NP-MRD: Showing NP-Card for 3-{1'-[1-(3,4-dimethyl-5-oxo-2h-furan-2-yl)propan-2-yl]-2,7'-dihydroxy-3'a,4,4,7a,7'a-pentamethyl-4'-oxo-decahydro-1'h-1,5'-spirobi[inden]-5-yloxy}-3-oxopropanoic acid (NP0209263)

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Record Information

Version

2.0

Created at

2022-09-05 06:36:15 UTC

Updated at

2022-09-05 06:36:15 UTC

NP-MRD ID

NP0209263

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-{1'-[1-(3,4-dimethyl-5-oxo-2h-furan-2-yl)propan-2-yl]-2,7'-dihydroxy-3'a,4,4,7a,7'a-pentamethyl-4'-oxo-decahydro-1'h-1,5'-spirobi[inden]-5-yloxy}-3-oxopropanoic acid

Description

3-{1'-[1-(3,4-Dimethyl-5-oxo-2,5-dihydrofuran-2-yl)propan-2-yl]-2,7'-dihydroxy-3'a,4,4,7a,7'a-pentamethyl-4'-oxo-hexadecahydro-1,5'-spirobi[indene]-5-yloxy}-3-oxopropanoic acid belongs to the class of organic compounds known as tricarboxylic acids and derivatives. These are carboxylic acids containing exactly three carboxyl groups. 3-{1'-[1-(3,4-dimethyl-5-oxo-2h-furan-2-yl)propan-2-yl]-2,7'-dihydroxy-3'a,4,4,7a,7'a-pentamethyl-4'-oxo-decahydro-1'h-1,5'-spirobi[inden]-5-yloxy}-3-oxopropanoic acid is found in Fomitopsis officinalis. Based on a literature review very few articles have been published on 3-{1'-[1-(3,4-dimethyl-5-oxo-2,5-dihydrofuran-2-yl)propan-2-yl]-2,7'-dihydroxy-3'a,4,4,7a,7'a-pentamethyl-4'-oxo-hexadecahydro-1,5'-spirobi[indene]-5-yloxy}-3-oxopropanoic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052208362D          

 43 47  0  0  0  0            999 V2000
    7.1522    4.4635    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4979    3.9610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  5 41  1  0  0  0  0
 41 42  1  0  0  0  0
  2 42  1  0  0  0  0
 42 43  2  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652309052208362D          

 43 47  0  0  0  0            999 V2000
    7.1522    4.4635    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4979    3.9610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5198    3.1363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1999    2.6693    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7422    2.8606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5082    2.0695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7061    1.8766    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1380    2.4748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4721    1.0855    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9746    0.4312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5076   -0.2489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7165   -0.0149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8245   -0.8328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0132   -0.4463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0352   -1.2710    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2880   -0.0529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2661    0.7718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9694    1.2031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9474    2.0278    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6946    0.8098    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7590    1.6322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2236   -0.8754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6550   -1.5787    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4215   -1.0683    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9902   -0.3651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1789   -0.2151    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1721   -1.0400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6347   -0.3515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0968    0.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9080    0.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1837    1.4901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6482    2.1177    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9950    1.6401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2707    2.4177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0819    2.5677    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7351    3.0452    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4388    1.1901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2500    1.0401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5257    0.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9191    0.9877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2397    3.5149    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7068    4.1950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4311    4.9726    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
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  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
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 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
  9 20  1  0  0  0  0
 12 20  1  0  0  0  0
 20 21  1  0  0  0  0
 16 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 26 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 34 36  1  0  0  0  0
 29 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 25 39  1  0  0  0  0
 16 39  1  0  0  0  0
 39 40  1  0  0  0  0
  5 41  1  0  0  0  0
 41 42  1  0  0  0  0
  2 42  1  0  0  0  0
 42 43  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0209263

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(CC1OC(=O)C(C)=C1C)C1CCC2(C)C(=O)C3(CC(O)C12C)C(O)CC1C3(C)CCC(OC(=O)CC(O)=O)C1(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C34H50O9/c1-17(13-21-18(2)19(3)28(40)42-21)20-9-11-32(7)29(41)34(16-24(36)33(20,32)8)23(35)14-22-30(4,5)25(10-12-31(22,34)6)43-27(39)15-26(37)38/h17,20-25,35-36H,9-16H2,1-8H3,(H,37,38)

