NP-MRD: Showing NP-Card for (1s,2s,4r,5r,10r,11s,13r,16s,17s,20s)-4,5,13,17-tetrahydroxy-16-[(2r)-2-hydroxy-4,5-dimethyl-6-oxo-3h-pyran-2-yl]-10,20-dimethyl-14-oxapentacyclo[11.6.1.0²,¹¹.0⁵,¹⁰.0¹⁷,²⁰]icos-7-en-9-one (NP0206398)

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Record Information

Version

2.0

Created at

2022-09-05 02:37:50 UTC

Updated at

2022-09-05 02:37:50 UTC

NP-MRD ID

NP0206398

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2s,4r,5r,10r,11s,13r,16s,17s,20s)-4,5,13,17-tetrahydroxy-16-[(2r)-2-hydroxy-4,5-dimethyl-6-oxo-3h-pyran-2-yl]-10,20-dimethyl-14-oxapentacyclo[11.6.1.0²,¹¹.0⁵,¹⁰.0¹⁷,²⁰]icos-7-en-9-one

Description

(1S,2S,4R,5R,10R,11S,13R,16S,17S,20S)-4,5,13,17-tetrahydroxy-16-[(2R)-2-hydroxy-4,5-dimethyl-6-oxo-3,6-dihydro-2H-pyran-2-yl]-10,20-dimethyl-14-oxapentacyclo[11.6.1.0²,¹¹.0⁵,¹⁰.0¹⁷,²⁰]Icos-7-en-9-one belongs to the class of organic compounds known as steroid lactones. These are sterol lipids containing a lactone moiety linked to the steroid skeleton. (1s,2s,4r,5r,10r,11s,13r,16s,17s,20s)-4,5,13,17-tetrahydroxy-16-[(2r)-2-hydroxy-4,5-dimethyl-6-oxo-3h-pyran-2-yl]-10,20-dimethyl-14-oxapentacyclo[11.6.1.0²,¹¹.0⁵,¹⁰.0¹⁷,²⁰]icos-7-en-9-one is found in Jaborosa caulescens. Based on a literature review very few articles have been published on (1S,2S,4R,5R,10R,11S,13R,16S,17S,20S)-4,5,13,17-tetrahydroxy-16-[(2R)-2-hydroxy-4,5-dimethyl-6-oxo-3,6-dihydro-2H-pyran-2-yl]-10,20-dimethyl-14-oxapentacyclo[11.6.1.0²,¹¹.0⁵,¹⁰.0¹⁷,²⁰]Icos-7-en-9-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052204372D          

 37 42  0  0  1  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1652309052204372D          

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    4.4663    2.4477    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6909    1.0365    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1712    1.6773    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7663    0.0067    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3175   -0.6855    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5205   -0.4726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4767    0.3512    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8937   -0.2326    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2466    0.6475    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0434    0.8616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0929    1.3834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  8 10  1  6  0  0  0
 10 11  1  1  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
 13 15  1  0  0  0  0
 16 15  1  6  0  0  0
 16 17  1  0  0  0  0
 17 18  1  1  0  0  0
 18 19  1  0  0  0  0
 19 20  1  6  0  0  0
 19 21  1  0  0  0  0
 21 22  1  1  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 16 28  1  0  0  0  0
 21 28  1  0  0  0  0
 28 29  1  6  0  0  0
 17 30  1  0  0  0  0
 30 31  1  6  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 10 33  1  0  0  0  0
 33 34  1  1  0  0  0
 33 35  1  0  0  0  0
 30 35  1  0  0  0  0
 13 35  1  0  0  0  0
 35 36  1  6  0  0  0
  8 37  1  0  0  0  0
  2 37  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0206398

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=C(C)C(=O)O[C@](O)(C1)[C@H]1CO[C@]2(O)C[C@H]3[C@@H](C[C@@H](O)[C@@]4(O)CC=CC(=O)[C@]34C)[C@@H]3CC[C@@]1(O)[C@@]23C

> <INCHI_IDENTIFIER>
InChI=1S/C28H38O9/c1-14-11-27(34,37-22(31)15(14)2)19-13-36-28(35)12-18-16(17-7-9-25(19,32)24(17,28)4)10-21(30)26(33)8-5-6-20(29)23(18,26)3/h5-6,16-19,21,30,32-35H,7-13H2,1-4H3/t16-,17-,18-,19-,21+,23-,24-,25-,26-,27+,28+/m0/s1

> <INCHI_KEY>
VRYOFCDLUFFOBU-UBJHLIQCSA-N

> <FORMULA>
C28H38O9

> <MOLECULAR_WEIGHT>
518.603

> <EXACT_MASS>
518.251582804

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
75

> <JCHEM_AVERAGE_POLARIZABILITY>
54.81074481028359

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2S,4R,5R,10R,11S,13R,16S,17S,20S)-4,5,13,17-tetrahydroxy-16-[(2R)-2-hydroxy-4,5-dimethyl-6-oxo-3,6-dihydro-2H-pyran-2-yl]-10,20-dimethyl-14-oxapentacyclo[11.6.1.0^{2,11}.0^{5,10}.0^{17,20}]icos-7-en-9-one

