NP-MRD: Showing NP-Card for (4z)-4-[(2e,4r,6e)-8-[(2r,4s,6r,8r,9s)-8-ethyl-4-hydroxy-9-methyl-1,7-dioxaspiro[5.5]undecan-2-yl]-4,6-dimethylocta-2,6-dien-1-ylidene]-6-hydroxy-7-methyl-3h-2-benzopyran-1-one (NP0141613)

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Record Information

Version

2.0

Created at

2022-09-01 19:58:38 UTC

Updated at

2022-09-01 19:58:38 UTC

NP-MRD ID

NP0141613

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(4z)-4-[(2e,4r,6e)-8-[(2r,4s,6r,8r,9s)-8-ethyl-4-hydroxy-9-methyl-1,7-dioxaspiro[5.5]undecan-2-yl]-4,6-dimethylocta-2,6-dien-1-ylidene]-6-hydroxy-7-methyl-3h-2-benzopyran-1-one

Description

(4Z)-4-[(2E,4R,6E)-8-[(2R,4S,6R,8R,9S)-8-ethyl-4-hydroxy-9-methyl-1,7-dioxaspiro[5.5]Undecan-2-yl]-4,6-dimethylocta-2,6-dien-1-ylidene]-6-hydroxy-7-methyl-3,4-dihydro-1H-2-benzopyran-1-one belongs to the class of organic compounds known as 2-benzopyrans. These are organic aromatic compounds that 1-benzopyran, a bicyclic compound made up of a benzene ring fused to a pyran, so that the oxygen atom is at the 2-position. (4z)-4-[(2e,4r,6e)-8-[(2r,4s,6r,8r,9s)-8-ethyl-4-hydroxy-9-methyl-1,7-dioxaspiro[5.5]undecan-2-yl]-4,6-dimethylocta-2,6-dien-1-ylidene]-6-hydroxy-7-methyl-3h-2-benzopyran-1-one is found in Streptomyces bingchenggensis. Based on a literature review very few articles have been published on (4Z)-4-[(2E,4R,6E)-8-[(2R,4S,6R,8R,9S)-8-ethyl-4-hydroxy-9-methyl-1,7-dioxaspiro[5.5]Undecan-2-yl]-4,6-dimethylocta-2,6-dien-1-ylidene]-6-hydroxy-7-methyl-3,4-dihydro-1H-2-benzopyran-1-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309012221582D          

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M  END

     RDKit          3D

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M  END


  Mrv1652309012221582D          

 38 41  0  0  1  0            999 V2000
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   -8.5737   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8592   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8592    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -8.5737    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447    4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302    5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158    4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013    4.5375    0.0000 C   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    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.4315   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  1  0  0  0
  3  4  1  0  0  0  0
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  3  8  1  0  0  0  0
  8  9  1  6  0  0  0
  5 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  1  0  0  0
 11 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
 16 17  2  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
 20 21  1  1  0  0  0
 20 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  2  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
 36 37  2  0  0  0  0
 30 37  1  0  0  0  0
 25 37  1  0  0  0  0
 14 38  1  0  0  0  0
  5 38  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0141613

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@H]1O[C@]2(CC[C@@H]1C)C[C@@H](O)C[C@@H](C\C=C(/C)C[C@@H](C)\C=C\C=C1/COC(=O)C3=CC(C)=C(O)C=C13)O2

> <INCHI_IDENTIFIER>
InChI=1S/C32H44O6/c1-6-30-22(4)12-13-32(38-30)18-25(33)16-26(37-32)11-10-21(3)14-20(2)8-7-9-24-19-36-31(35)28-15-23(5)29(34)17-27(24)28/h7-10,15,17,20,22,25-26,30,33-34H,6,11-14,16,18-19H2,1-5H3/b8-7+,21-10+,24-9+/t20-,22-,25-,26+,30+,32+/m0/s1

> <INCHI_KEY>
SRECUTFLUZBTIJ-XPUZEOAGSA-N

> <FORMULA>
C32H44O6

> <MOLECULAR_WEIGHT>
524.698

> <EXACT_MASS>
524.313789137

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
82

> <JCHEM_AVERAGE_POLARIZABILITY>
59.945625710501794

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(4Z)-4-[(2E,4R,6E)-8-[(2R,4S,6R,8R,9S)-8-ethyl-4-hydroxy-9-methyl-1,7-dioxaspiro[5.5]undecan-2-yl]-4,6-dimethylocta-2,6-dien-1-ylidene]-6-hydroxy-7-methyl-3,4-dihydro-1H-2-benzopyran-1-one