> <INCHI_KEY>
UDBAOVMCUDEARR-UHFFFAOYSA-N

> <FORMULA>
C34H50O9

> <MOLECULAR_WEIGHT>
602.765

> <EXACT_MASS>
602.34548319

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
93

> <JCHEM_AVERAGE_POLARIZABILITY>
65.86918897663168

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3-{1'-[1-(3,4-dimethyl-5-oxo-2,5-dihydrofuran-2-yl)propan-2-yl]-2,7'-dihydroxy-3'a,4,4,7a,7'a-pentamethyl-4'-oxo-hexadecahydro-1,5'-spirobi[indene]-5-yloxy}-3-oxopropanoic acid

> <JCHEM_LOGP>
4.987367837333332

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
13.587084392946874

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.113010847581585

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9606616525825764

> <JCHEM_POLAR_SURFACE_AREA>
147.43

> <JCHEM_REFRACTIVITY>
157.1819

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
3-{1'-[1-(3,4-dimethyl-5-oxo-2H-furan-2-yl)propan-2-yl]-2,7'-dihydroxy-3'a,4,4,7a,7'a-pentamethyl-4'-oxo-decahydro-1'H-1,5'-spirobi[indene]-5-yloxy}-3-oxopropanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0      13.351   8.332   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.129   7.394   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      12.170   5.854   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      13.440   4.983   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.719   5.340   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.282   3.863   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.785   3.503   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.724   4.620   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.348   2.026   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.286   0.805   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.414  -0.465   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.937  -0.028   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.139  -1.555   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.625  -0.833   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       5.666  -2.373   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       4.271  -0.099   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.230   1.441   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.543   2.246   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       5.502   3.785   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       6.896   1.512   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.017   3.047   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.151  -1.634   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       4.956  -2.947   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       2.654  -1.994   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.848  -0.681   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.334  -0.401   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.321  -1.941   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -1.185  -0.656   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -0.181   1.050   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -1.695   1.330   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      -2.210   2.782   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      -1.210   3.953   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      -3.724   3.062   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -4.239   4.513   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      -5.753   4.793   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0      -3.239   5.684   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       0.819   2.221   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       2.333   1.941   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       2.848   0.490   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       3.582   1.844   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       9.781   6.561   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0      10.653   7.831   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      10.138   9.282   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   42                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   41                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   20                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14   20                                             
CONECT   13   12                                                            
CONECT   14   12   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   22   39                                             
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18    9   12   21                                             
CONECT   21   20                                                            
CONECT   22   16   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26   39                                                  
CONECT   26   25   27   28   29                                             
CONECT   27   26                                                            
CONECT   28   26                                                            
CONECT   29   26   30   37                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34                                                       
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34                                                            
CONECT   37   29   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   25   16   40                                             
CONECT   40   39                                                            
CONECT   41    5   42                                                       
CONECT   42   41    2   43                                                  
CONECT   43   42                                                            
MASTER        0    0    0    0    0    0    0    0   43    0   94    0
END

View in JSmol

Synonyms

Value	Source
3-{1'-[1-(3,4-dimethyl-5-oxo-2,5-dihydrofuran-2-yl)propan-2-yl]-2,7'-dihydroxy-3'a,4,4,7a,7'a-pentamethyl-4'-oxo-hexadecahydro-1,5'-spirobi[indene]-5-yloxy}-3-oxopropanoate	Generator

Chemical Formula

C₃₄H₅₀O₉

Average Mass

602.7650 Da

Monoisotopic Mass

602.34548 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(CC1OC(=O)C(C)=C1C)C1CCC2(C)C(=O)C3(CC(O)C12C)C(O)CC1C3(C)CCC(OC(=O)CC(O)=O)C1(C)C

InChI Identifier

InChI=1S/C34H50O9/c1-17(13-21-18(2)19(3)28(40)42-21)20-9-11-32(7)29(41)34(16-24(36)33(20,32)8)23(35)14-22-30(4,5)25(10-12-31(22,34)6)43-27(39)15-26(37)38/h17,20-25,35-36H,9-16H2,1-8H3,(H,37,38)

InChI Key

UDBAOVMCUDEARR-UHFFFAOYSA-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
Fomitopsis officinalis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tricarboxylic acids and derivatives. These are carboxylic acids containing exactly three carboxyl groups.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Tricarboxylic acids and derivatives

