NP-MRD: Showing NP-Card for Liacylindrolide (NP0058756)

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Record Information

Version

2.0

Created at

2022-04-28 04:06:14 UTC

Updated at

2022-04-28 04:06:14 UTC

NP-MRD ID

NP0058756

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Liacylindrolide

Description

(2E)-3-{[(3aR,4R,11aS)-6,10-dimethyl-3-methylidene-2-oxo-2H,3H,3aH,4H,5H,8H,9H,11aH-cyclodeca[b]furan-4-yl]oxy}-2-ethylidene-3-oxopropyl (2E)-2-(hydroxymethyl)but-2-enoate 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. Liacylindrolide is found in Liatris cylindracea. Based on a literature review very few articles have been published on (2E)-3-{[(3aR,4R,11aS)-6,10-dimethyl-3-methylidene-2-oxo-2H,3H,3aH,4H,5H,8H,9H,11aH-cyclodeca[b]furan-4-yl]oxy}-2-ethylidene-3-oxopropyl (2E)-2-(hydroxymethyl)but-2-enoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282206062D          

 32 33  0  0  1  0            999 V2000
    4.7983    1.8420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6124    1.7084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9037    0.9365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3809    0.2983    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5668    0.4320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2755    1.2038    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4614    1.3375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1701    2.1093    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6929    2.7476    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5070    2.6139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4015    3.5194    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9243    4.1576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7384    4.0240    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6330    4.9295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8189    5.0631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5276    5.8350    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1558    5.5677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8645    6.3395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3873    6.9778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2014    6.8441    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0960    7.7496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6188    8.3878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3275    9.1597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2819    7.8833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9906    8.6551    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3460    2.0708    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8304    2.7149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1279    1.2751    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3561    0.9838    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8173    0.8219    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0440   -0.2062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0002    1.6330    0.0000 C   0  0  0  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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  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
  1 10  1  0  0  0  0
  9 11  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  2  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
 14 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 21 24  1  0  0  0  0
 24 25  1  0  0  0  0
  8 26  1  6  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
  7 30  1  6  0  0  0
  5 31  1  0  0  0  0
  1 32  1  0  0  0  0
M  END

     RDKit          3D

 64 65  0  0  0  0  0  0  0  0999 V2000
   -0.7044   -0.5386   -2.9985 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6568   -1.0082   -2.2325 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9921   -2.3987   -1.9727 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.7994   -1.1235   -1.4343 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.9445   -0.9610   -0.5476 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6708    0.1190   -0.3363 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8302    0.1665    0.6144 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4918    1.4499   -0.9635 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5144    2.3638   -0.3841 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1925    2.2036    1.0527 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4796    1.2849    1.6687 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3232    1.3649    3.1999 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7691    0.1118    1.1077 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0666    0.2977   -0.1828 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7741   -0.3345   -0.0767 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3678    0.4375   -0.0361 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2944    1.6901   -0.0902 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7078   -0.1629    0.0718 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7828   -1.4737    0.1249 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0750   -2.1965    0.2380 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8762    0.7086    0.1180 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1132    0.0827    0.2235 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3194    0.7618    0.2836 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3131    2.0104    0.2421 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6020    0.0448    0.3947 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7006    0.7704    0.4470 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0393    0.1772    0.5570 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6253   -1.4134    0.4422 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8436   -2.0155    0.5436 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6646   -0.2237   -1.4121 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.5758    0.5282   -3.0938 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0289   -1.1700   -3.5495 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1098   -1.1944   -2.5288 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2543   -1.8441    0.0238 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.7498    0.4991    0.0685 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.4686    1.9932   -1.1110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0143    3.3999   -0.4527 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6323    2.5914   -1.0264 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6046    2.9685    1.7728 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6906    2.3129    3.5726 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7325    0.4569    3.6461 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2214    1.3509    3.3512 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3619   -0.8272    1.2043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9187   -0.1113    1.8517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8086    1.3977   -0.2218 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8402   -2.0407    0.0825 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6244   -1.9656    1.1604 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6565   -1.9746   -0.7017 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8338   -3.3042    0.2451 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7299    1.4177    0.9766 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8237    1.3648   -0.7928 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6371    1.8730    0.4077 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.3046   -0.4585   -0.3014 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1709   -0.4042    1.4885 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.8116    0.9857    0.6221 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0101   -1.7977    1.3125 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0935   -1.7898   -0.4759 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0208   -2.6107   -0.2184 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8828    0.6527   -2.0986 H   0  0  0  0  0  0  0  0  0  0  0  0
 29 28  1  0
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  2  1  2  3
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 32  6  1  0
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 29 59  1  0
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 31 63  1  0
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  9 37  1  0
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  6 35  1  6
  1 33  1  0
  1 34  1  0
 32 64  1  6
M  END


