NP-MRD: Showing NP-Card for (5z)-5-[(2e,4e)-9-(4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-7-methylnona-2,4,6-trien-8-yn-1-ylidene]-3-[2-(1,2,4-trihydroxy-2,6,6-trimethylcyclohexyl)ethenyl]furan-2-one (NP0194148)

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Record Information

Version

2.0

Created at

2022-09-04 11:45:39 UTC

Updated at

2022-09-04 11:45:39 UTC

NP-MRD ID

NP0194148

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(5z)-5-[(2e,4e)-9-(4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-7-methylnona-2,4,6-trien-8-yn-1-ylidene]-3-[2-(1,2,4-trihydroxy-2,6,6-trimethylcyclohexyl)ethenyl]furan-2-one

Description

(5Z)-5-[(2E,4E)-9-(4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-7-methylnona-2,4,6-trien-8-yn-1-ylidene]-3-[2-(1,2,4-trihydroxy-2,6,6-trimethylcyclohexyl)ethenyl]-2,5-dihydrofuran-2-one belongs to the class of organic compounds known as terpene lactones. (5z)-5-[(2e,4e)-9-(4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-7-methylnona-2,4,6-trien-8-yn-1-ylidene]-3-[2-(1,2,4-trihydroxy-2,6,6-trimethylcyclohexyl)ethenyl]furan-2-one is found in Mytilus edulis. These are prenol lipids containing a lactone ring (5Z)-5-[(2E,4E)-9-(4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-7-methylnona-2,4,6-trien-8-yn-1-ylidene]-3-[2-(1,2,4-trihydroxy-2,6,6-trimethylcyclohexyl)ethenyl]-2,5-dihydrofuran-2-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004201503432D          

 40 42  0  0  0  0            999 V2000
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 31 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  1  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1533004201503432D          

 40 42  0  0  0  0            999 V2000
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   -5.7920   -4.8861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6125   -4.7999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0974   -5.4673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3559   -5.8289    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6705   -4.8738    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9866   -4.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0061   -4.1202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4710   -5.0734    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6984   -5.8665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4989   -6.0660    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1253   -6.4599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3248   -6.2603    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5402   -6.5153    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0974   -7.0534    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4656    2.0009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1801    2.4134    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8946    2.8259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6091    2.4134    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6091    1.5884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3235    2.8259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3235    3.6509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0380    4.0634    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6091    4.0634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8946    3.6509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4574    4.3505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0701    3.6797    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
  3  4  1  4  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
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
  9 14  1  0  0  0  0
 15 13  1  4  0  0  0
 15 16  2  0  0  0  0
 16 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
 19 21  1  0  0  0  0
 19 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 17 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
  2 29  1  0  0  0  0
 29 30  3  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 35 37  1  0  0  0  0
 37 38  1  0  0  0  0
 31 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0194148

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=C\C=C\C=C\C=C1/OC(=O)C(C=CC2(O)C(C)(C)CC(O)CC2(C)O)=C1)C#CC1=C(C)CC(O)CC1(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C34H44O6/c1-23(14-15-29-24(2)18-26(35)20-31(29,3)4)12-10-8-9-11-13-28-19-25(30(37)40-28)16-17-34(39)32(5,6)21-27(36)22-33(34,7)38/h8-13,16-17,19,26-27,35-36,38-39H,18,20-22H2,1-7H3/b10-8+,11-9+,17-16?,23-12?,28-13-

> <INCHI_KEY>
DCKASVXEXOVCAV-AWYDGTGXSA-N

> <FORMULA>
C34H44O6

> <MOLECULAR_WEIGHT>
548.72

> <EXACT_MASS>
548.313789137

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
84

> <JCHEM_AVERAGE_POLARIZABILITY>
64.11745291787491

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(5Z)-5-[(2E,4E)-9-(4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-7-methylnona-2,4,6-trien-8-yn-1-ylidene]-3-[2-(1,2,4-trihydroxy-2,6,6-trimethylcyclohexyl)ethenyl]-2,5-dihydrofuran-2-one

