NP-MRD: Showing NP-Card for 3-[5-hydroxy-3-methoxy-1-(phenylimino)hexyl]-5-(propan-2-ylidene)pyrrole-2,4-diol (NP0189149)

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Record Information

Version

2.0

Created at

2022-09-04 05:35:31 UTC

Updated at

2022-09-04 05:35:31 UTC

NP-MRD ID

NP0189149

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-[5-hydroxy-3-methoxy-1-(phenylimino)hexyl]-5-(propan-2-ylidene)pyrrole-2,4-diol

Description

4-[5-Hydroxy-3-methoxy-1-(phenylimino)hexyl]-2-(propan-2-ylidene)-2H-pyrrole-3,5-diol belongs to the class of organic compounds known as benzene and substituted derivatives. These are aromatic compounds containing one monocyclic ring system consisting of benzene. Based on a literature review very few articles have been published on 4-[5-hydroxy-3-methoxy-1-(phenylimino)hexyl]-2-(propan-2-ylidene)-2H-pyrrole-3,5-diol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042207352D          

 26 27  0  0  0  0            999 V2000
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -2.0625    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1904   -0.3401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3654   -0.3401    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4454    0.4445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9605    1.1120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1400    1.0257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2960    1.8657    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2704    0.4445    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5253   -0.3401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3099   -0.5950    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.0625    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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  4  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
  7 12  1  0  0  0  0
  5 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 16 20  1  0  0  0  0
 20 21  2  0  0  0  0
 13 21  1  0  0  0  0
 21 22  1  0  0  0  0
  3 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
M  END

     RDKit          3D

 52 53  0  0  0  0  0  0  0  0999 V2000
   -3.3983    1.0993    1.6713 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5941   -0.0012    1.5882 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3887   -0.4479    0.2735 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9691   -0.7280    0.0065 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0538    0.4736    0.2088 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5034    1.5560    0.5580 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3018    2.8417    0.8763 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0454    3.3073    2.1718 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1331    4.6263    2.4386 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0736    5.5855    1.4573 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1785    5.1353    0.1799 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3622    3.8180   -0.1207 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3594    0.1707   -0.0574 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8484   -1.0185   -0.4415 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1621   -2.2100   -0.6730 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2930   -0.8580   -0.5867 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1642   -1.7970   -0.9533 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5983   -1.4552   -1.0483 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7169   -3.1715   -1.2653 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5402    0.4916   -0.2553 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4534    1.1091    0.0529 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4456    2.4657    0.4196 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1563   -1.7877    0.1779 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0639   -2.4319   -1.1679 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9078   -3.7216   -1.0812 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7699   -2.9115   -1.4666 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0992    2.0057    1.1625 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4526    0.8967    1.3521 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4923    1.3537    2.7697 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8317    0.2048   -0.4830 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5990   -1.5362    0.6504 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7612   -0.9963   -1.0549 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0110    2.5884    2.9810 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3345    4.9959    3.4538 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2128    6.6308    1.6509 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2258    5.9067   -0.6057 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5551    3.5595   -1.1527 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0443   -2.4759   -1.6590 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1694   -2.2855   -0.5514 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8358   -0.4822   -0.5841 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8865   -1.4296   -2.1148 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2522   -3.2111   -2.2557 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5981   -3.8567   -1.2590 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0465   -3.5749   -0.4514 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7567    3.1789   -0.2398 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2026   -1.6608    0.5208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7054   -2.5029    0.9194 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3888   -1.7933   -2.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1153   -4.0688   -2.0994 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2999   -4.4370   -0.5052 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8854   -3.4873   -0.5772 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6285   -3.6631   -0.8308 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3 23  1  0
 23 24  1  0
 24 25  1  0
 24 26  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
  5 13  1  0
 13 14  2  0
 14 15  1  0
 14 16  1  0
 16 20  1  0
 20 21  2  0
 21 22  1  0
 16 17  2  3
 17 18  1  0
 17 19  1  0
 12  7  1  0
 21 13  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  3 30  1  6
 23 46  1  0
 23 47  1  0
 24 48  1  6
 25 49  1  0
 25 50  1  0
 25 51  1  0
 26 52  1  0
  4 31  1  0
  4 32  1  0
  8 33  1  0
  9 34  1  0
 10 35  1  0
 11 36  1  0
 12 37  1  0
 15 38  1  0
 22 45  1  0
 18 39  1  0
 18 40  1  0
 18 41  1  0
 19 42  1  0
 19 43  1  0
 19 44  1  0
M  END


  Mrv1652309042207352D          

 26 27  0  0  0  0            999 V2000
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -2.0625    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1904   -0.3401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3654   -0.3401    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4454    0.4445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9605    1.1120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1400    1.0257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2960    1.8657    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2704    0.4445    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5253   -0.3401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3099   -0.5950    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.0625    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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  4  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
  7 12  1  0  0  0  0
  5 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 16 20  1  0  0  0  0
 20 21  2  0  0  0  0
 13 21  1  0  0  0  0
 21 22  1  0  0  0  0
  3 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0189149

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(CC(C)O)CC(=NC1=CC=CC=C1)C1=C(O)C(N=C1O)=C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C20H26N2O4/c1-12(2)18-19(24)17(20(25)22-18)16(11-15(26-4)10-13(3)23)21-14-8-6-5-7-9-14/h5-9,13,15,23-24H,10-11H2,1-4H3,(H,22,25)

