NP-MRD: Showing NP-Card for (3r)-3-[(2e)-3-[(1s,3r,4r)-4-ethenyl-4-methyl-3-(prop-1-en-2-yl)cyclohexyl]but-2-en-1-yl]-2,2-dimethyloxirane (NP0274264)

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Record Information

Version

2.0

Created at

2022-09-08 21:35:48 UTC

Updated at

2022-09-08 21:35:48 UTC

NP-MRD ID

NP0274264

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3r)-3-[(2e)-3-[(1s,3r,4r)-4-ethenyl-4-methyl-3-(prop-1-en-2-yl)cyclohexyl]but-2-en-1-yl]-2,2-dimethyloxirane

Description

17,18-Epoxy-8,10,13(15)-lobatriene belongs to the class of organic compounds known as elemane sesquiterpenoids. These are sesquiterpenoids with a structure based on the elemane skeleton. Elemane is a monocyclic compound consisting of a cyclohexane ring substituted with a methyl group, an ethyl group, and two 1-methylethyl groups at the 1-, 1-, 2-, and 4-position, respectively. Thus, 17,18-epoxy-8,10,13(15)-lobatriene is considered to be an isoprenoid. (3r)-3-[(2e)-3-[(1s,3r,4r)-4-ethenyl-4-methyl-3-(prop-1-en-2-yl)cyclohexyl]but-2-en-1-yl]-2,2-dimethyloxirane is found in Lobophytum pauciflorum. Based on a literature review very few articles have been published on 17,18-epoxy-8,10,13(15)-lobatriene.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 53 54  0  0  0  0  0  0  0  0999 V2000
   -3.3352    1.7281   -2.3824 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9472    0.4769   -2.2461 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1891   -0.2580   -0.9364 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.6827   -0.4498   -0.9030 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5343   -1.6104   -1.0249 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2031   -1.6331   -0.2949 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5390   -0.3093   -0.5405 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9473   -0.3932   -0.3562 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6506   -1.2977   -1.2904 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6057    0.2726    0.5296 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0136    0.3284    0.8578 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0542   -0.3393    0.0668 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2778   -0.0266   -1.2448 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3098    0.3591   -0.3281 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5500   -0.4687   -0.5605 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4943    1.8235   -0.0718 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2160    0.7373    0.2390 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7382    0.5614    0.1928 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.2173    0.1240    1.5298 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9452   -0.9195    1.8394 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8515    1.0032    2.7359 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1451    2.2367   -3.3461 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8430    2.3234   -1.6222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4723   -0.0138   -3.0815 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0052   -1.5144   -0.9636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1931    0.0134   -0.0506 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1798    0.0140   -1.8071 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1654   -2.4527   -0.7001 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3026   -1.8058   -2.0918 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5725   -2.4545   -0.6231 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4180   -1.6977    0.8113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6756   -0.0903   -1.6257 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3836   -1.8865   -0.7612 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9437   -2.0763   -1.7338 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9849   -0.7608   -2.2061 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9481    0.9483    1.1662 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1788    0.0488    1.9723 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3528    1.4358    0.9213 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2942   -1.3849    0.4617 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1840   -0.5484    0.3385 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0878   -0.0106   -1.4229 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2663   -1.5091   -0.8370 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8022    2.4073   -0.7234 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5214    2.1135   -0.3755 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3984    2.1030    0.9951 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9137    1.7590   -0.0125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9620    0.6138    1.3330 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1358    1.6025    0.0723 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2282   -1.0730    2.9115 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3169   -1.6954    1.2145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9869    0.5688    3.2639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6991    1.0430    3.4235 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6355    2.0337    2.3842 H   0  0  0  0  0  0  0  0  0  0  0  0
 21 19  1  0
 19 20  2  3
 19 18  1  0
 18 17  1  0
 17  7  1  0
  7  6  1  0
  6  5  1  0
  5  3  1  0
  3  4  1  0
  3  2  1  6
  2  1  2  3
  7  8  1  0
  8  9  1  0
  8 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
  3 18  1  0
 14 12  1  0
 21 51  1  0
 21 52  1  0
 21 53  1  0
 20 49  1  0
 20 50  1  0
 18 48  1  6
 17 46  1  0
 17 47  1  0
  7 32  1  6
  6 30  1  0
  6 31  1  0
  5 28  1  0
  5 29  1  0
  4 25  1  0
  4 26  1  0
  4 27  1  0
  2 24  1  0
  1 22  1  0
  1 23  1  0
  9 33  1  0
  9 34  1  0
  9 35  1  0
 10 36  1  0
 11 37  1  0
 11 38  1  0
 12 39  1  6
 15 40  1  0
 15 41  1  0
 15 42  1  0
 16 43  1  0
 16 44  1  0
 16 45  1  0
M  END


