MiMeDB: Showing metabocard for Paspaline (MMDBc0008860)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-15 01:33:58 UTC

Update Date

2024-10-17 17:05:16 UTC

Metabolite ID

MMDBc0008860

Metabolite Identification

Common Name

Paspaline

Description

2-[(1S,2S,5S,7S,10S,11R,14S)-1,2,10-trimethyl-6-oxa-23-azahexacyclo[12.10.0.0²,¹¹.0⁵,¹⁰.0¹⁶,²⁴.0¹⁷,²²]tetracosa-16(24),17,19,21-tetraen-7-yl]propan-2-ol belongs to the class of organic compounds known as naphthopyrans. Naphthopyrans are compounds containing a pyran ring fused to a naphthalene moiety. Furan is a 6 membered-ring non-aromatic ring with five carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings. 2-[(1S,2S,5S,7S,10S,11R,14S)-1,2,10-trimethyl-6-oxa-23-azahexacyclo[12.10.0.0²,¹¹.0⁵,¹⁰.0¹⁶,²⁴.0¹⁷,²²]tetracosa-16(24),17,19,21-tetraen-7-yl]propan-2-ol is an extremely weak basic (essentially neutral) compound (based on its pKa). 2-[(1S,2S,5S,7S,10S,11R,14S)-1,2,10-trimethyl-6-oxa-23-azahexacyclo[12.10.0.0²,¹¹.0⁵,¹⁰.0¹⁶,²⁴.0¹⁷,²²]tetracosa-16(24),17,19,21-tetraen-7-yl]propan-2-ol is a potentially toxic compound.

Structure

MOL SDF PDB SMILES InChI


  Mrv0541 08291401162D          

 35 40  0  0  1  0            999 V2000
   10.8055   -3.0133    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2195   -1.9225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1267   -4.0969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1189   -2.6496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7779   -2.6867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5545   -3.2761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6377   -2.4553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2238   -3.7585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3901   -2.1169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6219   -4.7736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3743   -4.4352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6315   -3.4201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6238   -1.9728    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8791   -3.7585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8714   -2.3112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1463   -4.4657    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9526   -4.2912    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9762   -3.4201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7311   -3.7528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0594   -2.5993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4574   -3.6144    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.7147   -2.5993    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.2930   -2.4553    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2809   -3.1377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4671   -2.2609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2099   -3.2761    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.7882   -3.1320    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.0358   -3.4704    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8657   -2.4247    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   10.1287   -1.5085    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.0454   -2.1169    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7050   -3.9528    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5406   -2.7936    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7978   -1.7785    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9623   -2.9377    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  7  6  2  0  0  0  0
  8  6  1  0  0  0  0
  9  7  1  0  0  0  0
 11 10  1  0  0  0  0
 14 12  1  0  0  0  0
 15 13  1  0  0  0  0
 17 10  1  0  0  0  0
 17 16  1  0  0  0  0
 18  8  2  0  0  0  0
 19 16  1  0  0  0  0
 19 18  1  0  0  0  0
 20  9  2  0  0  0  0
 20 18  1  0  0  0  0
 21 11  1  0  0  0  0
 22 12  1  0  0  0  0
 23 13  1  0  0  0  0
 24 19  2  0  0  0  0
 25  1  1  0  0  0  0
 25  2  1  0  0  0  0
 22 25  1  6  0  0  0
 26  3  1  6  0  0  0
 26 14  1  0  0  0  0
 26 21  1  0  0  0  0
 26 23  1  0  0  0  0
 27  4  1  6  0  0  0
 27 15  1  0  0  0  0
 27 21  1  0  0  0  0
 28  5  1  1  0  0  0
 28 17  1  0  0  0  0
 28 24  1  0  0  0  0
 28 27  1  0  0  0  0
 29 20  1  0  0  0  0
 29 24  1  0  0  0  0
 30 25  1  0  0  0  0
 31 22  1  0  0  0  0
 31 23  1  0  0  0  0
 17 32  1  6  0  0  0
 21 33  1  1  0  0  0
 22 34  1  1  0  0  0
 23 35  1  1  0  0  0
M  END