> <JCHEM_LOGP>
1.7953331383333304

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.802220453222624

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.201989725070598

> <JCHEM_PKA_STRONGEST_BASIC>
-3.258134932128563

> <JCHEM_POLAR_SURFACE_AREA>
153.75

> <JCHEM_REFRACTIVITY>
131.8806

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,4R,5R,10R,11S,13R,16S,17S,20S)-4,5,13,17-tetrahydroxy-16-[(2R)-2-hydroxy-4,5-dimethyl-6-oxo-3H-pyran-2-yl]-10,20-dimethyl-14-oxapentacyclo[11.6.1.0^{2,11}.0^{5,10}.0^{17,20}]icos-7-en-9-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      -1.925   4.594   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.630   3.083   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.791   2.071   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.248   2.572   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.496   0.560   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -3.658  -0.451   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0      -1.040   0.060   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       0.122   1.071   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       0.916  -0.249   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       1.559   1.624   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.799   3.145   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       3.236   3.698   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       4.433   2.730   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       4.884   4.203   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       6.265   2.889   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.235   1.693   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.685   0.255   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.655  -0.941   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.176  -0.699   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      10.146  -1.895   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       9.726   0.739   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      10.696  -0.457   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      11.247   0.981   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      11.798   2.419   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      10.828   3.615   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       9.307   3.373   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       8.337   4.569   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       8.756   1.935   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       7.786   3.131   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.164   0.013   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.326  -1.280   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       2.838  -0.882   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       2.756   0.656   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       1.668  -0.434   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       4.194   1.209   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       5.681   1.608   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      -0.173   2.582   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   37                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   10   37                                             
CONECT    9    8                                                            
CONECT   10    8   11   33                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15   35                                             
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17   28                                                  
CONECT   17   16   18   30                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   23   28                                             
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   16   21   29                                             
CONECT   29   28                                                            
CONECT   30   17   31   35                                                  
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   10   34   35                                             
CONECT   34   33                                                            
CONECT   35   33   30   13   36                                             
CONECT   36   35                                                            
CONECT   37    8    2                                                       
MASTER        0    0    0    0    0    0    0    0   37    0   84    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₈H₃₈O₉

Average Mass

518.6030 Da

Monoisotopic Mass

518.25158 Da

IUPAC Name

Traditional Name

(1S,2S,4R,5R,10R,11S,13R,16S,17S,20S)-4,5,13,17-tetrahydroxy-16-[(2R)-2-hydroxy-4,5-dimethyl-6-oxo-3H-pyran-2-yl]-10,20-dimethyl-14-oxapentacyclo[11.6.1.0^{2,11}.0^{5,10}.0^{17,20}]icos-7-en-9-one

CAS Registry Number

Not Available

SMILES

CC1=C(C)C(=O)O[C@](O)(C1)[C@H]1CO[C@]2(O)C[C@H]3[C@@H](C[C@@H](O)[C@@]4(O)CC=CC(=O)[C@]34C)[C@@H]3CC[C@@]1(O)[C@@]23C

InChI Identifier

InChI=1S/C28H38O9/c1-14-11-27(34,37-22(31)15(14)2)19-13-36-28(35)12-18-16(17-7-9-25(19,32)24(17,28)4)10-21(30)26(33)8-5-6-20(29)23(18,26)3/h5-6,16-19,21,30,32-35H,7-13H2,1-4H3/t16-,17-,18-,19-,21+,23-,24-,25-,26-,27+,28+/m0/s1

InChI Key

VRYOFCDLUFFOBU-UBJHLIQCSA-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
Jaborosa caulescens	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as steroid lactones. These are sterol lipids containing a lactone moiety linked to the steroid skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroid lactones

Direct Parent

Steroid lactones

Alternative Parents

Substituents

22-hydroxysteroid
Steroid lactone
12-hydroxysteroid
6-hydroxysteroid
5-hydroxysteroid
Hydroxysteroid
1-oxosteroid
Oxosteroid
17-hydroxysteroid
Naphthopyran
Iridoid-skeleton
Naphthalene
Dihydropyranone
Cyclohexenone
Pyran
Oxane
Alpha,beta-unsaturated carboxylic ester
Cyclic alcohol
Tertiary alcohol
Enoate ester
Carboxylic acid ester
Secondary alcohol
Lactone
Ketone
Hemiacetal
Organoheterocyclic compound
Polyol
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Oxacycle
Carbonyl group
Alcohol
Organooxygen compound
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
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	ChemAxon
pKa (Strongest Acidic)	11.2	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	153.75 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	131.88 m³·mol⁻¹	ChemAxon
Polarizability	54.81 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