> <INCHI_KEY>
OWHMOWSDDNPFFS-UHFFFAOYSA-N

> <FORMULA>
C20H26N2O4

> <MOLECULAR_WEIGHT>
358.438

> <EXACT_MASS>
358.189257325

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
39.63465120332952

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-[5-hydroxy-3-methoxy-1-(phenylimino)hexyl]-2-(propan-2-ylidene)-2H-pyrrole-3,5-diol

> <JCHEM_LOGP>
2.5607991623333337

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
10.430357408572313

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.669610166128613

> <JCHEM_PKA_STRONGEST_BASIC>
2.608040240199869

> <JCHEM_POLAR_SURFACE_AREA>
94.64

> <JCHEM_REFRACTIVITY>
105.0999

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
3-[5-hydroxy-3-methoxy-1-(phenylimino)hexyl]-5-(propan-2-ylidene)pyrrole-2,4-diol

> <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      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -2.667  -1.540   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.001  -3.850   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -5.335  -3.080   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0      -6.668  -3.850   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0      -6.668  -5.390   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -5.335  -6.160   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -5.335  -7.700   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -6.668  -8.470   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -8.002  -7.700   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -8.002  -6.160   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -5.335  -1.540   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -4.089  -0.635   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -2.549  -0.635   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -4.565   0.830   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -3.660   2.076   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -2.128   1.915   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -4.286   3.483   0.000  0.00  0.00           C+0
HETATM   20  N   UNK     0      -6.105   0.830   0.000  0.00  0.00           N+0
HETATM   21  C   UNK     0      -6.581  -0.635   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -8.045  -1.111   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -1.334  -3.850   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.000  -1.540   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       1.334  -3.850   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   23                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   13                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   12                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11    7                                                       
CONECT   13    5   14   21                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   20                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   16   21                                                       
CONECT   21   20   13   22                                                  
CONECT   22   21                                                            
CONECT   23    3   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   54    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₆N₂O₄

Average Mass

358.4380 Da

Monoisotopic Mass

358.18926 Da

IUPAC Name

4-[5-hydroxy-3-methoxy-1-(phenylimino)hexyl]-2-(propan-2-ylidene)-2H-pyrrole-3,5-diol

Traditional Name

3-[5-hydroxy-3-methoxy-1-(phenylimino)hexyl]-5-(propan-2-ylidene)pyrrole-2,4-diol

CAS Registry Number

Not Available

SMILES

COC(CC(C)O)CC(=NC1=CC=CC=C1)C1=C(O)C(N=C1O)=C(C)C

InChI Identifier

InChI=1S/C20H26N2O4/c1-12(2)18-19(24)17(20(25)22-18)16(11-15(26-4)10-13(3)23)21-14-8-6-5-7-9-14/h5-9,13,15,23-24H,10-11H2,1-4H3,(H,22,25)

InChI Key

OWHMOWSDDNPFFS-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 benzene and substituted derivatives. These are aromatic compounds containing one monocyclic ring system consisting of benzene.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Not Available

Direct Parent

Benzene and substituted derivatives

Alternative Parents

Substituents

Monocyclic benzene moiety
Vinylogous acid
Secondary ketimine
Pyrroline
Azomethine
Secondary carboxylic acid amide
Secondary alcohol
Lactam
Ketimine
Carboxamide group
Azacycle
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Ether
Enol
Dialkyl ether
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Imine
Carbonyl group
Alcohol
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic 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	2.56	ChemAxon
pKa (Strongest Acidic)	4.67	ChemAxon
pKa (Strongest Basic)	2.61	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	94.64 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	105.1 m³·mol⁻¹	ChemAxon
Polarizability	39.63 Å³	ChemAxon
Number of Rings	2	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

162815635

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-[5-hydroxy-3-methoxy-1-(phenylimino)hexyl]-5-(propan-2-ylidene)pyrrole-2,4-diol (NP0189149)

MOL for NP0189149 (3-[5-hydroxy-3-methoxy-1-(phenylimino)hexyl]-5-(propan-2-ylidene)pyrrole-2,4-diol)

3D MOL for NP0189149 (3-[5-hydroxy-3-methoxy-1-(phenylimino)hexyl]-5-(propan-2-ylidene)pyrrole-2,4-diol)

3D SDF for NP0189149 (3-[5-hydroxy-3-methoxy-1-(phenylimino)hexyl]-5-(propan-2-ylidene)pyrrole-2,4-diol)

3D-SDF for NP0189149 (3-[5-hydroxy-3-methoxy-1-(phenylimino)hexyl]-5-(propan-2-ylidene)pyrrole-2,4-diol)

PDB for NP0189149 (3-[5-hydroxy-3-methoxy-1-(phenylimino)hexyl]-5-(propan-2-ylidene)pyrrole-2,4-diol)

3D PDB for NP0189149 (3-[5-hydroxy-3-methoxy-1-(phenylimino)hexyl]-5-(propan-2-ylidene)pyrrole-2,4-diol)

SMILES for NP0189149 (3-[5-hydroxy-3-methoxy-1-(phenylimino)hexyl]-5-(propan-2-ylidene)pyrrole-2,4-diol)

INCHI for NP0189149 (3-[5-hydroxy-3-methoxy-1-(phenylimino)hexyl]-5-(propan-2-ylidene)pyrrole-2,4-diol)

Structure for NP0189149 (3-[5-hydroxy-3-methoxy-1-(phenylimino)hexyl]-5-(propan-2-ylidene)pyrrole-2,4-diol)

3D Structure for NP0189149 (3-[5-hydroxy-3-methoxy-1-(phenylimino)hexyl]-5-(propan-2-ylidene)pyrrole-2,4-diol)