  Mrv1652304282206062D          

 32 33  0  0  1  0            999 V2000
    4.7983    1.8420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6124    1.7084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9037    0.9365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3809    0.2983    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5668    0.4320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2755    1.2038    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4614    1.3375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1701    2.1093    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.6929    2.7476    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5070    2.6139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4015    3.5194    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9243    4.1576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7384    4.0240    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6330    4.9295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8189    5.0631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5276    5.8350    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1558    5.5677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8645    6.3395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3873    6.9778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2014    6.8441    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0960    7.7496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6188    8.3878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3275    9.1597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2819    7.8833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9906    8.6551    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3460    2.0708    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8304    2.7149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1279    1.2751    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3561    0.9838    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8173    0.8219    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0440   -0.2062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0002    1.6330    0.0000 C   0  0  0  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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  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
  1 10  1  0  0  0  0
  9 11  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  2  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
 14 17  1  0  0  0  0
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 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
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 24 25  1  0  0  0  0
  8 26  1  6  0  0  0
 26 27  2  0  0  0  0
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 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
  7 30  1  6  0  0  0
  5 31  1  0  0  0  0
  1 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0058756

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C=C(/CO)C(=O)OC\C(=C/C)C(=O)O[C@@H]1C\C(C)=C\CC\C(C)=C\[C@@H]2OC(=O)C(=C)[C@H]12

> <INCHI_IDENTIFIER>
InChI=1S/C25H32O7/c1-6-18(13-26)24(28)30-14-19(7-2)25(29)32-21-12-16(4)10-8-9-15(3)11-20-22(21)17(5)23(27)31-20/h6-7,10-11,20-22,26H,5,8-9,12-14H2,1-4H3/b15-11+,16-10+,18-6+,19-7+/t20-,21+,22-/m0/s1

> <INCHI_KEY>
MZDDYPUIJFFVAN-GJMSYHLOSA-N

> <FORMULA>
C25H32O7

> <MOLECULAR_WEIGHT>
444.524

> <EXACT_MASS>
444.21480337

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
64

> <JCHEM_AVERAGE_POLARIZABILITY>
47.55752841245753

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2E)-3-{[(3aR,4R,11aS)-6,10-dimethyl-3-methylidene-2-oxo-2H,3H,3aH,4H,5H,8H,9H,11aH-cyclodeca[b]furan-4-yl]oxy}-2-ethylidene-3-oxopropyl (2E)-2-(hydroxymethyl)but-2-enoate

