NP-MRD: Showing NP-Card for 4,26-dimethoxy-2-oxa-11,15,20-triazatricyclo[22.3.1.1³,⁷]nonacosa-1(28),3(29),4,6,8,10,20,22,24,26-decaene-10,21,27-triol (NP0165701)

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Record Information

Version

2.0

Created at

2022-09-03 00:54:45 UTC

Updated at

2022-09-03 00:54:45 UTC

NP-MRD ID

NP0165701

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4,26-dimethoxy-2-oxa-11,15,20-triazatricyclo[22.3.1.1³,⁷]nonacosa-1(28),3(29),4,6,8,10,20,22,24,26-decaene-10,21,27-triol

Description

4,26-Dimethoxy-2-oxa-11,15,20-triazatricyclo[22.3.1.1³,⁷]Nonacosa-1(28),3,5,7(29),8,10,20,22,24,26-decaene-10,21,27-triol belongs to the class of organic compounds known as diarylethers. These are organic compounds containing the dialkyl ether functional group, with the formula ROR', where R and R' are aryl groups. 4,26-dimethoxy-2-oxa-11,15,20-triazatricyclo[22.3.1.1³,⁷]nonacosa-1(28),3(29),4,6,8,10,20,22,24,26-decaene-10,21,27-triol is found in Brassica napus. Based on a literature review very few articles have been published on 4,26-dimethoxy-2-oxa-11,15,20-triazatricyclo[22.3.1.1³,⁷]Nonacosa-1(28),3,5,7(29),8,10,20,22,24,26-decaene-10,21,27-triol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032202542D          

 36 38  0  0  0  0            999 V2000
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  6 36  1  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652309032202542D          

 36 38  0  0  0  0            999 V2000
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 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 23 24  1  4  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 32 31  1  4  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 35 33  1  4  0  0  0
 35 36  2  0  0  0  0
  6 36  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0165701

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C2C=C1OC1=CC(=CC(OC)=C1O)C=CC(O)=NCCCCNCCCN=C(O)C=C2

> <INCHI_IDENTIFIER>
InChI=1S/C27H33N3O6/c1-34-21-9-6-19-7-10-25(31)30-15-5-13-28-12-3-4-14-29-26(32)11-8-20-17-23(35-2)27(33)24(18-20)36-22(21)16-19/h6-11,16-18,28,33H,3-5,12-15H2,1-2H3,(H,29,32)(H,30,31)

> <INCHI_KEY>
PXTQTPSOXAZCQC-UHFFFAOYSA-N

> <FORMULA>
C27H33N3O6

> <MOLECULAR_WEIGHT>
495.576

> <EXACT_MASS>
495.236935795

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
69

> <JCHEM_AVERAGE_POLARIZABILITY>
52.393054238579836

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4,26-dimethoxy-2-oxa-11,15,20-triazatricyclo[22.3.1.1^{3,7}]nonacosa-1(28),3(29),4,6,8,10,20,22,24,26-decaene-10,21,27-triol

> <ALOGPS_LOGP>
3.34

> <JCHEM_LOGP>
0.42946129444924996

> <ALOGPS_LOGS>
-5.10

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
4.480641854779483

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.8880705101860498

> <JCHEM_PKA_STRONGEST_BASIC>
10.665861060009306

> <JCHEM_POLAR_SURFACE_AREA>
125.13000000000001

> <JCHEM_REFRACTIVITY>
140.8219

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.93e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4,26-dimethoxy-2-oxa-11,15,20-triazatricyclo[22.3.1.1^{3,7}]nonacosa-1(28),3(29),4,6,8,10,20,22,24,26-decaene-10,21,27-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       6.668  -5.390   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.336  -5.390   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.669  -4.620   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.669  -3.080   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.336  -2.310   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.002  -3.080   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       6.668  -2.310   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       4.001  -6.930   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       5.961  -6.027   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.261  -0.626   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.230   0.518   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -1.302   0.357   0.000  0.00  0.00           O+0
HETATM   23  N   UNK     0       1.000   1.852   0.000  0.00  0.00           N+0
HETATM   24  C   UNK     0       2.506   1.532   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   28  N   UNK     0       8.002   1.540   0.000  0.00  0.00           N+0
HETATM   29  C   UNK     0       9.336   2.310   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      10.669   1.540   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      12.003   2.310   0.000  0.00  0.00           C+0
HETATM   32  N   UNK     0      13.337   1.540   0.000  0.00  0.00           N+0
HETATM   33  C   UNK     0      13.337   0.000   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      14.670  -0.770   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      12.003  -0.770   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      12.003  -2.310   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                                                       
CONECT    6    5    7   36                                                  
CONECT    7    6    8                                                       
CONECT    8    7    3    9                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   17                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   19                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   17                                                  
CONECT   15   14   16                                                       
CONECT   16   15                                                            
CONECT   17   14   10   18                                                  
CONECT   18   17                                                            
CONECT   19   12   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   36                                                       
CONECT   36   35    6                                                       
MASTER        0    0    0    0    0    0    0    0   36    0   76    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₇H₃₃N₃O₆

