NP-MRD: Showing NP-Card for 11-methoxy-3,3-dimethyl-7,12-dimethylidene-10-oxatricyclo[6.4.0.0²,⁴]dodecan-9-yl acetate (NP0292933)

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Record Information

Version

2.0

Created at

2022-09-10 00:41:39 UTC

Updated at

2022-09-10 00:41:39 UTC

NP-MRD ID

NP0292933

Secondary Accession Numbers

None

Natural Product Identification

Common Name

11-methoxy-3,3-dimethyl-7,12-dimethylidene-10-oxatricyclo[6.4.0.0²,⁴]dodecan-9-yl acetate

Description

11-Methoxy-3,3-dimethyl-7,12-dimethylidene-10-oxatricyclo[6.4.0.0²,⁴]Dodecan-9-yl acetate belongs to the class of organic compounds known as aromadendrane sesquiterpenoids. These are sesquiterpenoids with a structure based on an aromadendrane (a cyclopropa[e]azulene derivative) skeleton. Some aromadendrane sesquiterpenoids are found in essential oils. Certain aromadendrane Sesquiterpenoids from the Leaves of Xylopia brasiliensis were found to possess antifungal activities. 11-methoxy-3,3-dimethyl-7,12-dimethylidene-10-oxatricyclo[6.4.0.0²,⁴]dodecan-9-yl acetate is found in Plagiochila parvifolia and Plagiochila semidecurrens. 11-Methoxy-3,3-dimethyl-7,12-dimethylidene-10-oxatricyclo[6.4.0.0²,⁴]Dodecan-9-yl acetate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 48 50  0  0  0  0  0  0  0  0999 V2000
    0.1342    2.5764   -1.4657 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4457    1.7335   -0.5258 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2807    0.8831    0.3562 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6618    0.5332    0.4007 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2305    0.2166   -0.9000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.5338   -1.2362   -1.0115 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4133   -2.1703   -0.6869 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4289   -1.6096    0.2919 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4093   -2.2519    1.4280 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4772   -0.4705    0.1557 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6769   -0.3675    0.9817 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7048   -1.2775    0.6709 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2662   -2.0831    1.6135 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3684   -3.0671    1.2829 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8634   -2.0170    2.8048 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1708    0.9594    0.9310 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9428    1.5914   -0.2857 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6043    0.9462   -1.2858 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5894    1.7512   -1.8459 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9342    1.1183    0.0431 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2134    0.4277    0.5772 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2097    2.5479   -0.1778 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8763    2.8065   -1.7757 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8927    3.1408   -2.0373 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0175    1.2593    1.4085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7961   -0.2715    1.2124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9409    0.6746   -1.8542 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9794   -1.5033   -2.0187 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3583   -1.4672   -0.3002 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7669   -3.1553   -0.3316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8451   -2.3566   -1.6215 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2278   -1.9801    2.2377 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0716   -3.1144    1.5762 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8222   -0.5135   -0.9232 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4174   -0.4759    2.0512 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9133   -4.0854    1.3503 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7797   -2.8570    0.2851 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1220   -3.0135    2.0953 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3246    2.6178   -0.1592 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1341    1.2267   -2.6651 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3338    2.0827   -1.0668 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2086    2.6869   -2.2953 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7941   -0.0273   -0.2223 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8026    1.1374    1.2023 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9141   -0.3764    1.3132 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5006    2.6938   -1.2596 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0588    2.8922    0.4389 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3822    3.2444    0.0071 H   0  0  0  0  0  0  0  0  0  0  0  0
 19 18  1  0
 18 17  1  0
 17 16  1  0
 16 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  2  0
 11 10  1  0
 10  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  3
  5 20  1  0
 20 21  1  0
 20 22  1  0
  3  2  1  0
  2  1  2  3
  2 17  1  0
  8 10  1  0
 20  4  1  0
 19 40  1  0
 19 41  1  0
 19 42  1  0
 17 39  1  1
 11 35  1  1
 14 36  1  0
 14 37  1  0
 14 38  1  0
 10 34  1  6
  3 25  1  1
  4 26  1  1
  5 27  1  6
  6 28  1  0
  6 29  1  0
  7 30  1  0
  7 31  1  0
  9 32  1  0
  9 33  1  0
 21 43  1  0
 21 44  1  0
 21 45  1  0
 22 46  1  0
 22 47  1  0
 22 48  1  0
  1 23  1  0
  1 24  1  0
M  END