> <ALOGPS_LOGP>
6.20

> <JCHEM_LOGP>
6.799196512333333

> <ALOGPS_LOGS>
-5.71

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.002003707830486

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.732603472542005

> <JCHEM_PKA_STRONGEST_BASIC>
-2.7979236803507854

> <JCHEM_POLAR_SURFACE_AREA>
85.22000000000001

> <JCHEM_REFRACTIVITY>
152.7477

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.02e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(4Z)-4-[(2E,4R,6E)-8-[(2R,4S,6R,8R,9S)-8-ethyl-4-hydroxy-9-methyl-1,7-dioxaspiro[5.5]undecan-2-yl]-4,6-dimethylocta-2,6-dien-1-ylidene]-6-hydroxy-7-methyl-3H-2-benzopyran-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 01-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   01-SEP-22         0                                  
HETATM    1  C   UNK     0     -28.007  -0.770   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -26.674   0.000   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -25.340  -0.770   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0     -24.006   0.000   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0     -22.673  -0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0     -22.673  -2.310   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0     -24.006  -3.080   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0     -25.340  -2.310   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0     -26.674  -3.080   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0     -22.673   0.770   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0     -21.339   1.540   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0     -21.339   3.080   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0     -20.005   0.770   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0     -20.005  -0.770   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0     -18.672  -1.540   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0     -17.338  -0.770   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0     -16.004  -1.540   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0     -16.004  -3.080   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0     -14.670  -0.770   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0     -14.670   0.770   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0     -16.004   1.540   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0     -13.337   1.540   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0     -13.337   3.080   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0     -12.003   3.850   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0     -12.003   5.390   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0     -13.337   6.160   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0     -13.337   7.700   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0     -12.003   8.470   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0     -12.003  10.010   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0     -10.669   7.700   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -9.336   8.470   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -8.002   7.700   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -6.668   8.470   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -8.002   6.160   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      -6.668   5.390   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      -9.336   5.390   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0     -10.669   6.160   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0     -21.339  -1.540   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   10   38                                             
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    3    9                                                  
CONECT    9    8                                                            
CONECT   10    5   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15   38                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   37                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31   37                                                  
CONECT   31   30   32                                                       
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37                                                       
CONECT   37   36   30   25                                                  
CONECT   38   14    5                                                       
MASTER        0    0    0    0    0    0    0    0   38    0   82    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₂H₄₄O₆

Average Mass

524.6980 Da

Monoisotopic Mass

524.31379 Da

IUPAC Name

(4Z)-4-[(2E,4R,6E)-8-[(2R,4S,6R,8R,9S)-8-ethyl-4-hydroxy-9-methyl-1,7-dioxaspiro[5.5]undecan-2-yl]-4,6-dimethylocta-2,6-dien-1-ylidene]-6-hydroxy-7-methyl-3,4-dihydro-1H-2-benzopyran-1-one

Traditional Name

(4Z)-4-[(2E,4R,6E)-8-[(2R,4S,6R,8R,9S)-8-ethyl-4-hydroxy-9-methyl-1,7-dioxaspiro[5.5]undecan-2-yl]-4,6-dimethylocta-2,6-dien-1-ylidene]-6-hydroxy-7-methyl-3H-2-benzopyran-1-one

CAS Registry Number

Not Available

SMILES

CC[C@H]1O[C@]2(CC[C@@H]1C)C[C@@H](O)C[C@@H](C\C=C(/C)C[C@@H](C)\C=C\C=C1/COC(=O)C3=CC(C)=C(O)C=C13)O2

InChI Identifier

InChI=1S/C32H44O6/c1-6-30-22(4)12-13-32(38-30)18-25(33)16-26(37-32)11-10-21(3)14-20(2)8-7-9-24-19-36-31(35)28-15-23(5)29(34)17-27(24)28/h7-10,15,17,20,22,25-26,30,33-34H,6,11-14,16,18-19H2,1-5H3/b8-7+,21-10+,24-9+/t20-,22-,25-,26+,30+,32+/m0/s1

InChI Key

SRECUTFLUZBTIJ-XPUZEOAGSA-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
Streptomyces bingchenggensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 2-benzopyrans. These are organic aromatic compounds that 1-benzopyran, a bicyclic compound made up of a benzene ring fused to a pyran, so that the oxygen atom is at the 2-position.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

2-benzopyrans

Direct Parent

2-benzopyrans

Alternative Parents

Substituents

2-benzopyran
1-hydroxy-2-unsubstituted benzenoid
Ketal
Oxane
Benzenoid
Carboxylic acid ester
Lactone
Secondary alcohol
Monocarboxylic acid or derivatives
Acetal
Carboxylic acid derivative
Oxacycle
Organic oxygen compound
Organooxygen compound
Alcohol
Organic oxide
Hydrocarbon derivative
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	6.2	ALOGPS
logP	6.8	ChemAxon
logS	-5.7	ALOGPS
pKa (Strongest Acidic)	8.73	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	85.22 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	152.75 m³·mol⁻¹	ChemAxon
Polarizability	59.95 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	No	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

