NP-MRD: Showing NP-Card for brevipsidone A (NP0037577)

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Record Information

Version

2.0

Created at

2021-06-20 20:28:12 UTC

Updated at

2021-06-30 00:09:51 UTC

NP-MRD ID

NP0037577

Secondary Accession Numbers

None

Natural Product Identification

Common Name

brevipsidone A

Provided By

JEOL Database JEOL Logo

Description

brevipsidone A is found in Garcinia brevipedicellata (Clusiaceae). brevipsidone A was first documented in 2008 (Ngoupayo, J.,et al.). Based on a literature review very few articles have been published on 5,12-dihydroxy-4-methoxy-16,16-dimethyl-13-(3-methylbut-2-en-1-yl)-2,9,15-trioxatetracyclo[9.8.0.0³,⁸.0¹⁴,¹⁹]Nonadeca-1(11),3(8),4,6,12,14(19),17-heptaen-10-one.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306202122283D          

 55 58  0  0  0  0            999 V2000
    3.3202    3.2961    2.0061 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1382    2.7744    2.6205 O   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652306202122283D          

 55 58  0  0  0  0            999 V2000
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    2.9976   -2.1462    4.2417 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0315   -1.1094   -2.1983 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3410   -2.6734   -1.9818 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2389   -2.8803    0.3361 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9476    0.1394   -0.4971 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9079   -0.2557   -1.8586 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4054   -1.1574   -1.6173 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0426   -1.3865    1.5609 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2140   -2.9477    1.5287 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6362   -2.6923    0.5102 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5396   -3.6652   -0.6470 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3784    4.1666   -1.4672 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1281    2.6525   -2.0159 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5526    3.1133   -2.6364 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6143    3.3558    1.0091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3879    1.8802    0.3945 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9917    1.7517    1.4476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1782    4.0971   -0.1469 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8564    2.8127    0.2134 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  7  2  0  0  0  0
  8 25  1  0  0  0  0
  4  3  2  0  0  0  0
  9 10  1  0  0  0  0
  3  9  1  0  0  0  0
 25 23  1  0  0  0  0
 13 26  1  0  0  0  0
 12 31  1  0  0  0  0
 31 30  2  0  0  0  0
 30 27  1  0  0  0  0
 27 26  1  0  0  0  0
 10 11  1  0  0  0  0
 23 24  2  0  0  0  0
 23 22  1  0  0  0  0
  4  5  1  0  0  0  0
 22 11  2  0  0  0  0
  3  2  1  0  0  0  0
  8  7  1  0  0  0  0
  2  1  1  0  0  0  0
 14 15  1  0  0  0  0
  6  4  1  0  0  0  0
 15 16  1  0  0  0  0
  9  8  2  0  0  0  0
 16 17  2  3  0  0  0
 22 20  1  0  0  0  0
 17 18  1  0  0  0  0
 11 12  1  0  0  0  0
 17 19  1  0  0  0  0
 13 14  1  0  0  0  0
 27 28  1  6  0  0  0
 14 20  2  0  0  0  0
 27 29  1  0  0  0  0
 13 12  2  0  0  0  0
 20 21  1  0  0  0  0
  6 36  1  0  0  0  0
  7 37  1  0  0  0  0
 31 55  1  0  0  0  0
 30 54  1  0  0  0  0
  5 35  1  0  0  0  0
  1 32  1  0  0  0  0
  1 33  1  0  0  0  0
  1 34  1  0  0  0  0
 15 38  1  0  0  0  0
 15 39  1  0  0  0  0
 16 40  1  0  0  0  0
 18 41  1  0  0  0  0
 18 42  1  0  0  0  0
 18 43  1  0  0  0  0
 19 44  1  0  0  0  0
 19 45  1  0  0  0  0
 19 46  1  0  0  0  0
 28 48  1  0  0  0  0
 28 49  1  0  0  0  0
 28 50  1  0  0  0  0
 29 51  1  0  0  0  0
 29 52  1  0  0  0  0
 29 53  1  0  0  0  0
 21 47  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0037577

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C(OC([H])([H])[H])C2=C(OC(=O)C3=C(O2)C2=C(OC(C([H])=C2[H])(C([H])([H])[H])C([H])([H])[H])C(=C3O[H])C([H])([H])C([H])=C(C([H])([H])[H])C([H])([H])[H])C([H])=C1[H]

