MiMeDB: Showing metabocard for 1,1,1-tris(3-indolyl)methane (MMDBc0014542)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-15 05:33:25 UTC

Update Date

2022-08-31 06:37:48 UTC

MiMeDB ID

MMDBc0014542

Metabolite Identification

Common Name

1,1,1-tris(3-indolyl)methane

Description

Structure

MOL SDF PDB SMILES InChI


  Mrv1533004241501572D          

 28 33  0  0  0  0            999 V2000
    1.2643   -5.2201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5498   -4.8076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5498   -3.9826    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2643   -3.5701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4358   -2.7631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2563   -2.6769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5919   -3.4305    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9788   -3.9826    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9788   -4.8076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8838   -2.1500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0768   -2.3215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2587   -3.0752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0792   -2.9890    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2508   -2.1820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9652   -1.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9652   -0.9445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2508   -0.5320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5363   -0.9445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5363   -1.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -1.3654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -0.0305    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -1.1104    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
  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
  4  8  1  0  0  0  0
  8  9  2  0  0  0  0
  1  9  1  0  0  0  0
  5 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  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 11 19  1  0  0  0  0
 14 19  1  0  0  0  0
 10 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  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
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 20 28  1  0  0  0  0
 23 28  1  0  0  0  0
M  END


  Mrv1533004241501572D          

 28 33  0  0  0  0            999 V2000
    1.2643   -5.2201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5498   -4.8076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5498   -3.9826    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2643   -3.5701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4358   -2.7631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2563   -2.6769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5919   -3.4305    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9788   -3.9826    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9788   -4.8076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8838   -2.1500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0768   -2.3215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2587   -3.0752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0792   -2.9890    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2508   -2.1820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9652   -1.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9652   -0.9445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2508   -0.5320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5363   -0.9445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5363   -1.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -1.3654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -0.0305    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -1.1104    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
  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
  4  8  1  0  0  0  0
  8  9  2  0  0  0  0
  1  9  1  0  0  0  0
  5 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  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 11 19  1  0  0  0  0
 14 19  1  0  0  0  0
 10 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  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
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 20 28  1  0  0  0  0
 23 28  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0014542

> <DATABASE_NAME>
MIME

> <SMILES>
N1C=C(C(C2=CNC3=CC=CC=C23)C2=CNC3=CC=CC=C23)C2=CC=CC=C12

> <INCHI_IDENTIFIER>
InChI=1S/C25H19N3/c1-4-10-22-16(7-1)19(13-26-22)25(20-14-27-23-11-5-2-8-17(20)23)21-15-28-24-12-6-3-9-18(21)24/h1-15,25-28H

> <INCHI_KEY>
AXZRNKFNIAOZEK-UHFFFAOYSA-N

> <FORMULA>
C25H19N3

> <MOLECULAR_WEIGHT>
361.448

> <EXACT_MASS>
361.157897624

> <JCHEM_ACCEPTOR_COUNT>
0

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
40.74149465771008

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3-[bis(1H-indol-3-yl)methyl]-1H-indole

> <ALOGPS_LOGP>
5.92

> <JCHEM_LOGP>
5.782148891

> <ALOGPS_LOGS>
-6.69

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
16.35232303307558

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.814982360255485

> <JCHEM_POLAR_SURFACE_AREA>
47.37

> <JCHEM_REFRACTIVITY>
113.69830000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
7.35e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-[bis(1H-indol-3-yl)methyl]-1H-indole

