NP-MRD: Showing NP-Card for Gaudichaudione E (NP0084056)

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Record Information

Version

2.0

Created at

2022-04-29 04:54:39 UTC

Updated at

2022-04-29 04:54:39 UTC

NP-MRD ID

NP0084056

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Gaudichaudione E

Description

Gaudichaudione E is found in Garcinia gaudichaudii. Based on a literature review very few articles have been published on 2-(1-Methyl-1-hydroxyethyl)-4-hydroxy-9-[(E)-3-formyl-2-butenyl]-11-(3-methyl-2-butenyl)-13,13-dimethyl-9beta,9abeta,7beta-(epoxy[1,2,3]propanetriyl)-2,3,9,9a-tetrahydro-5H-furo[3,2-b]xanthene-5,8(7H)-dione.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292206542D          

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M  END

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M  END


  Mrv1652304292206542D          

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    2.2294   -1.4315    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4802   -2.0045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7185   -1.6875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6122   -0.8694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0632   -2.1886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1695   -3.0068    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1043   -1.3601    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8445   -1.4182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7046   -1.1426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0639   -2.3762    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0863   -0.7674    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2742   -0.1229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0669    1.8754    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  3  2  1  1  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  8 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
 14 16  1  0  0  0  0
 14 17  1  0  0  0  0
 13 18  1  0  0  0  0
 10 18  1  0  0  0  0
 11 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 19 25  2  0  0  0  0
  7 25  1  0  0  0  0
 25 26  1  0  0  0  0
 27 26  1  6  0  0  0
  5 27  1  0  0  0  0
 27 28  1  0  0  0  0
  2 28  1  0  0  0  0
 28 29  1  1  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 33 34  2  0  0  0  0
 28 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 36 39  1  0  0  0  0
 27 39  1  0  0  0  0
 39 40  1  1  0  0  0
  3 40  1  0  0  0  0
  6 41  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0084056

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCC1=C2O[C@]34[C@@H]5C[C@H](C=C3C(=O)C2=C(O)C2=C1OC(C2)C(C)(C)O)C(=O)[C@@]4(C\C=C(/C)C=O)OC5(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C33H38O8/c1-16(2)8-9-19-27-20(14-23(39-27)30(4,5)38)25(35)24-26(36)21-12-18-13-22-31(6,7)41-32(29(18)37,11-10-17(3)15-34)33(21,22)40-28(19)24/h8,10,12,15,18,22-23,35,38H,9,11,13-14H2,1-7H3/b17-10+/t18-,22+,23?,32+,33-/m0/s1

> <INCHI_KEY>
QOSIIPFIQGNGLK-VQTOALDMSA-N

> <FORMULA>
C33H38O8

> <MOLECULAR_WEIGHT>
562.659

> <EXACT_MASS>
562.256668184

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
79

> <JCHEM_AVERAGE_POLARIZABILITY>
60.788136696010284

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2E)-4-[(1R,2R,16R,18S)-11-hydroxy-8-(2-hydroxypropan-2-yl)-20,20-dimethyl-5-(3-methylbut-2-en-1-yl)-13,17-dioxo-3,7,19-trioxahexacyclo[14.4.1.0^{2,14}.0^{2,18}.0^{4,12}.0^{6,10}]henicosa-4,6(10),11,14-tetraen-18-yl]-2-methylbut-2-enal

> <ALOGPS_LOGP>
4.19

> <JCHEM_LOGP>
4.935883481000001

> <ALOGPS_LOGS>
-5.16

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.74301657133

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.843415885609975

> <JCHEM_PKA_STRONGEST_BASIC>
-3.106445716807631

> <JCHEM_POLAR_SURFACE_AREA>
119.36000000000001

> <JCHEM_REFRACTIVITY>
154.9095

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.89e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2E)-4-[(1R,2R,16R,18S)-11-hydroxy-8-(2-hydroxypropan-2-yl)-20,20-dimethyl-5-(3-methylbut-2-en-1-yl)-13,17-dioxo-3,7,19-trioxahexacyclo[14.4.1.0^{2,14}.0^{2,18}.0^{4,12}.0^{6,10}]henicosa-4,6(10),11,14-tetraen-18-yl]-2-methylbut-2-enal

