NP-MRD: Showing NP-Card for (1r,14s)-6,20,25-trimethoxy-15-methyl-23-oxa-15,30-diazaheptacyclo[22.6.2.1³,⁷.1⁸,¹².1¹⁴,¹⁸.0²⁷,³¹.0²²,³³]pentatriaconta-3,5,7(35),8(34),9,11,18(33),19,21,24(32),25,27(31)-dodecaene-9,21-diol (NP0213126)

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Record Information

Version

2.0

Created at

2022-09-05 12:00:49 UTC

Updated at

2022-09-05 12:00:49 UTC

NP-MRD ID

NP0213126

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,14s)-6,20,25-trimethoxy-15-methyl-23-oxa-15,30-diazaheptacyclo[22.6.2.1³,⁷.1⁸,¹².1¹⁴,¹⁸.0²⁷,³¹.0²²,³³]pentatriaconta-3,5,7(35),8(34),9,11,18(33),19,21,24(32),25,27(31)-dodecaene-9,21-diol

Description

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052214002D          

 44 50  0  0  1  0            999 V2000
    0.9906   -0.4972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2691    0.2794    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.3594    1.2031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652309052214002D          

 44 50  0  0  1  0            999 V2000
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    2.0037    4.0384    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7348    4.7031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5364    4.8980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8197    5.6728    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6324    5.8148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1618    5.1821    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9745    5.3241    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8784    4.4072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0658    4.2652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5431    3.6762    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1611    2.9450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6033    2.2485    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4276    2.2833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8096    3.0145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3674    3.7109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7494    4.4421    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5737    4.4769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1822    1.3547    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5162    0.8678    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0495    0.2383    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.7710   -0.5382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9592   -0.6853    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8616    4.8511    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4944    5.3805    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0868    5.1344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4540    4.6051    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  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 13 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 10 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  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  2  0  0  0  0
 21 27  1  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
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 28 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 30 36  1  0  0  0  0
 36 37  1  0  0  0  0
  6 37  1  0  0  0  0
 37 38  1  1  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
  5 40  1  0  0  0  0
 19 41  1  6  0  0  0
 41 42  1  0  0  0  0
 41 43  1  0  0  0  0
 43 44  1  0  0  0  0
 17 44  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0213126

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC2=C3[C@H](CC4=CC=C(O)C(=C4)C4=CC(C[C@H]5NCCC6=C5C=C(OC3=C1O)C(OC)=C6)=CC=C4OC)N(C)CC2

> <INCHI_IDENTIFIER>
InChI=1S/C36H38N2O6/c1-38-12-10-23-18-33(43-4)35(40)36-34(23)28(38)16-21-5-7-29(39)25(13-21)26-14-20(6-8-30(26)41-2)15-27-24-19-32(44-36)31(42-3)17-22(24)9-11-37-27/h5-8,13-14,17-19,27-28,37,39-40H,9-12,15-16H2,1-4H3/t27-,28?/m1/s1

> <INCHI_KEY>
WNWKGLOUHHZEQB-QXPUDEPPSA-N

> <FORMULA>
C36H38N2O6

> <MOLECULAR_WEIGHT>
594.708

> <EXACT_MASS>
594.272986952

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
82

> <JCHEM_AVERAGE_POLARIZABILITY>
66.36783714814727

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,14S)-6,20,25-trimethoxy-15-methyl-23-oxa-15,30-diazaheptacyclo[22.6.2.1^{3,7}.1^{8,12}.1^{14,18}.0^{27,31}.0^{22,33}]pentatriaconta-3,5,7(35),8(34),9,11,18(33),19,21,24(32),25,27(31)-dodecaene-9,21-diol

