NP-MRD: Showing NP-Card for (1r,2r,2'r,4r,4as,5r,5's,6r,8ar)-5'-(furan-3-yl)-2',4-dihydroxy-2,4a,5,8a-tetrakis(hydroxymethyl)-6-{[(2e)-2-methylbut-2-enoyl]oxy}-hexahydrospiro[naphthalene-1,3'-oxolan]-5-ylacetic acid (NP0208308)

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Record Information

Version

1.0

Created at

2022-09-05 05:15:27 UTC

Updated at

2022-09-05 05:15:27 UTC

NP-MRD ID

NP0208308

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2r,2'r,4r,4as,5r,5's,6r,8ar)-5'-(furan-3-yl)-2',4-dihydroxy-2,4a,5,8a-tetrakis(hydroxymethyl)-6-{[(2e)-2-methylbut-2-enoyl]oxy}-hexahydrospiro[naphthalene-1,3'-oxolan]-5-ylacetic acid

Description

Musabalbisiane C belongs to the class of organic compounds known as colensane and clerodane diterpenoids. These are diterpenoids with a structure based on the clerodane or the colensane skeleton. Clerodanes arise from labdanes by two methyl migrations. Musabalbisiane C is an extremely weak basic (essentially neutral) compound (based on its pKa). Outside of the human body, Musabalbisiane C has been detected, but not quantified in, fruits. It was first documented in 2000 (PMID: 11413487). This could make musabalbisiane C a potential biomarker for the consumption of these foods (PMID: 16902246) (PMID: 17374880) (PMID: 20044567).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv0541 01291301542D          

 40 43  0  0  0  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv0541 01291301542D          

 40 43  0  0  0  0            999 V2000
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   -7.1511   -6.8187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1739   -3.0006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9937   -2.9077    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3199   -3.9368    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3430   -4.9918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6286   -4.5793    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6694   -2.2299    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0819   -0.9604    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7493   -1.4453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4944   -2.2299    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4145   -1.4453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3444   -5.4044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0588   -5.8169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3443   -4.5794    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7733   -5.4044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0588   -6.6419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7733   -7.0544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9533   -6.6264    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  1  6  1  0  0  0  0
 10  6  1  0  0  0  0
  6  5  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
 10  9  1  0  0  0  0
 10 11  1  1  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 10 14  1  0  0  0  0
  7 15  1  1  0  0  0
  5 16  1  1  0  0  0
  3 17  1  6  0  0  0
  4 18  1  0  0  0  0
 16 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
  4 23  1  6  0  0  0
  6 24  1  1  0  0  0
 24 25  1  0  0  0  0
 14 26  1  1  0  0  0
  9 27  1  6  0  0  0
 27 28  1  0  0  0  0
 12 29  1  1  0  0  0
 32 29  1  0  0  0  0
 29 33  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 30 33  1  0  0  0  0
 17 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  2  0  0  0  0
 35 37  1  0  0  0  0
 35 38  2  0  0  0  0
 38 39  1  0  0  0  0
 23 40  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0208308

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C=C(/C)C(=O)O[C@@H]1CC[C@]2(CO)[C@@]3(C[C@H](O[C@H]3O)C3=COC=C3)[C@H](CO)C[C@@H](O)[C@]2(CO)[C@@]1(CO)CC(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C28H40O12/c1-3-16(2)23(36)40-21-4-6-26(14-31)27(9-19(39-24(27)37)17-5-7-38-12-17)18(11-29)8-20(33)28(26,15-32)25(21,13-30)10-22(34)35/h3,5,7,12,18-21,24,29-33,37H,4,6,8-11,13-15H2,1-2H3,(H,34,35)/b16-3+/t18-,19-,20+,21+,24+,25+,26-,27-,28+/m0/s1

> <INCHI_KEY>
CPJNTZBFGMGXON-DFBMNNFESA-N

> <FORMULA>
C28H40O12

> <MOLECULAR_WEIGHT>
568.61

> <EXACT_MASS>
568.251976744

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_AVERAGE_POLARIZABILITY>
58.134241772200006

