NP-MRD: Showing NP-Card for 5,17,20,22,29-pentahydroxy-9,11,26,28-tetramethyl-2,10,27-trioxaheptacyclo[15.12.0.0¹,²⁵.0³,¹⁶.0⁶,¹⁵.0⁸,¹³.0¹⁸,²³]nonacosa-3,5,8(13),15,18,20,22-heptaene-7,14,24-trione (NP0214470)

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Record Information

Version

2.0

Created at

2022-09-05 13:46:35 UTC

Updated at

2022-09-05 13:46:36 UTC

NP-MRD ID

NP0214470

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5,17,20,22,29-pentahydroxy-9,11,26,28-tetramethyl-2,10,27-trioxaheptacyclo[15.12.0.0¹,²⁵.0³,¹⁶.0⁶,¹⁵.0⁸,¹³.0¹⁸,²³]nonacosa-3,5,8(13),15,18,20,22-heptaene-7,14,24-trione

Description

5,17,20,22,29-Pentahydroxy-9,11,26,28-tetramethyl-2,10,27-trioxaheptacyclo[15.12.0.0¹,²⁵.0³,¹⁶.0⁶,¹⁵.0⁸,¹³.0¹⁸,²³]Nonacosa-3(16),4,6(15),8(13),18(23),19,21-heptaene-7,14,24-trione belongs to the class of organic compounds known as quassinoids. These are a group of compounds chemically degraded from triterpenes. According to their basic skeleton, quassinoids are categorized into five distinct groups, C-18, C-19, C-20, C-22 and C-25 types. The C-20 quassinoids can be further classified into two types, tetracyclic and the pentacyclic. The tetracyclic variety does not have oxygenation at C-20, while the pentacyclic quassinoids possess additional oxygenation at C-20 that allows for the formation of an additional ring. 5,17,20,22,29-pentahydroxy-9,11,26,28-tetramethyl-2,10,27-trioxaheptacyclo[15.12.0.0¹,²⁵.0³,¹⁶.0⁶,¹⁵.0⁸,¹³.0¹⁸,²³]nonacosa-3,5,8(13),15,18,20,22-heptaene-7,14,24-trione is found in Uroleucon nigrotuberculatum. 5,17,20,22,29-Pentahydroxy-9,11,26,28-tetramethyl-2,10,27-trioxaheptacyclo[15.12.0.0¹,²⁵.0³,¹⁶.0⁶,¹⁵.0⁸,¹³.0¹⁸,²³]Nonacosa-3(16),4,6(15),8(13),18(23),19,21-heptaene-7,14,24-trione is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004231523582D          

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M  END

     RDKit          3D

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M  END


  Mrv1533004231523582D          

 41 47  0  0  0  0            999 V2000
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    0.4236    0.7697    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1610    1.3518    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2200    0.9850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4318    1.7823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8472    2.3644    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2282    1.9976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8129    1.4155    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6093    1.6307    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6011    0.6181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8046    0.4029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5928   -0.3945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4074   -0.2637    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0437   -1.0854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8588   -1.2127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3766   -0.5704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0793    0.1991    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  2  8  1  0  0  0  0
  5  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  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
 23 25  1  0  0  0  0
 17 25  1  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
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
 34 35  2  0  0  0  0
 28 35  1  0  0  0  0
 35 36  1  0  0  0  0
 17 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 15 38  1  0  0  0  0
 38 39  2  0  0  0  0
 11 39  1  0  0  0  0
 39 40  1  0  0  0  0
  4 40  1  0  0  0  0
 40 41  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0214470

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1CC2=C(C(C)O1)C(=O)C1=C(O)C=C3OC45C(O)C(C)OC(C)C4C(=O)C4=C(O)C=C(O)C=C4C5(O)C3=C1C2=O

> <INCHI_IDENTIFIER>
InChI=1S/C30H28O11/c1-9-5-14-19(10(2)39-9)26(35)21-17(33)8-18-24(22(21)25(14)34)29(38)15-6-13(31)7-16(32)20(15)27(36)23-11(3)40-12(4)28(37)30(23,29)41-18/h6-12,23,28,31-33,37-38H,5H2,1-4H3

> <INCHI_KEY>
PALHHCRJJXZADT-UHFFFAOYSA-N

> <FORMULA>
C30H28O11

> <MOLECULAR_WEIGHT>
564.543

> <EXACT_MASS>
564.163161722

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
69

> <JCHEM_AVERAGE_POLARIZABILITY>
56.648137904247804

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
5,17,20,22,29-pentahydroxy-9,11,26,28-tetramethyl-2,10,27-trioxaheptacyclo[15.12.0.0¹,²⁵.0³,¹⁶.0⁶,¹⁵.0⁸,¹³.0¹⁸,²³]nonacosa-3,5,8(13),15,18,20,22-heptaene-7,14,24-trione

