NP-MRD: Showing NP-Card for 23-hydroxy-17,18-dimethoxy-7,10-dioxa-4,14-diazaheptacyclo[10.8.3.2¹¹,¹⁴.0¹,¹³.0⁶,⁸.0⁶,²³.0¹⁵,²⁰]pentacosa-15(20),16,18-triene-21,24-dione (NP0217866)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-05 18:20:59 UTC

Updated at

2022-09-05 18:20:59 UTC

NP-MRD ID

NP0217866

Secondary Accession Numbers

None

Natural Product Identification

Common Name

23-hydroxy-17,18-dimethoxy-7,10-dioxa-4,14-diazaheptacyclo[10.8.3.2¹¹,¹⁴.0¹,¹³.0⁶,⁸.0⁶,²³.0¹⁵,²⁰]pentacosa-15(20),16,18-triene-21,24-dione

Description

23-Hydroxy-17,18-dimethoxy-7,10-dioxa-4,14-diazaheptacyclo[10.8.3.2¹¹,¹⁴.0¹,¹³.0⁶,⁸.0⁶,²³.0¹⁵,²⁰]Pentacosa-15,17,19-triene-21,24-dione belongs to the class of organic compounds known as carbazoles. Carbazoles are compounds containing a three ring system containing a pyrrole ring fused on either side to a benzene ring. 23-hydroxy-17,18-dimethoxy-7,10-dioxa-4,14-diazaheptacyclo[10.8.3.2¹¹,¹⁴.0¹,¹³.0⁶,⁸.0⁶,²³.0¹⁵,²⁰]pentacosa-15(20),16,18-triene-21,24-dione is found in Strychnos icaja. 23-Hydroxy-17,18-dimethoxy-7,10-dioxa-4,14-diazaheptacyclo[10.8.3.2¹¹,¹⁴.0¹,¹³.0⁶,⁸.0⁶,²³.0¹⁵,²⁰]Pentacosa-15,17,19-triene-21,24-dione is a very strong basic compound (based on its pKa).

Structure

MOL SDF PDB SMILES InChI


  Mrv1533004161514262D          

 32 38  0  0  0  0            999 V2000
    4.3379   -1.0255    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3262   -0.2006    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6060    0.2017    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8974   -0.2209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1772    0.1815    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2670    0.0203    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8448    0.6599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0749    0.6472    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3294   -0.1763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1151   -0.7846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8811   -0.6801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3478   -1.3604    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1887   -0.6298    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9101   -0.1704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9024    0.6455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2481    1.0423    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2184    0.1245    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6180   -0.7776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2104   -1.3210    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1130   -1.1361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5819   -0.3120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3578    0.8135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0198    1.6137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5059    2.2803    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1112    1.6949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5325    0.9890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1608    1.5236    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1655    1.0064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8740    1.4290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5943    1.0266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3028    1.4492    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2912    2.2741    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
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  6 11  1  0  0  0  0
 11 12  2  0  0  0  0
  9 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  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
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
  7 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
  8 26  1  0  0  0  0
 17 26  1  0  0  0  0
 26 27  1  0  0  0  0
 22 28  1  0  0  0  0
  5 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
  3 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
M  END


  Mrv1533004161514262D          

 32 38  0  0  0  0            999 V2000
    4.3379   -1.0255    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3262   -0.2006    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6060    0.2017    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8974   -0.2209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1772    0.1815    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2670    0.0203    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8448    0.6599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0749    0.6472    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3294   -0.1763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1151   -0.7846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8811   -0.6801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3478   -1.3604    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1887   -0.6298    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9101   -0.1704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9024    0.6455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2481    1.0423    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2184    0.1245    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6180   -0.7776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2104   -1.3210    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1130   -1.1361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5819   -0.3120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3578    0.8135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0198    1.6137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5059    2.2803    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1112    1.6949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5325    0.9890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1608    1.5236    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1655    1.0064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8740    1.4290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5943    1.0266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3028    1.4492    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2912    2.2741    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
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  6 11  1  0  0  0  0
 11 12  2  0  0  0  0
  9 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  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
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
  7 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
  8 26  1  0  0  0  0
 17 26  1  0  0  0  0
 26 27  1  0  0  0  0
 22 28  1  0  0  0  0
  5 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
  3 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0217866

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC2=C(C=C1OC)C13CCNCC45OC4COC4CC(=O)N2C1C4C5(O)CC3=O

> <INCHI_IDENTIFIER>
InChI=1S/C23H26N2O7/c1-29-13-5-11-12(6-14(13)30-2)25-18(27)7-15-19-20(25)21(11)3-4-24-10-23(17(32-23)9-31-15)22(19,28)8-16(21)26/h5-6,15,17,19-20,24,28H,3-4,7-10H2,1-2H3

