NP-MRD: Showing NP-Card for Garciduol A (NP0084018)

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Record Information

Version

2.0

Created at

2022-04-29 04:53:07 UTC

Updated at

2022-04-29 04:53:08 UTC

NP-MRD ID

NP0084018

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Garciduol A

Description

2-(3-Benzoyl-2,4-dihydroxy-6-methoxyphenyl)-1,4,8-trihydroxy-9H-xanthen-9-one belongs to the class of organic compounds known as xanthones. These are polycyclic aromatic compounds containing a xanthene moiety conjugated to a ketone group at carbon 9. Xanthene is a tricyclic compound made up of two benzene rings linearly fused to each other through a pyran ring. Garciduol A is found in Garcinia bracteata and Garcinia dulcis . Based on a literature review very few articles have been published on 2-(3-benzoyl-2,4-dihydroxy-6-methoxyphenyl)-1,4,8-trihydroxy-9H-xanthen-9-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292206532D          

 36 40  0  0  0  0            999 V2000
    2.1434    2.0625    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
    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 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    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
    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
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 O   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
    0.7145   -1.2375    0.0000 O   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
   -0.7145    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 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
   -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 C   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 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  3  9  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  2 11  1  0  0  0  0
 11 12  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 20 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
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 22 27  1  0  0  0  0
 21 28  2  0  0  0  0
 20 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  2  0  0  0  0
 17 32  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 16 35  2  0  0  0  0
 11 35  1  0  0  0  0
 35 36  1  0  0  0  0
M  END

     RDKit          3D

 54 58  0  0  0  0  0  0  0  0999 V2000
   -0.4908   -2.9245   -3.4023 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0813   -1.9357   -2.4966 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0253   -1.2567   -1.6981 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3459   -1.5848   -1.8284 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2659   -0.8909   -1.0179 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5694   -1.2881   -1.1863 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8894    0.0813   -0.1295 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8068    0.7515    0.7535 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3208    1.0126    1.9333 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1550    1.1792    0.5327 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6243    1.5700   -0.7019 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9404    1.9674   -0.8300 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8197    1.9890    0.2486 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3529    1.5979    1.4898 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0371    1.2053    1.5938 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5371    0.3734   -0.0377 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0940    1.3263    0.8209 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5749   -0.2966   -0.8260 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8296    0.0638   -0.6728 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4179    1.0504   -1.4217 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7378    1.4101   -1.2982 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3252    2.4071   -2.0569 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5452    0.7536   -0.3693 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8113    1.0940   -0.2455 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5875    0.4901    0.6210 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9336    0.8494    0.7547 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7449    0.2124    1.6665 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2821   -0.7967    2.4825 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9629   -1.1543    2.3565 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4178   -2.1620    3.1412 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1324   -0.5181    1.4389 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7946   -0.8864    1.3165 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4100   -1.7946    2.0623 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9812   -0.2502    0.4049 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6605   -0.5893    0.2609 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0879   -1.5583    0.9978 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0006   -3.7888   -2.9252 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2313   -2.5172   -4.1480 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3929   -3.2701   -3.9845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6762   -2.3552   -2.5325 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3136   -0.9796   -0.6387 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9740    1.5702   -1.5903 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3316    2.2801   -1.7944 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8463    2.3013    0.1293 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9943    1.5952    2.3679 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7140    0.9003    2.6030 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4559    1.9480    1.4563 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7808    1.5629   -2.1489 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2761    2.6848   -1.9861 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2962    1.6548    0.1004 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7864    0.5208    1.7402 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9496   -1.2776    3.1895 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0045   -2.6323    3.8101 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3198   -2.1890    1.6948 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3 18  2  0
 18 16  1  0
 16 17  1  0
 16  7  2  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
  7  5  1  0
  5  6  1  0
  5  4  2  0
 18 19  1  0
 19 35  2  0
 35 36  1  0
 35 34  1  0
 34 23  2  0
 23 24  1  0
 24 25  1  0
 25 31  2  0
 31 29  1  0
 29 30  1  0
 29 28  2  0
 28 27  1  0
 27 26  2  0
 31 32  1  0
 32 33  2  0
 23 21  1  0
 21 22  1  0
 21 20  2  0
  4  3  1  0
 20 19  1  0
 15 10  1  0
 32 34  1  0
 26 25  1  0
  1 37  1  0
  1 38  1  0
  1 39  1  0
 17 47  1  0
 11 42  1  0
 12 43  1  0
 13 44  1  0
 14 45  1  0
 15 46  1  0
  6 41  1  0
  4 40  1  0
 36 54  1  0
 30 53  1  0
 28 52  1  0
 27 51  1  0
 26 50  1  0
 22 49  1  0
 20 48  1  0
M  END


  Mrv1652304292206532D          

 36 40  0  0  0  0            999 V2000
    2.1434    2.0625    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
    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 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    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
    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
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 O   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
    0.7145   -1.2375    0.0000 O   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
   -0.7145    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 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
   -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 C   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 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  3  9  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  2 11  1  0  0  0  0
 11 12  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 20 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
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 22 27  1  0  0  0  0
 21 28  2  0  0  0  0
 20 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  2  0  0  0  0
 17 32  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 16 35  2  0  0  0  0
 11 35  1  0  0  0  0
 35 36  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0084018