> <INCHI_IDENTIFIER>
InChI=1S/C24H24O7/c1-12(2)6-7-13-18(26)17-20(14-10-11-24(3,4)31-19(13)14)30-22-16(29-23(17)27)9-8-15(25)21(22)28-5/h6,8-11,25-26H,7H2,1-5H3

> <INCHI_KEY>
VPYHBRQMDZZLDV-UHFFFAOYSA-N

> <FORMULA>
C24H24O7

> <MOLECULAR_WEIGHT>
424.449

> <EXACT_MASS>
424.152203113

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
44.08638220312654

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5,12-dihydroxy-4-methoxy-16,16-dimethyl-13-(3-methylbut-2-en-1-yl)-2,9,15-trioxatetracyclo[9.8.0.0^{3,8}.0^{14,19}]nonadeca-1(11),3(8),4,6,12,14(19),17-heptaen-10-one

> <ALOGPS_LOGP>
4.73

> <JCHEM_LOGP>
5.476111088

> <ALOGPS_LOGS>
-4.81

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.80140185371632

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.139332909127482

> <JCHEM_PKA_STRONGEST_BASIC>
-3.7894793593682112

> <JCHEM_POLAR_SURFACE_AREA>
94.45000000000002

> <JCHEM_REFRACTIVITY>
117.10489999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.63e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5,12-dihydroxy-4-methoxy-16,16-dimethyl-13-(3-methylbut-2-en-1-yl)-2,9,15-trioxatetracyclo[9.8.0.0^{3,8}.0^{14,19}]nonadeca-1(11),3(8),4,6,12,14(19),17-heptaen-10-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 55 58  0  0  0  0  0  0  0  0999 V2000
    3.3202    3.2961    2.0061 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1382    2.7744    2.6205 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3367    1.4687    2.9957 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5187    1.2079    4.3571 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4827    2.2244    5.2696 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7507   -0.0835    4.8160 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7893   -1.1353    3.9017 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5569   -0.8784    2.5482 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3081    0.4099    2.0860 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0821    0.6550    0.7575 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9430    0.0488    0.2739 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1314    0.8625   -0.1313 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2883    0.2644   -0.6571 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3651   -1.1284   -0.8436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6110   -1.7643   -1.4296 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6143   -2.1380   -0.3691 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8786   -1.6960   -0.2166 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5615   -0.6894   -1.0998 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7369   -2.2116    0.9091 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2684   -1.9156   -0.4564 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3605   -3.2710   -0.6714 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8753   -1.3378    0.1238 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9970   -2.2206    0.4933 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2195   -3.2236   -0.1823 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6868   -1.9794    1.6736 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3727    0.9994   -1.0643 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5046    2.3541   -0.5931 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.1783    3.1235   -1.7357 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4247    2.3444    0.6331 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1942    3.0157   -0.2504 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0733    2.3199   -0.0417 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1734    4.3711    1.8646 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1986    3.1561    2.6463 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4894    2.8478    1.0222 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2067    3.0183    4.7729 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9100   -0.2661    5.8750 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9976   -2.1462    4.2417 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0315   -1.1094   -2.1983 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3410   -2.6734   -1.9818 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2389   -2.8803    0.3361 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9476    0.1394   -0.4971 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9079   -0.2557   -1.8586 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4054   -1.1574   -1.6173 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0426   -1.3865    1.5609 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2140   -2.9477    1.5287 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6362   -2.6923    0.5102 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5396   -3.6652   -0.6470 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3784    4.1666   -1.4672 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1281    2.6525   -2.0159 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5526    3.1133   -2.6364 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6143    3.3558    1.0091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3879    1.8802    0.3945 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9917    1.7517    1.4476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1782    4.0971   -0.1469 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8564    2.8127    0.2134 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  7  2  0
  8 25  1  0
  4  3  2  0
  9 10  1  0
  3  9  1  0
 25 23  1  0
 13 26  1  0
 12 31  1  0
 31 30  2  0
 30 27  1  0
 27 26  1  0
 10 11  1  0
 23 24  2  0
 23 22  1  0
  4  5  1  0
 22 11  2  0
  3  2  1  0
  8  7  1  0
  2  1  1  0
 14 15  1  0
  6  4  1  0
 15 16  1  0
  9  8  2  0
 16 17  2  3
 22 20  1  0
 17 18  1  0
 11 12  1  0
 17 19  1  0
 13 14  1  0
 27 28  1  6
 14 20  2  0
 27 29  1  0
 13 12  2  0
 20 21  1  0
  6 36  1  0
  7 37  1  0
 31 55  1  0
 30 54  1  0
  5 35  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
 15 38  1  0
 15 39  1  0
 16 40  1  0
 18 41  1  0
 18 42  1  0
 18 43  1  0
 19 44  1  0
 19 45  1  0
 19 46  1  0
 28 48  1  0
 28 49  1  0
 28 50  1  0
 29 51  1  0
 29 52  1  0
 29 53  1  0
 21 47  1  0
M  END

