NP-MRD: Showing NP-Card for (1's,2s,2'r,3's,4r,5'r,7'r,8's,9's,12'r)-2',4,12'-trihydroxy-4-[(1r)-1-hydroxyethyl]-12'-isopropyl-8'-methoxy-7'-methyl-4',10'-dioxaspiro[oxolane-2,6'-tetracyclo[7.2.1.0²,⁷.0³,⁵]dodecane]-5,11'-dione (NP0174816)

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Record Information

Version

2.0

Created at

2022-09-03 12:08:47 UTC

Updated at

2022-09-03 12:08:47 UTC

NP-MRD ID

NP0174816

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1's,2s,2'r,3's,4r,5'r,7'r,8's,9's,12'r)-2',4,12'-trihydroxy-4-[(1r)-1-hydroxyethyl]-12'-isopropyl-8'-methoxy-7'-methyl-4',10'-dioxaspiro[oxolane-2,6'-tetracyclo[7.2.1.0²,⁷.0³,⁵]dodecane]-5,11'-dione

Description

Picrodendrin F belongs to the class of organic compounds known as gamma butyrolactones. Gamma butyrolactones are compounds containing a gamma butyrolactone moiety, which consists of an aliphatic five-member ring with four carbon atoms, one oxygen atom, and bears a ketone group on the carbon adjacent to the oxygen atom. (1's,2s,2'r,3's,4r,5'r,7'r,8's,9's,12'r)-2',4,12'-trihydroxy-4-[(1r)-1-hydroxyethyl]-12'-isopropyl-8'-methoxy-7'-methyl-4',10'-dioxaspiro[oxolane-2,6'-tetracyclo[7.2.1.0²,⁷.0³,⁵]dodecane]-5,11'-dione is found in Picrodendron baccatum. Based on a literature review very few articles have been published on Picrodendrin F.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032214082D          

 30 34  0  0  1  0            999 V2000
   -0.3069   -0.8654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6815    0.0660    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2554    0.4662    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0267    0.1734    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7365    0.5938    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8504    1.4110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6695    1.6948    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2825    2.0094    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3841    1.0594    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9380    1.6483    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8109    0.5184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4804    1.2506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9927   -0.4501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4605    1.9385    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8273    2.7905    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0514    2.5855    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6867    3.1119    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8249    2.2985    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7910    1.4742    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8608    0.7033    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5306    0.3629    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6073   -0.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3467   -0.1426    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6060   -0.9934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2097   -0.0946    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0425    1.0099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8381    1.3499    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5854    1.6967    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0035    1.2517    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3297    0.4723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  1  0  0  0
  3  4  1  0  0  0  0
  4  5  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  8  6  1  1  0  0  0
  8  9  1  0  0  0  0
  4  9  1  0  0  0  0
  9 10  1  6  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
  8 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  0  0  0  0
 16 17  1  6  0  0  0
 18 17  1  6  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  6  0  0  0
 21 23  1  1  0  0  0
 23 24  1  0  0  0  0
 23 25  1  1  0  0  0
 21 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 19 28  1  6  0  0  0
 19 29  1  0  0  0  0
  3 29  1  0  0  0  0
 14 29  1  0  0  0  0
 29 30  1  6  0  0  0
M  END