78437428

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

24778285

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (4z)-4-[(2e,4r,6e)-8-[(2r,4s,6r,8r,9s)-8-ethyl-4-hydroxy-9-methyl-1,7-dioxaspiro[5.5]undecan-2-yl]-4,6-dimethylocta-2,6-dien-1-ylidene]-6-hydroxy-7-methyl-3h-2-benzopyran-1-one (NP0141613)

MOL for NP0141613 ((4z)-4-[(2e,4r,6e)-8-[(2r,4s,6r,8r,9s)-8-ethyl-4-hydroxy-9-methyl-1,7-dioxaspiro[5.5]undecan-2-yl]-4,6-dimethylocta-2,6-dien-1-ylidene]-6-hydroxy-7-methyl-3h-2-benzopyran-1-one)

3D MOL for NP0141613 ((4z)-4-[(2e,4r,6e)-8-[(2r,4s,6r,8r,9s)-8-ethyl-4-hydroxy-9-methyl-1,7-dioxaspiro[5.5]undecan-2-yl]-4,6-dimethylocta-2,6-dien-1-ylidene]-6-hydroxy-7-methyl-3h-2-benzopyran-1-one)

3D SDF for NP0141613 ((4z)-4-[(2e,4r,6e)-8-[(2r,4s,6r,8r,9s)-8-ethyl-4-hydroxy-9-methyl-1,7-dioxaspiro[5.5]undecan-2-yl]-4,6-dimethylocta-2,6-dien-1-ylidene]-6-hydroxy-7-methyl-3h-2-benzopyran-1-one)

3D-SDF for NP0141613 ((4z)-4-[(2e,4r,6e)-8-[(2r,4s,6r,8r,9s)-8-ethyl-4-hydroxy-9-methyl-1,7-dioxaspiro[5.5]undecan-2-yl]-4,6-dimethylocta-2,6-dien-1-ylidene]-6-hydroxy-7-methyl-3h-2-benzopyran-1-one)

PDB for NP0141613 ((4z)-4-[(2e,4r,6e)-8-[(2r,4s,6r,8r,9s)-8-ethyl-4-hydroxy-9-methyl-1,7-dioxaspiro[5.5]undecan-2-yl]-4,6-dimethylocta-2,6-dien-1-ylidene]-6-hydroxy-7-methyl-3h-2-benzopyran-1-one)

3D PDB for NP0141613 ((4z)-4-[(2e,4r,6e)-8-[(2r,4s,6r,8r,9s)-8-ethyl-4-hydroxy-9-methyl-1,7-dioxaspiro[5.5]undecan-2-yl]-4,6-dimethylocta-2,6-dien-1-ylidene]-6-hydroxy-7-methyl-3h-2-benzopyran-1-one)

SMILES for NP0141613 ((4z)-4-[(2e,4r,6e)-8-[(2r,4s,6r,8r,9s)-8-ethyl-4-hydroxy-9-methyl-1,7-dioxaspiro[5.5]undecan-2-yl]-4,6-dimethylocta-2,6-dien-1-ylidene]-6-hydroxy-7-methyl-3h-2-benzopyran-1-one)

INCHI for NP0141613 ((4z)-4-[(2e,4r,6e)-8-[(2r,4s,6r,8r,9s)-8-ethyl-4-hydroxy-9-methyl-1,7-dioxaspiro[5.5]undecan-2-yl]-4,6-dimethylocta-2,6-dien-1-ylidene]-6-hydroxy-7-methyl-3h-2-benzopyran-1-one)

Structure for NP0141613 ((4z)-4-[(2e,4r,6e)-8-[(2r,4s,6r,8r,9s)-8-ethyl-4-hydroxy-9-methyl-1,7-dioxaspiro[5.5]undecan-2-yl]-4,6-dimethylocta-2,6-dien-1-ylidene]-6-hydroxy-7-methyl-3h-2-benzopyran-1-one)

3D Structure for NP0141613 ((4z)-4-[(2e,4r,6e)-8-[(2r,4s,6r,8r,9s)-8-ethyl-4-hydroxy-9-methyl-1,7-dioxaspiro[5.5]undecan-2-yl]-4,6-dimethylocta-2,6-dien-1-ylidene]-6-hydroxy-7-methyl-3h-2-benzopyran-1-one)