NP-MRD: Showing NP-Card for 27-methoxy-22-methyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.2¹⁶,¹⁹.1⁴,³⁰.1¹⁰,¹⁴.0³,⁸.0²⁵,³³.0²⁸,³²]heptatriaconta-1,3(8),4,6,10,12,14(37),16,18,25(33),26,28(32),30(34),35-tetradecaene-13,26-diol (NP0181979)

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Record Information

Version

2.0

Created at

2022-09-03 20:35:10 UTC

Updated at

2022-09-03 20:35:10 UTC

NP-MRD ID

NP0181979

Secondary Accession Numbers

None

Natural Product Identification

Common Name

27-methoxy-22-methyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.2¹⁶,¹⁹.1⁴,³⁰.1¹⁰,¹⁴.0³,⁸.0²⁵,³³.0²⁸,³²]heptatriaconta-1,3(8),4,6,10,12,14(37),16,18,25(33),26,28(32),30(34),35-tetradecaene-13,26-diol

Description

27-Methoxy-22-methyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.2¹⁶,¹⁹.1⁴,³⁰.1¹⁰,¹⁴.0³,⁸.0²⁵,³³.0²⁸,³²]Heptatriaconta-1(30),2,4(34),5,7,10(37),11,13,16,18,25(33),26,28(32),35-tetradecaene-13,26-diol belongs to the class of organic compounds known as dibenzo-p-dioxins. Dibenzo-p-dioxins are compounds containing a dibenzo-p-dioxin moiety, which consists of two benzene connected by a para-dioxin ring. 27-methoxy-22-methyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.2¹⁶,¹⁹.1⁴,³⁰.1¹⁰,¹⁴.0³,⁸.0²⁵,³³.0²⁸,³²]heptatriaconta-1,3(8),4,6,10,12,14(37),16,18,25(33),26,28(32),30(34),35-tetradecaene-13,26-diol is found in Cocculus pendulus. 27-Methoxy-22-methyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.2¹⁶,¹⁹.1⁴,³⁰.1¹⁰,¹⁴.0³,⁸.0²⁵,³³.0²⁸,³²]Heptatriaconta-1(30),2,4(34),5,7,10(37),11,13,16,18,25(33),26,28(32),35-tetradecaene-13,26-diol is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004251516292D          

 42 49  0  0  0  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1533004251516292D          

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    4.4155   -3.8351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9038   -4.5200    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.5794   -5.2875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7555   -5.3830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2396   -4.7188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4038   -4.8218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8752   -4.1642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0373   -4.2599    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5152   -3.5960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8240   -2.8117    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6670   -2.7331    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1913   -3.3897    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0254   -3.2882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5648   -3.9418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2934   -2.1206    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9726   -2.0972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2536   -1.3127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6952   -0.6910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9690    0.0873    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9512    0.7351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1124    0.7068    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
  4  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
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  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
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 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
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 28 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 22 35  2  0  0  0  0
 26 35  1  0  0  0  0
 31 36  1  0  0  0  0
  6 36  2  0  0  0  0
 11 36  1  0  0  0  0
 20 37  2  0  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 18 39  1  0  0  0  0
 39 40  1  0  0  0  0
 16 41  1  0  0  0  0
 41 42  2  0  0  0  0
 13 42  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0181979

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(O)C2=C3C(CC4=CC=C(OC5=CC(CC6=C7C=C8OC3=C1OC8=CC7=CC=N6)=CC=C5O)C=C4)N(C)CC2

> <INCHI_IDENTIFIER>
InChI=1S/C34H28N2O6/c1-36-12-10-22-30-25(36)14-18-3-6-21(7-4-18)40-27-15-19(5-8-26(27)37)13-24-23-17-29-28(16-20(23)9-11-35-24)42-34(32(30)41-29)33(39-2)31(22)38/h3-9,11,15-17,25,37-38H,10,12-14H2,1-2H3

> <INCHI_KEY>
DWAZEYVNMOERBJ-UHFFFAOYSA-N

> <FORMULA>
C34H28N2O6

> <MOLECULAR_WEIGHT>
560.606

> <EXACT_MASS>
560.19473663

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
70

> <JCHEM_AVERAGE_POLARIZABILITY>
59.58075947069057

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
27-methoxy-22-methyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.2¹⁶,¹⁹.1⁴,³⁰.1¹⁰,¹⁴.0³,⁸.0²⁵,³³.0²⁸,³²]heptatriaconta-1,3(8),4,6,10,12,14(37),16,18,25(33),26,28(32),30(34),35-tetradecaene-13,26-diol

