NP-MRD: Showing NP-Card for n-{3-methoxy-5-[2-(2-methylpropyl)-5-oxo-2h-pyrrol-1-yl]-5-oxopent-3-en-1-yl}-6,6-dimethylheptanimidic acid (NP0323244)

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Record Information

Version

2.0

Created at

2022-09-12 02:32:32 UTC

Updated at

2022-09-12 02:32:32 UTC

NP-MRD ID

NP0323244

Secondary Accession Numbers

None

Natural Product Identification

Common Name

n-{3-methoxy-5-[2-(2-methylpropyl)-5-oxo-2h-pyrrol-1-yl]-5-oxopent-3-en-1-yl}-6,6-dimethylheptanimidic acid

Description

N-{3-methoxy-5-[2-(2-methylpropyl)-5-oxo-2,5-dihydro-1H-pyrrol-1-yl]-5-oxopent-3-en-1-yl}-6,6-dimethylheptanimidic acid belongs to the class of organic compounds known as n-acyl amines. N-acyl amines are compounds containing a fatty acid moiety linked to an amine group through an ester linkage. Based on a literature review very few articles have been published on N-{3-methoxy-5-[2-(2-methylpropyl)-5-oxo-2,5-dihydro-1H-pyrrol-1-yl]-5-oxopent-3-en-1-yl}-6,6-dimethylheptanimidic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122204322D          

 29 29  0  0  0  0            999 V2000
    0.5678    4.4143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5678    3.5893    0.0000 O   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 N   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  0  0  0  0  0  0  0  0  0  0
    0.1553   -0.1553    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 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4974    0.3323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2820    0.5872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3259   -0.4747    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
   -0.8612    4.4143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5757    4.8268    0.0000 N   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
   -0.8612    6.0643    0.0000 O   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
   -2.2901    6.8893    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
   -3.0046    8.1268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7191    8.5393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4335    8.9518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3066    9.2538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1316    7.8248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  4  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
  3 17  1  0  0  0  0
 17 18  1  0  0  0  0
 19 18  1  4  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 26 29  1  0  0  0  0
M  END

     RDKit          3D

 67 67  0  0  0  0  0  0  0  0999 V2000
   -1.3436    3.8563   -1.2043 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0678    2.9027   -0.4609 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6788    1.5754   -0.4396 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4433    0.5158   -0.5123 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7885    0.1848   -0.6289 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9758   -1.1484   -0.6262 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0304    0.8293   -0.7495 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3695    2.1721   -0.9545 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6220    3.2039   -1.0078 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8270    2.2531   -1.1173 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3432    1.0650   -1.0111 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3166    0.0870   -0.7582 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.4772   -0.6522    0.5458 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7331   -1.4475    0.6585 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8486   -2.4979   -0.4555 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0096   -0.7195    0.7701 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1601    1.4630   -0.3136 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3130    0.0597   -0.2787 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7704    0.0819   -0.1472 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2889   -0.2274    0.9797 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4569   -0.5717    2.0328 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7870   -0.2174    1.1597 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4110    0.2050   -0.1401 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9156    0.2502   -0.0717 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5061   -1.0961    0.2687 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0032   -1.0663    0.3420 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5116   -0.1043    1.3921 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4950   -2.4626    0.6564 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6139   -0.6428   -0.9767 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8506    4.8448   -1.0732 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3454    3.5336   -2.2648 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2876    3.9098   -0.8425 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7420   -0.4256   -0.4574 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3828    3.1708   -1.2987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4373    0.8378   -1.1207 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2008   -0.6355   -1.6009 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5197    0.1269    1.3665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6439   -1.2965    0.8189 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6605   -2.1088    1.6018 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2159   -1.9625   -1.3510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6432   -3.2093   -0.1568 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8624   -2.9754   -0.5950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9471    0.3410    1.1037 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6284   -1.1966    1.6025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6914   -0.8504   -0.1221 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2534    2.0105   -1.2137 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1425    2.0655    0.5603 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0402   -0.4925   -1.2262 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0831   -0.4771    0.5881 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3785   -1.5176    2.3826 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0698   -1.2259    1.4895 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0645    0.4903    1.9665 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0156    1.2129   -0.3798 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0810   -0.4942   -0.9466 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2659    1.0574    0.5674 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2664    0.4939   -1.1121 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2325   -1.7852   -0.5600 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0759   -1.4713    1.2182 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5849    0.9116    0.9738 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5662   -0.4277    1.6165 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9567   -0.1711    2.3365 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6418   -3.1811    0.7514 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0226   -2.5000    1.6313 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1227   -2.8662   -0.1665 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2197   -1.2677   -1.7991 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3974    0.4380   -1.1189 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7063   -0.7576   -0.9208 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 26 28  1  0
 26 29  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  5  7  1  0
  7 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
 12 11  1  0
 11 10  2  0
 10  8  1  0
  8  9  2  0
  8  7  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
 17 46  1  0
 17 47  1  0
 18 48  1  0
 18 49  1  0
 21 50  1  0
 22 51  1  0
 22 52  1  0
 23 53  1  0
 23 54  1  0
 24 55  1  0
 24 56  1  0
 25 57  1  0
 25 58  1  0
 27 59  1  0
 27 60  1  0
 27 61  1  0
 28 62  1  0
 28 63  1  0
 28 64  1  0
 29 65  1  0
 29 66  1  0
 29 67  1  0
  4 33  1  0
 12 36  1  6
 13 37  1  0
 13 38  1  0
 14 39  1  0
 15 40  1  0
 15 41  1  0
 15 42  1  0
 16 43  1  0
 16 44  1  0
 16 45  1  0
 11 35  1  0
 10 34  1  0
M  END


