NP-MRD: Showing NP-Card for 4,5,19,20-tetramethoxy-10-methyl-2,17-dioxa-10,25-diazaheptacyclo[26.2.2.2¹³,¹⁶.1³,⁷.1¹⁸,²².0¹¹,³⁶.0²⁶,³³]hexatriaconta-1(30),3,5,7(36),13,15,18,20,22(33),28,31,34-dodecaene (NP0309414)

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Record Information

Version

2.0

Created at

2022-09-11 03:59:50 UTC

Updated at

2022-09-11 03:59:50 UTC

NP-MRD ID

NP0309414

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4,5,19,20-tetramethoxy-10-methyl-2,17-dioxa-10,25-diazaheptacyclo[26.2.2.2¹³,¹⁶.1³,⁷.1¹⁸,²².0¹¹,³⁶.0²⁶,³³]hexatriaconta-1(30),3,5,7(36),13,15,18,20,22(33),28,31,34-dodecaene

Description

N-Desmethylcycleanine 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. 4,5,19,20-tetramethoxy-10-methyl-2,17-dioxa-10,25-diazaheptacyclo[26.2.2.2¹³,¹⁶.1³,⁷.1¹⁸,²².0¹¹,³⁶.0²⁶,³³]hexatriaconta-1(30),3,5,7(36),13,15,18,20,22(33),28,31,34-dodecaene is found in Stephania pierrei. N-Desmethylcycleanine is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004191513562D          

 45 51  0  0  0  0            999 V2000
   11.1105    6.1646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6810    5.5687    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4502    4.7766    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0210    4.1756    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8010    3.3542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3971    2.7571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1966    1.9463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4011    1.7268    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   10.7832    2.2973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1792    1.6846    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


  Mrv1533004191513562D          

 45 51  0  0  0  0            999 V2000
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   11.6810    5.5687    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   10.1792    1.6846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4879    1.1718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9132    1.7703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0968    1.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8052    0.8188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9483    0.9921    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1229    1.2940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8601    0.4986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4212   -0.1062    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1779   -0.8945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0583    0.2989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8276   -0.4932    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3981   -1.0891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4875    0.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7076    1.7213    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1115    2.3185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3119    3.1292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1074    3.3487    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.3020    4.1504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7254    2.7782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3294    3.3910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0206    3.9037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2969    4.7033    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1249    4.8687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7034    4.2567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5603    4.0834    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.3857    3.7815    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6485    4.5769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0874    5.1817    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.3307    5.9700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9822    3.1449    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4117    3.4756    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5954    3.3052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5264    1.9306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3836    0.2068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2116    0.3723    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
 11 12  2  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  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 17 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 20 23  2  0  0  0  0
 23 24  1  0  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
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
  3 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 36 40  1  0  0  0  0
  5 40  2  0  0  0  0
  9 40  1  0  0  0  0
 34 41  1  0  0  0  0
 41 42  2  0  0  0  0
 31 42  1  0  0  0  0
 29 43  1  0  0  0  0
 16 43  1  0  0  0  0
 24 43  2  0  0  0  0
 14 44  1  0  0  0  0
 44 45  2  0  0  0  0
 11 45  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0309414

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC2=C3C(CC4=CC=C(OC5=C(OC)C(OC)=CC6=C5C(CC5=CC=C(OC3=C1OC)C=C5)N(C)CC6)C=C4)NCC2

> <INCHI_IDENTIFIER>
InChI=1S/C37H40N2O6/c1-39-17-15-25-21-31(41-3)35(43-5)37-33(25)29(39)19-23-8-12-26(13-9-23)44-36-32-24(20-30(40-2)34(36)42-4)14-16-38-28(32)18-22-6-10-27(45-37)11-7-22/h6-13,20-21,28-29,38H,14-19H2,1-5H3

> <INCHI_KEY>
ZYKGNXPEWXZKGA-UHFFFAOYSA-N

> <FORMULA>
C37H40N2O6

> <MOLECULAR_WEIGHT>
608.735

> <EXACT_MASS>
608.288637016

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
85

> <JCHEM_AVERAGE_POLARIZABILITY>
66.64564900913786

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4,5,19,20-tetramethoxy-10-methyl-2,17-dioxa-10,25-diazaheptacyclo[26.2.2.2¹³,¹⁶.1³,⁷.1¹⁸,²².0¹¹,³⁶.0²⁶,³³]hexatriaconta-1(30),3,5,7(36),13,15,18,20,22(33),28,31,34-dodecaene

