NP-MRD: Showing NP-Card for 1,5,8-trimethyl-13-oxo-12-oxatricyclo[6.3.2.0²,⁷]tridec-5-en-3-yl 2-methylbut-2-enoate (NP0330737)

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Record Information

Version

2.0

Created at

2022-09-12 16:22:47 UTC

Updated at

2022-09-12 16:22:47 UTC

NP-MRD ID

NP0330737

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1,5,8-trimethyl-13-oxo-12-oxatricyclo[6.3.2.0²,⁷]tridec-5-en-3-yl 2-methylbut-2-enoate

Description

1,5,8-Trimethyl-13-oxo-12-oxatricyclo[6.3.2.0²,⁷]Tridec-5-en-3-yl 2-methylbut-2-enoate belongs to the class of organic compounds known as lactones. These are cyclic esters of hydroxy carboxylic acids, containing a 1-oxacycloalkan-2-one structure, or analogues having unsaturation or heteroatoms replacing one or more carbon atoms of the ring. 1,5,8-trimethyl-13-oxo-12-oxatricyclo[6.3.2.0²,⁷]tridec-5-en-3-yl 2-methylbut-2-enoate is found in Acritopappus longifolius. 1,5,8-Trimethyl-13-oxo-12-oxatricyclo[6.3.2.0²,⁷]Tridec-5-en-3-yl 2-methylbut-2-enoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 52 54  0  0  0  0  0  0  0  0999 V2000
    5.3992    1.8105   -0.7513 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1204    1.1060   -0.4941 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0043    0.2290    0.4908 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1760   -0.0589    1.3590 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7664   -0.4546    0.7416 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6992   -1.2796    1.6869 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6088   -0.2425   -0.0308 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4568   -0.9485    0.2851 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2938   -1.9824   -0.8468 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0456   -2.6163   -0.8373 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1501   -4.0916   -0.8434 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0931   -1.7935   -0.8235 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7072   -0.3596   -0.8194 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8057   -0.1936    0.4094 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7879    1.2226    0.7748 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5167    1.7361    1.3880 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8604    1.5494    1.7906 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1139    0.7865    1.6876 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7154    0.5746    0.3652 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8225    0.6091   -0.8162 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.6770    0.3325   -2.0538 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2162    1.9544   -0.9824 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6925    2.8915   -1.6441 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0137    2.1296   -0.3219 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2027    2.7610   -1.2742 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8871    1.9689    0.2314 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0103    1.1468   -1.3951 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2602    1.2960   -1.1063 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0727   -1.0969    1.7382 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2197    0.5949    2.2462 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1296   -0.0316    0.7967 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6465   -1.6124    1.1832 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4950   -1.4918   -1.8281 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1230   -2.7101   -0.7147 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2717   -4.4416   -1.8906 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9717   -4.4626   -0.1898 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2147   -4.5323   -0.4581 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0991   -2.1806   -0.8165 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0512   -0.1430   -1.6903 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4045   -0.7372    1.2105 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2415    2.7369    1.8433 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2603    2.0011    0.6157 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8663    1.1352    2.2206 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3924    1.2911    2.7887 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0515    2.6469    1.8512 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0683   -0.1972    2.2482 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8733    1.3585    2.3114 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5468    1.3160    0.1630 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2555   -0.4193    0.3467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9869    0.0584   -2.8854 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4119   -0.4613   -1.8311 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1560    1.2956   -2.3401 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
 14 15  1  0
 15 16  1  1
 15 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  6
 20 22  1  0
 22 23  2  0
 22 24  1  0
 14  8  1  0
 24 15  1  0
 20 13  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  2 28  1  0
  4 29  1  0
  4 30  1  0
  4 31  1  0
  8 32  1  1
  9 33  1  0
  9 34  1  0
 11 35  1  0
 11 36  1  0
 11 37  1  0
 12 38  1  0
 13 39  1  6
 14 40  1  1
 16 41  1  0
 16 42  1  0
 16 43  1  0
 17 44  1  0
 17 45  1  0
 18 46  1  0
 18 47  1  0
 19 48  1  0
 19 49  1  0
 21 50  1  0
 21 51  1  0
 21 52  1  0
M  END


  Mrv1533004171508242D          

 24 26  0  0  0  0            999 V2000
    2.8845   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8845   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5989   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3134   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5989   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3134   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8845   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8845   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5989    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5989    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8845    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1700    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1700   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5250   -0.5144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7086   -1.3187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7207   -0.3308    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3627    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7207    1.1558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5250    1.3394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7086    2.1437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3705    0.7215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5517    0.8223    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3705    0.1035    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3134    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  4  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
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
  8 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 12 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 14 23  1  0  0  0  0
 10 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0330737

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC=C(C)C(=O)OC1CC(C)=CC2C1C1(C)CCCC2(C)C(=O)O1

> <INCHI_IDENTIFIER>
InChI=1S/C20H28O4/c1-6-13(3)17(21)23-15-11-12(2)10-14-16(15)20(5)9-7-8-19(14,4)18(22)24-20/h6,10,14-16H,7-9,11H2,1-5H3

> <INCHI_KEY>
KREPOBCVKLZNPY-UHFFFAOYSA-N

> <FORMULA>
C20H28O4

> <MOLECULAR_WEIGHT>
332.44

> <EXACT_MASS>
332.198759382

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
36.99646919331389

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1,5,8-trimethyl-13-oxo-12-oxatricyclo[6.3.2.0²,⁷]tridec-5-en-3-yl 2-methylbut-2-enoate

