NP-MRD: Showing NP-Card for 1-[9,17-dihydroxy-21-(2-hydroxypropyl)-6,20-dimethoxy-7,19-dioxo-12,14-dioxahexacyclo[13.8.0.0²,¹¹.0³,⁸.0⁴,²².0¹⁸,²³]tricosa-1(23),2(11),3(8),4(22),5,9,15,17,20-nonaen-5-yl]propan-2-yl acetate (NP0147893)

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Record Information

Version

2.0

Created at

2022-09-02 03:34:42 UTC

Updated at

2022-09-02 03:34:42 UTC

NP-MRD ID

NP0147893

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-[9,17-dihydroxy-21-(2-hydroxypropyl)-6,20-dimethoxy-7,19-dioxo-12,14-dioxahexacyclo[13.8.0.0²,¹¹.0³,⁸.0⁴,²².0¹⁸,²³]tricosa-1(23),2(11),3(8),4(22),5,9,15,17,20-nonaen-5-yl]propan-2-yl acetate

Description

1-[9,17-Dihydroxy-21-(2-hydroxypropyl)-6,20-dimethoxy-7,19-dioxo-12,14-dioxahexacyclo[13.8.0.0²,¹¹.0³,⁸.0⁴,²².0¹⁸,²³]Tricosa-1(15),2(11),3(8),4(22),5,9,16,18(23),20-nonaen-5-yl]propan-2-yl acetate belongs to the class of organic compounds known as perylenequinones. These are heterocyclic compounds characterized by two 8-hydroxy-1,4-dihydronaphthalen-1-one moieties joined together one or two CC-bonds. 1-[9,17-Dihydroxy-21-(2-hydroxypropyl)-6,20-dimethoxy-7,19-dioxo-12,14-dioxahexacyclo[13.8.0.0²,¹¹.0³,⁸.0⁴,²².0¹⁸,²³]Tricosa-1(15),2(11),3(8),4(22),5,9,16,18(23),20-nonaen-5-yl]propan-2-yl acetate is a strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004261512402D          

 42 47  0  0  0  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1533004261512402D          

 42 47  0  0  0  0            999 V2000
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    3.5635    2.0563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2806    2.4642    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1346    2.0656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4228    2.4827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7057    2.0748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7003    1.2498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1186   -0.4094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1133   -1.2344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3961   -1.6422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8251   -1.6515    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8197   -2.4764    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1026   -2.8843    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5315   -2.8936    0.0000 C   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  2  0  0  0  0
  4  5  1  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
  4  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 12 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
  3 30  1  0  0  0  0
 30 31  2  0  0  0  0
 29 32  2  0  0  0  0
  9 32  1  0  0  0  0
 32 33  1  0  0  0  0
 25 33  2  0  0  0  0
 33 34  1  0  0  0  0
 21 34  2  0  0  0  0
 34 35  1  0  0  0  0
 10 35  1  0  0  0  0
 17 35  2  0  0  0  0
 11 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 37 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
 40 42  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0147893

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(CC(C)O)C2=C3C(CC(C)OC(C)=O)=C(OC)C(=O)C4=C3C3=C(OCOC5=C3C2=C(C(O)=C5)C1=O)C=C4O

> <INCHI_IDENTIFIER>
InChI=1S/C31H28O11/c1-11(32)6-14-20-21-15(7-12(2)42-13(3)33)31(39-5)29(37)23-17(35)9-19-25(27(21)23)24-18(40-10-41-19)8-16(34)22(26(20)24)28(36)30(14)38-4/h8-9,11-12,32,34-35H,6-7,10H2,1-5H3

> <INCHI_KEY>
KGRDKNXMYLHGRI-UHFFFAOYSA-N

> <FORMULA>
C31H28O11

> <MOLECULAR_WEIGHT>
576.554

> <EXACT_MASS>
576.163161722

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
70

> <JCHEM_AVERAGE_POLARIZABILITY>
57.86067756945609

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
1-[9,17-dihydroxy-21-(2-hydroxypropyl)-6,20-dimethoxy-7,19-dioxo-12,14-dioxahexacyclo[13.8.0.0²,¹¹.0³,⁸.0⁴,²².0¹⁸,²³]tricosa-1(15),2(11),3(8),4(22),5,9,16,18(23),20-nonaen-5-yl]propan-2-yl acetate

