NP-MRD: Showing NP-Card for methyl 3,4,10-trihydroxy-1,16-dimethyl-11,19-dioxo-6,12,20-trioxahexacyclo[13.7.0.0²,⁸.0⁵,⁹.0⁸,¹³.0¹⁷,²¹]docosa-17,21-diene-5-carboxylate (NP0200434)

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Record Information

Version

2.0

Created at

2022-09-04 19:17:05 UTC

Updated at

2022-09-04 19:17:05 UTC

NP-MRD ID

NP0200434

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 3,4,10-trihydroxy-1,16-dimethyl-11,19-dioxo-6,12,20-trioxahexacyclo[13.7.0.0²,⁸.0⁵,⁹.0⁸,¹³.0¹⁷,²¹]docosa-17,21-diene-5-carboxylate

Description

15-Deacetylsergeolide belongs to the class of organic compounds known as quassinoids. These are a group of compounds chemically degraded from triterpenes. According to their basic skeleton, quassinoids are categorized into five distinct groups, C-18, C-19, C-20, C-22 and C-25 types. The C-20 quassinoids can be further classified into two types, tetracyclic and the pentacyclic. The tetracyclic variety does not have oxygenation at C-20, while the pentacyclic quassinoids possess additional oxygenation at C-20 that allows for the formation of an additional ring. methyl 3,4,10-trihydroxy-1,16-dimethyl-11,19-dioxo-6,12,20-trioxahexacyclo[13.7.0.0²,⁸.0⁵,⁹.0⁸,¹³.0¹⁷,²¹]docosa-17,21-diene-5-carboxylate is found in Picrolemma sprucei. methyl 3,4,10-trihydroxy-1,16-dimethyl-11,19-dioxo-6,12,20-trioxahexacyclo[13.7.0.0²,⁸.0⁵,⁹.0⁸,¹³.0¹⁷,²¹]docosa-17,21-diene-5-carboxylate was first documented in 1984 (PMID: 6533270). Based on a literature review very few articles have been published on 15-Deacetylsergeolide.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042221172D          

 33 38  0  0  0  0            999 V2000
   -0.3336    1.7775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0910    1.0701    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9158    1.0841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3162    1.8055    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3404    0.3768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5947    0.1311    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9427   -0.6394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0427   -0.6904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3855   -1.4843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1818   -1.7441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7874   -1.1876    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5831   -1.4056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7922   -2.2036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1697   -0.8255    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9933   -0.8732    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2932   -0.1046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0913    0.1045    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6549    0.4181    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9606   -0.0274    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1649    0.1905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5783   -0.3896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3595    0.4059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7736   -0.1900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6915    0.6257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3597    1.1095    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9467    0.9563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8050    1.7690    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8664   -2.1276    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0517   -2.0012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5226   -2.6342    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7851   -1.2292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0169   -1.0359    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4500   -0.5906    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
  3  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
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 14 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 11 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
  8 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
  5 26  1  0  0  0  0
 26 27  1  0  0  0  0
  9 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 29 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
  5 33  1  0  0  0  0
  8 33  1  0  0  0  0
M  END

