NP-MRD: Showing NP-Card for (2r,2as,4ar,7r,7as,7br)-2a,4a,7-trihydroxy-3-(hydroxymethyl)-6,6,7b-trimethyl-1h,2h,5h,7h,7ah-cyclobuta[e]inden-2-yl 2-hydroxy-4-methoxy-6-methylbenzoate (NP0170026)

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Record Information

Version

2.0

Created at

2022-09-03 06:05:28 UTC

Updated at

2022-09-03 06:05:29 UTC

NP-MRD ID

NP0170026

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,2as,4ar,7r,7as,7br)-2a,4a,7-trihydroxy-3-(hydroxymethyl)-6,6,7b-trimethyl-1h,2h,5h,7h,7ah-cyclobuta[e]inden-2-yl 2-hydroxy-4-methoxy-6-methylbenzoate

Description

Melleolide C belongs to the class of organic compounds known as melleolides and analogues. Melleolides and analogues are compounds with a structure characterized by the presence of a 2-hydroxy-4-methoxy-6-methylbenzoic acid derivative linked to a 3,6,6,7b-tetramethyl-cyclobuta[e]indene moiety. (2r,2as,4ar,7r,7as,7br)-2a,4a,7-trihydroxy-3-(hydroxymethyl)-6,6,7b-trimethyl-1h,2h,5h,7h,7ah-cyclobuta[e]inden-2-yl 2-hydroxy-4-methoxy-6-methylbenzoate is found in Armillaria. Based on a literature review very few articles have been published on melleolide C.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032208052D          

 32 35  0  0  1  0            999 V2000
   -4.1164   -1.7959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8734   -1.0075    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0691   -0.8238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8261   -0.0354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0218    0.1484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7788    0.9368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4606   -0.4563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6563   -0.2725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4133    0.5159    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0950   -0.8772    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7092   -0.6934    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1480    0.0052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8467   -0.4336    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0897    0.3548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6711   -0.4642    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2455    0.1279    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1041    0.9407    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9862   -0.2354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2702    0.5392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7863   -0.4368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8695   -1.0521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0567   -1.1935    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5165   -1.8786    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6180   -1.8922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7935   -1.8615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3548   -2.5601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5303   -2.5295    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4079   -1.1322    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8032   -1.6935    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7036   -1.2447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1423   -1.8493    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5079   -1.4284    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
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 11 10  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
 15 13  1  1  0  0  0
 15 16  1  0  0  0  0
 16 17  1  1  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 18 21  1  0  0  0  0
 21 22  1  0  0  0  0
 15 22  1  0  0  0  0
 22 23  1  6  0  0  0
 22 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 25 28  1  0  0  0  0
 11 28  1  0  0  0  0
 13 28  1  0  0  0  0
 28 29  1  1  0  0  0
  7 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  2  0  0  0  0
  3 32  1  0  0  0  0
M  END

