NP-MRD: Showing NP-Card for (-)-Leuconicine F (NP0081631)

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Record Information

Version

2.0

Created at

2022-04-29 02:38:31 UTC

Updated at

2022-04-29 02:38:31 UTC

NP-MRD ID

NP0081631

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(-)-Leuconicine F

Description

CHEMBL1086393 belongs to the class of organic compounds known as carbazoles. Carbazoles are compounds containing a three ring system containing a pyrrole ring fused on either side to a benzene ring. (-)-Leuconicine F is found in Leuconotis sp. Based on a literature review very few articles have been published on CHEMBL1086393.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292204382D          

 28 33  0  0  1  0            999 V2000
    2.8271    1.0827    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7552    0.2027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9775   -0.2373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1598    0.1762    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5432    0.6567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0411    1.2772    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6146    1.9470    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2620    2.6928    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3184    2.4482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0099    1.9545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7724    1.7189    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5536    0.8561    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2478    0.6602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4787   -0.1319    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0278   -1.0599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7561   -1.4547    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4714   -1.0261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1849   -1.4402    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4887   -0.1872    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.0822    0.4102    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7024    1.1425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1467    1.8377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9708    1.8005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3507    1.0681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9064    0.3730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7738   -2.2795    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4970   -2.6765    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0684   -2.7073    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  6  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  1  0  0  0
  6  5  1  6  0  0  0
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
  1 10  1  0  0  0  0
  7 11  1  0  0  0  0
 11 12  1  0  0  0  0
  4 12  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  1  0  0  0  0
  3 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
  2 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
  1 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  2  0  0  0  0
 20 25  1  0  0  0  0
 16 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
M  END

     RDKit          3D

 51 56  0  0  0  0  0  0  0  0999 V2000
    4.2879    1.4571   -0.6728 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9140    1.5125   -0.0433 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6136    0.1692    0.6322 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6552   -0.8979   -0.3678 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7642   -1.9923   -0.3226 N   0  0  2  0  0  4  0  0  0  0  0  0
    2.3195   -3.1881   -0.1071 O   0  0  0  0  0  1  0  0  0  0  0  0
    1.1563   -2.0456   -1.6811 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2211   -0.8475   -1.6154 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4371   -1.1244   -0.2097 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7607   -1.6706   -0.4885 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1703   -2.9315   -0.8474 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4741   -3.1453   -1.2316 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3544   -2.0982   -1.2534 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9277   -0.8138   -0.8820 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6391   -0.5835   -0.4949 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9397    0.5213    0.0718 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7253    0.1755    0.4185 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2262    0.8926    1.1085 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1552    2.1598    1.4709 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4392    2.6040    1.1263 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8805    3.9419    1.4899 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1594    4.4301    1.1657 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0880    4.6859    2.1162 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3214    1.7852    0.4327 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4837    2.1581    0.1117 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4837    0.2390    1.5517 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0145   -1.2111    1.8432 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5902   -1.8421    0.5217 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2136    1.0399   -1.6897 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9358    0.7363   -0.1003 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7509    2.4750   -0.6557 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1569    1.7875   -0.7746 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9530    2.3226    0.7212 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5390    0.0089    1.3113 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6677   -0.3939   -1.3911 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7011   -1.3657   -0.3502 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9062   -1.8296   -2.4563 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6642   -2.9837   -1.8833 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5563   -0.9183   -2.3764 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6992    0.1087   -1.5716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4627   -3.7601   -0.8273 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7627   -4.1492   -1.5074 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3709   -2.2898   -1.5607 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6042    0.0093   -0.8950 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5105    2.8002    2.0063 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2934    4.9801    0.3034 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9653    4.2435    1.7821 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8046    0.6714    2.5473 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1204   -1.2109    2.4945 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8577   -1.7568    2.2585 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2440   -2.8660    0.7718 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  5  1  0
  5  6  1  1
  5  7  1  0
  7  8  1  0
  9  8  1  6
  9 28  1  0
 28 27  1  0
 27 26  1  0
 26 18  1  0
 18 17  2  0
 17 16  1  0
 16 15  1  0
 15 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 16 24  1  0
 24 25  2  0
 24 20  1  0
 20 19  2  0
 20 21  1  0
 21 22  1  0
 21 23  2  0
 26  3  1  0
 19 18  1  0
 28  5  1  0
 14 15  1  0
 17  9  1  0
 10  9  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  2 32  1  0
  2 33  1  0
  3 34  1  1
  4 35  1  0
  4 36  1  0
  7 37  1  0
  7 38  1  0
  8 39  1  0
  8 40  1  0
 28 51  1  1
 27 49  1  0
 27 50  1  0
 26 48  1  1
 11 41  1  0
 12 42  1  0
 13 43  1  0
 14 44  1  0
 19 45  1  0
 22 46  1  0
 22 47  1  0
M  CHG  2   5   1   6  -1
M  END


