NP-MRD: Showing NP-Card for 7-hydroxy-7-methyl-1-[(3,4,5-trihydroxy-6-{[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}oxan-2-yl)methoxy]-1h,4ah,5h,6h,7ah-cyclopenta[c]pyran-4-carbaldehyde (NP0228957)

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Record Information

Version

2.0

Created at

2022-09-06 08:49:20 UTC

Updated at

2022-09-06 08:49:21 UTC

NP-MRD ID

NP0228957

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7-hydroxy-7-methyl-1-[(3,4,5-trihydroxy-6-{[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}oxan-2-yl)methoxy]-1h,4ah,5h,6h,7ah-cyclopenta[c]pyran-4-carbaldehyde

Description

7-Hydroxy-7-methyl-1-[(3,4,5-trihydroxy-6-{[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}oxan-2-yl)methoxy]-1H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyran-4-carbaldehyde belongs to the class of organic compounds known as iridoids and derivatives. These are monoterpenes containing a skeleton structurally characterized by the presence of a cylopentane fused to a pyran ( forming a 4,7-dimethylcyclopenta[c]pyran), or a derivative where the pentane moiety is open. 7-hydroxy-7-methyl-1-[(3,4,5-trihydroxy-6-{[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}oxan-2-yl)methoxy]-1h,4ah,5h,6h,7ah-cyclopenta[c]pyran-4-carbaldehyde is found in Pedicularis plicata. 7-Hydroxy-7-methyl-1-[(3,4,5-trihydroxy-6-{[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}oxan-2-yl)methoxy]-1H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyran-4-carbaldehyde is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171518262D          

 36 39  0  0  0  0            999 V2000
   -0.8580    0.3820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435   -0.0305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1921    0.7232    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6284   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435   -1.3654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    0.9521    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701    1.3646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701    2.1896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    2.6021    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    3.4271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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 33 34  2  0  0  0  0
  6 34  1  0  0  0  0
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 35 36  2  0  0  0  0
M  END

     RDKit          3D

 70 73  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1533004171518262D          

 36 39  0  0  0  0            999 V2000
   -0.8580    0.3820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435   -0.0305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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 10 11  1  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
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 19 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 15 24  1  0  0  0  0
 24 25  1  0  0  0  0
 13 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 11 30  1  0  0  0  0
 30 31  1  0  0  0  0
  8 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
  6 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0228957

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(O)CCC2C1C(OCC1OC(OC3C(O)OC(CO)C(O)C3O)C(O)C(O)C1O)OC=C2C=O

> <INCHI_IDENTIFIER>
InChI=1S/C22H34O14/c1-22(31)3-2-9-8(4-23)6-32-20(12(9)22)33-7-11-14(26)15(27)17(29)21(35-11)36-18-16(28)13(25)10(5-24)34-19(18)30/h4,6,9-21,24-31H,2-3,5,7H2,1H3

> <INCHI_KEY>
WILPSDUESCCQEW-UHFFFAOYSA-N

> <FORMULA>
C22H34O14

> <MOLECULAR_WEIGHT>
522.5

> <EXACT_MASS>
522.194855775

> <JCHEM_ACCEPTOR_COUNT>
14

> <JCHEM_ATOM_COUNT>
70

> <JCHEM_AVERAGE_POLARIZABILITY>
49.92074903821978

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
7-hydroxy-7-methyl-1-[(3,4,5-trihydroxy-6-{[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}oxan-2-yl)methoxy]-1H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyran-4-carbaldehyde

> <ALOGPS_LOGP>
-1.80

> <JCHEM_LOGP>
-3.9691417586666664

> <ALOGPS_LOGS>
-1.01

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.156032421198525

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.267478090821314

> <JCHEM_PKA_STRONGEST_BASIC>
-2.969803499781979

> <JCHEM_POLAR_SURFACE_AREA>
225.05999999999997

> <JCHEM_REFRACTIVITY>
113.99900000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.14e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
7-hydroxy-7-methyl-1-[(3,4,5-trihydroxy-6-{[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}oxan-2-yl)methoxy]-1H,4aH,5H,6H,7aH-cyclopenta[c]pyran-4-carbaldehyde

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0      -1.602   0.713   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.268  -0.057   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       0.358   1.350   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      -1.173  -1.303   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.268  -2.549   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.197  -2.073   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.197  -0.533   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.530   0.237   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       2.530   1.777   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       3.864   2.547   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.864   4.087   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       2.530   4.857   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       2.530   6.397   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       1.197   7.167   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -0.137   6.397   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.471   7.167   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -1.471   8.707   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0      -2.804   6.397   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      -2.804   4.857   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -4.138   4.087   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -4.138   2.547   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -1.471   4.087   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -1.471   2.547   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -0.137   4.857   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       1.197   4.087   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       3.864   7.167   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       3.864   8.707   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       5.198   6.397   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       6.531   7.167   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       5.198   4.857   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       6.531   4.087   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       3.864  -0.533   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       3.864  -2.073   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       2.530  -2.843   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       2.530  -4.383   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       3.864  -5.153   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4    7                                             
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   34                                                  
CONECT    7    6    2    8                                                  
CONECT    8    7    9   32                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   30                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   26                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   24                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20   22                                                  
CONECT   20   19   21                                                       
CONECT   21   20                                                            
CONECT   22   19   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   15   25                                                  
CONECT   25   24                                                            
CONECT   26   13   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   11   31                                                  
CONECT   31   30                                                            
CONECT   32    8   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33    6   35                                                  
CONECT   35   34   36                                                       
CONECT   36   35                                                            
MASTER        0    0    0    0    0    0    0    0   36    0   78    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₃₄O₁₄

