NP-MRD: Showing NP-Card for 2-Methyl-2-[2-[(acetyloxy)methyl]oxiranyl]-4-methoxy-5-methylphenyl ester (NP0057714)

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Record Information

Version

2.0

Created at

2022-04-28 03:07:26 UTC

Updated at

2022-04-28 03:07:26 UTC

NP-MRD ID

NP0057714

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-Methyl-2-[2-[(acetyloxy)methyl]oxiranyl]-4-methoxy-5-methylphenyl ester

Description

2-[(2S)-2-[(acetyloxy)methyl]oxiran-2-yl]-4-methoxy-5-methylphenyl (2E)-2-methylbut-2-enoate belongs to the class of organic compounds known as phenol esters. These are aromatic compounds containing a benzene ring substituted by a hydroxyl group and an ester group. 2-Methyl-2-[2-[(acetyloxy)methyl]oxiranyl]-4-methoxy-5-methylphenyl ester is found in Mikania purpurascens. Based on a literature review very few articles have been published on 2-[(2S)-2-[(acetyloxy)methyl]oxiran-2-yl]-4-methoxy-5-methylphenyl (2E)-2-methylbut-2-enoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 46 47  0  0  0  0  0  0  0  0999 V2000
    4.7898    2.9184   -0.6195 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7423    1.8917   -0.4111 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4446    1.4056    0.7864 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1793    1.8985    1.9713 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3925    0.3880    0.9164 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1289   -0.0565    2.0605 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6982   -0.0846   -0.1653 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6960   -1.0457   -0.0787 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0788   -2.3935   -0.0909 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1442   -3.4081   -0.0090 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5863   -4.8330   -0.0251 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1994   -3.1244    0.0879 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1680   -4.0911    0.1719 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5360   -3.8841    0.2715 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5559   -1.7921    0.0982 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6365   -0.7702    0.0172 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0391    0.6846    0.0251 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1150    1.4073   -1.2640 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9494    2.5275   -1.1760 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3098    2.4528   -0.9658 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1542    3.6760   -0.8677 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8617    1.3396   -0.8530 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8654    1.0747    1.1905 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4475    1.3657    1.1289 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2931    3.9076   -0.6131 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5746    2.8734    0.1656 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2746    2.7152   -1.5916 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1709    1.4940   -1.2497 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1836    1.4171    2.0070 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5967    1.6433    2.8836 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2627    3.0084    1.8949 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1122   -2.6458   -0.1649 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4724   -5.2961    0.9750 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6564   -4.9230   -0.3033 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0332   -5.4100   -0.8204 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0453   -4.8684    0.1449 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9542   -3.2040   -0.4914 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8620   -3.5140    1.2715 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6068   -1.4807    0.1729 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1005    1.7620   -1.5677 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5150    0.7324   -2.0532 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4939    3.7708    0.1907 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0472    3.5957   -1.5170 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5559    4.5526   -1.1512 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3948    2.0315    1.2420 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0979    0.2909    1.9616 H   0  0  0  0  0  0  0  0  0  0  0  0
 14 13  1  0
 13 12  1  0
 12 10  2  0
 10 11  1  0
 10  9  1  0
  9  8  2  0
  8  7  1  0
  7  5  1  0
  5  6  2  0
  5  3  1  0
  3  4  1  0
  3  2  2  0
  2  1  1  0
  8 16  1  0
 16 15  2  0
 16 17  1  0
 17 18  1  6
 18 19  1  0
 19 20  1  0
 20 21  1  0
 20 22  2  0
 17 23  1  0
 23 24  1  0
 15 12  1  0
 24 17  1  0
 14 36  1  0
 14 37  1  0
 14 38  1  0
 11 33  1  0
 11 34  1  0
 11 35  1  0
  9 32  1  0
  4 29  1  0
  4 30  1  0
  4 31  1  0
  2 28  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
 15 39  1  0
 18 40  1  0
 18 41  1  0
 21 42  1  0
 21 43  1  0
 21 44  1  0
 23 45  1  0
 23 46  1  0
M  END


  Mrv1652304282205072D          

 24 25  0  0  1  0            999 V2000
    0.8189   -0.1571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1869    0.3732    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3302    1.1856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1054    1.4678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7374    0.9375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5941    0.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2261   -0.4053    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6386   -1.1197    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8136   -1.1197    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8581    0.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7149    0.9375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3468    1.4678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2036    2.2803    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1221    1.1856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2487    2.2803    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0239    2.5624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3018    1.7159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6756   -0.9696    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0996   -1.2518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7316   -0.7215    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2429   -2.0642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0181   -2.3464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1614   -3.1589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3891   -2.5945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  7  6  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  7  9  1  0  0  0  0
  7 10  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
  4 15  1  0  0  0  0
 15 16  1  0  0  0  0
  3 17  1  0  0  0  0
  1 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 21 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0057714

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(C)C=C(OC(=O)C(\C)=C\C)C(=C1)[C@@]1(COC(C)=O)CO1

> <INCHI_IDENTIFIER>
InChI=1S/C18H22O6/c1-6-11(2)17(20)24-16-7-12(3)15(21-5)8-14(16)18(10-23-18)9-22-13(4)19/h6-8H,9-10H2,1-5H3/b11-6+/t18-/m1/s1

> <INCHI_KEY>
FZEGVWGMVBZRSI-PMQIGOLDSA-N

> <FORMULA>
C18H22O6

> <MOLECULAR_WEIGHT>
334.368

> <EXACT_MASS>
334.141638428

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
46

> <JCHEM_AVERAGE_POLARIZABILITY>
34.78725370647031

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-[(2S)-2-[(acetyloxy)methyl]oxiran-2-yl]-4-methoxy-5-methylphenyl (2E)-2-methylbut-2-enoate