HEADER    PROTEIN                                 20-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-JUN-21         0                                  
HETATM    1  C   UNK     0       3.320   3.296   2.006  0.00  0.00           C+0
HETATM    2  O   UNK     0       2.138   2.774   2.620  0.00  0.00           O+0
HETATM    3  C   UNK     0       2.337   1.469   2.996  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.519   1.208   4.357  0.00  0.00           C+0
HETATM    5  O   UNK     0       2.483   2.224   5.270  0.00  0.00           O+0
HETATM    6  C   UNK     0       2.751  -0.084   4.816  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.789  -1.135   3.902  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.557  -0.878   2.548  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.308   0.410   2.086  0.00  0.00           C+0
HETATM   10  O   UNK     0       2.082   0.655   0.758  0.00  0.00           O+0
HETATM   11  C   UNK     0       0.943   0.049   0.274  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.131   0.863  -0.131  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.288   0.264  -0.657  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.365  -1.128  -0.844  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.611  -1.764  -1.430  0.00  0.00           C+0
HETATM   16  C   UNK     0      -3.614  -2.138  -0.369  0.00  0.00           C+0
HETATM   17  C   UNK     0      -4.879  -1.696  -0.217  0.00  0.00           C+0
HETATM   18  C   UNK     0      -5.561  -0.689  -1.100  0.00  0.00           C+0
HETATM   19  C   UNK     0      -5.737  -2.212   0.909  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.268  -1.916  -0.456  0.00  0.00           C+0
HETATM   21  O   UNK     0      -0.361  -3.271  -0.671  0.00  0.00           O+0
HETATM   22  C   UNK     0       0.875  -1.338   0.124  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.997  -2.221   0.493  0.00  0.00           C+0
HETATM   24  O   UNK     0       2.220  -3.224  -0.182  0.00  0.00           O+0
HETATM   25  O   UNK     0       2.687  -1.979   1.674  0.00  0.00           O+0
HETATM   26  O   UNK     0      -2.373   0.999  -1.064  0.00  0.00           O+0
HETATM   27  C   UNK     0      -2.505   2.354  -0.593  0.00  0.00           C+0
HETATM   28  C   UNK     0      -3.178   3.123  -1.736  0.00  0.00           C+0
HETATM   29  C   UNK     0      -3.425   2.344   0.633  0.00  0.00           C+0
HETATM   30  C   UNK     0      -1.194   3.016  -0.250  0.00  0.00           C+0
HETATM   31  C   UNK     0      -0.073   2.320  -0.042  0.00  0.00           C+0
HETATM   32  H   UNK     0       3.173   4.371   1.865  0.00  0.00           H+0
HETATM   33  H   UNK     0       4.199   3.156   2.646  0.00  0.00           H+0
HETATM   34  H   UNK     0       3.489   2.848   1.022  0.00  0.00           H+0
HETATM   35  H   UNK     0       2.207   3.018   4.773  0.00  0.00           H+0
HETATM   36  H   UNK     0       2.910  -0.266   5.875  0.00  0.00           H+0
HETATM   37  H   UNK     0       2.998  -2.146   4.242  0.00  0.00           H+0
HETATM   38  H   UNK     0      -3.031  -1.109  -2.198  0.00  0.00           H+0
HETATM   39  H   UNK     0      -2.341  -2.673  -1.982  0.00  0.00           H+0
HETATM   40  H   UNK     0      -3.239  -2.880   0.336  0.00  0.00           H+0
HETATM   41  H   UNK     0      -5.948   0.139  -0.497  0.00  0.00           H+0
HETATM   42  H   UNK     0      -4.908  -0.256  -1.859  0.00  0.00           H+0
HETATM   43  H   UNK     0      -6.405  -1.157  -1.617  0.00  0.00           H+0
HETATM   44  H   UNK     0      -6.043  -1.387   1.561  0.00  0.00           H+0
HETATM   45  H   UNK     0      -5.214  -2.948   1.529  0.00  0.00           H+0
HETATM   46  H   UNK     0      -6.636  -2.692   0.510  0.00  0.00           H+0
HETATM   47  H   UNK     0       0.540  -3.665  -0.647  0.00  0.00           H+0
HETATM   48  H   UNK     0      -3.378   4.167  -1.467  0.00  0.00           H+0
HETATM   49  H   UNK     0      -4.128   2.652  -2.016  0.00  0.00           H+0
HETATM   50  H   UNK     0      -2.553   3.113  -2.636  0.00  0.00           H+0
HETATM   51  H   UNK     0      -3.614   3.356   1.009  0.00  0.00           H+0
HETATM   52  H   UNK     0      -4.388   1.880   0.395  0.00  0.00           H+0
HETATM   53  H   UNK     0      -2.992   1.752   1.448  0.00  0.00           H+0
