NP-MRD: Showing NP-Card for Acutifolin A (NP0025992)

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Record Information

Version

2.0

Created at

2021-06-19 17:58:06 UTC

Updated at

2021-06-29 23:51:15 UTC

NP-MRD ID

NP0025992

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Acutifolin A

Provided By

JEOL Database JEOL Logo

Description

Acutifolin A is found in Brosimum acutifolium and Broussonetia acutifolium. Acutifolin A was first documented in 2001 (Takahashi, J., et al.). Based on a literature review very few articles have been published on (+)-acutifolin a.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306192119583D          

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M  END

     RDKit          3D

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M  END


  Mrv1652306192119583D          

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  3 28  1  0  0  0  0
  3 29  1  0  0  0  0
  3 30  1  0  0  0  0
 20 44  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0025992

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C([H])C([H])=C(C([H])=C1[H])[C@]1([H])C([H])([H])C([H])([H])[C@]2(O[H])C([H])=C([H])C(=O)[C@]1(C2=O)C([H])([H])C([H])=C(C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C20H22O4/c1-13(2)7-12-20-16(14-3-5-15(21)6-4-14)8-10-19(24,18(20)23)11-9-17(20)22/h3-7,9,11,16,21,24H,8,10,12H2,1-2H3/t16-,19-,20-/m0/s1

> <INCHI_KEY>
LDQGHYBYTNQNFR-VDGAXYAQSA-N

> <FORMULA>
C20H22O4

> <MOLECULAR_WEIGHT>
326.392

> <EXACT_MASS>
326.151809188

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
46

> <JCHEM_AVERAGE_POLARIZABILITY>
34.69080441188443

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,5S,8S)-5-hydroxy-8-(4-hydroxyphenyl)-1-(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione

> <ALOGPS_LOGP>
2.84

> <JCHEM_LOGP>
4.0265422483333335

> <ALOGPS_LOGS>
-4.05

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.588366835255556

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.500531242149862

> <JCHEM_PKA_STRONGEST_BASIC>
-3.8538037138970127

> <JCHEM_POLAR_SURFACE_AREA>
74.6

> <JCHEM_REFRACTIVITY>
93.70879999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.89e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(+)-acutifolin A

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 46 48  0  0  0  0  0  0  0  0999 V2000
    0.8500    2.8784    0.5127 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4874    2.5328    1.1105 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6511    2.9890    2.5383 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4931    1.8939    0.4796 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5350    1.3923   -0.9470 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9452   -0.0935   -1.1544 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8493   -0.3934   -2.6657 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0003    0.0964   -3.4077 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8182   -1.3497   -3.2764 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7489   -1.9608   -2.5299 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9219   -1.7285   -1.0588 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.3011   -1.8572   -0.7644 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1201   -2.7109   -0.2058 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6075   -2.5742   -0.4156 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1265   -1.1052   -0.2784 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3909   -1.0503   -0.4012 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1561   -0.6636    0.7126 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5502   -0.6166    0.6476 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1945   -0.9602   -0.5310 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5555   -0.8938   -0.5569 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4659   -1.3611   -1.6433 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0699   -1.4130   -1.5740 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4092   -0.3130   -0.7621 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1524    0.5337   -0.2668 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6561    2.4850    1.1409 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9629    3.9662    0.4563 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0017    2.4799   -0.4917 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1032    2.5156    3.1753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6353    2.7368    2.9470 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5322    4.0754    2.6051 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4211    1.7527    1.0350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2490    2.0317   -1.4856 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5737    1.5676   -1.4381 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7133   -1.5330   -4.3405 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4229   -2.6746   -2.9989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5751   -1.0152   -0.3454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3506   -2.5404    0.8548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4311   -3.7433   -0.4113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3324   -2.9870   -1.3936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0947   -3.2018    0.3253 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3604   -0.8484    0.7670 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6735   -0.3844    1.6473 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1281   -0.3074    1.5136 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8570   -1.1228   -1.4512 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9590   -1.6370   -2.5701 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5315   -1.7432   -2.4582 H   0  0  0  0  0  0  0  0  0  0  0  0
 14 15  1  0
 23 24  2  0
 15  6  1  0
 16 17  2  0
 17 18  1  0
  6  7  1  0
 18 19  2  0
 11 10  1  0
 19 21  1  0
 23 11  1  0
 21 22  2  0
 22 16  1  0
 15 16  1  0
 11 12  1  1
 23  6  1  0
  6  5  1  6
  7  9  1  0
  5  4  1  0
 11 13  1  0
  4  2  2  3
  9 10  2  0
  2  1  1  0
 13 14  1  0
  2  3  1  0
  7  8  2  0
 19 20  1  0
 13 37  1  0
 13 38  1  0
 14 39  1  0
 14 40  1  0
 15 41  1  1
  9 34  1  0
 10 35  1  0
 17 42  1  0
 18 43  1  0
 21 45  1  0
 22 46  1  0
 12 36  1  0
  5 32  1  0
  5 33  1  0
  4 31  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  3 28  1  0
  3 29  1  0
  3 30  1  0
 20 44  1  0
M  END

