NP-MRD: Showing NP-Card for neocroalbidinone (NP0042419)

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Record Information

Version

2.0

Created at

2021-06-21 00:05:18 UTC

Updated at

2021-06-30 00:17:29 UTC

NP-MRD ID

NP0042419

Secondary Accession Numbers

None

Natural Product Identification

Common Name

neocroalbidinone

Provided By

JEOL Database JEOL Logo

Description

neocroalbidinone is found in Crotalaria albida. neocroalbidinone was first documented in 2013 (Sun, Q.-H., et al.).

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306212102053D          

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     RDKit          3D

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    3.8496    0.8700   -1.2788 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0567    2.3911   -1.6597 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4066    1.2491   -2.9582 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6848   -1.3071   -1.8108 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6097   -1.7743   -0.4874 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6685   -2.6954   -2.0011 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8084   -0.7377   -3.7538 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0262    0.2458    2.9611 H   0  0  0  0  0  0  0  0  0  0  0  0
 18 19  1  0  0  0  0
 16 26  1  0  0  0  0
 19 21  1  0  0  0  0
 26  8  1  0  0  0  0
  7  5  1  0  0  0  0
  8  9  1  0  0  0  0
  5  3  1  0  0  0  0
  9 10  1  0  0  0  0
  3 23  1  0  0  0  0
 23 21  1  0  0  0  0
 10 11  1  0  0  0  0
 21 22  1  0  0  0  0
 11 26  1  0  0  0  0
 23 24  1  0  0  0  0
 16 17  1  0  0  0  0
  3  2  1  6  0  0  0
 23 25  1  6  0  0  0
 26 53  1  1  0  0  0
  3  4  1  0  0  0  0
 11 12  1  0  0  0  0
 14 15  1  0  0  0  0
  8  7  1  0  0  0  0
 19 20  2  0  0  0  0
 12 14  1  0  0  0  0
  2  1  1  0  0  0  0
 17 18  1  0  0  0  0
  5  6  2  0  0  0  0
 14 16  1  0  0  0  0
 12 13  2  0  0  0  0
 14 40  1  1  0  0  0
 16 42  1  6  0  0  0
  8 35  1  1  0  0  0
  9 36  1  0  0  0  0
  9 37  1  0  0  0  0
 10 38  1  0  0  0  0
 10 39  1  0  0  0  0
 17 43  1  0  0  0  0
 17 44  1  0  0  0  0
 21 45  1  6  0  0  0
 22 46  1  0  0  0  0
 22 47  1  0  0  0  0
 22 48  1  0  0  0  0
 24 49  1  0  0  0  0
 24 50  1  0  0  0  0
 24 51  1  0  0  0  0
  2 30  1  0  0  0  0
  2 31  1  0  0  0  0
 25 52  1  0  0  0  0
  4 32  1  0  0  0  0
  4 33  1  0  0  0  0
  4 34  1  0  0  0  0
 15 41  1  0  0  0  0
  1 27  1  0  0  0  0
  1 28  1  0  0  0  0
  1 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0042419

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]O[C@@]1([H])C(=O)N2C([H])([H])C([H])([H])[C@@]3([H])OC(=O)[C@](C([H])([H])[H])(C([H])([H])C([H])([H])[H])[C@](O[H])(C([H])([H])[H])[C@@]([H])(C(=O)OC([H])([H])[C@@]1([H])[C@@]23[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C18H27NO7/c1-5-17(3)16(23)26-11-6-7-19-12(11)10(13(20)14(19)21)8-25-15(22)9(2)18(17,4)24/h9-13,20,24H,5-8H2,1-4H3/t9-,10+,11-,12-,13-,17+,18+/m1/s1

> <INCHI_KEY>
HCELONNSPUFZFZ-WYHMLUIOSA-N

> <FORMULA>
C18H27NO7

> <MOLECULAR_WEIGHT>
369.414

> <EXACT_MASS>
369.178752213

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
37.409744689465185

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,4R,5S,6S,10R,11R,16R)-4-ethyl-5,11-dihydroxy-4,5,6-trimethyl-2,8-dioxa-13-azatricyclo[8.5.1.0^{13,16}]hexadecane-3,7,12-trione