HETATM   54  H   UNK     0      -1.178   4.097  -0.147  0.00  0.00           H+0
HETATM   55  H   UNK     0       0.856   2.813   0.213  0.00  0.00           H+0
CONECT    1    2   32   33   34                                             
CONECT    2    3    1                                                       
CONECT    3    4    9    2                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4   35                                                       
CONECT    6    7    4   36                                                  
CONECT    7    6    8   37                                                  
CONECT    8   25    7    9                                                  
CONECT    9   10    3    8                                                  
CONECT   10    9   11                                                       
CONECT   11   10   22   12                                                  
CONECT   12   31   11   13                                                  
CONECT   13   26   14   12                                                  
CONECT   14   15   13   20                                                  
CONECT   15   14   16   38   39                                             
CONECT   16   15   17   40                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17   41   42   43                                             
CONECT   19   17   44   45   46                                             
CONECT   20   22   14   21                                                  
CONECT   21   20   47                                                       
CONECT   22   23   11   20                                                  
CONECT   23   25   24   22                                                  
CONECT   24   23                                                            
CONECT   25    8   23                                                       
CONECT   26   13   27                                                       
CONECT   27   30   26   28   29                                             
CONECT   28   27   48   49   50                                             
CONECT   29   27   51   52   53                                             
CONECT   30   31   27   54                                                  
CONECT   31   12   30   55                                                  
CONECT   32    1                                                            
CONECT   33    1                                                            
CONECT   34    1                                                            
CONECT   35    5                                                            
CONECT   36    6                                                            
CONECT   37    7                                                            
CONECT   38   15                                                            
CONECT   39   15                                                            
CONECT   40   16                                                            
CONECT   41   18                                                            
CONECT   42   18                                                            
CONECT   43   18                                                            
CONECT   44   19                                                            
CONECT   45   19                                                            
CONECT   46   19                                                            
CONECT   47   21                                                            
CONECT   48   28                                                            
CONECT   49   28                                                            
CONECT   50   28                                                            
CONECT   51   29                                                            
CONECT   52   29                                                            
CONECT   53   29                                                            
CONECT   54   30                                                            
CONECT   55   31                                                            
MASTER        0    0    0    0    0    0    0    0   55    0  116    0
END

