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
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  2  0  0  0  0
 15 22  1  0  0  0  0
 22 23  1  0  0  0  0
 12 23  1  0  0  0  0
 23 24  2  0  0  0  0
 13 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  2  0  0  0  0
 25 31  1  0  0  0  0
 10 31  1  0  0  0  0
 28 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
 33 36  1  0  0  0  0
 36 37  2  0  0  0  0
 27 37  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0272536

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCC\C(C)=C\C1OC2=C(OC3=CC(O)=CC(O)=C3C2=O)C2=CC3=C(OC(C)(C)C=C3)C(O)=C12

> <INCHI_IDENTIFIER>
InChI=1S/C30H30O7/c1-15(2)7-6-8-16(3)11-21-23-19(12-17-9-10-30(4,5)37-27(17)25(23)33)28-29(36-21)26(34)24-20(32)13-18(31)14-22(24)35-28/h7,9-14,21,31-33H,6,8H2,1-5H3/b16-11+

> <INCHI_KEY>
DZZXWKNORXMNFI-LFIBNONCSA-N

> <FORMULA>
C30H30O7

> <MOLECULAR_WEIGHT>
502.563

> <EXACT_MASS>
502.199153306

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
67

> <JCHEM_AVERAGE_POLARIZABILITY>
54.59209278210725

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
13-[(1E)-2,6-dimethylhepta-1,5-dien-1-yl]-8,10,14-trihydroxy-2,2-dimethyl-11,13-dihydro-2H-1,6,12-trioxapentaphen-11-one

> <JCHEM_LOGP>
6.305270313000001

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
7.928850445285042

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.377298093598055

> <JCHEM_PKA_STRONGEST_BASIC>
-4.655234662426598

> <JCHEM_POLAR_SURFACE_AREA>
105.45000000000002

> <JCHEM_REFRACTIVITY>
145.17149999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
13-[(1E)-2,6-dimethylhepta-1,5-dien-1-yl]-8,10,14-trihydroxy-2,2-dimethyl-13H-1,6,12-trioxapentaphen-11-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0      -0.206  -9.899   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.564  -8.566   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.206  -7.232   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.104  -8.566   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.874  -7.232   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.414  -7.232   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.184  -5.898   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.724  -5.898   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.414  -4.565   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.184  -3.231   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       6.724  -3.231   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       7.494  -1.897   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.724  -0.564   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       7.494   0.770   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       9.034   0.770   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.804   2.104   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      11.344   2.104   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      12.114   3.437   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      12.114   0.770   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      11.344  -0.564   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      12.114  -1.897   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       9.804  -0.564   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.034  -1.897   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       9.804  -3.231   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       5.184  -0.564   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.414   0.770   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.874   0.770   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.104  -0.564   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.874  -1.897   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       2.104  -3.231   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       4.414  -1.897   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       0.564  -0.564   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      -0.206   0.770   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -1.386  -0.220   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -1.386   1.760   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       0.564   2.104   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       2.104   2.104   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                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11   31                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   23                                                  
CONECT   13   12   14   25                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   22                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   15   23                                                  
CONECT   23   22   12   24                                                  
CONECT   24   23                                                            
CONECT   25   13   26   31                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   37                                                  
CONECT   28   27   29   32                                                  
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   25   10                                                  
CONECT   32   28   33                                                       
CONECT   33   32   34   35   36                                             
CONECT   34   33                                                            
CONECT   35   33                                                            
CONECT   36   33   37                                                       
CONECT   37   36   27                                                       
MASTER        0    0    0    0    0    0    0    0   37    0   82    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₃₀O₇

Average Mass

502.5630 Da

Monoisotopic Mass

502.19915 Da

IUPAC Name

13-[(1E)-2,6-dimethylhepta-1,5-dien-1-yl]-8,10,14-trihydroxy-2,2-dimethyl-11,13-dihydro-2H-1,6,12-trioxapentaphen-11-one

Traditional Name

13-[(1E)-2,6-dimethylhepta-1,5-dien-1-yl]-8,10,14-trihydroxy-2,2-dimethyl-13H-1,6,12-trioxapentaphen-11-one

