NP-MRD: Showing NP-Card for methyl (1s,9s,10r,12s)-20-oxo-19-oxa-8,16-diazahexacyclo[8.8.2.2⁹,¹².0¹,⁹.0²,⁷.0¹²,¹⁶]docosa-2,4,6,13-tetraene-8-carboxylate (NP0223007)

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Record Information

Version

2.0

Created at

2022-09-06 00:59:03 UTC

Updated at

2022-09-06 00:59:04 UTC

NP-MRD ID

NP0223007

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (1s,9s,10r,12s)-20-oxo-19-oxa-8,16-diazahexacyclo[8.8.2.2⁹,¹².0¹,⁹.0²,⁷.0¹²,¹⁶]docosa-2,4,6,13-tetraene-8-carboxylate

Description

Methyl (1S,9S,10R,12S)-20-oxo-19-oxa-8,16-diazahexacyclo[8.8.2.2⁹,¹².0¹,⁹.0²,⁷.0¹²,¹⁶]Docosa-2,4,6,13-tetraene-8-carboxylate belongs to the class of organic compounds known as indolecarboxylic acids. Indolecarboxylic acids are compounds containing a carboxylic acid group linked to an indole. Based on a literature review very few articles have been published on methyl (1S,9S,10R,12S)-20-oxo-19-oxa-8,16-diazahexacyclo[8.8.2.2⁹,¹².0¹,⁹.0²,⁷.0¹²,¹⁶]Docosa-2,4,6,13-tetraene-8-carboxylate.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309062202592D          

 27 32  0  0  1  0            999 V2000
   -0.6992   -1.2934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5888   -0.4759    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1744   -0.1627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8273   -0.6670    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2848    0.6549    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3817    1.2334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1940    1.0891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7251    1.7204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4439    2.4960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6317    2.6403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1005    2.0090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8000    2.0327    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5182    2.5689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3990    2.5130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1506    2.0361    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.7688    2.6226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4695    2.1680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2660    1.3425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4303    1.1544    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8181    0.4627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8858    0.4978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0975    1.0439    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8874    1.2970    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6519    1.2000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2522    1.7171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8042    2.3303    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4388    1.3969    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  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 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
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 15  1  1  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  5  1  6  0  0  0
 12 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 19 24  1  0  0  0  0
 23 25  1  6  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 12 27  1  6  0  0  0
M  END


  Mrv1652309062202592D          

 27 32  0  0  1  0            999 V2000
   -0.6992   -1.2934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5888   -0.4759    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1744   -0.1627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8273   -0.6670    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2848    0.6549    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3817    1.2334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1940    1.0891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7251    1.7204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4439    2.4960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6317    2.6403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1005    2.0090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8000    2.0327    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5182    2.5689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3990    2.5130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1506    2.0361    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.7688    2.6226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4695    2.1680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2660    1.3425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4303    1.1544    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8181    0.4627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8858    0.4978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0975    1.0439    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8874    1.2970    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6519    1.2000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2522    1.7171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8042    2.3303    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4388    1.3969    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  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 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
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 15  1  1  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  5  1  6  0  0  0
 12 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 19 24  1  0  0  0  0
 23 25  1  6  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 12 27  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0223007

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)N1C2=CC=CC=C2[C@@]23CCN4CC=C[C@@]44CC[C@@]12[C@@H](C4)C(=O)O3

> <INCHI_IDENTIFIER>
InChI=1S/C21H22N2O4/c1-26-18(25)23-16-6-3-2-5-14(16)21-10-12-22-11-4-7-19(22)8-9-20(21,23)15(13-19)17(24)27-21/h2-7,15H,8-13H2,1H3/t15-,19-,20-,21-/m0/s1

> <INCHI_KEY>
GLOIILVAVSJIEX-ZEWNOJEFSA-N

> <FORMULA>
C21H22N2O4

> <MOLECULAR_WEIGHT>
366.417

> <EXACT_MASS>
366.157957196

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
49

> <JCHEM_AVERAGE_POLARIZABILITY>
38.47145202995189

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (1S,9S,10R,12S)-20-oxo-19-oxa-8,16-diazahexacyclo[8.8.2.2^{9,12}.0^{1,9}.0^{2,7}.0^{12,16}]docosa-2,4,6,13-tetraene-8-carboxylate

> <JCHEM_LOGP>
1.9950590509999993

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_BASIC>
9.82271467028367

> <JCHEM_POLAR_SURFACE_AREA>
59.08

> <JCHEM_REFRACTIVITY>
98.09659999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1S,9S,10R,12S)-20-oxo-19-oxa-8,16-diazahexacyclo[8.8.2.2^{9,12}.0^{1,9}.0^{2,7}.0^{12,16}]docosa-2,4,6,13-tetraene-8-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0      -1.305  -2.414   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -1.099  -0.888   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       0.326  -0.304   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       1.544  -1.245   0.000  0.00  0.00           O+0
HETATM    5  N   UNK     0       0.532   1.223   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0      -0.713   2.302   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.229   2.033   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -3.220   3.211   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.695   4.659   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.179   4.929   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.188   3.750   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.493   3.794   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.834   4.795   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.478   4.691   0.000  0.00  0.00           C+0
HETATM   15  N   UNK     0       5.881   3.801   0.000  0.00  0.00           N+0
HETATM   16  C   UNK     0       7.035   4.896   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.343   4.047   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.963   2.506   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.403   2.155   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.260   0.864   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.520   0.929   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.049   1.949   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.523   2.421   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.950   2.240   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.337   3.205   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       3.368   4.350   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       0.819   2.608   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   22                                                  
CONECT    6    5    7   11                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10    6   12                                                  
CONECT   12   11   13   22   27                                             
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   19                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   15   20   24                                             
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21    5   12   23                                             
CONECT   23   22   24   25                                                  
CONECT   24   23   19                                                       
CONECT   25   23   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   12                                                       
MASTER        0    0    0    0    0    0    0    0   27    0   64    0
END

