NP-MRD: Showing NP-Card for N-p-coumaroyl-N'-caffeoylputrescine (NP0140186)

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Record Information

Version

2.0

Created at

2022-06-29 20:50:01 UTC

Updated at

2022-06-29 20:50:01 UTC

NP-MRD ID

NP0140186

Secondary Accession Numbers

None

Natural Product Identification

Common Name

N-p-coumaroyl-N'-caffeoylputrescine

Description

N-p-coumaroyl-N'-caffeoylputrescine belongs to the class of organic compounds known as coumaric acids and derivatives. These are aromatic compounds containing Aromatic compounds containing a cinnamic acid moiety (or a derivative thereof) hydroxylated at the C2 (ortho-), C3 (meta-), or C4 (para-) carbon atom of the benzene ring. N-p-coumaroyl-N'-caffeoylputrescine was first documented in 2011 (PMID: 21842649). Based on a literature review very few articles have been published on N-p-coumaroyl-N'-caffeoylputrescine.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652306292222502D          

 29 30  0  0  0  0            999 V2000
   -3.5724   -7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -6.1875    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -5.7750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -7.0125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -7.4250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 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
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
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 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 21 26  1  0  0  0  0
 24 27  1  0  0  0  0
 23 28  1  0  0  0  0
  3 29  1  0  0  0  0
M  END

     RDKit          3D

 53 54  0  0  0  0  0  0  0  0999 V2000
    3.0774    1.6845   -0.7980 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8070    0.6366   -0.6993 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1928    0.8634   -0.3111 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0073   -0.1405   -0.1857 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4099    0.0271    0.2015 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2301   -1.0828    0.3189 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5481   -0.9917    0.6768 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1310    0.2266    0.9415 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4642    0.3696    1.3082 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.3177    1.3259    0.8251 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9715    1.2545    0.4614 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2625   -0.6274   -0.9581 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.8744   -0.7598   -1.3320 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0056   -0.2535   -0.2302 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4847   -0.3899   -0.5948 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2464    0.1531    0.5940 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6799    0.0859    0.3868 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5670    0.5502    1.3942 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0728    1.0138    2.4541 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0205    0.5186    1.2661 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6407    0.0573    0.2063 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0866    0.0291    0.0861 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9559    0.4724    1.0473 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3467    0.4133    0.8600 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9017   -0.0906   -0.2931 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.2816   -0.1416   -0.4617 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0345   -0.5393   -1.2663 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6037   -1.0463   -2.4268 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6714   -0.4822   -1.0846 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5382    1.8966   -0.1261 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6843   -1.1512   -0.3627 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8073   -2.0571    0.1187 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1578   -1.8958    0.7569 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.7525    0.3493    2.2740 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7612    2.3076    1.0314 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3867    2.1762    0.3895 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8416   -1.4821   -0.8864 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7485   -0.1045   -2.2434 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6166   -1.7862   -1.6522 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1094   -0.8653    0.7043 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1389    0.8145   -0.0175 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7573   -1.4443   -0.7495 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.9026    1.1682    0.8411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0047   -0.5001    1.4585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0119   -0.3155   -0.5272 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6051    0.8971    2.0927 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0214   -0.3175   -0.6107 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5613    0.8805    1.9788 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0032    0.7749    1.6460 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.7142   -0.5071   -1.2992 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9784   -1.3793   -3.1497 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9886   -0.8331   -1.8456 H   0  0  0  0  0  0  0  0  0  0  0  0
  9  8  1  0
  8  7  2  0
  7  6  1  0
  6  5  2  0
  5  4  1  0
  4  3  2  0
  3  2  1  0
  2  1  2  0
  2 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  2  0
 21 22  1  0
 22 29  2  0
 29 27  1  0
 27 28  1  0
 27 25  2  0
 25 26  1  0
 25 24  1  0
 24 23  2  0
  5 11  1  0
 11 10  2  0
 10  8  1  0
 23 22  1  0
  9 34  1  0
  7 33  1  0
  6 32  1  0
  4 31  1  0
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 20 47  1  0
 21 48  1  0
 29 53  1  0
 28 52  1  0
 26 51  1  0
 24 50  1  0
 23 49  1  0
 11 36  1  0
 10 35  1  0
M  END


  Mrv1652306292222502D          

 29 30  0  0  0  0            999 V2000
   -3.5724   -7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -6.1875    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -5.7750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -7.0125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -7.4250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 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
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 21 26  1  0  0  0  0
 24 27  1  0  0  0  0
 23 28  1  0  0  0  0
  3 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0140186

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC1=CC=C(\C=C\C(=O)NCCCCNC(=O)\C=C\C2=CC(O)=C(O)C=C2)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C22H24N2O5/c25-18-8-3-16(4-9-18)6-11-21(28)23-13-1-2-14-24-22(29)12-7-17-5-10-19(26)20(27)15-17/h3-12,15,25-27H,1-2,13-14H2,(H,23,28)(H,24,29)/b11-6+,12-7+