> <ALOGPS_LOGP>
4.90

> <JCHEM_LOGP>
4.275687136000001

> <ALOGPS_LOGS>
-4.21

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-6.668424740334313

> <JCHEM_POLAR_SURFACE_AREA>
52.60000000000001

> <JCHEM_REFRACTIVITY>
92.98249999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.03e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1,5,8-trimethyl-13-oxo-12-oxatricyclo[6.3.2.0²,⁷]tridec-5-en-3-yl 2-methylbut-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0       5.384  -6.930   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.384  -5.390   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.718  -4.620   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.052  -5.390   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.718  -3.080   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       8.052  -2.310   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       5.384  -2.310   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       5.384  -0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.718   0.000   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.718   1.540   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.384   2.310   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.051   1.540   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.051  -0.000   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.847  -0.960   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.189  -2.462   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.345  -0.617   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.677   0.770   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.345   2.157   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.847   2.500   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.189   4.002   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.558   1.347   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       1.030   1.535   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       2.558   0.193   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       8.052   2.310   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   13                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   24                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   19                                                  
CONECT   13   12    8   14                                                  
CONECT   14   13   15   16   23                                             
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   12   20   21                                             
CONECT   20   19                                                            
CONECT   21   19   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   14                                                       
CONECT   24   10                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   52    0
END

View in JSmol

Synonyms

Value	Source
1,5,8-Trimethyl-13-oxo-12-oxatricyclo[6.3.2.0,]tridec-5-en-3-yl 2-methylbut-2-enoic acid	Generator
1,5,8-Trimethyl-13-oxo-12-oxatricyclo[6.3.2.0²,⁷]tridec-5-en-3-yl 2-methylbut-2-enoic acid	Generator

Chemical Formula

C₂₀H₂₈O₄

Average Mass

332.4400 Da

Monoisotopic Mass

332.19876 Da

IUPAC Name

1,5,8-trimethyl-13-oxo-12-oxatricyclo[6.3.2.0²,⁷]tridec-5-en-3-yl 2-methylbut-2-enoate

Traditional Name

1,5,8-trimethyl-13-oxo-12-oxatricyclo[6.3.2.0²,⁷]tridec-5-en-3-yl 2-methylbut-2-enoate

CAS Registry Number

Not Available

SMILES

CC=C(C)C(=O)OC1CC(C)=CC2C1C1(C)CCCC2(C)C(=O)O1

InChI Identifier

InChI=1S/C20H28O4/c1-6-13(3)17(21)23-15-11-12(2)10-14-16(15)20(5)9-7-8-19(14,4)18(22)24-20/h6,10,14-16H,7-9,11H2,1-5H3

InChI Key

KREPOBCVKLZNPY-UHFFFAOYSA-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
Acritopappus longifolius	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as lactones. These are cyclic esters of hydroxy carboxylic acids, containing a 1-oxacycloalkan-2-one structure, or analogues having unsaturation or heteroatoms replacing one or more carbon atoms of the ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Lactones

Sub Class

Not Available

Direct Parent

Lactones

Alternative Parents

Substituents

Caprolactone
Delta valerolactone
Fatty acid ester
Delta_valerolactone
Oxepane
Dicarboxylic acid or derivatives
Oxane
Fatty acyl
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Lactone
Carboxylic acid ester
Oxacycle
Carboxylic acid derivative
Organic oxygen compound
Organooxygen compound
Hydrocarbon derivative
Organic oxide
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	4.9	ALOGPS
logP	4.28	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Basic)	-6.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	52.6 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	92.98 m³·mol⁻¹	ChemAxon
Polarizability	37 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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1,5,8-trimethyl-13-oxo-12-oxatricyclo[6.3.2.0²,⁷]tridec-5-en-3-yl 2-methylbut-2-enoate (NP0330737)

MOL for NP0330737 (1,5,8-trimethyl-13-oxo-12-oxatricyclo[6.3.2.0²,⁷]tridec-5-en-3-yl 2-methylbut-2-enoate)

3D MOL for NP0330737 (1,5,8-trimethyl-13-oxo-12-oxatricyclo[6.3.2.0²,⁷]tridec-5-en-3-yl 2-methylbut-2-enoate)

3D SDF for NP0330737 (1,5,8-trimethyl-13-oxo-12-oxatricyclo[6.3.2.0²,⁷]tridec-5-en-3-yl 2-methylbut-2-enoate)

3D-SDF for NP0330737 (1,5,8-trimethyl-13-oxo-12-oxatricyclo[6.3.2.0²,⁷]tridec-5-en-3-yl 2-methylbut-2-enoate)

PDB for NP0330737 (1,5,8-trimethyl-13-oxo-12-oxatricyclo[6.3.2.0²,⁷]tridec-5-en-3-yl 2-methylbut-2-enoate)

3D PDB for NP0330737 (1,5,8-trimethyl-13-oxo-12-oxatricyclo[6.3.2.0²,⁷]tridec-5-en-3-yl 2-methylbut-2-enoate)

SMILES for NP0330737 (1,5,8-trimethyl-13-oxo-12-oxatricyclo[6.3.2.0²,⁷]tridec-5-en-3-yl 2-methylbut-2-enoate)

INCHI for NP0330737 (1,5,8-trimethyl-13-oxo-12-oxatricyclo[6.3.2.0²,⁷]tridec-5-en-3-yl 2-methylbut-2-enoate)

Structure for NP0330737 (1,5,8-trimethyl-13-oxo-12-oxatricyclo[6.3.2.0²,⁷]tridec-5-en-3-yl 2-methylbut-2-enoate)

3D Structure for NP0330737 (1,5,8-trimethyl-13-oxo-12-oxatricyclo[6.3.2.0²,⁷]tridec-5-en-3-yl 2-methylbut-2-enoate)