NP-MRD: Showing NP-Card for Penicillactam (NP0010559)

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Record Information

Version

2.0

Created at

2021-01-05 20:02:11 UTC

Updated at

2021-07-15 17:06:26 UTC

NP-MRD ID

NP0010559

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Penicillactam

Provided By

NPAtlas

Description

Penicillactam is found in Penicillium sp. F11. Penicillactam was first documented in 2012 (PMID: 22248032). Based on a literature review very few articles have been published on Penicillactam.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242107393D          

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M  END

     RDKit          3D

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  Mrv1652306242107393D          

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M  END
> <DATABASE_ID>
NP0010559

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]O[C@@]1(OC(=O)C2=C([H])C([H])=C([H])C([H])=C2N([H])C1=O)C([H])([H])[C@]1(N([H])C(=O)C2=C([H])C([H])=C([H])C([H])=C2N([H])C1=O)C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C20H17N3O6/c1-19(17(26)21-13-8-4-2-6-11(13)15(24)23-19)10-20(28)18(27)22-14-9-5-3-7-12(14)16(25)29-20/h2-9,28H,10H2,1H3,(H,21,26)(H,22,27)(H,23,24)/t19-,20-/m1/s1

> <INCHI_KEY>
FAPNBQQEEOZITN-UHFFFAOYSA-N

> <FORMULA>
C20H17N3O6

> <MOLECULAR_WEIGHT>
395.371

> <EXACT_MASS>
395.111735279

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
46

> <JCHEM_AVERAGE_POLARIZABILITY>
38.72545310250737

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3R)-3-hydroxy-3-{[(3R)-3-methyl-2,5-dioxo-2,3,4,5-tetrahydro-1H-1,4-benzodiazepin-3-yl]methyl}-1,2,3,5-tetrahydro-4,1-benzoxazepine-2,5-dione

> <ALOGPS_LOGP>
1.12

> <JCHEM_LOGP>
2.920325551

> <ALOGPS_LOGS>
-3.38

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.4458006803114

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.750447363300657

> <JCHEM_PKA_STRONGEST_BASIC>
-1.517101295129407

> <JCHEM_POLAR_SURFACE_AREA>
133.82999999999998

> <JCHEM_REFRACTIVITY>
102.9533

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.67e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3R)-3-hydroxy-3-{[(3R)-3-methyl-2,5-dioxo-1,4-dihydro-1,4-benzodiazepin-3-yl]methyl}-1H-4,1-benzoxazepine-2,5-dione

