NP-MRD: Showing NP-Card for methyl (1s,2r,4r,7e,9r,10r,11s)-9-(acetyloxy)-4-methyl-10-{[(2z)-2-methylbut-2-enoyl]oxy}-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-ene-8-carboxylate (NP0301174)

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Record Information

Version

2.0

Created at

2022-09-10 13:58:30 UTC

Updated at

2022-09-10 13:58:30 UTC

NP-MRD ID

NP0301174

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (1s,2r,4r,7e,9r,10r,11s)-9-(acetyloxy)-4-methyl-10-{[(2z)-2-methylbut-2-enoyl]oxy}-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-ene-8-carboxylate

Description

Fluctuanin belongs to the class of organic compounds known as germacranolides and derivatives. These are sesquiterpene lactones with a structure based on the germacranolide skeleton, characterized by a gamma lactone fused to a 1,7-dimethylcyclodec-1-ene moiety. methyl (1s,2r,4r,7e,9r,10r,11s)-9-(acetyloxy)-4-methyl-10-{[(2z)-2-methylbut-2-enoyl]oxy}-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-ene-8-carboxylate is found in Melampodium longipilum and Smallanthus sonchifolius. methyl (1s,2r,4r,7e,9r,10r,11s)-9-(acetyloxy)-4-methyl-10-{[(2z)-2-methylbut-2-enoyl]oxy}-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-ene-8-carboxylate was first documented in 2003 (PMID: 14586103). Based on a literature review a small amount of articles have been published on Fluctuanin (PMID: 26125943) (PMID: 18239309).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102215582D          

 32 34  0  0  1  0            999 V2000
    5.1775    0.4639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6520    0.9520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7534    1.8715    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4963    2.2302    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0265    2.2618    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4307    1.6911    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7894    0.9481    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3253    0.2660    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0890   -0.0461    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7411    0.4592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6296    1.2766    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5048    0.1470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6163   -0.6704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1569    0.6523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0454    1.4697    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6839   -0.4769    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5067   -0.5378    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8653   -1.2808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6881   -1.3417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5367   -2.2856    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2198   -1.1590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5785   -1.9020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4012   -1.9629    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1144   -2.5841    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4730   -3.3270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3971   -1.0981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0384   -0.3552    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5025    0.3269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1439    1.0699    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4009    0.7112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7852    1.8129    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6080    1.7520    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
  7  2  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  2  0  0  0  0
 14 15  1  0  0  0  0
  8 16  1  0  0  0  0
 16 17  1  6  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 16 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 21 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  6  0  0  0
 29 31  1  0  0  0  0
 32 31  1  6  0  0  0
  6 32  1  0  0  0  0
 29 32  1  0  0  0  0
M  END

