NP-MRD: Showing NP-Card for Oliganthin A (NP0084291)

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Record Information

Version

2.0

Created at

2022-04-29 05:04:12 UTC

Updated at

2022-04-29 05:04:12 UTC

NP-MRD ID

NP0084291

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Oliganthin A

Description

Oliganthin A belongs to the class of organic compounds known as pyranoxanthones. These are organic aromatic compounds containing a pyran or a hydrogenated derivative fused to a xanthone ring system. Oliganthin A is found in Garcinia oligantha. Based on a literature review very few articles have been published on Oliganthin A.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292207042D          

 35 38  0  0  0  0            999 V2000
    2.1434   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5316   -1.0445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3441   -0.9012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8744   -1.5332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6868   -1.3900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5922   -2.3085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4710   -1.0445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7532   -1.8197    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5656   -1.9630    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8478   -2.7382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0959   -1.3310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8125    0.6817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2822    1.6002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 O   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
  3  4  1  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
  9 11  1  0  0  0  0
 11 12  1  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
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 12 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 11 23  2  0  0  0  0
  6 24  2  0  0  0  0
 12 24  1  0  0  0  0
 24 25  1  0  0  0  0
  3 25  1  0  0  0  0
 25 26  2  0  0  0  0
  4 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
  2 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
 32 35  1  0  0  0  0
 28 35  1  0  0  0  0
M  END

     RDKit          3D

 65 68  0  0  0  0  0  0  0  0999 V2000
   -6.0152    3.4569    1.1203 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5747    3.0829    1.1025 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7170    3.6794    2.1558 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0428    2.2703    0.2196 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6094    1.9466    0.2647 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3586    0.4557    0.4668 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9893   -0.2896   -0.7088 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7876   -1.7456   -0.5932 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1652   -2.4726   -1.4927 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5871   -1.9139   -2.7404 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0034   -3.9491   -1.2958 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1285    0.0398    1.6736 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3803    0.2623    1.7096 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5526   -0.6079    2.8254 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3156   -0.9805    3.9418 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2774   -0.8593    2.8361 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7143   -1.4919    3.9607 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4028   -0.5019    1.7066 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8752   -0.7801    1.7728 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7036   -0.4864    0.7982 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0563   -0.8042    0.9186 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9486   -0.5169   -0.0687 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5235    0.1007   -1.2177 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1756    0.4314   -1.3677 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8191    1.0393   -2.5243 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2800    0.1385   -0.3670 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0607    0.4353   -0.4471 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4966    0.9920   -1.4609 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9400    0.1171    0.6011 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5156    0.3772   -2.2229 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7873    0.0659   -2.0826 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2876   -0.5894   -0.8840 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.4051    0.2635   -0.2650 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9330   -1.9363   -1.1827 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2801   -0.8317    0.0539 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3429    3.4391    2.1886 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6385    2.8343    0.4827 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0726    4.5245    0.8082 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2711    4.3810    2.8178 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9566    4.3117    1.6405 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2446    2.9020    2.8140 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6673    1.8456   -0.5409 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1639    2.5073    1.1362 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1446    2.3238   -0.6743 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6013    0.1162   -1.6338 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1011   -0.0743   -0.7293 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1810   -2.2323    0.2907 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1605   -1.1000   -3.1843 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5535   -1.5243   -2.5350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4769   -2.6973   -3.5264 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9276   -4.1761   -1.5327 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2627   -4.2695   -0.2745 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6083   -4.4720   -2.0746 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9895   -0.6351    4.8527 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2991   -2.3949    3.8620 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3616   -1.2925    1.8398 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9831    1.3573   -2.8595 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1753    0.8728   -3.1453 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4958    0.3075   -2.8954 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0991   -0.3445    0.3179 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9069    1.0721    0.2826 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9235    0.7282   -1.1405 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9639   -1.7617   -1.5416 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9143   -2.5397   -0.2455 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3687   -2.4067   -2.0066 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
  6  5  1  6
  6  7  1  0
  7  8  1  0
  8  9  2  3
  9 10  1  0
  9 11  1  0
  6 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  1  0
 14 16  2  0
 16 17  1  0
 16 18  1  0
 18 29  2  0
 29 27  1  0
 27 28  2  0
 27 26  1  0
 26 24  2  0
 24 25  1  0
 24 23  1  0
 23 22  2  0
 22 35  1  0
 35 32  1  0
 32 33  1  1
 32 34  1  0
 32 31  1  0
 31 30  2  0
 22 21  1  0
 21 20  2  0
 20 19  1  0
 29  6  1  0
 20 26  1  0
 19 18  1  0
 30 23  1  0
  1 36  1  0
  1 37  1  0
  1 38  1  0
  3 39  1  0
  3 40  1  0
  3 41  1  0
  4 42  1  0
  5 43  1  0
  5 44  1  0
  7 45  1  0
  7 46  1  0
  8 47  1  0
 10 48  1  0
 10 49  1  0
 10 50  1  0
 11 51  1  0
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 11 53  1  0
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 17 55  1  0
 25 57  1  0
 33 60  1  0
 33 61  1  0
 33 62  1  0
 34 63  1  0
 34 64  1  0
 34 65  1  0
 31 59  1  0
 30 58  1  0
 21 56  1  0
M  END