> <ALOGPS_LOGP>
0.25

> <JCHEM_LOGP>
-0.010945610000000864

> <ALOGPS_LOGS>
-1.31

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.900212400038566

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.763434676830244

> <JCHEM_PKA_STRONGEST_BASIC>
-3.2955347886297064

> <JCHEM_POLAR_SURFACE_AREA>
113.37000000000002

> <JCHEM_REFRACTIVITY>
88.52090000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.81e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,4R,5S,6S,10R,11R,16R)-4-ethyl-5,11-dihydroxy-4,5,6-trimethyl-2,8-dioxa-13-azatricyclo[8.5.1.0^{13,16}]hexadecane-3,7,12-trione

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 53 55  0  0  0  0  0  0  0  0999 V2000
   -1.3288   -3.4598   -2.9417 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0329   -2.7637   -2.9246 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1263   -1.4563   -2.0505 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9788   -0.4938   -2.5478 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1204   -1.8790   -0.5955 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2447   -2.9458   -0.1167 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7489   -0.9051    0.1155 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8603   -1.1486    1.5185 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1858   -1.8675    1.8360 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5323   -1.4000    3.2418 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0393   -0.0475    3.2271 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7397    1.1068    3.4948 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7895    1.2247    4.1027 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9747    2.2390    2.8056 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7926    3.2700    2.2935 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2613    1.4873    1.6603 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0474    2.2687    1.1656 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3470    1.8455   -0.1506 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3418    0.9234   -0.2429 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8802    0.3800    0.7109 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7008    0.6910   -1.6980 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0843    1.3251   -1.9158 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5784   -0.7958   -2.1788 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6857   -1.6883   -1.5740 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8462   -0.7400   -3.6080 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9224    0.1560    2.3336 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2474   -4.4139   -3.4735 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0795   -2.8630   -3.4675 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6939   -3.6723   -1.9331 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2916   -2.5399   -3.9664 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7646   -3.5022   -2.5783 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9793   -0.9084   -2.3824 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9765    0.4630   -2.0197 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8700   -0.2839   -3.6172 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0148   -1.7390    1.8971 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9613   -1.5558    1.1248 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0974   -2.9558    1.7659 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9702   -1.9589    3.9965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6023   -1.4421    3.4601 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2665    2.6645    3.5263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5038    3.4007    2.9518 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9637    1.3335    0.8293 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7922    2.2242    1.8698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3064    3.3286    1.0633 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0252    1.2932   -2.3202 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8496    0.8700   -1.2788 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0567    2.3911   -1.6597 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4066    1.2491   -2.9582 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6848   -1.3071   -1.8108 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6097   -1.7743   -0.4874 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6685   -2.6954   -2.0011 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8084   -0.7377   -3.7538 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0262    0.2458    2.9611 H   0  0  0  0  0  0  0  0  0  0  0  0
 18 19  1  0
 16 26  1  0
 19 21  1  0
 26  8  1  0
  7  5  1  0
  8  9  1  0
  5  3  1  0
  9 10  1  0
  3 23  1  0
 23 21  1  0
 10 11  1  0
 21 22  1  0
 11 26  1  0
 23 24  1  0
 16 17  1  0
  3  2  1  6
 23 25  1  6
 26 53  1  1
  3  4  1  0
 11 12  1  0
 14 15  1  0
  8  7  1  0
 19 20  2  0
 12 14  1  0
  2  1  1  0
 17 18  1  0
  5  6  2  0
 14 16  1  0
 12 13  2  0
 14 40  1  1
 16 42  1  6
  8 35  1  1
  9 36  1  0
  9 37  1  0
 10 38  1  0
 10 39  1  0
 17 43  1  0
 17 44  1  0
 21 45  1  6
 22 46  1  0
 22 47  1  0
 22 48  1  0
 24 49  1  0
 24 50  1  0
 24 51  1  0
  2 30  1  0
  2 31  1  0
 25 52  1  0
  4 32  1  0
  4 33  1  0
  4 34  1  0
 15 41  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
M  END

