NP-MRD: Showing NP-Card for (1s,3r)-3-hydroxy-3,5,5-trimethyl-4-[(3e,5e)-3-methyl-7-oxoocta-1,3,5-trien-1-ylidene]cyclohexyl acetate (NP0265588)

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Record Information

Version

2.0

Created at

2022-09-08 09:37:21 UTC

Updated at

2022-09-08 09:37:22 UTC

NP-MRD ID

NP0265588

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,3r)-3-hydroxy-3,5,5-trimethyl-4-[(3e,5e)-3-methyl-7-oxoocta-1,3,5-trien-1-ylidene]cyclohexyl acetate

Description

Apo-13'-fucoxanthinone belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. Thus, apo-13'-fucoxanthinone is considered to be an isoprenoid. Based on a literature review very few articles have been published on Apo-13'-fucoxanthinone.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 52 52  0  0  0  0  0  0  0  0999 V2000
    5.7192    3.0082   -1.1340 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5814    1.6187   -0.6433 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6049    0.9281   -0.5041 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2355    1.1213   -0.3434 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0468   -0.1108    0.0980 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6953   -0.6132    0.4002 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4674   -1.8149    0.8349 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6770   -2.6939    1.0215 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1981   -2.3812    1.1512 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1580   -1.6443    0.8366 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8081   -0.8347    0.4768 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3002   -1.0326   -0.8830 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1849   -2.5063   -1.2865 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3996   -0.2834   -1.8759 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7064   -0.5707   -1.0453 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2250    0.3009    0.0437 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.1294    1.2364   -0.5464 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4750    1.2716   -0.2227 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4018    2.2678   -0.8608 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8781    0.4338    0.6255 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2126    1.0725    0.8082 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2180    0.1135    1.4799 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1445    0.8430    2.1975 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9815   -0.5766    2.4517 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7572    3.3856   -1.0634 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4046    3.1087   -2.1886 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1101    3.6468   -0.4524 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3609    1.7414   -0.4727 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9086   -0.7500    0.2350 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8545    0.0508    0.2525 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3741   -2.1117    1.6563 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1023   -3.0037    0.0560 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4324   -3.6171    1.5844 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9314   -3.2897    1.5951 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4218   -2.5434   -2.3675 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9568   -3.0696   -0.7537 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1584   -2.8758   -1.1217 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0540    0.6040   -1.4265 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0200   -0.0477   -2.7706 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4238   -0.9439   -2.2196 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7950   -0.0841   -2.0521 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3596   -1.4881   -1.1408 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7680   -0.3591    0.7715 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8466    1.8691   -1.7829 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2391    2.4108   -0.1342 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8854    3.2286   -1.0383 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6917    1.8464    0.2350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7305    1.5816    1.6457 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6609    0.1339    2.4496 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2881    1.7012    1.6521 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5656    1.1953    3.1779 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5429   -1.4736    2.5938 H   0  0  0  0  0  0  0  0  0  0  0  0
 19 18  1  0
 18 20  2  0
 18 17  1  0
 17 16  1  0
 16 15  1  0
 15 12  1  0
 12 13  1  0
 12 14  1  0
 12 11  1  0
 11 10  2  0
 10  9  2  0
  9  7  1  0
  7  8  1  0
  7  6  2  0
  6  5  1  0
  5  4  2  0
  4  2  1  0
  2  1  1  0
  2  3  2  0
 11 22  1  0
 22 23  1  0
 22 24  1  1
 22 21  1  0
 21 16  1  0
 19 44  1  0
 19 45  1  0
 19 46  1  0
 16 43  1  1
 15 41  1  0
 15 42  1  0
 13 35  1  0
 13 36  1  0
 13 37  1  0
 14 38  1  0
 14 39  1  0
 14 40  1  0
  9 34  1  0
  8 31  1  0
  8 32  1  0
  8 33  1  0
  6 30  1  0
  5 29  1  0
  4 28  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
 23 49  1  0
 23 50  1  0
 23 51  1  0
 24 52  1  0
 21 47  1  0
 21 48  1  0
M  END


  Mrv1652309082211372D          

 24 24  0  0  1  0            999 V2000
    5.0013    5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    1.6500    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
    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  0  0  0  0  0  0  0  0  0  0
    2.2414    0.1433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7111   -0.7752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.0000    0.0000 C   0  0  0  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
   -1.4289    0.8250    0.0000 O   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
    0.3272    1.9659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1018    1.9659    0.0000 O   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  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 12 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  6  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 16 21  1  0  0  0  0
 21 22  1  0  0  0  0
 11 22  1  0  0  0  0
 22 23  1  6  0  0  0
 22 24  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0265588

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)O[C@H]1CC(C)(C)C(=C=C\C(C)=C\C=C\C(C)=O)[C@](C)(O)C1

> <INCHI_IDENTIFIER>
InChI=1S/C20H28O4/c1-14(8-7-9-15(2)21)10-11-18-19(4,5)12-17(24-16(3)22)13-20(18,6)23/h7-10,17,23H,12-13H2,1-6H3/b9-7+,14-8+/t11?,17-,20+/m0/s1