  Mrv1652304292207042D          

 35 38  0  0  0  0            999 V2000
    2.1434   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5316   -1.0445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3441   -0.9012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8744   -1.5332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6868   -1.3900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5922   -2.3085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4710   -1.0445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7532   -1.8197    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5656   -1.9630    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8478   -2.7382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0959   -1.3310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8125    0.6817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2822    1.6002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 O   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
  3  4  1  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
  9 11  1  0  0  0  0
 11 12  1  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
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 12 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 11 23  2  0  0  0  0
  6 24  2  0  0  0  0
 12 24  1  0  0  0  0
 24 25  1  0  0  0  0
  3 25  1  0  0  0  0
 25 26  2  0  0  0  0
  4 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
  2 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
 32 35  1  0  0  0  0
 28 35  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0084291

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCC1(CC=C(C)C)C(=O)C(O)=C(O)C2=C1C(=O)C1=C(O)C3=C(OC(C)(C)C=C3)C=C1O2

> <INCHI_IDENTIFIER>
InChI=1S/C28H30O7/c1-14(2)7-11-28(12-8-15(3)4)20-22(30)19-18(34-25(20)23(31)24(32)26(28)33)13-17-16(21(19)29)9-10-27(5,6)35-17/h7-10,13,29,31-32H,11-12H2,1-6H3

> <INCHI_KEY>
PBHSSDRLJOYTHW-UHFFFAOYSA-N

> <FORMULA>
C28H30O7

> <MOLECULAR_WEIGHT>
478.541

> <EXACT_MASS>
478.199153306

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
65

> <JCHEM_AVERAGE_POLARIZABILITY>
51.3990517174529

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
5,9,10-trihydroxy-2,2-dimethyl-7,7-bis(3-methylbut-2-en-1-yl)-2,6,7,8-tetrahydro-1,11-dioxatetracene-6,8-dione

> <ALOGPS_LOGP>
3.69

> <JCHEM_LOGP>
5.331827440666668

> <ALOGPS_LOGS>
-4.66

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
7.246996685564688

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.9803422405936657

> <JCHEM_PKA_STRONGEST_BASIC>
-4.638279772814912

> <JCHEM_POLAR_SURFACE_AREA>
113.29

> <JCHEM_REFRACTIVITY>
138.0805

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.05e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5,9,10-trihydroxy-2,2-dimethyl-7,7-bis(3-methylbut-2-en-1-yl)-1,11-dioxatetracene-6,8-dione