> <ALOGPS_LOGP>
4.82

> <JCHEM_LOGP>
6.095214697333333

> <ALOGPS_LOGS>
-5.67

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
2

> <JCHEM_PKA_STRONGEST_BASIC>
8.673593215443786

> <JCHEM_POLAR_SURFACE_AREA>
70.65

> <JCHEM_REFRACTIVITY>
174.8198999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.29e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4,5,19,20-tetramethoxy-10-methyl-2,17-dioxa-10,25-diazaheptacyclo[26.2.2.2¹³,¹⁶.1³,⁷.1¹⁸,²².0¹¹,³⁶.0²⁶,³³]hexatriaconta-1(30),3,5,7(36),13,15,18,20,22(33),28,31,34-dodecaene

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 19-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-APR-15         0                                  
HETATM    1  C   UNK     0      20.740  11.507   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      21.805  10.395   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      21.374   8.916   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      22.439   7.794   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      22.028   6.261   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      23.141   5.147   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      22.767   3.633   0.000  0.00  0.00           C+0
HETATM    8  N   UNK     0      21.282   3.223   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0      20.129   4.288   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      19.001   3.145   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      17.711   2.187   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      16.638   3.305   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      15.114   2.987   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      14.570   1.528   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      12.970   1.852   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      11.429   2.416   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.939   0.931   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      11.986  -0.198   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      11.532  -1.670   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.442   0.558   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       9.011  -0.921   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      10.076  -2.033   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.377   1.680   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       8.788   3.213   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       7.675   4.328   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.049   5.841   0.000  0.00  0.00           C+0
HETATM   27  N   UNK     0       9.534   6.251   0.000  0.00  0.00           N+0
HETATM   28  C   UNK     0       9.897   7.747   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      10.687   5.186   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      11.815   6.330   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      13.105   7.287   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      13.621   8.779   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      15.167   9.088   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      16.246   7.946   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      17.846   7.622   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      19.387   7.059   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      19.877   8.544   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      18.830   9.673   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0      19.284  11.144   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      20.500   5.870   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      15.702   6.488   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      14.178   6.170   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      10.316   3.604   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      15.649   0.386   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      17.195   0.695   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   37                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   40                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   40                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   45                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   44                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   43                                                  
CONECT   17   16   18   20                                                  
CONECT   18   17   19                                                       
CONECT   19   18                                                            
CONECT   20   17   21   23                                                  
CONECT   21   20   22                                                       
CONECT   22   21                                                            
CONECT   23   20   24                                                       
CONECT   24   23   25   43                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   43                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32   42                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35   41                                                  
CONECT   35   34   36                                                       
CONECT   36   35   37   40                                                  
CONECT   37   36    3   38                                                  
CONECT   38   37   39                                                       
CONECT   39   38                                                            
CONECT   40   36    5    9                                                  
CONECT   41   34   42                                                       
CONECT   42   41   31                                                       
CONECT   43   29   16   24                                                  
CONECT   44   14   45                                                       
CONECT   45   44   11                                                       
MASTER        0    0    0    0    0    0    0    0   45    0  102    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₇H₄₀N₂O₆

Average Mass

608.7350 Da

Monoisotopic Mass

608.28864 Da

IUPAC Name

4,5,19,20-tetramethoxy-10-methyl-2,17-dioxa-10,25-diazaheptacyclo[26.2.2.2¹³,¹⁶.1³,⁷.1¹⁸,²².0¹¹,³⁶.0²⁶,³³]hexatriaconta-1(30),3,5,7(36),13,15,18,20,22(33),28,31,34-dodecaene

Traditional Name

4,5,19,20-tetramethoxy-10-methyl-2,17-dioxa-10,25-diazaheptacyclo[26.2.2.2¹³,¹⁶.1³,⁷.1¹⁸,²².0¹¹,³⁶.0²⁶,³³]hexatriaconta-1(30),3,5,7(36),13,15,18,20,22(33),28,31,34-dodecaene

CAS Registry Number

Not Available

SMILES

COC1=CC2=C3C(CC4=CC=C(OC5=C(OC)C(OC)=CC6=C5C(CC5=CC=C(OC3=C1OC)C=C5)N(C)CC6)C=C4)NCC2

InChI Identifier

InChI=1S/C37H40N2O6/c1-39-17-15-25-21-31(41-3)35(43-5)37-33(25)29(39)19-23-8-12-26(13-9-23)44-36-32-24(20-30(40-2)34(36)42-4)14-16-38-28(32)18-22-6-10-27(45-37)11-7-22/h6-13,20-21,28-29,38H,14-19H2,1-5H3

