NP-MRD: Showing NP-Card for (1s,2s,4r,5s,6r,7e,10r,11r,12s)-5,6-dihydroxy-4,8,12-trimethyl-13-oxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-en-10-yl (2e)-2-methylbut-2-enoate (NP0191639)

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Record Information

Version

2.0

Created at

2022-09-04 08:40:16 UTC

Updated at

2022-09-04 08:40:16 UTC

NP-MRD ID

NP0191639

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2s,4r,5s,6r,7e,10r,11r,12s)-5,6-dihydroxy-4,8,12-trimethyl-13-oxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-en-10-yl (2e)-2-methylbut-2-enoate

Description

(1S,2S,4R,5S,6R,7E,10R,11R,12S)-5,6-dihydroxy-4,8,12-trimethyl-13-oxo-3,14-dioxatricyclo[9.3.0.0²,⁴]Tetradec-7-en-10-yl 2-methylbut-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. (1s,2s,4r,5s,6r,7e,10r,11r,12s)-5,6-dihydroxy-4,8,12-trimethyl-13-oxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-en-10-yl (2e)-2-methylbut-2-enoate is found in Eupatorium perfoliatum. Based on a literature review very few articles have been published on (1S,2S,4R,5S,6R,7E,10R,11R,12S)-5,6-dihydroxy-4,8,12-trimethyl-13-oxo-3,14-dioxatricyclo[9.3.0.0²,⁴]Tetradec-7-en-10-yl 2-methylbut-2-enoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042210402D          

 27 29  0  0  1  0            999 V2000
    2.4813    2.2408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9765    1.5883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1590    1.6992    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8462    2.4626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6542    1.0466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1633    1.1575    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9669    0.2832    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7844    0.1723    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1425    0.9155    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9600    0.8047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1072   -0.0071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6866    1.1955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2828    0.6253    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0093    1.0161    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4300   -0.1865    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.2475   -0.2974    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0719   -0.9297    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8733   -1.1254    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0471   -1.7544    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3453   -1.3206    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5278   -1.2097    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1698   -1.9529    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3522   -1.8420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7820   -2.4383    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2051   -1.0303    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4618   -0.6722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9316   -0.6395    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  8  7  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
 13 15  1  0  0  0  0
 15 16  1  6  0  0  0
 15 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  0  0  0  0
 20 19  1  1  0  0  0
 17 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  1  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  1  1  0  0  0
 27 25  1  6  0  0  0
 21 27  1  0  0  0  0
  8 27  1  0  0  0  0
M  END

     RDKit          3D

 55 57  0  0  0  0  0  0  0  0999 V2000
    5.7642    1.5205   -0.8814 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3429    1.0510   -0.7280 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0493    0.0290    0.0585 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1495   -0.6509    0.7913 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6760   -0.4451    0.2233 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3614   -1.3997    0.9515 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6808    0.1902   -0.4562 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2846   -0.1754   -0.3837 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2268   -0.7453   -1.6265 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6710   -2.1898   -1.5359 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3895   -3.1738   -1.8894 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8978   -2.5274   -1.1650 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9910   -1.5930   -0.7926 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.2396   -2.1515   -1.0917 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9387   -1.2103    0.6704 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7380   -2.1757    1.3412 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3991    0.1683    0.9457 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.8743    0.1794    1.4182 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6108    0.8752    1.8688 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8865    1.3172    0.4760 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6057    1.5373   -0.2512 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3158    2.9683   -0.2397 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0596    3.1205   -0.2880 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6552    3.9625   -0.9924 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5386    2.0856    0.6537 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3546    2.6212    2.0424 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3913    0.9244    0.3200 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7912    2.5975   -1.1536 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2290    1.4661    0.1378 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3195    0.9243   -1.6059 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5306    1.5381   -1.2569 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4778   -0.0575    1.6766 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9834   -0.8345    0.1098 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7975   -1.6431    1.1589 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3301   -1.0581    0.3442 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6620   -0.7499   -2.3388 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9803   -0.1670   -2.1921 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9122   -2.8374   -2.8279 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1569   -3.1237   -1.0964 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0240   -4.1842   -2.0941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1349   -3.5819   -1.1269 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9756   -0.6495   -1.3708 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2254   -3.1125   -0.7930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9240   -1.4276    1.0863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6761   -2.0898    1.0142 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5304   -0.2162    0.6275 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9336   -0.4867    2.3014 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1709    1.1859    1.7381 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5276    2.2556    0.5006 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6588    1.3564   -1.3338 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5987    1.8347    0.5320 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8497    3.6196    2.0692 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9314    1.9815    2.7444 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6832    2.7766    2.3422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6931    0.5705    1.3676 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  3  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 10 12  2  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  1
 17 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  2  0
 23 25  1  0
 25 26  1  0
 25 27  1  0
 27  8  1  0
 20 17  1  0
 27 21  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  2 31  1  0
  4 32  1  0
  4 33  1  0
  4 34  1  0
  8 35  1  1
  9 36  1  0
  9 37  1  0
 11 38  1  0
 11 39  1  0
 11 40  1  0
 12 41  1  0
 13 42  1  6
 14 43  1  0
 15 44  1  1
 16 45  1  0
 18 46  1  0
 18 47  1  0
 18 48  1  0
 20 49  1  1
 21 50  1  6
 25 51  1  6
 26 52  1  0
 26 53  1  0
 26 54  1  0
 27 55  1  1
M  END


