NP-MRD: Showing NP-Card for Crepidiaside E (NP0063659)

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Record Information

Version

2.0

Created at

2022-04-28 08:02:11 UTC

Updated at

2022-04-28 08:02:11 UTC

NP-MRD ID

NP0063659

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Crepidiaside E

Description

(2R,3S,4S,5S,6S)-2-{[(3aR,4S,9aR,9bS)-4-hydroxy-6-methyl-3-methylidene-2-oxo-2H,3H,3aH,4H,5H,7H,9aH,9bH-azuleno[4,5-b]furan-9-yl]methoxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl 2-(4-hydroxyphenyl)acetate belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond. Crepidiaside E is found in Cichorium pumilum and Crepidiastrum keiskeanum. Based on a literature review very few articles have been published on (2R,3S,4S,5S,6S)-2-{[(3aR,4S,9aR,9bS)-4-hydroxy-6-methyl-3-methylidene-2-oxo-2H,3H,3aH,4H,5H,7H,9aH,9bH-azuleno[4,5-b]furan-9-yl]methoxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl 2-(4-hydroxyphenyl)acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282210022D          

 40 44  0  0  1  0            999 V2000
    2.7444    1.0885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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 37 40  1  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652304282210022D          

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   -2.4047   -2.3172    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3010   -3.2247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8250   -3.8620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5351   -4.6344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0591   -5.2716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8729   -5.1365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1628   -4.3641    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6388   -3.7268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3969   -5.7737    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  1  3  1  0  0  0  0
  3  4  2  0  0  0  0
  5  3  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  1  0  0  0
  1  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  1  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
  5 12  1  0  0  0  0
 12 13  1  6  0  0  0
 10 14  1  0  0  0  0
  9 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
  8 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 20 19  1  1  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 20 25  1  0  0  0  0
 24 26  1  6  0  0  0
 26 27  1  0  0  0  0
 23 28  1  6  0  0  0
 22 29  1  1  0  0  0
 21 30  1  1  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
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 34 39  1  0  0  0  0
 37 40  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0063659

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=C2CC=C(CO[C@@H]3O[C@@H](CO)[C@@H](O)[C@H](O)[C@@H]3OC(=O)CC3=CC=C(O)C=C3)[C@@H]2[C@@H]2OC(=O)C(=C)[C@@H]2[C@@H](O)C1

> <INCHI_IDENTIFIER>
InChI=1S/C29H34O11/c1-13-9-19(32)22-14(2)28(36)40-26(22)23-16(5-8-18(13)23)12-37-29-27(25(35)24(34)20(11-30)38-29)39-21(33)10-15-3-6-17(31)7-4-15/h3-7,19-20,22-27,29-32,34-35H,2,8-12H2,1H3/t19-,20-,22+,23-,24+,25-,26+,27-,29+/m0/s1

> <INCHI_KEY>
RTXSNWYVOKAJIF-JLDBJBMBSA-N

> <FORMULA>
C29H34O11

> <MOLECULAR_WEIGHT>
558.58

> <EXACT_MASS>
558.210111915

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
74

> <JCHEM_AVERAGE_POLARIZABILITY>
55.23583182022976

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,3S,4S,5S,6S)-2-{[(3aR,4S,9aR,9bS)-4-hydroxy-6-methyl-3-methylidene-2-oxo-2H,3H,3aH,4H,5H,7H,9aH,9bH-azuleno[4,5-b]furan-9-yl]methoxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl 2-(4-hydroxyphenyl)acetate