HEADER    PROTEIN                                 19-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-JUN-21         0                                  
HETATM    1  C   UNK     0       0.850   2.878   0.513  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.487   2.533   1.111  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.651   2.989   2.538  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.493   1.894   0.480  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.535   1.392  -0.947  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.945  -0.094  -1.154  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.849  -0.393  -2.666  0.00  0.00           C+0
HETATM    8  O   UNK     0      -1.000   0.096  -3.408  0.00  0.00           O+0
HETATM    9  C   UNK     0      -2.818  -1.350  -3.276  0.00  0.00           C+0
HETATM   10  C   UNK     0      -3.749  -1.961  -2.530  0.00  0.00           C+0
HETATM   11  C   UNK     0      -3.922  -1.728  -1.059  0.00  0.00           C+0
HETATM   12  O   UNK     0      -5.301  -1.857  -0.764  0.00  0.00           O+0
HETATM   13  C   UNK     0      -3.120  -2.711  -0.206  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.607  -2.574  -0.416  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.127  -1.105  -0.278  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.391  -1.050  -0.401  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.156  -0.664   0.713  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.550  -0.617   0.648  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.195  -0.960  -0.531  0.00  0.00           C+0
HETATM   20  O   UNK     0       4.556  -0.894  -0.557  0.00  0.00           O+0
HETATM   21  C   UNK     0       2.466  -1.361  -1.643  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.070  -1.413  -1.574  0.00  0.00           C+0
HETATM   23  C   UNK     0      -3.409  -0.313  -0.762  0.00  0.00           C+0
HETATM   24  O   UNK     0      -4.152   0.534  -0.267  0.00  0.00           O+0
HETATM   25  H   UNK     0       1.656   2.485   1.141  0.00  0.00           H+0
HETATM   26  H   UNK     0       0.963   3.966   0.456  0.00  0.00           H+0
HETATM   27  H   UNK     0       1.002   2.480  -0.492  0.00  0.00           H+0
HETATM   28  H   UNK     0       0.103   2.516   3.175  0.00  0.00           H+0
HETATM   29  H   UNK     0      -1.635   2.737   2.947  0.00  0.00           H+0
HETATM   30  H   UNK     0      -0.532   4.075   2.605  0.00  0.00           H+0
HETATM   31  H   UNK     0      -2.421   1.753   1.035  0.00  0.00           H+0
HETATM   32  H   UNK     0      -2.249   2.032  -1.486  0.00  0.00           H+0
HETATM   33  H   UNK     0      -0.574   1.568  -1.438  0.00  0.00           H+0
HETATM   34  H   UNK     0      -2.713  -1.533  -4.340  0.00  0.00           H+0
HETATM   35  H   UNK     0      -4.423  -2.675  -2.999  0.00  0.00           H+0
HETATM   36  H   UNK     0      -5.575  -1.015  -0.345  0.00  0.00           H+0
HETATM   37  H   UNK     0      -3.351  -2.540   0.855  0.00  0.00           H+0
HETATM   38  H   UNK     0      -3.431  -3.743  -0.411  0.00  0.00           H+0
HETATM   39  H   UNK     0      -1.332  -2.987  -1.394  0.00  0.00           H+0
HETATM   40  H   UNK     0      -1.095  -3.202   0.325  0.00  0.00           H+0
HETATM   41  H   UNK     0      -1.360  -0.848   0.767  0.00  0.00           H+0
HETATM   42  H   UNK     0       0.674  -0.384   1.647  0.00  0.00           H+0
HETATM   43  H   UNK     0       3.128  -0.307   1.514  0.00  0.00           H+0
HETATM   44  H   UNK     0       4.857  -1.123  -1.451  0.00  0.00           H+0
HETATM   45  H   UNK     0       2.959  -1.637  -2.570  0.00  0.00           H+0