     RDKit          3D

 59 64  0  0  0  0  0  0  0  0999 V2000
    6.4528    0.2363    0.2709 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0822    0.4150    0.5797 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1218   -0.3870    0.0250 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4966   -1.2888   -0.7688 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6921   -0.2659    0.2945 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3391    0.7631    1.1383 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0646    1.2171    0.7894 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5396    0.3208   -0.2878 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0605   -0.9658    0.2424 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7969   -1.5317    1.3212 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8549   -0.8009    2.4901 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2309   -1.6179    0.8206 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3139   -2.5259   -0.2299 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5162   -0.9212    0.5228 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9866   -2.3624    0.7046 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9346   -0.1593    1.7022 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1157    0.4478    1.7537 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6955    1.2154    2.7684 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9518    1.6465    2.3658 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8057    2.3501    2.9582 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1480    1.1078    1.0241 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0747    0.4062    0.6646 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7248   -0.3471   -0.5567 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.2961    0.3079   -1.8015 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2340   -0.3877   -0.6942 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7634    1.0096   -1.0435 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2878    0.9548   -1.3342 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2244    2.2029   -1.7007 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5816    2.2072   -2.0434 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0175    3.2227   -2.6371 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4797    1.0775   -1.7301 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6427    1.6275   -1.2076 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8833   -0.0296   -0.9609 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.5974   -0.0402   -0.7928 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0478    1.1502    0.4691 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8867   -0.6069    0.8626 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1599    2.2563    0.3753 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3940    1.3329    1.6631 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0502   -1.6865   -0.6299 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5202   -2.5670    1.6006 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7837   -1.3706    3.3051 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8877   -1.9148    1.6480 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1159   -3.0997   -0.1762 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7223   -2.6702   -0.0740 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1576   -3.0926    0.6051 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4834   -2.5103    1.6844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3124   -0.0597    2.5765 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0045    1.2231    0.3733 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1940   -1.3515   -0.4928 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2952    1.3975   -1.7531 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3340   -0.0179   -1.9990 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6745   -0.0124   -2.6622 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0129   -1.0112   -1.5934 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9482    1.7461   -0.2661 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2699    1.3084   -1.9827 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1951    0.3088   -2.2591 H   0  0  0  0  0  0  0  0  0  0  0  0
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    3.3979    2.4590   -0.7024 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7570   -0.9725   -1.5431 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
  5  3  1  6
  5  6  1  0
  6  7  1  0
  8  7  1  1
  8 33  1  0
 33 31  1  0
 31 32  1  0
 31 29  1  0
 29 30  2  0
 29 28  1  0
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 25 23  1  0
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 23 22  1  0
 22 21  2  0
 21 19  1  0
 19 20  2  0
 19 18  1  0
 18 17  1  0
 17 16  2  0
 16 14  1  0
 14 15  1  1
 14  9  1  0
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 10 12  1  0
 12 13  1  0
 33  5  1  0
 14 25  1  0
 12  5  1  0
 27  8  1  0
 17 22  1  0
  9  8  1  0
  1 34  1  0
  1 35  1  0
  1 36  1  0
  7 37  1  0
  7 38  1  0
 33 59  1  6
 31 57  1  6
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 25 53  1  6
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 21 48  1  0
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  9 39  1  6
 10 40  1  1
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 13 43  1  0
M  END


  Mrv1652309042221172D          

 33 38  0  0  0  0            999 V2000
   -0.3336    1.7775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0910    1.0701    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9158    1.0841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3162    1.8055    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3404    0.3768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5947    0.1311    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9427   -0.6394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0427   -0.6904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3855   -1.4843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1818   -1.7441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7874   -1.1876    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5831   -1.4056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7922   -2.2036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1697   -0.8255    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9933   -0.8732    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2932   -0.1046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0913    0.1045    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6549    0.4181    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9606   -0.0274    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1649    0.1905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5783   -0.3896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3595    0.4059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7736   -0.1900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6915    0.6257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3597    1.1095    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9467    0.9563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8050    1.7690    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8664   -2.1276    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0517   -2.0012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5226   -2.6342    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7851   -1.2292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0169   -1.0359    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4500   -0.5906    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
  3  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
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
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  8 23  1  0  0  0  0
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  5 26  1  0  0  0  0
 26 27  1  0  0  0  0
  9 28  1  0  0  0  0
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 29 30  2  0  0  0  0
 29 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
  5 33  1  0  0  0  0
  8 33  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0200434

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C12OCC34C1C(O)C(=O)OC3CC1C(C)C3=CC(=O)OC3=CC1(C)C4C(O)C2O

> <INCHI_IDENTIFIER>
InChI=1S/C23H26O10/c1-8-9-4-13(24)32-11(9)6-21(2)10(8)5-12-22-7-31-23(20(29)30-3,18(27)14(25)16(21)22)17(22)15(26)19(28)33-12/h4,6,8,10,12,14-18,25-27H,5,7H2,1-3H3

> <INCHI_KEY>
NPWJHTWCKHUSAM-UHFFFAOYSA-N

> <FORMULA>
C23H26O10

> <MOLECULAR_WEIGHT>
462.451

> <EXACT_MASS>
462.152597037

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
45.4800620111819

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl 3,4,10-trihydroxy-1,16-dimethyl-11,19-dioxo-6,12,20-trioxahexacyclo[13.7.0.0^{2,8}.0^{5,9}.0^{8,13}.0^{17,21}]docosa-17,21-diene-5-carboxylate