HEADER    PROTEIN                                 21-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   21-JUN-21         0                                  
HETATM    1  C   UNK     0      -1.329  -3.460  -2.942  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.033  -2.764  -2.925  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.126  -1.456  -2.050  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.979  -0.494  -2.548  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.120  -1.879  -0.596  0.00  0.00           C+0
HETATM    6  O   UNK     0       0.245  -2.946  -0.117  0.00  0.00           O+0
HETATM    7  O   UNK     0      -0.749  -0.905   0.116  0.00  0.00           O+0
HETATM    8  C   UNK     0      -0.860  -1.149   1.519  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.186  -1.867   1.836  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.532  -1.400   3.242  0.00  0.00           C+0
HETATM   11  N   UNK     0      -2.039  -0.048   3.227  0.00  0.00           N+0
HETATM   12  C   UNK     0      -2.740   1.107   3.495  0.00  0.00           C+0
HETATM   13  O   UNK     0      -3.789   1.225   4.103  0.00  0.00           O+0
HETATM   14  C   UNK     0      -1.975   2.239   2.806  0.00  0.00           C+0
HETATM   15  O   UNK     0      -2.793   3.270   2.293  0.00  0.00           O+0
HETATM   16  C   UNK     0      -1.261   1.487   1.660  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.047   2.269   1.166  0.00  0.00           C+0
HETATM   18  O   UNK     0       0.347   1.845  -0.151  0.00  0.00           O+0
HETATM   19  C   UNK     0       1.342   0.923  -0.243  0.00  0.00           C+0
HETATM   20  O   UNK     0       1.880   0.380   0.711  0.00  0.00           O+0
HETATM   21  C   UNK     0       1.701   0.691  -1.698  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.084   1.325  -1.916  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.578  -0.796  -2.179  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.686  -1.688  -1.574  0.00  0.00           C+0
HETATM   25  O   UNK     0       1.846  -0.740  -3.608  0.00  0.00           O+0
HETATM   26  C   UNK     0      -0.922   0.156   2.334  0.00  0.00           C+0
HETATM   27  H   UNK     0      -1.247  -4.414  -3.474  0.00  0.00           H+0
HETATM   28  H   UNK     0      -2.079  -2.863  -3.467  0.00  0.00           H+0
HETATM   29  H   UNK     0      -1.694  -3.672  -1.933  0.00  0.00           H+0
HETATM   30  H   UNK     0       0.292  -2.540  -3.966  0.00  0.00           H+0
HETATM   31  H   UNK     0       0.765  -3.502  -2.578  0.00  0.00           H+0
HETATM   32  H   UNK     0      -1.979  -0.908  -2.382  0.00  0.00           H+0
HETATM   33  H   UNK     0      -0.977   0.463  -2.020  0.00  0.00           H+0
HETATM   34  H   UNK     0      -0.870  -0.284  -3.617  0.00  0.00           H+0
HETATM   35  H   UNK     0      -0.015  -1.739   1.897  0.00  0.00           H+0
HETATM   36  H   UNK     0      -2.961  -1.556   1.125  0.00  0.00           H+0
HETATM   37  H   UNK     0      -2.097  -2.956   1.766  0.00  0.00           H+0
HETATM   38  H   UNK     0      -1.970  -1.959   3.997  0.00  0.00           H+0
HETATM   39  H   UNK     0      -3.602  -1.442   3.460  0.00  0.00           H+0
HETATM   40  H   UNK     0      -1.266   2.664   3.526  0.00  0.00           H+0
HETATM   41  H   UNK     0      -3.504   3.401   2.952  0.00  0.00           H+0
HETATM   42  H   UNK     0      -1.964   1.333   0.829  0.00  0.00           H+0
HETATM   43  H   UNK     0       0.792   2.224   1.870  0.00  0.00           H+0
HETATM   44  H   UNK     0      -0.306   3.329   1.063  0.00  0.00           H+0
HETATM   45  H   UNK     0       1.025   1.293  -2.320  0.00  0.00           H+0
HETATM   46  H   UNK     0       3.850   0.870  -1.279  0.00  0.00           H+0
HETATM   47  H   UNK     0       3.057   2.391  -1.660  0.00  0.00           H+0
HETATM   48  H   UNK     0       3.407   1.249  -2.958  0.00  0.00           H+0
HETATM   49  H   UNK     0       3.685  -1.307  -1.811  0.00  0.00           H+0
HETATM   50  H   UNK     0       2.610  -1.774  -0.487  0.00  0.00           H+0
HETATM   51  H   UNK     0       2.668  -2.695  -2.001  0.00  0.00           H+0
HETATM   52  H   UNK     0       2.808  -0.738  -3.754  0.00  0.00           H+0
HETATM   53  H   UNK     0      -0.026   0.246   2.961  0.00  0.00           H+0
CONECT    1    2   27   28   29                                             
CONECT    2    3    1   30   31                                             
CONECT    3    5   23    2    4                                             
CONECT    4    3   32   33   34                                             
CONECT    5    7    3    6                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8   26    9    7   35                                             
CONECT    9    8   10   36   37                                             
CONECT   10    9   11   38   39                                             
CONECT   11   10   26   12                                                  
CONECT   12   11   14   13                                                  
CONECT   13   12                                                            
CONECT   14   15   12   16   40                                             
CONECT   15   14   41                                                       
CONECT   16   26   17   14   42                                             
CONECT   17   16   18   43   44                                             
CONECT   18   19   17                                                       
CONECT   19   18   21   20                                                  
CONECT   20   19                                                            
CONECT   21   19   23   22   45                                             
CONECT   22   21   46   47   48                                             
CONECT   23    3   21   24   25                                             
CONECT   24   23   49   50   51                                             
CONECT   25   23   52                                                       
CONECT   26   16    8   11   53                                             
CONECT   27    1                                                            
CONECT   28    1                                                            
CONECT   29    1                                                            
CONECT   30    2                                                            
CONECT   31    2                                                            
CONECT   32    4                                                            
CONECT   33    4                                                            
CONECT   34    4                                                            
CONECT   35    8                                                            
CONECT   36    9                                                            
CONECT   37    9                                                            
CONECT   38   10                                                            
CONECT   39   10                                                            
CONECT   40   14                                                            
CONECT   41   15                                                            
CONECT   42   16                                                            
CONECT   43   17                                                            
CONECT   44   17                                                            
CONECT   45   21                                                            
CONECT   46   22                                                            
CONECT   47   22                                                            
CONECT   48   22                                                            
CONECT   49   24                                                            
CONECT   50   24                                                            
CONECT   51   24                                                            
CONECT   52   25                                                            
CONECT   53   26                                                            
MASTER        0    0    0    0    0    0    0    0   53    0  110    0
END

