NP-MRD: Showing NP-Card for 9,20,25-trimethoxy-15,30-dimethyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.2³,⁶.1⁸,¹².1¹⁴,¹⁸.0²⁷,³¹.0²²,³³]hexatriaconta-3,5,8(34),9,11,18(33),19,21,24,26,31,35-dodecaen-21-ol (NP0248081)

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Record Information

Version

2.0

Created at

2022-09-07 10:11:46 UTC

Updated at

2022-09-07 10:11:46 UTC

NP-MRD ID

NP0248081

Secondary Accession Numbers

None

Natural Product Identification

Common Name

9,20,25-trimethoxy-15,30-dimethyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.2³,⁶.1⁸,¹².1¹⁴,¹⁸.0²⁷,³¹.0²²,³³]hexatriaconta-3,5,8(34),9,11,18(33),19,21,24,26,31,35-dodecaen-21-ol

Description

Fangchinoline, also known as thalrugosine or limacine, belongs to the class of organic compounds known as lignans, neolignans and related compounds. These are plant products of low molecular weight formed primarily from oxidative coupling of two p-propylphenol moieties. They can also be described as micromolecules with two phenylpropanoid units coupled together. They can be attached in various manners, like C5-C5', C8-C8'. Most known natural lignans are oxidized at C9 and C9´ and, based upon the way in which oxygen is incorporated into the skeleton and on the cyclization patterns, a wide range of lignans of very different structural types can be formed. Fangchinoline is a very strong basic compound (based on its pKa). 9,20,25-trimethoxy-15,30-dimethyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.2³,⁶.1⁸,¹².1¹⁴,¹⁸.0²⁷,³¹.0²²,³³]hexatriaconta-3,5,8(34),9,11,18(33),19,21,24,26,31,35-dodecaen-21-ol is found in Abuta grandifolia, Berberis fendleri, Cyclea barbata, Dehaasia incrassata, Hypserpa nitida, Laurelia sempervirens, Berberis repens, Pycnarrhena longifolia, Stephania cephalantha, Stephania hernandifolia, Stephania rotunda, Stephania tetrandra, Thalictrum minus, Thalictrum pubescens and Thalictrum sachalinense. Fangchinoline is an isolate of Stephania tetrandra that has anticancer activity.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004151516342D          

 45 51  0  0  0  0            999 V2000
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   -0.1243   -1.9688    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.9143   -0.9221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1574   -0.0114    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


  Mrv1533004151516342D          

 45 51  0  0  0  0            999 V2000
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   -0.1243   -1.9688    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1206   -1.1730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9143   -0.9221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1574   -0.0114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0316    0.3096    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6611   -0.3940    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8365   -0.3698    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9924   -1.1238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7677   -1.2426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1421   -0.5403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7940   -1.0021    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4434   -0.5551    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1820   -0.9226    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2332   -1.7460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4071    0.2529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1300    0.6504    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7471    0.7143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6671    0.8626    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3444    0.2289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2753   -0.6437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8508   -1.2749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7481   -2.1563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2537   -2.8937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5739   -3.4484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1263   -4.1716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2727   -4.1566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8076   -3.4442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0052   -3.0219    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2946   -2.4685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4219   -1.6373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2881   -2.7620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1188   -2.7604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4463   -2.6218    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.3763   -3.4438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2014   -2.2863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2800   -1.4628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6176   -0.9460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7717   -0.1135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1533    0.4441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3469    1.2461    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1383    1.4794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9510    0.2683    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  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  1  0  0  0  0
 16 17  1  0  0  0  0
 15 18  2  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 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  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
  3 32  1  0  0  0  0
 32 33  2  0  0  0  0
  6 33  1  0  0  0  0
 30 34  1  0  0  0  0
 34 35  2  0  0  0  0
 27 35  1  0  0  0  0
 25 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 24 40  2  0  0  0  0
 40 41  1  0  0  0  0
 41 42  2  0  0  0  0
 22 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 20 45  2  0  0  0  0
  8 45  1  0  0  0  0
 13 45  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0248081

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C2CC3N(C)CCC4=CC(OC)=C(O)C(OC5=CC6=C(CCN(C)C6CC6=CC=C(OC1=C2)C=C6)C=C5OC)=C34

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

> <INCHI_KEY>
IIQSJHUEZBTSAT-UHFFFAOYSA-N

> <FORMULA>
C37H40N2O6

> <MOLECULAR_WEIGHT>
608.735

> <EXACT_MASS>
608.288637016

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
85

> <JCHEM_AVERAGE_POLARIZABILITY>
67.02940305446222

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
9,20,25-trimethoxy-15,30-dimethyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.2³,⁶.1⁸,¹².1¹⁴,¹⁸.0²⁷,³¹.0²²,³³]hexatriaconta-3,5,8(34),9,11,18,20,22(33),24(32),25,27(31),35-dodecaen-21-ol