  Mrv1652309042210402D          

 27 29  0  0  1  0            999 V2000
    2.4813    2.2408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9765    1.5883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1590    1.6992    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8462    2.4626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6542    1.0466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1633    1.1575    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9669    0.2832    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7844    0.1723    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1425    0.9155    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9600    0.8047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1072   -0.0071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6866    1.1955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2828    0.6253    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0093    1.0161    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4300   -0.1865    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.2475   -0.2974    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0719   -0.9297    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8733   -1.1254    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0471   -1.7544    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3453   -1.3206    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5278   -1.2097    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1698   -1.9529    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3522   -1.8420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7820   -2.4383    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2051   -1.0303    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4618   -0.6722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9316   -0.6395    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  8  7  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
 13 15  1  0  0  0  0
 15 16  1  6  0  0  0
 15 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  0  0  0  0
 20 19  1  1  0  0  0
 17 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  1  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  1  1  0  0  0
 27 25  1  6  0  0  0
 21 27  1  0  0  0  0
  8 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0191639

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C20H28O7/c1-6-10(3)18(23)25-13-8-9(2)7-12(21)16(22)20(5)17(27-20)15-14(13)11(4)19(24)26-15/h6-7,11-17,21-22H,8H2,1-5H3/b9-7+,10-6+/t11-,12+,13+,14+,15-,16-,17-,20+/m0/s1

> <INCHI_KEY>
NJLPUPGLCFTKPE-NVQLDWBNSA-N

> <FORMULA>
C20H28O7

> <MOLECULAR_WEIGHT>
380.437

> <EXACT_MASS>
380.183503242

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
40.138900474801524

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2S,4R,5S,6R,7E,10R,11R,12S)-5,6-dihydroxy-4,8,12-trimethyl-13-oxo-3,14-dioxatricyclo[9.3.0.0^{2,4}]tetradec-7-en-10-yl (2E)-2-methylbut-2-enoate

> <JCHEM_LOGP>
1.8035135746666677

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.634047100397535

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.862782933241494

> <JCHEM_PKA_STRONGEST_BASIC>
-3.3523229113880664

> <JCHEM_POLAR_SURFACE_AREA>
105.59

> <JCHEM_REFRACTIVITY>
96.719

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,4R,5S,6R,7E,10R,11R,12S)-5,6-dihydroxy-4,8,12-trimethyl-13-oxo-3,14-dioxatricyclo[9.3.0.0^{2,4}]tetradec-7-en-10-yl (2E)-2-methylbut-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       4.632   4.183   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.689   2.965   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.163   3.172   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.580   4.597   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.221   1.954   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -0.305   2.161   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       1.805   0.529   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       3.331   0.322   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.999   1.709   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.525   1.502   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.800  -0.013   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.882   2.232   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.995   1.167   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       9.351   1.897   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       8.269  -0.348   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       9.795  -0.555   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       7.601  -1.735   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.097  -2.101   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       7.555  -3.275   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       6.245  -2.465   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.719  -2.258   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       4.050  -3.645   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       2.524  -3.438   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       1.460  -4.551   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       2.249  -1.923   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.862  -1.255   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       3.606  -1.194   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   27                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   19   20                                             
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   17   21                                                  
CONECT   21   20   22   27                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   21    8                                                  
MASTER        0    0    0    0    0    0    0    0   27    0   58    0
END

View in JSmol

Synonyms

Value	Source
(1S,2S,4R,5S,6R,7E,10R,11R,12S)-5,6-Dihydroxy-4,8,12-trimethyl-13-oxo-3,14-dioxatricyclo[9.3.0.0,]tetradec-7-en-10-yl 2-methylbut-2-enoic acid	Generator