     RDKit          3D

 64 67  0  0  0  0  0  0  0  0999 V2000
    7.9160   -2.1716   -1.1149 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5803   -2.5293   -0.8299 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5705   -1.5826   -0.7339 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7907   -0.2369   -0.9072 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7786    0.6733   -0.8071 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0847    2.0937   -1.0037 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.4166    1.2768   -0.4245 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6808    2.5153   -0.5955 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1358    0.9686   -0.1548 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0567    1.8624   -0.0407 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5918    1.7190    1.3298 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9375    1.5038    0.6406 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8148    2.7486    0.8184 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6092    0.3104    1.1543 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.0827    0.2139    0.8020 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.3180    0.2526   -0.5510 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4066   -1.1591    1.4068 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7354   -1.6729    0.9615 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3749   -0.9842    2.9062 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2490   -1.9770    0.9027 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0791   -1.0076    0.7379 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0595   -1.4699    1.5955 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6155   -1.0037   -0.6770 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2380    0.1037   -1.3022 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7928   -0.0146   -2.7193 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5034    0.4080   -2.9038 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2442    1.4163   -0.6575 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7093    2.4330   -1.5257 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2419   -1.0485   -0.3507 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0245   -1.5936   -0.0693 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2885   -1.9855   -0.4545 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4874   -3.0712   -1.4286 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9410   -1.4071   -1.9210 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3791   -1.7422   -0.2118 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7968    0.0840   -1.1269 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5721    2.5162   -1.8920 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9114    2.7259   -0.1075 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1832    2.2210   -1.2523 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3332    2.9167   -0.1959 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2429    0.8407    1.9064 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5526    2.6152    1.9624 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2484    3.6687    0.6230 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2856    2.6917    1.8053 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6392    2.6196    0.0651 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5812    0.3422    2.2838 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6490    1.0096    1.2925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0691   -0.5809   -1.0317 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1421   -2.3087    1.7901 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6353   -2.3092    0.0742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4267   -0.8210    0.8232 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3601   -1.2378    3.3129 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1448   -1.6311    3.4112 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5779    0.0584    3.2236 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0443   -2.7618    1.6364 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4827   -2.4815   -0.0582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8374   -2.4040    1.3455 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5871   -1.9549   -1.2181 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9710   -1.0275   -3.1289 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4630    0.6786   -3.3053 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5046    1.3708   -3.0753 H   0  0  0  0  0  0  0  0  0  0  0  0
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    4.0855   -3.0446   -0.3126 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  5  7  2  0
  7  8  1  0
  8  9  2  0
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 13 14  1  6
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 18 20  1  0
 18 21  1  0
 21 22  1  0
 22 23  1  1
 22 24  1  0
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 25 26  1  0
 26 27  1  0
 25 28  1  0
 28 29  1  6
  7 30  1  0
 30 31  1  0
 30 32  2  0
 32  3  1  0
 28 11  1  0
 28 13  1  0
 22 15  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  4 36  1  0
  6 37  1  0
  6 38  1  0
  6 39  1  0
 11 40  1  6
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 12 42  1  0
 14 43  1  0
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 16 47  1  1
 17 48  1  0
 19 49  1  0
 19 50  1  0
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 20 52  1  0
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 20 54  1  0
 21 55  1  0
 21 56  1  0
 23 57  1  0
 24 58  1  0
 26 59  1  0
 26 60  1  0
 27 61  1  0
 29 62  1  0
 31 63  1  0
 32 64  1  0
M  END


  Mrv1652309032208052D          

 32 35  0  0  1  0            999 V2000
   -4.1164   -1.7959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8734   -1.0075    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0691   -0.8238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8261   -0.0354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0218    0.1484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7788    0.9368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4606   -0.4563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6563   -0.2725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4133    0.5159    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0950   -0.8772    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7092   -0.6934    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1480    0.0052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8467   -0.4336    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0897    0.3548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6711   -0.4642    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2455    0.1279    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1041    0.9407    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9862   -0.2354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2702    0.5392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7863   -0.4368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8695   -1.0521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0567   -1.1935    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5165   -1.8786    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6180   -1.8922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7935   -1.8615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3548   -2.5601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5303   -2.5295    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4079   -1.1322    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8032   -1.6935    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7036   -1.2447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1423   -1.8493    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5079   -1.4284    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
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
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 11 28  1  0  0  0  0
 13 28  1  0  0  0  0
 28 29  1  1  0  0  0
  7 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  2  0  0  0  0
  3 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0170026

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(C)=C(C(=O)O[C@@H]2C[C@]3(C)[C@H]4[C@@H](O)C(C)(C)C[C@@]4(O)C=C(CO)[C@]23O)C(O)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C24H32O8/c1-12-6-14(31-5)7-15(26)17(12)20(28)32-16-9-22(4)18-19(27)21(2,3)11-23(18,29)8-13(10-25)24(16,22)30/h6-8,16,18-19,25-27,29-30H,9-11H2,1-5H3/t16-,18-,19-,22-,23+,24+/m1/s1

> <INCHI_KEY>
XXMVVKDVYBWXPQ-QSNWBFGMSA-N

> <FORMULA>
C24H32O8

> <MOLECULAR_WEIGHT>
448.512

> <EXACT_MASS>
448.20971799

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
64

> <JCHEM_AVERAGE_POLARIZABILITY>
46.84369609041577

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R,2aS,4aR,7R,7aS,7bR)-2a,4a,7-trihydroxy-3-(hydroxymethyl)-6,6,7b-trimethyl-1H,2H,2aH,4aH,5H,6H,7H,7aH,7bH-cyclobuta[e]inden-2-yl 2-hydroxy-4-methoxy-6-methylbenzoate

