NP-MRD: Showing NP-Card for (2s,3r,4s,5s,6r)-2-{[(1s,2r,4s,5s,6r,10s)-5-{[(1e)-2-(4-hydroxy-3-methoxyphenyl)ethenyl]oxy}-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-10-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol (NP0227374)

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Record Information

Version

2.0

Created at

2022-09-06 06:40:40 UTC

Updated at

2022-09-06 06:40:40 UTC

NP-MRD ID

NP0227374

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s,3r,4s,5s,6r)-2-{[(1s,2r,4s,5s,6r,10s)-5-{[(1e)-2-(4-hydroxy-3-methoxyphenyl)ethenyl]oxy}-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-10-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

Description

CHEMBL463912 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. (2s,3r,4s,5s,6r)-2-{[(1s,2r,4s,5s,6r,10s)-5-{[(1e)-2-(4-hydroxy-3-methoxyphenyl)ethenyl]oxy}-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-10-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol is found in Stereospermum colais. Based on a literature review very few articles have been published on CHEMBL463912.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062208402D          

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M  END

     RDKit          3D

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M  END


  Mrv1652309062208402D          

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 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 32 31  1  1  0  0  0
  9 32  1  0  0  0  0
 15 32  1  0  0  0  0
  5 33  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
  3 35  1  0  0  0  0
 35 36  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0227374

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(\C=C\O[C@@H]2[C@@H]3O[C@@]3(CO)[C@@H]3[C@H]2C=CO[C@H]3O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)=CC=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C24H30O12/c1-31-14-8-11(2-3-13(14)27)4-6-32-20-12-5-7-33-22(16(12)24(10-26)21(20)36-24)35-23-19(30)18(29)17(28)15(9-25)34-23/h2-8,12,15-23,25-30H,9-10H2,1H3/b6-4+/t12-,15-,16-,17-,18+,19-,20+,21+,22+,23+,24+/m1/s1

> <INCHI_KEY>
PZQJSFUXSDAPFA-KXANSVNUSA-N

> <FORMULA>
C24H30O12

> <MOLECULAR_WEIGHT>
510.492

> <EXACT_MASS>
510.173726406

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_ATOM_COUNT>
66

> <JCHEM_AVERAGE_POLARIZABILITY>
37.35986686965755

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,3R,4S,5S,6R)-2-{[(1S,2R,4S,5S,6R,10S)-5-{[(E)-2-(4-hydroxy-3-methoxyphenyl)ethenyl]oxy}-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.0^{2,4}]dec-7-en-10-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

> <JCHEM_LOGP>
-1.1421003259999996

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.204828014903917

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.82217118312139

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810847601929344

> <JCHEM_POLAR_SURFACE_AREA>
180.05999999999997

> <JCHEM_REFRACTIVITY>
119.84750000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3R,4S,5S,6R)-2-{[(1S,2R,4S,5S,6R,10S)-5-{[(E)-2-(4-hydroxy-3-methoxyphenyl)ethenyl]oxy}-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.0^{2,4}]dec-7-en-10-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0      13.236   4.259   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      11.849   3.590   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      10.576   4.457   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.189   3.787   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.916   4.654   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.529   3.984   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.256   4.851   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       3.869   4.182   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       3.755   2.646   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.931   1.651   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       5.874   0.433   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       4.348   0.226   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.395  -1.314   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       5.752  -2.042   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       2.812   0.339   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.700  -0.726   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       2.066  -2.222   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       0.954  -3.287   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       1.320  -4.783   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       0.208  -5.848   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.575  -7.343   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       2.053  -7.774   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -1.270  -5.417   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -2.383  -6.482   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -1.637  -3.921   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -3.115  -3.491   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -0.524  -2.856   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -0.891  -1.360   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       0.221  -0.295   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      -0.145   1.201   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       0.967   2.266   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       2.446   1.835   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       8.030   6.190   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       9.417   6.859   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      10.690   5.992   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      12.077   6.662   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   35                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   33                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   32                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10   12                                                       
CONECT   12   11   10   13   15                                             
CONECT   13   12   14                                                       
CONECT   14   13                                                            
CONECT   15   12   16   32                                                  
CONECT   16   15   17   29                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   27                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   23                                                  
CONECT   21   20   22                                                       
CONECT   22   21                                                            
CONECT   23   20   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   18   28                                                  
CONECT   28   27                                                            
CONECT   29   16   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31    9   15                                                  
CONECT   33    5   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34    3   36                                                  
CONECT   36   35                                                            
MASTER        0    0    0    0    0    0    0    0   36    0   80    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₃₀O₁₂