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-[(1R,2R,2'R,4R,4aS,5R,5'S,6R,8aR)-5'-(furan-3-yl)-2',4-dihydroxy-2,4a,5,8a-tetrakis(hydroxymethyl)-6-{[(2E)-2-methylbut-2-enoyl]oxy}-octahydro-2H-spiro[naphthalene-1,3'-oxolane]-5-yl]acetic acid

> <ALOGPS_LOGP>
-0.53

> <JCHEM_LOGP>
-1.148204747000002

> <ALOGPS_LOGS>
-1.76

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
11.90440897750674

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.042923216656388

> <JCHEM_PKA_STRONGEST_BASIC>
-2.6066561070473266

> <JCHEM_POLAR_SURFACE_AREA>
207.35

> <JCHEM_REFRACTIVITY>
138.5726

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
9.88e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,2'R,4R,4aS,5R,5'S,6R,8aR)-5'-(furan-3-yl)-2',4-dihydroxy-2,4a,5,8a-tetrakis(hydroxymethyl)-6-{[(2E)-2-methylbut-2-enoyl]oxy}-hexahydrospiro[naphthalene-1,3'-oxolane]-5-ylacetic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-JAN-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-JAN-13         0                                  
HETATM    1  C   UNK     0     -11.575  -7.778   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -12.909  -8.548   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -12.909 -10.088   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0     -11.575 -10.858   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0     -10.241 -10.088   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0     -10.241  -8.548   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -8.908 -10.858   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -7.574 -10.088   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -7.574  -8.548   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -8.908  -7.778   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0     -10.154  -6.873   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -9.678  -5.408   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -8.138  -5.408   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -7.662  -6.873   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -8.908 -12.398   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0     -10.315 -16.395   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0     -14.242 -10.858   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0     -11.648 -14.452   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -8.990 -17.180   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0     -13.761 -15.955   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0     -13.616 -17.488   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0     -15.162 -15.315   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0     -13.349 -12.728   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0     -11.525  -5.601   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0     -13.055  -5.428   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0      -6.197  -7.349   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -6.240  -9.318   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -4.907  -8.548   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0     -10.583  -4.162   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0     -11.353  -1.793   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0     -12.599  -2.698   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0     -12.123  -4.162   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0     -10.107  -2.698   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0     -15.576 -10.088   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0     -16.910 -10.858   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0     -15.576  -8.548   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0     -18.243 -10.088   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0     -16.910 -12.398   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0     -18.243 -13.168   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0     -14.846 -12.369   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4   17                                                  
CONECT    4    3    5   18   23                                             
CONECT    5    4    6    7   16                                             
CONECT    6    1   10    5   24                                             
CONECT    7    5    8   15                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   27                                                  
CONECT   10    6    9   11   14                                             
CONECT   11   10   12                                                       
CONECT   12   11   13   29                                                  
CONECT   13   12   14                                                       
CONECT   14   13   10   26                                                  
CONECT   15    7                                                            
CONECT   16    5   19                                                       
CONECT   17    3   34                                                       
CONECT   18    4   20                                                       
CONECT   19   16                                                            
CONECT   20   18   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23    4   40                                                       
CONECT   24    6   25                                                       
CONECT   25   24                                                            
CONECT   26   14                                                            
CONECT   27    9   28                                                       
CONECT   28   27                                                            
CONECT   29   12   32   33                                                  
CONECT   30   31   33                                                       
CONECT   31   30   32                                                       
CONECT   32   29   31                                                       
CONECT   33   29   30                                                       
CONECT   34   17   35   36                                                  
CONECT   35   34   37   38                                                  
CONECT   36   34                                                            
CONECT   37   35                                                            
CONECT   38   35   39                                                       
CONECT   39   38                                                            
CONECT   40   23                                                            
MASTER        0    0    0    0    0    0    0    0   40    0   86    0
END

View in JSmol

Synonyms

Value	Source
3-(1,3-Dioxobutyl)oxazolidin-2-one	HMDB
3-Acetoacetyl-1,3-oxazolidin-2-one	HMDB
2-[(1R,2R,2'r,4R,4AS,5R,5's,6R,8ar)-5'-(furan-3-yl)-2',4-dihydroxy-2,4a,5,8a-tetrakis(hydroxymethyl)-6-[(2-methylbut-2-enoyl)oxy]-octahydro-2H-spiro[naphthalene-1,3'-oxolane]-5-yl]acetate	Generator