     RDKit          3D

 58 62  0  0  0  0  0  0  0  0999 V2000
    0.0273   -2.9297    1.1290 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0050   -2.0555    0.0482 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7807   -0.9377    0.3010 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0411   -1.1466   -0.5350 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7605   -0.9795   -1.9395 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3690    0.2150   -2.3868 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8418    0.5364   -3.4751 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2774    1.0359   -1.0947 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9727   -0.0093   -0.2964 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1312   -0.3427   -1.0804 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4547    0.2472    1.0442 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2218   -1.0124    1.5171 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5118    1.3521    1.1240 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8126    1.2089   -0.9255 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5814    2.5615   -0.5927 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0115    0.9463   -2.1896 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1697    1.5804   -2.4522 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2012    0.2413   -1.8485 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2988    0.3478   -0.3680 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1751   -0.6559    0.3025 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5814   -0.0260    0.3166 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2225   -0.2674    1.5087 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4015   -0.4933   -0.8370 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7631    0.2029   -0.7069 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6725   -1.8582   -0.7976 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2700    1.4015    0.1720 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1326    2.3170    0.2115 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9127    1.6095   -0.0123 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1319    0.3780    0.1210 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0479    1.1814    1.4280 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4408   -2.4168    2.0152 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7207   -3.7725    0.9149 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9855   -3.2880    1.4101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1402   -1.0405    1.3531 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4340   -2.1395   -0.3086 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8243    1.9763   -1.2157 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7983    0.3883   -0.9365 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7084    0.3519    1.8514 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7521   -0.7944    2.4673 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4470   -1.7979    1.6986 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9695   -1.3014    0.7701 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5619    1.7947    2.1325 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2402    2.0771    0.3309 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5192    0.9464    0.8932 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4051    3.1123   -1.3812 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5691    0.7024   -3.1426 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6903   -0.5292   -2.4362 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8927   -0.6669    1.3770 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2616   -1.6295   -0.1757 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0076    0.4849    2.1342 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9842   -0.2160   -1.8141 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7457    1.1863   -1.2037 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5627   -0.4707   -1.1096 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9780    0.3038    0.3770 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4891   -2.0006   -1.3365 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8478    1.9519    1.3881 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8962    1.6745    1.5967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3422    0.4646    2.2232 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  1  0
  9 10  1  6
  9 11  1  0
 11 12  1  0
 11 13  1  0
  8 14  1  0
 14 15  1  1
 14 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  1
 21 23  1  0
 23 24  1  0
 23 25  1  0
 21 26  1  0
 26 27  2  0
 26 28  1  0
 19 29  1  0
 29 30  1  1
 29  3  1  0
  9  4  1  0
 29 14  1  0
 18 16  1  0
 19 28  1  6
  1 31  1  0
  1 32  1  0
  1 33  1  0
  3 34  1  1
  4 35  1  6
  8 36  1  6
 10 37  1  0
 11 38  1  0
 12 39  1  0
 12 40  1  0
 12 41  1  0
 13 42  1  0
 13 43  1  0
 13 44  1  0
 15 45  1  0
 16 46  1  6
 18 47  1  6
 20 48  1  0
 20 49  1  0
 22 50  1  0
 23 51  1  6
 24 52  1  0
 24 53  1  0
 24 54  1  0
 25 55  1  0
 30 56  1  0
 30 57  1  0
 30 58  1  0
M  END


  Mrv1652309032214082D          

 30 34  0  0  1  0            999 V2000
   -0.3069   -0.8654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6815    0.0660    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2554    0.4662    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0267    0.1734    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7365    0.5938    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8504    1.4110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6695    1.6948    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2825    2.0094    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3841    1.0594    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9380    1.6483    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8109    0.5184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4804    1.2506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9927   -0.4501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4605    1.9385    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8273    2.7905    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0514    2.5855    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6867    3.1119    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8249    2.2985    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7910    1.4742    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8608    0.7033    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5306    0.3629    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6073   -0.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3467   -0.1426    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6060   -0.9934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2097   -0.0946    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0425    1.0099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8381    1.3499    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5854    1.6967    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0035    1.2517    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3297    0.4723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  1  0  0  0
  3  4  1  0  0  0  0
  4  5  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  8  6  1  1  0  0  0
  8  9  1  0  0  0  0
  4  9  1  0  0  0  0
  9 10  1  6  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
  8 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  0  0  0  0
 16 17  1  6  0  0  0
 18 17  1  6  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  6  0  0  0
 21 23  1  1  0  0  0
 23 24  1  0  0  0  0
 23 25  1  1  0  0  0
 21 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 19 28  1  6  0  0  0
 19 29  1  0  0  0  0
  3 29  1  0  0  0  0
 14 29  1  0  0  0  0
 29 30  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0174816

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CO[C@@H]1[C@@H]2OC(=O)[C@@H]([C@]2(O)C(C)C)[C@]2(O)[C@H]3O[C@H]3[C@]3(C[C@@](O)([C@@H](C)O)C(=O)O3)[C@]12C

> <INCHI_IDENTIFIER>
InChI=1S/C20H28O10/c1-7(2)19(25)9-14(22)29-12(19)10(27-5)16(4)18(11-13(28-11)20(9,16)26)6-17(24,8(3)21)15(23)30-18/h7-13,21,24-26H,6H2,1-5H3/t8-,9+,10-,11-,12+,13+,16+,17-,18-,19-,20+/m1/s1

