NP-MRD: Showing NP-Card for [2-(1h-indol-3-ylmethyl)-1h-indol-3-yl]acetic acid (NP0214279)

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Record Information

Version

2.0

Created at

2022-09-05 13:32:14 UTC

Updated at

2022-09-05 13:32:14 UTC

NP-MRD ID

NP0214279

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[2-(1h-indol-3-ylmethyl)-1h-indol-3-yl]acetic acid

Description

2-(Indol-3-ylmethyl)indol-3-ylacetic acid, also known as 2-IMIAC, belongs to the class of organic compounds known as indole-3-acetic acid derivatives. Indole-3-acetic acid derivatives are compounds containing an acetic acid (or a derivative) linked to the C3 carbon atom of an indole. Based on a literature review very few articles have been published on 2-(Indol-3-ylmethyl)indol-3-ylacetic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 39 42  0  0  0  0  0  0  0  0999 V2000
   -2.6716    2.6379   -0.9513 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5566    2.8295    0.2935 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8617    4.1015    0.7463 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1262    1.8034    1.2487 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7797    0.5230    0.5703 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6187    0.2681   -0.1647 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3846    1.3178   -0.4124 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6492    0.8243   -0.9824 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9945    0.7788   -2.3212 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2035    0.2369   -2.4709 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.6694   -0.0807   -1.2435 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8827   -0.6521   -0.8858 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1220   -0.8578    0.4506 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1886   -0.5076    1.3900 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9827    0.0617    1.0182 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7090    0.2815   -0.3108 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6649   -1.0081   -0.5836 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8140   -1.5657   -0.1417 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3474   -2.8339   -0.3015 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5639   -3.1847    0.2367 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2595   -2.2278    0.9574 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7560   -0.9485    1.1386 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5260   -0.6215    0.5843 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7773    4.4789    0.8359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2267    2.1060    1.8574 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9599    1.6048    1.9631 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0163    2.0744   -1.1267 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5348    1.8718    0.5435 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3302    1.1450   -3.0976 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7099    0.0806   -3.3581 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6181   -0.9316   -1.6201 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0589   -1.3040    0.7522 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4255   -0.6881    2.4486 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2528    0.3313    1.8008 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0777   -1.4643   -1.1569 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7830   -3.5723   -0.8801 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9356   -4.1842    0.0787 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2304   -2.5146    1.3826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3187   -0.2094    1.7116 H   0  0  0  0  0  0  0  0  0  0  0  0
  3  2  1  0
  2  1  2  0
  2  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
  6 17  1  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  2  0
 23  5  1  0
 16  8  1  0
 23 18  1  0
 16 11  1  0
  3 24  1  0
  4 25  1  0
  4 26  1  0
  7 27  1  0
  7 28  1  0
  9 29  1  0
 10 30  1  0
 12 31  1  0
 13 32  1  0
 14 33  1  0
 15 34  1  0
 17 35  1  0
 19 36  1  0
 20 37  1  0
 21 38  1  0
 22 39  1  0
M  END


  Mrv1652309052215322D          

 23 26  0  0  0  0            999 V2000
    3.6959   -4.3649    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9509   -3.5803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7578   -3.4088    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3988   -2.9672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6538   -2.1826    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1688   -1.5151    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3438   -1.5151    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9313   -2.2296    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2669   -2.9833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6538   -3.5353    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.9393   -3.1228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1547   -3.3777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4584   -2.8257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2869   -2.0187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4978   -1.7638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1109   -2.3158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6538   -0.8477    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.4384   -1.1026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1529   -0.6901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8673   -1.1026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8673   -1.9276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1529   -2.3401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4384   -1.9276    0.0000 C   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
  2  4  1  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
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
  8 16  1  0  0  0  0
 11 16  1  0  0  0  0
  6 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
  5 23  1  0  0  0  0
 18 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0214279

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC(=O)CC1=C(CC2=CNC3=CC=CC=C23)NC2=CC=CC=C12

> <INCHI_IDENTIFIER>
InChI=1S/C19H16N2O2/c22-19(23)10-15-14-6-2-4-8-17(14)21-18(15)9-12-11-20-16-7-3-1-5-13(12)16/h1-8,11,20-21H,9-10H2,(H,22,23)

> <INCHI_KEY>
OKSIBGLOGCEKNP-UHFFFAOYSA-N

> <FORMULA>
C19H16N2O2

> <MOLECULAR_WEIGHT>
304.349

> <EXACT_MASS>
304.121177763

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
32.505798399410146

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-{2-[(1H-indol-3-yl)methyl]-1H-indol-3-yl}acetic acid

