NP-MRD: Showing NP-Card for (-)-Limacine (NP0067540)

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Record Information

Version

2.0

Created at

2022-04-28 12:24:23 UTC

Updated at

2022-04-28 12:24:23 UTC

NP-MRD ID

NP0067540

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(-)-Limacine

Description

Limacine, also known as fangchinoline or thaligine, 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. (-)-Limacine is found in Abuta grandifolia, Anisocycla jollyana (Pierre) Diels, Arcangelisia flava (L.)Merr., Archangelicia flava, Curarea candicans Barneby & Kurkoff , Cyclea barbata Miers , Cyclea peltata Diels , Gyrocarpus americanus, Hypserpa nitida, Isopyrum thalictroides, Limacia cuspidata, Pachygone dasycarpa, Pycnarrhena longifolia, Pycnarrhena longifolia (Decne ex.Miq.) Becc., Pycnarrhena novoguineensis, Spirospermum penduliflorum, Spirospermum penduliflorum Thou., Stephania japonica, Stephania rotunda, Stephania tetrandra and Strychnopsis thouarsii. (-)-Limacine was first documented in 2012 (PMID: 22033647). Based on a literature review very few articles have been published on Limacine (PMID: 34348525).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282214242D          

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M  END

     RDKit          3D

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M  END


  Mrv1652304282214242D          

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    2.6995    0.7302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2439    1.3650    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9225    2.1530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0951    2.2733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9723    0.8850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6326    0.3156    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.3636    0.7362    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.1035    0.3562    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1330   -0.4700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4299   -0.9280    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6824   -0.5406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9929   -1.0344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0061   -1.8762    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7776   -2.2228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4726   -1.7661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8432   -3.0452    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5881   -3.3997    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2220   -2.2566    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5284   -2.7987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6696   -2.9557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0184   -2.3600    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6702   -1.5554    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2275   -2.6464    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0359   -3.4521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6409   -4.0114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4409   -3.7723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9989   -4.3986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8080   -4.2360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0625   -3.4509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8732   -3.2980    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3569   -4.8519    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1647   -4.6846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3882   -2.0972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3440    1.5610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9871    1.4029    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8104    1.4565    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  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
 12 13  2  0  0  0  0
  8 13  1  0  0  0  0
 11 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 15 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
 19 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 22 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
  1 31  1  0  0  0  0
 30 32  1  6  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 29 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 28 38  1  0  0  0  0
 38 39  1  0  0  0  0
 37 40  1  0  0  0  0
 40 41  1  0  0  0  0
 32 42  1  0  0  0  0
 16 43  1  0  0  0  0
  4 44  1  0  0  0  0
 44 45  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0067540

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C2C[C@H]3N(C)CCC4=CC(OC)=C(O)C(OC5=CC6=C(CCN(C)[C@@H]6CC6=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/t28-,29-/m1/s1

> <INCHI_KEY>
IIQSJHUEZBTSAT-FQLXRVMXSA-N

> <FORMULA>
C37H40N2O6

> <MOLECULAR_WEIGHT>
608.735

> <EXACT_MASS>
608.288637016

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
85

> <JCHEM_AVERAGE_POLARIZABILITY>
66.54962094551917

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,14R)-9,20,25-trimethoxy-15,30-dimethyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.2^{3,6}.1^{8,12}.1^{14,18}.0^{27,31}.0^{22,33}]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>
6.050110928197637

> <ALOGPS_LOGS>
-4.85

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
2

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.198443731818413

> <JCHEM_PKA_STRONGEST_BASIC>
9.259350589897657

> <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>
(1R,14R)-9,20,25-trimethoxy-15,30-dimethyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.2^{3,6}.1^{8,12}.1^{14,18}.0^{27,31}.0^{22,33}]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                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       0.228  -1.624   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.348  -1.440   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.042  -0.039   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.161   1.238   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.404   1.159   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.041  -0.284   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       1.417   2.402   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       2.889   3.047   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.522   1.615   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.039   1.363   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.055   2.548   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.455   4.019   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.911   4.244   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.415   1.652   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.648   0.589   0.000  0.00  0.00           C+0
HETATM   16  N   UNK     0      10.012   1.374   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0      11.393   0.665   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      11.448  -0.877   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      10.136  -1.732   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.740  -1.009   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.453  -1.931   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.478  -3.502   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.918  -4.149   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      10.216  -3.297   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       9.041  -5.684   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      10.431  -6.346   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       6.014  -4.212   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       4.720  -5.224   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.117  -5.517   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       1.901  -4.405   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       1.251  -2.903   0.000  0.00  0.00           C+0
HETATM   32  N   UNK     0       0.425  -4.940   0.000  0.00  0.00           N+0
HETATM   33  C   UNK     0       0.067  -6.444   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       1.196  -7.488   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       2.690  -7.042   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       3.731  -8.211   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       5.242  -7.907   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       5.717  -6.442   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       7.230  -6.156   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0       6.266  -9.057   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       7.774  -8.745   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -0.725  -3.915   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       9.975   2.914   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0      -1.843   2.619   0.000  0.00  0.00           O+0
HETATM   45  C   UNK     0      -3.379   2.719   0.000  0.00  0.00           C+0
CONECT    1    2    6   31                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   44                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8                                                       
CONECT    8    7    9   13                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   14                                                  
CONECT   12   11   13                                                       
CONECT   13   12    8                                                       
CONECT   14   11   15                                                       
CONECT   15   14   16   20                                                  
CONECT   16   15   17   43                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   24                                                  
CONECT   20   19   15   21                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   27                                                  
CONECT   23   22   24   25                                                  
CONECT   24   23   19                                                       
CONECT   25   23   26                                                       
CONECT   26   25                                                            
CONECT   27   22   28                                                       
CONECT   28   27   29   38                                                  
CONECT   29   28   30   35                                                  
CONECT   30   29   31   32                                                  
CONECT   31   30    1                                                       
CONECT   32   30   33   42                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   29   36                                                  
CONECT   36   35   37                                                       
CONECT   37   36   38   40                                                  
CONECT   38   37   28   39                                                  
CONECT   39   38                                                            
CONECT   40   37   41                                                       
CONECT   41   40                                                            
CONECT   42   32                                                            
CONECT   43   16                                                            
CONECT   44    4   45                                                       
CONECT   45   44                                                            
MASTER        0    0    0    0    0    0    0    0   45    0  102    0
END

