NP-MRD: Showing NP-Card for (1r,2r)-2-hydroxy-1-{[(2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}propane-1,2,3-tricarboxylic acid (NP0197507)

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Record Information

Version

2.0

Created at

2022-09-04 15:47:11 UTC

Updated at

2022-09-04 15:47:11 UTC

NP-MRD ID

NP0197507

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2r)-2-hydroxy-1-{[(2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}propane-1,2,3-tricarboxylic acid

Description

(1R,2R)-2-hydroxy-1-{[(2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}propane-1,2,3-tricarboxylic acid belongs to the class of organic compounds known as tetracarboxylic acids and derivatives. These are carboxylic acids containing exactly four carboxyl groups. (1r,2r)-2-hydroxy-1-{[(2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}propane-1,2,3-tricarboxylic acid is found in Dactylis glomerata. Based on a literature review very few articles have been published on (1R,2R)-2-hydroxy-1-{[(2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}propane-1,2,3-tricarboxylic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042217472D          

 27 27  0  0  1  0            999 V2000
   -1.5732    7.4912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1995    6.7557    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6497    6.0643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2760    5.3288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7262    4.6374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3525    3.9019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8026    3.2105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8791    1.7836    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6051    2.4309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2314    1.6953    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6816    1.0040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3079    0.2684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5054    1.0481    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5924    1.6512    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5482    0.8274    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4162    1.6070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7899    0.8715    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6137    0.8274    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3397    0.1801    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6365    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0549    2.9251    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3720    2.8487    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5500    4.6816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9236    5.4171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4735    6.1085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8472    6.8440    0.0000 O   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  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
  8 10  1  0  0  0  0
 11 10  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 11 15  1  0  0  0  0
 15 16  1  6  0  0  0
 15 17  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 15 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
  5 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
  3 26  1  0  0  0  0
 26 27  1  0  0  0  0
M  END

     RDKit          3D

 43 43  0  0  0  0  0  0  0  0999 V2000
    3.9667    0.9182   -4.1172 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9222    0.4104   -3.1956 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5332    0.0720   -1.9010 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2413    0.2195   -1.4956 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9032   -0.1321   -0.1932 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5276    0.0441    0.1820 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0899   -0.2497    1.3734 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3274   -0.0360    1.6626 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7682   -0.3110    2.7949 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2253    0.4572    0.7545 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5838    0.6298    1.1312 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8720    2.1093    1.1267 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9874    2.5077    1.4863 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8992    3.0183    0.7237 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5147   -0.1599    0.2889 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5057    0.2197   -1.0641 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9270   -0.0401    0.7791 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0966   -0.5140    2.1689 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9626    0.1597    3.2001 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4409   -1.8503    2.3416 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0585   -1.5975    0.3798 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7650   -2.2232   -0.6670 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9523   -2.2533    1.5896 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8305   -0.6186    0.6824 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1544   -0.7681    0.2614 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4922   -0.4211   -1.0261 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8009   -0.5645   -1.4553 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3606    1.7100   -3.6610 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3821    0.0327   -4.4572 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5489    1.3259   -4.9802 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4991    0.6037   -2.1829 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7905    0.4356   -0.5316 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7041   -0.6398    2.1633 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6862    0.3095    2.1739 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2041    3.3816    1.3315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0609    1.1253   -1.0684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3715    0.9638    0.7021 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6255   -0.6780    0.1602 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2049   -2.3007    1.8598 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2480   -2.9415    1.8042 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5852   -0.8921    1.6881 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8960   -1.1520    0.9453 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0587   -0.3105   -2.4061 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 14  1  0
 12 13  2  0
 11 15  1  0
 15 16  1  6
 15 17  1  0
 17 18  1  0
 18 20  1  0
 18 19  2  0
 15 21  1  0
 21 23  1  0
 21 22  2  0
  5 24  2  0
 24 25  1  0
 25 26  2  0
 26 27  1  0
 26  3  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  4 31  1  0
  6 32  1  0
  7 33  1  0
 11 34  1  1
 14 35  1  0
 16 36  1  0
 17 37  1  0
 17 38  1  0
 20 39  1  0
 23 40  1  0
 24 41  1  0
 25 42  1  0
 27 43  1  0
M  END


  Mrv1652309042217472D          

 27 27  0  0  1  0            999 V2000
   -1.5732    7.4912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1995    6.7557    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6497    6.0643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2760    5.3288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7262    4.6374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3525    3.9019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8026    3.2105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8791    1.7836    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6051    2.4309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2314    1.6953    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6816    1.0040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3079    0.2684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5054    1.0481    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5924    1.6512    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5482    0.8274    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4162    1.6070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7899    0.8715    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6137    0.8274    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3397    0.1801    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6365    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0549    2.9251    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3720    2.8487    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5500    4.6816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9236    5.4171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4735    6.1085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8472    6.8440    0.0000 O   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  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
  8 10  1  0  0  0  0
 11 10  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 11 15  1  0  0  0  0
 15 16  1  6  0  0  0
 15 17  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 15 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
  5 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
  3 26  1  0  0  0  0
 26 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0197507

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(\C=C\C(=O)O[C@@H](C(O)=O)[C@](O)(CC(O)=O)C(O)=O)=CC=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C16H16O11/c1-26-10-6-8(2-4-9(10)17)3-5-12(20)27-13(14(21)22)16(25,15(23)24)7-11(18)19/h2-6,13,17,25H,7H2,1H3,(H,18,19)(H,21,22)(H,23,24)/b5-3+/t13-,16+/m0/s1