Chemical Formula

C₂₈H₄₀O₁₂

Average Mass

568.6100 Da

Monoisotopic Mass

568.25198 Da

IUPAC Name

2-[(1R,2R,2'R,4R,4aS,5R,5'S,6R,8aR)-5'-(furan-3-yl)-2',4-dihydroxy-2,4a,5,8a-tetrakis(hydroxymethyl)-6-{[(2E)-2-methylbut-2-enoyl]oxy}-octahydro-2H-spiro[naphthalene-1,3'-oxolane]-5-yl]acetic acid

Traditional Name

(1R,2R,2'R,4R,4aS,5R,5'S,6R,8aR)-5'-(furan-3-yl)-2',4-dihydroxy-2,4a,5,8a-tetrakis(hydroxymethyl)-6-{[(2E)-2-methylbut-2-enoyl]oxy}-hexahydrospiro[naphthalene-1,3'-oxolane]-5-ylacetic acid

CAS Registry Number

Not Available

SMILES

C\C=C(/C)C(=O)O[C@@H]1CC[C@]2(CO)[C@@]3(C[C@H](O[C@H]3O)C3=COC=C3)[C@H](CO)C[C@@H](O)[C@]2(CO)[C@@]1(CO)CC(O)=O

InChI Identifier

InChI=1S/C28H40O12/c1-3-16(2)23(36)40-21-4-6-26(14-31)27(9-19(39-24(27)37)17-5-7-38-12-17)18(11-29)8-20(33)28(26,15-32)25(21,13-30)10-22(34)35/h3,5,7,12,18-21,24,29-33,37H,4,6,8-11,13-15H2,1-2H3,(H,34,35)/b16-3+/t18-,19-,20+,21+,24+,25+,26-,27-,28+/m0/s1

InChI Key

CPJNTZBFGMGXON-DFBMNNFESA-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 colensane and clerodane diterpenoids. These are diterpenoids with a structure based on the clerodane or the colensane skeleton. Clerodanes arise from labdanes by two methyl migrations.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Colensane and clerodane diterpenoids

Alternative Parents

Substituents

Clerodane diterpenoid
Fatty acid ester
Dicarboxylic acid or derivatives
Fatty acyl
Cyclic alcohol
Heteroaromatic compound
Furan
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tetrahydrofuran
Carboxylic acid ester
Secondary alcohol
Hemiacetal
Carboxylic acid derivative
Carboxylic acid
Oxacycle
Organoheterocyclic compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Carbonyl group
Alcohol
Primary alcohol
Organooxygen compound
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	-0.53	ALOGPS
logP	-1.1	ChemAxon
logS	-1.8	ALOGPS
pKa (Strongest Acidic)	4.04	ChemAxon
pKa (Strongest Basic)	-2.6	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	207.35 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	138.57 m³·mol⁻¹	ChemAxon
Polarizability	58.13 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

HMDB0038682

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB018086

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

131752424

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. [PubMed:11413487 ]
Watson AD: Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Lipidomics: a global approach to lipid analysis in biological systems. J Lipid Res. 2006 Oct;47(10):2101-11. Epub 2006 Aug 10. [PubMed:16902246 ]
Sethi JK, Vidal-Puig AJ: Thematic review series: adipocyte biology. Adipose tissue function and plasticity orchestrate nutritional adaptation. J Lipid Res. 2007 Jun;48(6):1253-62. Epub 2007 Mar 20. [PubMed:17374880 ]
Lingwood D, Simons K: Lipid rafts as a membrane-organizing principle. Science. 2010 Jan 1;327(5961):46-50. doi: 10.1126/science.1174621. [PubMed:20044567 ]
LOTUS database [Link]

Showing NP-Card for (1r,2r,2'r,4r,4as,5r,5's,6r,8ar)-5'-(furan-3-yl)-2',4-dihydroxy-2,4a,5,8a-tetrakis(hydroxymethyl)-6-{[(2e)-2-methylbut-2-enoyl]oxy}-hexahydrospiro[naphthalene-1,3'-oxolan]-5-ylacetic acid (NP0208308)