HETATM   46  H   UNK     0       0.532  -1.743  -2.458  0.00  0.00           H+0
CONECT    1    2   25   26   27                                             
CONECT    2    4    1    3                                                  
CONECT    3    2   28   29   30                                             
CONECT    4    5    2   31                                                  
CONECT    5    6    4   32   33                                             
CONECT    6   15    7   23    5                                             
CONECT    7    6    9    8                                                  
CONECT    8    7                                                            
CONECT    9    7   10   34                                                  
CONECT   10   11    9   35                                                  
CONECT   11   10   23   12   13                                             
CONECT   12   11   36                                                       
CONECT   13   11   14   37   38                                             
CONECT   14   15   13   39   40                                             
CONECT   15   14    6   16   41                                             
CONECT   16   17   22   15                                                  
CONECT   17   16   18   42                                                  
CONECT   18   17   19   43                                                  
CONECT   19   18   21   20                                                  
CONECT   20   19   44                                                       
CONECT   21   19   22   45                                                  
CONECT   22   21   16   46                                                  
CONECT   23   24   11    6                                                  
CONECT   24   23                                                            
CONECT   25    1                                                            
CONECT   26    1                                                            
CONECT   27    1                                                            
CONECT   28    3                                                            
CONECT   29    3                                                            
CONECT   30    3                                                            
CONECT   31    4                                                            
CONECT   32    5                                                            
CONECT   33    5                                                            
CONECT   34    9                                                            
CONECT   35   10                                                            
CONECT   36   12                                                            
CONECT   37   13                                                            
CONECT   38   13                                                            
CONECT   39   14                                                            
CONECT   40   14                                                            
CONECT   41   15                                                            
CONECT   42   17                                                            
CONECT   43   18                                                            
CONECT   44   20                                                            
CONECT   45   21                                                            
CONECT   46   22                                                            
MASTER        0    0    0    0    0    0    0    0   46    0   96    0
END