> <ALOGPS_LOGP>
1.11

> <JCHEM_LOGP>
1.668975393333334

> <ALOGPS_LOGS>
-3.12

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.86551010760936

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.762842871934216

> <JCHEM_PKA_STRONGEST_BASIC>
-2.7719665684205426

> <JCHEM_POLAR_SURFACE_AREA>
136.68

> <JCHEM_REFRACTIVITY>
116.37979999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.44e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R,2aS,4aR,7R,7aS,7bR)-2a,4a,7-trihydroxy-3-(hydroxymethyl)-6,6,7b-trimethyl-1H,2H,5H,7H,7aH-cyclobuta[e]inden-2-yl 2-hydroxy-4-methoxy-6-methylbenzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0      -7.684  -3.352   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -7.230  -1.881   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -5.729  -1.538   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -5.275  -0.066   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -3.774   0.277   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -3.321   1.749   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.726  -0.852   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.225  -0.509   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -0.771   0.963   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0      -0.177  -1.637   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       1.324  -1.294   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.143   0.010   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.447  -0.809   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.901   0.662   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.986  -0.867   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.058   0.239   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       5.794   1.756   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       7.441  -0.439   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.971   1.006   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.934  -0.815   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.223  -1.964   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.706  -2.228   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       6.564  -3.507   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       4.887  -3.532   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.348  -3.475   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.529  -4.779   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       0.990  -4.722   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       2.628  -2.113   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       1.499  -3.161   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      -3.180  -2.323   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      -2.132  -3.452   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      -4.681  -2.666   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   32                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   30                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   28                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15   28                                             
CONECT   14   13                                                            
CONECT   15   13   16   22                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20   21                                             
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   18   22                                                       
CONECT   22   21   15   23   24                                             
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26   28                                                  
CONECT   26   25   27                                                       
CONECT   27   26                                                            
CONECT   28   25   11   13   29                                             
CONECT   29   28                                                            
CONECT   30    7   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30    3                                                       
MASTER        0    0    0    0    0    0    0    0   32    0   70    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₃₂O₈

Average Mass

448.5120 Da

Monoisotopic Mass

448.20972 Da

IUPAC Name

(2R,2aS,4aR,7R,7aS,7bR)-2a,4a,7-trihydroxy-3-(hydroxymethyl)-6,6,7b-trimethyl-1H,2H,2aH,4aH,5H,6H,7H,7aH,7bH-cyclobuta[e]inden-2-yl 2-hydroxy-4-methoxy-6-methylbenzoate

Traditional Name

(2R,2aS,4aR,7R,7aS,7bR)-2a,4a,7-trihydroxy-3-(hydroxymethyl)-6,6,7b-trimethyl-1H,2H,5H,7H,7aH-cyclobuta[e]inden-2-yl 2-hydroxy-4-methoxy-6-methylbenzoate

CAS Registry Number

Not Available

SMILES

COC1=CC(C)=C(C(=O)O[C@@H]2C[C@]3(C)[C@H]4[C@@H](O)C(C)(C)C[C@@]4(O)C=C(CO)[C@]23O)C(O)=C1

InChI Identifier

InChI=1S/C24H32O8/c1-12-6-14(31-5)7-15(26)17(12)20(28)32-16-9-22(4)18-19(27)21(2,3)11-23(18,29)8-13(10-25)24(16,22)30/h6-8,16,18-19,25-27,29-30H,9-11H2,1-5H3/t16-,18-,19-,22-,23+,24+/m1/s1

InChI Key

XXMVVKDVYBWXPQ-QSNWBFGMSA-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
Armillaria	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as melleolides and analogues. Melleolides and analogues are compounds with a structure characterized by the presence of a 2-hydroxy-4-methoxy-6-methylbenzoic acid derivative linked to a 3,6,6,7b-tetramethyl-cyclobuta[e]indene moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Melleolides and analogues