> <ALOGPS_LOGP>
5.57

> <JCHEM_LOGP>
6.0587464941127624

> <ALOGPS_LOGS>
-4.85

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
2

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.167045339722147

> <JCHEM_PKA_STRONGEST_BASIC>
9.250389909798063

> <JCHEM_POLAR_SURFACE_AREA>
72.86000000000001

> <JCHEM_REFRACTIVITY>
175.63229999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
8.68e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
9,20,25-trimethoxy-15,30-dimethyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.2³,⁶.1⁸,¹².1¹⁴,¹⁸.0²⁷,³¹.0²²,³³]hexatriaconta-3,5,8(34),9,11,18,20,22(33),24(32),25,27(31),35-dodecaen-21-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 15-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   15-APR-15         0                                  
HETATM    1  C   UNK     0      -1.163  -6.551   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       0.350  -6.266   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       0.860  -4.813   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.232  -3.675   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.225  -2.190   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.707  -1.721   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.160  -0.021   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.792   0.578   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0       3.101  -0.735   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0       1.561  -0.690   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.719  -2.098   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.166  -2.320   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.865  -1.009   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.082  -1.871   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.294  -1.036   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       9.673  -1.722   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       9.769  -3.259   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.227   0.472   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       9.576   1.214   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       6.995   1.333   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       8.712   1.610   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       9.976   0.427   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.847  -1.202   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      10.922  -2.380   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      10.730  -4.025   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       9.807  -5.402   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       8.538  -6.437   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       7.702  -7.787   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.109  -7.759   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.241  -6.429   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       3.743  -5.641   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       2.417  -4.608   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       2.654  -3.056   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       6.138  -5.156   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       7.688  -5.153   0.000  0.00  0.00           C+0
HETATM   36  N   UNK     0      12.033  -4.894   0.000  0.00  0.00           N+0
HETATM   37  C   UNK     0      11.902  -6.428   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      13.443  -4.268   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      13.589  -2.731   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      12.353  -1.766   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      12.640  -0.212   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      11.486   0.829   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      11.848   2.326   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0      13.325   2.762   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       5.508   0.501   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   32                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   33                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   45                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   45                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   18                                                  
CONECT   16   15   17                                                       
CONECT   17   16                                                            
CONECT   18   15   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   45                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   42                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   40                                                  
CONECT   25   24   26   36                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   35                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31   34                                                  
CONECT   31   30   32                                                       
CONECT   32   31    3   33                                                  
CONECT   33   32    6                                                       
CONECT   34   30   35                                                       
CONECT   35   34   27                                                       
CONECT   36   25   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   24   41                                                  
CONECT   41   40   42                                                       
CONECT   42   41   22   43                                                  
CONECT   43   42   44                                                       
CONECT   44   43                                                            
CONECT   45   20    8   13                                                  
MASTER        0    0    0    0    0    0    0    0   45    0  102    0
END

View in JSmol

Synonyms

Value	Source
Thalrugosine	MeSH
7-O-Demethyl-tetrandrine	MeSH
Thaligine	MeSH
Isofangchinoline	MeSH
(1beta)-Isomer OF fangchinoline	MeSH
Limacine	MeSH
7-O-Demethyltetrandrine	MeSH

Chemical Formula

C₃₇H₄₀N₂O₆

Average Mass

608.7350 Da

Monoisotopic Mass

608.28864 Da

IUPAC Name

9,20,25-trimethoxy-15,30-dimethyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.2³,⁶.1⁸,¹².1¹⁴,¹⁸.0²⁷,³¹.0²²,³³]hexatriaconta-3,5,8(34),9,11,18,20,22(33),24(32),25,27(31),35-dodecaen-21-ol

Traditional Name

CAS Registry Number

Not Available

SMILES

COC1=CC=C2CC3N(C)CCC4=CC(OC)=C(O)C(OC5=CC6=C(CCN(C)C6CC6=CC=C(OC1=C2)C=C6)C=C5OC)=C34

InChI Identifier

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

InChI Key

IIQSJHUEZBTSAT-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
Abuta grandifolia	LOTUS Database	35616633
Berberis fendleri	LOTUS Database	35616633
Cyclea barbata	LOTUS Database	35616633
Dehaasia incrassata	LOTUS Database	35616633
Hypserpa nitida	LOTUS Database	35616633
Laurelia sempervirens	LOTUS Database	35616633
Mahonia repens	LOTUS Database	35616633
Pycnarrhena longifolia	LOTUS Database	35616633
Stephania cephalantha	LOTUS Database	35616633
Stephania hernandifolia	LOTUS Database	35616633
Stephania rotunda	LOTUS Database	35616633
Stephania tetrandra	LOTUS Database	35616633
Thalictrum minus	LOTUS Database	35616633
Thalictrum polygamum	LOTUS Database	35616633
Thalictrum sachalinense	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as lignans, neolignans and related compounds. These are plant products of low molecular weight formed primarily from oxidative coupling of two p-propylphenol moieties. They can also be described as micromolecules with two phenylpropanoid units coupled together. They can be attached in various manners, like C5-C5', C8-C8'. Most known natural lignans are oxidized at C9 and C9´ and, based upon the way in which oxygen is incorporated into the skeleton and on the cyclization patterns, a wide range of lignans of very different structural types can be formed.

