NP-MRD: Showing NP-Card for 15-hydroxy-8,10-dioxa-13,19-diazaoctacyclo[12.8.2.1¹,¹⁵.0²,¹⁹.0³,¹⁴.0³,¹⁷.0⁴,¹².0⁷,¹¹]pentacosa-4,6,11-triene-16,18-dione (NP0218756)

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Record Information

Version

2.0

Created at

2022-09-05 19:31:41 UTC

Updated at

2022-09-05 19:31:41 UTC

NP-MRD ID

NP0218756

Secondary Accession Numbers

None

Natural Product Identification

Common Name

15-hydroxy-8,10-dioxa-13,19-diazaoctacyclo[12.8.2.1¹,¹⁵.0²,¹⁹.0³,¹⁴.0³,¹⁷.0⁴,¹².0⁷,¹¹]pentacosa-4,6,11-triene-16,18-dione

Description

15-Hydroxy-8,10-dioxa-13,19-diazaoctacyclo[12.8.2.1¹,¹⁵.0²,¹⁹.0³,¹⁴.0³,¹⁷.0⁴,¹².0⁷,¹¹]Pentacosa-4(12),5,7(11)-triene-16,18-dione belongs to the class of organic compounds known as aspidofractine alkaloids. These are alkaloids with a structure that is based on the hexacyclic aspidofractine core. These compounds are related to the Aspidosperma group by formation of a C-2 to C-18 bond. 15-Hydroxy-8,10-dioxa-13,19-diazaoctacyclo[12.8.2.1¹,¹⁵.0²,¹⁹.0³,¹⁴.0³,¹⁷.0⁴,¹².0⁷,¹¹]Pentacosa-4(12),5,7(11)-triene-16,18-dione is a moderately basic compound (based on its pKa).

Structure

MOL SDF PDB SMILES InChI


  Mrv1533004161523202D          

 28 35  0  0  0  0            999 V2000
    1.0345   -1.1733    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0684   -0.3490    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0469   -0.0737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0239    0.5416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7443    1.0506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8017    1.8975    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0845    2.3342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6985    1.9226    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5823    1.1208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3457    0.7733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9271    0.8284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5738    1.7646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1017    2.3986    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0098   -0.1765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6647   -0.6782    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1559    1.3108    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2561    2.1297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0153    2.4524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6744    1.9562    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4842    2.1141    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8845    1.3927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3222    0.7890    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5743    1.1373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8151    0.8146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5059    0.0643    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5290   -0.1293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9094   -0.8841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0057   -0.5467    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  1  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
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  4  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
  8 12  1  0  0  0  0
 12 13  2  0  0  0  0
 11 14  1  0  0  0  0
  2 14  1  0  0  0  0
 14 15  2  0  0  0  0
 10 16  1  0  0  0  0
 16 17  2  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  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 19 23  1  0  0  0  0
 23 24  2  0  0  0  0
 16 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
  2 26  1  0  0  0  0
 10 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
  4 28  1  0  0  0  0
M  END


  Mrv1533004161523202D          

 28 35  0  0  0  0            999 V2000
    1.0345   -1.1733    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0684   -0.3490    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0469   -0.0737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0239    0.5416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7443    1.0506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8017    1.8975    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0845    2.3342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6985    1.9226    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5823    1.1208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3457    0.7733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9271    0.8284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5738    1.7646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1017    2.3986    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0098   -0.1765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6647   -0.6782    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1559    1.3108    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2561    2.1297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0153    2.4524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6744    1.9562    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4842    2.1141    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8845    1.3927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3222    0.7890    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5743    1.1373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8151    0.8146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5059    0.0643    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5290   -0.1293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9094   -0.8841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0057   -0.5467    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  1  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
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  4  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
  8 12  1  0  0  0  0
 12 13  2  0  0  0  0
 11 14  1  0  0  0  0
  2 14  1  0  0  0  0
 14 15  2  0  0  0  0
 10 16  1  0  0  0  0
 16 17  2  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  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 19 23  1  0  0  0  0
 23 24  2  0  0  0  0
 16 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
  2 26  1  0  0  0  0
 10 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
  4 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0218756

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC12CC34CCCN5C3C3(C(C5=O)C1=O)C1=CC=C5OCOC5=C1NC23CC4

> <INCHI_IDENTIFIER>
InChI=1S/C21H20N2O5/c24-15-12-16(25)23-7-1-4-18-5-6-20(19(15,26)8-18)21(12,17(18)23)10-2-3-11-14(13(10)22-20)28-9-27-11/h2-3,12,17,22,26H,1,4-9H2

