MiMeDB: Showing metabocard for Neofipiperzine C (MMDBc0003918)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-14 22:09:06 UTC

Update Date

2025-10-07 16:04:48 UTC

Metabolite ID

MMDBc0003918

Metabolite Identification

Common Name

Neofipiperzine C

Description

Neofipiperzine C is a diketopiperazine alkaloid, a chemical class known for its diverse biological activities. This compound has been identified as a metabolite derived from marine-derived fungi, specifically from the strain Penicillium brasilianum. In a study focused on isolating bioactive diketopiperazine alkaloids, researchers discovered neofipiperzine C alongside two novel related compounds, penipiperazine A and its new metabolite. The presence of neofipiperzine C in this context highlights its significance in the realm of natural products and potential pharmacological applications. Diketopiperazines, including neofipiperzine C, are of interest due to their ability to interact with various biological targets, which may lead to the development of new therapeutic agents. As research continues, understanding the specific mechanisms of action and biological effects of neofipiperzine C could provide insights into its utility in drug discovery and development. The exploration of such metabolites from marine fungi emphasizes the rich biodiversity of these organisms and their potential contributions to medicinal chemistry (PMID:38315417 ).

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152100092D          

 39 43  0  0  1  0            999 V2000
    3.8314   -0.9646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2408   -0.7293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9549    0.8586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0866   -0.3006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4749    1.9560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3352    2.8644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9545    2.1325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8893    3.4561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0651    3.4924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3323    0.3736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7567    3.4526    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5597    0.6628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8265    2.0285    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7957    0.7270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4682   -0.4401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2700    2.7242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6216    2.7967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1407    2.2684    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0023    2.0648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9179    1.5429    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8078    2.6608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6856    1.8450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1624    3.1746    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5047    1.7546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7492    3.3864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4411    0.2132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3947    2.8726    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4238    1.4766    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0185    3.0843    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2724    2.0567    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2846    3.9905    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3825    0.9387    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8714    4.2023    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9273   -0.4323    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5169    3.6885    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0942    2.6879    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3476    1.4697    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5634    1.0291    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9301    3.4767    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  7  6  1  0  0  0  0
  9  8  2  0  0  0  0
 11  6  1  0  0  0  0
 12 10  1  0  0  0  0
 15  1  1  0  0  0  0
 15  2  1  0  0  0  0
 15 10  2  0  0  0  0
 16  8  1  0  0  0  0
 16 13  2  0  0  0  0
 17  9  1  0  0  0  0
 18  7  1  0  0  0  0
 19 13  1  0  0  0  0
 19 17  2  0  0  0  0
 20 14  1  6  0  0  0
 21 17  1  0  0  0  0
 22 20  1  0  0  0  0
 22 21  2  0  0  0  0
 23 21  1  0  0  0  0
 24 18  1  0  0  0  0
 26  3  1  0  0  0  0
 26  4  1  0  0  0  0
 26 14  1  0  0  0  0
 27 23  1  0  0  0  0
 27 25  1  0  0  0  0
 28 12  1  0  0  0  0
 28 19  1  0  0  0  0
 28 22  1  0  0  0  0
 29 11  1  0  0  0  0
 29 18  1  0  0  0  0
 29 25  1  0  0  0  0
 30 20  1  0  0  0  0
 30 24  1  0  0  0  0
 30 27  1  0  0  0  0
 23 31  1  1  0  0  0
 32 24  2  0  0  0  0
 33 25  2  0  0  0  0
 34 26  1  0  0  0  0
 27 35  1  1  0  0  0
 36  5  1  0  0  0  0
 36 16  1  0  0  0  0
 18 37  1  1  0  0  0
 20 38  1  1  0  0  0
 23 39  1  6  0  0  0
M  END