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(C(O)=C(C(=O)C2=CC=CC=C2)C(O)=C1)C1=C(O)C2=C(OC3=C(C(O)=CC=C3)C2=O)C(O)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C27H18O9/c1-35-18-11-15(29)21(23(31)12-6-3-2-4-7-12)25(33)19(18)13-10-16(30)27-22(24(13)32)26(34)20-14(28)8-5-9-17(20)36-27/h2-11,28-30,32-33H,1H3

> <INCHI_KEY>
MLZDXLKUYJKGMA-UHFFFAOYSA-N

> <FORMULA>
C27H18O9

> <MOLECULAR_WEIGHT>
486.432

> <EXACT_MASS>
486.09508216

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
47.92977647129982

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-(3-benzoyl-2,4-dihydroxy-6-methoxyphenyl)-1,4,8-trihydroxy-9H-xanthen-9-one

> <ALOGPS_LOGP>
4.04

> <JCHEM_LOGP>
6.990720745666666

> <ALOGPS_LOGS>
-4.38

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
7.509722367568919

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.66081145984938

> <JCHEM_PKA_STRONGEST_BASIC>
-3.7747721205294344

> <JCHEM_POLAR_SURFACE_AREA>
153.75

> <JCHEM_REFRACTIVITY>
128.89570000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.05e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-(3-benzoyl-2,4-dihydroxy-6-methoxyphenyl)-1,4,8-trihydroxyxanthen-9-one

> <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   3.850   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       6.668   3.850   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       8.002  -0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       4.001  -0.770   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       1.334  -2.310   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -2.667  -0.000   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -4.001   2.310   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -5.335   1.540   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -6.668   2.310   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -8.002   1.540   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -9.336   2.310   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -9.336   3.850   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -8.002   4.620   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -6.668   3.850   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -5.335  -0.000   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -4.001   3.850   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -5.335   4.620   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      -2.667   4.620   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      -0.000   4.620   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      -0.000   6.160   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       1.334   3.850   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   11                                                  
CONECT    3    2    4    9                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    3    8   10                                                  
CONECT   10    9   12                                                       
CONECT   11    2   12   35                                                  
CONECT   12   11   10   13                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17   35                                                  
CONECT   17   16   18   32                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   29                                                  
CONECT   21   20   22   28                                                  
CONECT   22   21   23   27                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   22                                                       
CONECT   28   21                                                            
CONECT   29   20   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32                                                       
CONECT   32   17   31   33                                                  
CONECT   33   32   34                                                       
CONECT   34   33                                                            
CONECT   35   16   11   36                                                  
CONECT   36   35                                                            
MASTER        0    0    0    0    0    0    0    0   36    0   80    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₇H₁₈O₉

Average Mass

486.4320 Da

Monoisotopic Mass

486.09508 Da

IUPAC Name

2-(3-benzoyl-2,4-dihydroxy-6-methoxyphenyl)-1,4,8-trihydroxy-9H-xanthen-9-one

Traditional Name

2-(3-benzoyl-2,4-dihydroxy-6-methoxyphenyl)-1,4,8-trihydroxyxanthen-9-one

CAS Registry Number

Not Available

SMILES

COC1=C(C(O)=C(C(=O)C2=CC=CC=C2)C(O)=C1)C1=C(O)C2=C(OC3=C(C(O)=CC=C3)C2=O)C(O)=C1

InChI Identifier

InChI=1S/C27H18O9/c1-35-18-11-15(29)21(23(31)12-6-3-2-4-7-12)25(33)19(18)13-10-16(30)27-22(24(13)32)26(34)20-14(28)8-5-9-17(20)36-27/h2-11,28-30,32-33H,1H3

InChI Key

MLZDXLKUYJKGMA-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 bracteata (nom. inval.)	Plant	KNApSAcK
Garcinia dulcis	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as xanthones. These are polycyclic aromatic compounds containing a xanthene moiety conjugated to a ketone group at carbon 9. Xanthene is a tricyclic compound made up of two benzene rings linearly fused to each other through a pyran ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

Xanthones

Alternative Parents

Substituents

Xanthone
Biphenol
Benzophenone
Aryl-phenylketone
Diphenylmethane
Chromone
Methoxyphenol
Phenoxy compound
Methoxybenzene
Aryl ketone
Resorcinol
Phenol ether
Benzoyl
Anisole
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Pyranone
Phenol
Alkyl aryl ether
Benzenoid
Pyran
Monocyclic benzene moiety
Heteroaromatic compound
Vinylogous acid
Ketone
Oxacycle
Polyol
Ether
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
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	4.04	ALOGPS
logP	6.99	ChemAxon
logS	-4.4	ALOGPS
pKa (Strongest Acidic)	6.66	ChemAxon
pKa (Strongest Basic)	-3.8	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	153.75 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	128.9 m³·mol⁻¹	ChemAxon
Polarizability	47.93 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00053203

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

163196014

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Garciduol A (NP0084018)

MOL for NP0084018 (Garciduol A)

3D MOL for NP0084018 (Garciduol A)

3D SDF for NP0084018 (Garciduol A)

3D-SDF for NP0084018 (Garciduol A)

PDB for NP0084018 (Garciduol A)

3D PDB for NP0084018 (Garciduol A)

SMILES for NP0084018 (Garciduol A)

INCHI for NP0084018 (Garciduol A)

Structure for NP0084018 (Garciduol A)

3D Structure for NP0084018 (Garciduol A)