NP-MRD: Showing NP-Card for 5,6,11,15-tetrahydroxy-4-(hydroxymethyl)-8,12-dimethyl-7-oxo-14-(prop-1-en-2-yl)-3-oxatetracyclo[9.4.0.0²,⁴.0⁶,¹⁰]pentadec-8-en-14-yl (2e,4e)-deca-2,4-dienoate (NP0163906)

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Record Information

Version

2.0

Created at

2022-09-02 22:39:58 UTC

Updated at

2022-09-02 22:39:58 UTC

NP-MRD ID

NP0163906

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5,6,11,15-tetrahydroxy-4-(hydroxymethyl)-8,12-dimethyl-7-oxo-14-(prop-1-en-2-yl)-3-oxatetracyclo[9.4.0.0²,⁴.0⁶,¹⁰]pentadec-8-en-14-yl (2e,4e)-deca-2,4-dienoate

Description

Isovesiculosin belongs to the class of organic compounds known as rhamnofolane and daphnane diterpenoids. These are diterpenoids with a structure based on one the rhamnofolane or daphnane skeleton. The rhamnofolane and daphnane skeletons are closely related, being formally derived from casbane by two cyclizations (6,10 and 5,14) followed by cleavage of the 1,15 (daphnane) or 2,15 (rhamnofolane) cyclopropane bonds. 5,6,11,15-tetrahydroxy-4-(hydroxymethyl)-8,12-dimethyl-7-oxo-14-(prop-1-en-2-yl)-3-oxatetracyclo[9.4.0.0²,⁴.0⁶,¹⁰]pentadec-8-en-14-yl (2e,4e)-deca-2,4-dienoate is found in Diarthron vesiculosum. 5,6,11,15-tetrahydroxy-4-(hydroxymethyl)-8,12-dimethyl-7-oxo-14-(prop-1-en-2-yl)-3-oxatetracyclo[9.4.0.0²,⁴.0⁶,¹⁰]pentadec-8-en-14-yl (2e,4e)-deca-2,4-dienoate was first documented in 1985 (PMID: 3839255). Based on a literature review very few articles have been published on Isovesiculosin.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032200392D          

 39 42  0  0  0  0            999 V2000
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    3.0135    4.2800    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4849    2.9524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

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M  END


  Mrv1652309032200392D          

 39 42  0  0  0  0            999 V2000
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    2.3301    1.0245    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9752    0.9137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4088    1.6156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2335    1.5909    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4701    0.2537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0578   -0.3253    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2626   -0.5448    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5409   -1.3215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3527   -1.4687    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5089   -0.8804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4843   -1.7051    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7766   -0.5005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7890   -1.3254    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0561   -0.9023    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9576   -1.7214    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4513   -0.3412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6418   -0.5006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7980    0.4074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6171    0.3090    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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  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
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
  4 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
  4 23  1  0  0  0  0
 23 24  1  0  0  0  0
 22 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 27 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
 34 35  2  0  0  0  0
 34 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  2  0  0  0  0
 38 39  1  0  0  0  0
 32 39  1  0  0  0  0
 20 39  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0163906

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCC\C=C\C=C\C(=O)OC1(CC(C)C2(O)C3C=C(C)C(=O)C3(O)C(O)C3(CO)OC3C2C1O)C(C)=C

> <INCHI_IDENTIFIER>
InChI=1S/C30H42O9/c1-6-7-8-9-10-11-12-13-21(32)38-27(17(2)3)15-19(5)29(36)20-14-18(4)23(33)30(20,37)26(35)28(16-31)25(39-28)22(29)24(27)34/h10-14,19-20,22,24-26,31,34-37H,2,6-9,15-16H2,1,3-5H3/b11-10+,13-12+

> <INCHI_KEY>
YVVNYYRTWOFPMR-AQASXUMVSA-N

> <FORMULA>
C30H42O9

> <MOLECULAR_WEIGHT>
546.657

> <EXACT_MASS>
546.282882932

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
81

> <JCHEM_AVERAGE_POLARIZABILITY>
60.24915176270037

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
5,6,11,15-tetrahydroxy-4-(hydroxymethyl)-8,12-dimethyl-7-oxo-14-(prop-1-en-2-yl)-3-oxatetracyclo[9.4.0.0^{2,4}.0^{6,10}]pentadec-8-en-14-yl (2E,4E)-deca-2,4-dienoate

