NP-MRD: Showing NP-Card for 3-[(2r)-4-[(2e,4e,6e,8e,10e)-dodeca-2,4,6,8,10-pentaenoyl]-3-hydroxy-1-methyl-5-oxo-2h-pyrrol-2-yl]propanoic acid (NP0301016)

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Record Information

Version

2.0

Created at

2022-09-10 13:44:11 UTC

Updated at

2022-09-10 13:44:11 UTC

NP-MRD ID

NP0301016

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-[(2r)-4-[(2e,4e,6e,8e,10e)-dodeca-2,4,6,8,10-pentaenoyl]-3-hydroxy-1-methyl-5-oxo-2h-pyrrol-2-yl]propanoic acid

Description

3-[(2r)-4-[(2e,4e,6e,8e,10e)-dodeca-2,4,6,8,10-pentaenoyl]-3-hydroxy-1-methyl-5-oxo-2h-pyrrol-2-yl]propanoic acid is found in Fuligo septica.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102215442D          

 26 26  0  0  1  0            999 V2000
   -3.7191    8.5393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0046    8.1268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0046    7.3018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2901    6.8893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2901    6.0643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5757    5.6518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5757    4.8268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8612    4.4143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8612    3.5893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1467    3.1768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1467    2.3518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5678    1.9393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2822    2.3518    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5678    1.1143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2352    0.6294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0198    0.8843    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9803   -0.1553    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4652   -0.8227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2857   -0.7365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7706   -1.4039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5911   -1.3177    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4350   -2.1576    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1553   -0.1553    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3297   -0.8227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0997    0.6294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8843    0.8843    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  1  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 17 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 14 25  1  0  0  0  0
 25 26  2  0  0  0  0
M  END

     RDKit          3D

 49 49  0  0  0  0  0  0  0  0999 V2000
   11.2535    1.0860    0.1638 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0517    0.3667   -0.3695 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8317    0.6778    0.0214 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6695   -0.0260   -0.5016 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4739    0.3047   -0.0971 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2991   -0.3804   -0.6022 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0745   -0.0767   -0.2198 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8935   -0.7911   -0.7509 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6789   -0.4609   -0.3477 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4782   -1.1200   -0.8277 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7068   -0.7081   -0.3551 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9024   -1.3362   -0.8084 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8338   -2.2840   -1.6573 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2334   -0.9141   -0.3164 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5302    0.0235    0.5452 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6524    0.8580    1.2332 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0491    0.1285    0.7158 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.4632    1.4882    0.3078 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9190    1.7639    0.3473 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7244    1.0795   -0.6730 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1306    0.6078   -1.6992 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0887    0.9314   -0.5599 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5592   -1.0337    0.1488 N   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8527   -1.7231    0.2740 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4934   -1.6258   -0.6238 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5743   -2.5839   -1.4328 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.8819    2.0773    0.5554 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.9608    1.2214   -0.6785 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.6559    0.4712    0.9811 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1981   -0.4219   -1.0900 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6922    1.4666    0.7399 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7657   -0.8312   -1.2299 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3439    1.0955    0.6214 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4294   -1.1697   -1.3190 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9301    0.7107    0.4973 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0224   -1.5815   -1.4669 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6265    0.3425    0.3732 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4637   -1.9231   -1.5417 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7088    0.1066    0.3706 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6462    0.9062    2.2547 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1309    0.0549    1.8618 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9744    2.2809    0.9691 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1298    1.6961   -0.7534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1499    2.8683    0.3112 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3472    1.4527    1.3447 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4704    0.8250    0.3826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6484   -2.7665    0.6850 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5102   -1.2280    0.9838 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2453   -1.9060   -0.7278 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  2  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 22  1  0
 20 21  2  0
 17 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  2  0
 25 14  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  2 30  1  0
  3 31  1  0
  4 32  1  0
  5 33  1  0
  6 34  1  0
  7 35  1  0
  8 36  1  0
  9 37  1  0
 10 38  1  0
 11 39  1  0
 16 40  1  0
 17 41  1  1
 18 42  1  0
 18 43  1  0
 19 44  1  0
 19 45  1  0
 22 46  1  0
 24 47  1  0
 24 48  1  0
 24 49  1  0
M  END


