MiMeDB: Showing metabocard for Lysiformine (MMDBc0022920)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-15 12:58:49 UTC

Update Date

2022-08-31 06:48:06 UTC

Metabolite ID

MMDBc0022920

Metabolite Identification

Common Name

Lysiformine

Description

Lysiformine belongs to the class of organic compounds known as 3-alkylindoles. 3-alkylindoles are compounds containing an indole moiety that carries an alkyl chain at the 3-position. Based on a literature review very few articles have been published on Lysiformine.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152114582D          

 26 30  0  0  0  0            999 V2000
   -3.4536   -2.0964    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
   -3.4536   -2.9214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7391   -1.6839    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7391   -3.3339    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9851   -1.0568    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0768   -0.1006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7551   -2.5089    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1809   -1.3268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2400   -1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1781   -0.8853    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0247   -2.0964    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
    0.8838    0.0709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    0.8555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0247   -2.9214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4358   -0.5422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3739   -1.4984    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2400   -3.1763    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    2.1904    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2428   -0.3707    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  3  1  2  0  0  0  0
  4  2  2  0  0  0  0
  5  1  1  0  0  0  0
  6  2  1  0  0  0  0
  7  3  1  0  0  0  0
  8  4  1  0  0  0  0
 14  9  1  0  0  0  0
 14 11  2  0  0  0  0
 15  9  1  0  0  0  0
 15 10  1  0  0  0  0
 16  5  2  0  0  0  0
 16 14  1  0  0  0  0
 17  6  2  0  0  0  0
 18 10  2  0  0  0  0
 19 12  2  0  0  0  0
 19 17  1  0  0  0  0
 19 18  1  0  0  0  0
 20  7  2  0  0  0  0
 20 16  1  0  0  0  0
 21  8  2  0  0  0  0
 21 17  1  0  0  0  0
 22 13  2  0  0  0  0
 22 18  1  0  0  0  0
 23 13  1  0  0  0  0
 23 15  2  0  0  0  0
 24 11  1  0  0  0  0
 24 20  1  0  0  0  0
 25 12  1  0  0  0  0
 25 21  1  0  0  0  0
 26 22  1  0  0  0  0
M  END


  Mrv1652305152114582D          

 26 30  0  0  0  0            999 V2000
   -3.4536   -2.0964    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
   -3.4536   -2.9214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7391   -1.6839    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7391   -3.3339    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9851   -1.0568    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0768   -0.1006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7551   -2.5089    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1809   -1.3268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2400   -1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1781   -0.8853    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0247   -2.0964    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
    0.8838    0.0709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    0.8555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0247   -2.9214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4358   -0.5422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3739   -1.4984    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2400   -3.1763    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    2.1904    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2428   -0.3707    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  3  1  2  0  0  0  0
  4  2  2  0  0  0  0
  5  1  1  0  0  0  0
  6  2  1  0  0  0  0
  7  3  1  0  0  0  0
  8  4  1  0  0  0  0
 14  9  1  0  0  0  0
 14 11  2  0  0  0  0
 15  9  1  0  0  0  0
 15 10  1  0  0  0  0
 16  5  2  0  0  0  0
 16 14  1  0  0  0  0
 17  6  2  0  0  0  0
 18 10  2  0  0  0  0
 19 12  2  0  0  0  0
 19 17  1  0  0  0  0
 19 18  1  0  0  0  0
 20  7  2  0  0  0  0
 20 16  1  0  0  0  0
 21  8  2  0  0  0  0
 21 17  1  0  0  0  0
 22 13  2  0  0  0  0
 22 18  1  0  0  0  0
 23 13  1  0  0  0  0
 23 15  2  0  0  0  0
 24 11  1  0  0  0  0
 24 20  1  0  0  0  0
 25 12  1  0  0  0  0
 25 21  1  0  0  0  0
 26 22  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0022920

> <DATABASE_NAME>
MIME

> <SMILES>
OC1=CN=C(CC2=CNC3=CC=CC=C23)C=C1C1=CNC2=CC=CC=C12

> <INCHI_IDENTIFIER>
InChI=1S/C22H17N3O/c26-22-13-23-15(9-14-11-24-20-7-3-1-5-16(14)20)10-18(22)19-12-25-21-8-4-2-6-17(19)21/h1-8,10-13,24-26H,9H2

> <INCHI_KEY>
DCDRAIPBJLUPLW-UHFFFAOYSA-N

> <FORMULA>
C22H17N3O

> <MOLECULAR_WEIGHT>
339.398

> <EXACT_MASS>
339.137162179

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
43

> <JCHEM_AVERAGE_POLARIZABILITY>
37.146547204115116

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-(1H-indol-3-yl)-6-[(1H-indol-3-yl)methyl]pyridin-3-ol