> <ALOGPS_LOGP>
3.18

> <JCHEM_LOGP>
2.285595647666667

> <ALOGPS_LOGS>
-2.86

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.154359446919713

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.484978552516287

> <JCHEM_PKA_STRONGEST_BASIC>
-3.7146946864968724

> <JCHEM_POLAR_SURFACE_AREA>
180.05

> <JCHEM_REFRACTIVITY>
142.18990000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
7.71e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5,17,20,22,29-pentahydroxy-9,11,26,28-tetramethyl-2,10,27-trioxaheptacyclo[15.12.0.0¹,²⁵.0³,¹⁶.0⁶,¹⁵.0⁸,¹³.0¹⁸,²³]nonacosa-3,5,8(13),15,18,20,22-heptaene-7,14,24-trione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 23-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-APR-15         0                                  
HETATM    1  C   UNK     0      11.279   0.858   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.313  -0.341   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.791  -0.103   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.825  -1.302   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.380  -2.739   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.901  -2.977   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.456  -4.413   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      10.868  -1.778   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       7.413  -3.938   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       7.968  -5.374   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       5.891  -3.700   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.925  -4.899   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       5.480  -6.336   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       3.403  -4.662   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.848  -3.225   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       1.786  -2.458   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       1.487  -1.138   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.091  -2.627   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       2.183  -3.713   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -0.395  -3.028   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -0.791  -4.517   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -1.487  -1.942   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -1.091  -0.453   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -2.183   0.633   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.395  -0.052   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.791   1.437   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -0.301   2.523   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       2.277   1.839   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.673   3.327   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       1.581   4.414   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       4.159   3.729   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       5.251   2.642   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       6.737   3.044   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       4.855   1.154   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       3.369   0.752   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       2.973  -0.736   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       4.494  -0.492   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       3.815  -2.026   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       5.336  -2.264   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       6.303  -1.065   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       5.748   0.372   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    8                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   40                                                  
CONECT    5    4    6    9                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    2                                                       
CONECT    9    5   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   39                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16   38                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   25   36                                             
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   17   26                                                  
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29   35                                                  
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32                                                       
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35                                                       
CONECT   35   34   28   36                                                  
CONECT   36   35   17   37   38                                             
CONECT   37   36                                                            
CONECT   38   36   15   39                                                  
CONECT   39   38   11   40                                                  
CONECT   40   39    4   41                                                  
CONECT   41   40                                                            
MASTER        0    0    0    0    0    0    0    0   41    0   94    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₂₈O₁₁

Average Mass

564.5430 Da

Monoisotopic Mass

564.16316 Da

IUPAC Name

5,17,20,22,29-pentahydroxy-9,11,26,28-tetramethyl-2,10,27-trioxaheptacyclo[15.12.0.0¹,²⁵.0³,¹⁶.0⁶,¹⁵.0⁸,¹³.0¹⁸,²³]nonacosa-3,5,8(13),15,18,20,22-heptaene-7,14,24-trione

Traditional Name

5,17,20,22,29-pentahydroxy-9,11,26,28-tetramethyl-2,10,27-trioxaheptacyclo[15.12.0.0¹,²⁵.0³,¹⁶.0⁶,¹⁵.0⁸,¹³.0¹⁸,²³]nonacosa-3,5,8(13),15,18,20,22-heptaene-7,14,24-trione

CAS Registry Number

Not Available

SMILES

CC1CC2=C(C(C)O1)C(=O)C1=C(O)C=C3OC45C(O)C(C)OC(C)C4C(=O)C4=C(O)C=C(O)C=C4C5(O)C3=C1C2=O

InChI Identifier

InChI=1S/C30H28O11/c1-9-5-14-19(10(2)39-9)26(35)21-17(33)8-18-24(22(21)25(14)34)29(38)15-6-13(31)7-16(32)20(15)27(36)23-11(3)40-12(4)28(37)30(23,29)41-18/h6-12,23,28,31-33,37-38H,5H2,1-4H3

InChI Key

PALHHCRJJXZADT-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
Uroleucon nigrotuberculatum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as quassinoids. These are a group of compounds chemically degraded from triterpenes. According to their basic skeleton, quassinoids are categorized into five distinct groups, C-18, C-19, C-20, C-22 and C-25 types. The C-20 quassinoids can be further classified into two types, tetracyclic and the pentacyclic. The tetracyclic variety does not have oxygenation at C-20, while the pentacyclic quassinoids possess additional oxygenation at C-20 that allows for the formation of an additional ring.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Quassinoids