> <ALOGPS_LOGP>
3.16

> <JCHEM_LOGP>
3.146879713333333

> <ALOGPS_LOGS>
-4.49

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.148420518574212

> <JCHEM_POLAR_SURFACE_AREA>
74.36000000000001

> <JCHEM_REFRACTIVITY>
87.9748

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.08e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-[(2S)-2-[(acetyloxy)methyl]oxiran-2-yl]-4-methoxy-5-methylphenyl (2E)-2-methylbut-2-enoate

> <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       1.529  -0.293   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.349   0.697   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.616   2.213   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.063   2.740   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.243   1.750   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.976   0.233   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.155  -0.756   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.925  -2.090   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       3.385  -2.090   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       5.335   0.233   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       5.068   1.750   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       6.247   2.740   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       5.980   4.257   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       7.695   2.213   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       2.331   4.257   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       3.778   4.783   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.563   3.203   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       1.261  -1.810   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -0.186  -2.337   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -1.366  -1.347   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -0.453  -3.853   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.900  -4.380   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -2.168  -5.897   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.726  -4.843   0.000  0.00  0.00           C+0
CONECT    1    2    6   18                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4   17                                                  
CONECT    4    3    5   15                                                  
CONECT    5    4    6                                                       
CONECT    6    5    1    7                                                  
CONECT    7    6    8    9   10                                             
CONECT    8    7    9                                                       
CONECT    9    8    7                                                       
CONECT   10    7   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15    4   16                                                       
CONECT   16   15                                                            
CONECT   17    3                                                            
CONECT   18    1   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   24                                                  
CONECT   22   21   23                                                       
CONECT   23   22                                                            
CONECT   24   21                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   50    0
END

View in JSmol

Synonyms

Value	Source
2-[(2S)-2-[(Acetyloxy)methyl]oxiran-2-yl]-4-methoxy-5-methylphenyl (2E)-2-methylbut-2-enoic acid	Generator

Chemical Formula

C₁₈H₂₂O₆

Average Mass

334.3680 Da

Monoisotopic Mass

334.14164 Da

IUPAC Name

2-[(2S)-2-[(acetyloxy)methyl]oxiran-2-yl]-4-methoxy-5-methylphenyl (2E)-2-methylbut-2-enoate

Traditional Name

2-[(2S)-2-[(acetyloxy)methyl]oxiran-2-yl]-4-methoxy-5-methylphenyl (2E)-2-methylbut-2-enoate

CAS Registry Number

Not Available

SMILES

COC1=C(C)C=C(OC(=O)C(\C)=C\C)C(=C1)[C@@]1(COC(C)=O)CO1

InChI Identifier

InChI=1S/C18H22O6/c1-6-11(2)17(20)24-16-7-12(3)15(21-5)8-14(16)18(10-23-18)9-22-13(4)19/h6-8H,9-10H2,1-5H3/b11-6+/t18-/m1/s1

InChI Key

FZEGVWGMVBZRSI-PMQIGOLDSA-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
Mikania purpurascens	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenol esters. These are aromatic compounds containing a benzene ring substituted by a hydroxyl group and an ester group.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Phenol esters

Sub Class

Not Available

Direct Parent

Phenol esters

Alternative Parents

Substituents

Phenol ester
Phenoxy compound
Methoxybenzene
Phenol ether
Anisole
Toluene
Fatty acid ester
Alkyl aryl ether
Fatty acyl
Dicarboxylic acid or derivatives
Monocyclic benzene moiety
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic 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	3.16	ALOGPS
logP	3.15	ChemAxon
logS	-4.5	ALOGPS
pKa (Strongest Basic)	-4.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	74.36 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	87.97 m³·mol⁻¹	ChemAxon
Polarizability	34.79 Å³	ChemAxon
Number of Rings	2	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

162974468

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 2-Methyl-2-[2-[(acetyloxy)methyl]oxiranyl]-4-methoxy-5-methylphenyl ester (NP0057714)

MOL for NP0057714 (2-Methyl-2-[2-[(acetyloxy)methyl]oxiranyl]-4-methoxy-5-methylphenyl ester)

3D MOL for NP0057714 (2-Methyl-2-[2-[(acetyloxy)methyl]oxiranyl]-4-methoxy-5-methylphenyl ester)

3D SDF for NP0057714 (2-Methyl-2-[2-[(acetyloxy)methyl]oxiranyl]-4-methoxy-5-methylphenyl ester)

3D-SDF for NP0057714 (2-Methyl-2-[2-[(acetyloxy)methyl]oxiranyl]-4-methoxy-5-methylphenyl ester)

PDB for NP0057714 (2-Methyl-2-[2-[(acetyloxy)methyl]oxiranyl]-4-methoxy-5-methylphenyl ester)

3D PDB for NP0057714 (2-Methyl-2-[2-[(acetyloxy)methyl]oxiranyl]-4-methoxy-5-methylphenyl ester)

SMILES for NP0057714 (2-Methyl-2-[2-[(acetyloxy)methyl]oxiranyl]-4-methoxy-5-methylphenyl ester)

INCHI for NP0057714 (2-Methyl-2-[2-[(acetyloxy)methyl]oxiranyl]-4-methoxy-5-methylphenyl ester)

Structure for NP0057714 (2-Methyl-2-[2-[(acetyloxy)methyl]oxiranyl]-4-methoxy-5-methylphenyl ester)

3D Structure for NP0057714 (2-Methyl-2-[2-[(acetyloxy)methyl]oxiranyl]-4-methoxy-5-methylphenyl ester)