Average Mass

495.5760 Da

Monoisotopic Mass

495.23694 Da

IUPAC Name

4,26-dimethoxy-2-oxa-11,15,20-triazatricyclo[22.3.1.1^{3,7}]nonacosa-1(28),3(29),4,6,8,10,20,22,24,26-decaene-10,21,27-triol

Traditional Name

4,26-dimethoxy-2-oxa-11,15,20-triazatricyclo[22.3.1.1^{3,7}]nonacosa-1(28),3(29),4,6,8,10,20,22,24,26-decaene-10,21,27-triol

CAS Registry Number

Not Available

SMILES

COC1=CC=C2C=C1OC1=CC(=CC(OC)=C1O)C=CC(O)=NCCCCNCCCN=C(O)C=C2

InChI Identifier

InChI=1S/C27H33N3O6/c1-34-21-9-6-19-7-10-25(31)30-15-5-13-28-12-3-4-14-29-26(32)11-8-20-17-23(35-2)27(33)24(18-20)36-22(21)16-19/h6-11,16-18,28,33H,3-5,12-15H2,1-2H3,(H,29,32)(H,30,31)

InChI Key

PXTQTPSOXAZCQC-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
Brassica napus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diarylethers. These are organic compounds containing the dialkyl ether functional group, with the formula ROR', where R and R' are aryl groups.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Ethers

Direct Parent

Diarylethers

Alternative Parents

Substituents

Diaryl ether
Anisole
Alkyl aryl ether
Benzenoid
Cyclic carboximidic acid
Secondary aliphatic amine
Polyol
Secondary amine
Oxacycle
Propargyl-type 1,3-dipolar organic compound
Organic 1,3-dipolar compound
Organoheterocyclic compound
Azacycle
Organopnictogen compound
Organic nitrogen compound
Hydrocarbon derivative
Organonitrogen 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	3.34	ALOGPS
logP	0.43	ChemAxon
logS	-5.1	ALOGPS
pKa (Strongest Acidic)	3.89	ChemAxon
pKa (Strongest Basic)	10.67	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	125.13 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	140.82 m³·mol⁻¹	ChemAxon
Polarizability	52.39 Å³	ChemAxon
Number of Rings	3	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

162911971

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4,26-dimethoxy-2-oxa-11,15,20-triazatricyclo[22.3.1.1³,⁷]nonacosa-1(28),3(29),4,6,8,10,20,22,24,26-decaene-10,21,27-triol (NP0165701)

MOL for NP0165701 (4,26-dimethoxy-2-oxa-11,15,20-triazatricyclo[22.3.1.1³,⁷]nonacosa-1(28),3(29),4,6,8,10,20,22,24,26-decaene-10,21,27-triol)

3D MOL for NP0165701 (4,26-dimethoxy-2-oxa-11,15,20-triazatricyclo[22.3.1.1³,⁷]nonacosa-1(28),3(29),4,6,8,10,20,22,24,26-decaene-10,21,27-triol)

3D SDF for NP0165701 (4,26-dimethoxy-2-oxa-11,15,20-triazatricyclo[22.3.1.1³,⁷]nonacosa-1(28),3(29),4,6,8,10,20,22,24,26-decaene-10,21,27-triol)

3D-SDF for NP0165701 (4,26-dimethoxy-2-oxa-11,15,20-triazatricyclo[22.3.1.1³,⁷]nonacosa-1(28),3(29),4,6,8,10,20,22,24,26-decaene-10,21,27-triol)

PDB for NP0165701 (4,26-dimethoxy-2-oxa-11,15,20-triazatricyclo[22.3.1.1³,⁷]nonacosa-1(28),3(29),4,6,8,10,20,22,24,26-decaene-10,21,27-triol)

3D PDB for NP0165701 (4,26-dimethoxy-2-oxa-11,15,20-triazatricyclo[22.3.1.1³,⁷]nonacosa-1(28),3(29),4,6,8,10,20,22,24,26-decaene-10,21,27-triol)

SMILES for NP0165701 (4,26-dimethoxy-2-oxa-11,15,20-triazatricyclo[22.3.1.1³,⁷]nonacosa-1(28),3(29),4,6,8,10,20,22,24,26-decaene-10,21,27-triol)

INCHI for NP0165701 (4,26-dimethoxy-2-oxa-11,15,20-triazatricyclo[22.3.1.1³,⁷]nonacosa-1(28),3(29),4,6,8,10,20,22,24,26-decaene-10,21,27-triol)

Structure for NP0165701 (4,26-dimethoxy-2-oxa-11,15,20-triazatricyclo[22.3.1.1³,⁷]nonacosa-1(28),3(29),4,6,8,10,20,22,24,26-decaene-10,21,27-triol)

3D Structure for NP0165701 (4,26-dimethoxy-2-oxa-11,15,20-triazatricyclo[22.3.1.1³,⁷]nonacosa-1(28),3(29),4,6,8,10,20,22,24,26-decaene-10,21,27-triol)