NP-MRD: Showing NP-Card for (1s,2s,5s,6s,9s,10s,13s,16s,18r)-16-{[(2s,3r,4s,5r)-4,5-dihydroxy-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-2-yl]oxy}-10-hydroxy-2,6,13,17,17-pentamethyl-6-(4-methylpentyl)-7-oxapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-11-en-8-one (NP0198107)

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Record Information

Version

2.0

Created at

2022-09-04 16:29:40 UTC

Updated at

2022-09-04 16:29:41 UTC

NP-MRD ID

NP0198107

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2s,5s,6s,9s,10s,13s,16s,18r)-16-{[(2s,3r,4s,5r)-4,5-dihydroxy-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-2-yl]oxy}-10-hydroxy-2,6,13,17,17-pentamethyl-6-(4-methylpentyl)-7-oxapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-11-en-8-one

Description

SCHEMBL6259817 belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. (1s,2s,5s,6s,9s,10s,13s,16s,18r)-16-{[(2s,3r,4s,5r)-4,5-dihydroxy-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-2-yl]oxy}-10-hydroxy-2,6,13,17,17-pentamethyl-6-(4-methylpentyl)-7-oxapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-11-en-8-one is found in Bohadschia bivittata. Based on a literature review very few articles have been published on SCHEMBL6259817.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042218292D          

 53 59  0  0  1  0            999 V2000
   -2.6434    0.8190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.7847   -0.2673    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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 12 53  1  0  0  0  0
M  END

     RDKit          3D

119125  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1652309042218292D          

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  7 53  1  0  0  0  0
 12 53  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0198107

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)CCC[C@]1(C)OC(=O)[C@@]23[C@@H]1CC[C@@]2(C)[C@@H]1CC[C@H]2C(C)(C)[C@H](CC[C@]2(C)C1=C[C@@H]3O)O[C@@H]1OC[C@@H](O)[C@H](O)[C@H]1O[C@@H]1O[C@H](C)[C@@H](O)[C@H](O)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C41H66O12/c1-20(2)10-9-15-40(8)26-13-17-39(7)22-11-12-25-37(4,5)28(14-16-38(25,6)23(22)18-27(43)41(26,39)36(48)53-40)51-35-33(30(45)24(42)19-49-35)52-34-32(47)31(46)29(44)21(3)50-34/h18,20-22,24-35,42-47H,9-17,19H2,1-8H3/t21-,22-,24-,25+,26-,27+,28+,29-,30+,31+,32-,33-,34+,35+,38-,39+,40+,41+/m1/s1

> <INCHI_KEY>
GOYXWSSENLVERY-YZRCTGSKSA-N

> <FORMULA>
C41H66O12

> <MOLECULAR_WEIGHT>
750.967

> <EXACT_MASS>
750.455427565

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
119

> <JCHEM_AVERAGE_POLARIZABILITY>
83.99607369070873

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2S,5S,6S,9S,10S,13S,16S,18R)-16-{[(2S,3R,4S,5R)-4,5-dihydroxy-3-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-2-yl]oxy}-10-hydroxy-2,6,13,17,17-pentamethyl-6-(4-methylpentyl)-7-oxapentacyclo[10.8.0.0^{2,9}.0^{5,9}.0^{13,18}]icos-11-en-8-one