  Mrv1652305152100092D          

 39 43  0  0  1  0            999 V2000
    3.8314   -0.9646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2408   -0.7293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9549    0.8586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0866   -0.3006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4749    1.9560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3352    2.8644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9545    2.1325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8893    3.4561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0651    3.4924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3323    0.3736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7567    3.4526    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5597    0.6628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8265    2.0285    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7957    0.7270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4682   -0.4401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2700    2.7242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6216    2.7967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1407    2.2684    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0023    2.0648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9179    1.5429    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8078    2.6608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6856    1.8450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1624    3.1746    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5047    1.7546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7492    3.3864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4411    0.2132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3947    2.8726    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4238    1.4766    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0185    3.0843    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2724    2.0567    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2846    3.9905    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3825    0.9387    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8714    4.2023    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9273   -0.4323    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5169    3.6885    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0942    2.6879    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3476    1.4697    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5634    1.0291    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9301    3.4767    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  7  6  1  0  0  0  0
  9  8  2  0  0  0  0
 11  6  1  0  0  0  0
 12 10  1  0  0  0  0
 15  1  1  0  0  0  0
 15  2  1  0  0  0  0
 15 10  2  0  0  0  0
 16  8  1  0  0  0  0
 16 13  2  0  0  0  0
 17  9  1  0  0  0  0
 18  7  1  0  0  0  0
 19 13  1  0  0  0  0
 19 17  2  0  0  0  0
 20 14  1  6  0  0  0
 21 17  1  0  0  0  0
 22 20  1  0  0  0  0
 22 21  2  0  0  0  0
 23 21  1  0  0  0  0
 24 18  1  0  0  0  0
 26  3  1  0  0  0  0
 26  4  1  0  0  0  0
 26 14  1  0  0  0  0
 27 23  1  0  0  0  0
 27 25  1  0  0  0  0
 28 12  1  0  0  0  0
 28 19  1  0  0  0  0
 28 22  1  0  0  0  0
 29 11  1  0  0  0  0
 29 18  1  0  0  0  0
 29 25  1  0  0  0  0
 30 20  1  0  0  0  0
 30 24  1  0  0  0  0
 30 27  1  0  0  0  0
 23 31  1  1  0  0  0
 32 24  2  0  0  0  0
 33 25  2  0  0  0  0
 34 26  1  0  0  0  0
 27 35  1  1  0  0  0
 36  5  1  0  0  0  0
 36 16  1  0  0  0  0
 18 37  1  1  0  0  0
 20 38  1  1  0  0  0
 23 39  1  6  0  0  0
M  END
> <DATABASE_ID>
MMDBc0003918

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@@]12CCCN1C(=O)[C@@]1(O)N(C2=O)[C@@]([H])(CC(C)(C)O)C2=C(C3=C(C=C(OC)C=C3)N2CC=C(C)C)[C@]1([H])O

> <INCHI_IDENTIFIER>
InChI=1S/C27H35N3O6/c1-15(2)10-12-28-19-13-16(36-5)8-9-17(19)21-22(28)20(14-26(3,4)34)30-24(32)18-7-6-11-29(18)25(33)27(30,35)23(21)31/h8-10,13,18,20,23,31,34-35H,6-7,11-12,14H2,1-5H3/t18-,20-,23-,27+/m0/s1

> <INCHI_KEY>
PHYQSJPYTFUFQL-LRAXRWESSA-N

> <FORMULA>
C27H35N3O6

> <MOLECULAR_WEIGHT>
497.592

> <EXACT_MASS>
497.252585859

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
71

> <JCHEM_AVERAGE_POLARIZABILITY>
54.29463167362526

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2S,12S,15S)-1,2-dihydroxy-12-(2-hydroxy-2-methylpropyl)-7-methoxy-10-(3-methylbut-2-en-1-yl)-10,13,19-triazapentacyclo[11.7.0.0^{3,11}.0^{4,9}.0^{15,19}]icosa-3(11),4(9),5,7-tetraene-14,20-dione