> <ALOGPS_LOGP>
2.92

> <JCHEM_LOGP>
2.5132619553333333

> <ALOGPS_LOGS>
-3.54

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.054150786365014

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.638485156654916

> <JCHEM_PKA_STRONGEST_BASIC>
-3.1497128696477246

> <JCHEM_POLAR_SURFACE_AREA>
157.05

> <JCHEM_REFRACTIVITY>
145.02990000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.59e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5,6,11,15-tetrahydroxy-4-(hydroxymethyl)-8,12-dimethyl-7-oxo-14-(prop-1-en-2-yl)-3-oxatetracyclo[9.4.0.0^{2,4}.0^{6,10}]pentadec-8-en-14-yl (2E,4E)-deca-2,4-dienoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0      10.112   3.830   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.962   4.855   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.275   6.363   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.500   4.372   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       7.278   5.896   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       5.847   6.465   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       5.625   7.989   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       4.638   5.511   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.208   6.081   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.999   5.127   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.568   5.696   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.641   4.742   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.071   5.312   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -3.280   4.357   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -4.711   4.927   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -5.920   3.973   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.961   4.418   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.151   3.108   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.612   3.154   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.881   1.752   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       4.349   1.912   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       7.420   1.706   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.230   3.016   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       9.769   2.970   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       8.344   0.473   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       9.441  -0.607   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       7.957  -1.017   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       8.476  -2.467   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       9.992  -2.742   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       6.550  -1.643   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       6.504  -3.183   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       5.183  -0.934   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       5.206  -2.474   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       3.838  -1.684   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       3.654  -3.213   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       2.709  -0.637   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       1.198  -0.935   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       3.356   0.761   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       4.885   0.577   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   17   23                                             
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15                                                            
CONECT   17    4   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   22   39                                             
CONECT   21   20                                                            
CONECT   22   20   23   25                                                  
CONECT   23   22    4   24                                                  
CONECT   24   23                                                            
CONECT   25   22   26   27                                                  
CONECT   26   25   27                                                       
CONECT   27   26   25   28   30                                             
CONECT   28   27   29                                                       
CONECT   29   28                                                            
CONECT   30   27   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33   34   39                                             
CONECT   33   32                                                            
CONECT   34   32   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   39                                                       
CONECT   39   38   32   20                                                  
MASTER        0    0    0    0    0    0    0    0   39    0   84    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₄₂O₉

Average Mass

546.6570 Da

Monoisotopic Mass

546.28288 Da

IUPAC Name

5,6,11,15-tetrahydroxy-4-(hydroxymethyl)-8,12-dimethyl-7-oxo-14-(prop-1-en-2-yl)-3-oxatetracyclo[9.4.0.0^{2,4}.0^{6,10}]pentadec-8-en-14-yl (2E,4E)-deca-2,4-dienoate

Traditional Name

5,6,11,15-tetrahydroxy-4-(hydroxymethyl)-8,12-dimethyl-7-oxo-14-(prop-1-en-2-yl)-3-oxatetracyclo[9.4.0.0^{2,4}.0^{6,10}]pentadec-8-en-14-yl (2E,4E)-deca-2,4-dienoate

CAS Registry Number

Not Available

SMILES

CCCCC\C=C\C=C\C(=O)OC1(CC(C)C2(O)C3C=C(C)C(=O)C3(O)C(O)C3(CO)OC3C2C1O)C(C)=C

InChI Identifier

InChI=1S/C30H42O9/c1-6-7-8-9-10-11-12-13-21(32)38-27(17(2)3)15-19(5)29(36)20-14-18(4)23(33)30(20,37)26(35)28(16-31)25(39-28)22(29)24(27)34/h10-14,19-20,22,24-26,31,34-37H,2,6-9,15-16H2,1,3-5H3/b11-10+,13-12+

InChI Key

YVVNYYRTWOFPMR-AQASXUMVSA-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
Diarthron vesiculosum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as rhamnofolane and daphnane diterpenoids. These are diterpenoids with a structure based on one the rhamnofolane or daphnane skeleton. The rhamnofolane and daphnane skeletons are closely related, being formally derived from casbane by two cyclizations (6,10 and 5,14) followed by cleavage of the 1,15 (daphnane) or 2,15 (rhamnofolane) cyclopropane bonds.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Rhamnofolane and daphnane diterpenoids

Alternative Parents

Substituents

Daphnane diterpenoid
Fatty acid ester
Fatty acyl
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tertiary alcohol
Cyclic alcohol
Secondary alcohol
Ketone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Polyol
Monocarboxylic acid or derivatives
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	2.92	ALOGPS
logP	2.51	ChemAxon
logS	-3.5	ALOGPS
pKa (Strongest Acidic)	11.64	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	157.05 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	145.03 m³·mol⁻¹	ChemAxon
Polarizability	60.25 Å³	ChemAxon
Number of Rings	4	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