  Mrv1652309082223352D          

 21 22  0  0  1  0            999 V2000
   -0.6283   -0.9012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1842   -1.0445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2448   -1.0445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    3.7125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1105    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020    4.4270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1712    5.1028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7752    5.1028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  3  2  1  1  0  0  0
  3  4  1  6  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  6  0  0  0
  8  9  1  0  0  0  0
  8 10  2  0  0  0  0
 10 11  1  0  0  0  0
 12 11  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
  7 17  1  0  0  0  0
 17 18  1  0  0  0  0
  3 18  1  0  0  0  0
 18 19  1  6  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0274264

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=C)[C@H]1C[C@H](CC[C@]1(C)C=C)C(\C)=C\C[C@H]1OC1(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C20H32O/c1-8-20(7)12-11-16(13-17(20)14(2)3)15(4)9-10-18-19(5,6)21-18/h8-9,16-18H,1-2,10-13H2,3-7H3/b15-9+/t16-,17+,18+,20-/m0/s1

> <INCHI_KEY>
PLMPUHCOGGTVIR-JZXJGBJOSA-N

> <FORMULA>
C20H32O

> <MOLECULAR_WEIGHT>
288.475

> <EXACT_MASS>
288.24531565

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
36.29088121401277

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3R)-3-[(2E)-3-[(1S,3R,4R)-4-ethenyl-4-methyl-3-(prop-1-en-2-yl)cyclohexyl]but-2-en-1-yl]-2,2-dimethyloxirane

> <JCHEM_LOGP>
5.360026344666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.224607503663974

> <JCHEM_POLAR_SURFACE_AREA>
12.53

> <JCHEM_REFRACTIVITY>
91.93879999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(3R)-3-[(2E)-3-[(1S,3R,4R)-4-ethenyl-4-methyl-3-(prop-1-en-2-yl)cyclohexyl]but-2-en-1-yl]-2,2-dimethyloxirane

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0      -1.173  -1.682   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.344  -1.950   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.324  -1.950   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.000   0.000   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.000   1.540   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.000   4.620   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.667   6.160   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.334   6.930   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -0.206   6.930   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       0.564   8.264   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.320   9.525   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.447   9.525   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.335  -0.000   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5   18                                             
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   17                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12   14                                                       
CONECT   14   13   12   15   16                                             
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17    7   18                                                       
CONECT   18   17    3   19                                                  
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   44    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₃₂O

Average Mass

288.4750 Da

Monoisotopic Mass

288.24532 Da

IUPAC Name

(3R)-3-[(2E)-3-[(1S,3R,4R)-4-ethenyl-4-methyl-3-(prop-1-en-2-yl)cyclohexyl]but-2-en-1-yl]-2,2-dimethyloxirane

Traditional Name

(3R)-3-[(2E)-3-[(1S,3R,4R)-4-ethenyl-4-methyl-3-(prop-1-en-2-yl)cyclohexyl]but-2-en-1-yl]-2,2-dimethyloxirane

