NP-MRD: Showing NP-Card for 10-(acetyloxy)-1,2,6-trimethyl-8-methylidenetricyclo[5.3.1.0²,⁶]undecan-9-yl acetate (NP0216404)

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Record Information

Version

2.0

Created at

2022-09-05 16:20:53 UTC

Updated at

2022-09-05 16:20:53 UTC

NP-MRD ID

NP0216404

Secondary Accession Numbers

None

Natural Product Identification

Common Name

10-(acetyloxy)-1,2,6-trimethyl-8-methylidenetricyclo[5.3.1.0²,⁶]undecan-9-yl acetate

Description

9-(Acetyloxy)-2,6,7-trimethyl-10-methylidenetricyclo[5.3.1.0²,⁶]Undecan-8-yl acetate belongs to the class of organic compounds known as dicarboxylic acids and derivatives. These are organic compounds containing exactly two carboxylic acid groups. 10-(acetyloxy)-1,2,6-trimethyl-8-methylidenetricyclo[5.3.1.0²,⁶]undecan-9-yl acetate is found in Marsupella emarginata. 9-(Acetyloxy)-2,6,7-trimethyl-10-methylidenetricyclo[5.3.1.0²,⁶]Undecan-8-yl acetate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 51 53  0  0  0  0  0  0  0  0999 V2000
    0.2760   -2.9878    0.5635 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2335   -1.8246   -0.0713 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3440   -0.8746    0.0744 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4566   -1.4231   -0.6384 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6014   -1.8399   -0.0254 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7101   -2.3969   -0.8314 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7408   -1.7632    1.2130 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0409    0.5263   -0.3433 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2771    1.4764    0.6720 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2249    2.4763    0.5616 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4709    3.4775    1.6362 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8960    2.5163   -0.5100 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3368    0.7193   -0.9142 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3401    2.0115   -1.6736 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5717   -0.4374   -1.8878 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9676   -1.5384   -0.9182 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9598   -0.8297   -0.0397 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1525   -1.5127    1.2838 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3353   -0.7405   -0.6934 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8466    0.5579   -0.0665 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6394    1.4533   -0.3038 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4412    0.5647    0.0610 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0799    0.9371    1.4761 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1265   -3.2217    1.1795 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5155   -3.7338    0.4957 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6440   -0.8838    1.1487 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6590   -3.5137   -0.9095 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6753   -2.0964   -0.3507 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7400   -2.0072   -1.8561 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7564    0.7787   -1.1749 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3721    3.1798    2.2185 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6220    3.5752    2.3116 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7155    4.4683    1.1658 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0179    2.0106   -2.5493 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6933    2.1395   -2.1120 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4845    2.8529   -0.9929 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3670   -0.2072   -2.6068 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3935   -0.7160   -2.3534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3653   -2.4223   -1.4145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5138   -2.5431    1.0820 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9347   -0.9887    1.8523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2581   -1.5917    1.8958 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2218   -0.5673   -1.7628 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9654   -1.6049   -0.4235 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7033    0.9148   -0.6743 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0999    0.4454    0.9886 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7099    2.3320    0.3576 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6479    1.7279   -1.3568 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8253    2.0073    1.5429 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3397    0.2936    1.9406 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0290    0.8241    2.0784 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  1  0
  5  7  2  0
  5  4  1  0
  4  3  1  0
  3  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 10 12  2  0
  8 13  1  0
 13 14  1  6
 13 15  1  0
 15 16  1  0
 16  2  1  0
  2  1  2  3
 16 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  1
  2  3  1  0
 22 17  1  0
 22 13  1  0
  6 27  1  0
  6 28  1  0
  6 29  1  0
  3 26  1  1
  8 30  1  6
 11 31  1  0
 11 32  1  0
 11 33  1  0
 14 34  1  0
 14 35  1  0
 14 36  1  0
 15 37  1  0
 15 38  1  0
 16 39  1  6
  1 24  1  0
  1 25  1  0
 18 40  1  0
 18 41  1  0
 18 42  1  0
 19 43  1  0
 19 44  1  0
 20 45  1  0
 20 46  1  0
 21 47  1  0
 21 48  1  0
 23 49  1  0
 23 50  1  0
 23 51  1  0
M  END


  Mrv1533004171505572D          

 23 25  0  0  0  0            999 V2000
    6.5774    1.7450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7524    1.7450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3399    2.4594    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3399    1.0305    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5149    1.0305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1569    1.7738    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6713    2.4188    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3699    3.1868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5541    3.3097    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8843    3.8318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3526    1.9574    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1690    2.7617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1209    1.0305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3526    0.1036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1569    0.2872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6713   -0.3578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7076    0.6180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5603   -0.1938    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9230    0.3631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4380    1.0305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9230    1.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7076    1.4430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5603    2.2547    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  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  2  0  0  0  0
  8 10  1  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
  5 15  1  0  0  0  0
 15 16  2  0  0  0  0
 14 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 11 22  1  0  0  0  0
 17 22  1  0  0  0  0
 22 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0216404

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC1C(OC(C)=O)C2(C)CC(C1=C)C1(C)CCCC21C

> <INCHI_IDENTIFIER>
InChI=1S/C19H28O4/c1-11-14-10-18(5,19(6)9-7-8-17(14,19)4)16(23-13(3)21)15(11)22-12(2)20/h14-16H,1,7-10H2,2-6H3