RDKit          3D

53 55  0  0  0  0  0  0  0  0999 V2000
   -1.3288   -3.4598   -2.9417 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₂₇NO₇

Average Mass

369.4140 Da

Monoisotopic Mass

369.17875 Da

IUPAC Name

(1R,4R,5S,6S,10R,11R,16R)-4-ethyl-5,11-dihydroxy-4,5,6-trimethyl-2,8-dioxa-13-azatricyclo[8.5.1.0^{13,16}]hexadecane-3,7,12-trione

Traditional Name

(1R,4R,5S,6S,10R,11R,16R)-4-ethyl-5,11-dihydroxy-4,5,6-trimethyl-2,8-dioxa-13-azatricyclo[8.5.1.0^{13,16}]hexadecane-3,7,12-trione

CAS Registry Number

Not Available

SMILES

[H]O[C@@]1([H])C(=O)N2C([H])([H])C([H])([H])[C@@]3([H])OC(=O)[C@](C([H])([H])[H])(C([H])([H])C([H])([H])[H])[C@](O[H])(C([H])([H])[H])[C@@]([H])(C(=O)OC([H])([H])[C@@]1([H])[C@@]23[H])C([H])([H])[H]

InChI Identifier

InChI=1S/C18H27NO7/c1-5-17(3)16(23)26-11-6-7-19-12(11)10(13(20)14(19)21)8-25-15(22)9(2)18(17,4)24/h9-13,20,24H,5-8H2,1-4H3/t9-,10+,11-,12-,13-,17+,18+/m1/s1

InChI Key

HCELONNSPUFZFZ-WYHMLUIOSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Crotalaria albida	JEOL database	Sun, Q.-H., et al, Phytochem. Lett. 6, 449 (2013)

Chemical Taxonomy

Classification

Not classified

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	0.25	ALOGPS
logP	-0.011	ChemAxon
logS	-1.3	ALOGPS
pKa (Strongest Acidic)	12.76	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	113.37 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	88.52 m³·mol⁻¹	ChemAxon
Polarizability	37.41 Å³	ChemAxon
Number of Rings	3	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

Not Available

References

General References

Sun, Q.-H., et al. (2013). Sun, Q.-H., et al, Phytochem. Lett. 6, 449 (2013). Phytochem..

Showing NP-Card for neocroalbidinone (NP0042419)

MOL for NP0042419 (neocroalbidinone)

3D MOL for NP0042419 (neocroalbidinone)

3D SDF for NP0042419 (neocroalbidinone)

3D-SDF for NP0042419 (neocroalbidinone)

PDB for NP0042419 (neocroalbidinone)

3D PDB for NP0042419 (neocroalbidinone)

SMILES for NP0042419 (neocroalbidinone)

INCHI for NP0042419 (neocroalbidinone)

Structure for NP0042419 (neocroalbidinone)

3D Structure for NP0042419 (neocroalbidinone)