> <JCHEM_LOGP>
5.23034072944219

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
2

> <JCHEM_PKA>
9.889682756150561

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.736694862899835

> <JCHEM_PKA_STRONGEST_BASIC>
9.282162980657992

> <JCHEM_POLAR_SURFACE_AREA>
92.65

> <JCHEM_REFRACTIVITY>
171.21389999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,14S)-6,20,25-trimethoxy-15-methyl-23-oxa-15,30-diazaheptacyclo[22.6.2.1^{3,7}.1^{8,12}.1^{14,18}.0^{27,31}.0^{22,33}]pentatriaconta-3,5,7(35),8(34),9,11,18(33),19,21,24(32),25,27(31)-dodecaene-9,21-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0       1.849  -0.928   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       2.369   0.522   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       3.884   0.796   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.880  -0.379   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.395  -0.104   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.915   1.345   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.919   2.520   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.404   2.246   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       3.188   3.537   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       2.824   5.033   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.643   4.045   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       1.908   2.528   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       0.197   4.574   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -0.985   3.586   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -2.431   4.115   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.068   6.091   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.113   7.079   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.559   6.550   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.740   7.538   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.105   8.779   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.601   9.143   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.130  10.589   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.647  10.854   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.635   9.673   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      11.152   9.938   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       9.106   8.227   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       7.589   7.962   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      10.347   6.862   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       9.634   5.497   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      10.460   4.197   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      11.998   4.262   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      12.711   5.627   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      11.886   6.927   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      12.599   8.292   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      14.138   8.357   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       9.674   2.529   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       8.430   1.620   0.000  0.00  0.00           C+0
HETATM   38  N   UNK     0       9.426   0.445   0.000  0.00  0.00           N+0
HETATM   39  C   UNK     0       8.906  -1.005   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       7.391  -1.279   0.000  0.00  0.00           C+0
HETATM   41  N   UNK     0       3.475   9.055   0.000  0.00  0.00           N+0
HETATM   42  C   UNK     0       4.656  10.044   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       2.029   9.584   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       0.848   8.596   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   40                                                  
CONECT    6    5    7   37                                                  
CONECT    7    6    8                                                       
CONECT    8    7    3    9                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   18                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   16                                                  
CONECT   14   13   15                                                       
CONECT   15   14                                                            
CONECT   16   13   17                                                       
CONECT   17   16   18   44                                                  
CONECT   18   17   10   19                                                  
CONECT   19   18   20   41                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   27                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   28                                                  
CONECT   27   26   21                                                       
CONECT   28   26   29   33                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31   36                                                  
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   28   34                                                  
CONECT   34   33   35                                                       
CONECT   35   34                                                            
CONECT   36   30   37                                                       
CONECT   37   36    6   38                                                  
CONECT   38   37   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39    5                                                       
CONECT   41   19   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41   44                                                       
CONECT   44   43   17                                                       
MASTER        0    0    0    0    0    0    0    0   44    0  100    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₆H₃₈N₂O₆

Average Mass

594.7080 Da

Monoisotopic Mass

594.27299 Da

IUPAC Name

(1R,14S)-6,20,25-trimethoxy-15-methyl-23-oxa-15,30-diazaheptacyclo[22.6.2.1^{3,7}.1^{8,12}.1^{14,18}.0^{27,31}.0^{22,33}]pentatriaconta-3,5,7(35),8(34),9,11,18(33),19,21,24(32),25,27(31)-dodecaene-9,21-diol

Traditional Name

CAS Registry Number

Not Available

SMILES

COC1=CC2=C3[C@H](CC4=CC=C(O)C(=C4)C4=CC(C[C@H]5NCCC6=C5C=C(OC3=C1O)C(OC)=C6)=CC=C4OC)N(C)CC2

InChI Identifier

InChI=1S/C36H38N2O6/c1-38-12-10-23-18-33(43-4)35(40)36-34(23)28(38)16-21-5-7-29(39)25(13-21)26-14-20(6-8-30(26)41-2)15-27-24-19-32(44-36)31(42-3)17-22(24)9-11-37-27/h5-8,13-14,17-19,27-28,37,39-40H,9-12,15-16H2,1-4H3/t27-,28?/m1/s1

InChI Key

WNWKGLOUHHZEQB-QXPUDEPPSA-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
Guatteria guianensis	LOTUS Database	35616633

Chemical Taxonomy

Classification

Not classified

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	5.23	ChemAxon
pKa (Strongest Acidic)	8.74	ChemAxon
pKa (Strongest Basic)	9.28	ChemAxon
Physiological Charge	2	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	92.65 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	171.21 m³·mol⁻¹	ChemAxon
Polarizability	66.37 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

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,14s)-6,20,25-trimethoxy-15-methyl-23-oxa-15,30-diazaheptacyclo[22.6.2.1³,⁷.1⁸,¹².1¹⁴,¹⁸.0²⁷,³¹.0²²,³³]pentatriaconta-3,5,7(35),8(34),9,11,18(33),19,21,24(32),25,27(31)-dodecaene-9,21-diol (NP0213126)