> <INCHI_KEY>
WBQTULHCTLHEOG-OLARYOTISA-N

> <FORMULA>
C20H28O10

> <MOLECULAR_WEIGHT>
428.434

> <EXACT_MASS>
428.168247102

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
41.02418706718208

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1'S,2S,2'R,3'S,4R,5'R,7'R,8'S,9'S,12'R)-2',4,12'-trihydroxy-4-[(1R)-1-hydroxyethyl]-8'-methoxy-7'-methyl-12'-(propan-2-yl)-4',10'-dioxaspiro[oxolane-2,6'-tetracyclo[7.2.1.0^{2,7}.0^{3,5}]dodecane]-5,11'-dione

> <ALOGPS_LOGP>
-0.05

> <JCHEM_LOGP>
-1.4639807129999995

> <ALOGPS_LOGS>
-1.59

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.541738577881006

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.351356673933447

> <JCHEM_PKA_STRONGEST_BASIC>
-3.2359754365322955

> <JCHEM_POLAR_SURFACE_AREA>
155.28

> <JCHEM_REFRACTIVITY>
95.04959999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.11e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1'S,2S,2'R,3'S,4R,5'R,7'R,8'S,9'S,12'R)-2',4,12'-trihydroxy-4-[(1R)-1-hydroxyethyl]-12'-isopropyl-8'-methoxy-7'-methyl-4',10'-dioxaspiro[oxolane-2,6'-tetracyclo[7.2.1.0^{2,7}.0^{3,5}]dodecane]-5,11'-dione

> <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      -0.573  -1.615   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -1.272   0.123   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       0.477   0.870   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.917   0.324   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       3.242   1.109   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       3.454   2.634   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       4.983   3.164   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       2.394   3.751   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.584   1.978   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       1.751   3.077   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       1.514   0.968   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.897   2.334   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.853  -0.840   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.860   3.619   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       1.544   5.209   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -0.096   4.826   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -1.282   5.809   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -1.540   4.291   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.477   2.752   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.607   1.313   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -2.857   0.677   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -3.000  -1.003   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -4.380  -0.266   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -4.865  -1.854   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -5.991  -0.177   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      -3.813   1.885   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -5.298   2.520   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0      -2.959   3.167   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       0.006   2.337   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -0.615   0.882   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   29                                                  
CONECT    4    3    5    9                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   14                                                  
CONECT    9    8    4   10   11                                             
CONECT   10    9                                                            
CONECT   11    9   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14    8   15   16   29                                             
CONECT   15   14                                                            
CONECT   16   14   17   18                                                  
CONECT   17   16   18                                                       
CONECT   18   17   16   19                                                  
CONECT   19   18   20   28   29                                             
CONECT   20   19   21                                                       
CONECT   21   20   22   23   26                                             
CONECT   22   21                                                            
CONECT   23   21   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23                                                            
CONECT   26   21   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   19                                                       
CONECT   29   19    3   14   30                                             
CONECT   30   29                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   68    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₈O₁₀

Average Mass

428.4340 Da

Monoisotopic Mass

428.16825 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CO[C@@H]1[C@@H]2OC(=O)[C@@H]([C@]2(O)C(C)C)[C@]2(O)[C@H]3O[C@H]3[C@]3(C[C@@](O)([C@@H](C)O)C(=O)O3)[C@]12C

InChI Identifier

InChI=1S/C20H28O10/c1-7(2)19(25)9-14(22)29-12(19)10(27-5)16(4)18(11-13(28-11)20(9,16)26)6-17(24,8(3)21)15(23)30-18/h7-13,21,24-26H,6H2,1-5H3/t8-,9+,10-,11-,12+,13+,16+,17-,18-,19-,20+/m1/s1

InChI Key

WBQTULHCTLHEOG-OLARYOTISA-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
Picrodendron baccatum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as gamma butyrolactones. Gamma butyrolactones are compounds containing a gamma butyrolactone moiety, which consists of an aliphatic five-member ring with four carbon atoms, one oxygen atom, and bears a ketone group on the carbon adjacent to the oxygen atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Lactones

Sub Class

Gamma butyrolactones

Direct Parent

Gamma butyrolactones

Alternative Parents

Substituents

Oxepane
Dicarboxylic acid or derivatives
Gamma butyrolactone
Oxane
Cyclic alcohol
Tertiary alcohol
Tetrahydrofuran
Carboxylic acid ester
Secondary alcohol
Polyol
Oxacycle
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Hydrocarbon derivative
Organooxygen compound
Organic oxide
Organic oxygen compound
Alcohol
Carbonyl group
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

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

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

101615680

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1's,2s,2'r,3's,4r,5'r,7'r,8's,9's,12'r)-2',4,12'-trihydroxy-4-[(1r)-1-hydroxyethyl]-12'-isopropyl-8'-methoxy-7'-methyl-4',10'-dioxaspiro[oxolane-2,6'-tetracyclo[7.2.1.0²,⁷.0³,⁵]dodecane]-5,11'-dione (NP0174816)