162897849

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,2s,4r,5r,10r,11s,13r,16s,17s,20s)-4,5,13,17-tetrahydroxy-16-[(2r)-2-hydroxy-4,5-dimethyl-6-oxo-3h-pyran-2-yl]-10,20-dimethyl-14-oxapentacyclo[11.6.1.0²,¹¹.0⁵,¹⁰.0¹⁷,²⁰]icos-7-en-9-one (NP0206398)

MOL for NP0206398 ((1s,2s,4r,5r,10r,11s,13r,16s,17s,20s)-4,5,13,17-tetrahydroxy-16-[(2r)-2-hydroxy-4,5-dimethyl-6-oxo-3h-pyran-2-yl]-10,20-dimethyl-14-oxapentacyclo[11.6.1.0²,¹¹.0⁵,¹⁰.0¹⁷,²⁰]icos-7-en-9-one)

3D MOL for NP0206398 ((1s,2s,4r,5r,10r,11s,13r,16s,17s,20s)-4,5,13,17-tetrahydroxy-16-[(2r)-2-hydroxy-4,5-dimethyl-6-oxo-3h-pyran-2-yl]-10,20-dimethyl-14-oxapentacyclo[11.6.1.0²,¹¹.0⁵,¹⁰.0¹⁷,²⁰]icos-7-en-9-one)

3D SDF for NP0206398 ((1s,2s,4r,5r,10r,11s,13r,16s,17s,20s)-4,5,13,17-tetrahydroxy-16-[(2r)-2-hydroxy-4,5-dimethyl-6-oxo-3h-pyran-2-yl]-10,20-dimethyl-14-oxapentacyclo[11.6.1.0²,¹¹.0⁵,¹⁰.0¹⁷,²⁰]icos-7-en-9-one)

3D-SDF for NP0206398 ((1s,2s,4r,5r,10r,11s,13r,16s,17s,20s)-4,5,13,17-tetrahydroxy-16-[(2r)-2-hydroxy-4,5-dimethyl-6-oxo-3h-pyran-2-yl]-10,20-dimethyl-14-oxapentacyclo[11.6.1.0²,¹¹.0⁵,¹⁰.0¹⁷,²⁰]icos-7-en-9-one)

PDB for NP0206398 ((1s,2s,4r,5r,10r,11s,13r,16s,17s,20s)-4,5,13,17-tetrahydroxy-16-[(2r)-2-hydroxy-4,5-dimethyl-6-oxo-3h-pyran-2-yl]-10,20-dimethyl-14-oxapentacyclo[11.6.1.0²,¹¹.0⁵,¹⁰.0¹⁷,²⁰]icos-7-en-9-one)

3D PDB for NP0206398 ((1s,2s,4r,5r,10r,11s,13r,16s,17s,20s)-4,5,13,17-tetrahydroxy-16-[(2r)-2-hydroxy-4,5-dimethyl-6-oxo-3h-pyran-2-yl]-10,20-dimethyl-14-oxapentacyclo[11.6.1.0²,¹¹.0⁵,¹⁰.0¹⁷,²⁰]icos-7-en-9-one)

SMILES for NP0206398 ((1s,2s,4r,5r,10r,11s,13r,16s,17s,20s)-4,5,13,17-tetrahydroxy-16-[(2r)-2-hydroxy-4,5-dimethyl-6-oxo-3h-pyran-2-yl]-10,20-dimethyl-14-oxapentacyclo[11.6.1.0²,¹¹.0⁵,¹⁰.0¹⁷,²⁰]icos-7-en-9-one)

INCHI for NP0206398 ((1s,2s,4r,5r,10r,11s,13r,16s,17s,20s)-4,5,13,17-tetrahydroxy-16-[(2r)-2-hydroxy-4,5-dimethyl-6-oxo-3h-pyran-2-yl]-10,20-dimethyl-14-oxapentacyclo[11.6.1.0²,¹¹.0⁵,¹⁰.0¹⁷,²⁰]icos-7-en-9-one)

Structure for NP0206398 ((1s,2s,4r,5r,10r,11s,13r,16s,17s,20s)-4,5,13,17-tetrahydroxy-16-[(2r)-2-hydroxy-4,5-dimethyl-6-oxo-3h-pyran-2-yl]-10,20-dimethyl-14-oxapentacyclo[11.6.1.0²,¹¹.0⁵,¹⁰.0¹⁷,²⁰]icos-7-en-9-one)

3D Structure for NP0206398 ((1s,2s,4r,5r,10r,11s,13r,16s,17s,20s)-4,5,13,17-tetrahydroxy-16-[(2r)-2-hydroxy-4,5-dimethyl-6-oxo-3h-pyran-2-yl]-10,20-dimethyl-14-oxapentacyclo[11.6.1.0²,¹¹.0⁵,¹⁰.0¹⁷,²⁰]icos-7-en-9-one)