  Mrv1652304292204382D          

 28 33  0  0  1  0            999 V2000
    2.8271    1.0827    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7552    0.2027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9775   -0.2373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1598    0.1762    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5432    0.6567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0411    1.2772    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6146    1.9470    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2620    2.6928    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3184    2.4482    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0099    1.9545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7724    1.7189    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5536    0.8561    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2478    0.6602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4787   -0.1319    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0278   -1.0599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7561   -1.4547    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4714   -1.0261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1849   -1.4402    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4887   -0.1872    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.0822    0.4102    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7024    1.1425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1467    1.8377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9708    1.8005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3507    1.0681    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9064    0.3730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7738   -2.2795    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4970   -2.6765    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0684   -2.7073    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  6  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  1  0  0  0
  6  5  1  6  0  0  0
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
  1 10  1  0  0  0  0
  7 11  1  0  0  0  0
 11 12  1  0  0  0  0
  4 12  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  1  0  0  0  0
  3 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
  2 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
  1 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  2  0  0  0  0
 20 25  1  0  0  0  0
 16 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0081631

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC[C@@H]1CN2(=O)CC[C@@]34[C@@H]2C[C@@H]1C1=C3N(C2=C4C=CC=C2)C(=O)C(=C1)C(N)=O

> <INCHI_IDENTIFIER>
InChI=1S/C22H23N3O3/c1-2-12-11-25(28)8-7-22-16-5-3-4-6-17(16)24-19(22)14(13(12)10-18(22)25)9-15(20(23)26)21(24)27/h3-6,9,12-13,18H,2,7-8,10-11H2,1H3,(H2,23,26)/t12-,13+,18+,22-,25?/m1/s1

> <INCHI_KEY>
GDXGWPRFCUUOJJ-TZSLYKAUSA-N

> <FORMULA>
C22H23N3O3

> <MOLECULAR_WEIGHT>
377.444

> <EXACT_MASS>
377.173941613

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
51

> <JCHEM_AVERAGE_POLARIZABILITY>
40.283543085773076

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,13S,14S,19S)-14-ethyl-9,16-dioxo-8,16lambda5-diazahexacyclo[11.5.2.1^{1,8}.0^{2,7}.0^{16,19}.0^{12,21}]henicosa-2(7),3,5,10,12(21)-pentaene-10-carboxamide

> <ALOGPS_LOGP>
0.88

> <JCHEM_LOGP>
0.03418296800000126

> <ALOGPS_LOGS>
-4.30

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.408179010059516

> <JCHEM_PKA_STRONGEST_BASIC>
1.9698113463021993

> <JCHEM_POLAR_SURFACE_AREA>
90.28

> <JCHEM_REFRACTIVITY>
106.39189999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.87e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,13S,14S,19S)-14-ethyl-9,16-dioxo-8,16lambda5-diazahexacyclo[11.5.2.1^{1,8}.0^{2,7}.0^{16,19}.0^{12,21}]henicosa-2(7),3,5,10,12(21)-pentaene-10-carboxamide