RDKit          3D

46 48  0  0  0  0  0  0  0  0999 V2000
    0.8500    2.8784    0.5127 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4874    2.5328    1.1105 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6511    2.9890    2.5383 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4931    1.8939    0.4796 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5350    1.3923   -0.9470 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9452   -0.0935   -1.1544 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8493   -0.3934   -2.6657 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0003    0.0964   -3.4077 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8182   -1.3497   -3.2764 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7489   -1.9608   -2.5299 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9219   -1.7285   -1.0588 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.3011   -1.8572   -0.7644 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1201   -2.7109   -0.2058 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6075   -2.5742   -0.4156 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1265   -1.1052   -0.2784 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3909   -1.0503   -0.4012 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1561   -0.6636    0.7126 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5502   -0.6166    0.6476 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1945   -0.9602   -0.5310 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5555   -0.8938   -0.5569 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4659   -1.3611   -1.6433 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0699   -1.4130   -1.5740 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4092   -0.3130   -0.7621 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1524    0.5337   -0.2668 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6561    2.4850    1.1409 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9629    3.9662    0.4563 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0017    2.4799   -0.4917 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1032    2.5156    3.1753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6353    2.7368    2.9470 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5322    4.0754    2.6051 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4211    1.7527    1.0350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2490    2.0317   -1.4856 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5737    1.5676   -1.4381 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7133   -1.5330   -4.3405 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4229   -2.6746   -2.9989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5751   -1.0152   -0.3454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3506   -2.5404    0.8548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4311   -3.7433   -0.4113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3324   -2.9870   -1.3936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0947   -3.2018    0.3253 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3604   -0.8484    0.7670 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6735   -0.3844    1.6473 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1281   -0.3074    1.5136 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8570   -1.1228   -1.4512 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9590   -1.6370   -2.5701 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5315   -1.7432   -2.4582 H   0  0  0  0  0  0  0  0  0  0  0  0
 14 15  1  0
 23 24  2  0
 15  6  1  0
 16 17  2  0
 17 18  1  0
  6  7  1  0
 18 19  2  0
 11 10  1  0
 19 21  1  0
 23 11  1  0
 21 22  2  0
 22 16  1  0
 15 16  1  0
 11 12  1  1
 23  6  1  0
  6  5  1  6
  7  9  1  0
  5  4  1  0
 11 13  1  0
  4  2  2  3
  9 10  2  0
  2  1  1  0
 13 14  1  0
  2  3  1  0
  7  8  2  0
 19 20  1  0
 13 37  1  0
 13 38  1  0
 14 39  1  0
 14 40  1  0
 15 41  1  1
  9 34  1  0
 10 35  1  0
 17 42  1  0
 18 43  1  0
 21 45  1  0
 22 46  1  0
 12 36  1  0
  5 32  1  0
  5 33  1  0
  4 31  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  3 28  1  0
  3 29  1  0
  3 30  1  0
 20 44  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₂O₄

Average Mass

326.3920 Da

Monoisotopic Mass

326.15181 Da

IUPAC Name

(1S,5S,8S)-5-hydroxy-8-(4-hydroxyphenyl)-1-(3-methylbut-2-en-1-yl)bicyclo[3.3.1]non-3-ene-2,9-dione

Traditional Name

(+)-acutifolin A

CAS Registry Number

Not Available

SMILES

[H]OC1=C([H])C([H])=C(C([H])=C1[H])[C@]1([H])C([H])([H])C([H])([H])[C@]2(O[H])C([H])=C([H])C(=O)[C@]1(C2=O)C([H])([H])C([H])=C(C([H])([H])[H])C([H])([H])[H]

InChI Identifier

InChI=1S/C20H22O4/c1-13(2)7-12-20-16(14-3-5-15(21)6-4-14)8-10-19(24,18(20)23)11-9-17(20)22/h3-7,9,11,16,21,24H,8,10,12H2,1-2H3/t16-,19-,20-/m0/s1

InChI Key

LDQGHYBYTNQNFR-VDGAXYAQSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
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, 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, 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, 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
Brosimum acutifolium	JEOL database	Takahashi, J., et al, J. Nat. Prod. 64, 1493 (2001)
Broussonetia acutifolium	Plant	KNApSAcK

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	2.84	ALOGPS
logP	4.03	ChemAxon
logS	-4	ALOGPS
pKa (Strongest Acidic)	9.5	ChemAxon
pKa (Strongest Basic)	-3.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	74.6 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	93.71 m³·mol⁻¹	ChemAxon
Polarizability	34.69 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

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

9242517

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Takahashi, J., et al. (2001). Takahashi, J., et al, J. Nat. Prod. 64, 1493 (2001). J. Nat. Prod..

Showing NP-Card for Acutifolin A (NP0025992)

MOL for NP0025992 (Acutifolin A)

3D MOL for NP0025992 (Acutifolin A)

3D SDF for NP0025992 (Acutifolin A)

3D-SDF for NP0025992 (Acutifolin A)

PDB for NP0025992 (Acutifolin A)

3D PDB for NP0025992 (Acutifolin A)

SMILES for NP0025992 (Acutifolin A)

INCHI for NP0025992 (Acutifolin A)

Structure for NP0025992 (Acutifolin A)

3D Structure for NP0025992 (Acutifolin A)