NP-MRD: Showing NP-Card for Orthopappolide methacrylate (NP0058361)

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Record Information

Version

2.0

Created at

2022-04-28 03:43:17 UTC

Updated at

2022-04-28 03:43:18 UTC

NP-MRD ID

NP0058361

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Orthopappolide methacrylate

Description

(1S,3R,5R,6S,10R,11S,14S)-14-methoxy-3-methyl-9-methylidene-8-oxo-4,7,15-trioxatetracyclo[11.2.1.0³,⁵.0⁶,¹⁰]Hexadec-13(16)-en-11-yl 2-methylprop-2-enoate 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. Orthopappolide methacrylate is found in Elephantopus angustifolius and Orthopappus angustifolius. Based on a literature review very few articles have been published on (1S,3R,5R,6S,10R,11S,14S)-14-methoxy-3-methyl-9-methylidene-8-oxo-4,7,15-trioxatetracyclo[11.2.1.0³,⁵.0⁶,¹⁰]Hexadec-13(16)-en-11-yl 2-methylprop-2-enoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282205432D          

 27 30  0  0  1  0            999 V2000
    1.9606   -0.3387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2187    0.0221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1602    0.8450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8436    1.3072    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5855    0.9464    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6440    0.1235    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3638   -0.3518    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4445   -1.0602    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7611   -1.5224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0192   -1.1616    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0345   -1.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6463   -0.5720    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1708   -0.4582    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4808    0.3064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1279   -0.5981    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9067   -1.7436    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4448   -0.0751    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8811    0.6250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7040    0.6835    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3501    1.2564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5487    2.0571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7850    2.1301    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0431    2.4909    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3597    2.0287    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9846    3.3138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2426    3.6746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6680    3.7759    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  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
  1 10  1  0  0  0  0
 10 11  1  6  0  0  0
 11 12  1  0  0  0  0
  2 12  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  1  0  0  0  0
  8 15  1  0  0  0  0
  7 15  1  1  0  0  0
  8 16  1  1  0  0  0
  6 17  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
  5 20  1  1  0  0  0
 20 21  2  0  0  0  0
  4 22  1  6  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
M  END

     RDKit          3D

 51 54  0  0  0  0  0  0  0  0999 V2000
    4.6680    0.9976   -1.6332 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5384   -0.0733   -0.8953 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7352   -0.8921   -0.6058 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2679   -0.4625   -0.3659 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0954   -1.4820    0.3599 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1503    0.2966   -0.6453 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8639   -0.0175   -0.1509 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3242    1.1238    0.6287 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0138    1.0156    1.2185 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7220    0.0308    1.6753 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1566    0.4700    1.3976 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9718   -0.5630    0.7245 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0746   -1.6206    0.1207 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8270   -2.8326    0.9669 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3234   -1.9744   -1.2311 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2877   -1.1225   -0.9347 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8626   -1.5549   -1.1033 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7562   -2.3496   -2.2570 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5775   -2.2137   -2.7000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2976   -3.1233   -3.1721 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8897   -0.7875   -2.4737 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7708   -0.1115   -3.1970 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0317   -0.3920   -1.3518 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0610    1.6922    0.7545 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9327    2.2175    1.4325 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4720    3.3801    0.9029 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3878    4.3847    1.8839 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6449    1.3079   -2.0485 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8684    1.6827   -1.9055 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9719   -0.8533    0.4823 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6478   -1.9336   -0.9852 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6461   -0.4796   -1.1089 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8934   -0.9296    0.4970 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0414    1.2519    1.5023 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4726    2.1098    0.0831 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6321   -0.9380    2.1715 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6440    0.7045    2.3921 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6148   -0.1689   -0.0959 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6404   -1.1026    1.4601 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4551   -3.6810    0.5649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7910   -3.1917    0.9468 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2217   -2.7054    2.0097 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4788   -0.0634   -1.2683 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4959   -2.1849   -0.2671 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3269   -0.5568   -4.0065 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8821    0.9384   -2.9129 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5836    0.4668   -1.7098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1255    2.3648    2.5037 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0137    5.3319    1.4424 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6992    4.0375    2.7099 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3610    4.5570    2.3838 H   0  0  0  0  0  0  0  0  0  0  0  0
 27 26  1  0
 26 25  1  0
 25 24  1  0
 24 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  1
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 19 21  1  0
 21 22  2  3
 21 23  1  0
 23  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
  7  6  1  0
  6  4  1  0
  4  5  2  0
  4  2  1  0
  2  3  1  0
  2  1  2  3
  9 25  1  0
 10 11  1  0
 16 13  1  0
 23 17  1  0
 27 49  1  0
 27 50  1  0
 27 51  1  0
 25 48  1  1
 11 37  1  1
 12 38  1  0
 12 39  1  0
 14 40  1  0
 14 41  1  0
 14 42  1  0
 16 43  1  6
 17 44  1  1
 22 45  1  0
 22 46  1  0
 23 47  1  6
  7 33  1  1
  8 34  1  0
  8 35  1  0
 10 36  1  0
  3 30  1  0
  3 31  1  0
  3 32  1  0
  1 28  1  0
  1 29  1  0
M  END