> <ALOGPS_LOGP>
4.68

> <JCHEM_LOGP>
4.262467404

> <ALOGPS_LOGS>
-5.16

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.947317572244014

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.977135767817938

> <JCHEM_PKA_STRONGEST_BASIC>
4.794732675276399

> <JCHEM_POLAR_SURFACE_AREA>
64.7

> <JCHEM_REFRACTIVITY>
102.5046

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.37e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-(1H-indol-3-yl)-6-(1H-indol-3-ylmethyl)pyridin-3-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 15-MAY-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   15-MAY-21         0                                  
HETATM    1  C   UNK     0      -6.447  -3.913   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.258   2.073   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -6.447  -5.453   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.258   3.613   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -5.113  -3.143   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.924   1.303   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -5.113  -6.223   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.924   4.383   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.839  -1.973   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.143  -0.188   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.410  -4.683   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.220   2.843   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.204  -2.477   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.315  -3.437   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.333  -1.652   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -3.779  -3.913   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.590   2.073   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.650   0.132   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.126   1.597   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -3.779  -5.453   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.590   3.613   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.680  -1.012   0.000  0.00  0.00           C+0
HETATM   23  N   UNK     0       0.698  -2.797   0.000  0.00  0.00           N+0
HETATM   24  N   UNK     0      -2.315  -5.929   0.000  0.00  0.00           N+0
HETATM   25  N   UNK     0       2.126   4.089   0.000  0.00  0.00           N+0
HETATM   26  O   UNK     0       4.187  -0.692   0.000  0.00  0.00           O+0
CONECT    1    3    5                                                       
CONECT    2    4    6                                                       
CONECT    3    1    7                                                       
CONECT    4    2    8                                                       
CONECT    5    1   16                                                       
CONECT    6    2   17                                                       
CONECT    7    3   20                                                       
CONECT    8    4   21                                                       
CONECT    9   14   15                                                       
CONECT   10   15   18                                                       
CONECT   11   14   24                                                       
CONECT   12   19   25                                                       
CONECT   13   22   23                                                       
CONECT   14    9   11   16                                                  
CONECT   15    9   10   23                                                  
CONECT   16    5   14   20                                                  
CONECT   17    6   19   21                                                  
CONECT   18   10   19   22                                                  
CONECT   19   12   17   18                                                  
CONECT   20    7   16   24                                                  
CONECT   21    8   17   25                                                  
CONECT   22   13   18   26                                                  
CONECT   23   13   15                                                       
CONECT   24   11   20                                                       
CONECT   25   12   21                                                       
CONECT   26   22                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   60    0
END

Synonyms

Not Available

Molecular Formula

C₂₂H₁₇N₃O

Average Mass

339.398

Monoisotopic Mass

339.137162179

IUPAC Name

4-(1H-indol-3-yl)-6-[(1H-indol-3-yl)methyl]pyridin-3-ol

Traditional Name

4-(1H-indol-3-yl)-6-(1H-indol-3-ylmethyl)pyridin-3-ol

CAS Registry Number

Not Available

SMILES

OC1=CN=C(CC2=CNC3=CC=CC=C23)C=C1C1=CNC2=CC=CC=C12

InChI Identifier

InChI=1S/C22H17N3O/c26-22-13-23-15(9-14-11-24-20-7-3-1-5-16(14)20)10-18(22)19-12-25-21-8-4-2-6-17(19)21/h1-8,10-13,24-26H,9H2

InChI Key

DCDRAIPBJLUPLW-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 3-alkylindoles. 3-Alkylindoles are compounds containing an indole moiety that carries an alkyl chain at the 3-position.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Indoles

Direct Parent

3-alkylindoles

Alternative Parents

Substituents

3-alkylindole
Hydroxypyridine
Benzenoid
Substituted pyrrole
Pyridine
Heteroaromatic compound
Pyrrole
Azacycle
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.0024 g/L	ALOGPS
logP	4.68	ALOGPS
logP	4.26	ChemAxon
logS	-5.2	ALOGPS
pKa (Strongest Acidic)	8.98	ChemAxon
pKa (Strongest Basic)	4.79	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	64.7 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	102.5 m³·mol⁻¹	ChemAxon
Polarizability	37.15 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

Protein ID	Protein Name	Protein Type	Uniprot ID	Species

Human Pathways

Pathways

Name	SMPDB/PathBank

Metabolic Reactions

Not Available

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Evidence Type	Host and Biospecimen	Data Source	Reference

Microbial Sources

Superkingdom/Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
Bacteria	Firmicutes	1	Human	Metabolic reconstruction

Exposure Sources

Source Type	Source Sub-type	Species	Data Source	Reference

Host Biospecimen and Location

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

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

71048926

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139590265

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

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 Lysiformine (MMDBc0022920)

MOL for #<Metabolite:0x00007f46cc021678>

3D MOL for #<Metabolite:0x00007f46cc021678>

3D SDF for #<Metabolite:0x00007f46cc021678>

3D-SDF for #<Metabolite:0x00007f46cc021678>

PDB for #<Metabolite:0x00007f46cc021678>

3D PDB for #<Metabolite:0x00007f46cc021678>

SMILES for #<Metabolite:0x00007f46cc021678>

INCHI for #<Metabolite:0x00007f46cc021678>

Structure for #<Metabolite:0x00007f46cc021678>

3D Structure for #<Metabolite:0x00007f46cc021678>