  Mrv0541 08291401162D          

 35 40  0  0  1  0            999 V2000
   10.8055   -3.0133    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2195   -1.9225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1267   -4.0969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1189   -2.6496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7779   -2.6867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5545   -3.2761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6377   -2.4553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2238   -3.7585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3901   -2.1169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6219   -4.7736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3743   -4.4352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6315   -3.4201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6238   -1.9728    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8791   -3.7585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8714   -2.3112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1463   -4.4657    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9526   -4.2912    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9762   -3.4201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7311   -3.7528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0594   -2.5993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4574   -3.6144    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.7147   -2.5993    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.2930   -2.4553    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2809   -3.1377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4671   -2.2609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2099   -3.2761    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.7882   -3.1320    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.0358   -3.4704    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8657   -2.4247    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   10.1287   -1.5085    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.0454   -2.1169    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7050   -3.9528    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5406   -2.7936    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7978   -1.7785    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9623   -2.9377    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  7  6  2  0  0  0  0
  8  6  1  0  0  0  0
  9  7  1  0  0  0  0
 11 10  1  0  0  0  0
 14 12  1  0  0  0  0
 15 13  1  0  0  0  0
 17 10  1  0  0  0  0
 17 16  1  0  0  0  0
 18  8  2  0  0  0  0
 19 16  1  0  0  0  0
 19 18  1  0  0  0  0
 20  9  2  0  0  0  0
 20 18  1  0  0  0  0
 21 11  1  0  0  0  0
 22 12  1  0  0  0  0
 23 13  1  0  0  0  0
 24 19  2  0  0  0  0
 25  1  1  0  0  0  0
 25  2  1  0  0  0  0
 22 25  1  6  0  0  0
 26  3  1  6  0  0  0
 26 14  1  0  0  0  0
 26 21  1  0  0  0  0
 26 23  1  0  0  0  0
 27  4  1  6  0  0  0
 27 15  1  0  0  0  0
 27 21  1  0  0  0  0
 28  5  1  1  0  0  0
 28 17  1  0  0  0  0
 28 24  1  0  0  0  0
 28 27  1  0  0  0  0
 29 20  1  0  0  0  0
 29 24  1  0  0  0  0
 30 25  1  0  0  0  0
 31 22  1  0  0  0  0
 31 23  1  0  0  0  0
 17 32  1  6  0  0  0
 21 33  1  1  0  0  0
 22 34  1  1  0  0  0
 23 35  1  1  0  0  0
M  END
> <DATABASE_ID>
MMDBc0008860

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@]12CC3=C(NC4=CC=CC=C34)[C@]1(C)[C@@]1(C)CC[C@]3([H])O[C@@]([H])(CC[C@@]3(C)[C@]1([H])CC2)C(C)(C)O

> <INCHI_IDENTIFIER>
InChI=1S/C28H39NO2/c1-25(2,30)22-12-14-26(3)21-11-10-17-16-19-18-8-6-7-9-20(18)29-24(19)28(17,5)27(21,4)15-13-23(26)31-22/h6-9,17,21-23,29-30H,10-16H2,1-5H3/t17-,21-,22-,23-,26-,27-,28+/m0/s1

> <INCHI_KEY>
WLAIEIMDXUAGPY-HSECPPETSA-N

> <FORMULA>
C28H39NO2

> <MOLECULAR_WEIGHT>
421.6148

> <EXACT_MASS>
421.298079497

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
70

> <JCHEM_AVERAGE_POLARIZABILITY>
51.52545461834933

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-[(1S,2S,5S,7S,10S,11R,14S)-1,2,10-trimethyl-6-oxa-23-azahexacyclo[12.10.0.0²,¹¹.0⁵,¹⁰.0¹⁶,²⁴.0¹⁷,²²]tetracosa-16(24),17,19,21-tetraen-7-yl]propan-2-ol