     RDKit          3D

 60 62  0  0  0  0  0  0  0  0999 V2000
   -1.2022   -3.1238    1.7143 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2111   -2.2639    1.8223 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2595   -1.5826    3.0257 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4424   -1.3238    4.0498 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6216   -1.2802    2.8180 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9998   -1.7153    1.4996 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7154   -1.7690    0.7553 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2448   -0.6275   -0.0283 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2087   -0.7451   -0.0827 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8817   -1.0966   -1.2056 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1751   -1.3382   -2.2354 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3224   -1.2025   -1.2668 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9057   -1.6375   -2.5869 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1679   -0.9647   -0.3098 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7138   -0.5318    1.0218 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6188    0.7492    0.3601 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5067    1.2737    1.1067 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4465    1.6831    2.4029 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6723    2.2026    3.0734 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6203    1.6262    3.0273 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9147    1.6897   -0.7750 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0554    2.8956   -0.7960 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8432    3.0983    0.0534 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2211    3.8518   -1.7706 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5534    5.0331   -1.8671 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8111    1.5860   -1.7034 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8254    0.5784   -2.0231 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8453    0.3010   -0.9419 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4791   -1.0596   -0.3905 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3179   -2.1221   -1.4199 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4048   -1.5820    0.6391 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0948   -0.9543    0.9256 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7923   -3.4258    2.5369 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4142   -3.5334    0.7385 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3288   -2.7771    1.6708 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8007   -2.6693    0.0581 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5168   -0.8488   -1.1075 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9021   -1.1672   -2.7048 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9651   -2.7463   -2.5216 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2447   -1.2829   -3.3978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2396   -1.0882   -0.4936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5950   -0.0495    1.5456 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3913   -1.3559    1.6531 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9844    0.2974    0.9445 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4002    0.7544    1.1092 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0247    1.5456    3.8773 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4379    3.1938    3.5280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4961    2.3554    2.3485 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1235    5.8665   -1.5174 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4475    4.9683   -1.2290 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7782    5.2476   -2.9296 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8574    2.4338   -2.4532 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4123   -0.3754   -2.4073 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4699    0.9097   -2.9117 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7699    1.0407   -0.1160 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8753    0.2588   -1.3589 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7866   -3.1013   -1.1776 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2756   -2.2626   -1.7529 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8713   -1.7937   -2.3489 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4282   -0.0429    1.5250 H   0  0  0  0  0  0  0  0  0  0  0  0
 25 24  1  0
 24 22  1  0
 22 23  2  0
 22 21  1  0
 21 26  2  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  6
 29 31  1  0
 31 32  1  0
 32  6  1  0
  6  5  1  0
  5  3  1  0
  3  4  2  0
  3  2  1  0
  2  1  2  3
  2  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
 12 13  1  0
 12 14  2  0
 14 15  1  0
  8 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  2  0
 16 21  1  0
 32 29  1  0
  7  6  1  0
 25 49  1  0
 25 50  1  0
 25 51  1  0
 26 52  1  0
 27 53  1  0
 27 54  1  0
 28 55  1  0
 28 56  1  0
 30 57  1  0
 30 58  1  0
 30 59  1  0
 32 60  1  1
  6 35  1  1
  1 33  1  0
  1 34  1  0
  7 36  1  6
  8 37  1  6
 13 38  1  0
 13 39  1  0
 13 40  1  0
 14 41  1  0
 15 42  1  0
 15 43  1  0
 15 44  1  0
 16 45  1  1
 19 46  1  0
 19 47  1  0
 19 48  1  0
M  END


  Mrv1652309102215582D          

 32 34  0  0  1  0            999 V2000
    5.1775    0.4639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6520    0.9520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7534    1.8715    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4963    2.2302    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0265    2.2618    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4307    1.6911    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7894    0.9481    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3253    0.2660    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0890   -0.0461    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7411    0.4592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6296    1.2766    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5048    0.1470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6163   -0.6704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1569    0.6523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0454    1.4697    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6839   -0.4769    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5067   -0.5378    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8653   -1.2808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6881   -1.3417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5367   -2.2856    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2198   -1.1590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5785   -1.9020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4012   -1.9629    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1144   -2.5841    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4730   -3.3270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3971   -1.0981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0384   -0.3552    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5025    0.3269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1439    1.0699    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4009    0.7112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7852    1.8129    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6080    1.7520    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
  7  2  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  2  0  0  0  0
 14 15  1  0  0  0  0
  8 16  1  0  0  0  0
 16 17  1  6  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 16 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 21 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  6  0  0  0
 29 31  1  0  0  0  0
 32 31  1  6  0  0  0
  6 32  1  0  0  0  0
 29 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0301174

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C1=C/CC[C@@]2(C)O[C@@H]2[C@H]2OC(=O)C(=C)[C@H]2[C@@H](OC(=O)C(\C)=C/C)[C@@H]\1OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C23H28O9/c1-7-11(2)20(25)30-17-15-12(3)21(26)31-18(15)19-23(5,32-19)10-8-9-14(22(27)28-6)16(17)29-13(4)24/h7,9,15-19H,3,8,10H2,1-2,4-6H3/b11-7-,14-9+/t15-,16+,17+,18-,19+,23+/m0/s1