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 46 49  0  0  0  0  0  0  0  0999 V2000
   -0.2564    2.5984   -1.1274 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1168    1.5154   -0.5306 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4188    0.7314    0.5423 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8298    0.0332    0.0518 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5309   -0.8661   -0.9730 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7631    0.9504   -0.4673 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1108    0.8817   -0.7254 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5692    1.6670   -1.5846 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0708    0.0027   -0.1176 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3229    0.1032   -0.6727 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3772   -0.6691   -0.2137 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1660   -1.5571    0.8217 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9068   -1.6677    1.3903 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8736   -0.8882    0.9160 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6531   -1.1259    1.6082 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.3572   -0.7665    1.1836 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4490   -1.2260    1.9303 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5455    0.5891   -1.5497 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5048   -0.4479   -1.4941 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4232   -1.3765   -2.3637 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5965   -0.5609   -0.5231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2219   -1.7767   -0.5762 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2883   -2.0783    0.2712 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7238   -1.1468    1.1755 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1123    0.0839    1.2496 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0577    0.3650    0.4026 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5168    1.6754    0.5855 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2809    2.1939    0.1149 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1983    3.4516    0.2954 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8947    3.4600   -1.4371 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2499    2.2620   -2.0701 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4377    2.9711   -0.3758 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2241    1.3532    1.4368 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1176   -0.0676    0.8698 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3028   -1.7778   -0.6144 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5295    0.7994   -1.4992 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3520   -0.5672   -0.6716 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0042   -2.1488    1.1624 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7389   -2.3559    2.1943 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7592   -1.6216    2.5264 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0736    0.7061   -2.4640 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8630   -2.4958   -1.2957 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7822   -3.0280    0.2348 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5539   -1.3470    1.8532 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4518    0.8389    1.9698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1319    2.3306    1.1474 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6
  2  3  1  0
  3  4  1  0
  4  5  1  6
  4  6  1  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
  2 18  1  0
 18 19  1  0
 19 20  2  0
 19 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  2  0
 24 25  1  0
 25 26  2  0
 26 27  1  0
 27 28  1  0
 28 29  2  0
 28  2  1  0
 16  4  1  0
 26 21  1  0
 14  9  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  3 33  1  0
  3 34  1  0
  5 35  1  0
 10 36  1  0
 11 37  1  0
 12 38  1  0
 13 39  1  0
 15 40  1  0
 18 41  1  0
 22 42  1  0
 23 43  1  0
 24 44  1  0
 25 45  1  0
 27 46  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0      -0.256   2.598  -1.127  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.117   1.515  -0.531  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.419   0.731   0.542  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.830   0.033   0.052  0.00  0.00           C+0
HETATM    5  O   UNK     0       0.531  -0.866  -0.973  0.00  0.00           O+0
HETATM    6  O   UNK     0       1.763   0.950  -0.467  0.00  0.00           O+0
HETATM    7  C   UNK     0       3.111   0.882  -0.725  0.00  0.00           C+0
HETATM    8  O   UNK     0       3.569   1.667  -1.585  0.00  0.00           O+0
HETATM    9  C   UNK     0       4.071   0.003  -0.118  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.323   0.103  -0.673  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.377  -0.669  -0.214  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.166  -1.557   0.822  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.907  -1.668   1.390  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.874  -0.888   0.916  0.00  0.00           C+0
HETATM   15  N   UNK     0       2.653  -1.126   1.608  0.00  0.00           N+0
HETATM   16  C   UNK     0       1.357  -0.767   1.184  0.00  0.00           C+0
HETATM   17  O   UNK     0       0.449  -1.226   1.930  0.00  0.00           O+0