> <ALOGPS_LOGP>
5.26

> <JCHEM_LOGP>
3.9361744810000006

> <ALOGPS_LOGS>
-5.36

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.459953465003839

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.896781177249277

> <JCHEM_PKA_STRONGEST_BASIC>
-1.1704723592086674

> <JCHEM_POLAR_SURFACE_AREA>
107.22000000000001

> <JCHEM_REFRACTIVITY>
166.30990000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.39e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(5Z)-5-[(2E,4E)-9-(4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-7-methylnona-2,4,6-trien-8-yn-1-ylidene]-3-[2-(1,2,4-trihydroxy-2,6,6-trimethylcyclohexyl)ethenyl]furan-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 20-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-APR-15         0                                  
HETATM    1  C   UNK     0      -3.802   3.735   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.136   2.965   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -5.136   1.425   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -6.469   0.655   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -6.469  -0.885   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -7.803  -1.655   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -7.803  -3.195   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -9.137  -3.965   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -9.137  -5.505   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -7.891  -6.410   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -8.367  -7.875   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -7.461  -9.121   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -9.907  -7.875   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0     -10.382  -6.410   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0     -10.812  -9.121   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0     -12.343  -8.960   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0     -13.249 -10.206   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0     -11.864 -10.881   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0     -14.318  -9.098   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0     -13.042  -8.237   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0     -14.945  -7.691   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0     -15.813  -9.470   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0     -16.237 -10.951   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0     -17.731 -11.323   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0     -15.167 -12.059   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0     -13.673 -11.686   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0     -12.208 -12.162   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0     -13.249 -13.166   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -6.469   3.735   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -7.803   4.505   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -9.137   5.275   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0     -10.470   4.505   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0     -10.470   2.965   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0     -11.804   5.275   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0     -11.804   6.815   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0     -13.138   7.585   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0     -10.470   7.585   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      -9.137   6.815   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      -8.320   8.121   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      -7.598   6.869   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   29                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   15                                                  
CONECT   14   13    9                                                       
CONECT   15   13   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19   26                                             
CONECT   18   17                                                            
CONECT   19   17   20   21   22                                             
CONECT   20   19                                                            
CONECT   21   19                                                            
CONECT   22   19   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   17   27   28                                             
CONECT   27   26                                                            
CONECT   28   26                                                            
CONECT   29    2   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32   38                                                  
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35                                                       
CONECT   35   34   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35   38                                                       
CONECT   38   37   31   39   40                                             
CONECT   39   38                                                            
CONECT   40   38                                                            
MASTER        0    0    0    0    0    0    0    0   40    0   84    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₄H₄₄O₆

Average Mass

548.7200 Da

Monoisotopic Mass

548.31379 Da

IUPAC Name

(5Z)-5-[(2E,4E)-9-(4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-7-methylnona-2,4,6-trien-8-yn-1-ylidene]-3-[2-(1,2,4-trihydroxy-2,6,6-trimethylcyclohexyl)ethenyl]-2,5-dihydrofuran-2-one

Traditional Name

(5Z)-5-[(2E,4E)-9-(4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-7-methylnona-2,4,6-trien-8-yn-1-ylidene]-3-[2-(1,2,4-trihydroxy-2,6,6-trimethylcyclohexyl)ethenyl]furan-2-one

CAS Registry Number

Not Available

SMILES

CC(=C\C=C\C=C\C=C1/OC(=O)C(C=CC2(O)C(C)(C)CC(O)CC2(C)O)=C1)C#CC1=C(C)CC(O)CC1(C)C

InChI Identifier

InChI=1S/C34H44O6/c1-23(14-15-29-24(2)18-26(35)20-31(29,3)4)12-10-8-9-11-13-28-19-25(30(37)40-28)16-17-34(39)32(5,6)21-27(36)22-33(34,7)38/h8-13,16-17,19,26-27,35-36,38-39H,18,20-22H2,1-7H3/b10-8+,11-9+,17-16?,23-12?,28-13-