MOL for NP0208308 ((1r,2r,2'r,4r,4as,5r,5's,6r,8ar)-5'-(furan-3-yl)-2',4-dihydroxy-2,4a,5,8a-tetrakis(hydroxymethyl)-6-{[(2e)-2-methylbut-2-enoyl]oxy}-hexahydrospiro[naphthalene-1,3'-oxolan]-5-ylacetic acid)

3D MOL for NP0208308 ((1r,2r,2'r,4r,4as,5r,5's,6r,8ar)-5'-(furan-3-yl)-2',4-dihydroxy-2,4a,5,8a-tetrakis(hydroxymethyl)-6-{[(2e)-2-methylbut-2-enoyl]oxy}-hexahydrospiro[naphthalene-1,3'-oxolan]-5-ylacetic acid)

3D SDF for NP0208308 ((1r,2r,2'r,4r,4as,5r,5's,6r,8ar)-5'-(furan-3-yl)-2',4-dihydroxy-2,4a,5,8a-tetrakis(hydroxymethyl)-6-{[(2e)-2-methylbut-2-enoyl]oxy}-hexahydrospiro[naphthalene-1,3'-oxolan]-5-ylacetic acid)

3D-SDF for NP0208308 ((1r,2r,2'r,4r,4as,5r,5's,6r,8ar)-5'-(furan-3-yl)-2',4-dihydroxy-2,4a,5,8a-tetrakis(hydroxymethyl)-6-{[(2e)-2-methylbut-2-enoyl]oxy}-hexahydrospiro[naphthalene-1,3'-oxolan]-5-ylacetic acid)

PDB for NP0208308 ((1r,2r,2'r,4r,4as,5r,5's,6r,8ar)-5'-(furan-3-yl)-2',4-dihydroxy-2,4a,5,8a-tetrakis(hydroxymethyl)-6-{[(2e)-2-methylbut-2-enoyl]oxy}-hexahydrospiro[naphthalene-1,3'-oxolan]-5-ylacetic acid)

3D PDB for NP0208308 ((1r,2r,2'r,4r,4as,5r,5's,6r,8ar)-5'-(furan-3-yl)-2',4-dihydroxy-2,4a,5,8a-tetrakis(hydroxymethyl)-6-{[(2e)-2-methylbut-2-enoyl]oxy}-hexahydrospiro[naphthalene-1,3'-oxolan]-5-ylacetic acid)

SMILES for NP0208308 ((1r,2r,2'r,4r,4as,5r,5's,6r,8ar)-5'-(furan-3-yl)-2',4-dihydroxy-2,4a,5,8a-tetrakis(hydroxymethyl)-6-{[(2e)-2-methylbut-2-enoyl]oxy}-hexahydrospiro[naphthalene-1,3'-oxolan]-5-ylacetic acid)

INCHI for NP0208308 ((1r,2r,2'r,4r,4as,5r,5's,6r,8ar)-5'-(furan-3-yl)-2',4-dihydroxy-2,4a,5,8a-tetrakis(hydroxymethyl)-6-{[(2e)-2-methylbut-2-enoyl]oxy}-hexahydrospiro[naphthalene-1,3'-oxolan]-5-ylacetic acid)

Structure for NP0208308 ((1r,2r,2'r,4r,4as,5r,5's,6r,8ar)-5'-(furan-3-yl)-2',4-dihydroxy-2,4a,5,8a-tetrakis(hydroxymethyl)-6-{[(2e)-2-methylbut-2-enoyl]oxy}-hexahydrospiro[naphthalene-1,3'-oxolan]-5-ylacetic acid)

3D Structure for NP0208308 ((1r,2r,2'r,4r,4as,5r,5's,6r,8ar)-5'-(furan-3-yl)-2',4-dihydroxy-2,4a,5,8a-tetrakis(hydroxymethyl)-6-{[(2e)-2-methylbut-2-enoyl]oxy}-hexahydrospiro[naphthalene-1,3'-oxolan]-5-ylacetic acid)