> <JCHEM_LOGP>
3.757536335999999

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.769071267017452

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.12169514864474

> <JCHEM_PKA_STRONGEST_BASIC>
-3.2198545378505754

> <JCHEM_POLAR_SURFACE_AREA>
184.6

> <JCHEM_REFRACTIVITY>
192.55030000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,5S,6S,9S,10S,13S,16S,18R)-16-{[(2S,3R,4S,5R)-4,5-dihydroxy-3-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-2-yl]oxy}-10-hydroxy-2,6,13,17,17-pentamethyl-6-(4-methylpentyl)-7-oxapentacyclo[10.8.0.0^{2,9}.0^{5,9}.0^{13,18}]icos-11-en-8-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0      -4.934   1.529   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -3.772   0.519   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.066  -0.993   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.316   1.020   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.154   0.010   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.302   0.511   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.465  -0.499   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.339  -1.549   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       2.348   0.763   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       3.821   0.313   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       5.051   1.240   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       3.848  -1.227   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.449   0.190   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       3.522   1.420   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       5.978   0.378   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.905  -0.852   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.303  -2.269   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.230  -3.499   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.759  -3.311   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.360  -1.894   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      10.889  -1.706   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      10.808  -3.244   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      12.389  -2.052   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      11.490  -0.288   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      13.019  -0.100   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      13.620   1.317   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      12.693   2.547   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      13.295   3.965   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      14.824   4.153   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      15.425   5.570   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      15.751   2.923   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      17.279   3.111   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      15.149   1.505   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      16.076   0.275   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      17.604   0.463   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      18.206   1.881   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      19.734   2.069   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      20.336   3.486   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      20.661   0.839   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      22.190   1.027   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      20.060  -0.579   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0      20.987  -1.809   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0      18.531  -0.767   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0      17.930  -2.184   0.000  0.00  0.00           O+0
HETATM   45  C   UNK     0      10.563   0.942   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       9.035   0.754   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       8.433  -0.664   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       7.506   0.566   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0       4.775  -2.457   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0       5.568  -3.777   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0       3.892  -3.719   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0       2.419  -3.268   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0       2.392  -1.729   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9   53                                             
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   49   53                                             
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17   47                                                  
CONECT   17   16   18   49                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   47                                                  
CONECT   21   20   22   23   24                                             
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   21   25   45                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   33                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   26   34                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36   43                                                  
CONECT   36   35   37                                                       
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41   35   44                                                  
CONECT   44   43                                                            
CONECT   45   24   46                                                       
CONECT   46   45   47                                                       
CONECT   47   46   16   20   48                                             
CONECT   48   47                                                            
CONECT   49   17   12   50   51                                             
CONECT   50   49                                                            
CONECT   51   49   52                                                       
CONECT   52   51   53                                                       
CONECT   53   52    7   12                                                  
MASTER        0    0    0    0    0    0    0    0   53    0  118    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₁H₆₆O₁₂

Average Mass

750.9670 Da

Monoisotopic Mass

750.45543 Da

IUPAC Name

(1S,2S,5S,6S,9S,10S,13S,16S,18R)-16-{[(2S,3R,4S,5R)-4,5-dihydroxy-3-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-2-yl]oxy}-10-hydroxy-2,6,13,17,17-pentamethyl-6-(4-methylpentyl)-7-oxapentacyclo[10.8.0.0^{2,9}.0^{5,9}.0^{13,18}]icos-11-en-8-one

Traditional Name

CAS Registry Number

Not Available

SMILES

CC(C)CCC[C@]1(C)OC(=O)[C@@]23[C@@H]1CC[C@@]2(C)[C@@H]1CC[C@H]2C(C)(C)[C@H](CC[C@]2(C)C1=C[C@@H]3O)O[C@@H]1OC[C@@H](O)[C@H](O)[C@H]1O[C@@H]1O[C@H](C)[C@@H](O)[C@H](O)[C@H]1O

InChI Identifier

InChI=1S/C41H66O12/c1-20(2)10-9-15-40(8)26-13-17-39(7)22-11-12-25-37(4,5)28(14-16-38(25,6)23(22)18-27(43)41(26,39)36(48)53-40)51-35-33(30(45)24(42)19-49-35)52-34-32(47)31(46)29(44)21(3)50-34/h18,20-22,24-35,42-47H,9-17,19H2,1-8H3/t21-,22-,24-,25+,26-,27+,28+,29-,30+,31+,32-,33-,34+,35+,38-,39+,40+,41+/m1/s1

InChI Key

GOYXWSSENLVERY-YZRCTGSKSA-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
Bohadschia bivittata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Triterpenoids

