NP-MRD: Showing NP-Card for Methyl uguenenoate (NP0073621)

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Record Information

Version

2.0

Created at

2022-04-28 18:51:02 UTC

Updated at

2022-04-28 18:51:02 UTC

NP-MRD ID

NP0073621

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Methyl uguenenoate

Description

Methyl 2-[(1S,2R,4S,7S,8R,11S,12R,13R,16S)-7-(furan-3-yl)-12-(hydroxymethyl)-1,8,15,15-tetramethyl-5,18-dioxo-3,6,14-trioxapentacyclo[9.7.0.0²,⁴.0²,⁸.0¹²,¹⁶]Octadecan-13-yl]acetate belongs to the class of organic compounds known as steroid lactones. These are sterol lipids containing a lactone moiety linked to the steroid skeleton. Methyl uguenenoate is found in Vepris uguenensis. Based on a literature review very few articles have been published on methyl 2-[(1S,2R,4S,7S,8R,11S,12R,13R,16S)-7-(furan-3-yl)-12-(hydroxymethyl)-1,8,15,15-tetramethyl-5,18-dioxo-3,6,14-trioxapentacyclo[9.7.0.0²,⁴.0²,⁸.0¹²,¹⁶]Octadecan-13-yl]acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282220512D          

 36 41  0  0  1  0            999 V2000
    0.1827   -0.2182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3492   -0.8489    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0976    0.5577    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4342    1.1884    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2463    1.0432    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5266    0.2673    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9948   -0.3634    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8069   -0.5086    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3387    0.1221    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8705    0.7528    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5902    1.5287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7781    1.6739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6826    0.6076    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9629   -0.1684    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4311   -0.7991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6190   -0.6539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0872   -1.2846    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7875   -0.1416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0168    0.6509    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3340    1.1139    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3072    1.9385    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0079    2.3740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7354    1.9849    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9811    3.1985    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6817    3.6340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9089   -0.9576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.4850    1.4085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8741    2.1360    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    0.9660    1.8191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1539    1.9643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6169    2.6472    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1105    3.2985    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6654    3.0182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6386    2.1937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  1  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
  1  7  1  0  0  0  0
  7  8  1  6  0  0  0
  6  8  1  6  0  0  0
  6  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  1  0  0  0
 11 12  1  0  0  0  0
  5 12  1  0  0  0  0
 10 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  1  0  0  0
 15 16  1  0  0  0  0
  9 16  1  0  0  0  0
 16 17  2  0  0  0  0
 14 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 13 20  1  0  0  0  0
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 22 24  1  0  0  0  0
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 18 26  1  0  0  0  0
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 13 28  1  6  0  0  0
 28 29  1  0  0  0  0
  9 30  1  1  0  0  0
  5 31  1  6  0  0  0
  4 32  1  6  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 32 36  1  0  0  0  0
M  END

     RDKit          3D

 70 75  0  0  0  0  0  0  0  0999 V2000
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    0.2682   -0.4708   -1.9028 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0337   -0.1398    0.5947 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4234    1.2352    0.9752 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5615    1.7927    0.1894 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.4392    0.3320    0.7634 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.6442   -0.6796    2.6052 H   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0
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  3  5  1  0
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M  END


  Mrv1652304282220512D          

 36 41  0  0  1  0            999 V2000
    0.1827   -0.2182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  2  0  0  0  0
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 20 21  1  1  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 18 26  1  0  0  0  0
 18 27  1  0  0  0  0
 13 28  1  6  0  0  0
 28 29  1  0  0  0  0
  9 30  1  1  0  0  0
  5 31  1  6  0  0  0
  4 32  1  6  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 32 36  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0073621

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C[C@H]1OC(C)(C)[C@H]2CC(=O)[C@@]3(C)[C@@H](CC[C@]4(C)[C@H](OC(=O)[C@H]5O[C@@]345)C3=COC=C3)[C@@]12CO