> <ALOGPS_LOGP>
6.30

> <JCHEM_LOGP>
5.6359221396666666

> <ALOGPS_LOGS>
-7.32

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
16.860463551856473

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.324846174098045

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0935564409641225

> <JCHEM_POLAR_SURFACE_AREA>
45.25

> <JCHEM_REFRACTIVITY>
125.02669999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.02e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-[(1S,2S,5S,7S,10S,11R,14S)-1,2,10-trimethyl-6-oxa-23-azahexacyclo[12.10.0.0²,¹¹.0⁵,¹⁰.0¹⁶,²⁴.0¹⁷,²²]tetracosa-16(24),17,19,21-tetraen-7-yl]propan-2-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-AUG-14   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-AUG-14         0                                  
HETATM    1  C   UNK     0      20.170  -5.625   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      20.943  -3.589   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      15.170  -7.647   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.422  -4.946   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.785  -5.015   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.768  -6.115   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.924  -4.583   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.018  -7.016   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.328  -3.952   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      12.361  -8.911   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      13.765  -8.279   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      17.979  -6.384   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      14.231  -3.683   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      16.574  -7.016   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      12.827  -4.314   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.606  -8.336   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      11.112  -8.010   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.422  -6.384   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.831  -7.005   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.577  -4.852   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      13.921  -6.747   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      18.134  -4.852   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      15.480  -4.583   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.858  -5.857   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      19.539  -4.220   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      15.325  -6.115   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      12.671  -5.846   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      11.267  -6.478   0.000  0.00  0.00           C+0
HETATM   29  N   UNK     0       9.083  -4.526   0.000  0.00  0.00           N+0
HETATM   30  O   UNK     0      18.907  -2.816   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0      16.885  -3.952   0.000  0.00  0.00           O+0
HETATM   32  H   UNK     0      12.516  -7.379   0.000  0.00  0.00           H+0
HETATM   33  H   UNK     0      14.076  -5.215   0.000  0.00  0.00           H+0
HETATM   34  H   UNK     0      18.289  -3.320   0.000  0.00  0.00           H+0
HETATM   35  H   UNK     0      16.730  -5.484   0.000  0.00  0.00           H+0
CONECT    1   25                                                            
CONECT    2   25                                                            
CONECT    3   26                                                            
CONECT    4   27                                                            
CONECT    5   28                                                            
CONECT    6    7    8                                                       
CONECT    7    6    9                                                       
CONECT    8    6   18                                                       
CONECT    9    7   20                                                       
CONECT   10   11   17                                                       
CONECT   11   10   21                                                       
CONECT   12   14   22                                                       
CONECT   13   15   23                                                       
CONECT   14   12   26                                                       
CONECT   15   13   27                                                       
CONECT   16   17   19                                                       
CONECT   17   10   16   28   32                                             
CONECT   18    8   19   20                                                  
CONECT   19   16   18   24                                                  
CONECT   20    9   18   29                                                  
CONECT   21   11   26   27   33                                             
CONECT   22   12   25   31   34                                             
CONECT   23   13   26   31   35                                             
CONECT   24   19   28   29                                                  
CONECT   25    1    2   22   30                                             
CONECT   26    3   14   21   23                                             
CONECT   27    4   15   21   28                                             
CONECT   28    5   17   24   27                                             
CONECT   29   20   24                                                       
CONECT   30   25                                                            
CONECT   31   22   23                                                       
CONECT   32   17                                                            
CONECT   33   21                                                            
CONECT   34   22                                                            
CONECT   35   23                                                            
MASTER        0    0    0    0    0    0    0    0   35    0   80    0
END

Synonyms

Not Available

Molecular Formula

C₂₈H₃₉NO₂

Average Mass

421.6148

Monoisotopic Mass

421.298079497

IUPAC Name

2-[(1S,2S,5S,7S,10S,11R,14S)-1,2,10-trimethyl-6-oxa-23-azahexacyclo[12.10.0.0²,¹¹.0⁵,¹⁰.0¹⁶,²⁴.0¹⁷,²²]tetracosa-16(24),17,19,21-tetraen-7-yl]propan-2-ol