> <ALOGPS_LOGP>
3.13

> <JCHEM_LOGP>
3.7768203566666676

> <ALOGPS_LOGS>
-4.49

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
7.026439881331792

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.424400233228942

> <JCHEM_PKA_STRONGEST_BASIC>
3.1870105496423258

> <JCHEM_POLAR_SURFACE_AREA>
158.04999999999998

> <JCHEM_REFRACTIVITY>
151.25879999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.89e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-[9,17-dihydroxy-21-(2-hydroxypropyl)-6,20-dimethoxy-7,19-dioxo-12,14-dioxahexacyclo[13.8.0.0²,¹¹.0³,⁸.0⁴,²².0¹⁸,²³]tricosa-1(15),2(11),3(8),4(22),5,9,16,18(23),20-nonaen-5-yl]propan-2-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 26-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   26-APR-15         0                                  
HETATM    1  C   UNK     0       9.309   2.281   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       7.971   1.520   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       6.642   2.299   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.303   1.537   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.293  -0.003   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.622  -0.781   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.961  -0.020   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       6.612  -2.321   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       3.975   2.316   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.636   1.554   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.626   0.014   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.287  -0.747   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       1.277  -2.287   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -0.061  -3.048   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.041   0.032   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -1.380  -0.730   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -0.031   1.572   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.360   2.350   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -2.699   1.589   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -1.350   3.890   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -0.113   4.445   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -0.557   5.919   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       0.319   7.186   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       1.855   7.291   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       2.895   6.156   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.004   6.936   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.333   6.157   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       6.672   6.918   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       5.323   4.617   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       6.652   3.839   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       7.990   4.600   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       3.985   3.856   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       2.656   4.634   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       1.317   3.873   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       1.307   2.333   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       3.955  -0.764   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       3.945  -2.304   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       2.606  -3.066   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       5.273  -3.083   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0       5.263  -4.623   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       3.925  -5.384   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       6.592  -5.401   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   30                                                  
CONECT    4    3    5    9                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6                                                            
CONECT    9    4   10   32                                                  
CONECT   10    9   11   35                                                  
CONECT   11   10   12   36                                                  
CONECT   12   11   13   15                                                  
CONECT   13   12   14                                                       
CONECT   14   13                                                            
CONECT   15   12   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   35                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22   34                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   33                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   32                                                  
CONECT   30   29    3   31                                                  
CONECT   31   30                                                            
CONECT   32   29    9   33                                                  
CONECT   33   32   25   34                                                  
CONECT   34   33   21   35                                                  
CONECT   35   34   10   17                                                  
CONECT   36   11   37                                                       
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40                                                       
CONECT   40   39   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40                                                            
MASTER        0    0    0    0    0    0    0    0   42    0   94    0
END

View in JSmol

Synonyms

Value	Source
1-[9,17-Dihydroxy-21-(2-hydroxypropyl)-6,20-dimethoxy-7,19-dioxo-12,14-dioxahexacyclo[13.8.0.0,.0,.0,.0,]tricosa-1(15),2(11),3(8),4(22),5,9,16,18(23),20-nonaen-5-yl]propan-2-yl acetic acid	Generator
1-[9,17-Dihydroxy-21-(2-hydroxypropyl)-6,20-dimethoxy-7,19-dioxo-12,14-dioxahexacyclo[13.8.0.0²,¹¹.0³,⁸.0⁴,²².0¹⁸,²³]tricosa-1(15),2(11),3(8),4(22),5,9,16,18(23),20-nonaen-5-yl]propan-2-yl acetic acid	Generator

Chemical Formula

C₃₁H₂₈O₁₁

Average Mass

576.5540 Da

Monoisotopic Mass

576.16316 Da

IUPAC Name

1-[9,17-dihydroxy-21-(2-hydroxypropyl)-6,20-dimethoxy-7,19-dioxo-12,14-dioxahexacyclo[13.8.0.0²,¹¹.0³,⁸.0⁴,²².0¹⁸,²³]tricosa-1(15),2(11),3(8),4(22),5,9,16,18(23),20-nonaen-5-yl]propan-2-yl acetate

Traditional Name

CAS Registry Number

Not Available

SMILES

COC1=C(CC(C)O)C2=C3C(CC(C)OC(C)=O)=C(OC)C(=O)C4=C3C3=C(OCOC5=C3C2=C(C(O)=C5)C1=O)C=C4O

InChI Identifier

InChI=1S/C31H28O11/c1-11(32)6-14-20-21-15(7-12(2)42-13(3)33)31(39-5)29(37)23-17(35)9-19-25(27(21)23)24-18(40-10-41-19)8-16(34)22(26(20)24)28(36)30(14)38-4/h8-9,11-12,32,34-35H,6-7,10H2,1-5H3

InChI Key

KGRDKNXMYLHGRI-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as perylenequinones. These are heterocyclic compounds characterized by two 8-hydroxy-1,4-dihydronaphthalen-1-one moieties joined together one or two CC-bonds.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Perylenequinones