> <INCHI_KEY>
JKQYQVNQRKCWEJ-UHFFFAOYSA-N

> <FORMULA>
C19H28O4

> <MOLECULAR_WEIGHT>
320.429

> <EXACT_MASS>
320.198759382

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
51

> <JCHEM_AVERAGE_POLARIZABILITY>
35.15529143803468

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
9-(acetyloxy)-2,6,7-trimethyl-10-methylidenetricyclo[5.3.1.0²,⁶]undecan-8-yl acetate

> <ALOGPS_LOGP>
4.51

> <JCHEM_LOGP>
2.904563487

> <ALOGPS_LOGS>
-5.09

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-6.7139928592134135

> <JCHEM_POLAR_SURFACE_AREA>
52.6

> <JCHEM_REFRACTIVITY>
85.57440000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.58e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
9-(acetyloxy)-2,6,7-trimethyl-10-methylidenetricyclo[5.3.1.0²,⁶]undecan-8-yl acetate

> <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      12.278   3.257   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.738   3.257   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       9.968   4.591   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       9.968   1.924   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       8.428   1.924   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.760   3.311   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       8.720   4.515   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       8.157   5.949   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       6.634   6.178   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       9.117   7.153   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.258   3.654   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.916   5.155   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.826   1.924   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.258   0.193   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.760   0.536   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.720  -0.668   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.054   1.154   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.779  -0.362   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.590   0.678   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.684   1.924   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.590   3.169   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.054   2.694   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.779   4.209   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   15                                                  
CONECT    6    5    7   11                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    6   12   13   22                                             
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15   17                                                  
CONECT   15   14    5   16                                                  
CONECT   16   15                                                            
CONECT   17   14   18   19   22                                             
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   11   17   23                                             
CONECT   23   22                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   50    0
END

View in JSmol

Synonyms

Value	Source
9-(Acetyloxy)-2,6,7-trimethyl-10-methylidenetricyclo[5.3.1.0,]undecan-8-yl acetic acid	Generator
9-(Acetyloxy)-2,6,7-trimethyl-10-methylidenetricyclo[5.3.1.0²,⁶]undecan-8-yl acetic acid	Generator

Chemical Formula

C₁₉H₂₈O₄

Average Mass

320.4290 Da

Monoisotopic Mass

320.19876 Da

IUPAC Name

9-(acetyloxy)-2,6,7-trimethyl-10-methylidenetricyclo[5.3.1.0²,⁶]undecan-8-yl acetate

Traditional Name

9-(acetyloxy)-2,6,7-trimethyl-10-methylidenetricyclo[5.3.1.0²,⁶]undecan-8-yl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)OC1C(OC(C)=O)C2(C)CC(C1=C)C1(C)CCCC21C

InChI Identifier

InChI=1S/C19H28O4/c1-11-14-10-18(5,19(6)9-7-8-17(14,19)4)16(23-13(3)21)15(11)22-12(2)20/h14-16H,1,7-10H2,2-6H3

InChI Key

JKQYQVNQRKCWEJ-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
Marsupella emarginata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as dicarboxylic acids and derivatives. These are organic compounds containing exactly two carboxylic acid groups.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Dicarboxylic acids and derivatives

Direct Parent

Dicarboxylic acids and derivatives

Alternative Parents

Substituents

Dicarboxylic acid or derivatives
Carboxylic acid ester
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic 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	4.51	ALOGPS
logP	2.9	ChemAxon
logS	-5.1	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	4	ChemAxon
Refractivity	85.57 m³·mol⁻¹	ChemAxon
Polarizability	35.16 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 10-(acetyloxy)-1,2,6-trimethyl-8-methylidenetricyclo[5.3.1.0²,⁶]undecan-9-yl acetate (NP0216404)

MOL for NP0216404 (10-(acetyloxy)-1,2,6-trimethyl-8-methylidenetricyclo[5.3.1.0²,⁶]undecan-9-yl acetate)

3D MOL for NP0216404 (10-(acetyloxy)-1,2,6-trimethyl-8-methylidenetricyclo[5.3.1.0²,⁶]undecan-9-yl acetate)

3D SDF for NP0216404 (10-(acetyloxy)-1,2,6-trimethyl-8-methylidenetricyclo[5.3.1.0²,⁶]undecan-9-yl acetate)

3D-SDF for NP0216404 (10-(acetyloxy)-1,2,6-trimethyl-8-methylidenetricyclo[5.3.1.0²,⁶]undecan-9-yl acetate)

PDB for NP0216404 (10-(acetyloxy)-1,2,6-trimethyl-8-methylidenetricyclo[5.3.1.0²,⁶]undecan-9-yl acetate)

3D PDB for NP0216404 (10-(acetyloxy)-1,2,6-trimethyl-8-methylidenetricyclo[5.3.1.0²,⁶]undecan-9-yl acetate)

SMILES for NP0216404 (10-(acetyloxy)-1,2,6-trimethyl-8-methylidenetricyclo[5.3.1.0²,⁶]undecan-9-yl acetate)

INCHI for NP0216404 (10-(acetyloxy)-1,2,6-trimethyl-8-methylidenetricyclo[5.3.1.0²,⁶]undecan-9-yl acetate)

Structure for NP0216404 (10-(acetyloxy)-1,2,6-trimethyl-8-methylidenetricyclo[5.3.1.0²,⁶]undecan-9-yl acetate)

3D Structure for NP0216404 (10-(acetyloxy)-1,2,6-trimethyl-8-methylidenetricyclo[5.3.1.0²,⁶]undecan-9-yl acetate)