> <JCHEM_LOGP>
3.6644057819999993

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
15.744400881619619

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.696094791832146

> <JCHEM_POLAR_SURFACE_AREA>
68.88

> <JCHEM_REFRACTIVITY>
89.30730000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
[2-(1H-indol-3-ylmethyl)-1H-indol-3-yl]acetic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  O   UNK     0       6.899  -8.148   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       7.375  -6.683   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       8.881  -6.363   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       6.344  -5.539   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.820  -4.074   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.915  -2.828   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.375  -2.828   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.605  -4.162   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.232  -5.569   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0       3.087  -6.599   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0       1.753  -5.829   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.289  -6.305   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.856  -5.275   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.535  -3.768   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.929  -3.292   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.074  -4.323   0.000  0.00  0.00           C+0
HETATM   17  N   UNK     0       6.820  -1.582   0.000  0.00  0.00           N+0
HETATM   18  C   UNK     0       8.285  -2.058   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.619  -1.288   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      10.952  -2.058   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      10.952  -3.598   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       9.619  -4.368   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.285  -3.598   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   23                                                  
CONECT    6    5    7   17                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   16                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   16                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15    8   11                                                  
CONECT   17    6   18                                                       
CONECT   18   17   19   23                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22    5   18                                                  
MASTER        0    0    0    0    0    0    0    0   23    0   52    0
END

View in JSmol

Synonyms

Value	Source
2-(indol-3-Ylmethyl)indol-3-ylacetate	Generator
2-IMIAC	MeSH

Chemical Formula

C₁₉H₁₆N₂O₂

Average Mass

304.3490 Da

Monoisotopic Mass

304.12118 Da

IUPAC Name

2-{2-[(1H-indol-3-yl)methyl]-1H-indol-3-yl}acetic acid

Traditional Name

[2-(1H-indol-3-ylmethyl)-1H-indol-3-yl]acetic acid

CAS Registry Number

Not Available

SMILES

OC(=O)CC1=C(CC2=CNC3=CC=CC=C23)NC2=CC=CC=C12

InChI Identifier

InChI=1S/C19H16N2O2/c22-19(23)10-15-14-6-2-4-8-17(14)21-18(15)9-12-11-20-16-7-3-1-5-13(12)16/h1-8,11,20-21H,9-10H2,(H,22,23)

InChI Key

OKSIBGLOGCEKNP-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 indole-3-acetic acid derivatives. Indole-3-acetic acid derivatives are compounds containing an acetic acid (or a derivative) linked to the C3 carbon atom of an indole.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Indolyl carboxylic acids and derivatives

Direct Parent

Indole-3-acetic acid derivatives

Alternative Parents

Substituents

Indole-3-acetic acid derivative
3-alkylindole
Indole
Substituted pyrrole
Benzenoid
Heteroaromatic compound
Pyrrole
Azacycle
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Carbonyl group
Organopnictogen compound
Organooxygen compound
Organonitrogen compound
Organic oxygen compound
Organic nitrogen compound
Hydrocarbon derivative
Organic oxide
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic 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	3.66	ChemAxon
pKa (Strongest Acidic)	4.7	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	68.88 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	89.31 m³·mol⁻¹	ChemAxon
Polarizability	32.51 Å³	ChemAxon
Number of Rings	4	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

114518

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

129287

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for [2-(1h-indol-3-ylmethyl)-1h-indol-3-yl]acetic acid (NP0214279)

MOL for NP0214279 ([2-(1h-indol-3-ylmethyl)-1h-indol-3-yl]acetic acid)

3D MOL for NP0214279 ([2-(1h-indol-3-ylmethyl)-1h-indol-3-yl]acetic acid)

3D SDF for NP0214279 ([2-(1h-indol-3-ylmethyl)-1h-indol-3-yl]acetic acid)

3D-SDF for NP0214279 ([2-(1h-indol-3-ylmethyl)-1h-indol-3-yl]acetic acid)

PDB for NP0214279 ([2-(1h-indol-3-ylmethyl)-1h-indol-3-yl]acetic acid)

3D PDB for NP0214279 ([2-(1h-indol-3-ylmethyl)-1h-indol-3-yl]acetic acid)

SMILES for NP0214279 ([2-(1h-indol-3-ylmethyl)-1h-indol-3-yl]acetic acid)

INCHI for NP0214279 ([2-(1h-indol-3-ylmethyl)-1h-indol-3-yl]acetic acid)

Structure for NP0214279 ([2-(1h-indol-3-ylmethyl)-1h-indol-3-yl]acetic acid)

3D Structure for NP0214279 ([2-(1h-indol-3-ylmethyl)-1h-indol-3-yl]acetic acid)