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0       5.277   2.021   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.143   0.378   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.691  -0.443   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.165   0.329   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.881   1.226   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.810   2.384   0.000  0.00  0.00           C+0
HETATM    7  N   UNK     0       3.014   3.634   0.000  0.00  0.00           N+0
HETATM    8  O   UNK     0       2.356   5.027   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       4.328   4.570   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.618   3.648   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.442   3.209   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.033   1.598   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.462   1.232   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.894  -0.246   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.785  -1.978   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.145  -2.715   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.480  -1.915   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       7.812  -2.688   0.000  0.00  0.00           O+0
HETATM   19  N   UNK     0       6.512  -0.349   0.000  0.00  0.00           N+0
HETATM   20  C   UNK     0       7.620   0.766   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.911   2.133   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.740   3.430   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.279   3.361   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.988   1.994   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       9.159   0.696   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.178  -4.255   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       6.528  -4.996   0.000  0.00  0.00           O+0
HETATM   28  N   UNK     0       3.861  -5.054   0.000  0.00  0.00           N+0
CONECT    1    2    6   10   21                                             
CONECT    2    1    3   19                                                  
CONECT    3    2    4   15                                                  
CONECT    4    3    5   12                                                  
CONECT    5    4    6                                                       
CONECT    6    5    1    7                                                  
CONECT    7    6    8    9   11                                             
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9    1                                                       
CONECT   11    7   12                                                       
CONECT   12   11    4   13                                                  
CONECT   13   12   14                                                       
CONECT   14   13                                                            
CONECT   15    3   16                                                       
CONECT   16   15   17   26                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17    2   20                                                  
CONECT   20   19   21   25                                                  
CONECT   21   20    1   22                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   20                                                       
CONECT   26   16   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₂₃N₃O₃

Average Mass

377.4440 Da

Monoisotopic Mass

377.17394 Da

IUPAC Name

(1R,13S,14S,19S)-14-ethyl-9,16-dioxo-8,16lambda5-diazahexacyclo[11.5.2.1^{1,8}.0^{2,7}.0^{16,19}.0^{12,21}]henicosa-2(7),3,5,10,12(21)-pentaene-10-carboxamide

Traditional Name

(1R,13S,14S,19S)-14-ethyl-9,16-dioxo-8,16lambda5-diazahexacyclo[11.5.2.1^{1,8}.0^{2,7}.0^{16,19}.0^{12,21}]henicosa-2(7),3,5,10,12(21)-pentaene-10-carboxamide

CAS Registry Number

Not Available

SMILES

CC[C@@H]1CN2(=O)CC[C@@]34[C@@H]2C[C@@H]1C1=C3N(C2=C4C=CC=C2)C(=O)C(=C1)C(N)=O

InChI Identifier

InChI=1S/C22H23N3O3/c1-2-12-11-25(28)8-7-22-16-5-3-4-6-17(16)24-19(22)14(13(12)10-18(22)25)9-15(20(23)26)21(24)27/h3-6,9,12-13,18H,2,7-8,10-11H2,1H3,(H2,23,26)/t12-,13+,18+,22-,25?/m1/s1

InChI Key

GDXGWPRFCUUOJJ-TZSLYKAUSA-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
Leuconotis sp.	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as carbazoles. Carbazoles are compounds containing a three ring system containing a pyrrole ring fused on either side to a benzene ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Carbazoles

Direct Parent

Carbazoles

Alternative Parents

Substituents

Carbazole
Quinoline-3-carboxamide
Quinolone
Indolizidine
Pyridine carboxylic acid or derivatives
Pyridinone
Pyridine
N-alkylpyrrolidine
Piperidine
Benzenoid
Pyrrolidine
Trialkyl amine oxide
Heteroaromatic compound
Vinylogous amide
Carboxamide group
Lactam
Primary carboxylic acid amide
N-oxide
Carboxylic acid derivative
Azacycle
Trisubstituted n-oxide
Organooxygen compound
Organonitrogen compound
Hydrocarbon derivative
Organic oxide
Organic nitrogen compound
Organic salt
Organic zwitterion
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	0.88	ALOGPS
logP	0.034	ChemAxon
logS	-4.3	ALOGPS
pKa (Strongest Acidic)	15.41	ChemAxon
pKa (Strongest Basic)	1.97	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	90.28 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	106.39 m³·mol⁻¹	ChemAxon
Polarizability	40.28 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

Not Available

Chemspider ID

24665266

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

46881270

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (-)-Leuconicine F (NP0081631)

MOL for NP0081631 ((-)-Leuconicine F)

3D MOL for NP0081631 ((-)-Leuconicine F)

3D SDF for NP0081631 ((-)-Leuconicine F)

3D-SDF for NP0081631 ((-)-Leuconicine F)

PDB for NP0081631 ((-)-Leuconicine F)

3D PDB for NP0081631 ((-)-Leuconicine F)

SMILES for NP0081631 ((-)-Leuconicine F)

INCHI for NP0081631 ((-)-Leuconicine F)

Structure for NP0081631 ((-)-Leuconicine F)

3D Structure for NP0081631 ((-)-Leuconicine F)