HETATM   18  N   UNK     0      -1.546   0.589  -1.550  0.00  0.00           N+0
HETATM   19  C   UNK     0      -2.505  -0.448  -1.494  0.00  0.00           C+0
HETATM   20  O   UNK     0      -2.423  -1.377  -2.364  0.00  0.00           O+0
HETATM   21  C   UNK     0      -3.596  -0.561  -0.523  0.00  0.00           C+0
HETATM   22  C   UNK     0      -4.222  -1.777  -0.576  0.00  0.00           C+0
HETATM   23  C   UNK     0      -5.288  -2.078   0.271  0.00  0.00           C+0
HETATM   24  C   UNK     0      -5.724  -1.147   1.176  0.00  0.00           C+0
HETATM   25  C   UNK     0      -5.112   0.084   1.250  0.00  0.00           C+0
HETATM   26  C   UNK     0      -4.058   0.365   0.403  0.00  0.00           C+0
HETATM   27  N   UNK     0      -3.517   1.675   0.586  0.00  0.00           N+0
HETATM   28  C   UNK     0      -2.281   2.194   0.115  0.00  0.00           C+0
HETATM   29  O   UNK     0      -2.198   3.452   0.295  0.00  0.00           O+0
HETATM   30  H   UNK     0      -0.895   3.460  -1.437  0.00  0.00           H+0
HETATM   31  H   UNK     0       0.250   2.262  -2.070  0.00  0.00           H+0
HETATM   32  H   UNK     0       0.438   2.971  -0.376  0.00  0.00           H+0
HETATM   33  H   UNK     0      -0.224   1.353   1.437  0.00  0.00           H+0
HETATM   34  H   UNK     0      -1.118  -0.068   0.870  0.00  0.00           H+0
HETATM   35  H   UNK     0       0.303  -1.778  -0.614  0.00  0.00           H+0
HETATM   36  H   UNK     0       5.529   0.799  -1.499  0.00  0.00           H+0
HETATM   37  H   UNK     0       7.352  -0.567  -0.672  0.00  0.00           H+0
HETATM   38  H   UNK     0       7.004  -2.149   1.162  0.00  0.00           H+0
HETATM   39  H   UNK     0       4.739  -2.356   2.194  0.00  0.00           H+0
HETATM   40  H   UNK     0       2.759  -1.622   2.526  0.00  0.00           H+0
HETATM   41  H   UNK     0      -1.074   0.706  -2.464  0.00  0.00           H+0
HETATM   42  H   UNK     0      -3.863  -2.496  -1.296  0.00  0.00           H+0
HETATM   43  H   UNK     0      -5.782  -3.028   0.235  0.00  0.00           H+0
HETATM   44  H   UNK     0      -6.554  -1.347   1.853  0.00  0.00           H+0
HETATM   45  H   UNK     0      -5.452   0.839   1.970  0.00  0.00           H+0
HETATM   46  H   UNK     0      -4.132   2.331   1.147  0.00  0.00           H+0
CONECT    1    2   30   31   32                                             
CONECT    2    1    3   18   28                                             
CONECT    3    2    4   33   34                                             
CONECT    4    3    5    6   16                                             
CONECT    5    4   35                                                       
CONECT    6    4    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   14                                                  
CONECT   10    9   11   36                                                  
CONECT   11   10   12   37                                                  
CONECT   12   11   13   38                                                  
CONECT   13   12   14   39                                                  
CONECT   14   13   15    9                                                  
CONECT   15   14   16   40                                                  
CONECT   16   15   17    4                                                  
CONECT   17   16                                                            
CONECT   18    2   19   41                                                  
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   26                                                  
CONECT   22   21   23   42                                                  
CONECT   23   22   24   43                                                  
CONECT   24   23   25   44                                                  
CONECT   25   24   26   45                                                  
CONECT   26   25   27   21                                                  
CONECT   27   26   28   46                                                  
CONECT   28   27   29    2                                                  
CONECT   29   28                                                            
CONECT   30    1                                                            
CONECT   31    1                                                            
CONECT   32    1                                                            
CONECT   33    3                                                            
CONECT   34    3                                                            
CONECT   35    5                                                            
CONECT   36   10                                                            
CONECT   37   11                                                            
CONECT   38   12                                                            
CONECT   39   13                                                            
CONECT   40   15                                                            
CONECT   41   18                                                            
CONECT   42   22                                                            
CONECT   43   23                                                            
CONECT   44   24                                                            
CONECT   45   25                                                            
CONECT   46   27                                                            
MASTER        0    0    0    0    0    0    0    0   46    0   98    0
END