Traditional Name

2-[(1S,2S,5S,7S,10S,11R,14S)-1,2,10-trimethyl-6-oxa-23-azahexacyclo[12.10.0.0²,¹¹.0⁵,¹⁰.0¹⁶,²⁴.0¹⁷,²²]tetracosa-16(24),17,19,21-tetraen-7-yl]propan-2-ol

CAS Registry Number

Not Available

SMILES

[H][C@]12CC3=C(NC4=CC=CC=C34)[C@]1(C)[C@@]1(C)CC[C@]3([H])O[C@@]([H])(CC[C@@]3(C)[C@]1([H])CC2)C(C)(C)O

InChI Identifier

InChI=1S/C28H39NO2/c1-25(2,30)22-12-14-26(3)21-11-10-17-16-19-18-8-6-7-9-20(18)29-24(19)28(17,5)27(21,4)15-13-23(26)31-22/h6-9,17,21-23,29-30H,10-16H2,1-5H3/t17-,21-,22-,23-,26-,27-,28+/m0/s1

InChI Key

WLAIEIMDXUAGPY-HSECPPETSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as naphthopyrans. Naphthopyrans are compounds containing a pyran ring fused to a naphthalene moiety. Furan is a 6 membered-ring non-aromatic ring with five carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Naphthopyrans

Sub Class

Not Available

Direct Parent

Naphthopyrans

Alternative Parents

Substituents

Naphthopyran
Naphthalene
3-alkylindole
Indole
Indole or derivatives
Oxane
Pyran
Benzenoid
Heteroaromatic compound
Tertiary alcohol
Pyrrole
Ether
Dialkyl ether
Azacycle
Oxacycle
Alcohol
Organooxygen compound
Organonitrogen compound
Hydrocarbon derivative
Organopnictogen compound
Organic oxygen compound
Organic nitrogen compound
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	2.0e-05 g/L	ALOGPS
logP	6.3	ALOGPS
logP	5.64	ChemAxon
logS	-7.3	ALOGPS
pKa (Strongest Acidic)	14.32	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	45.25 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	125.03 m³·mol⁻¹	ChemAxon
Polarizability	51.53 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Spectrum Type	Description	Splash Key	Deposition Date	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	splash10-00di-0003900000-ce5ced2a3e9c7be017b8	2016-06-03	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-015i-0119100000-9b6ffa195d91e2eab6e5	2016-06-03	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-02a9-5389000000-d97c710f5a8a01a8bea5	2016-06-03	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	splash10-00di-0001900000-091f4a2324c7c12bddb1	2016-08-03	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	splash10-00di-2208900000-1c08cf6c909ff015af93	2016-08-03	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	splash10-00si-1109000000-465cb760412ff872e51b	2016-08-03	View Spectrum

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

Metabolic Reactions

Not Available

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	8	Human feces	Metabolic reconstruction

Exposure Sources

Source Type	Activity	Data Source	Reference
Not Available	Mycotoxins	U.S. Environmental Protection Agency	CompTox
Cosmetics	Not Available	U.S. Environmental Protection Agency	CompTox
Domestics	Not Available	U.S. Environmental Protection Agency	CompTox

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

Not Available

KEGG Compound ID

C20530

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

115028

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

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 Paspaline (MMDBc0008860)

MOL for #<Metabolite:0x00007fdb716cc420>

3D MOL for #<Metabolite:0x00007fdb716cc420>

3D SDF for #<Metabolite:0x00007fdb716cc420>

3D-SDF for #<Metabolite:0x00007fdb716cc420>

PDB for #<Metabolite:0x00007fdb716cc420>

3D PDB for #<Metabolite:0x00007fdb716cc420>

SMILES for #<Metabolite:0x00007fdb716cc420>

INCHI for #<Metabolite:0x00007fdb716cc420>

Structure for #<Metabolite:0x00007fdb716cc420>

3D Structure for #<Metabolite:0x00007fdb716cc420>