> <INCHI_KEY>
NDUQQMKMMARZRU-GNXRPPCSSA-N

> <FORMULA>
C22H24N2O5

> <MOLECULAR_WEIGHT>
396.443

> <EXACT_MASS>
396.168521881

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
43.82649684490451

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2E)-N-{4-[(2E)-3-(3,4-dihydroxyphenyl)prop-2-enamido]butyl}-3-(4-hydroxyphenyl)prop-2-enamide

> <ALOGPS_LOGP>
2.55

> <JCHEM_LOGP>
2.600740925666666

> <ALOGPS_LOGS>
-4.83

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.632475726165913

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.007998962445777

> <JCHEM_PKA_STRONGEST_BASIC>
-0.007960962308620756

> <JCHEM_POLAR_SURFACE_AREA>
118.89000000000001

> <JCHEM_REFRACTIVITY>
113.0413

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.93e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2E)-N-{4-[(2E)-3-(3,4-dihydroxyphenyl)prop-2-enamido]butyl}-3-(4-hydroxyphenyl)prop-2-enamide

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-JUN-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-JUN-22         0                                  
HETATM    1  C   UNK     0      -6.668 -13.090   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -8.002 -13.860   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -9.336 -13.090   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -9.336 -11.550   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -8.002 -10.780   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -6.668 -11.550   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -5.335 -10.780   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -4.001 -11.550   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.667 -10.780   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -2.667  -9.240   0.000  0.00  0.00           O+0
HETATM   11  N   UNK     0      -1.334 -11.550   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0       0.000 -10.780   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.334 -11.550   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.667 -10.780   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.001 -11.550   0.000  0.00  0.00           C+0
HETATM   16  N   UNK     0       5.335 -10.780   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0       6.668 -11.550   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       6.668 -13.090   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       8.002 -10.780   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.002  -9.240   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.336  -8.470   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       9.336  -6.930   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      10.669  -6.160   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      12.003  -6.930   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      12.003  -8.470   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      10.669  -9.240   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      13.337  -6.160   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0      10.669  -4.620   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0     -10.669 -13.860   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4   29                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    1    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   26                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   28                                                  
CONECT   24   23   25   27                                                  
CONECT   25   24   26                                                       
CONECT   26   25   21                                                       
CONECT   27   24                                                            
CONECT   28   23                                                            
CONECT   29    3                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₂₄N₂O₅

Average Mass

396.4430 Da

Monoisotopic Mass

396.16852 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

OC1=CC=C(\C=C\C(=O)NCCCCNC(=O)\C=C\C2=CC(O)=C(O)C=C2)C=C1

InChI Identifier

InChI=1S/C22H24N2O5/c25-18-8-3-16(4-9-18)6-11-21(28)23-13-1-2-14-24-22(29)12-7-17-5-10-19(26)20(27)15-17/h3-12,15,25-27H,1-2,13-14H2,(H,23,28)(H,24,29)/b11-6+,12-7+

InChI Key

NDUQQMKMMARZRU-GNXRPPCSSA-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 coumaric acids and derivatives. These are aromatic compounds containing Aromatic compounds containing a cinnamic acid moiety (or a derivative thereof) hydroxylated at the C2 (ortho-), C3 (meta-), or C4 (para-) carbon atom of the benzene ring.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Cinnamic acids and derivatives

Sub Class

Hydroxycinnamic acids and derivatives

Direct Parent

Coumaric acids and derivatives

Alternative Parents

Substituents

Cinnamic acid amide
Coumaric acid or derivatives
Catechol
Styrene
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Monocyclic benzene moiety
Benzenoid
Secondary carboxylic acid amide
Carboxamide group
Carboxylic acid derivative
Organic oxygen compound
Carbonyl group
Organooxygen compound
Organonitrogen compound
Organic nitrogen compound
Hydrocarbon derivative
Organic oxide
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic 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

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

28425446

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

45783040

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Zhang J, Li X, Ren L, Fang C, Wang F: [Chemical constituents from Exochorda racemosa]. Zhongguo Zhong Yao Za Zhi. 2011 May;36(9):1198-201. [PubMed:21842649 ]

Showing NP-Card for N-p-coumaroyl-N'-caffeoylputrescine (NP0140186)

MOL for NP0140186 (N-p-coumaroyl-N'-caffeoylputrescine)

3D MOL for NP0140186 (N-p-coumaroyl-N'-caffeoylputrescine)

3D SDF for NP0140186 (N-p-coumaroyl-N'-caffeoylputrescine)

3D-SDF for NP0140186 (N-p-coumaroyl-N'-caffeoylputrescine)

PDB for NP0140186 (N-p-coumaroyl-N'-caffeoylputrescine)

3D PDB for NP0140186 (N-p-coumaroyl-N'-caffeoylputrescine)

SMILES for NP0140186 (N-p-coumaroyl-N'-caffeoylputrescine)

INCHI for NP0140186 (N-p-coumaroyl-N'-caffeoylputrescine)

Structure for NP0140186 (N-p-coumaroyl-N'-caffeoylputrescine)

3D Structure for NP0140186 (N-p-coumaroyl-N'-caffeoylputrescine)