> <ALOGPS_LOGP>
0.86

> <JCHEM_LOGP>
0.4908613580000006

> <ALOGPS_LOGS>
-3.18

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.691748966584115

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.496146665738289

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9245636540438644

> <JCHEM_POLAR_SURFACE_AREA>
172.21

> <JCHEM_REFRACTIVITY>
139.46279999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.69e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3S,4S,5S,6S)-2-{[(3aR,4S,9aR,9bS)-4-hydroxy-6-methyl-3-methylidene-2-oxo-3aH,4H,5H,7H,9aH,9bH-azuleno[4,5-b]furan-9-yl]methoxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl (4-hydroxyphenyl)acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       5.123   2.032   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       6.327   1.072   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       5.192   3.570   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.477   4.419   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.750   4.111   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.790   2.907   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       3.638   1.622   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       1.250   2.907   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.290   4.111   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.632   5.613   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.020   6.281   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.407   5.613   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       4.611   6.573   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -0.572   6.573   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.152   3.570   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.083   2.032   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.402   1.622   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.943   0.180   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -0.035  -1.009   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -1.555  -0.757   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -2.533  -1.946   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -4.052  -1.694   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -4.593  -0.252   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -3.615   0.937   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -2.096   0.685   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      -4.156   2.379   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -3.178   3.569   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0      -6.112   0.000   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      -5.030  -2.884   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      -1.992  -3.388   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      -2.970  -4.578   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      -4.489  -4.325   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      -2.429  -6.019   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -3.407  -7.209   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -2.866  -8.651   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -3.844  -9.840   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      -5.363  -9.588   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      -5.904  -8.146   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      -4.926  -6.957   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      -6.341 -10.778   0.000  0.00  0.00           O+0
CONECT    1    2    3    7                                                  
CONECT    2    1                                                            
CONECT    3    1    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   12                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6    1                                                       
CONECT    8    6    9   17                                                  
CONECT    9    8   10   15                                                  
CONECT   10    9   11   14                                                  
CONECT   11   10   12                                                       
CONECT   12   11    5   13                                                  
CONECT   13   12                                                            
CONECT   14   10                                                            
CONECT   15    9   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16    8   18                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   25                                                  
CONECT   21   20   22   30                                                  
CONECT   22   21   23   29                                                  
CONECT   23   22   24   28                                                  
CONECT   24   23   25   26                                                  
CONECT   25   24   20                                                       
CONECT   26   24   27                                                       
CONECT   27   26                                                            
CONECT   28   23                                                            
CONECT   29   22                                                            
CONECT   30   21   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34                                                       
CONECT   34   33   35   39                                                  
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38   40                                                  
CONECT   38   37   39                                                       
CONECT   39   38   34                                                       
CONECT   40   37                                                            
MASTER        0    0    0    0    0    0    0    0   40    0   88    0
END

View in JSmol

Synonyms

Value	Source
(2R,3S,4S,5S,6S)-2-{[(3ar,4S,9ar,9BS)-4-hydroxy-6-methyl-3-methylidene-2-oxo-2H,3H,3ah,4H,5H,7H,9ah,9BH-azuleno[4,5-b]furan-9-yl]methoxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl 2-(4-hydroxyphenyl)acetic acid	Generator

Chemical Formula

C₂₉H₃₄O₁₁

Average Mass

558.5800 Da

Monoisotopic Mass

558.21011 Da

IUPAC Name

Traditional Name

(2R,3S,4S,5S,6S)-2-{[(3aR,4S,9aR,9bS)-4-hydroxy-6-methyl-3-methylidene-2-oxo-3aH,4H,5H,7H,9aH,9bH-azuleno[4,5-b]furan-9-yl]methoxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl (4-hydroxyphenyl)acetate

CAS Registry Number

Not Available

SMILES

CC1=C2CC=C(CO[C@@H]3O[C@@H](CO)[C@@H](O)[C@H](O)[C@@H]3OC(=O)CC3=CC=C(O)C=C3)[C@@H]2[C@@H]2OC(=O)C(=C)[C@@H]2[C@@H](O)C1

InChI Identifier

InChI=1S/C29H34O11/c1-13-9-19(32)22-14(2)28(36)40-26(22)23-16(5-8-18(13)23)12-37-29-27(25(35)24(34)20(11-30)38-29)39-21(33)10-15-3-6-17(31)7-4-15/h3-7,19-20,22-27,29-32,34-35H,2,8-12H2,1H3/t19-,20-,22+,23-,24+,25-,26+,27-,29+/m0/s1

InChI Key

RTXSNWYVOKAJIF-JLDBJBMBSA-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
Cichorium pumilum	Plant	KNApSAcK
Crepidiastrum keiskeanum	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

O-glycosyl compounds

Alternative Parents

Substituents

Hexose monosaccharide
O-glycosyl compound
1-hydroxy-2-unsubstituted benzenoid
Phenol
Benzenoid
Oxane
Monosaccharide
Gamma butyrolactone
Dicarboxylic acid or derivatives
Monocyclic benzene moiety
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tetrahydrofuran
Secondary alcohol
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Acetal
Organic oxide
Hydrocarbon derivative
Primary alcohol
Carbonyl group
Alcohol
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	0.86	ALOGPS
logP	0.49	ChemAxon
logS	-3.2	ALOGPS
pKa (Strongest Acidic)	9.5	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	172.21 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	139.46 m³·mol⁻¹	ChemAxon
Polarizability	55.24 Å³	ChemAxon
Number of Rings	5	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

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

163010708

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Crepidiaside E (NP0063659)

MOL for NP0063659 (Crepidiaside E)

3D MOL for NP0063659 (Crepidiaside E)

3D SDF for NP0063659 (Crepidiaside E)

3D-SDF for NP0063659 (Crepidiaside E)

PDB for NP0063659 (Crepidiaside E)

3D PDB for NP0063659 (Crepidiaside E)

SMILES for NP0063659 (Crepidiaside E)

INCHI for NP0063659 (Crepidiaside E)

Structure for NP0063659 (Crepidiaside E)

3D Structure for NP0063659 (Crepidiaside E)