NP-MRD: Showing NP-Card for (3r,3'r,4's,4'ar,5'as)-4'-ethenyl-2-hydroxy-3'-{[(2r,3s,4r,5r,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4',4'a,5',5'a,7',8'-hexahydro-3'h-spiro[indole-3,6'-pyrano[3,4-f]indolizin]-10'-one (NP0211441)

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Record Information

Version

2.0

Created at

2022-09-05 09:43:25 UTC

Updated at

2022-09-05 09:43:25 UTC

NP-MRD ID

NP0211441

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3r,3'r,4's,4'ar,5'as)-4'-ethenyl-2-hydroxy-3'-{[(2r,3s,4r,5r,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4',4'a,5',5'a,7',8'-hexahydro-3'h-spiro[indole-3,6'-pyrano[3,4-f]indolizin]-10'-one

Description

(3R,3'R,4'S,4'aR,5'aS)-4'-ethenyl-2-hydroxy-3'-{[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3',4',4'a,5',5'a,7',8',10'-octahydrospiro[indole-3,6'-pyrano[3,4-f]indolizine]-10'-one 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. (3r,3'r,4's,4'ar,5'as)-4'-ethenyl-2-hydroxy-3'-{[(2r,3s,4r,5r,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4',4'a,5',5'a,7',8'-hexahydro-3'h-spiro[indole-3,6'-pyrano[3,4-f]indolizin]-10'-one is found in Alangium javanicum. Based on a literature review very few articles have been published on (3R,3'R,4'S,4'aR,5'aS)-4'-ethenyl-2-hydroxy-3'-{[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3',4',4'a,5',5'a,7',8',10'-octahydrospiro[indole-3,6'-pyrano[3,4-f]indolizine]-10'-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052211432D          

 37 42  0  0  1  0            999 V2000
    3.1601    0.1125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6566    0.7714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.2000    1.0730    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -0.1153    0.5147    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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  1  2  2  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652309052211432D          

 37 42  0  0  1  0            999 V2000
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  4  5  1  1  0  0  0
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  9 10  1  0  0  0  0
  8 11  1  0  0  0  0
 11 12  1  6  0  0  0
 11 13  1  0  0  0  0
 13 14  1  1  0  0  0
 13 15  1  0  0  0  0
  6 15  1  0  0  0  0
 15 16  1  6  0  0  0
  4 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 25 24  1  1  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 29 34  1  0  0  0  0
 25 34  1  0  0  0  0
 25 35  1  0  0  0  0
 35 22  1  6  0  0  0
 35 36  1  0  0  0  0
 37 36  1  6  0  0  0
 19 37  1  0  0  0  0
  3 37  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0211441

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC[C@@H]1O[C@H](O[C@H]2OC=C3[C@H](C[C@@H]4N(CC[C@]44C(O)=NC5=CC=CC=C45)C3=O)[C@@H]2C=C)[C@@H](O)[C@H](O)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C26H30N2O9/c1-2-12-13-9-18-26(15-5-3-4-6-16(15)27-25(26)34)7-8-28(18)22(33)14(13)11-35-23(12)37-24-21(32)20(31)19(30)17(10-29)36-24/h2-6,11-13,17-21,23-24,29-32H,1,7-10H2,(H,27,34)/t12-,13+,17-,18-,19-,20+,21-,23+,24+,26+/m0/s1

> <INCHI_KEY>
UXDQUMNIWFOBFX-GDHPVAJASA-N

> <FORMULA>
C26H30N2O9

> <MOLECULAR_WEIGHT>
514.531

> <EXACT_MASS>
514.195130554

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
67

> <JCHEM_AVERAGE_POLARIZABILITY>
51.2185324562783

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3R,3'R,4'S,4'aR,5'aS)-4'-ethenyl-2-hydroxy-3'-{[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-3',4',4'a,5',5'a,7',8',10'-octahydrospiro[indole-3,6'-pyrano[3,4-f]indolizine]-10'-one