> <JCHEM_LOGP>
-1.3784914760000004

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.888611458369613

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.186356313314333

> <JCHEM_PKA_STRONGEST_BASIC>
-3.325963400946863

> <JCHEM_POLAR_SURFACE_AREA>
148.82

> <JCHEM_REFRACTIVITY>
108.88550000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
methyl 3,4,10-trihydroxy-1,16-dimethyl-11,19-dioxo-6,12,20-trioxahexacyclo[13.7.0.0^{2,8}.0^{5,9}.0^{8,13}.0^{17,21}]docosa-17,21-diene-5-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0      -0.623   3.318   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       0.170   1.998   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       1.710   2.024   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       2.457   3.370   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       2.502   0.703   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       1.110   0.245   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       1.760  -1.194   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.813  -1.289   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.453  -2.771   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.939  -3.256   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.070  -2.217   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.555  -2.624   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.945  -4.113   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.650  -1.541   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      11.187  -1.630   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      11.747  -0.195   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      13.237   0.195   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0      10.556   0.780   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       9.260  -0.051   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.774   0.356   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.679  -0.727   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.271   0.758   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.177  -0.355   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.024   1.168   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       6.272   2.071   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       3.634   1.785   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       3.369   3.302   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       3.484  -3.972   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       1.963  -3.736   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       0.976  -4.917   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       1.466  -2.295   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      -0.032  -1.934   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       2.707  -1.103   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   26   33                                             
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   23   33                                             
CONECT    9    8   10   28                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   21                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   19                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   14   20                                                  
CONECT   20   19   21                                                       
CONECT   21   20   11   22   23                                             
CONECT   22   21                                                            
CONECT   23   21    8   24                                                  
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24    5   27                                                  
CONECT   27   26                                                            
CONECT   28    9   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31    5    8                                                  
MASTER        0    0    0    0    0    0    0    0   33    0   76    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₂₆O₁₀

Average Mass

462.4510 Da

Monoisotopic Mass

462.15260 Da

IUPAC Name

methyl 3,4,10-trihydroxy-1,16-dimethyl-11,19-dioxo-6,12,20-trioxahexacyclo[13.7.0.0^{2,8}.0^{5,9}.0^{8,13}.0^{17,21}]docosa-17,21-diene-5-carboxylate

Traditional Name

methyl 3,4,10-trihydroxy-1,16-dimethyl-11,19-dioxo-6,12,20-trioxahexacyclo[13.7.0.0^{2,8}.0^{5,9}.0^{8,13}.0^{17,21}]docosa-17,21-diene-5-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)C12OCC34C1C(O)C(=O)OC3CC1C(C)C3=CC(=O)OC3=CC1(C)C4C(O)C2O

InChI Identifier

InChI=1S/C23H26O10/c1-8-9-4-13(24)32-11(9)6-21(2)10(8)5-12-22-7-31-23(20(29)30-3,18(27)14(25)16(21)22)17(22)15(26)19(28)33-12/h4,6,8,10,12,14-18,25-27H,5,7H2,1-3H3

InChI Key

NPWJHTWCKHUSAM-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, 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
Picrolemma sprucei	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as quassinoids. These are a group of compounds chemically degraded from triterpenes. According to their basic skeleton, quassinoids are categorized into five distinct groups, C-18, C-19, C-20, C-22 and C-25 types. The C-20 quassinoids can be further classified into two types, tetracyclic and the pentacyclic. The tetracyclic variety does not have oxygenation at C-20, while the pentacyclic quassinoids possess additional oxygenation at C-20 that allows for the formation of an additional ring.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Quassinoids

Alternative Parents

Substituents

C-20 quassinoid skeleton
Quassinoid
Naphthopyran
Naphthofuran
Naphthalene
Furopyran
Tricarboxylic acid or derivatives
Delta valerolactone
Oxepane
Delta_valerolactone
Beta-hydroxy acid
Hydroxy acid
Pyran
Oxane
2-furanone
Methyl ester
Tetrahydrofuran
Enol ester
Dihydrofuran
Furan
Cyclic alcohol
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Carboxylic acid ester
Secondary alcohol
Lactone
Ether
Organoheterocyclic compound
Dialkyl ether
Oxacycle
Carboxylic acid derivative
Polyol
Hydrocarbon derivative
Alcohol
Carbonyl group
Organic oxide
Organooxygen compound
Organic oxygen compound
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	-1.4	ChemAxon
pKa (Strongest Acidic)	12.19	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	148.82 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	108.89 m³·mol⁻¹	ChemAxon
Polarizability	45.48 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