> <INCHI_KEY>
QAEWENIBBUMYIB-QFMIGQRISA-N

> <FORMULA>
C16H16O11

> <MOLECULAR_WEIGHT>
384.293

> <EXACT_MASS>
384.069261335

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
43

> <JCHEM_AVERAGE_POLARIZABILITY>
34.72157650392327

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,2R)-2-hydroxy-1-{[(2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}propane-1,2,3-tricarboxylic acid

> <JCHEM_LOGP>
0.5348082180000003

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-3

> <JCHEM_PKA>
4.303190612133933

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.86266134569989

> <JCHEM_PKA_STRONGEST_BASIC>
-4.5894545120764745

> <JCHEM_POLAR_SURFACE_AREA>
187.88999999999996

> <JCHEM_REFRACTIVITY>
84.9739

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R)-2-hydroxy-1-{[(2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}propane-1,2,3-tricarboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0      -2.937  13.984   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -2.239  12.611   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -3.079  11.320   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.382   9.947   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -3.222   8.657   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.525   7.284   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -3.365   5.993   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.667   4.620   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -3.508   3.329   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0      -1.130   4.538   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -0.432   3.165   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.272   1.874   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -0.575   0.501   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0      -2.810   1.956   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       1.106   3.082   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       1.023   1.544   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       2.644   3.000   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.341   1.627   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       4.879   1.544   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       2.501   0.336   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       1.188   4.620   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -0.102   5.460   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       2.561   5.318   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -4.760   8.739   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -5.457  10.112   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -4.617  11.402   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -5.315  12.775   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   26                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   24                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   15                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15   11   16   17   21                                             
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   15   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24    5   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25    3   27                                                  
CONECT   27   26                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   54    0
END

View in JSmol

Synonyms

Value	Source
(1R,2R)-2-Hydroxy-1-{[(2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}propane-1,2,3-tricarboxylate	Generator

Chemical Formula

C₁₆H₁₆O₁₁

Average Mass

384.2930 Da

Monoisotopic Mass

384.06926 Da

IUPAC Name

(1R,2R)-2-hydroxy-1-{[(2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}propane-1,2,3-tricarboxylic acid

Traditional Name

(1R,2R)-2-hydroxy-1-{[(2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}propane-1,2,3-tricarboxylic acid

CAS Registry Number

Not Available

SMILES

COC1=CC(\C=C\C(=O)O[C@@H](C(O)=O)[C@](O)(CC(O)=O)C(O)=O)=CC=C1O

InChI Identifier

InChI=1S/C16H16O11/c1-26-10-6-8(2-4-9(10)17)3-5-12(20)27-13(14(21)22)16(25,15(23)24)7-11(18)19/h2-6,13,17,25H,7H2,1H3,(H,18,19)(H,21,22)(H,23,24)/b5-3+/t13-,16+/m0/s1

InChI Key

QAEWENIBBUMYIB-QFMIGQRISA-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
Dactylis glomerata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tetracarboxylic acids and derivatives. These are carboxylic acids containing exactly four carboxyl groups.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Tetracarboxylic acids and derivatives

Direct Parent

Tetracarboxylic acids and derivatives

Alternative Parents

Substituents

Tetracarboxylic acid or derivatives
Cinnamic acid or derivatives
Coumaric acid or derivatives
Hydroxycinnamic acid or derivatives
Cinnamic acid ester
Methoxyphenol
Phenoxy compound
Anisole
Methoxybenzene
Phenol ether
Styrene
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Fatty acid ester
Phenol
Alpha-hydroxy acid
Fatty acyl
Benzenoid
Hydroxy acid
Monocyclic benzene moiety
Monosaccharide
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Tertiary alcohol
Carboxylic acid ester
Ether
Carboxylic acid
Carbonyl group
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Alcohol
Organic oxygen compound
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
logP	0.53	ChemAxon
pKa (Strongest Acidic)	2.86	ChemAxon
pKa (Strongest Basic)	-4.6	ChemAxon
Physiological Charge	-3	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	187.89 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	84.97 m³·mol⁻¹	ChemAxon
Polarizability	34.72 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

163189266

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,2r)-2-hydroxy-1-{[(2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}propane-1,2,3-tricarboxylic acid (NP0197507)

MOL for NP0197507 ((1r,2r)-2-hydroxy-1-{[(2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}propane-1,2,3-tricarboxylic acid)

3D MOL for NP0197507 ((1r,2r)-2-hydroxy-1-{[(2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}propane-1,2,3-tricarboxylic acid)

3D SDF for NP0197507 ((1r,2r)-2-hydroxy-1-{[(2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}propane-1,2,3-tricarboxylic acid)

3D-SDF for NP0197507 ((1r,2r)-2-hydroxy-1-{[(2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}propane-1,2,3-tricarboxylic acid)

PDB for NP0197507 ((1r,2r)-2-hydroxy-1-{[(2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}propane-1,2,3-tricarboxylic acid)

3D PDB for NP0197507 ((1r,2r)-2-hydroxy-1-{[(2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}propane-1,2,3-tricarboxylic acid)

SMILES for NP0197507 ((1r,2r)-2-hydroxy-1-{[(2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}propane-1,2,3-tricarboxylic acid)

INCHI for NP0197507 ((1r,2r)-2-hydroxy-1-{[(2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}propane-1,2,3-tricarboxylic acid)

Structure for NP0197507 ((1r,2r)-2-hydroxy-1-{[(2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}propane-1,2,3-tricarboxylic acid)

3D Structure for NP0197507 ((1r,2r)-2-hydroxy-1-{[(2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}propane-1,2,3-tricarboxylic acid)