Sub Class

Not Available

Direct Parent

Perylenequinones

Alternative Parents

Substituents

Perylenequinone
Phenanthrol
Anthracene
Phenanthrene
2-naphthol
1-naphthol
Anisole
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Vinylogous acid
Carboxylic acid ester
Secondary alcohol
Acetal
Organoheterocyclic compound
Oxacycle
Monocarboxylic acid or derivatives
Ether
Carboxylic acid derivative
Organooxygen compound
Carbonyl group
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Alcohol
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	3.13	ALOGPS
logP	3.78	ChemAxon
logS	-4.5	ALOGPS
pKa (Strongest Acidic)	6.42	ChemAxon
pKa (Strongest Basic)	3.19	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	158.05 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	151.26 m³·mol⁻¹	ChemAxon
Polarizability	57.86 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	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 1-[9,17-dihydroxy-21-(2-hydroxypropyl)-6,20-dimethoxy-7,19-dioxo-12,14-dioxahexacyclo[13.8.0.0²,¹¹.0³,⁸.0⁴,²².0¹⁸,²³]tricosa-1(23),2(11),3(8),4(22),5,9,15,17,20-nonaen-5-yl]propan-2-yl acetate (NP0147893)

MOL for NP0147893 (1-[9,17-dihydroxy-21-(2-hydroxypropyl)-6,20-dimethoxy-7,19-dioxo-12,14-dioxahexacyclo[13.8.0.0²,¹¹.0³,⁸.0⁴,²².0¹⁸,²³]tricosa-1(23),2(11),3(8),4(22),5,9,15,17,20-nonaen-5-yl]propan-2-yl acetate)

3D MOL for NP0147893 (1-[9,17-dihydroxy-21-(2-hydroxypropyl)-6,20-dimethoxy-7,19-dioxo-12,14-dioxahexacyclo[13.8.0.0²,¹¹.0³,⁸.0⁴,²².0¹⁸,²³]tricosa-1(23),2(11),3(8),4(22),5,9,15,17,20-nonaen-5-yl]propan-2-yl acetate)

3D SDF for NP0147893 (1-[9,17-dihydroxy-21-(2-hydroxypropyl)-6,20-dimethoxy-7,19-dioxo-12,14-dioxahexacyclo[13.8.0.0²,¹¹.0³,⁸.0⁴,²².0¹⁸,²³]tricosa-1(23),2(11),3(8),4(22),5,9,15,17,20-nonaen-5-yl]propan-2-yl acetate)

3D-SDF for NP0147893 (1-[9,17-dihydroxy-21-(2-hydroxypropyl)-6,20-dimethoxy-7,19-dioxo-12,14-dioxahexacyclo[13.8.0.0²,¹¹.0³,⁸.0⁴,²².0¹⁸,²³]tricosa-1(23),2(11),3(8),4(22),5,9,15,17,20-nonaen-5-yl]propan-2-yl acetate)

PDB for NP0147893 (1-[9,17-dihydroxy-21-(2-hydroxypropyl)-6,20-dimethoxy-7,19-dioxo-12,14-dioxahexacyclo[13.8.0.0²,¹¹.0³,⁸.0⁴,²².0¹⁸,²³]tricosa-1(23),2(11),3(8),4(22),5,9,15,17,20-nonaen-5-yl]propan-2-yl acetate)

3D PDB for NP0147893 (1-[9,17-dihydroxy-21-(2-hydroxypropyl)-6,20-dimethoxy-7,19-dioxo-12,14-dioxahexacyclo[13.8.0.0²,¹¹.0³,⁸.0⁴,²².0¹⁸,²³]tricosa-1(23),2(11),3(8),4(22),5,9,15,17,20-nonaen-5-yl]propan-2-yl acetate)

SMILES for NP0147893 (1-[9,17-dihydroxy-21-(2-hydroxypropyl)-6,20-dimethoxy-7,19-dioxo-12,14-dioxahexacyclo[13.8.0.0²,¹¹.0³,⁸.0⁴,²².0¹⁸,²³]tricosa-1(23),2(11),3(8),4(22),5,9,15,17,20-nonaen-5-yl]propan-2-yl acetate)

INCHI for NP0147893 (1-[9,17-dihydroxy-21-(2-hydroxypropyl)-6,20-dimethoxy-7,19-dioxo-12,14-dioxahexacyclo[13.8.0.0²,¹¹.0³,⁸.0⁴,²².0¹⁸,²³]tricosa-1(23),2(11),3(8),4(22),5,9,15,17,20-nonaen-5-yl]propan-2-yl acetate)

Structure for NP0147893 (1-[9,17-dihydroxy-21-(2-hydroxypropyl)-6,20-dimethoxy-7,19-dioxo-12,14-dioxahexacyclo[13.8.0.0²,¹¹.0³,⁸.0⁴,²².0¹⁸,²³]tricosa-1(23),2(11),3(8),4(22),5,9,15,17,20-nonaen-5-yl]propan-2-yl acetate)

3D Structure for NP0147893 (1-[9,17-dihydroxy-21-(2-hydroxypropyl)-6,20-dimethoxy-7,19-dioxo-12,14-dioxahexacyclo[13.8.0.0²,¹¹.0³,⁸.0⁴,²².0¹⁸,²³]tricosa-1(23),2(11),3(8),4(22),5,9,15,17,20-nonaen-5-yl]propan-2-yl acetate)