> <INCHI_IDENTIFIER>
InChI=1S/C27H34O9/c1-23(2)16-10-17(29)25(4)15(26(16,13-28)18(35-23)11-19(30)32-5)6-8-24(3)20(14-7-9-33-12-14)34-22(31)21-27(24,25)36-21/h7,9,12,15-16,18,20-21,28H,6,8,10-11,13H2,1-5H3/t15-,16-,18-,20-,21-,24-,25-,26-,27-/m1/s1

> <INCHI_KEY>
XCLFXSUTXZKNFU-RLIIIGMDSA-N

> <FORMULA>
C27H34O9

> <MOLECULAR_WEIGHT>
502.56

> <EXACT_MASS>
502.220282675

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
70

> <JCHEM_AVERAGE_POLARIZABILITY>
51.88687594130249

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl 2-[(1S,2R,4S,7S,8R,11S,12R,13R,16S)-7-(furan-3-yl)-12-(hydroxymethyl)-1,8,15,15-tetramethyl-5,18-dioxo-3,6,14-trioxapentacyclo[9.7.0.0^{2,4}.0^{2,8}.0^{12,16}]octadecan-13-yl]acetate

> <ALOGPS_LOGP>
2.83

> <JCHEM_LOGP>
1.9386140723333318

> <ALOGPS_LOGS>
-3.69

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
17.239972656423365

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.999689194915788

> <JCHEM_PKA_STRONGEST_BASIC>
-2.796346335814146

> <JCHEM_POLAR_SURFACE_AREA>
124.8

> <JCHEM_REFRACTIVITY>
122.98049999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.03e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl [(1S,2R,4S,7S,8R,11S,12R,13R,16S)-7-(furan-3-yl)-12-(hydroxymethyl)-1,8,15,15-tetramethyl-5,18-dioxo-3,6,14-trioxapentacyclo[9.7.0.0^{2,4}.0^{2,8}.0^{12,16}]octadecan-13-yl]acetate

> <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       0.341  -0.407   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -0.652  -1.585   0.000  0.00  0.00           O+0
HETATM    3  O   UNK     0      -0.182   1.041   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       0.810   2.218   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.326   1.947   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.850   0.499   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.857  -0.678   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       3.373  -0.949   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       4.366   0.228   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.358   1.405   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.835   2.854   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.319   3.125   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.874   1.134   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.398  -0.314   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.405  -1.492   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.889  -1.221   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       3.896  -2.398   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       8.937  -0.264   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       9.365   1.215   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       8.090   2.079   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.040   3.618   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       9.348   4.431   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      10.706   3.705   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       9.298   5.971   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      10.606   6.784   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       9.163  -1.787   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      10.357  -0.859   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.505   2.629   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       7.232   3.987   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       4.254  -1.308   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       1.803   3.396   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       0.287   3.667   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       1.151   4.941   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       0.206   6.157   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      -1.242   5.634   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -1.192   4.095   0.000  0.00  0.00           C+0
CONECT    1    2    3    7                                                  
CONECT    2    1                                                            
CONECT    3    1    4                                                       
CONECT    4    3    5   32                                                  
CONECT    5    4    6   12   31                                             
CONECT    6    5    7    8    9                                             
CONECT    7    6    1    8                                                  
CONECT    8    7    6                                                       
CONECT    9    6   10   16   30                                             
CONECT   10    9   11   13                                                  
CONECT   11   10   12                                                       
CONECT   12   11    5                                                       
CONECT   13   10   14   20   28                                             
CONECT   14   13   15   18                                                  
CONECT   15   14   16                                                       
CONECT   16   15    9   17                                                  
CONECT   17   16                                                            
CONECT   18   14   19   26   27                                             
CONECT   19   18   20                                                       
CONECT   20   19   13   21                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24                                                            
CONECT   26   18                                                            
CONECT   27   18                                                            
CONECT   28   13   29                                                       
CONECT   29   28                                                            
CONECT   30    9                                                            
CONECT   31    5                                                            
CONECT   32    4   33   36                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   32                                                       
MASTER        0    0    0    0    0    0    0    0   36    0   82    0
END