  Mrv1533004241512492D          

 22 24  0  0  0  0            999 V2000
    2.6745   -0.8783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0927   -0.1672    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6860    0.5506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1042    1.2617    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6975    1.9795    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1157    2.6906    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9407    2.6840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3590    3.3951    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3474    1.9662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8725    1.9862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4543    1.2750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6375    1.1587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0373    1.7247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1056    2.5468    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7909    3.0061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5773    2.7565    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1433    3.3568    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1528    0.9218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9607    0.7548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2721    0.1055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8610    0.5573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4428   -0.1539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  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  2  0  0  0  0
  7  9  1  0  0  0  0
  5 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 10 16  1  0  0  0  0
 16 17  2  0  0  0  0
 13 18  1  0  0  0  0
 12 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 11 21  1  0  0  0  0
  3 21  1  0  0  0  0
 21 22  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0292933

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1OC(OC(C)=O)C2C(C3C(CCC2=C)C3(C)C)C1=C

> <INCHI_IDENTIFIER>
InChI=1S/C18H26O4/c1-9-7-8-12-15(18(12,4)5)14-10(2)16(20-6)22-17(13(9)14)21-11(3)19/h12-17H,1-2,7-8H2,3-6H3

> <INCHI_KEY>
XZWTYQVMLSCUGD-UHFFFAOYSA-N

> <FORMULA>
C18H26O4

> <MOLECULAR_WEIGHT>
306.402

> <EXACT_MASS>
306.183109317

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
48

> <JCHEM_AVERAGE_POLARIZABILITY>
34.21391439754721

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
11-methoxy-3,3-dimethyl-7,12-dimethylidene-10-oxatricyclo[6.4.0.0²,⁴]dodecan-9-yl acetate

> <ALOGPS_LOGP>
2.33

> <JCHEM_LOGP>
3.0258047513333337

> <ALOGPS_LOGS>
-3.61

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.118653899032017

> <JCHEM_POLAR_SURFACE_AREA>
44.760000000000005

> <JCHEM_REFRACTIVITY>
82.4091

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.51e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
11-methoxy-3,3-dimethyl-7,12-dimethylidene-10-oxatricyclo[6.4.0.0²,⁴]dodecan-9-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0       4.992  -1.639   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       5.773  -0.312   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       5.014   1.028   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       5.795   2.355   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       5.035   3.695   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       5.816   5.023   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       7.356   5.010   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       8.137   6.338   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       8.115   3.670   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.495   3.708   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.715   2.380   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.190   2.163   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.070   3.219   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.197   4.754   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.476   5.611   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.944   5.146   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.001   6.266   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.285   1.721   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.793   1.409   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.508   0.197   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.474   1.040   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.693  -0.287   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   21                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   10                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    5   11   16                                                  
CONECT   11   10   12   21                                                  
CONECT   12   11   13   18                                                  
CONECT   13   12   14   18                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   10   17                                                  
CONECT   17   16                                                            
CONECT   18   13   12   19   20                                             
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   11    3   22                                                  
CONECT   22   21                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   48    0
END

View in JSmol

Synonyms

Value	Source
11-Methoxy-3,3-dimethyl-7,12-dimethylidene-10-oxatricyclo[6.4.0.0,]dodecan-9-yl acetic acid	Generator
11-Methoxy-3,3-dimethyl-7,12-dimethylidene-10-oxatricyclo[6.4.0.0²,⁴]dodecan-9-yl acetic acid	Generator