  Mrv1652309102215442D          

 26 26  0  0  1  0            999 V2000
   -3.7191    8.5393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0046    8.1268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0046    7.3018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2901    6.8893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2901    6.0643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5757    5.6518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5757    4.8268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8612    4.4143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8612    3.5893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1467    3.1768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1467    2.3518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5678    1.9393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2822    2.3518    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5678    1.1143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2352    0.6294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0198    0.8843    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9803   -0.1553    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4652   -0.8227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2857   -0.7365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7706   -1.4039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5911   -1.3177    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4350   -2.1576    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1553   -0.1553    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3297   -0.8227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0997    0.6294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8843    0.8843    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  1  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 17 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 14 25  1  0  0  0  0
 25 26  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0301016

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C=C\C=C\C=C\C=C\C=C\C(=O)C1=C(O)[C@@H](CCC(O)=O)N(C)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C20H23NO5/c1-3-4-5-6-7-8-9-10-11-12-16(22)18-19(25)15(13-14-17(23)24)21(2)20(18)26/h3-12,15,25H,13-14H2,1-2H3,(H,23,24)/b4-3+,6-5+,8-7+,10-9+,12-11+/t15-/m1/s1

> <INCHI_KEY>
MCZKTQVSHDNNLH-XJCMFISFSA-N

> <FORMULA>
C20H23NO5

> <MOLECULAR_WEIGHT>
357.406

> <EXACT_MASS>
357.157622845

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
49

> <JCHEM_AVERAGE_POLARIZABILITY>
40.14147140503002

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-[(2R)-4-[(2E,4E,6E,8E,10E)-dodeca-2,4,6,8,10-pentaenoyl]-3-hydroxy-1-methyl-5-oxo-2,5-dihydro-1H-pyrrol-2-yl]propanoic acid

> <JCHEM_LOGP>
2.3590344436666664

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
4.373653105721806

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.6321705405999984

> <JCHEM_PKA_STRONGEST_BASIC>
-0.9963062254260912

> <JCHEM_POLAR_SURFACE_AREA>
94.91

> <JCHEM_REFRACTIVITY>
106.41639999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
3-[(2R)-4-[(2E,4E,6E,8E,10E)-dodeca-2,4,6,8,10-pentaenoyl]-3-hydroxy-1-methyl-5-oxo-2H-pyrrol-2-yl]propanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0      -6.942  15.940   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.609  15.170   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -5.609  13.630   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.275  12.860   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -4.275  11.320   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.941  10.550   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.941   9.010   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.608   8.240   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.608   6.700   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.274   5.930   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.274   4.390   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.060   3.620   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       2.393   4.390   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       1.060   2.080   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.306   1.175   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       3.770   1.651   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       1.830  -0.290   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.735  -1.536   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.267  -1.375   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.172  -2.621   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       6.703  -2.460   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       4.545  -4.027   0.000  0.00  0.00           O+0
HETATM   23  N   UNK     0       0.290  -0.290   0.000  0.00  0.00           N+0
HETATM   24  C   UNK     0      -0.615  -1.536   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -0.186   1.175   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -1.651   1.651   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   25                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   23                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   17   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   14   26                                                  
CONECT   26   25                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   52    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₃NO₅

Average Mass

357.4060 Da

Monoisotopic Mass

357.15762 Da

IUPAC Name

3-[(2R)-4-[(2E,4E,6E,8E,10E)-dodeca-2,4,6,8,10-pentaenoyl]-3-hydroxy-1-methyl-5-oxo-2,5-dihydro-1H-pyrrol-2-yl]propanoic acid

Traditional Name

3-[(2R)-4-[(2E,4E,6E,8E,10E)-dodeca-2,4,6,8,10-pentaenoyl]-3-hydroxy-1-methyl-5-oxo-2H-pyrrol-2-yl]propanoic acid