Average Mass

510.4920 Da

Monoisotopic Mass

510.17373 Da

IUPAC Name

(2S,3R,4S,5S,6R)-2-{[(1S,2R,4S,5S,6R,10S)-5-{[(E)-2-(4-hydroxy-3-methoxyphenyl)ethenyl]oxy}-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.0^{2,4}]dec-7-en-10-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

Traditional Name

(2S,3R,4S,5S,6R)-2-{[(1S,2R,4S,5S,6R,10S)-5-{[(E)-2-(4-hydroxy-3-methoxyphenyl)ethenyl]oxy}-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.0^{2,4}]dec-7-en-10-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

CAS Registry Number

Not Available

SMILES

COC1=CC(\C=C\O[C@@H]2[C@@H]3O[C@@]3(CO)[C@@H]3[C@H]2C=CO[C@H]3O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)=CC=C1O

InChI Identifier

InChI=1S/C24H30O12/c1-31-14-8-11(2-3-13(14)27)4-6-32-20-12-5-7-33-22(16(12)24(10-26)21(20)36-24)35-23-19(30)18(29)17(28)15(9-25)34-23/h2-8,12,15-23,25-30H,9-10H2,1H3/b6-4+/t12-,15-,16-,17-,18+,19-,20+,21+,22+,23+,24+/m1/s1

InChI Key

PZQJSFUXSDAPFA-KXANSVNUSA-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
Stereospermum colais	LOTUS Database	35616633

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
Methoxyphenol
Phenoxy compound
Anisole
Methoxybenzene
Styrene
Phenol ether
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Phenol
Monocyclic benzene moiety
Benzenoid
Monosaccharide
Oxane
Secondary alcohol
Organoheterocyclic compound
Ether
Oxirane
Dialkyl ether
Acetal
Oxacycle
Polyol
Hydrocarbon derivative
Alcohol
Primary 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	-1.1	ChemAxon
pKa (Strongest Acidic)	9.82	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	12	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	180.06 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	119.85 m³·mol⁻¹	ChemAxon
Polarizability	37.36 Å³	ChemAxon
Number of Rings	5	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

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

23339303

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

44566578

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2s,3r,4s,5s,6r)-2-{[(1s,2r,4s,5s,6r,10s)-5-{[(1e)-2-(4-hydroxy-3-methoxyphenyl)ethenyl]oxy}-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-10-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol (NP0227374)

MOL for NP0227374 ((2s,3r,4s,5s,6r)-2-{[(1s,2r,4s,5s,6r,10s)-5-{[(1e)-2-(4-hydroxy-3-methoxyphenyl)ethenyl]oxy}-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-10-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D MOL for NP0227374 ((2s,3r,4s,5s,6r)-2-{[(1s,2r,4s,5s,6r,10s)-5-{[(1e)-2-(4-hydroxy-3-methoxyphenyl)ethenyl]oxy}-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-10-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D SDF for NP0227374 ((2s,3r,4s,5s,6r)-2-{[(1s,2r,4s,5s,6r,10s)-5-{[(1e)-2-(4-hydroxy-3-methoxyphenyl)ethenyl]oxy}-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-10-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D-SDF for NP0227374 ((2s,3r,4s,5s,6r)-2-{[(1s,2r,4s,5s,6r,10s)-5-{[(1e)-2-(4-hydroxy-3-methoxyphenyl)ethenyl]oxy}-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-10-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

PDB for NP0227374 ((2s,3r,4s,5s,6r)-2-{[(1s,2r,4s,5s,6r,10s)-5-{[(1e)-2-(4-hydroxy-3-methoxyphenyl)ethenyl]oxy}-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-10-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D PDB for NP0227374 ((2s,3r,4s,5s,6r)-2-{[(1s,2r,4s,5s,6r,10s)-5-{[(1e)-2-(4-hydroxy-3-methoxyphenyl)ethenyl]oxy}-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-10-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

SMILES for NP0227374 ((2s,3r,4s,5s,6r)-2-{[(1s,2r,4s,5s,6r,10s)-5-{[(1e)-2-(4-hydroxy-3-methoxyphenyl)ethenyl]oxy}-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-10-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

INCHI for NP0227374 ((2s,3r,4s,5s,6r)-2-{[(1s,2r,4s,5s,6r,10s)-5-{[(1e)-2-(4-hydroxy-3-methoxyphenyl)ethenyl]oxy}-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-10-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

Structure for NP0227374 ((2s,3r,4s,5s,6r)-2-{[(1s,2r,4s,5s,6r,10s)-5-{[(1e)-2-(4-hydroxy-3-methoxyphenyl)ethenyl]oxy}-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-10-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D Structure for NP0227374 ((2s,3r,4s,5s,6r)-2-{[(1s,2r,4s,5s,6r,10s)-5-{[(1e)-2-(4-hydroxy-3-methoxyphenyl)ethenyl]oxy}-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-10-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)