Chemical Formula

C₁₈H₂₆O₄

Average Mass

306.4020 Da

Monoisotopic Mass

306.18311 Da

IUPAC Name

11-methoxy-3,3-dimethyl-7,12-dimethylidene-10-oxatricyclo[6.4.0.0²,⁴]dodecan-9-yl acetate

Traditional Name

11-methoxy-3,3-dimethyl-7,12-dimethylidene-10-oxatricyclo[6.4.0.0²,⁴]dodecan-9-yl acetate

CAS Registry Number

Not Available

SMILES

COC1OC(OC(C)=O)C2C(C3C(CCC2=C)C3(C)C)C1=C

InChI Identifier

InChI=1S/C18H26O4/c1-9-7-8-12-15(18(12,4)5)14-10(2)16(20-6)22-17(13(9)14)21-11(3)19/h12-17H,1-2,7-8H2,3-6H3

InChI Key

XZWTYQVMLSCUGD-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
Plagiochila parvifolia	LOTUS Database	35616633
Plagiochila semidecurrens	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as aromadendrane sesquiterpenoids. These are sesquiterpenoids with a structure based on an aromadendrane (a cyclopropa[e]azulene derivative) skeleton. Some aromadendrane sesquiterpenoids are found in essential oils. Certain aromadendrane Sesquiterpenoids from the Leaves of Xylopia brasiliensis were found to possess antifungal activities.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Aromadendrane sesquiterpenoids

Alternative Parents

Substituents

Aromadendrane sesquiterpenoid
Oxane
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Acetal
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	2.33	ALOGPS
logP	3.03	ChemAxon
logS	-3.6	ALOGPS
pKa (Strongest Basic)	-4.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	44.76 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	82.41 m³·mol⁻¹	ChemAxon
Polarizability	34.21 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 11-methoxy-3,3-dimethyl-7,12-dimethylidene-10-oxatricyclo[6.4.0.0²,⁴]dodecan-9-yl acetate (NP0292933)

MOL for NP0292933 (11-methoxy-3,3-dimethyl-7,12-dimethylidene-10-oxatricyclo[6.4.0.0²,⁴]dodecan-9-yl acetate)

3D MOL for NP0292933 (11-methoxy-3,3-dimethyl-7,12-dimethylidene-10-oxatricyclo[6.4.0.0²,⁴]dodecan-9-yl acetate)

3D SDF for NP0292933 (11-methoxy-3,3-dimethyl-7,12-dimethylidene-10-oxatricyclo[6.4.0.0²,⁴]dodecan-9-yl acetate)

3D-SDF for NP0292933 (11-methoxy-3,3-dimethyl-7,12-dimethylidene-10-oxatricyclo[6.4.0.0²,⁴]dodecan-9-yl acetate)

PDB for NP0292933 (11-methoxy-3,3-dimethyl-7,12-dimethylidene-10-oxatricyclo[6.4.0.0²,⁴]dodecan-9-yl acetate)

3D PDB for NP0292933 (11-methoxy-3,3-dimethyl-7,12-dimethylidene-10-oxatricyclo[6.4.0.0²,⁴]dodecan-9-yl acetate)

SMILES for NP0292933 (11-methoxy-3,3-dimethyl-7,12-dimethylidene-10-oxatricyclo[6.4.0.0²,⁴]dodecan-9-yl acetate)

INCHI for NP0292933 (11-methoxy-3,3-dimethyl-7,12-dimethylidene-10-oxatricyclo[6.4.0.0²,⁴]dodecan-9-yl acetate)

Structure for NP0292933 (11-methoxy-3,3-dimethyl-7,12-dimethylidene-10-oxatricyclo[6.4.0.0²,⁴]dodecan-9-yl acetate)

3D Structure for NP0292933 (11-methoxy-3,3-dimethyl-7,12-dimethylidene-10-oxatricyclo[6.4.0.0²,⁴]dodecan-9-yl acetate)