  Mrv1652304282205432D          

 27 30  0  0  1  0            999 V2000
    1.9606   -0.3387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2187    0.0221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1602    0.8450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8436    1.3072    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5855    0.9464    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6440    0.1235    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3638   -0.3518    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4445   -1.0602    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7611   -1.5224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0192   -1.1616    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0345   -1.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6463   -0.5720    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1708   -0.4582    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4808    0.3064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1279   -0.5981    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9067   -1.7436    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4448   -0.0751    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8811    0.6250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7040    0.6835    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3501    1.2564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5487    2.0571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7850    2.1301    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0431    2.4909    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3597    2.0287    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9846    3.3138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2426    3.6746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6680    3.7759    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  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
  1 10  1  0  0  0  0
 10 11  1  6  0  0  0
 11 12  1  0  0  0  0
  2 12  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  1  0  0  0  0
  8 15  1  0  0  0  0
  7 15  1  1  0  0  0
  8 16  1  1  0  0  0
  6 17  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
  5 20  1  1  0  0  0
 20 21  2  0  0  0  0
  4 22  1  6  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0058361

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CO[C@H]1O[C@H]2C[C@@]3(C)O[C@@H]3[C@H]3OC(=O)C(=C)[C@@H]3[C@H](CC1=C2)OC(=O)C(C)=C

> <INCHI_IDENTIFIER>
InChI=1S/C20H24O7/c1-9(2)17(21)25-13-7-11-6-12(24-19(11)23-5)8-20(4)16(27-20)15-14(13)10(3)18(22)26-15/h6,12-16,19H,1,3,7-8H2,2,4-5H3/t12-,13+,14-,15+,16-,19+,20-/m1/s1

> <INCHI_KEY>
QGGGTLQHMHIOKZ-VLCBXQEZSA-N

> <FORMULA>
C20H24O7

> <MOLECULAR_WEIGHT>
376.405

> <EXACT_MASS>
376.152203113

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
51

> <JCHEM_AVERAGE_POLARIZABILITY>
38.556503502885114

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,3R,5R,6S,10R,11S,14S)-14-methoxy-3-methyl-9-methylidene-8-oxo-4,7,15-trioxatetracyclo[11.2.1.0^{3,5}.0^{6,10}]hexadec-13(16)-en-11-yl 2-methylprop-2-enoate