MOL for NP0174816 ((1's,2s,2'r,3's,4r,5'r,7'r,8's,9's,12'r)-2',4,12'-trihydroxy-4-[(1r)-1-hydroxyethyl]-12'-isopropyl-8'-methoxy-7'-methyl-4',10'-dioxaspiro[oxolane-2,6'-tetracyclo[7.2.1.0²,⁷.0³,⁵]dodecane]-5,11'-dione)

3D MOL for NP0174816 ((1's,2s,2'r,3's,4r,5'r,7'r,8's,9's,12'r)-2',4,12'-trihydroxy-4-[(1r)-1-hydroxyethyl]-12'-isopropyl-8'-methoxy-7'-methyl-4',10'-dioxaspiro[oxolane-2,6'-tetracyclo[7.2.1.0²,⁷.0³,⁵]dodecane]-5,11'-dione)

3D SDF for NP0174816 ((1's,2s,2'r,3's,4r,5'r,7'r,8's,9's,12'r)-2',4,12'-trihydroxy-4-[(1r)-1-hydroxyethyl]-12'-isopropyl-8'-methoxy-7'-methyl-4',10'-dioxaspiro[oxolane-2,6'-tetracyclo[7.2.1.0²,⁷.0³,⁵]dodecane]-5,11'-dione)

3D-SDF for NP0174816 ((1's,2s,2'r,3's,4r,5'r,7'r,8's,9's,12'r)-2',4,12'-trihydroxy-4-[(1r)-1-hydroxyethyl]-12'-isopropyl-8'-methoxy-7'-methyl-4',10'-dioxaspiro[oxolane-2,6'-tetracyclo[7.2.1.0²,⁷.0³,⁵]dodecane]-5,11'-dione)

PDB for NP0174816 ((1's,2s,2'r,3's,4r,5'r,7'r,8's,9's,12'r)-2',4,12'-trihydroxy-4-[(1r)-1-hydroxyethyl]-12'-isopropyl-8'-methoxy-7'-methyl-4',10'-dioxaspiro[oxolane-2,6'-tetracyclo[7.2.1.0²,⁷.0³,⁵]dodecane]-5,11'-dione)

3D PDB for NP0174816 ((1's,2s,2'r,3's,4r,5'r,7'r,8's,9's,12'r)-2',4,12'-trihydroxy-4-[(1r)-1-hydroxyethyl]-12'-isopropyl-8'-methoxy-7'-methyl-4',10'-dioxaspiro[oxolane-2,6'-tetracyclo[7.2.1.0²,⁷.0³,⁵]dodecane]-5,11'-dione)

SMILES for NP0174816 ((1's,2s,2'r,3's,4r,5'r,7'r,8's,9's,12'r)-2',4,12'-trihydroxy-4-[(1r)-1-hydroxyethyl]-12'-isopropyl-8'-methoxy-7'-methyl-4',10'-dioxaspiro[oxolane-2,6'-tetracyclo[7.2.1.0²,⁷.0³,⁵]dodecane]-5,11'-dione)

INCHI for NP0174816 ((1's,2s,2'r,3's,4r,5'r,7'r,8's,9's,12'r)-2',4,12'-trihydroxy-4-[(1r)-1-hydroxyethyl]-12'-isopropyl-8'-methoxy-7'-methyl-4',10'-dioxaspiro[oxolane-2,6'-tetracyclo[7.2.1.0²,⁷.0³,⁵]dodecane]-5,11'-dione)

Structure for NP0174816 ((1's,2s,2'r,3's,4r,5'r,7'r,8's,9's,12'r)-2',4,12'-trihydroxy-4-[(1r)-1-hydroxyethyl]-12'-isopropyl-8'-methoxy-7'-methyl-4',10'-dioxaspiro[oxolane-2,6'-tetracyclo[7.2.1.0²,⁷.0³,⁵]dodecane]-5,11'-dione)

3D Structure for NP0174816 ((1's,2s,2'r,3's,4r,5'r,7'r,8's,9's,12'r)-2',4,12'-trihydroxy-4-[(1r)-1-hydroxyethyl]-12'-isopropyl-8'-methoxy-7'-methyl-4',10'-dioxaspiro[oxolane-2,6'-tetracyclo[7.2.1.0²,⁷.0³,⁵]dodecane]-5,11'-dione)