  Mrv1652309122204322D          

 29 29  0  0  0  0            999 V2000
    0.5678    4.4143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5678    3.5893    0.0000 O   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 N   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  0  0  0  0  0  0  0  0  0  0
    0.1553   -0.1553    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 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4974    0.3323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2820    0.5872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3259   -0.4747    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
   -0.8612    4.4143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5757    4.8268    0.0000 N   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
   -0.8612    6.0643    0.0000 O   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
   -2.2901    6.8893    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
   -3.0046    8.1268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7191    8.5393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4335    8.9518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3066    9.2538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1316    7.8248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  4  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
  7 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
  3 17  1  0  0  0  0
 17 18  1  0  0  0  0
 19 18  1  4  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 26 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0323244

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(CCN=C(O)CCCCC(C)(C)C)=CC(=O)N1C(CC(C)C)C=CC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C23H38N2O4/c1-17(2)15-18-10-11-21(27)25(18)22(28)16-19(29-6)12-14-24-20(26)9-7-8-13-23(3,4)5/h10-11,16-18H,7-9,12-15H2,1-6H3,(H,24,26)

> <INCHI_KEY>
VKIGEMQNRQJTHS-UHFFFAOYSA-N

> <FORMULA>
C23H38N2O4

> <MOLECULAR_WEIGHT>
406.567

> <EXACT_MASS>
406.283157712

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
67

> <JCHEM_AVERAGE_POLARIZABILITY>
47.983894790701484

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
N-{3-methoxy-5-[2-(2-methylpropyl)-5-oxo-2,5-dihydro-1H-pyrrol-1-yl]-5-oxopent-3-en-1-yl}-6,6-dimethylheptanimidic acid

> <JCHEM_LOGP>
4.194957868999999

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.813688132870917

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.441381567005436

> <JCHEM_PKA_STRONGEST_BASIC>
4.334798907089903

> <JCHEM_POLAR_SURFACE_AREA>
79.2

> <JCHEM_REFRACTIVITY>
118.13789999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
N-{3-methoxy-5-[2-(2-methylpropyl)-5-oxo-2H-pyrrol-1-yl]-5-oxopent-3-en-1-yl}-6,6-dimethylheptanimidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0       1.060   8.240   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       1.060   6.700   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -0.274   5.930   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.274   4.390   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.060   3.620   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       2.393   4.390   0.000  0.00  0.00           O+0
HETATM    7  N   UNK     0       1.060   2.080   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0       2.306   1.175   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       3.770   1.651   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       1.830  -0.290   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.290  -0.290   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.186   1.175   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.651   1.651   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.795   0.620   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -4.260   1.096   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.475  -0.886   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.608   6.700   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.608   8.240   0.000  0.00  0.00           C+0
HETATM   19  N   UNK     0      -2.941   9.010   0.000  0.00  0.00           N+0
HETATM   20  C   UNK     0      -2.941  10.550   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -1.608  11.320   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -4.275  11.320   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -4.275  12.860   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -5.609  13.630   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -5.609  15.170   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -6.942  15.940   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -8.276  16.710   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -6.172  17.274   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -7.712  14.606   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   17                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   12                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11    7   13                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17    3   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   28   29                                             
CONECT   27   26                                                            
CONECT   28   26                                                            
CONECT   29   26                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   58    0
END

View in JSmol

Synonyms

Value	Source
N-{3-methoxy-5-[2-(2-methylpropyl)-5-oxo-2,5-dihydro-1H-pyrrol-1-yl]-5-oxopent-3-en-1-yl}-6,6-dimethylheptanimidate	Generator