> <JCHEM_LOGP>
-0.14546506533333278

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.207016197354495

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.179436985317975

> <JCHEM_PKA_STRONGEST_BASIC>
1.1117612810679365

> <JCHEM_POLAR_SURFACE_AREA>
161.51

> <JCHEM_REFRACTIVITY>
129.16199999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(3R,3'R,4'S,4'aR,5'aS)-4'-ethenyl-2-hydroxy-3'-{[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4',4'a,5',5'a,7',8'-hexahydro-3'H-spiro[indole-3,6'-pyrano[3,4-f]indolizine]-10'-one

> <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       5.899   0.210   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.826   1.440   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.224   2.857   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.695   3.045   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       3.769   1.815   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       2.240   2.003   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       1.313   0.773   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -0.215   0.961   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.142  -0.269   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -2.671  -0.081   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -0.817   2.378   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -2.346   2.566   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       0.110   3.608   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -0.492   5.026   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       1.638   3.421   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       2.565   4.650   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       4.094   4.463   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       5.020   5.693   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.549   5.505   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.476   6.735   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       6.874   8.152   0.000  0.00  0.00           O+0
HETATM   22  N   UNK     0       9.004   6.547   0.000  0.00  0.00           N+0
HETATM   23  C   UNK     0      10.167   7.557   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      11.487   6.764   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      11.140   5.264   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      12.674   5.398   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      13.467   6.718   0.000  0.00  0.00           O+0
HETATM   28  N   UNK     0      13.276   3.980   0.000  0.00  0.00           N+0
HETATM   29  C   UNK     0      12.114   2.970   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      12.087   1.430   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      10.740   0.684   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       9.420   1.477   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       9.447   3.017   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      10.794   3.763   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       9.606   5.130   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       8.679   3.900   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       7.151   4.087   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   37                                                  
CONECT    4    3    5   17                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   15                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   11                                                  
CONECT    9    8   10                                                       
CONECT   10    9                                                            
CONECT   11    8   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13    6   16                                                  
CONECT   16   15                                                            
CONECT   17    4   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   37                                                  
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   35                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   34   35                                             
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   30   34                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   29   25                                                  
CONECT   35   25   22   36                                                  
CONECT   36   35   37                                                       
CONECT   37   36   19    3                                                  
MASTER        0    0    0    0    0    0    0    0   37    0   84    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₆H₃₀N₂O₉

Average Mass

514.5310 Da

Monoisotopic Mass

514.19513 Da

IUPAC Name

Traditional Name

(3R,3'R,4'S,4'aR,5'aS)-4'-ethenyl-2-hydroxy-3'-{[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4',4'a,5',5'a,7',8'-hexahydro-3'H-spiro[indole-3,6'-pyrano[3,4-f]indolizine]-10'-one

CAS Registry Number

Not Available

SMILES

OC[C@@H]1O[C@H](O[C@H]2OC=C3[C@H](C[C@@H]4N(CC[C@]44C(O)=NC5=CC=CC=C45)C3=O)[C@@H]2C=C)[C@@H](O)[C@H](O)[C@H]1O

InChI Identifier

InChI=1S/C26H30N2O9/c1-2-12-13-9-18-26(15-5-3-4-6-16(15)27-25(26)34)7-8-28(18)22(33)14(13)11-35-23(12)37-24-21(32)20(31)19(30)17(10-29)36-24/h2-6,11-13,17-21,23-24,29-32H,1,7-10H2,(H,27,34)/t12-,13+,17-,18-,19-,20+,21-,23+,24+,26+/m0/s1

InChI Key

UXDQUMNIWFOBFX-GDHPVAJASA-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
Alangium javanicum	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
Indole or derivatives
Dihydroindole
Indolizidine
Delta-lactam
Piperidinone
Monosaccharide
Oxane
Piperidine
Benzenoid
Pyrrolidine
Vinylogous ester
Tertiary carboxylic acid amide
Secondary alcohol
Secondary carboxylic acid amide
Carboxamide group
Lactam
Polyol
Organoheterocyclic compound
Carboxylic acid derivative
Oxacycle
Acetal
Azacycle
Organic oxide
Organopnictogen compound
Organic nitrogen compound
Hydrocarbon derivative
Carbonyl group
Alcohol
Primary alcohol
Organonitrogen compound
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	-0.15	ChemAxon
pKa (Strongest Acidic)	4.18	ChemAxon
pKa (Strongest Basic)	1.11	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	161.51 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	129.16 m³·mol⁻¹	ChemAxon
Polarizability	51.22 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	No	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