> <ALOGPS_LOGP>
3.31

> <JCHEM_LOGP>
4.335337002666665

> <ALOGPS_LOGS>
-4.58

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.886246127014672

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8485559440437687

> <JCHEM_POLAR_SURFACE_AREA>
99.13000000000001

> <JCHEM_REFRACTIVITY>
122.72609999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.17e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2E)-3-{[(3aR,4R,11aS)-6,10-dimethyl-3-methylidene-2-oxo-3aH,4H,5H,8H,9H,11aH-cyclodeca[b]furan-4-yl]oxy}-2-ethylidene-3-oxopropyl (2E)-2-(hydroxymethyl)but-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       8.957   3.438   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.476   3.189   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      11.020   1.748   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.044   0.557   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.525   0.806   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.981   2.247   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.461   2.497   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.917   3.937   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.893   5.129   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.413   4.879   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       6.350   6.570   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       7.325   7.761   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       8.845   7.511   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       6.782   9.202   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.262   9.451   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.718  10.892   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.758  10.393   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       7.214  11.834   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       8.190  13.025   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       9.709  12.776   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       7.646  14.466   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.622  15.657   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.078  17.098   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.126  14.715   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       5.582  16.156   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       4.379   3.866   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       3.417   5.068   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.972   2.380   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       2.531   1.836   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       5.259   1.534   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       7.549  -0.385   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       7.467   3.048   0.000  0.00  0.00           C+0
CONECT    1    2   10   32                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   31                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   30                                                  
CONECT    8    7    9   26                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9    1                                                       
CONECT   11    9   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   17                                                  
CONECT   15   14   16                                                       
CONECT   16   15                                                            
CONECT   17   14   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   24                                                  
CONECT   22   21   23                                                       
CONECT   23   22                                                            
CONECT   24   21   25                                                       
CONECT   25   24                                                            
CONECT   26    8   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28    7                                                       
CONECT   31    5                                                            
CONECT   32    1                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   66    0
END

View in JSmol

Synonyms

Value	Source
(2E)-3-{[(3ar,4R,11as)-6,10-dimethyl-3-methylidene-2-oxo-2H,3H,3ah,4H,5H,8H,9H,11ah-cyclodeca[b]furan-4-yl]oxy}-2-ethylidene-3-oxopropyl (2E)-2-(hydroxymethyl)but-2-enoic acid	Generator

Chemical Formula

C₂₅H₃₂O₇

Average Mass

444.5240 Da

Monoisotopic Mass

444.21480 Da

IUPAC Name

(2E)-3-{[(3aR,4R,11aS)-6,10-dimethyl-3-methylidene-2-oxo-2H,3H,3aH,4H,5H,8H,9H,11aH-cyclodeca[b]furan-4-yl]oxy}-2-ethylidene-3-oxopropyl (2E)-2-(hydroxymethyl)but-2-enoate

Traditional Name

(2E)-3-{[(3aR,4R,11aS)-6,10-dimethyl-3-methylidene-2-oxo-3aH,4H,5H,8H,9H,11aH-cyclodeca[b]furan-4-yl]oxy}-2-ethylidene-3-oxopropyl (2E)-2-(hydroxymethyl)but-2-enoate

CAS Registry Number

Not Available

SMILES

C\C=C(/CO)C(=O)OC\C(=C/C)C(=O)O[C@@H]1C\C(C)=C\CC\C(C)=C\[C@@H]2OC(=O)C(=C)[C@H]12

InChI Identifier

InChI=1S/C25H32O7/c1-6-18(13-26)24(28)30-14-19(7-2)25(29)32-21-12-16(4)10-8-9-15(3)11-20-22(21)17(5)23(27)31-20/h6-7,10-11,20-22,26H,5,8-9,12-14H2,1-4H3/b15-11+,16-10+,18-6+,19-7+/t20-,21+,22-/m0/s1

InChI Key

MZDDYPUIJFFVAN-GJMSYHLOSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Liatris cylindracea	Plant	KNApSAcK

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
Tricarboxylic acid or derivatives
Fatty acid ester
Beta-hydroxy acid
Fatty acyl
Hydroxy acid
Gamma butyrolactone
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tetrahydrofuran
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Carbonyl group
Alcohol
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	3.31	ALOGPS
logP	4.34	ChemAxon
logS	-4.6	ALOGPS
pKa (Strongest Acidic)	14.89	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	99.13 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	122.73 m³·mol⁻¹	ChemAxon
Polarizability	47.56 Å³	ChemAxon
Number of Rings	2	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

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

162938215

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Liacylindrolide (NP0058756)

MOL for NP0058756 (Liacylindrolide)

3D MOL for NP0058756 (Liacylindrolide)

3D SDF for NP0058756 (Liacylindrolide)

3D-SDF for NP0058756 (Liacylindrolide)

PDB for NP0058756 (Liacylindrolide)

3D PDB for NP0058756 (Liacylindrolide)

SMILES for NP0058756 (Liacylindrolide)

INCHI for NP0058756 (Liacylindrolide)

Structure for NP0058756 (Liacylindrolide)

3D Structure for NP0058756 (Liacylindrolide)