NP-MRD: Showing NP-Card for (2r)-3-{[(2e,4e,6e,8e,10e,12e)-1-hydroxy-13-{2-[(1-hydroxyethylidene)amino]-3-methoxyphenyl}trideca-2,4,6,8,10,12-hexaen-1-ylidene]amino}-2-methylpropanoic acid (NP0283641)

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Record Information

Version

2.0

Created at

2022-09-09 10:59:17 UTC

Updated at

2022-09-09 10:59:17 UTC

NP-MRD ID

NP0283641

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r)-3-{[(2e,4e,6e,8e,10e,12e)-1-hydroxy-13-{2-[(1-hydroxyethylidene)amino]-3-methoxyphenyl}trideca-2,4,6,8,10,12-hexaen-1-ylidene]amino}-2-methylpropanoic acid

Description

(2R)-3-{[(2E,4E,6E,8E,10E,12E)-1-hydroxy-13-{2-[(1-hydroxyethylidene)amino]-3-methoxyphenyl}trideca-2,4,6,8,10,12-hexaen-1-ylidene]amino}-2-methylpropanoic acid belongs to the class of organic compounds known as methoxyanilines. These are organic compound containing an aniline group substituted at one or more positions by a methoxy group. (2r)-3-{[(2e,4e,6e,8e,10e,12e)-1-hydroxy-13-{2-[(1-hydroxyethylidene)amino]-3-methoxyphenyl}trideca-2,4,6,8,10,12-hexaen-1-ylidene]amino}-2-methylpropanoic acid is found in Physarum rigidum. Based on a literature review very few articles have been published on (2R)-3-{[(2E,4E,6E,8E,10E,12E)-1-hydroxy-13-{2-[(1-hydroxyethylidene)amino]-3-methoxyphenyl}trideca-2,4,6,8,10,12-hexaen-1-ylidene]amino}-2-methylpropanoic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092212592D          

 33 33  0  0  1  0            999 V2000
    0.0000    2.4750    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
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   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   -1.2375    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   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8592   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5737   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5737   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2881   -1.2375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0026   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0026   -2.4750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -9.2881   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7171   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7171   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  -11.4315   -2.4750    0.0000 O   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    1.2375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.0000    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  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
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 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
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 15 16  1  0  0  0  0
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 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
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 20 22  2  0  0  0  0
 22 23  1  4  0  0  0
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  3 29  1  0  0  0  0
 30 29  1  4  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
M  END

     RDKit          3D

 63 63  0  0  0  0  0  0  0  0999 V2000
  -10.9158   -2.3313    0.1890 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5428   -2.2477    0.1519 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.0710   -0.7496    2.2141 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7213   -0.5979    1.7267 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7494    0.0559    2.3268 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4406    0.0927    1.6555 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6276    0.7768    2.0890 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8269    0.6878    1.2867 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9681    1.3185    1.4469 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0571    1.1245    0.5760 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1970    1.4338    0.2617 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4604    1.7383   -0.1278 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3417    2.6155    0.2668 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6290    2.5888   -0.4678 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4616    3.6644   -0.0493 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.9859    1.7956   -1.2909 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.0789    0.7834   -2.1397 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1582    0.4140   -3.2631 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.0655    1.5554   -4.2690 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6671   -0.7899   -3.9792 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6054   -0.8026   -5.2832 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.1841   -1.8629   -3.3234 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2987   -1.8790    0.9412 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8164   -2.0903   -0.4251 N   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5596   -1.0022   -1.1182 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7472    0.3390   -0.5161 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1203   -1.1198   -2.4013 O   0  0  0  0  0  0  0  0  0  0  0  0
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  -11.3685   -2.8394   -0.6802 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.2698   -2.7107    1.1661 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1858   -1.7384    2.6673 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5437   -1.1854    4.4730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1593   -1.1025    3.9458 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6386   -1.7741    0.5233 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3919   -0.3500    3.1576 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4728   -1.0616    0.7689 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9503    0.5435    3.2719 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2994   -0.4759    0.7359 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5597    1.3301    2.9729 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8328   -0.0128    0.4147 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0163    1.9861    2.2878 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6278    0.5817   -0.4286 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4283    0.0598   -0.0259 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8775    1.1549   -1.0165 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1126    3.2749    1.0709 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6207    4.4316   -0.6903 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0348   -0.2125   -1.4792 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1667    0.6103   -2.5362 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1188    0.1490   -2.9503 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2011    1.1546   -5.3286 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.8258    0.9695   -0.6054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1999   -1.3165   -2.7455 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
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  3  4  2  0
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 23 24  1  0
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 26 28  1  0
 26 27  2  0
  7 29  2  0
 29 30  1  0
 30 31  2  0
 31 32  1  0
 31 33  1  0
 29  3  1  0
  1 34  1  0
  1 35  1  0
  1 36  1  0
  4 37  1  0
  5 38  1  0
  6 39  1  0
  8 40  1  0
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 11 43  1  0
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 25 57  1  0
 25 58  1  0
 28 59  1  0
 32 60  1  0
 32 61  1  0
 32 62  1  0
 33 63  1  0
M  END