> <INCHI_KEY>
FRJDOHXLSCQTIL-IGWVAYMQSA-N

> <FORMULA>
C23H28O9

> <MOLECULAR_WEIGHT>
448.468

> <EXACT_MASS>
448.173332482

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
43.85077054586376

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (1S,2R,4R,7E,9R,10R,11S)-9-(acetyloxy)-4-methyl-10-{[(2Z)-2-methylbut-2-enoyl]oxy}-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.0^{2,4}]tetradec-7-ene-8-carboxylate

> <JCHEM_LOGP>
3.0321172846666657

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.240144824047126

> <JCHEM_POLAR_SURFACE_AREA>
117.73

> <JCHEM_REFRACTIVITY>
110.7987

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1S,2R,4R,7E,9R,10R,11S)-9-(acetyloxy)-4-methyl-10-{[(2Z)-2-methylbut-2-enoyl]oxy}-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.0^{2,4}]tetradec-7-ene-8-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0       9.665   0.866   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.684   1.777   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.873   3.493   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      10.260   4.163   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0       7.516   4.222   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       6.404   3.157   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.074   1.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.207   0.497   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       7.633  -0.086   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       8.850   0.857   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       8.642   2.383   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      10.276   0.274   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.484  -1.251   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      11.493   1.218   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      11.285   2.744   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.877  -0.890   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       8.412  -1.004   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       9.082  -2.391   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      10.618  -2.504   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       8.468  -4.266   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       6.010  -2.163   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.680  -3.550   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       8.216  -3.664   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       5.813  -4.824   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       6.483  -6.210   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.475  -2.050   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       3.805  -0.663   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.671   0.610   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.002   1.997   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.615   1.328   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       3.332   3.384   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       4.868   3.270   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7   32                                                  
CONECT    7    6    2    8                                                  
CONECT    8    7    9   16                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14                                                            
CONECT   16    8   17   21                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   16   22   26                                                  
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24                                                            
CONECT   26   21   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30   31   32                                             
CONECT   30   29                                                            
CONECT   31   29   32                                                       
CONECT   32   31    6   29                                                  
MASTER        0    0    0    0    0    0    0    0   32    0   68    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₂₈O₉

Average Mass

448.4680 Da

Monoisotopic Mass

448.17333 Da

IUPAC Name

methyl (1S,2R,4R,7E,9R,10R,11S)-9-(acetyloxy)-4-methyl-10-{[(2Z)-2-methylbut-2-enoyl]oxy}-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.0^{2,4}]tetradec-7-ene-8-carboxylate

Traditional Name

methyl (1S,2R,4R,7E,9R,10R,11S)-9-(acetyloxy)-4-methyl-10-{[(2Z)-2-methylbut-2-enoyl]oxy}-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.0^{2,4}]tetradec-7-ene-8-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)C1=C/CC[C@@]2(C)O[C@@H]2[C@H]2OC(=O)C(=C)[C@H]2[C@@H](OC(=O)C(\C)=C/C)[C@@H]\1OC(C)=O

InChI Identifier

InChI=1S/C23H28O9/c1-7-11(2)20(25)30-17-15-12(3)21(26)31-18(15)19-23(5,32-19)10-8-9-14(22(27)28-6)16(17)29-13(4)24/h7,9,15-19H,3,8,10H2,1-2,4-6H3/b11-7-,14-9+/t15-,16+,17+,18-,19+,23+/m0/s1

InChI Key

FRJDOHXLSCQTIL-IGWVAYMQSA-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
Melampodium longipilum	LOTUS Database	35616633
Smallanthus sonchifolius	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as germacranolides and derivatives. These are sesquiterpene lactones with a structure based on the germacranolide skeleton, characterized by a gamma lactone fused to a 1,7-dimethylcyclodec-1-ene moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Germacranolides and derivatives

Alternative Parents

Substituents

Germacranolide
Sesquiterpenoid
Germacrane sesquiterpenoid
Tetracarboxylic acid or derivatives
Fatty acid ester
Fatty acyl
Gamma butyrolactone
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Methyl ester
Tetrahydrofuran
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
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
logP	3.03	ChemAxon
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	117.73 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	110.8 m³·mol⁻¹	ChemAxon
Polarizability	43.85 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00011880