RDKit          3D

55 58  0  0  0  0  0  0  0  0999 V2000
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    1.9970   -2.2206    0.4933 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2195   -3.2236   -0.1823 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.5046    2.3541   -0.5931 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.1783    3.1235   -1.7357 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4247    2.3444    0.6331 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1942    3.0157   -0.2504 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0733    2.3199   -0.0417 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.9100   -0.2661    5.8750 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9976   -2.1462    4.2417 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.3410   -2.6734   -1.9818 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2389   -2.8803    0.3361 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9476    0.1394   -0.4971 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9079   -0.2557   -1.8586 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4054   -1.1574   -1.6173 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0426   -1.3865    1.5609 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2140   -2.9477    1.5287 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6362   -2.6923    0.5102 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5396   -3.6652   -0.6470 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3784    4.1666   -1.4672 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1281    2.6525   -2.0159 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.6143    3.3558    1.0091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3879    1.8802    0.3945 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9917    1.7517    1.4476 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.8564    2.8127    0.2134 H   0  0  0  0  0  0  0  0  0  0  0  0
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  6 36  1  0
  7 37  1  0
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 30 54  1  0
  5 35  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
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 16 40  1  0
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 29 51  1  0
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 29 53  1  0
 21 47  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₂₄O₇

Average Mass

424.4490 Da

Monoisotopic Mass

424.15220 Da

IUPAC Name

5,12-dihydroxy-4-methoxy-16,16-dimethyl-13-(3-methylbut-2-en-1-yl)-2,9,15-trioxatetracyclo[9.8.0.0^{3,8}.0^{14,19}]nonadeca-1(11),3(8),4,6,12,14(19),17-heptaen-10-one

Traditional Name

5,12-dihydroxy-4-methoxy-16,16-dimethyl-13-(3-methylbut-2-en-1-yl)-2,9,15-trioxatetracyclo[9.8.0.0^{3,8}.0^{14,19}]nonadeca-1(11),3(8),4,6,12,14(19),17-heptaen-10-one

CAS Registry Number

Not Available

SMILES

[H]OC1=C(OC([H])([H])[H])C2=C(OC(=O)C3=C(O2)C2=C(OC(C([H])=C2[H])(C([H])([H])[H])C([H])([H])[H])C(=C3O[H])C([H])([H])C([H])=C(C([H])([H])[H])C([H])([H])[H])C([H])=C1[H]

InChI Identifier

InChI=1S/C24H24O7/c1-12(2)6-7-13-18(26)17-20(14-10-11-24(3,4)31-19(13)14)30-22-16(29-23(17)27)9-8-15(25)21(22)28-5/h6,8-11,25-26H,7H2,1-5H3

InChI Key

VPYHBRQMDZZLDV-UHFFFAOYSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Garcinia brevipedicellata	KNApSAcK Database	22123792
Garcinia brevipedicellata (Clusiaceae)	JEOL database	Ngoupayo, J.,et al, Chem. Pharm. Bull. 56, 1466 (2008)

Chemical Taxonomy

Description

This compound belongs to the class of organic compounds known as 2,2-dimethyl-1-benzopyrans. These are organic compounds containing a 1-benzopyran moiety that carries two methyl groups at the 2-position.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

2,2-dimethyl-1-benzopyrans

Alternative Parents

Substituents

2,2-dimethyl-1-benzopyran
Diaryl ether
Anisole
Phenol ether
1-hydroxy-2-unsubstituted benzenoid
1,4-dioxepine
Alkyl aryl ether
Phenol
Dioxepine
Benzenoid
Vinylogous acid
Carboxylic acid ester
Lactone
Oxacycle
Carboxylic acid derivative
Ether
Organooxygen compound
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
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	4.73	ALOGPS
logP	5.48	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	9.14	ChemAxon
pKa (Strongest Basic)	-3.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	94.45 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	117.1 m³·mol⁻¹	ChemAxon
Polarizability	44.09 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	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

C00029849

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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Ngoupayo, J.,et al. (2008). Ngoupayo, J.,et al, Chem. Pharm. Bull. 56, 1466 (2008). Chem. Pharm. Bull..

Showing NP-Card for brevipsidone A (NP0037577)

MOL for NP0037577 (brevipsidone A)

3D MOL for NP0037577 (brevipsidone A)

3D SDF for NP0037577 (brevipsidone A)

3D-SDF for NP0037577 (brevipsidone A)

PDB for NP0037577 (brevipsidone A)

3D PDB for NP0037577 (brevipsidone A)

SMILES for NP0037577 (brevipsidone A)

INCHI for NP0037577 (brevipsidone A)

Structure for NP0037577 (brevipsidone A)

3D Structure for NP0037577 (brevipsidone A)