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  O   UNK     0      -0.082  -1.452   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       1.321  -0.443   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.469   1.105   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.832   1.978   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.219   1.233   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.726   1.846   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.971   0.918   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.404   1.480   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       8.782   3.037   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       9.608   0.520   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.378  -1.003   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      10.756  -1.692   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      11.837  -0.595   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      13.487  -0.810   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      13.675  -2.411   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      15.083  -1.016   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      14.048   0.699   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      11.127   0.772   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.945  -1.565   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.542  -3.158   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.489  -4.471   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.858  -5.876   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.326  -6.032   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.759  -7.124   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.741  -0.605   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       5.273  -1.126   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       3.857  -0.384   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.983  -1.014   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.162  -2.672   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.763  -3.742   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       1.341  -3.150   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       1.143  -1.623   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       0.118  -4.085   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       0.316  -5.613   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0       2.061  -2.539   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       3.443  -2.647   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       5.049  -2.133   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       3.853  -4.436   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       2.028  -1.432   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       0.512  -0.229   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       5.725   3.501   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   28                                                  
CONECT    3    2    4   40                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   27                                                  
CONECT    6    5    7   41                                                  
CONECT    7    6    8   25                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   18                                                  
CONECT   11   10   12   19                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   18                                                  
CONECT   14   13   15   16   17                                             
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17   14                                                            
CONECT   18   13   10                                                       
CONECT   19   11   20   25                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25   19    7   26                                                  
CONECT   26   25   27                                                       
CONECT   27   26    5   28   39                                             
CONECT   28   27    2   29   35                                             
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34                                                       
CONECT   34   33                                                            
CONECT   35   28   36                                                       
CONECT   36   35   37   38   39                                             
CONECT   37   36                                                            
CONECT   38   36                                                            
CONECT   39   36   27   40                                                  
CONECT   40   39    3                                                       
CONECT   41    6                                                            
MASTER        0    0    0    0    0    0    0    0   41    0   92    0
END

View in JSmol

Synonyms

Value	Source
2-(1-Methyl-1-hydroxyethyl)-4-hydroxy-9-[(e)-3-formyl-2-butenyl]-11-(3-methyl-2-butenyl)-13,13-dimethyl-9b,9abeta,7b-(epoxy[1,2,3]propanetriyl)-2,3,9,9a-tetrahydro-5H-furo[3,2-b]xanthene-5,8(7H)-dione	Generator
2-(1-Methyl-1-hydroxyethyl)-4-hydroxy-9-[(e)-3-formyl-2-butenyl]-11-(3-methyl-2-butenyl)-13,13-dimethyl-9β,9abeta,7β-(epoxy[1,2,3]propanetriyl)-2,3,9,9a-tetrahydro-5H-furo[3,2-b]xanthene-5,8(7H)-dione	Generator

Chemical Formula

C₃₃H₃₈O₈

Average Mass

562.6590 Da

Monoisotopic Mass

562.25667 Da

IUPAC Name

(2E)-4-[(1R,2R,16R,18S)-11-hydroxy-8-(2-hydroxypropan-2-yl)-20,20-dimethyl-5-(3-methylbut-2-en-1-yl)-13,17-dioxo-3,7,19-trioxahexacyclo[14.4.1.0^{2,14}.0^{2,18}.0^{4,12}.0^{6,10}]henicosa-4,6(10),11,14-tetraen-18-yl]-2-methylbut-2-enal

Traditional Name

CAS Registry Number

Not Available

SMILES

CC(C)=CCC1=C2O[C@]34[C@@H]5C[C@H](C=C3C(=O)C2=C(O)C2=C1OC(C2)C(C)(C)O)C(=O)[C@@]4(C\C=C(/C)C=O)OC5(C)C

InChI Identifier

InChI=1S/C33H38O8/c1-16(2)8-9-19-27-20(14-23(39-27)30(4,5)38)25(35)24-26(36)21-12-18-13-22-31(6,7)41-32(29(18)37,11-10-17(3)15-34)33(21,22)40-28(19)24/h8,10,12,15,18,22-23,35,38H,9,11,13-14H2,1-7H3/b17-10+/t18-,22+,23?,32+,33-/m0/s1

InChI Key

QOSIIPFIQGNGLK-VQTOALDMSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Garcinia gaudichaudii	Plant	KNApSAcK

Chemical Taxonomy

Classification

Not classified

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	4.19	ALOGPS
logP	4.94	ChemAxon
logS	-5.2	ALOGPS
pKa (Strongest Acidic)	8.84	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	119.36 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	154.91 m³·mol⁻¹	ChemAxon
Polarizability	60.79 Å³	ChemAxon
Number of Rings	6	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

C00053247

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

102533558

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Gaudichaudione E (NP0084056)

MOL for NP0084056 (Gaudichaudione E)

3D MOL for NP0084056 (Gaudichaudione E)

3D SDF for NP0084056 (Gaudichaudione E)

3D-SDF for NP0084056 (Gaudichaudione E)

PDB for NP0084056 (Gaudichaudione E)

3D PDB for NP0084056 (Gaudichaudione E)

SMILES for NP0084056 (Gaudichaudione E)

INCHI for NP0084056 (Gaudichaudione E)

Structure for NP0084056 (Gaudichaudione E)

3D Structure for NP0084056 (Gaudichaudione E)