Alternative Parents

Substituents

Triterpenoid
Steroidal glycoside
Steroid lactone
12-hydroxysteroid
Hydroxysteroid
Steroid
Disaccharide
Glycosyl compound
O-glycosyl compound
Gamma butyrolactone
Oxane
Tetrahydrofuran
Secondary alcohol
Lactone
Carboxylic acid ester
Acetal
Monocarboxylic acid or derivatives
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Polyol
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Carbonyl group
Alcohol
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	3.76	ChemAxon
pKa (Strongest Acidic)	12.12	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	184.6 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	192.55 m³·mol⁻¹	ChemAxon
Polarizability	84 Å³	ChemAxon
Number of Rings	7	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

10244713

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

21607583

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,5s,6s,9s,10s,13s,16s,18r)-16-{[(2s,3r,4s,5r)-4,5-dihydroxy-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-2-yl]oxy}-10-hydroxy-2,6,13,17,17-pentamethyl-6-(4-methylpentyl)-7-oxapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-11-en-8-one (NP0198107)

MOL for NP0198107 ((1s,2s,5s,6s,9s,10s,13s,16s,18r)-16-{[(2s,3r,4s,5r)-4,5-dihydroxy-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-2-yl]oxy}-10-hydroxy-2,6,13,17,17-pentamethyl-6-(4-methylpentyl)-7-oxapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-11-en-8-one)

3D MOL for NP0198107 ((1s,2s,5s,6s,9s,10s,13s,16s,18r)-16-{[(2s,3r,4s,5r)-4,5-dihydroxy-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-2-yl]oxy}-10-hydroxy-2,6,13,17,17-pentamethyl-6-(4-methylpentyl)-7-oxapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-11-en-8-one)

3D SDF for NP0198107 ((1s,2s,5s,6s,9s,10s,13s,16s,18r)-16-{[(2s,3r,4s,5r)-4,5-dihydroxy-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-2-yl]oxy}-10-hydroxy-2,6,13,17,17-pentamethyl-6-(4-methylpentyl)-7-oxapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-11-en-8-one)

3D-SDF for NP0198107 ((1s,2s,5s,6s,9s,10s,13s,16s,18r)-16-{[(2s,3r,4s,5r)-4,5-dihydroxy-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-2-yl]oxy}-10-hydroxy-2,6,13,17,17-pentamethyl-6-(4-methylpentyl)-7-oxapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-11-en-8-one)

PDB for NP0198107 ((1s,2s,5s,6s,9s,10s,13s,16s,18r)-16-{[(2s,3r,4s,5r)-4,5-dihydroxy-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-2-yl]oxy}-10-hydroxy-2,6,13,17,17-pentamethyl-6-(4-methylpentyl)-7-oxapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-11-en-8-one)

3D PDB for NP0198107 ((1s,2s,5s,6s,9s,10s,13s,16s,18r)-16-{[(2s,3r,4s,5r)-4,5-dihydroxy-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-2-yl]oxy}-10-hydroxy-2,6,13,17,17-pentamethyl-6-(4-methylpentyl)-7-oxapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-11-en-8-one)

SMILES for NP0198107 ((1s,2s,5s,6s,9s,10s,13s,16s,18r)-16-{[(2s,3r,4s,5r)-4,5-dihydroxy-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-2-yl]oxy}-10-hydroxy-2,6,13,17,17-pentamethyl-6-(4-methylpentyl)-7-oxapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-11-en-8-one)

INCHI for NP0198107 ((1s,2s,5s,6s,9s,10s,13s,16s,18r)-16-{[(2s,3r,4s,5r)-4,5-dihydroxy-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-2-yl]oxy}-10-hydroxy-2,6,13,17,17-pentamethyl-6-(4-methylpentyl)-7-oxapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-11-en-8-one)

Structure for NP0198107 ((1s,2s,5s,6s,9s,10s,13s,16s,18r)-16-{[(2s,3r,4s,5r)-4,5-dihydroxy-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-2-yl]oxy}-10-hydroxy-2,6,13,17,17-pentamethyl-6-(4-methylpentyl)-7-oxapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-11-en-8-one)

3D Structure for NP0198107 ((1s,2s,5s,6s,9s,10s,13s,16s,18r)-16-{[(2s,3r,4s,5r)-4,5-dihydroxy-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-2-yl]oxy}-10-hydroxy-2,6,13,17,17-pentamethyl-6-(4-methylpentyl)-7-oxapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-11-en-8-one)