RDKit          3D

46 49  0  0  0  0  0  0  0  0999 V2000
   -0.2564    2.5984   -1.1274 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1168    1.5154   -0.5306 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4188    0.7314    0.5423 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8298    0.0332    0.0518 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5309   -0.8661   -0.9730 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7631    0.9504   -0.4673 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1108    0.8817   -0.7254 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5692    1.6670   -1.5846 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0708    0.0027   -0.1176 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3229    0.1032   -0.6727 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3772   -0.6691   -0.2137 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1660   -1.5571    0.8217 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9068   -1.6677    1.3903 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8736   -0.8882    0.9160 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6531   -1.1259    1.6082 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.3572   -0.7665    1.1836 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4490   -1.2260    1.9303 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5455    0.5891   -1.5497 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5048   -0.4479   -1.4941 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4232   -1.3765   -2.3637 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5965   -0.5609   -0.5231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2219   -1.7767   -0.5762 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2883   -2.0783    0.2712 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7238   -1.1468    1.1755 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1123    0.0839    1.2496 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0577    0.3650    0.4026 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5168    1.6754    0.5855 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2809    2.1939    0.1149 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1983    3.4516    0.2954 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8947    3.4600   -1.4371 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2499    2.2620   -2.0701 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4377    2.9711   -0.3758 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2241    1.3532    1.4368 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1176   -0.0676    0.8698 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3028   -1.7778   -0.6144 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5295    0.7994   -1.4992 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3520   -0.5672   -0.6716 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0042   -2.1488    1.1624 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7389   -2.3559    2.1943 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7592   -1.6216    2.5264 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0736    0.7061   -2.4640 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8630   -2.4958   -1.2957 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7822   -3.0280    0.2348 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5539   -1.3470    1.8532 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4518    0.8389    1.9698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1319    2.3306    1.1474 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6
  2  3  1  0
  3  4  1  0
  4  5  1  6
  4  6  1  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
  2 18  1  0
 18 19  1  0
 19 20  2  0
 19 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  2  0
 24 25  1  0
 25 26  2  0
 26 27  1  0
 27 28  1  0
 28 29  2  0
 28  2  1  0
 16  4  1  0
 26 21  1  0
 14  9  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  3 33  1  0
  3 34  1  0
  5 35  1  0
 10 36  1  0
 11 37  1  0
 12 38  1  0
 13 39  1  0
 15 40  1  0
 18 41  1  0
 22 42  1  0
 23 43  1  0
 24 44  1  0
 25 45  1  0
 27 46  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₂₀H₁₇N₃O₆

Average Mass

395.3710 Da

Monoisotopic Mass

395.11174 Da

IUPAC Name

(3R)-3-hydroxy-3-{[(3R)-3-methyl-2,5-dioxo-2,3,4,5-tetrahydro-1H-1,4-benzodiazepin-3-yl]methyl}-1,2,3,5-tetrahydro-4,1-benzoxazepine-2,5-dione

Traditional Name

(3R)-3-hydroxy-3-{[(3R)-3-methyl-2,5-dioxo-1,4-dihydro-1,4-benzodiazepin-3-yl]methyl}-1H-4,1-benzoxazepine-2,5-dione

CAS Registry Number

Not Available

SMILES

CC1(CC2(O)OC(=O)C3=CC=CC=C3NC2=O)NC(=O)C2=CC=CC=C2NC1=O

InChI Identifier

InChI=1S/C20H17N3O6/c1-19(17(26)21-13-8-4-2-6-11(13)15(24)23-19)10-20(28)18(27)22-14-9-5-3-7-12(14)16(25)29-20/h2-9,28H,10H2,1H3,(H,21,26)(H,22,27)(H,23,24)

InChI Key

FAPNBQQEEOZITN-UHFFFAOYSA-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
Penicillium sp. F11	NPAtlas	22248032

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	1.12	ALOGPS
logP	2.92	ChemAxon
logS	-3.4	ALOGPS
pKa (Strongest Acidic)	9.75	ChemAxon
pKa (Strongest Basic)	-1.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	133.83 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	102.95 m³·mol⁻¹	ChemAxon
Polarizability	38.73 Å³	ChemAxon
Number of Rings	4	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

NPAtlas ID

NPA012752

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

29212420

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

57337607

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Zhuang P, Tang XX, Yi ZW, Qiu YK, Wu Z: Two new compounds from marine-derived fungus Penicillium sp. F11. J Asian Nat Prod Res. 2012;14(3):197-203. doi: 10.1080/10286020.2011.634279. Epub 2012 Jan 16. [PubMed:22248032 ]

Showing NP-Card for Penicillactam (NP0010559)

MOL for NP0010559 (Penicillactam)

3D MOL for NP0010559 (Penicillactam)

3D SDF for NP0010559 (Penicillactam)

3D-SDF for NP0010559 (Penicillactam)

PDB for NP0010559 (Penicillactam)

3D PDB for NP0010559 (Penicillactam)

SMILES for NP0010559 (Penicillactam)

INCHI for NP0010559 (Penicillactam)

Structure for NP0010559 (Penicillactam)

3D Structure for NP0010559 (Penicillactam)