Chemical Formula

C₂₀H₂₈O₇

Average Mass

380.4370 Da

Monoisotopic Mass

380.18350 Da

IUPAC Name

(1S,2S,4R,5S,6R,7E,10R,11R,12S)-5,6-dihydroxy-4,8,12-trimethyl-13-oxo-3,14-dioxatricyclo[9.3.0.0^{2,4}]tetradec-7-en-10-yl (2E)-2-methylbut-2-enoate

Traditional Name

(1S,2S,4R,5S,6R,7E,10R,11R,12S)-5,6-dihydroxy-4,8,12-trimethyl-13-oxo-3,14-dioxatricyclo[9.3.0.0^{2,4}]tetradec-7-en-10-yl (2E)-2-methylbut-2-enoate

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C20H28O7/c1-6-10(3)18(23)25-13-8-9(2)7-12(21)16(22)20(5)17(27-20)15-14(13)11(4)19(24)26-15/h6-7,11-17,21-22H,8H2,1-5H3/b9-7+,10-6+/t11-,12+,13+,14+,15-,16-,17-,20+/m0/s1

InChI Key

NJLPUPGLCFTKPE-NVQLDWBNSA-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
Eupatorium perfoliatum	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
Germacrane sesquiterpenoid
Sesquiterpenoid
Fatty acid ester
Dicarboxylic acid or derivatives
Gamma butyrolactone
Fatty acyl
Alpha,beta-unsaturated carboxylic ester
Tetrahydrofuran
Enoate ester
Secondary alcohol
1,2-diol
Lactone
Carboxylic acid ester
Carboxylic acid derivative
Organoheterocyclic compound
Dialkyl ether
Oxirane
Ether
Oxacycle
Organooxygen compound
Organic oxygen compound
Carbonyl group
Organic oxide
Hydrocarbon derivative
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	1.8	ChemAxon
pKa (Strongest Acidic)	12.86	ChemAxon
pKa (Strongest Basic)	-3.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	105.59 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	96.72 m³·mol⁻¹	ChemAxon
Polarizability	40.14 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	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

162881705

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,2s,4r,5s,6r,7e,10r,11r,12s)-5,6-dihydroxy-4,8,12-trimethyl-13-oxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-en-10-yl (2e)-2-methylbut-2-enoate (NP0191639)

MOL for NP0191639 ((1s,2s,4r,5s,6r,7e,10r,11r,12s)-5,6-dihydroxy-4,8,12-trimethyl-13-oxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-en-10-yl (2e)-2-methylbut-2-enoate)

3D MOL for NP0191639 ((1s,2s,4r,5s,6r,7e,10r,11r,12s)-5,6-dihydroxy-4,8,12-trimethyl-13-oxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-en-10-yl (2e)-2-methylbut-2-enoate)

3D SDF for NP0191639 ((1s,2s,4r,5s,6r,7e,10r,11r,12s)-5,6-dihydroxy-4,8,12-trimethyl-13-oxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-en-10-yl (2e)-2-methylbut-2-enoate)

3D-SDF for NP0191639 ((1s,2s,4r,5s,6r,7e,10r,11r,12s)-5,6-dihydroxy-4,8,12-trimethyl-13-oxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-en-10-yl (2e)-2-methylbut-2-enoate)

PDB for NP0191639 ((1s,2s,4r,5s,6r,7e,10r,11r,12s)-5,6-dihydroxy-4,8,12-trimethyl-13-oxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-en-10-yl (2e)-2-methylbut-2-enoate)

3D PDB for NP0191639 ((1s,2s,4r,5s,6r,7e,10r,11r,12s)-5,6-dihydroxy-4,8,12-trimethyl-13-oxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-en-10-yl (2e)-2-methylbut-2-enoate)

SMILES for NP0191639 ((1s,2s,4r,5s,6r,7e,10r,11r,12s)-5,6-dihydroxy-4,8,12-trimethyl-13-oxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-en-10-yl (2e)-2-methylbut-2-enoate)

INCHI for NP0191639 ((1s,2s,4r,5s,6r,7e,10r,11r,12s)-5,6-dihydroxy-4,8,12-trimethyl-13-oxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-en-10-yl (2e)-2-methylbut-2-enoate)

Structure for NP0191639 ((1s,2s,4r,5s,6r,7e,10r,11r,12s)-5,6-dihydroxy-4,8,12-trimethyl-13-oxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-en-10-yl (2e)-2-methylbut-2-enoate)

3D Structure for NP0191639 ((1s,2s,4r,5s,6r,7e,10r,11r,12s)-5,6-dihydroxy-4,8,12-trimethyl-13-oxo-3,14-dioxatricyclo[9.3.0.0²,⁴]tetradec-7-en-10-yl (2e)-2-methylbut-2-enoate)