> <ALOGPS_LOGP>
1.23

> <JCHEM_LOGP>
2.4086629429999986

> <ALOGPS_LOGS>
-2.61

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-3.8379025532804927

> <JCHEM_POLAR_SURFACE_AREA>
83.59

> <JCHEM_REFRACTIVITY>
93.7975

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.28e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,3R,5R,6S,10R,11S,14S)-14-methoxy-3-methyl-9-methylidene-8-oxo-4,7,15-trioxatetracyclo[11.2.1.0^{3,5}.0^{6,10}]hexadec-13(16)-en-11-yl 2-methylprop-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       3.660  -0.632   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.275   0.041   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.166   1.577   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.441   2.440   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.826   1.767   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.936   0.231   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.279  -0.657   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.430  -1.979   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.154  -2.842   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.769  -2.168   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       1.931  -2.427   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       1.206  -1.068   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -0.319  -0.855   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -0.897   0.572   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       7.705  -1.116   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       7.292  -3.255   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       6.430  -0.140   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       7.245   1.167   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       8.781   1.276   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       6.253   2.345   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.624   3.840   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       3.332   3.976   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       1.947   4.650   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       0.671   3.787   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       1.838   6.186   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.453   6.859   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       3.114   7.048   0.000  0.00  0.00           C+0
CONECT    1    2   10                                                       
CONECT    2    1    3   12                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   22                                                  
CONECT    5    4    6   20                                                  
CONECT    6    5    7   17                                                  
CONECT    7    6    8   15                                                  
CONECT    8    7    9   15   16                                             
CONECT    9    8   10                                                       
CONECT   10    9    1   11                                                  
CONECT   11   10   12                                                       
CONECT   12   11    2   13                                                  
CONECT   13   12   14                                                       
CONECT   14   13                                                            
CONECT   15    8    7                                                       
CONECT   16    8                                                            
CONECT   17    6   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18    5   21                                                  
CONECT   21   20                                                            
CONECT   22    4   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   60    0
END

View in JSmol

Synonyms

Value	Source
(1S,3R,5R,6S,10R,11S,14S)-14-Methoxy-3-methyl-9-methylidene-8-oxo-4,7,15-trioxatetracyclo[11.2.1.0,.0,]hexadec-13(16)-en-11-yl 2-methylprop-2-enoic acid	Generator

Chemical Formula

C₂₀H₂₄O₇

Average Mass

376.4050 Da

Monoisotopic Mass

376.15220 Da

IUPAC Name

(1S,3R,5R,6S,10R,11S,14S)-14-methoxy-3-methyl-9-methylidene-8-oxo-4,7,15-trioxatetracyclo[11.2.1.0^{3,5}.0^{6,10}]hexadec-13(16)-en-11-yl 2-methylprop-2-enoate

Traditional Name

(1S,3R,5R,6S,10R,11S,14S)-14-methoxy-3-methyl-9-methylidene-8-oxo-4,7,15-trioxatetracyclo[11.2.1.0^{3,5}.0^{6,10}]hexadec-13(16)-en-11-yl 2-methylprop-2-enoate

CAS Registry Number

Not Available

SMILES

CO[C@H]1O[C@H]2C[C@@]3(C)O[C@@H]3[C@H]3OC(=O)C(=C)[C@@H]3[C@H](CC1=C2)OC(=O)C(C)=C

InChI Identifier

InChI=1S/C20H24O7/c1-9(2)17(21)25-13-7-11-6-12(24-19(11)23-5)8-20(4)16(27-20)15-14(13)10(3)18(22)26-15/h6,12-16,19H,1,3,7-8H2,2,4-5H3/t12-,13+,14-,15+,16-,19+,20-/m1/s1

InChI Key

QGGGTLQHMHIOKZ-VLCBXQEZSA-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
Elephantopus angustifolius	Plant	KNApSAcK
Orthopappus angustifolius	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

Dicarboxylic acid or derivatives
Gamma butyrolactone
Dihydrofuran
Tetrahydrofuran
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Carboxylic acid ester
Ether
Oxirane
Dialkyl ether
Acetal
Carboxylic acid derivative
Oxacycle
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen 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	1.23	ALOGPS
logP	2.41	ChemAxon
logS	-2.6	ALOGPS
pKa (Strongest Basic)	-3.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	83.59 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	93.8 m³·mol⁻¹	ChemAxon
Polarizability	38.56 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

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

162922471

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Orthopappolide methacrylate (NP0058361)

MOL for NP0058361 (Orthopappolide methacrylate)

3D MOL for NP0058361 (Orthopappolide methacrylate)

3D SDF for NP0058361 (Orthopappolide methacrylate)

3D-SDF for NP0058361 (Orthopappolide methacrylate)

PDB for NP0058361 (Orthopappolide methacrylate)

3D PDB for NP0058361 (Orthopappolide methacrylate)

SMILES for NP0058361 (Orthopappolide methacrylate)

INCHI for NP0058361 (Orthopappolide methacrylate)

Structure for NP0058361 (Orthopappolide methacrylate)

3D Structure for NP0058361 (Orthopappolide methacrylate)