> <INCHI_KEY>
YROKDQUJJIAIBL-UHFFFAOYSA-N

> <FORMULA>
C23H26N2O7

> <MOLECULAR_WEIGHT>
442.468

> <EXACT_MASS>
442.174001185

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
45.12922800373665

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
23-hydroxy-17,18-dimethoxy-7,10-dioxa-4,14-diazaheptacyclo[10.8.3.2¹¹,¹⁴.0¹,¹³.0⁶,⁸.0⁶,²³.0¹⁵,²⁰]pentacosa-15(20),16,18-triene-21,24-dione

> <ALOGPS_LOGP>
-0.08

> <JCHEM_LOGP>
-0.8243370483333339

> <ALOGPS_LOGS>
-1.77

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
14.663919228744632

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.75865675216394

> <JCHEM_PKA_STRONGEST_BASIC>
8.809590520306331

> <JCHEM_POLAR_SURFACE_AREA>
109.86000000000001

> <JCHEM_REFRACTIVITY>
108.8132

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.51e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
23-hydroxy-17,18-dimethoxy-7,10-dioxa-4,14-diazaheptacyclo[10.8.3.2¹¹,¹⁴.0¹,¹³.0⁶,⁸.0⁶,²³.0¹⁵,²⁰]pentacosa-15(20),16,18-triene-21,24-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  C   UNK     0       8.097  -1.914   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       8.076  -0.374   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       6.731   0.377   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.408  -0.412   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.064   0.339   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0       2.365   0.038   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0       1.577   1.232   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.140   1.208   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.615  -0.329   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.215  -1.465   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.645  -1.270   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       2.516  -2.539   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0      -2.219  -1.176   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -3.565  -0.318   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -3.551   1.205   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -2.330   1.946   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -2.274   0.232   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.154  -1.452   0.000  0.00  0.00           C+0
HETATM   19  N   UNK     0       0.393  -2.466   0.000  0.00  0.00           N+0
HETATM   20  C   UNK     0       2.078  -2.121   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.953  -0.582   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.535   1.519   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.904   3.012   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       2.811   4.257   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       0.208   3.164   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -0.994   1.846   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -2.167   2.844   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       4.042   1.879   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       5.365   2.667   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       6.709   1.916   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       8.032   2.705   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       8.010   4.245   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   30                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   28                                                  
CONECT    6    5    7   11                                                  
CONECT    7    6    8   22                                                  
CONECT    8    7    9   26                                                  
CONECT    9    8   10   13                                                  
CONECT   10    9   11                                                       
CONECT   11   10    6   12                                                  
CONECT   12   11                                                            
CONECT   13    9   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15   17                                                       
CONECT   17   16   15   18   26                                             
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21    7   23   28                                             
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25    8   17   27                                             
CONECT   27   26                                                            
CONECT   28   22    5   29                                                  
CONECT   29   28   30                                                       
CONECT   30   29    3   31                                                  
CONECT   31   30   32                                                       
CONECT   32   31                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   76    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₂₆N₂O₇

Average Mass

442.4680 Da

Monoisotopic Mass

442.17400 Da

IUPAC Name

23-hydroxy-17,18-dimethoxy-7,10-dioxa-4,14-diazaheptacyclo[10.8.3.2¹¹,¹⁴.0¹,¹³.0⁶,⁸.0⁶,²³.0¹⁵,²⁰]pentacosa-15(20),16,18-triene-21,24-dione

Traditional Name

23-hydroxy-17,18-dimethoxy-7,10-dioxa-4,14-diazaheptacyclo[10.8.3.2¹¹,¹⁴.0¹,¹³.0⁶,⁸.0⁶,²³.0¹⁵,²⁰]pentacosa-15(20),16,18-triene-21,24-dione

CAS Registry Number

Not Available

SMILES

COC1=CC2=C(C=C1OC)C13CCNCC45OC4COC4CC(=O)N2C1C4C5(O)CC3=O

InChI Identifier

InChI=1S/C23H26N2O7/c1-29-13-5-11-12(6-14(13)30-2)25-18(27)7-15-19-20(25)21(11)3-4-24-10-23(17(32-23)9-31-15)22(19,28)8-16(21)26/h5-6,15,17,19-20,24,28H,3-4,7-10H2,1-2H3

InChI Key

YROKDQUJJIAIBL-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Strychnos icaja	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as carbazoles. Carbazoles are compounds containing a three ring system containing a pyrrole ring fused on either side to a benzene ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Carbazoles