  Mrv1652309092212592D          

 33 33  0  0  1  0            999 V2000
    0.0000    2.4750    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
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.7145   -1.2375    0.0000 C   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   -1.2375    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
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   -4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -8.5737   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5737   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2881   -1.2375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0026   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0026   -2.4750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -9.2881   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7171   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7171   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  -11.4315   -2.4750    0.0000 O   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    1.2375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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  2  3  1  0  0  0  0
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  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
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 26 27  2  0  0  0  0
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 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0283641

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=CC(\C=C\C=C\C=C\C=C\C=C\C=C\C(O)=NC[C@@H](C)C(O)=O)=C1N=C(C)O

> <INCHI_IDENTIFIER>
InChI=1S/C26H30N2O5/c1-20(26(31)32)19-27-24(30)18-13-11-9-7-5-4-6-8-10-12-15-22-16-14-17-23(33-3)25(22)28-21(2)29/h4-18,20H,19H2,1-3H3,(H,27,30)(H,28,29)(H,31,32)/b6-4+,7-5+,10-8+,11-9+,15-12+,18-13+/t20-/m1/s1

> <INCHI_KEY>
DDPBZJFKHOQWLE-MTHOHEPCSA-N

> <FORMULA>
C26H30N2O5

> <MOLECULAR_WEIGHT>
450.535

> <EXACT_MASS>
450.215472074

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
63

> <JCHEM_AVERAGE_POLARIZABILITY>
52.48255467650805

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R)-3-{[(2E,4E,6E,8E,10E,12E)-1-hydroxy-13-{2-[(1-hydroxyethylidene)amino]-3-methoxyphenyl}trideca-2,4,6,8,10,12-hexaen-1-ylidene]amino}-2-methylpropanoic acid

> <JCHEM_LOGP>
3.580746700647105

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
5.019064148188321

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.893281437883494

> <JCHEM_PKA_STRONGEST_BASIC>
7.034543604783257

> <JCHEM_POLAR_SURFACE_AREA>
111.71000000000001

> <JCHEM_REFRACTIVITY>
139.3333

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2R)-3-{[(2E,4E,6E,8E,10E,12E)-1-hydroxy-13-{2-[(1-hydroxyethylidene)amino]-3-methoxyphenyl}trideca-2,4,6,8,10,12-hexaen-1-ylidene]amino}-2-methylpropanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       1.334   3.850   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -8.002  -3.080   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -9.336  -2.310   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0     -10.669  -3.080   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0     -12.003  -2.310   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0     -13.337  -3.080   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0     -14.670  -2.310   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0     -16.004  -3.080   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0     -16.004  -4.620   0.000  0.00  0.00           O+0
HETATM   22  N   UNK     0     -17.338  -2.310   0.000  0.00  0.00           N+0
HETATM   23  C   UNK     0     -18.672  -3.080   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0     -18.672  -4.620   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0     -17.338  -5.390   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0     -20.005  -5.390   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0     -20.005  -6.930   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0     -21.339  -4.620   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   30  N   UNK     0      -1.334   2.310   0.000  0.00  0.00           N+0
HETATM   31  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -4.001   2.310   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      -2.667   0.000   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   29                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   29                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   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                                                       
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   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26                                                            
CONECT   29    7    3   30                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   66    0
END

View in JSmol

Synonyms

Value	Source
(2R)-3-{[(2E,4E,6E,8E,10E,12E)-1-hydroxy-13-{2-[(1-hydroxyethylidene)amino]-3-methoxyphenyl}trideca-2,4,6,8,10,12-hexaen-1-ylidene]amino}-2-methylpropanoate	Generator

Chemical Formula

C₂₆H₃₀N₂O₅

Average Mass

450.5350 Da

Monoisotopic Mass

450.21547 Da

IUPAC Name

(2R)-3-{[(2E,4E,6E,8E,10E,12E)-1-hydroxy-13-{2-[(1-hydroxyethylidene)amino]-3-methoxyphenyl}trideca-2,4,6,8,10,12-hexaen-1-ylidene]amino}-2-methylpropanoic acid

Traditional Name

(2R)-3-{[(2E,4E,6E,8E,10E,12E)-1-hydroxy-13-{2-[(1-hydroxyethylidene)amino]-3-methoxyphenyl}trideca-2,4,6,8,10,12-hexaen-1-ylidene]amino}-2-methylpropanoic acid

CAS Registry Number

Not Available

SMILES

COC1=CC=CC(\C=C\C=C\C=C\C=C\C=C\C=C\C(O)=NC[C@@H](C)C(O)=O)=C1N=C(C)O

InChI Identifier

InChI=1S/C26H30N2O5/c1-20(26(31)32)19-27-24(30)18-13-11-9-7-5-4-6-8-10-12-15-22-16-14-17-23(33-3)25(22)28-21(2)29/h4-18,20H,19H2,1-3H3,(H,27,30)(H,28,29)(H,31,32)/b6-4+,7-5+,10-8+,11-9+,15-12+,18-13+/t20-/m1/s1