162893351

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3r,3'r,4's,4'ar,5'as)-4'-ethenyl-2-hydroxy-3'-{[(2r,3s,4r,5r,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4',4'a,5',5'a,7',8'-hexahydro-3'h-spiro[indole-3,6'-pyrano[3,4-f]indolizin]-10'-one (NP0211441)

MOL for NP0211441 ((3r,3'r,4's,4'ar,5'as)-4'-ethenyl-2-hydroxy-3'-{[(2r,3s,4r,5r,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4',4'a,5',5'a,7',8'-hexahydro-3'h-spiro[indole-3,6'-pyrano[3,4-f]indolizin]-10'-one)

3D MOL for NP0211441 ((3r,3'r,4's,4'ar,5'as)-4'-ethenyl-2-hydroxy-3'-{[(2r,3s,4r,5r,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4',4'a,5',5'a,7',8'-hexahydro-3'h-spiro[indole-3,6'-pyrano[3,4-f]indolizin]-10'-one)

3D SDF for NP0211441 ((3r,3'r,4's,4'ar,5'as)-4'-ethenyl-2-hydroxy-3'-{[(2r,3s,4r,5r,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4',4'a,5',5'a,7',8'-hexahydro-3'h-spiro[indole-3,6'-pyrano[3,4-f]indolizin]-10'-one)

3D-SDF for NP0211441 ((3r,3'r,4's,4'ar,5'as)-4'-ethenyl-2-hydroxy-3'-{[(2r,3s,4r,5r,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4',4'a,5',5'a,7',8'-hexahydro-3'h-spiro[indole-3,6'-pyrano[3,4-f]indolizin]-10'-one)

PDB for NP0211441 ((3r,3'r,4's,4'ar,5'as)-4'-ethenyl-2-hydroxy-3'-{[(2r,3s,4r,5r,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4',4'a,5',5'a,7',8'-hexahydro-3'h-spiro[indole-3,6'-pyrano[3,4-f]indolizin]-10'-one)

3D PDB for NP0211441 ((3r,3'r,4's,4'ar,5'as)-4'-ethenyl-2-hydroxy-3'-{[(2r,3s,4r,5r,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4',4'a,5',5'a,7',8'-hexahydro-3'h-spiro[indole-3,6'-pyrano[3,4-f]indolizin]-10'-one)

SMILES for NP0211441 ((3r,3'r,4's,4'ar,5'as)-4'-ethenyl-2-hydroxy-3'-{[(2r,3s,4r,5r,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4',4'a,5',5'a,7',8'-hexahydro-3'h-spiro[indole-3,6'-pyrano[3,4-f]indolizin]-10'-one)

INCHI for NP0211441 ((3r,3'r,4's,4'ar,5'as)-4'-ethenyl-2-hydroxy-3'-{[(2r,3s,4r,5r,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4',4'a,5',5'a,7',8'-hexahydro-3'h-spiro[indole-3,6'-pyrano[3,4-f]indolizin]-10'-one)

Structure for NP0211441 ((3r,3'r,4's,4'ar,5'as)-4'-ethenyl-2-hydroxy-3'-{[(2r,3s,4r,5r,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4',4'a,5',5'a,7',8'-hexahydro-3'h-spiro[indole-3,6'-pyrano[3,4-f]indolizin]-10'-one)

3D Structure for NP0211441 ((3r,3'r,4's,4'ar,5'as)-4'-ethenyl-2-hydroxy-3'-{[(2r,3s,4r,5r,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4',4'a,5',5'a,7',8'-hexahydro-3'h-spiro[indole-3,6'-pyrano[3,4-f]indolizin]-10'-one)