> <ALOGPS_LOGP>
1.66

> <JCHEM_LOGP>
1.4471568430000006

> <ALOGPS_LOGS>
-2.75

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.533898788328564

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.136844465422453

> <JCHEM_PKA_STRONGEST_BASIC>
-2.654172878413437

> <JCHEM_POLAR_SURFACE_AREA>
115.47000000000001

> <JCHEM_REFRACTIVITY>
134.43110000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.91e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,12S,15S)-1,2-dihydroxy-12-(2-hydroxy-2-methylpropyl)-7-methoxy-10-(3-methylbut-2-en-1-yl)-10,13,19-triazapentacyclo[11.7.0.0^{3,11}.0^{4,9}.0^{15,19}]icosa-3(11),4(9),5,7-tetraene-14,20-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 15-MAY-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   15-MAY-21         0                                  
HETATM    1  C   UNK     0       7.152  -1.801   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.783  -1.361   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.516   1.603   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.762  -0.561   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      12.086   3.651   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.492   5.347   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.782   3.981   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.127   6.451   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.588   6.519   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.087   0.697   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.413   6.445   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.645   1.237   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.009   3.787   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.352   1.357   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.341  -0.821   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.837   5.085   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.760   5.221   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.263   4.234   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.471   3.854   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.580   2.880   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.241   4.967   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.013   3.444   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.036   5.926   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.942   3.275   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.398   6.321   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.557   0.398   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.603   5.362   0.000  0.00  0.00           C+0
HETATM   28  N   UNK     0       6.391   2.756   0.000  0.00  0.00           N+0
HETATM   29  N   UNK     0      -0.035   5.757   0.000  0.00  0.00           N+0
HETATM   30  N   UNK     0       2.375   3.839   0.000  0.00  0.00           N+0
HETATM   31  O   UNK     0       4.265   7.449   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       0.714   1.752   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0       1.627   7.844   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0       3.598  -0.807   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0       2.832   6.885   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0      11.376   5.017   0.000  0.00  0.00           O+0
HETATM   37  H   UNK     0      -0.649   2.743   0.000  0.00  0.00           H+0
HETATM   38  H   UNK     0       4.785   1.921   0.000  0.00  0.00           H+0
HETATM   39  H   UNK     0       5.469   6.490   0.000  0.00  0.00           H+0
CONECT    1   15                                                            
CONECT    2   15                                                            
CONECT    3   26                                                            
CONECT    4   26                                                            
CONECT    5   36                                                            
CONECT    6    7   11                                                       
CONECT    7    6   18                                                       
CONECT    8    9   16                                                       
CONECT    9    8   17                                                       
CONECT   10   12   15                                                       
CONECT   11    6   29                                                       
CONECT   12   10   28                                                       
CONECT   13   16   19                                                       
CONECT   14   20   26                                                       
CONECT   15    1    2   10                                                  
CONECT   16    8   13   36                                                  
CONECT   17    9   19   21                                                  
CONECT   18    7   24   29   37                                             
CONECT   19   13   17   28                                                  
CONECT   20   14   22   30   38                                             
CONECT   21   17   22   23                                                  
CONECT   22   20   21   28                                                  
CONECT   23   21   27   31   39                                             
CONECT   24   18   30   32                                                  
CONECT   25   27   29   33                                                  
CONECT   26    3    4   14   34                                             
CONECT   27   23   25   30   35                                             
CONECT   28   12   19   22                                                  
CONECT   29   11   18   25                                                  
CONECT   30   20   24   27                                                  
CONECT   31   23                                                            
CONECT   32   24                                                            
CONECT   33   25                                                            
CONECT   34   26                                                            
CONECT   35   27                                                            
CONECT   36    5   16                                                       
CONECT   37   18                                                            
CONECT   38   20                                                            
CONECT   39   23                                                            
MASTER        0    0    0    0    0    0    0    0   39    0   86    0
END

Synonyms

Not Available

Molecular Formula

C₂₇H₃₅N₃O₆

Average Mass

497.592

Monoisotopic Mass

497.252585859

IUPAC Name

(1R,2S,12S,15S)-1,2-dihydroxy-12-(2-hydroxy-2-methylpropyl)-7-methoxy-10-(3-methylbut-2-en-1-yl)-10,13,19-triazapentacyclo[11.7.0.0^{3,11}.0^{4,9}.0^{15,19}]icosa-3(11),4(9),5,7-tetraene-14,20-dione

Traditional Name

(1R,2S,12S,15S)-1,2-dihydroxy-12-(2-hydroxy-2-methylpropyl)-7-methoxy-10-(3-methylbut-2-en-1-yl)-10,13,19-triazapentacyclo[11.7.0.0^{3,11}.0^{4,9}.0^{15,19}]icosa-3(11),4(9),5,7-tetraene-14,20-dione