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0       2.360  -9.744   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.026  -8.974   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.026  -7.434   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.360  -6.664   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.680  -5.158   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.212  -4.997   0.000  0.00  0.00           C+0
HETATM    7  N   UNK     0       4.838  -6.404   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0       3.694  -7.434   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.694  -8.974   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.650  -4.013   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.143  -4.334   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.483  -5.740   0.000  0.00  0.00           C+0
HETATM   13  N   UNK     0      -2.015  -5.579   0.000  0.00  0.00           N+0
HETATM   14  C   UNK     0      -2.335  -4.073   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -3.668  -3.303   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -3.668  -1.763   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -2.335  -0.993   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.001  -1.763   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.001  -3.303   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.126  -2.549   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.220  -1.303   0.000  0.00  0.00           C+0
HETATM   22  N   UNK     0       2.126  -0.057   0.000  0.00  0.00           N+0
HETATM   23  C   UNK     0       3.590  -0.533   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.924   0.237   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.258  -0.533   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.258  -2.073   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.924  -2.843   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.590  -2.073   0.000  0.00  0.00           C+0
CONECT    1    2    9                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    8                                                  
CONECT    5    4    6   10                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    4    9                                                  
CONECT    9    8    1                                                       
CONECT   10    5   11   20                                                  
CONECT   11   10   12   19                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   19                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   11   14                                                  
CONECT   20   10   21   28                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   28                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   20   23                                                  
MASTER        0    0    0    0    0    0    0    0   28    0   66    0
END

Synonyms

Not Available

Chemical Formula

C₂₅H₁₉N₃

Average Molecular Weight

361.448

Monoisotopic Molecular Weight

361.157897624

IUPAC Name

3-[bis(1H-indol-3-yl)methyl]-1H-indole

Traditional Name

3-[bis(1H-indol-3-yl)methyl]-1H-indole

CAS Registry Number

Not Available

SMILES

N1C=C(C(C2=CNC3=CC=CC=C23)C2=CNC3=CC=CC=C23)C2=CC=CC=C12

InChI Identifier

InChI=1S/C25H19N3/c1-4-10-22-16(7-1)19(13-26-22)25(20-14-27-23-11-5-2-8-17(20)23)21-15-28-24-12-6-3-9-18(21)24/h1-15,25-28H

InChI Key

AXZRNKFNIAOZEK-UHFFFAOYSA-N

Chemical Taxonomy

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	7.4e-05 g/L	ALOGPS
logP	5.92	ALOGPS
logP	5.78	ChemAxon
logS	-6.7	ALOGPS
pKa (Strongest Acidic)	15.81	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	0	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	47.37 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	113.7 m³·mol⁻¹	ChemAxon
Polarizability	40.74 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Not Available

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Proteins

Human Pathways

Pathways

Name	SMPDB/PathBank

Metabolic Reactions

Not Available

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Related Health Condition	Evidence Type	Measured in Matrix	Data Source	Reference

Microbial Sources

Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
	Proteobacteria	1		Metabolic reconstruction

Exposure Sources

Source Type	Source Sub-type	Species	Data Source	Reference	Details

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Units	Age	Sex	Health Condition	Data Source	Reference

External Links

Not Available

References

Synthesis Reference

Not Available

General References

van Santen JA, Poynton EF, Iskakova D, McMann E, Alsup TA, Clark TN, Fergusson CH, Fewer DP, Hughes AH, McCadden CA, Parra J, Soldatou S, Rudolf JD, Janssen EM, Duncan KR, Linington RG: The Natural Products Atlas 2.0: a database of microbially-derived natural products. Nucleic Acids Res. 2022 Jan 7;50(D1):D1317-D1323. doi: 10.1093/nar/gkab941. [PubMed:34718710 ]

Showing metabocard for 1,1,1-tris(3-indolyl)methane (MMDBc0014542)

MOL for #<Metabolite:0x00007f0910dc2010>

3D MOL for #<Metabolite:0x00007f0910dc2010>

3D SDF for #<Metabolite:0x00007f0910dc2010>

3D-SDF for #<Metabolite:0x00007f0910dc2010>

PDB for #<Metabolite:0x00007f0910dc2010>

3D PDB for #<Metabolite:0x00007f0910dc2010>

SMILES for #<Metabolite:0x00007f0910dc2010>

INCHI for #<Metabolite:0x00007f0910dc2010>

Structure for #<Metabolite:0x00007f0910dc2010>

3D Structure for #<Metabolite:0x00007f0910dc2010>