MiMeDB: Showing metabocard for Tetrahydroindol 5 (MMDBc0027423)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-15 17:09:31 UTC

Update Date

2022-08-31 06:52:30 UTC

Metabolite ID

MMDBc0027423

Metabolite Identification

Common Name

Tetrahydroindol 5

Description

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152119092D          

 27 30  0  0  1  0            999 V2000
    0.7601    4.2184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4894    4.5722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7179    2.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1569    3.2623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3869    1.8102    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2949    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0150    3.4338    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9019    2.4777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5249    1.8646    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4630    2.8207    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0769    2.4777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8220    3.2623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789    1.2375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.7798   -0.2549    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4894    3.7472    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.7798    1.0799    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.2073    1.8965    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3440    2.9922    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5671    4.0469    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3319    1.6930    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2080    3.6053    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  1  1  1  0  0  0
  9  4  2  0  0  0  0
  9  5  1  0  0  0  0
 10  3  1  0  0  0  0
 11  3  1  0  0  0  0
 11  8  1  0  0  0  0
 12  9  1  0  0  0  0
 12 10  1  0  0  0  0
 14  8  1  0  0  0  0
 14 12  2  0  0  0  0
 15 13  2  0  0  0  0
 16 13  1  0  0  0  0
 17  6  2  0  0  0  0
 17 15  1  0  0  0  0
 18  6  1  0  0  0  0
 18 16  2  0  0  0  0
 19  7  2  0  0  0  0
 19 13  1  0  0  0  0
 20  2  1  0  0  0  0
 20  4  1  0  0  0  0
 20 14  1  0  0  0  0
 21  7  1  0  0  0  0
 10 21  1  6  0  0  0
 21 15  1  0  0  0  0
 22  5  2  0  0  0  0
 11 23  1  1  0  0  0
 24 16  1  0  0  0  0
  8 25  1  6  0  0  0
 10 26  1  1  0  0  0
 11 27  1  6  0  0  0
M  END


  Mrv1652305152119092D          

 27 30  0  0  1  0            999 V2000
    0.7601    4.2184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4894    4.5722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7179    2.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1569    3.2623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3869    1.8102    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2949    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0150    3.4338    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9019    2.4777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5249    1.8646    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4630    2.8207    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0769    2.4777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8220    3.2623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789    1.2375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.7798   -0.2549    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4894    3.7472    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.7798    1.0799    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.2073    1.8965    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3440    2.9922    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5671    4.0469    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3319    1.6930    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2080    3.6053    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  1  1  1  0  0  0
  9  4  2  0  0  0  0
  9  5  1  0  0  0  0
 10  3  1  0  0  0  0
 11  3  1  0  0  0  0
 11  8  1  0  0  0  0
 12  9  1  0  0  0  0
 12 10  1  0  0  0  0
 14  8  1  0  0  0  0
 14 12  2  0  0  0  0
 15 13  2  0  0  0  0
 16 13  1  0  0  0  0
 17  6  2  0  0  0  0
 17 15  1  0  0  0  0
 18  6  1  0  0  0  0
 18 16  2  0  0  0  0
 19  7  2  0  0  0  0
 19 13  1  0  0  0  0
 20  2  1  0  0  0  0
 20  4  1  0  0  0  0
 20 14  1  0  0  0  0
 21  7  1  0  0  0  0
 10 21  1  6  0  0  0
 21 15  1  0  0  0  0
 22  5  2  0  0  0  0
 11 23  1  1  0  0  0
 24 16  1  0  0  0  0
  8 25  1  6  0  0  0
 10 26  1  1  0  0  0
 11 27  1  6  0  0  0
M  END
> <DATABASE_ID>
MMDBc0027423

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@@]1(O)C[C@@]([H])(N2C=NC3=C2N=CN=C3O)C2=C(N(C)C=C2C=O)[C@]1([H])C

> <INCHI_IDENTIFIER>
InChI=1S/C16H17N5O3/c1-8-11(23)3-10(12-9(5-22)4-20(2)14(8)12)21-7-19-13-15(21)17-6-18-16(13)24/h4-8,10-11,23H,3H2,1-2H3,(H,17,18,24)/t8-,10-,11-/m1/s1

> <INCHI_KEY>
HIODDSQIKRMOBZ-FBIMIBRVSA-N

> <FORMULA>
C16H17N5O3

> <MOLECULAR_WEIGHT>
327.344

> <EXACT_MASS>
327.133139427

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
41

> <JCHEM_AVERAGE_POLARIZABILITY>
33.274871757676436

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(4R,6R,7S)-6-hydroxy-4-(6-hydroxy-9H-purin-9-yl)-1,7-dimethyl-4,5,6,7-tetrahydro-1H-indole-3-carbaldehyde

> <ALOGPS_LOGP>
0.67

> <JCHEM_LOGP>
0.6584631986666661

> <ALOGPS_LOGS>
-2.26

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.805603510088407

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.705632589211282

> <JCHEM_PKA_STRONGEST_BASIC>
0.07366682832322047

> <JCHEM_POLAR_SURFACE_AREA>
106.06

> <JCHEM_REFRACTIVITY>
87.84059999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.80e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(4R,6R,7S)-6-hydroxy-4-(6-hydroxypurin-9-yl)-1,7-dimethyl-4,5,6,7-tetrahydroindole-3-carbaldehyde