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

134692058

PDB ID

Not Available

ChEBI ID

141118

Good Scents ID

Not Available

References

General References

De Ford C, Ulloa JL, Catalan CAN, Grau A, Martino VS, Muschietti LV, Merfort I: The sesquiterpene lactone polymatin B from Smallanthus sonchifolius induces different cell death mechanisms in three cancer cell lines. Phytochemistry. 2015 Sep;117:332-339. doi: 10.1016/j.phytochem.2015.06.020. Epub 2015 Jun 27. [PubMed:26125943 ]
Hong SS, Lee SA, Han XH, Lee MH, Hwang JS, Park JS, Oh KW, Han K, Lee MK, Lee H, Kim W, Lee D, Hwang BY: Melampolides from the leaves of Smallanthus sonchifolius and their inhibitory activity of lps-induced nitric oxide production. Chem Pharm Bull (Tokyo). 2008 Feb;56(2):199-202. doi: 10.1248/cpb.56.199. [PubMed:18239309 ]
Lin F, Hasegawa M, Kodama O: Purification and identification of antimicrobial sesquiterpene lactones from yacon (Smallanthus sonchifolius) leaves. Biosci Biotechnol Biochem. 2003 Oct;67(10):2154-9. doi: 10.1271/bbb.67.2154. [PubMed:14586103 ]
LOTUS database [Link]

Showing NP-Card for methyl (1s,2r,4r,7e,9r,10r,11s)-9-(acetyloxy)-4-methyl-10-{[(2z)-2-methylbut-2-enoyl]oxy}-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-ene-8-carboxylate (NP0301174)

MOL for NP0301174 (methyl (1s,2r,4r,7e,9r,10r,11s)-9-(acetyloxy)-4-methyl-10-{[(2z)-2-methylbut-2-enoyl]oxy}-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-ene-8-carboxylate)

3D MOL for NP0301174 (methyl (1s,2r,4r,7e,9r,10r,11s)-9-(acetyloxy)-4-methyl-10-{[(2z)-2-methylbut-2-enoyl]oxy}-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-ene-8-carboxylate)

3D SDF for NP0301174 (methyl (1s,2r,4r,7e,9r,10r,11s)-9-(acetyloxy)-4-methyl-10-{[(2z)-2-methylbut-2-enoyl]oxy}-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-ene-8-carboxylate)

3D-SDF for NP0301174 (methyl (1s,2r,4r,7e,9r,10r,11s)-9-(acetyloxy)-4-methyl-10-{[(2z)-2-methylbut-2-enoyl]oxy}-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-ene-8-carboxylate)

PDB for NP0301174 (methyl (1s,2r,4r,7e,9r,10r,11s)-9-(acetyloxy)-4-methyl-10-{[(2z)-2-methylbut-2-enoyl]oxy}-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-ene-8-carboxylate)

3D PDB for NP0301174 (methyl (1s,2r,4r,7e,9r,10r,11s)-9-(acetyloxy)-4-methyl-10-{[(2z)-2-methylbut-2-enoyl]oxy}-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-ene-8-carboxylate)

SMILES for NP0301174 (methyl (1s,2r,4r,7e,9r,10r,11s)-9-(acetyloxy)-4-methyl-10-{[(2z)-2-methylbut-2-enoyl]oxy}-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-ene-8-carboxylate)

INCHI for NP0301174 (methyl (1s,2r,4r,7e,9r,10r,11s)-9-(acetyloxy)-4-methyl-10-{[(2z)-2-methylbut-2-enoyl]oxy}-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-ene-8-carboxylate)

Structure for NP0301174 (methyl (1s,2r,4r,7e,9r,10r,11s)-9-(acetyloxy)-4-methyl-10-{[(2z)-2-methylbut-2-enoyl]oxy}-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-ene-8-carboxylate)

3D Structure for NP0301174 (methyl (1s,2r,4r,7e,9r,10r,11s)-9-(acetyloxy)-4-methyl-10-{[(2z)-2-methylbut-2-enoyl]oxy}-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-ene-8-carboxylate)