NP-MRD: Showing NP-Card for (+)-Luguine (NP0050998)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-04-27 22:27:15 UTC

Updated at

2022-04-27 22:27:15 UTC

NP-MRD ID

NP0050998

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-Luguine

Description

(+)-Luguine belongs to the class of organic compounds known as phenanthridines and derivatives. These are polycyclic compounds containing a phenanthridine moiety, which is a tricyclic system with two benzene rings joined by a pyridine forming a non-linear skeleton. Hydrogenated derivatives are also included. (+)-Luguine is found in Corydalis incisa and Glaucium flavum var. vestitum . Based on a literature review very few articles have been published on (+)-Luguine.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282200272D          

 25 30  0  0  1  0            999 V2000
    5.9819   -0.0050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8010    0.0936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1251    0.8523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6301    1.5123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8110    1.4137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4869    0.6550    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6678    0.5564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1729    1.2164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4970    1.9751    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.3161    2.0737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3538    1.1178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0297    0.3592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5246   -0.3009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3437   -0.2023    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8387   -0.8623    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2106    0.2605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7156    0.9206    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0398    1.6792    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8588    1.7778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4184    2.2219    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7102    1.7987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8939    0.9944    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1049    2.1870    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8933    1.9440    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9058    1.1191    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  1  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  5 10  1  0  0  0  0
  8 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
  7 14  1  0  0  0  0
 14 15  1  6  0  0  0
 12 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 11 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
 17 22  1  0  0  0  0
  4 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
  3 25  1  0  0  0  0
M  END

     RDKit          3D

 38 43  0  0  0  0  0  0  0  0999 V2000
   -0.4067   -3.1317   -0.3898 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2242   -1.9646   -0.1581 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4505   -2.0663    0.6938 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3268   -0.9071    0.3333 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7020   -1.0000    0.3694 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4815    0.1237    0.1373 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8770    1.3218   -0.1271 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4903    1.4575   -0.1745 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7557    0.3169    0.0597 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2964    0.4413   -0.1195 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2609    1.6671   -0.1841 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5715    1.8931   -0.1619 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3771    0.7630   -0.0638 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7574    0.8952   -0.0165 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5840   -0.2020    0.0938 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0394   -1.4594    0.1595 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6685   -1.6272    0.1153 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8604   -0.5271    0.0043 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4784   -0.7021   -0.0295 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8964    0.2413    0.1161 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8845    1.6340   -0.1042 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5324    2.0436   -0.0647 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8347    2.3181   -0.3275 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0530    1.7712    0.1693 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8604    0.3538    0.1041 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5496   -3.4004   -1.3089 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7425   -1.8076   -1.2163 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9943   -3.0076    0.4010 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2276   -2.0871    1.7803 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2006   -1.9191    0.5727 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0100    2.4037   -0.3833 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0653    2.8451   -0.2113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6249   -2.3632    0.2466 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2407   -2.6171    0.1865 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3035    1.8737   -1.1032 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4629    2.1935    0.6536 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8640    2.1071   -0.4985 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1731    2.1247    1.1979 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  9  2  0
  9  8  1  0
  8  7  2  0
  7 23  1  0
 23 24  1  0
 24 25  1  0
 25  6  1  0
  6  5  2  0
  9 10  1  0
 10 19  2  0
 19 18  1  0
 18 17  2  0
 17 16  1  0
 16 15  2  0
 15 20  1  0
 20 21  1  0
 21 22  1  0
 22 14  1  0
 14 13  2  0
 13 12  1  0
 12 11  2  0
 19  2  1  0
 13 18  1  0
  5  4  1  0
 11 10  1  0
  6  7  1  0
 14 15  1  0
  1 26  1  0
  2 27  1  6
  3 28  1  0
  3 29  1  0
  8 31  1  0
 24 37  1  0
 24 38  1  0
  5 30  1  0
 17 34  1  0
 16 33  1  0
 21 35  1  0
 21 36  1  0
 12 32  1  0
M  END


  Mrv1652304282200272D          

 25 30  0  0  1  0            999 V2000
    5.9819   -0.0050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8010    0.0936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1251    0.8523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6301    1.5123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8110    1.4137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4869    0.6550    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6678    0.5564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1729    1.2164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4970    1.9751    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.3161    2.0737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3538    1.1178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0297    0.3592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5246   -0.3009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3437   -0.2023    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8387   -0.8623    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2106    0.2605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7156    0.9206    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0398    1.6792    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8588    1.7778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4184    2.2219    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7102    1.7987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8939    0.9944    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1049    2.1870    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8933    1.9440    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9058    1.1191    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  1  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  5 10  1  0  0  0  0
  8 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
  7 14  1  0  0  0  0
 14 15  1  6  0  0  0
 12 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 11 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
 17 22  1  0  0  0  0
  4 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
  3 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0050998

> <DATABASE_NAME>
NP-MRD

> <SMILES>
O[C@@H]1CC2=C(C=C3OCOC3=C2)C2=C1C1=CC=C3OCOC3=C1C=N2

> <INCHI_IDENTIFIER>
InChI=1S/C19H13NO5/c21-13-3-9-4-15-16(24-7-23-15)5-11(9)18-17(13)10-1-2-14-19(25-8-22-14)12(10)6-20-18/h1-2,4-6,13,21H,3,7-8H2/t13-/m1/s1