Alternative Parents

Substituents

Melleolide-skeleton
P-methoxybenzoic acid or derivatives
O-hydroxybenzoic acid ester
Methoxyphenol
Salicylic acid or derivatives
Benzoate ester
Benzoic acid or derivatives
Methoxybenzene
Phenoxy compound
Benzoyl
M-cresol
Phenol ether
Anisole
Toluene
1-hydroxy-4-unsubstituted benzenoid
Phenol
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
Monocyclic benzene moiety
Benzenoid
Vinylogous acid
Tertiary alcohol
Cyclic alcohol
Carboxylic acid ester
Secondary alcohol
Cyclobutanol
Polyol
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Ether
Organooxygen compound
Hydrocarbon derivative
Alcohol
Organic oxygen compound
Organic oxide
Primary alcohol
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic 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	1.11	ALOGPS
logP	1.67	ChemAxon
logS	-3.1	ALOGPS
pKa (Strongest Acidic)	9.76	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	136.68 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	116.38 m³·mol⁻¹	ChemAxon
Polarizability	46.84 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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

C00021461

Chemspider ID

24672558

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

14166114

PDB ID

Not Available

ChEBI ID

175591

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r,2as,4ar,7r,7as,7br)-2a,4a,7-trihydroxy-3-(hydroxymethyl)-6,6,7b-trimethyl-1h,2h,5h,7h,7ah-cyclobuta[e]inden-2-yl 2-hydroxy-4-methoxy-6-methylbenzoate (NP0170026)

MOL for NP0170026 ((2r,2as,4ar,7r,7as,7br)-2a,4a,7-trihydroxy-3-(hydroxymethyl)-6,6,7b-trimethyl-1h,2h,5h,7h,7ah-cyclobuta[e]inden-2-yl 2-hydroxy-4-methoxy-6-methylbenzoate)

3D MOL for NP0170026 ((2r,2as,4ar,7r,7as,7br)-2a,4a,7-trihydroxy-3-(hydroxymethyl)-6,6,7b-trimethyl-1h,2h,5h,7h,7ah-cyclobuta[e]inden-2-yl 2-hydroxy-4-methoxy-6-methylbenzoate)

3D SDF for NP0170026 ((2r,2as,4ar,7r,7as,7br)-2a,4a,7-trihydroxy-3-(hydroxymethyl)-6,6,7b-trimethyl-1h,2h,5h,7h,7ah-cyclobuta[e]inden-2-yl 2-hydroxy-4-methoxy-6-methylbenzoate)

3D-SDF for NP0170026 ((2r,2as,4ar,7r,7as,7br)-2a,4a,7-trihydroxy-3-(hydroxymethyl)-6,6,7b-trimethyl-1h,2h,5h,7h,7ah-cyclobuta[e]inden-2-yl 2-hydroxy-4-methoxy-6-methylbenzoate)

PDB for NP0170026 ((2r,2as,4ar,7r,7as,7br)-2a,4a,7-trihydroxy-3-(hydroxymethyl)-6,6,7b-trimethyl-1h,2h,5h,7h,7ah-cyclobuta[e]inden-2-yl 2-hydroxy-4-methoxy-6-methylbenzoate)

3D PDB for NP0170026 ((2r,2as,4ar,7r,7as,7br)-2a,4a,7-trihydroxy-3-(hydroxymethyl)-6,6,7b-trimethyl-1h,2h,5h,7h,7ah-cyclobuta[e]inden-2-yl 2-hydroxy-4-methoxy-6-methylbenzoate)

SMILES for NP0170026 ((2r,2as,4ar,7r,7as,7br)-2a,4a,7-trihydroxy-3-(hydroxymethyl)-6,6,7b-trimethyl-1h,2h,5h,7h,7ah-cyclobuta[e]inden-2-yl 2-hydroxy-4-methoxy-6-methylbenzoate)

INCHI for NP0170026 ((2r,2as,4ar,7r,7as,7br)-2a,4a,7-trihydroxy-3-(hydroxymethyl)-6,6,7b-trimethyl-1h,2h,5h,7h,7ah-cyclobuta[e]inden-2-yl 2-hydroxy-4-methoxy-6-methylbenzoate)

Structure for NP0170026 ((2r,2as,4ar,7r,7as,7br)-2a,4a,7-trihydroxy-3-(hydroxymethyl)-6,6,7b-trimethyl-1h,2h,5h,7h,7ah-cyclobuta[e]inden-2-yl 2-hydroxy-4-methoxy-6-methylbenzoate)

3D Structure for NP0170026 ((2r,2as,4ar,7r,7as,7br)-2a,4a,7-trihydroxy-3-(hydroxymethyl)-6,6,7b-trimethyl-1h,2h,5h,7h,7ah-cyclobuta[e]inden-2-yl 2-hydroxy-4-methoxy-6-methylbenzoate)