4585613

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5477991

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Powell RG, Weisleder D, Smith CR Jr: Daphnane diterpenes from Diarthron vesiculosum: vesiculosin and isovesiculosin. J Nat Prod. 1985 Jan-Feb;48(1):102-7. doi: 10.1021/np50037a018. [PubMed:3839255 ]
LOTUS database [Link]

Showing NP-Card for 5,6,11,15-tetrahydroxy-4-(hydroxymethyl)-8,12-dimethyl-7-oxo-14-(prop-1-en-2-yl)-3-oxatetracyclo[9.4.0.0²,⁴.0⁶,¹⁰]pentadec-8-en-14-yl (2e,4e)-deca-2,4-dienoate (NP0163906)

MOL for NP0163906 (5,6,11,15-tetrahydroxy-4-(hydroxymethyl)-8,12-dimethyl-7-oxo-14-(prop-1-en-2-yl)-3-oxatetracyclo[9.4.0.0²,⁴.0⁶,¹⁰]pentadec-8-en-14-yl (2e,4e)-deca-2,4-dienoate)

3D MOL for NP0163906 (5,6,11,15-tetrahydroxy-4-(hydroxymethyl)-8,12-dimethyl-7-oxo-14-(prop-1-en-2-yl)-3-oxatetracyclo[9.4.0.0²,⁴.0⁶,¹⁰]pentadec-8-en-14-yl (2e,4e)-deca-2,4-dienoate)

3D SDF for NP0163906 (5,6,11,15-tetrahydroxy-4-(hydroxymethyl)-8,12-dimethyl-7-oxo-14-(prop-1-en-2-yl)-3-oxatetracyclo[9.4.0.0²,⁴.0⁶,¹⁰]pentadec-8-en-14-yl (2e,4e)-deca-2,4-dienoate)

3D-SDF for NP0163906 (5,6,11,15-tetrahydroxy-4-(hydroxymethyl)-8,12-dimethyl-7-oxo-14-(prop-1-en-2-yl)-3-oxatetracyclo[9.4.0.0²,⁴.0⁶,¹⁰]pentadec-8-en-14-yl (2e,4e)-deca-2,4-dienoate)

PDB for NP0163906 (5,6,11,15-tetrahydroxy-4-(hydroxymethyl)-8,12-dimethyl-7-oxo-14-(prop-1-en-2-yl)-3-oxatetracyclo[9.4.0.0²,⁴.0⁶,¹⁰]pentadec-8-en-14-yl (2e,4e)-deca-2,4-dienoate)

3D PDB for NP0163906 (5,6,11,15-tetrahydroxy-4-(hydroxymethyl)-8,12-dimethyl-7-oxo-14-(prop-1-en-2-yl)-3-oxatetracyclo[9.4.0.0²,⁴.0⁶,¹⁰]pentadec-8-en-14-yl (2e,4e)-deca-2,4-dienoate)

SMILES for NP0163906 (5,6,11,15-tetrahydroxy-4-(hydroxymethyl)-8,12-dimethyl-7-oxo-14-(prop-1-en-2-yl)-3-oxatetracyclo[9.4.0.0²,⁴.0⁶,¹⁰]pentadec-8-en-14-yl (2e,4e)-deca-2,4-dienoate)

INCHI for NP0163906 (5,6,11,15-tetrahydroxy-4-(hydroxymethyl)-8,12-dimethyl-7-oxo-14-(prop-1-en-2-yl)-3-oxatetracyclo[9.4.0.0²,⁴.0⁶,¹⁰]pentadec-8-en-14-yl (2e,4e)-deca-2,4-dienoate)

Structure for NP0163906 (5,6,11,15-tetrahydroxy-4-(hydroxymethyl)-8,12-dimethyl-7-oxo-14-(prop-1-en-2-yl)-3-oxatetracyclo[9.4.0.0²,⁴.0⁶,¹⁰]pentadec-8-en-14-yl (2e,4e)-deca-2,4-dienoate)

3D Structure for NP0163906 (5,6,11,15-tetrahydroxy-4-(hydroxymethyl)-8,12-dimethyl-7-oxo-14-(prop-1-en-2-yl)-3-oxatetracyclo[9.4.0.0²,⁴.0⁶,¹⁰]pentadec-8-en-14-yl (2e,4e)-deca-2,4-dienoate)