> <INCHI_KEY>
BOKUSIZTGUYFFP-UHFFFAOYSA-N

> <FORMULA>
C21H20N2O5

> <MOLECULAR_WEIGHT>
380.4

> <EXACT_MASS>
380.137221752

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
48

> <JCHEM_AVERAGE_POLARIZABILITY>
38.225958562622566

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
15-hydroxy-8,10-dioxa-13,19-diazaoctacyclo[12.8.2.1¹,¹⁵.0²,¹⁹.0³,¹⁴.0³,¹⁷.0⁴,¹².0⁷,¹¹]pentacosa-4,6,11-triene-16,18-dione

> <ALOGPS_LOGP>
1.25

> <JCHEM_LOGP>
0.35225311366666745

> <ALOGPS_LOGS>
-1.35

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
8

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.79279861784203

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.272342746539683

> <JCHEM_PKA_STRONGEST_BASIC>
2.530088634063406

> <JCHEM_POLAR_SURFACE_AREA>
88.10000000000001

> <JCHEM_REFRACTIVITY>
96.2589

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.72e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
15-hydroxy-8,10-dioxa-13,19-diazaoctacyclo[12.8.2.1¹,¹⁵.0²,¹⁹.0³,¹⁴.0³,¹⁷.0⁴,¹².0⁷,¹¹]pentacosa-4,6,11-triene-16,18-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  O   UNK     0       1.931  -2.190   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       1.994  -0.652   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.088  -0.138   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.045   1.011   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.389   1.961   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.497   3.542   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.158   4.357   0.000  0.00  0.00           C+0
HETATM    8  N   UNK     0       1.304   3.589   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0       1.087   2.092   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.512   1.444   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.597   1.546   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.938   3.294   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       3.923   4.477   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       3.752  -0.329   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       4.974  -1.266   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       4.024   2.447   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.211   3.975   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.629   4.578   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.859   3.652   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       8.371   3.946   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       9.118   2.600   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       8.068   1.473   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       6.672   2.123   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.255   1.521   0.000  0.00  0.00           C+0
HETATM   25  N   UNK     0       4.678   0.120   0.000  0.00  0.00           N+0
HETATM   26  C   UNK     0       2.854  -0.241   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       1.697  -1.650   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       0.011  -1.020   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   14   26                                             
CONECT    3    2    4                                                       
CONECT    4    3    5    9   28                                             
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   12                                                  
CONECT    9    8    4   10                                                  
CONECT   10    9   11   16   26                                             
CONECT   11   10   12   14                                                  
CONECT   12   11    8   13                                                  
CONECT   13   12                                                            
CONECT   14   11    2   15                                                  
CONECT   15   14                                                            
CONECT   16   10   17   24                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   23                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   19   24                                                  
CONECT   24   23   16   25                                                  
CONECT   25   24   26                                                       
CONECT   26   25    2   10   27                                             
CONECT   27   26   28                                                       
CONECT   28   27    4                                                       
MASTER        0    0    0    0    0    0    0    0   28    0   70    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₂₀N₂O₅

Average Mass

380.4000 Da

Monoisotopic Mass

380.13722 Da

IUPAC Name

15-hydroxy-8,10-dioxa-13,19-diazaoctacyclo[12.8.2.1¹,¹⁵.0²,¹⁹.0³,¹⁴.0³,¹⁷.0⁴,¹².0⁷,¹¹]pentacosa-4,6,11-triene-16,18-dione

Traditional Name

15-hydroxy-8,10-dioxa-13,19-diazaoctacyclo[12.8.2.1¹,¹⁵.0²,¹⁹.0³,¹⁴.0³,¹⁷.0⁴,¹².0⁷,¹¹]pentacosa-4,6,11-triene-16,18-dione

CAS Registry Number

Not Available

SMILES

OC12CC34CCCN5C3C3(C(C5=O)C1=O)C1=CC=C5OCOC5=C1NC23CC4

InChI Identifier

InChI=1S/C21H20N2O5/c24-15-12-16(25)23-7-1-4-18-5-6-20(19(15,26)8-18)21(12,17(18)23)10-2-3-11-14(13(10)22-20)28-9-27-11/h2-3,12,17,22,26H,1,4-9H2

InChI Key

BOKUSIZTGUYFFP-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as aspidofractine alkaloids. These are alkaloids with a structure that is based on the hexacyclic aspidofractine core. These compounds are related to the Aspidosperma group by formation of a C-2 to C-18 bond.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Aspidofractine alkaloids