> <INCHI_KEY>
PKAFVNJHLLUZFP-CYBMUJFWSA-N

> <FORMULA>
C19H13NO5

> <MOLECULAR_WEIGHT>
335.315

> <EXACT_MASS>
335.079372523

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
38

> <JCHEM_AVERAGE_POLARIZABILITY>
34.60116509845999

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(12R)-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.0^{2,10}.0^{4,8}.0^{14,22}.0^{17,21}]tetracosa-1(13),2(10),3,8,14,16,21,23-octaen-12-ol

> <ALOGPS_LOGP>
2.50

> <JCHEM_LOGP>
2.3568985776666667

> <ALOGPS_LOGS>
-3.08

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.425930247544386

> <JCHEM_PKA_STRONGEST_BASIC>
4.633039250670229

> <JCHEM_POLAR_SURFACE_AREA>
70.04000000000002

> <JCHEM_REFRACTIVITY>
86.44500000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.79e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(12R)-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.0^{2,10}.0^{4,8}.0^{14,22}.0^{17,21}]tetracosa-1(13),2(10),3,8,14,16,21,23-octaen-12-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      11.166  -0.009   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.695   0.175   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      13.300   1.591   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      12.376   2.823   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.847   2.639   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.242   1.223   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.713   1.039   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.789   2.271   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0       8.394   3.687   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0       9.923   3.871   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.260   2.087   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.655   0.670   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.579  -0.562   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.108  -0.378   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       9.032  -1.610   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       4.126   0.486   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.203   1.718   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.808   3.135   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.336   3.319   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       2.648   4.148   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       1.326   3.357   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       1.669   1.856   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      13.262   4.082   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      14.734   3.629   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      14.757   2.089   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4   25                                                  
CONECT    4    3    5   23                                                  
CONECT    5    4    6   10                                                  
CONECT    6    5    1    7                                                  
CONECT    7    6    8   14                                                  
CONECT    8    7    9   11                                                  
CONECT    9    8   10                                                       
CONECT   10    9    5                                                       
CONECT   11    8   12   19                                                  
CONECT   12   11   13   16                                                  
CONECT   13   12   14                                                       
CONECT   14   13    7   15                                                  
CONECT   15   14                                                            
CONECT   16   12   17                                                       
CONECT   17   16   18   22                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18   11                                                       
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   17                                                       
CONECT   23    4   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24    3                                                       
MASTER        0    0    0    0    0    0    0    0   25    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₁₃NO₅

Average Mass

335.3150 Da

Monoisotopic Mass

335.07937 Da

IUPAC Name

(12R)-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.0^{2,10}.0^{4,8}.0^{14,22}.0^{17,21}]tetracosa-1(13),2(10),3,8,14,16,21,23-octaen-12-ol

Traditional Name

(12R)-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.0^{2,10}.0^{4,8}.0^{14,22}.0^{17,21}]tetracosa-1(13),2(10),3,8,14,16,21,23-octaen-12-ol

CAS Registry Number

Not Available

SMILES

O[C@@H]1CC2=C(C=C3OCOC3=C2)C2=C1C1=CC=C3OCOC3=C1C=N2

InChI Identifier

InChI=1S/C19H13NO5/c21-13-3-9-4-15-16(24-7-23-15)5-11(9)18-17(13)10-1-2-14-19(25-8-22-14)12(10)6-20-18/h1-2,4-6,13,21H,3,7-8H2/t13-/m1/s1

InChI Key

PKAFVNJHLLUZFP-CYBMUJFWSA-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	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	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	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	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	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	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	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	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	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	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	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	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	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	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	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	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	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	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
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
Corydalis incisa	Plant	KNApSAcK
Glaucium flavum var. vestitum	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenanthridines and derivatives. These are polycyclic compounds containing a phenanthridine moiety, which is a tricyclic system with two benzene rings joined by a pyridine forming a non-linear skeleton. Hydrogenated derivatives are also included.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Quinolines and derivatives

Sub Class

Benzoquinolines

Direct Parent

Phenanthridines and derivatives

Alternative Parents

Substituents

Phenanthridine
Isoquinoline
Naphthalene
Benzodioxole
Pyridine
Benzenoid
Heteroaromatic compound
Secondary alcohol
Azacycle
Acetal
Oxacycle
Alcohol
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Organopnictogen compound
Organic oxygen compound
Organic nitrogen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

phenanthridines (CHEBI:29 )
Isoquinoline alkaloids (C09575 )

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	2.5	ALOGPS
logP	2.36	ChemAxon
logS	-3.1	ALOGPS
pKa (Strongest Acidic)	14.43	ChemAxon
pKa (Strongest Basic)	4.63	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	70.04 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	86.44 m³·mol⁻¹	ChemAxon
Polarizability	34.6 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

C00001882

Chemspider ID

390775

KEGG Compound ID

C09575

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

442317

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for (+)-Luguine (NP0050998)

MOL for NP0050998 ((+)-Luguine)

3D MOL for NP0050998 ((+)-Luguine)

3D SDF for NP0050998 ((+)-Luguine)

3D-SDF for NP0050998 ((+)-Luguine)

PDB for NP0050998 ((+)-Luguine)

3D PDB for NP0050998 ((+)-Luguine)

SMILES for NP0050998 ((+)-Luguine)

INCHI for NP0050998 ((+)-Luguine)

Structure for NP0050998 ((+)-Luguine)

3D Structure for NP0050998 ((+)-Luguine)