InChI Key

DCKASVXEXOVCAV-AWYDGTGXSA-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
Mytilus edulis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Terpene lactones

Alternative Parents

Substituents

Terpene lactone
Cyclofarsesane sesquiterpenoid
Sesquiterpenoid
Cyclohexanol
2-furanone
Cyclitol or derivatives
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tertiary alcohol
Enol ester
Dihydrofuran
Cyclic alcohol
Secondary alcohol
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Polyol
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic 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	5.26	ALOGPS
logP	3.94	ChemAxon
logS	-5.4	ALOGPS
pKa (Strongest Acidic)	12.9	ChemAxon
pKa (Strongest Basic)	-1.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	107.22 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	166.31 m³·mol⁻¹	ChemAxon
Polarizability	64.12 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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 (5z)-5-[(2e,4e)-9-(4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-7-methylnona-2,4,6-trien-8-yn-1-ylidene]-3-[2-(1,2,4-trihydroxy-2,6,6-trimethylcyclohexyl)ethenyl]furan-2-one (NP0194148)

MOL for NP0194148 ((5z)-5-[(2e,4e)-9-(4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-7-methylnona-2,4,6-trien-8-yn-1-ylidene]-3-[2-(1,2,4-trihydroxy-2,6,6-trimethylcyclohexyl)ethenyl]furan-2-one)

3D MOL for NP0194148 ((5z)-5-[(2e,4e)-9-(4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-7-methylnona-2,4,6-trien-8-yn-1-ylidene]-3-[2-(1,2,4-trihydroxy-2,6,6-trimethylcyclohexyl)ethenyl]furan-2-one)

3D SDF for NP0194148 ((5z)-5-[(2e,4e)-9-(4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-7-methylnona-2,4,6-trien-8-yn-1-ylidene]-3-[2-(1,2,4-trihydroxy-2,6,6-trimethylcyclohexyl)ethenyl]furan-2-one)

3D-SDF for NP0194148 ((5z)-5-[(2e,4e)-9-(4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-7-methylnona-2,4,6-trien-8-yn-1-ylidene]-3-[2-(1,2,4-trihydroxy-2,6,6-trimethylcyclohexyl)ethenyl]furan-2-one)

PDB for NP0194148 ((5z)-5-[(2e,4e)-9-(4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-7-methylnona-2,4,6-trien-8-yn-1-ylidene]-3-[2-(1,2,4-trihydroxy-2,6,6-trimethylcyclohexyl)ethenyl]furan-2-one)

3D PDB for NP0194148 ((5z)-5-[(2e,4e)-9-(4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-7-methylnona-2,4,6-trien-8-yn-1-ylidene]-3-[2-(1,2,4-trihydroxy-2,6,6-trimethylcyclohexyl)ethenyl]furan-2-one)

SMILES for NP0194148 ((5z)-5-[(2e,4e)-9-(4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-7-methylnona-2,4,6-trien-8-yn-1-ylidene]-3-[2-(1,2,4-trihydroxy-2,6,6-trimethylcyclohexyl)ethenyl]furan-2-one)

INCHI for NP0194148 ((5z)-5-[(2e,4e)-9-(4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-7-methylnona-2,4,6-trien-8-yn-1-ylidene]-3-[2-(1,2,4-trihydroxy-2,6,6-trimethylcyclohexyl)ethenyl]furan-2-one)

Structure for NP0194148 ((5z)-5-[(2e,4e)-9-(4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-7-methylnona-2,4,6-trien-8-yn-1-ylidene]-3-[2-(1,2,4-trihydroxy-2,6,6-trimethylcyclohexyl)ethenyl]furan-2-one)

3D Structure for NP0194148 ((5z)-5-[(2e,4e)-9-(4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-7-methylnona-2,4,6-trien-8-yn-1-ylidene]-3-[2-(1,2,4-trihydroxy-2,6,6-trimethylcyclohexyl)ethenyl]furan-2-one)