Direct Parent

Carbazoles

Alternative Parents

Substituents

Carbazole
Quinolidine
Anisole
Alkyl aryl ether
Oxepane
Delta-lactam
Aralkylamine
Piperidinone
Piperidine
Benzenoid
Cyclic alcohol
Tertiary carboxylic acid amide
Tertiary alcohol
Ketone
Carboxamide group
Amino acid or derivatives
Lactam
Carboxylic acid derivative
Oxacycle
Azacycle
Dialkyl ether
Secondary aliphatic amine
Oxirane
Ether
Secondary amine
Organic nitrogen compound
Alcohol
Hydrocarbon derivative
Amine
Organic oxygen compound
Organopnictogen compound
Organic oxide
Carbonyl group
Organooxygen 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	-0.08	ALOGPS
logP	-0.82	ChemAxon
logS	-1.8	ALOGPS
pKa (Strongest Acidic)	12.76	ChemAxon
pKa (Strongest Basic)	8.81	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	109.86 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	108.81 m³·mol⁻¹	ChemAxon
Polarizability	45.13 Å³	ChemAxon
Number of Rings	7	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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 23-hydroxy-17,18-dimethoxy-7,10-dioxa-4,14-diazaheptacyclo[10.8.3.2¹¹,¹⁴.0¹,¹³.0⁶,⁸.0⁶,²³.0¹⁵,²⁰]pentacosa-15(20),16,18-triene-21,24-dione (NP0217866)

MOL for NP0217866 (23-hydroxy-17,18-dimethoxy-7,10-dioxa-4,14-diazaheptacyclo[10.8.3.2¹¹,¹⁴.0¹,¹³.0⁶,⁸.0⁶,²³.0¹⁵,²⁰]pentacosa-15(20),16,18-triene-21,24-dione)

3D MOL for NP0217866 (23-hydroxy-17,18-dimethoxy-7,10-dioxa-4,14-diazaheptacyclo[10.8.3.2¹¹,¹⁴.0¹,¹³.0⁶,⁸.0⁶,²³.0¹⁵,²⁰]pentacosa-15(20),16,18-triene-21,24-dione)

3D SDF for NP0217866 (23-hydroxy-17,18-dimethoxy-7,10-dioxa-4,14-diazaheptacyclo[10.8.3.2¹¹,¹⁴.0¹,¹³.0⁶,⁸.0⁶,²³.0¹⁵,²⁰]pentacosa-15(20),16,18-triene-21,24-dione)

3D-SDF for NP0217866 (23-hydroxy-17,18-dimethoxy-7,10-dioxa-4,14-diazaheptacyclo[10.8.3.2¹¹,¹⁴.0¹,¹³.0⁶,⁸.0⁶,²³.0¹⁵,²⁰]pentacosa-15(20),16,18-triene-21,24-dione)

PDB for NP0217866 (23-hydroxy-17,18-dimethoxy-7,10-dioxa-4,14-diazaheptacyclo[10.8.3.2¹¹,¹⁴.0¹,¹³.0⁶,⁸.0⁶,²³.0¹⁵,²⁰]pentacosa-15(20),16,18-triene-21,24-dione)

3D PDB for NP0217866 (23-hydroxy-17,18-dimethoxy-7,10-dioxa-4,14-diazaheptacyclo[10.8.3.2¹¹,¹⁴.0¹,¹³.0⁶,⁸.0⁶,²³.0¹⁵,²⁰]pentacosa-15(20),16,18-triene-21,24-dione)

SMILES for NP0217866 (23-hydroxy-17,18-dimethoxy-7,10-dioxa-4,14-diazaheptacyclo[10.8.3.2¹¹,¹⁴.0¹,¹³.0⁶,⁸.0⁶,²³.0¹⁵,²⁰]pentacosa-15(20),16,18-triene-21,24-dione)

INCHI for NP0217866 (23-hydroxy-17,18-dimethoxy-7,10-dioxa-4,14-diazaheptacyclo[10.8.3.2¹¹,¹⁴.0¹,¹³.0⁶,⁸.0⁶,²³.0¹⁵,²⁰]pentacosa-15(20),16,18-triene-21,24-dione)

Structure for NP0217866 (23-hydroxy-17,18-dimethoxy-7,10-dioxa-4,14-diazaheptacyclo[10.8.3.2¹¹,¹⁴.0¹,¹³.0⁶,⁸.0⁶,²³.0¹⁵,²⁰]pentacosa-15(20),16,18-triene-21,24-dione)

3D Structure for NP0217866 (23-hydroxy-17,18-dimethoxy-7,10-dioxa-4,14-diazaheptacyclo[10.8.3.2¹¹,¹⁴.0¹,¹³.0⁶,⁸.0⁶,²³.0¹⁵,²⁰]pentacosa-15(20),16,18-triene-21,24-dione)