CAS Registry Number

Not Available

SMILES

C\C=C\C=C\C=C\C=C\C=C\C(=O)C1=C(O)[C@@H](CCC(O)=O)N(C)C1=O

InChI Identifier

InChI=1S/C20H23NO5/c1-3-4-5-6-7-8-9-10-11-12-16(22)18-19(25)15(13-14-17(23)24)21(2)20(18)26/h3-12,15,25H,13-14H2,1-2H3,(H,23,24)/b4-3+,6-5+,8-7+,10-9+,12-11+/t15-/m1/s1

InChI Key

MCZKTQVSHDNNLH-XJCMFISFSA-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, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, 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
Fuligo septica	LOTUS Database	35616633

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	2.36	ChemAxon
pKa (Strongest Acidic)	3.63	ChemAxon
pKa (Strongest Basic)	-1	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	94.91 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	106.42 m³·mol⁻¹	ChemAxon
Polarizability	40.14 Å³	ChemAxon
Number of Rings	1	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

LOTUS database [Link]

Showing NP-Card for 3-[(2r)-4-[(2e,4e,6e,8e,10e)-dodeca-2,4,6,8,10-pentaenoyl]-3-hydroxy-1-methyl-5-oxo-2h-pyrrol-2-yl]propanoic acid (NP0301016)

MOL for NP0301016 (3-[(2r)-4-[(2e,4e,6e,8e,10e)-dodeca-2,4,6,8,10-pentaenoyl]-3-hydroxy-1-methyl-5-oxo-2h-pyrrol-2-yl]propanoic acid)

3D MOL for NP0301016 (3-[(2r)-4-[(2e,4e,6e,8e,10e)-dodeca-2,4,6,8,10-pentaenoyl]-3-hydroxy-1-methyl-5-oxo-2h-pyrrol-2-yl]propanoic acid)

3D SDF for NP0301016 (3-[(2r)-4-[(2e,4e,6e,8e,10e)-dodeca-2,4,6,8,10-pentaenoyl]-3-hydroxy-1-methyl-5-oxo-2h-pyrrol-2-yl]propanoic acid)

3D-SDF for NP0301016 (3-[(2r)-4-[(2e,4e,6e,8e,10e)-dodeca-2,4,6,8,10-pentaenoyl]-3-hydroxy-1-methyl-5-oxo-2h-pyrrol-2-yl]propanoic acid)

PDB for NP0301016 (3-[(2r)-4-[(2e,4e,6e,8e,10e)-dodeca-2,4,6,8,10-pentaenoyl]-3-hydroxy-1-methyl-5-oxo-2h-pyrrol-2-yl]propanoic acid)

3D PDB for NP0301016 (3-[(2r)-4-[(2e,4e,6e,8e,10e)-dodeca-2,4,6,8,10-pentaenoyl]-3-hydroxy-1-methyl-5-oxo-2h-pyrrol-2-yl]propanoic acid)

SMILES for NP0301016 (3-[(2r)-4-[(2e,4e,6e,8e,10e)-dodeca-2,4,6,8,10-pentaenoyl]-3-hydroxy-1-methyl-5-oxo-2h-pyrrol-2-yl]propanoic acid)

INCHI for NP0301016 (3-[(2r)-4-[(2e,4e,6e,8e,10e)-dodeca-2,4,6,8,10-pentaenoyl]-3-hydroxy-1-methyl-5-oxo-2h-pyrrol-2-yl]propanoic acid)

Structure for NP0301016 (3-[(2r)-4-[(2e,4e,6e,8e,10e)-dodeca-2,4,6,8,10-pentaenoyl]-3-hydroxy-1-methyl-5-oxo-2h-pyrrol-2-yl]propanoic acid)

3D Structure for NP0301016 (3-[(2r)-4-[(2e,4e,6e,8e,10e)-dodeca-2,4,6,8,10-pentaenoyl]-3-hydroxy-1-methyl-5-oxo-2h-pyrrol-2-yl]propanoic acid)