Chemical Formula

C₂₃H₃₈N₂O₄

Average Mass

406.5670 Da

Monoisotopic Mass

406.28316 Da

IUPAC Name

N-{3-methoxy-5-[2-(2-methylpropyl)-5-oxo-2,5-dihydro-1H-pyrrol-1-yl]-5-oxopent-3-en-1-yl}-6,6-dimethylheptanimidic acid

Traditional Name

N-{3-methoxy-5-[2-(2-methylpropyl)-5-oxo-2H-pyrrol-1-yl]-5-oxopent-3-en-1-yl}-6,6-dimethylheptanimidic acid

CAS Registry Number

Not Available

SMILES

COC(CCN=C(O)CCCCC(C)(C)C)=CC(=O)N1C(CC(C)C)C=CC1=O

InChI Identifier

InChI=1S/C23H38N2O4/c1-17(2)15-18-10-11-21(27)25(18)22(28)16-19(29-6)12-14-24-20(26)9-7-8-13-23(3,4)5/h10-11,16-18H,7-9,12-15H2,1-6H3,(H,24,26)

InChI Key

VKIGEMQNRQJTHS-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, 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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as n-acyl amines. N-acyl amines are compounds containing a fatty acid moiety linked to an amine group through an ester linkage.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty amides

Direct Parent

N-acyl amines

Alternative Parents

Substituents

Carboxylic acid imide, n-substituted
N-acyl-amine
Vinylogous ester
Pyrroline
Dicarboximide
Carboxylic acid imide
Secondary carboxylic acid amide
Carboxamide group
Azacycle
Organoheterocyclic compound
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

Not Available

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	4.19	ChemAxon
pKa (Strongest Acidic)	6.44	ChemAxon
pKa (Strongest Basic)	4.33	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	79.2 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	118.14 m³·mol⁻¹	ChemAxon
Polarizability	47.98 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

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

162815700

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for n-{3-methoxy-5-[2-(2-methylpropyl)-5-oxo-2h-pyrrol-1-yl]-5-oxopent-3-en-1-yl}-6,6-dimethylheptanimidic acid (NP0323244)

MOL for NP0323244 (n-{3-methoxy-5-[2-(2-methylpropyl)-5-oxo-2h-pyrrol-1-yl]-5-oxopent-3-en-1-yl}-6,6-dimethylheptanimidic acid)

3D MOL for NP0323244 (n-{3-methoxy-5-[2-(2-methylpropyl)-5-oxo-2h-pyrrol-1-yl]-5-oxopent-3-en-1-yl}-6,6-dimethylheptanimidic acid)

3D SDF for NP0323244 (n-{3-methoxy-5-[2-(2-methylpropyl)-5-oxo-2h-pyrrol-1-yl]-5-oxopent-3-en-1-yl}-6,6-dimethylheptanimidic acid)

3D-SDF for NP0323244 (n-{3-methoxy-5-[2-(2-methylpropyl)-5-oxo-2h-pyrrol-1-yl]-5-oxopent-3-en-1-yl}-6,6-dimethylheptanimidic acid)

PDB for NP0323244 (n-{3-methoxy-5-[2-(2-methylpropyl)-5-oxo-2h-pyrrol-1-yl]-5-oxopent-3-en-1-yl}-6,6-dimethylheptanimidic acid)

3D PDB for NP0323244 (n-{3-methoxy-5-[2-(2-methylpropyl)-5-oxo-2h-pyrrol-1-yl]-5-oxopent-3-en-1-yl}-6,6-dimethylheptanimidic acid)

SMILES for NP0323244 (n-{3-methoxy-5-[2-(2-methylpropyl)-5-oxo-2h-pyrrol-1-yl]-5-oxopent-3-en-1-yl}-6,6-dimethylheptanimidic acid)

INCHI for NP0323244 (n-{3-methoxy-5-[2-(2-methylpropyl)-5-oxo-2h-pyrrol-1-yl]-5-oxopent-3-en-1-yl}-6,6-dimethylheptanimidic acid)

Structure for NP0323244 (n-{3-methoxy-5-[2-(2-methylpropyl)-5-oxo-2h-pyrrol-1-yl]-5-oxopent-3-en-1-yl}-6,6-dimethylheptanimidic acid)

3D Structure for NP0323244 (n-{3-methoxy-5-[2-(2-methylpropyl)-5-oxo-2h-pyrrol-1-yl]-5-oxopent-3-en-1-yl}-6,6-dimethylheptanimidic acid)