View in JSmol

Synonyms

Value	Source
Methyl (1S,9S,10R,12S)-20-oxo-19-oxa-8,16-diazahexacyclo[8.8.2.2,.0,.0,.0,]docosa-2,4,6,13-tetraene-8-carboxylic acid	Generator

Chemical Formula

C₂₁H₂₂N₂O₄

Average Mass

366.4170 Da

Monoisotopic Mass

366.15796 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

COC(=O)N1C2=CC=CC=C2[C@@]23CCN4CC=C[C@@]44CC[C@@]12[C@@H](C4)C(=O)O3

InChI Identifier

InChI=1S/C21H22N2O4/c1-26-18(25)23-16-6-3-2-5-14(16)21-10-12-22-11-4-7-19(22)8-9-20(21,23)15(13-19)17(24)27-21/h2-7,15H,8-13H2,1H3/t15-,19-,20-,21-/m0/s1

InChI Key

GLOIILVAVSJIEX-ZEWNOJEFSA-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 indolecarboxylic acids. Indolecarboxylic acids are compounds containing a carboxylic acid group linked to an indole.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Indolecarboxylic acids and derivatives

Direct Parent

Indolecarboxylic acids

Alternative Parents

Substituents

Indolecarboxylic acid
Aralkylamine
Gamma butyrolactone
Benzenoid
Pyrroline
Tetrahydrofuran
Carbamic acid ester
Carboxylic acid ester
Lactone
Carbonic acid derivative
Tertiary amine
Tertiary aliphatic amine
Amino acid or derivatives
Monocarboxylic acid or derivatives
Oxacycle
Carboxylic acid derivative
Azacycle
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Organic oxide
Organic nitrogen compound
Amine
Carbonyl group
Organopnictogen compound
Organic oxygen 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

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

163193000

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (1s,9s,10r,12s)-20-oxo-19-oxa-8,16-diazahexacyclo[8.8.2.2⁹,¹².0¹,⁹.0²,⁷.0¹²,¹⁶]docosa-2,4,6,13-tetraene-8-carboxylate (NP0223007)

MOL for NP0223007 (methyl (1s,9s,10r,12s)-20-oxo-19-oxa-8,16-diazahexacyclo[8.8.2.2⁹,¹².0¹,⁹.0²,⁷.0¹²,¹⁶]docosa-2,4,6,13-tetraene-8-carboxylate)

3D MOL for NP0223007 (methyl (1s,9s,10r,12s)-20-oxo-19-oxa-8,16-diazahexacyclo[8.8.2.2⁹,¹².0¹,⁹.0²,⁷.0¹²,¹⁶]docosa-2,4,6,13-tetraene-8-carboxylate)

3D SDF for NP0223007 (methyl (1s,9s,10r,12s)-20-oxo-19-oxa-8,16-diazahexacyclo[8.8.2.2⁹,¹².0¹,⁹.0²,⁷.0¹²,¹⁶]docosa-2,4,6,13-tetraene-8-carboxylate)

3D-SDF for NP0223007 (methyl (1s,9s,10r,12s)-20-oxo-19-oxa-8,16-diazahexacyclo[8.8.2.2⁹,¹².0¹,⁹.0²,⁷.0¹²,¹⁶]docosa-2,4,6,13-tetraene-8-carboxylate)

PDB for NP0223007 (methyl (1s,9s,10r,12s)-20-oxo-19-oxa-8,16-diazahexacyclo[8.8.2.2⁹,¹².0¹,⁹.0²,⁷.0¹²,¹⁶]docosa-2,4,6,13-tetraene-8-carboxylate)

3D PDB for NP0223007 (methyl (1s,9s,10r,12s)-20-oxo-19-oxa-8,16-diazahexacyclo[8.8.2.2⁹,¹².0¹,⁹.0²,⁷.0¹²,¹⁶]docosa-2,4,6,13-tetraene-8-carboxylate)

SMILES for NP0223007 (methyl (1s,9s,10r,12s)-20-oxo-19-oxa-8,16-diazahexacyclo[8.8.2.2⁹,¹².0¹,⁹.0²,⁷.0¹²,¹⁶]docosa-2,4,6,13-tetraene-8-carboxylate)

INCHI for NP0223007 (methyl (1s,9s,10r,12s)-20-oxo-19-oxa-8,16-diazahexacyclo[8.8.2.2⁹,¹².0¹,⁹.0²,⁷.0¹²,¹⁶]docosa-2,4,6,13-tetraene-8-carboxylate)

Structure for NP0223007 (methyl (1s,9s,10r,12s)-20-oxo-19-oxa-8,16-diazahexacyclo[8.8.2.2⁹,¹².0¹,⁹.0²,⁷.0¹²,¹⁶]docosa-2,4,6,13-tetraene-8-carboxylate)

3D Structure for NP0223007 (methyl (1s,9s,10r,12s)-20-oxo-19-oxa-8,16-diazahexacyclo[8.8.2.2⁹,¹².0¹,⁹.0²,⁷.0¹²,¹⁶]docosa-2,4,6,13-tetraene-8-carboxylate)