> <ALOGPS_LOGP>
5.00

> <JCHEM_LOGP>
5.554514808

> <ALOGPS_LOGS>
-4.67

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
8

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.940893482140632

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.447003702037405

> <JCHEM_PKA_STRONGEST_BASIC>
5.998585581540055

> <JCHEM_POLAR_SURFACE_AREA>
93.51000000000002

> <JCHEM_REFRACTIVITY>
157.58619999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.20e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
27-methoxy-22-methyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.2¹⁶,¹⁹.1⁴,³⁰.1¹⁰,¹⁴.0³,⁸.0²⁵,³³.0²⁸,³²]heptatriaconta-1,3(8),4,6,10,12,14(37),16,18,25(33),26,28(32),30(34),35-tetradecaene-13,26-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0      -2.691  -8.562   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -1.166  -8.347   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -0.591  -6.919   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.555  -5.707   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -3.077  -5.947   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -1.004  -4.241   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.037  -3.059   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.577  -1.583   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0      -0.070  -1.268   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0       0.385   0.203   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.012  -2.394   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.004  -1.132   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.189  -0.063   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.068  -1.349   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.604  -1.292   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.373   0.065   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       7.798  -0.629   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       9.094  -1.542   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.642  -3.039   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.626  -4.269   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.030  -5.757   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.242  -7.159   0.000  0.00  0.00           C+0
HETATM   23  N   UNK     0       9.154  -8.437   0.000  0.00  0.00           N+0
HETATM   24  C   UNK     0       8.548  -9.870   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       7.010 -10.048   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.047  -8.808   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.487  -9.001   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.500  -7.773   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       1.936  -7.952   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       0.962  -6.713   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       1.538  -5.248   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       3.112  -5.102   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       4.090  -6.327   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       5.647  -6.138   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       6.654  -7.358   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       0.548  -3.958   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      11.149  -3.915   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      11.673  -2.450   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      10.631  -1.290   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      11.142   0.163   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       5.509   1.372   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       3.943   1.319   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   30                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7   36                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   36                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   42                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   41                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   39                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   37                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   35                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   35                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29   33                                                  
CONECT   29   28   30                                                       
CONECT   30   29    3   31                                                  
CONECT   31   30   32   36                                                  
CONECT   32   31   33                                                       
CONECT   33   32   28   34                                                  
CONECT   34   33   35                                                       
CONECT   35   34   22   26                                                  
CONECT   36   31    6   11                                                  
CONECT   37   20   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   18   40                                                  
CONECT   40   39                                                            
CONECT   41   16   42                                                       
CONECT   42   41   13                                                       
MASTER        0    0    0    0    0    0    0    0   42    0   98    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₄H₂₈N₂O₆

Average Mass

560.6060 Da

Monoisotopic Mass

560.19474 Da

IUPAC Name

Traditional Name

CAS Registry Number

Not Available

SMILES

COC1=C(O)C2=C3C(CC4=CC=C(OC5=CC(CC6=C7C=C8OC3=C1OC8=CC7=CC=N6)=CC=C5O)C=C4)N(C)CC2

InChI Identifier

InChI=1S/C34H28N2O6/c1-36-12-10-22-30-25(36)14-18-3-6-21(7-4-18)40-27-15-19(5-8-26(27)37)13-24-23-17-29-28(16-20(23)9-11-35-24)42-34(32(30)41-29)33(39-2)31(22)38/h3-9,11,15-17,25,37-38H,10,12-14H2,1-2H3

InChI Key

DWAZEYVNMOERBJ-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

Species Name	Source	Reference
Cocculus pendulus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as dibenzo-p-dioxins. Dibenzo-p-dioxins are compounds containing a dibenzo-p-dioxin moiety, which consists of two benzene connected by a para-dioxin ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzodioxins

Sub Class

Benzo-p-dioxins

Direct Parent

Dibenzo-p-dioxins

Alternative Parents

Substituents

Dibenzo-p-dioxin
Diaryl ether
Isoquinoline
Tetrahydroisoquinoline
Anisole
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
Aralkylamine
Pyridine
Benzenoid
Heteroaromatic compound
Tertiary amine
Tertiary aliphatic amine
Azacycle
Oxacycle
Ether
Organooxygen compound
Organonitrogen compound
Organic nitrogen compound
Hydrocarbon derivative
Organopnictogen compound
Organic oxygen compound
Amine
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	5	ALOGPS
logP	5.55	ChemAxon
logS	-4.7	ALOGPS
pKa (Strongest Acidic)	8.45	ChemAxon
pKa (Strongest Basic)	6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	93.51 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	157.59 m³·mol⁻¹	ChemAxon
Polarizability	59.58 Å³	ChemAxon
Number of Rings	8	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