> <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       1.419   7.874   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.647   8.535   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.340   3.801   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.893   6.090   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.322   3.379   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.454   1.540   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.417   0.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.895   6.410   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.417   4.625   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.846   3.481   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.864   5.265   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.877   4.625   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.787   0.000   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.401   6.090   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.787   1.540   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.121  -0.770   0.000  0.00  0.00           C+0
HETATM   17  N   UNK     0       6.121   2.310   0.000  0.00  0.00           N+0
HETATM   18  N   UNK     0       7.454   0.000   0.000  0.00  0.00           N+0
HETATM   19  N   UNK     0       3.322  -0.476   0.000  0.00  0.00           N+0
HETATM   20  N   UNK     0       4.647   6.995   0.000  0.00  0.00           N+0
HETATM   21  N   UNK     0       3.322   2.016   0.000  0.00  0.00           N+0
HETATM   22  O   UNK     0       7.854   3.540   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      -0.642   5.586   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       6.121  -2.310   0.000  0.00  0.00           O+0
HETATM   25  H   UNK     0       2.925   7.554   0.000  0.00  0.00           H+0
HETATM   26  H   UNK     0       4.353   3.160   0.000  0.00  0.00           H+0
HETATM   27  H   UNK     0       0.388   6.730   0.000  0.00  0.00           H+0
CONECT    1    8                                                            
CONECT    2   20                                                            
CONECT    3   10   11                                                       
CONECT    4    9   20                                                       
CONECT    5    9   22                                                       
CONECT    6   17   18                                                       
CONECT    7   19   21                                                       
CONECT    8    1   11   14   25                                             
CONECT    9    4    5   12                                                  
CONECT   10    3   12   21   26                                             
CONECT   11    3    8   23   27                                             
CONECT   12    9   10   14                                                  
CONECT   13   15   16   19                                                  
CONECT   14    8   12   20                                                  
CONECT   15   13   17   21                                                  
CONECT   16   13   18   24                                                  
CONECT   17    6   15                                                       
CONECT   18    6   16                                                       
CONECT   19    7   13                                                       
CONECT   20    2    4   14                                                  
CONECT   21    7   10   15                                                  
CONECT   22    5                                                            
CONECT   23   11                                                            
CONECT   24   16                                                            
CONECT   25    8                                                            
CONECT   26   10                                                            
CONECT   27   11                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   60    0
END

Synonyms

Not Available

Molecular Formula

C₁₆H₁₇N₅O₃

Average Mass

327.344

Monoisotopic Mass

327.133139427

IUPAC Name

(4R,6R,7S)-6-hydroxy-4-(6-hydroxy-9H-purin-9-yl)-1,7-dimethyl-4,5,6,7-tetrahydro-1H-indole-3-carbaldehyde

Traditional Name

(4R,6R,7S)-6-hydroxy-4-(6-hydroxypurin-9-yl)-1,7-dimethyl-4,5,6,7-tetrahydroindole-3-carbaldehyde

CAS Registry Number

Not Available

SMILES

[H][C@@]1(O)C[C@@]([H])(N2C=NC3=C2N=CN=C3O)C2=C(N(C)C=C2C=O)[C@]1([H])C

InChI Identifier

InChI=1S/C16H17N5O3/c1-8-11(23)3-10(12-9(5-22)4-20(2)14(8)12)21-7-19-13-15(21)17-6-18-16(13)24/h4-8,10-11,23H,3H2,1-2H3,(H,17,18,24)/t8-,10-,11-/m1/s1

InChI Key

HIODDSQIKRMOBZ-FBIMIBRVSA-N

Chemical Taxonomy

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	1.8 g/L	ALOGPS
logP	0.67	ALOGPS
logP	0.66	ChemAxon
logS	-2.3	ALOGPS
pKa (Strongest Acidic)	11.71	ChemAxon
pKa (Strongest Basic)	0.074	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	106.06 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	87.84 m³·mol⁻¹	ChemAxon
Polarizability	33.27 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

Spectra

Chromatographic Retention Times and Retention Indices

Retention Times

Not Available

Retention Indices

Not Available

Chromatographic Retention Times and Retention Indices

Retention Times

Not Available

Retention Indices

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

Microbial Pathways

Pathways

Not Available

Metabolic Reactions

Reactions

This table shows at most 20 reactions. For the full list of associated reactions:

See All Associated Reactions

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference

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	Cyanobacteria	1	Human feces	Metabolic reconstruction

Exposure Sources

Other Exposures

Source Type	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

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 Tetrahydroindol 5 (MMDBc0027423)

MOL for #<Metabolite:0x00007f1240fded10>

3D MOL for #<Metabolite:0x00007f1240fded10>

3D SDF for #<Metabolite:0x00007f1240fded10>

3D-SDF for #<Metabolite:0x00007f1240fded10>

PDB for #<Metabolite:0x00007f1240fded10>

3D PDB for #<Metabolite:0x00007f1240fded10>

SMILES for #<Metabolite:0x00007f1240fded10>

INCHI for #<Metabolite:0x00007f1240fded10>

Structure for #<Metabolite:0x00007f1240fded10>

3D Structure for #<Metabolite:0x00007f1240fded10>