MOL for NP0213126 ((1r,14s)-6,20,25-trimethoxy-15-methyl-23-oxa-15,30-diazaheptacyclo[22.6.2.1³,⁷.1⁸,¹².1¹⁴,¹⁸.0²⁷,³¹.0²²,³³]pentatriaconta-3,5,7(35),8(34),9,11,18(33),19,21,24(32),25,27(31)-dodecaene-9,21-diol)

3D MOL for NP0213126 ((1r,14s)-6,20,25-trimethoxy-15-methyl-23-oxa-15,30-diazaheptacyclo[22.6.2.1³,⁷.1⁸,¹².1¹⁴,¹⁸.0²⁷,³¹.0²²,³³]pentatriaconta-3,5,7(35),8(34),9,11,18(33),19,21,24(32),25,27(31)-dodecaene-9,21-diol)

3D SDF for NP0213126 ((1r,14s)-6,20,25-trimethoxy-15-methyl-23-oxa-15,30-diazaheptacyclo[22.6.2.1³,⁷.1⁸,¹².1¹⁴,¹⁸.0²⁷,³¹.0²²,³³]pentatriaconta-3,5,7(35),8(34),9,11,18(33),19,21,24(32),25,27(31)-dodecaene-9,21-diol)

3D-SDF for NP0213126 ((1r,14s)-6,20,25-trimethoxy-15-methyl-23-oxa-15,30-diazaheptacyclo[22.6.2.1³,⁷.1⁸,¹².1¹⁴,¹⁸.0²⁷,³¹.0²²,³³]pentatriaconta-3,5,7(35),8(34),9,11,18(33),19,21,24(32),25,27(31)-dodecaene-9,21-diol)

PDB for NP0213126 ((1r,14s)-6,20,25-trimethoxy-15-methyl-23-oxa-15,30-diazaheptacyclo[22.6.2.1³,⁷.1⁸,¹².1¹⁴,¹⁸.0²⁷,³¹.0²²,³³]pentatriaconta-3,5,7(35),8(34),9,11,18(33),19,21,24(32),25,27(31)-dodecaene-9,21-diol)

3D PDB for NP0213126 ((1r,14s)-6,20,25-trimethoxy-15-methyl-23-oxa-15,30-diazaheptacyclo[22.6.2.1³,⁷.1⁸,¹².1¹⁴,¹⁸.0²⁷,³¹.0²²,³³]pentatriaconta-3,5,7(35),8(34),9,11,18(33),19,21,24(32),25,27(31)-dodecaene-9,21-diol)

SMILES for NP0213126 ((1r,14s)-6,20,25-trimethoxy-15-methyl-23-oxa-15,30-diazaheptacyclo[22.6.2.1³,⁷.1⁸,¹².1¹⁴,¹⁸.0²⁷,³¹.0²²,³³]pentatriaconta-3,5,7(35),8(34),9,11,18(33),19,21,24(32),25,27(31)-dodecaene-9,21-diol)

INCHI for NP0213126 ((1r,14s)-6,20,25-trimethoxy-15-methyl-23-oxa-15,30-diazaheptacyclo[22.6.2.1³,⁷.1⁸,¹².1¹⁴,¹⁸.0²⁷,³¹.0²²,³³]pentatriaconta-3,5,7(35),8(34),9,11,18(33),19,21,24(32),25,27(31)-dodecaene-9,21-diol)

Structure for NP0213126 ((1r,14s)-6,20,25-trimethoxy-15-methyl-23-oxa-15,30-diazaheptacyclo[22.6.2.1³,⁷.1⁸,¹².1¹⁴,¹⁸.0²⁷,³¹.0²²,³³]pentatriaconta-3,5,7(35),8(34),9,11,18(33),19,21,24(32),25,27(31)-dodecaene-9,21-diol)

3D Structure for NP0213126 ((1r,14s)-6,20,25-trimethoxy-15-methyl-23-oxa-15,30-diazaheptacyclo[22.6.2.1³,⁷.1⁸,¹².1¹⁴,¹⁸.0²⁷,³¹.0²²,³³]pentatriaconta-3,5,7(35),8(34),9,11,18(33),19,21,24(32),25,27(31)-dodecaene-9,21-diol)