CAS Registry Number

Not Available

SMILES

CC(C)=CCC\C(C)=C\C1OC2=C(OC3=CC(O)=CC(O)=C3C2=O)C2=CC3=C(OC(C)(C)C=C3)C(O)=C12

InChI Identifier

InChI=1S/C30H30O7/c1-15(2)7-6-8-16(3)11-21-23-19(12-17-9-10-30(4,5)37-27(17)25(23)33)28-29(36-21)26(34)24-20(32)13-18(31)14-22(24)35-28/h7,9-14,21,31-33H,6,8H2,1-5H3/b16-11+

InChI Key

DZZXWKNORXMNFI-LFIBNONCSA-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
Macaranga sampsonii	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyranoflavonoids. Pyranoflavonoids are compounds containing a pyran ring fused to a 2-phenyl-1,4-benzopyran skeleton.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Pyranoflavonoids

Direct Parent

Pyranoflavonoids

Alternative Parents

Substituents

Pyranoflavonoid
Pyranochromene
2,2-dimethyl-1-benzopyran
Chromone
Benzopyran
1-benzopyran
2-benzopyran
Alkyl aryl ether
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Pyranone
Pyran
Benzenoid
Heteroaromatic compound
Vinylogous acid
Ether
Polyol
Oxacycle
Organoheterocyclic compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	6.31	ChemAxon
pKa (Strongest Acidic)	6.38	ChemAxon
pKa (Strongest Basic)	-4.7	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	105.45 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	145.17 m³·mol⁻¹	ChemAxon
Polarizability	54.59 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	No	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

42642884

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 13-[(1e)-2,6-dimethylhepta-1,5-dien-1-yl]-8,10,14-trihydroxy-2,2-dimethyl-13h-1,6,12-trioxapentaphen-11-one (NP0272536)

MOL for NP0272536 (13-[(1e)-2,6-dimethylhepta-1,5-dien-1-yl]-8,10,14-trihydroxy-2,2-dimethyl-13h-1,6,12-trioxapentaphen-11-one)

3D MOL for NP0272536 (13-[(1e)-2,6-dimethylhepta-1,5-dien-1-yl]-8,10,14-trihydroxy-2,2-dimethyl-13h-1,6,12-trioxapentaphen-11-one)

3D SDF for NP0272536 (13-[(1e)-2,6-dimethylhepta-1,5-dien-1-yl]-8,10,14-trihydroxy-2,2-dimethyl-13h-1,6,12-trioxapentaphen-11-one)

3D-SDF for NP0272536 (13-[(1e)-2,6-dimethylhepta-1,5-dien-1-yl]-8,10,14-trihydroxy-2,2-dimethyl-13h-1,6,12-trioxapentaphen-11-one)

PDB for NP0272536 (13-[(1e)-2,6-dimethylhepta-1,5-dien-1-yl]-8,10,14-trihydroxy-2,2-dimethyl-13h-1,6,12-trioxapentaphen-11-one)

3D PDB for NP0272536 (13-[(1e)-2,6-dimethylhepta-1,5-dien-1-yl]-8,10,14-trihydroxy-2,2-dimethyl-13h-1,6,12-trioxapentaphen-11-one)

SMILES for NP0272536 (13-[(1e)-2,6-dimethylhepta-1,5-dien-1-yl]-8,10,14-trihydroxy-2,2-dimethyl-13h-1,6,12-trioxapentaphen-11-one)

INCHI for NP0272536 (13-[(1e)-2,6-dimethylhepta-1,5-dien-1-yl]-8,10,14-trihydroxy-2,2-dimethyl-13h-1,6,12-trioxapentaphen-11-one)

Structure for NP0272536 (13-[(1e)-2,6-dimethylhepta-1,5-dien-1-yl]-8,10,14-trihydroxy-2,2-dimethyl-13h-1,6,12-trioxapentaphen-11-one)

3D Structure for NP0272536 (13-[(1e)-2,6-dimethylhepta-1,5-dien-1-yl]-8,10,14-trihydroxy-2,2-dimethyl-13h-1,6,12-trioxapentaphen-11-one)