CAS Registry Number

Not Available

SMILES

[H][C@@]12CCCN1C(=O)[C@@]1(O)N(C2=O)[C@@]([H])(CC(C)(C)O)C2=C(C3=C(C=C(OC)C=C3)N2CC=C(C)C)[C@]1([H])O

InChI Identifier

InChI=1S/C27H35N3O6/c1-15(2)10-12-28-19-13-16(36-5)8-9-17(19)21-22(28)20(14-26(3,4)34)30-24(32)18-7-6-11-29(18)25(33)27(30,35)23(21)31/h8-10,13,18,20,23,31,34-35H,6-7,11-12,14H2,1-5H3/t18-,20-,23-,27+/m0/s1

InChI Key

PHYQSJPYTFUFQL-LRAXRWESSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as beta carbolines. Beta carbolines are compounds containing a 9H-pyrido[3,4-b]indole moiety.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Pyridoindoles

Direct Parent

Beta carbolines

Alternative Parents

Substituents

Beta-carboline
N-alkylindole
3-alkylindole
Alpha-amino acid or derivatives
Indole
2,5-dioxopiperazine
Dioxopiperazine
Anisole
N-alkylpiperazine
Alkyl aryl ether
Benzenoid
Substituted pyrrole
Piperazine
1,4-diazinane
Heteroaromatic compound
Tertiary carboxylic acid amide
Tertiary alcohol
Pyrrolidine
Pyrrole
Secondary alcohol
Lactam
Carboxamide group
Azacycle
Ether
Carboxylic acid derivative
Alkanolamine
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.89 g/L	ALOGPS
logP	1.66	ALOGPS
logP	1.45	ChemAxon
logS	-2.8	ALOGPS
pKa (Strongest Acidic)	10.14	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	115.47 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	134.43 m³·mol⁻¹	ChemAxon
Polarizability	54.29 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Not Available

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Protein ID	Protein Name	Protein Type	Uniprot ID	Species

Human Pathways

Pathways

Name	SMPDB/PathBank

Microbial Pathways

Pathways

This table shows at most 5 pathways. For the full list of associated pathways:

See All Associated Bacterial Pathways

Name	SMPDB/PathBank	Species

Metabolic Reactions

Reactions

This table shows at most 20 reactions. For the full list of associated reactions:

See All Associated Reactions

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Evidence Type	Host and Biospecimen	Data Source	Reference

Microbial Sources

Superkingdom/Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
Eukaryota/Fungi	Ascomycota	1	Human feces	Metabolic reconstruction

Exposure Sources

Other Exposures

Source Type	Data Source	Reference

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Units	Age	Sex	Health Condition	Data Source	Reference

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

78440819

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139583978

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

CMMC Knowledgebase

Not Available

References

Synthesis Reference

Not Available

General References

van Santen JA, Poynton EF, Iskakova D, McMann E, Alsup TA, Clark TN, Fergusson CH, Fewer DP, Hughes AH, McCadden CA, Parra J, Soldatou S, Rudolf JD, Janssen EM, Duncan KR, Linington RG: The Natural Products Atlas 2.0: a database of microbially-derived natural products. Nucleic Acids Res. 2022 Jan 7;50(D1):D1317-D1323. doi: 10.1093/nar/gkab941. [PubMed:34718710 ]

Showing metabocard for Neofipiperzine C (MMDBc0003918)

MOL for #<Metabolite:0x00007fb4d6801cd0>

3D MOL for #<Metabolite:0x00007fb4d6801cd0>

3D SDF for #<Metabolite:0x00007fb4d6801cd0>

3D-SDF for #<Metabolite:0x00007fb4d6801cd0>

PDB for #<Metabolite:0x00007fb4d6801cd0>

3D PDB for #<Metabolite:0x00007fb4d6801cd0>

SMILES for #<Metabolite:0x00007fb4d6801cd0>

INCHI for #<Metabolite:0x00007fb4d6801cd0>

Structure for #<Metabolite:0x00007fb4d6801cd0>

3D Structure for #<Metabolite:0x00007fb4d6801cd0>