Kingdom

Organic compounds

Super Class

Lignans, neolignans and related compounds

Class

Not Available

Sub Class

Not Available

Direct Parent

Lignans, neolignans and related compounds

Alternative Parents

Substituents

Oxyneolignan skeleton
Diaryl ether
Tetrahydroisoquinoline
Anisole
Alkyl aryl ether
Aralkylamine
Benzenoid
Tertiary amine
Tertiary aliphatic amine
Ether
Oxacycle
Azacycle
Organoheterocyclic compound
Organonitrogen compound
Hydrocarbon derivative
Organic nitrogen compound
Organopnictogen compound
Organooxygen compound
Amine
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
logP	5.57	ALOGPS
logP	6.06	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	8.17	ChemAxon
pKa (Strongest Basic)	9.25	ChemAxon
Physiological Charge	2	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	72.86 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	175.63 m³·mol⁻¹	ChemAxon
Polarizability	67.03 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

Fangchinoline

METLIN ID

Not Available

PubChem Compound

321937

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 9,20,25-trimethoxy-15,30-dimethyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.2³,⁶.1⁸,¹².1¹⁴,¹⁸.0²⁷,³¹.0²²,³³]hexatriaconta-3,5,8(34),9,11,18(33),19,21,24,26,31,35-dodecaen-21-ol (NP0248081)

MOL for NP0248081 (9,20,25-trimethoxy-15,30-dimethyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.2³,⁶.1⁸,¹².1¹⁴,¹⁸.0²⁷,³¹.0²²,³³]hexatriaconta-3,5,8(34),9,11,18(33),19,21,24,26,31,35-dodecaen-21-ol)

3D MOL for NP0248081 (9,20,25-trimethoxy-15,30-dimethyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.2³,⁶.1⁸,¹².1¹⁴,¹⁸.0²⁷,³¹.0²²,³³]hexatriaconta-3,5,8(34),9,11,18(33),19,21,24,26,31,35-dodecaen-21-ol)

3D SDF for NP0248081 (9,20,25-trimethoxy-15,30-dimethyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.2³,⁶.1⁸,¹².1¹⁴,¹⁸.0²⁷,³¹.0²²,³³]hexatriaconta-3,5,8(34),9,11,18(33),19,21,24,26,31,35-dodecaen-21-ol)

3D-SDF for NP0248081 (9,20,25-trimethoxy-15,30-dimethyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.2³,⁶.1⁸,¹².1¹⁴,¹⁸.0²⁷,³¹.0²²,³³]hexatriaconta-3,5,8(34),9,11,18(33),19,21,24,26,31,35-dodecaen-21-ol)

PDB for NP0248081 (9,20,25-trimethoxy-15,30-dimethyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.2³,⁶.1⁸,¹².1¹⁴,¹⁸.0²⁷,³¹.0²²,³³]hexatriaconta-3,5,8(34),9,11,18(33),19,21,24,26,31,35-dodecaen-21-ol)

3D PDB for NP0248081 (9,20,25-trimethoxy-15,30-dimethyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.2³,⁶.1⁸,¹².1¹⁴,¹⁸.0²⁷,³¹.0²²,³³]hexatriaconta-3,5,8(34),9,11,18(33),19,21,24,26,31,35-dodecaen-21-ol)

SMILES for NP0248081 (9,20,25-trimethoxy-15,30-dimethyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.2³,⁶.1⁸,¹².1¹⁴,¹⁸.0²⁷,³¹.0²²,³³]hexatriaconta-3,5,8(34),9,11,18(33),19,21,24,26,31,35-dodecaen-21-ol)

INCHI for NP0248081 (9,20,25-trimethoxy-15,30-dimethyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.2³,⁶.1⁸,¹².1¹⁴,¹⁸.0²⁷,³¹.0²²,³³]hexatriaconta-3,5,8(34),9,11,18(33),19,21,24,26,31,35-dodecaen-21-ol)

Structure for NP0248081 (9,20,25-trimethoxy-15,30-dimethyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.2³,⁶.1⁸,¹².1¹⁴,¹⁸.0²⁷,³¹.0²²,³³]hexatriaconta-3,5,8(34),9,11,18(33),19,21,24,26,31,35-dodecaen-21-ol)

3D Structure for NP0248081 (9,20,25-trimethoxy-15,30-dimethyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.2³,⁶.1⁸,¹².1¹⁴,¹⁸.0²⁷,³¹.0²²,³³]hexatriaconta-3,5,8(34),9,11,18(33),19,21,24,26,31,35-dodecaen-21-ol)