Average Mass

522.5000 Da

Monoisotopic Mass

522.19486 Da

IUPAC Name

7-hydroxy-7-methyl-1-[(3,4,5-trihydroxy-6-{[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}oxan-2-yl)methoxy]-1H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyran-4-carbaldehyde

Traditional Name

7-hydroxy-7-methyl-1-[(3,4,5-trihydroxy-6-{[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}oxan-2-yl)methoxy]-1H,4aH,5H,6H,7aH-cyclopenta[c]pyran-4-carbaldehyde

CAS Registry Number

Not Available

SMILES

CC1(O)CCC2C1C(OCC1OC(OC3C(O)OC(CO)C(O)C3O)C(O)C(O)C1O)OC=C2C=O

InChI Identifier

InChI=1S/C22H34O14/c1-22(31)3-2-9-8(4-23)6-32-20(12(9)22)33-7-11-14(26)15(27)17(29)21(35-11)36-18-16(28)13(25)10(5-24)34-19(18)30/h4,6,9-21,24-31H,2-3,5,7H2,1H3

InChI Key

WILPSDUESCCQEW-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
Pedicularis plicata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as iridoids and derivatives. These are monoterpenes containing a skeleton structurally characterized by the presence of a cylopentane fused to a pyran ( forming a 4,7-dimethylcyclopenta[c]pyran), or a derivative where the pentane moiety is open.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Monoterpenoids

Direct Parent

Iridoids and derivatives

Alternative Parents

Substituents

Disaccharide
Glycosyl compound
Iridoid-skeleton
O-glycosyl compound
Bicyclic monoterpenoid
Oxane
Cyclic alcohol
Vinylogous ester
Tertiary alcohol
Hemiacetal
Secondary alcohol
Polyol
Organoheterocyclic compound
Oxacycle
Acetal
Alcohol
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Carbonyl group
Organic oxygen compound
Primary alcohol
Aldehyde
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
logP	-1.8	ALOGPS
logP	-4	ChemAxon
logS	-1	ALOGPS
pKa (Strongest Acidic)	11.27	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	14	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	225.06 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	114 m³·mol⁻¹	ChemAxon
Polarizability	49.92 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

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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 7-hydroxy-7-methyl-1-[(3,4,5-trihydroxy-6-{[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}oxan-2-yl)methoxy]-1h,4ah,5h,6h,7ah-cyclopenta[c]pyran-4-carbaldehyde (NP0228957)

MOL for NP0228957 (7-hydroxy-7-methyl-1-[(3,4,5-trihydroxy-6-{[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}oxan-2-yl)methoxy]-1h,4ah,5h,6h,7ah-cyclopenta[c]pyran-4-carbaldehyde)

3D MOL for NP0228957 (7-hydroxy-7-methyl-1-[(3,4,5-trihydroxy-6-{[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}oxan-2-yl)methoxy]-1h,4ah,5h,6h,7ah-cyclopenta[c]pyran-4-carbaldehyde)

3D SDF for NP0228957 (7-hydroxy-7-methyl-1-[(3,4,5-trihydroxy-6-{[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}oxan-2-yl)methoxy]-1h,4ah,5h,6h,7ah-cyclopenta[c]pyran-4-carbaldehyde)

3D-SDF for NP0228957 (7-hydroxy-7-methyl-1-[(3,4,5-trihydroxy-6-{[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}oxan-2-yl)methoxy]-1h,4ah,5h,6h,7ah-cyclopenta[c]pyran-4-carbaldehyde)

PDB for NP0228957 (7-hydroxy-7-methyl-1-[(3,4,5-trihydroxy-6-{[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}oxan-2-yl)methoxy]-1h,4ah,5h,6h,7ah-cyclopenta[c]pyran-4-carbaldehyde)

3D PDB for NP0228957 (7-hydroxy-7-methyl-1-[(3,4,5-trihydroxy-6-{[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}oxan-2-yl)methoxy]-1h,4ah,5h,6h,7ah-cyclopenta[c]pyran-4-carbaldehyde)

SMILES for NP0228957 (7-hydroxy-7-methyl-1-[(3,4,5-trihydroxy-6-{[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}oxan-2-yl)methoxy]-1h,4ah,5h,6h,7ah-cyclopenta[c]pyran-4-carbaldehyde)

INCHI for NP0228957 (7-hydroxy-7-methyl-1-[(3,4,5-trihydroxy-6-{[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}oxan-2-yl)methoxy]-1h,4ah,5h,6h,7ah-cyclopenta[c]pyran-4-carbaldehyde)

Structure for NP0228957 (7-hydroxy-7-methyl-1-[(3,4,5-trihydroxy-6-{[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}oxan-2-yl)methoxy]-1h,4ah,5h,6h,7ah-cyclopenta[c]pyran-4-carbaldehyde)

3D Structure for NP0228957 (7-hydroxy-7-methyl-1-[(3,4,5-trihydroxy-6-{[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}oxan-2-yl)methoxy]-1h,4ah,5h,6h,7ah-cyclopenta[c]pyran-4-carbaldehyde)