> <INCHI_KEY>
ZOBVTHBOBODYBD-IFTLXNJVSA-N

> <FORMULA>
C20H28O4

> <MOLECULAR_WEIGHT>
332.44

> <EXACT_MASS>
332.198759382

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
37.87151484494304

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,3R)-3-hydroxy-3,5,5-trimethyl-4-[(3E,5E)-3-methyl-7-oxoocta-1,3,5-trien-1-ylidene]cyclohexyl acetate

> <JCHEM_LOGP>
2.5157084846666677

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
19.727491112042333

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.073492429233358

> <JCHEM_PKA_STRONGEST_BASIC>
-3.204053990080636

> <JCHEM_POLAR_SURFACE_AREA>
63.60000000000001

> <JCHEM_REFRACTIVITY>
97.95449999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,3R)-3-hydroxy-3,5,5-trimethyl-4-[(3E,5E)-3-methyl-7-oxoocta-1,3,5-trien-1-ylidene]cyclohexyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

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       9.336  10.010   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.002   9.240   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       6.668  10.010   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       8.002   7.700   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.668   6.930   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.668   5.390   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.335   4.620   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.001   5.390   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.335   3.080   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.184   0.267   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.194  -1.447   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -1.334  -0.770   0.000  0.00  0.00           O+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  O   UNK     0      -2.667   1.540   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.611   3.670   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       2.057   3.670   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   22                                                  
CONECT   12   11   13   14   15                                             
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15   12   16                                                       
CONECT   16   15   17   21                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   16   22                                                       
CONECT   22   21   11   23   24                                             
CONECT   23   22                                                            
CONECT   24   22                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   48    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₈O₄

Average Mass

332.4400 Da

Monoisotopic Mass

332.19876 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(=O)O[C@H]1CC(C)(C)C(=C=C\C(C)=C\C=C\C(C)=O)[C@](C)(O)C1

InChI Identifier

InChI=1S/C20H28O4/c1-14(8-7-9-15(2)21)10-11-18-19(4,5)12-17(24-16(3)22)13-20(18,6)23/h7-10,17,23H,12-13H2,1-6H3/b9-7+,14-8+/t11?,17-,20+/m0/s1

InChI Key

ZOBVTHBOBODYBD-IFTLXNJVSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Sesquiterpenoids

Alternative Parents

Substituents

Cyclofarsesane sesquiterpenoid
Sesquiterpenoid
Acryloyl-group
Cyclic alcohol
Alpha,beta-unsaturated ketone
Tertiary alcohol
Enone
Carboxylic acid ester
Ketone
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Carbonyl group
Organooxygen compound
Alcohol
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic homomonocyclic 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

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

10476765

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

21774689

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,3r)-3-hydroxy-3,5,5-trimethyl-4-[(3e,5e)-3-methyl-7-oxoocta-1,3,5-trien-1-ylidene]cyclohexyl acetate (NP0265588)

MOL for NP0265588 ((1s,3r)-3-hydroxy-3,5,5-trimethyl-4-[(3e,5e)-3-methyl-7-oxoocta-1,3,5-trien-1-ylidene]cyclohexyl acetate)

3D MOL for NP0265588 ((1s,3r)-3-hydroxy-3,5,5-trimethyl-4-[(3e,5e)-3-methyl-7-oxoocta-1,3,5-trien-1-ylidene]cyclohexyl acetate)

3D SDF for NP0265588 ((1s,3r)-3-hydroxy-3,5,5-trimethyl-4-[(3e,5e)-3-methyl-7-oxoocta-1,3,5-trien-1-ylidene]cyclohexyl acetate)

3D-SDF for NP0265588 ((1s,3r)-3-hydroxy-3,5,5-trimethyl-4-[(3e,5e)-3-methyl-7-oxoocta-1,3,5-trien-1-ylidene]cyclohexyl acetate)

PDB for NP0265588 ((1s,3r)-3-hydroxy-3,5,5-trimethyl-4-[(3e,5e)-3-methyl-7-oxoocta-1,3,5-trien-1-ylidene]cyclohexyl acetate)

3D PDB for NP0265588 ((1s,3r)-3-hydroxy-3,5,5-trimethyl-4-[(3e,5e)-3-methyl-7-oxoocta-1,3,5-trien-1-ylidene]cyclohexyl acetate)

SMILES for NP0265588 ((1s,3r)-3-hydroxy-3,5,5-trimethyl-4-[(3e,5e)-3-methyl-7-oxoocta-1,3,5-trien-1-ylidene]cyclohexyl acetate)

INCHI for NP0265588 ((1s,3r)-3-hydroxy-3,5,5-trimethyl-4-[(3e,5e)-3-methyl-7-oxoocta-1,3,5-trien-1-ylidene]cyclohexyl acetate)

Structure for NP0265588 ((1s,3r)-3-hydroxy-3,5,5-trimethyl-4-[(3e,5e)-3-methyl-7-oxoocta-1,3,5-trien-1-ylidene]cyclohexyl acetate)

3D Structure for NP0265588 ((1s,3r)-3-hydroxy-3,5,5-trimethyl-4-[(3e,5e)-3-methyl-7-oxoocta-1,3,5-trien-1-ylidene]cyclohexyl acetate)