InChI Key

DDPBZJFKHOQWLE-MTHOHEPCSA-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
Physarum rigidum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as methoxyanilines. These are organic compound containing an aniline group substituted at one or more positions by a methoxy group.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Aniline and substituted anilines

Direct Parent

Methoxyanilines

Alternative Parents

Substituents

Methoxyaniline
Phenoxy compound
Anisole
Phenol ether
Styrene
Methoxybenzene
Alkyl aryl ether
Carboximidic acid
Carboximidic acid derivative
Carboxylic acid derivative
Carboxylic acid
Ether
Monocarboxylic acid or derivatives
Propargyl-type 1,3-dipolar organic compound
Organic 1,3-dipolar compound
Organic nitrogen compound
Organic oxygen compound
Organonitrogen compound
Organooxygen compound
Organopnictogen compound
Organic oxide
Carbonyl group
Hydrocarbon derivative
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	3.58	ChemAxon
pKa (Strongest Acidic)	3.89	ChemAxon
pKa (Strongest Basic)	7.03	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	111.71 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	139.33 m³·mol⁻¹	ChemAxon
Polarizability	52.48 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	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

163195020

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r)-3-{[(2e,4e,6e,8e,10e,12e)-1-hydroxy-13-{2-[(1-hydroxyethylidene)amino]-3-methoxyphenyl}trideca-2,4,6,8,10,12-hexaen-1-ylidene]amino}-2-methylpropanoic acid (NP0283641)

MOL for NP0283641 ((2r)-3-{[(2e,4e,6e,8e,10e,12e)-1-hydroxy-13-{2-[(1-hydroxyethylidene)amino]-3-methoxyphenyl}trideca-2,4,6,8,10,12-hexaen-1-ylidene]amino}-2-methylpropanoic acid)

3D MOL for NP0283641 ((2r)-3-{[(2e,4e,6e,8e,10e,12e)-1-hydroxy-13-{2-[(1-hydroxyethylidene)amino]-3-methoxyphenyl}trideca-2,4,6,8,10,12-hexaen-1-ylidene]amino}-2-methylpropanoic acid)

3D SDF for NP0283641 ((2r)-3-{[(2e,4e,6e,8e,10e,12e)-1-hydroxy-13-{2-[(1-hydroxyethylidene)amino]-3-methoxyphenyl}trideca-2,4,6,8,10,12-hexaen-1-ylidene]amino}-2-methylpropanoic acid)

3D-SDF for NP0283641 ((2r)-3-{[(2e,4e,6e,8e,10e,12e)-1-hydroxy-13-{2-[(1-hydroxyethylidene)amino]-3-methoxyphenyl}trideca-2,4,6,8,10,12-hexaen-1-ylidene]amino}-2-methylpropanoic acid)

PDB for NP0283641 ((2r)-3-{[(2e,4e,6e,8e,10e,12e)-1-hydroxy-13-{2-[(1-hydroxyethylidene)amino]-3-methoxyphenyl}trideca-2,4,6,8,10,12-hexaen-1-ylidene]amino}-2-methylpropanoic acid)

3D PDB for NP0283641 ((2r)-3-{[(2e,4e,6e,8e,10e,12e)-1-hydroxy-13-{2-[(1-hydroxyethylidene)amino]-3-methoxyphenyl}trideca-2,4,6,8,10,12-hexaen-1-ylidene]amino}-2-methylpropanoic acid)

SMILES for NP0283641 ((2r)-3-{[(2e,4e,6e,8e,10e,12e)-1-hydroxy-13-{2-[(1-hydroxyethylidene)amino]-3-methoxyphenyl}trideca-2,4,6,8,10,12-hexaen-1-ylidene]amino}-2-methylpropanoic acid)

INCHI for NP0283641 ((2r)-3-{[(2e,4e,6e,8e,10e,12e)-1-hydroxy-13-{2-[(1-hydroxyethylidene)amino]-3-methoxyphenyl}trideca-2,4,6,8,10,12-hexaen-1-ylidene]amino}-2-methylpropanoic acid)

Structure for NP0283641 ((2r)-3-{[(2e,4e,6e,8e,10e,12e)-1-hydroxy-13-{2-[(1-hydroxyethylidene)amino]-3-methoxyphenyl}trideca-2,4,6,8,10,12-hexaen-1-ylidene]amino}-2-methylpropanoic acid)

3D Structure for NP0283641 ((2r)-3-{[(2e,4e,6e,8e,10e,12e)-1-hydroxy-13-{2-[(1-hydroxyethylidene)amino]-3-methoxyphenyl}trideca-2,4,6,8,10,12-hexaen-1-ylidene]amino}-2-methylpropanoic acid)