CAS Registry Number

Not Available

SMILES

CC(=C)[C@H]1C[C@H](CC[C@]1(C)C=C)C(\C)=C\C[C@H]1OC1(C)C

InChI Identifier

InChI=1S/C20H32O/c1-8-20(7)12-11-16(13-17(20)14(2)3)15(4)9-10-18-19(5,6)21-18/h8-9,16-18H,1-2,10-13H2,3-7H3/b15-9+/t16-,17+,18+,20-/m0/s1

InChI Key

PLMPUHCOGGTVIR-JZXJGBJOSA-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
Lobophytum pauciflorum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as elemane sesquiterpenoids. These are sesquiterpenoids with a structure based on the elemane skeleton. Elemane is a monocyclic compound consisting of a cyclohexane ring substituted with a methyl group, an ethyl group, and two 1-methylethyl groups at the 1-, 1-, 2-, and 4-position, respectively.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Elemane sesquiterpenoids

Alternative Parents

Substituents

Elemane sesquiterpenoid
Oxacycle
Organoheterocyclic compound
Ether
Oxirane
Dialkyl ether
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

Lobane diterpenoids (LMPR0104460001 )

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	5.36	ChemAxon
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	12.53 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	91.94 m³·mol⁻¹	ChemAxon
Polarizability	36.29 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	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

24697760

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

42608262

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3r)-3-[(2e)-3-[(1s,3r,4r)-4-ethenyl-4-methyl-3-(prop-1-en-2-yl)cyclohexyl]but-2-en-1-yl]-2,2-dimethyloxirane (NP0274264)

MOL for NP0274264 ((3r)-3-[(2e)-3-[(1s,3r,4r)-4-ethenyl-4-methyl-3-(prop-1-en-2-yl)cyclohexyl]but-2-en-1-yl]-2,2-dimethyloxirane)

3D MOL for NP0274264 ((3r)-3-[(2e)-3-[(1s,3r,4r)-4-ethenyl-4-methyl-3-(prop-1-en-2-yl)cyclohexyl]but-2-en-1-yl]-2,2-dimethyloxirane)

3D SDF for NP0274264 ((3r)-3-[(2e)-3-[(1s,3r,4r)-4-ethenyl-4-methyl-3-(prop-1-en-2-yl)cyclohexyl]but-2-en-1-yl]-2,2-dimethyloxirane)

3D-SDF for NP0274264 ((3r)-3-[(2e)-3-[(1s,3r,4r)-4-ethenyl-4-methyl-3-(prop-1-en-2-yl)cyclohexyl]but-2-en-1-yl]-2,2-dimethyloxirane)

PDB for NP0274264 ((3r)-3-[(2e)-3-[(1s,3r,4r)-4-ethenyl-4-methyl-3-(prop-1-en-2-yl)cyclohexyl]but-2-en-1-yl]-2,2-dimethyloxirane)

3D PDB for NP0274264 ((3r)-3-[(2e)-3-[(1s,3r,4r)-4-ethenyl-4-methyl-3-(prop-1-en-2-yl)cyclohexyl]but-2-en-1-yl]-2,2-dimethyloxirane)

SMILES for NP0274264 ((3r)-3-[(2e)-3-[(1s,3r,4r)-4-ethenyl-4-methyl-3-(prop-1-en-2-yl)cyclohexyl]but-2-en-1-yl]-2,2-dimethyloxirane)

INCHI for NP0274264 ((3r)-3-[(2e)-3-[(1s,3r,4r)-4-ethenyl-4-methyl-3-(prop-1-en-2-yl)cyclohexyl]but-2-en-1-yl]-2,2-dimethyloxirane)

Structure for NP0274264 ((3r)-3-[(2e)-3-[(1s,3r,4r)-4-ethenyl-4-methyl-3-(prop-1-en-2-yl)cyclohexyl]but-2-en-1-yl]-2,2-dimethyloxirane)

3D Structure for NP0274264 ((3r)-3-[(2e)-3-[(1s,3r,4r)-4-ethenyl-4-methyl-3-(prop-1-en-2-yl)cyclohexyl]but-2-en-1-yl]-2,2-dimethyloxirane)