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 27-methoxy-22-methyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.2¹⁶,¹⁹.1⁴,³⁰.1¹⁰,¹⁴.0³,⁸.0²⁵,³³.0²⁸,³²]heptatriaconta-1,3(8),4,6,10,12,14(37),16,18,25(33),26,28(32),30(34),35-tetradecaene-13,26-diol (NP0181979)

MOL for NP0181979 (27-methoxy-22-methyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.2¹⁶,¹⁹.1⁴,³⁰.1¹⁰,¹⁴.0³,⁸.0²⁵,³³.0²⁸,³²]heptatriaconta-1,3(8),4,6,10,12,14(37),16,18,25(33),26,28(32),30(34),35-tetradecaene-13,26-diol)

3D MOL for NP0181979 (27-methoxy-22-methyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.2¹⁶,¹⁹.1⁴,³⁰.1¹⁰,¹⁴.0³,⁸.0²⁵,³³.0²⁸,³²]heptatriaconta-1,3(8),4,6,10,12,14(37),16,18,25(33),26,28(32),30(34),35-tetradecaene-13,26-diol)

3D SDF for NP0181979 (27-methoxy-22-methyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.2¹⁶,¹⁹.1⁴,³⁰.1¹⁰,¹⁴.0³,⁸.0²⁵,³³.0²⁸,³²]heptatriaconta-1,3(8),4,6,10,12,14(37),16,18,25(33),26,28(32),30(34),35-tetradecaene-13,26-diol)

3D-SDF for NP0181979 (27-methoxy-22-methyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.2¹⁶,¹⁹.1⁴,³⁰.1¹⁰,¹⁴.0³,⁸.0²⁵,³³.0²⁸,³²]heptatriaconta-1,3(8),4,6,10,12,14(37),16,18,25(33),26,28(32),30(34),35-tetradecaene-13,26-diol)

PDB for NP0181979 (27-methoxy-22-methyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.2¹⁶,¹⁹.1⁴,³⁰.1¹⁰,¹⁴.0³,⁸.0²⁵,³³.0²⁸,³²]heptatriaconta-1,3(8),4,6,10,12,14(37),16,18,25(33),26,28(32),30(34),35-tetradecaene-13,26-diol)

3D PDB for NP0181979 (27-methoxy-22-methyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.2¹⁶,¹⁹.1⁴,³⁰.1¹⁰,¹⁴.0³,⁸.0²⁵,³³.0²⁸,³²]heptatriaconta-1,3(8),4,6,10,12,14(37),16,18,25(33),26,28(32),30(34),35-tetradecaene-13,26-diol)

SMILES for NP0181979 (27-methoxy-22-methyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.2¹⁶,¹⁹.1⁴,³⁰.1¹⁰,¹⁴.0³,⁸.0²⁵,³³.0²⁸,³²]heptatriaconta-1,3(8),4,6,10,12,14(37),16,18,25(33),26,28(32),30(34),35-tetradecaene-13,26-diol)

INCHI for NP0181979 (27-methoxy-22-methyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.2¹⁶,¹⁹.1⁴,³⁰.1¹⁰,¹⁴.0³,⁸.0²⁵,³³.0²⁸,³²]heptatriaconta-1,3(8),4,6,10,12,14(37),16,18,25(33),26,28(32),30(34),35-tetradecaene-13,26-diol)

Structure for NP0181979 (27-methoxy-22-methyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.2¹⁶,¹⁹.1⁴,³⁰.1¹⁰,¹⁴.0³,⁸.0²⁵,³³.0²⁸,³²]heptatriaconta-1,3(8),4,6,10,12,14(37),16,18,25(33),26,28(32),30(34),35-tetradecaene-13,26-diol)

3D Structure for NP0181979 (27-methoxy-22-methyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.2¹⁶,¹⁹.1⁴,³⁰.1¹⁰,¹⁴.0³,⁸.0²⁵,³³.0²⁸,³²]heptatriaconta-1,3(8),4,6,10,12,14(37),16,18,25(33),26,28(32),30(34),35-tetradecaene-13,26-diol)