InChI Key

ZYKGNXPEWXZKGA-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
Stephania pierrei	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
Tetrahydroisoquinoline
Anisole
Alkyl aryl ether
Aralkylamine
Benzenoid
Tertiary aliphatic amine
Tertiary amine
Organoheterocyclic compound
Secondary amine
Secondary aliphatic amine
Azacycle
Oxacycle
Amine
Hydrocarbon derivative
Organonitrogen compound
Organopnictogen compound
Organic nitrogen 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	4.82	ALOGPS
logP	6.1	ChemAxon
logS	-5.7	ALOGPS
pKa (Strongest Basic)	8.67	ChemAxon
Physiological Charge	2	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	70.65 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	174.82 m³·mol⁻¹	ChemAxon
Polarizability	66.65 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

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

158567

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4,5,19,20-tetramethoxy-10-methyl-2,17-dioxa-10,25-diazaheptacyclo[26.2.2.2¹³,¹⁶.1³,⁷.1¹⁸,²².0¹¹,³⁶.0²⁶,³³]hexatriaconta-1(30),3,5,7(36),13,15,18,20,22(33),28,31,34-dodecaene (NP0309414)

MOL for NP0309414 (4,5,19,20-tetramethoxy-10-methyl-2,17-dioxa-10,25-diazaheptacyclo[26.2.2.2¹³,¹⁶.1³,⁷.1¹⁸,²².0¹¹,³⁶.0²⁶,³³]hexatriaconta-1(30),3,5,7(36),13,15,18,20,22(33),28,31,34-dodecaene)

3D MOL for NP0309414 (4,5,19,20-tetramethoxy-10-methyl-2,17-dioxa-10,25-diazaheptacyclo[26.2.2.2¹³,¹⁶.1³,⁷.1¹⁸,²².0¹¹,³⁶.0²⁶,³³]hexatriaconta-1(30),3,5,7(36),13,15,18,20,22(33),28,31,34-dodecaene)

3D SDF for NP0309414 (4,5,19,20-tetramethoxy-10-methyl-2,17-dioxa-10,25-diazaheptacyclo[26.2.2.2¹³,¹⁶.1³,⁷.1¹⁸,²².0¹¹,³⁶.0²⁶,³³]hexatriaconta-1(30),3,5,7(36),13,15,18,20,22(33),28,31,34-dodecaene)

3D-SDF for NP0309414 (4,5,19,20-tetramethoxy-10-methyl-2,17-dioxa-10,25-diazaheptacyclo[26.2.2.2¹³,¹⁶.1³,⁷.1¹⁸,²².0¹¹,³⁶.0²⁶,³³]hexatriaconta-1(30),3,5,7(36),13,15,18,20,22(33),28,31,34-dodecaene)

PDB for NP0309414 (4,5,19,20-tetramethoxy-10-methyl-2,17-dioxa-10,25-diazaheptacyclo[26.2.2.2¹³,¹⁶.1³,⁷.1¹⁸,²².0¹¹,³⁶.0²⁶,³³]hexatriaconta-1(30),3,5,7(36),13,15,18,20,22(33),28,31,34-dodecaene)

3D PDB for NP0309414 (4,5,19,20-tetramethoxy-10-methyl-2,17-dioxa-10,25-diazaheptacyclo[26.2.2.2¹³,¹⁶.1³,⁷.1¹⁸,²².0¹¹,³⁶.0²⁶,³³]hexatriaconta-1(30),3,5,7(36),13,15,18,20,22(33),28,31,34-dodecaene)

SMILES for NP0309414 (4,5,19,20-tetramethoxy-10-methyl-2,17-dioxa-10,25-diazaheptacyclo[26.2.2.2¹³,¹⁶.1³,⁷.1¹⁸,²².0¹¹,³⁶.0²⁶,³³]hexatriaconta-1(30),3,5,7(36),13,15,18,20,22(33),28,31,34-dodecaene)

INCHI for NP0309414 (4,5,19,20-tetramethoxy-10-methyl-2,17-dioxa-10,25-diazaheptacyclo[26.2.2.2¹³,¹⁶.1³,⁷.1¹⁸,²².0¹¹,³⁶.0²⁶,³³]hexatriaconta-1(30),3,5,7(36),13,15,18,20,22(33),28,31,34-dodecaene)

Structure for NP0309414 (4,5,19,20-tetramethoxy-10-methyl-2,17-dioxa-10,25-diazaheptacyclo[26.2.2.2¹³,¹⁶.1³,⁷.1¹⁸,²².0¹¹,³⁶.0²⁶,³³]hexatriaconta-1(30),3,5,7(36),13,15,18,20,22(33),28,31,34-dodecaene)

3D Structure for NP0309414 (4,5,19,20-tetramethoxy-10-methyl-2,17-dioxa-10,25-diazaheptacyclo[26.2.2.2¹³,¹⁶.1³,⁷.1¹⁸,²².0¹¹,³⁶.0²⁶,³³]hexatriaconta-1(30),3,5,7(36),13,15,18,20,22(33),28,31,34-dodecaene)