View in JSmol

Synonyms

Value	Source
Methyl 2-[(1S,2R,4S,7S,8R,11S,12R,13R,16S)-7-(furan-3-yl)-12-(hydroxymethyl)-1,8,15,15-tetramethyl-5,18-dioxo-3,6,14-trioxapentacyclo[9.7.0.0,.0,.0,]octadecan-13-yl]acetic acid	Generator

Chemical Formula

C₂₇H₃₄O₉

Average Mass

502.5600 Da

Monoisotopic Mass

502.22028 Da

IUPAC Name

methyl 2-[(1S,2R,4S,7S,8R,11S,12R,13R,16S)-7-(furan-3-yl)-12-(hydroxymethyl)-1,8,15,15-tetramethyl-5,18-dioxo-3,6,14-trioxapentacyclo[9.7.0.0^{2,4}.0^{2,8}.0^{12,16}]octadecan-13-yl]acetate

Traditional Name

methyl [(1S,2R,4S,7S,8R,11S,12R,13R,16S)-7-(furan-3-yl)-12-(hydroxymethyl)-1,8,15,15-tetramethyl-5,18-dioxo-3,6,14-trioxapentacyclo[9.7.0.0^{2,4}.0^{2,8}.0^{12,16}]octadecan-13-yl]acetate

CAS Registry Number

Not Available

SMILES

COC(=O)C[C@H]1OC(C)(C)[C@H]2CC(=O)[C@@]3(C)[C@@H](CC[C@]4(C)[C@H](OC(=O)[C@H]5O[C@@]345)C3=COC=C3)[C@@]12CO

InChI Identifier

InChI=1S/C27H34O9/c1-23(2)16-10-17(29)25(4)15(26(16,13-28)18(35-23)11-19(30)32-5)6-8-24(3)20(14-7-9-33-12-14)34-22(31)21-27(24,25)36-21/h7,9,12,15-16,18,20-21,28H,6,8,10-11,13H2,1-5H3/t15-,16-,18-,20-,21-,24-,25-,26-,27-/m1/s1

InChI Key

XCLFXSUTXZKNFU-RLIIIGMDSA-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
Vepris uguenensis	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as steroid lactones. These are sterol lipids containing a lactone moiety linked to the steroid skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroid lactones

Direct Parent

Steroid lactones

Alternative Parents

Substituents

Steroid lactone
2-oxosteroid
Oxosteroid
11-oxosteroid
Naphthopyran
Naphthalene
Delta_valerolactone
Dioxepane
Delta valerolactone
1,4-dioxepane
Pyran
Oxane
Dicarboxylic acid or derivatives
Heteroaromatic compound
Methyl ester
Tetrahydrofuran
Furan
Lactone
Ketone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Carbonyl group
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	2.83	ALOGPS
logP	1.94	ChemAxon
logS	-3.7	ALOGPS
pKa (Strongest Acidic)	15	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	124.8 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	122.98 m³·mol⁻¹	ChemAxon
Polarizability	51.89 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

163065423

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Methyl uguenenoate (NP0073621)

MOL for NP0073621 (Methyl uguenenoate)

3D MOL for NP0073621 (Methyl uguenenoate)

3D SDF for NP0073621 (Methyl uguenenoate)

3D-SDF for NP0073621 (Methyl uguenenoate)

PDB for NP0073621 (Methyl uguenenoate)

3D PDB for NP0073621 (Methyl uguenenoate)

SMILES for NP0073621 (Methyl uguenenoate)

INCHI for NP0073621 (Methyl uguenenoate)

Structure for NP0073621 (Methyl uguenenoate)

3D Structure for NP0073621 (Methyl uguenenoate)