111822

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

125729

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Polonsky J, Bhatnagar S, Moretti C: 15-Deacetylsergeolide, a potent antileukemic quassinoid from Picrolemma pseudocoffea. J Nat Prod. 1984 Nov-Dec;47(6):994-6. doi: 10.1021/np50036a014. [PubMed:6533270 ]
LOTUS database [Link]

Showing NP-Card for methyl 3,4,10-trihydroxy-1,16-dimethyl-11,19-dioxo-6,12,20-trioxahexacyclo[13.7.0.0²,⁸.0⁵,⁹.0⁸,¹³.0¹⁷,²¹]docosa-17,21-diene-5-carboxylate (NP0200434)

MOL for NP0200434 (methyl 3,4,10-trihydroxy-1,16-dimethyl-11,19-dioxo-6,12,20-trioxahexacyclo[13.7.0.0²,⁸.0⁵,⁹.0⁸,¹³.0¹⁷,²¹]docosa-17,21-diene-5-carboxylate)

3D MOL for NP0200434 (methyl 3,4,10-trihydroxy-1,16-dimethyl-11,19-dioxo-6,12,20-trioxahexacyclo[13.7.0.0²,⁸.0⁵,⁹.0⁸,¹³.0¹⁷,²¹]docosa-17,21-diene-5-carboxylate)

3D SDF for NP0200434 (methyl 3,4,10-trihydroxy-1,16-dimethyl-11,19-dioxo-6,12,20-trioxahexacyclo[13.7.0.0²,⁸.0⁵,⁹.0⁸,¹³.0¹⁷,²¹]docosa-17,21-diene-5-carboxylate)

3D-SDF for NP0200434 (methyl 3,4,10-trihydroxy-1,16-dimethyl-11,19-dioxo-6,12,20-trioxahexacyclo[13.7.0.0²,⁸.0⁵,⁹.0⁸,¹³.0¹⁷,²¹]docosa-17,21-diene-5-carboxylate)

PDB for NP0200434 (methyl 3,4,10-trihydroxy-1,16-dimethyl-11,19-dioxo-6,12,20-trioxahexacyclo[13.7.0.0²,⁸.0⁵,⁹.0⁸,¹³.0¹⁷,²¹]docosa-17,21-diene-5-carboxylate)

3D PDB for NP0200434 (methyl 3,4,10-trihydroxy-1,16-dimethyl-11,19-dioxo-6,12,20-trioxahexacyclo[13.7.0.0²,⁸.0⁵,⁹.0⁸,¹³.0¹⁷,²¹]docosa-17,21-diene-5-carboxylate)

SMILES for NP0200434 (methyl 3,4,10-trihydroxy-1,16-dimethyl-11,19-dioxo-6,12,20-trioxahexacyclo[13.7.0.0²,⁸.0⁵,⁹.0⁸,¹³.0¹⁷,²¹]docosa-17,21-diene-5-carboxylate)

INCHI for NP0200434 (methyl 3,4,10-trihydroxy-1,16-dimethyl-11,19-dioxo-6,12,20-trioxahexacyclo[13.7.0.0²,⁸.0⁵,⁹.0⁸,¹³.0¹⁷,²¹]docosa-17,21-diene-5-carboxylate)

Structure for NP0200434 (methyl 3,4,10-trihydroxy-1,16-dimethyl-11,19-dioxo-6,12,20-trioxahexacyclo[13.7.0.0²,⁸.0⁵,⁹.0⁸,¹³.0¹⁷,²¹]docosa-17,21-diene-5-carboxylate)

3D Structure for NP0200434 (methyl 3,4,10-trihydroxy-1,16-dimethyl-11,19-dioxo-6,12,20-trioxahexacyclo[13.7.0.0²,⁸.0⁵,⁹.0⁸,¹³.0¹⁷,²¹]docosa-17,21-diene-5-carboxylate)