Sub Class

Not Available

Direct Parent

Aspidofractine alkaloids

Alternative Parents

Substituents

Aspidofractine skeleton
Aspidosperma alkaloid
Carbazole
2,3-cyclopentanoindoline
Azaspirodecane
Quinolidine
Benzodioxole
Indole or derivatives
Dihydroindole
Indolizidine
Aralkylamine
Secondary aliphatic/aromatic amine
Benzenoid
N-alkylpyrrolidine
1,3-dicarbonyl compound
Pyrrolidone
2-pyrrolidone
Piperidine
Cyclic alcohol
Pyrrolidine
Tertiary carboxylic acid amide
Tertiary alcohol
Amino acid or derivatives
Carboxamide group
Ketone
Lactam
Secondary amine
Organoheterocyclic compound
Carboxylic acid derivative
Acetal
Oxacycle
Azacycle
Organooxygen compound
Carbonyl group
Organic oxide
Organopnictogen compound
Organic oxygen compound
Amine
Alcohol
Hydrocarbon derivative
Organic nitrogen compound
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	1.25	ALOGPS
logP	0.35	ChemAxon
logS	-1.4	ALOGPS
pKa (Strongest Acidic)	12.27	ChemAxon
pKa (Strongest Basic)	2.53	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	88.1 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	96.26 m³·mol⁻¹	ChemAxon
Polarizability	38.23 Å³	ChemAxon
Number of Rings	8	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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 15-hydroxy-8,10-dioxa-13,19-diazaoctacyclo[12.8.2.1¹,¹⁵.0²,¹⁹.0³,¹⁴.0³,¹⁷.0⁴,¹².0⁷,¹¹]pentacosa-4,6,11-triene-16,18-dione (NP0218756)

MOL for NP0218756 (15-hydroxy-8,10-dioxa-13,19-diazaoctacyclo[12.8.2.1¹,¹⁵.0²,¹⁹.0³,¹⁴.0³,¹⁷.0⁴,¹².0⁷,¹¹]pentacosa-4,6,11-triene-16,18-dione)

3D MOL for NP0218756 (15-hydroxy-8,10-dioxa-13,19-diazaoctacyclo[12.8.2.1¹,¹⁵.0²,¹⁹.0³,¹⁴.0³,¹⁷.0⁴,¹².0⁷,¹¹]pentacosa-4,6,11-triene-16,18-dione)

3D SDF for NP0218756 (15-hydroxy-8,10-dioxa-13,19-diazaoctacyclo[12.8.2.1¹,¹⁵.0²,¹⁹.0³,¹⁴.0³,¹⁷.0⁴,¹².0⁷,¹¹]pentacosa-4,6,11-triene-16,18-dione)

3D-SDF for NP0218756 (15-hydroxy-8,10-dioxa-13,19-diazaoctacyclo[12.8.2.1¹,¹⁵.0²,¹⁹.0³,¹⁴.0³,¹⁷.0⁴,¹².0⁷,¹¹]pentacosa-4,6,11-triene-16,18-dione)

PDB for NP0218756 (15-hydroxy-8,10-dioxa-13,19-diazaoctacyclo[12.8.2.1¹,¹⁵.0²,¹⁹.0³,¹⁴.0³,¹⁷.0⁴,¹².0⁷,¹¹]pentacosa-4,6,11-triene-16,18-dione)

3D PDB for NP0218756 (15-hydroxy-8,10-dioxa-13,19-diazaoctacyclo[12.8.2.1¹,¹⁵.0²,¹⁹.0³,¹⁴.0³,¹⁷.0⁴,¹².0⁷,¹¹]pentacosa-4,6,11-triene-16,18-dione)

SMILES for NP0218756 (15-hydroxy-8,10-dioxa-13,19-diazaoctacyclo[12.8.2.1¹,¹⁵.0²,¹⁹.0³,¹⁴.0³,¹⁷.0⁴,¹².0⁷,¹¹]pentacosa-4,6,11-triene-16,18-dione)

INCHI for NP0218756 (15-hydroxy-8,10-dioxa-13,19-diazaoctacyclo[12.8.2.1¹,¹⁵.0²,¹⁹.0³,¹⁴.0³,¹⁷.0⁴,¹².0⁷,¹¹]pentacosa-4,6,11-triene-16,18-dione)

Structure for NP0218756 (15-hydroxy-8,10-dioxa-13,19-diazaoctacyclo[12.8.2.1¹,¹⁵.0²,¹⁹.0³,¹⁴.0³,¹⁷.0⁴,¹².0⁷,¹¹]pentacosa-4,6,11-triene-16,18-dione)

3D Structure for NP0218756 (15-hydroxy-8,10-dioxa-13,19-diazaoctacyclo[12.8.2.1¹,¹⁵.0²,¹⁹.0³,¹⁴.0³,¹⁷.0⁴,¹².0⁷,¹¹]pentacosa-4,6,11-triene-16,18-dione)