View in JSmol

Synonyms

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

Chemical Formula

C₃₇H₄₀N₂O₆

Average Mass

608.7350 Da

Monoisotopic Mass

608.28864 Da

IUPAC Name

(1R,14R)-9,20,25-trimethoxy-15,30-dimethyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.2^{3,6}.1^{8,12}.1^{14,18}.0^{27,31}.0^{22,33}]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=C2C[C@H]3N(C)CCC4=CC(OC)=C(O)C(OC5=CC6=C(CCN(C)[C@@H]6CC6=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/t28-,29-/m1/s1

InChI Key

IIQSJHUEZBTSAT-FQLXRVMXSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Anisocycla jollyana (Pierre) Diels	Plant	KNApSAcK
Arcangelisia flava	Plant	KNApSAcK
Archangelicia flava	-	KNApSAcK
Curarea candicans Barneby & Kurkoff	Plant	KNApSAcK
Cyclea barbata	Plant	KNApSAcK
Cyclea peltata Diels	Plant	KNApSAcK
Gyrocarpus americanus	LOTUS Database	35616633
Hypserpa nitida	LOTUS Database	35616633
Isopyrum thalictroides	LOTUS Database	35616633
Limacia cuspidata	Plant	KNApSAcK
Pachygone dasycarpa	LOTUS Database	35616633
Pycnarrhena longifolia	LOTUS Database	35616633
Pycnarrhena longifolia (Decne ex.Miq.) Becc.	Plant	KNApSAcK
Pycnarrhena novoguineensis	Plant	KNApSAcK
Spirospermum penduliflorum	LOTUS Database	35616633
Spirospermum penduliflorum Thou.	Plant	KNApSAcK
Stephania japonica	LOTUS Database	35616633
Stephania rotunda	LOTUS Database	35616633
Stephania tetrandra	LOTUS Database	35616633
Strychnopsis thouarsii Baill.	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
Phenol ether
Alkyl aryl ether
Aralkylamine
Phenol
Benzenoid
Tertiary amine
Tertiary aliphatic amine
Organoheterocyclic compound
Azacycle
Oxacycle
Ether
Organooxygen compound
Organonitrogen compound
Hydrocarbon derivative
Organic oxygen compound
Organic nitrogen 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	5.57	ALOGPS
logP	6.05	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	8.2	ChemAxon
pKa (Strongest Basic)	9.26	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	66.55 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

C00025320

Chemspider ID

20100816

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Slug

METLIN ID

Not Available

PubChem Compound

7656034

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Yang LJ, Yang ZD, Li ZJ, Yang SH, Shu ZM: Stephtetrandrine A-D, bisbenzylisoquinoline alkaloids from Stephania tetrandra. Nat Prod Res. 2021 Aug 5:1-12. doi: 10.1080/14786419.2021.1961135. [PubMed:34348525 ]
Zaima K, Takeyama Y, Koga I, Saito A, Tamamoto H, Azziz SS, Mukhtar MR, Awang K, Hadi AH, Morita H: Vasorelaxant effect of isoquinoline derivatives from two species of Popowia perakensis and Phaeanthus crassipetalus on rat aortic artery. J Nat Med. 2012 Jul;66(3):421-7. doi: 10.1007/s11418-011-0600-4. Epub 2011 Oct 28. [PubMed:22033647 ]

Showing NP-Card for (-)-Limacine (NP0067540)

MOL for NP0067540 ((-)-Limacine)

3D MOL for NP0067540 ((-)-Limacine)

3D SDF for NP0067540 ((-)-Limacine)

3D-SDF for NP0067540 ((-)-Limacine)

PDB for NP0067540 ((-)-Limacine)

3D PDB for NP0067540 ((-)-Limacine)

SMILES for NP0067540 ((-)-Limacine)

INCHI for NP0067540 ((-)-Limacine)

Structure for NP0067540 ((-)-Limacine)

3D Structure for NP0067540 ((-)-Limacine)