Alternative Parents

Substituents

C-20 quassinoid skeleton
Quassinoid
Naphthopyran
Naphthalene
Furopyran
Delta valerolactone
Fatty acid ester
Cyclohexenone
Delta_valerolactone
Oxepane
Dicarboxylic acid or derivatives
Fatty acyl
Oxane
Pyran
Tetrahydrofuran
Cyclic alcohol
Furan
Secondary alcohol
Cyclic ketone
Carboxylic acid ester
Ketone
Lactone
Ether
Dialkyl ether
Polyol
Oxacycle
Carboxylic acid derivative
Organoheterocyclic compound
Hydrocarbon derivative
Organooxygen compound
Organic oxide
Alcohol
Organic oxygen compound
Carbonyl group
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	3.18	ALOGPS
logP	2.29	ChemAxon
logS	-2.9	ALOGPS
pKa (Strongest Acidic)	7.48	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	180.05 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	142.19 m³·mol⁻¹	ChemAxon
Polarizability	56.65 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	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

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 5,17,20,22,29-pentahydroxy-9,11,26,28-tetramethyl-2,10,27-trioxaheptacyclo[15.12.0.0¹,²⁵.0³,¹⁶.0⁶,¹⁵.0⁸,¹³.0¹⁸,²³]nonacosa-3,5,8(13),15,18,20,22-heptaene-7,14,24-trione (NP0214470)

MOL for NP0214470 (5,17,20,22,29-pentahydroxy-9,11,26,28-tetramethyl-2,10,27-trioxaheptacyclo[15.12.0.0¹,²⁵.0³,¹⁶.0⁶,¹⁵.0⁸,¹³.0¹⁸,²³]nonacosa-3,5,8(13),15,18,20,22-heptaene-7,14,24-trione)

3D MOL for NP0214470 (5,17,20,22,29-pentahydroxy-9,11,26,28-tetramethyl-2,10,27-trioxaheptacyclo[15.12.0.0¹,²⁵.0³,¹⁶.0⁶,¹⁵.0⁸,¹³.0¹⁸,²³]nonacosa-3,5,8(13),15,18,20,22-heptaene-7,14,24-trione)

3D SDF for NP0214470 (5,17,20,22,29-pentahydroxy-9,11,26,28-tetramethyl-2,10,27-trioxaheptacyclo[15.12.0.0¹,²⁵.0³,¹⁶.0⁶,¹⁵.0⁸,¹³.0¹⁸,²³]nonacosa-3,5,8(13),15,18,20,22-heptaene-7,14,24-trione)

3D-SDF for NP0214470 (5,17,20,22,29-pentahydroxy-9,11,26,28-tetramethyl-2,10,27-trioxaheptacyclo[15.12.0.0¹,²⁵.0³,¹⁶.0⁶,¹⁵.0⁸,¹³.0¹⁸,²³]nonacosa-3,5,8(13),15,18,20,22-heptaene-7,14,24-trione)

PDB for NP0214470 (5,17,20,22,29-pentahydroxy-9,11,26,28-tetramethyl-2,10,27-trioxaheptacyclo[15.12.0.0¹,²⁵.0³,¹⁶.0⁶,¹⁵.0⁸,¹³.0¹⁸,²³]nonacosa-3,5,8(13),15,18,20,22-heptaene-7,14,24-trione)

3D PDB for NP0214470 (5,17,20,22,29-pentahydroxy-9,11,26,28-tetramethyl-2,10,27-trioxaheptacyclo[15.12.0.0¹,²⁵.0³,¹⁶.0⁶,¹⁵.0⁸,¹³.0¹⁸,²³]nonacosa-3,5,8(13),15,18,20,22-heptaene-7,14,24-trione)

SMILES for NP0214470 (5,17,20,22,29-pentahydroxy-9,11,26,28-tetramethyl-2,10,27-trioxaheptacyclo[15.12.0.0¹,²⁵.0³,¹⁶.0⁶,¹⁵.0⁸,¹³.0¹⁸,²³]nonacosa-3,5,8(13),15,18,20,22-heptaene-7,14,24-trione)

INCHI for NP0214470 (5,17,20,22,29-pentahydroxy-9,11,26,28-tetramethyl-2,10,27-trioxaheptacyclo[15.12.0.0¹,²⁵.0³,¹⁶.0⁶,¹⁵.0⁸,¹³.0¹⁸,²³]nonacosa-3,5,8(13),15,18,20,22-heptaene-7,14,24-trione)

Structure for NP0214470 (5,17,20,22,29-pentahydroxy-9,11,26,28-tetramethyl-2,10,27-trioxaheptacyclo[15.12.0.0¹,²⁵.0³,¹⁶.0⁶,¹⁵.0⁸,¹³.0¹⁸,²³]nonacosa-3,5,8(13),15,18,20,22-heptaene-7,14,24-trione)

3D Structure for NP0214470 (5,17,20,22,29-pentahydroxy-9,11,26,28-tetramethyl-2,10,27-trioxaheptacyclo[15.12.0.0¹,²⁵.0³,¹⁶.0⁶,¹⁵.0⁸,¹³.0¹⁸,²³]nonacosa-3,5,8(13),15,18,20,22-heptaene-7,14,24-trione)