> <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  O   UNK     0       4.001  -2.310   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.335  -0.000   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       6.668   2.310   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.336   2.310   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       9.336   3.850   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      10.669   1.540   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      12.003   2.310   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      10.669  -0.000   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.336  -0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.326  -1.950   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      11.842  -1.682   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      12.832  -2.862   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      14.349  -2.595   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      12.305  -4.309   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.346  -1.950   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.873  -3.397   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      10.389  -3.664   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      10.916  -5.111   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      11.379  -2.485   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      12.003  -0.770   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       8.002   0.000   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       6.668  -2.310   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -1.517   1.273   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -0.527   2.987   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       1.334   2.310   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   29                                                  
CONECT    3    2    4   25                                                  
CONECT    4    3    5   27                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   24                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   23                                                  
CONECT   12   11   13   18   24                                             
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18   12   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   11                                                            
CONECT   24    6   12   25                                                  
CONECT   25   24    3   26                                                  
CONECT   26   25                                                            
CONECT   27    4   28                                                       
CONECT   28   27   29   35                                                  
CONECT   29   28    2   30                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33   34   35                                             
CONECT   33   32                                                            
CONECT   34   32                                                            
CONECT   35   32   28                                                       
MASTER        0    0    0    0    0    0    0    0   35    0   76    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₈H₃₀O₇

Average Mass

478.5410 Da

Monoisotopic Mass

478.19915 Da

IUPAC Name

5,9,10-trihydroxy-2,2-dimethyl-7,7-bis(3-methylbut-2-en-1-yl)-2,6,7,8-tetrahydro-1,11-dioxatetracene-6,8-dione

Traditional Name

5,9,10-trihydroxy-2,2-dimethyl-7,7-bis(3-methylbut-2-en-1-yl)-1,11-dioxatetracene-6,8-dione

CAS Registry Number

Not Available

SMILES

CC(C)=CCC1(CC=C(C)C)C(=O)C(O)=C(O)C2=C1C(=O)C1=C(O)C3=C(OC(C)(C)C=C3)C=C1O2

InChI Identifier

InChI=1S/C28H30O7/c1-14(2)7-11-28(12-8-15(3)4)20-22(30)19-18(34-25(20)23(31)24(32)26(28)33)13-17-16(21(19)29)9-10-27(5,6)35-17/h7-10,13,29,31-32H,11-12H2,1-6H3

InChI Key

PBHSSDRLJOYTHW-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, 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
Garcinia oligantha	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyranoxanthones. These are organic aromatic compounds containing a pyran or a hydrogenated derivative fused to a xanthone ring system.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

Pyranoxanthones

Alternative Parents

Substituents

Pyranoxanthone
Pyranochromene
2,2-dimethyl-1-benzopyran
Chromone
1-hydroxy-4-unsubstituted benzenoid
Alkyl aryl ether
Phenol
Pyranone
Benzenoid
Pyran
Heteroaromatic compound
Vinylogous acid
Enediol
Ketone
Cyclic ketone
Ether
Polyol
Oxacycle
Hydrocarbon derivative
Organooxygen compound
Organic oxygen compound
Organic oxide
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	3.69	ALOGPS
logP	5.33	ChemAxon
logS	-4.7	ALOGPS
pKa (Strongest Acidic)	3.98	ChemAxon
pKa (Strongest Basic)	-4.6	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	113.29 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	138.08 m³·mol⁻¹	ChemAxon
Polarizability	51.4 Å³	ChemAxon
Number of Rings	4	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

C00053600

Chemspider ID

28289566

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

135981986

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Oliganthin A (NP0084291)

MOL for NP0084291 (Oliganthin A)

3D MOL for NP0084291 (Oliganthin A)

3D SDF for NP0084291 (Oliganthin A)

3D-SDF for NP0084291 (Oliganthin A)

PDB for NP0084291 (Oliganthin A)

3D PDB for NP0084291 (Oliganthin A)

SMILES for NP0084291 (Oliganthin A)

INCHI for NP0084291 (Oliganthin A)

Structure for NP0084291 (Oliganthin A)

3D Structure for NP0084291 (Oliganthin A)