Direct Parent

Tricarboxylic acids and derivatives

Alternative Parents

Substituents

Tricarboxylic acid or derivatives
1,3-dicarbonyl compound
2-furanone
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Dihydrofuran
Cyclic alcohol
Secondary alcohol
Lactone
Ketone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Carboxylic acid
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
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

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

162969933

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-{1'-[1-(3,4-dimethyl-5-oxo-2h-furan-2-yl)propan-2-yl]-2,7'-dihydroxy-3'a,4,4,7a,7'a-pentamethyl-4'-oxo-decahydro-1'h-1,5'-spirobi[inden]-5-yloxy}-3-oxopropanoic acid (NP0209263)

MOL for NP0209263 (3-{1'-[1-(3,4-dimethyl-5-oxo-2h-furan-2-yl)propan-2-yl]-2,7'-dihydroxy-3'a,4,4,7a,7'a-pentamethyl-4'-oxo-decahydro-1'h-1,5'-spirobi[inden]-5-yloxy}-3-oxopropanoic acid)

3D MOL for NP0209263 (3-{1'-[1-(3,4-dimethyl-5-oxo-2h-furan-2-yl)propan-2-yl]-2,7'-dihydroxy-3'a,4,4,7a,7'a-pentamethyl-4'-oxo-decahydro-1'h-1,5'-spirobi[inden]-5-yloxy}-3-oxopropanoic acid)

3D SDF for NP0209263 (3-{1'-[1-(3,4-dimethyl-5-oxo-2h-furan-2-yl)propan-2-yl]-2,7'-dihydroxy-3'a,4,4,7a,7'a-pentamethyl-4'-oxo-decahydro-1'h-1,5'-spirobi[inden]-5-yloxy}-3-oxopropanoic acid)

3D-SDF for NP0209263 (3-{1'-[1-(3,4-dimethyl-5-oxo-2h-furan-2-yl)propan-2-yl]-2,7'-dihydroxy-3'a,4,4,7a,7'a-pentamethyl-4'-oxo-decahydro-1'h-1,5'-spirobi[inden]-5-yloxy}-3-oxopropanoic acid)

PDB for NP0209263 (3-{1'-[1-(3,4-dimethyl-5-oxo-2h-furan-2-yl)propan-2-yl]-2,7'-dihydroxy-3'a,4,4,7a,7'a-pentamethyl-4'-oxo-decahydro-1'h-1,5'-spirobi[inden]-5-yloxy}-3-oxopropanoic acid)

3D PDB for NP0209263 (3-{1'-[1-(3,4-dimethyl-5-oxo-2h-furan-2-yl)propan-2-yl]-2,7'-dihydroxy-3'a,4,4,7a,7'a-pentamethyl-4'-oxo-decahydro-1'h-1,5'-spirobi[inden]-5-yloxy}-3-oxopropanoic acid)

SMILES for NP0209263 (3-{1'-[1-(3,4-dimethyl-5-oxo-2h-furan-2-yl)propan-2-yl]-2,7'-dihydroxy-3'a,4,4,7a,7'a-pentamethyl-4'-oxo-decahydro-1'h-1,5'-spirobi[inden]-5-yloxy}-3-oxopropanoic acid)

INCHI for NP0209263 (3-{1'-[1-(3,4-dimethyl-5-oxo-2h-furan-2-yl)propan-2-yl]-2,7'-dihydroxy-3'a,4,4,7a,7'a-pentamethyl-4'-oxo-decahydro-1'h-1,5'-spirobi[inden]-5-yloxy}-3-oxopropanoic acid)

Structure for NP0209263 (3-{1'-[1-(3,4-dimethyl-5-oxo-2h-furan-2-yl)propan-2-yl]-2,7'-dihydroxy-3'a,4,4,7a,7'a-pentamethyl-4'-oxo-decahydro-1'h-1,5'-spirobi[inden]-5-yloxy}-3-oxopropanoic acid)

3D Structure for NP0209263 (3-{1'-[1-(3,4-dimethyl-5-oxo-2h-furan-2-yl)propan-2-yl]-2,7'-dihydroxy-3'a,4,4,7a,7'a-pentamethyl-4'-oxo-decahydro-1'h-1,5'-spirobi[inden]-5-yloxy}-3-oxopropanoic acid)