MiMeDB: Showing metabocard for Chrysotriazole A (MMDBc0001792)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-14 20:11:45 UTC

Update Date

2025-10-07 16:04:31 UTC

Metabolite ID

MMDBc0001792

Metabolite Identification

Common Name

Chrysotriazole A

Description

Chrysotriazole A is a triazole derivative that has been identified as a metabolite in various biological systems. Its chemical structure features a triazole ring, which is known for its role in medicinal chemistry and potential biological activities. Although specific biological functions of Chrysotriazole A remain underexplored, its presence in metabolic pathways suggests possible interactions with biological molecules. Limited studies have reported on its properties, including a focus on its synthesis and potential applications in drug development. For instance, research has indicated that triazole compounds can exhibit antifungal and antibacterial properties, which may hint at the biological relevance of Chrysotriazole A (PMID: 27609231 ). However, comprehensive data on its pharmacological effects and mechanisms of action are scarce, indicating a need for further investigation into its biological significance (PMID: 30541068 ). Overall, while Chrysotriazole A represents an interesting compound within the triazole class, the current literature provides only a preliminary understanding of its chemical and biological implications.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305142122112D          

 23 25  0  0  0  0            999 V2000
    6.7286    1.2802    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8602   -1.9055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0367    2.0009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3222    0.7634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3222    2.4134    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6078    1.1759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1594    0.7703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3748    0.5154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7512    0.7634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6010   -0.5887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3387   -1.3312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0367    1.1759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6078    2.0009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7725    0.2183    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2032   -0.2916    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8163   -0.8436    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7512   -0.0616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0837   -0.5465    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.1637   -1.3312    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4186   -0.5465    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1067    2.4134    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5571    0.4732    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6448   -1.6506    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  5  3  1  0  0  0  0
  6  4  2  0  0  0  0
  8  7  2  0  0  0  0
 12  3  2  0  0  0  0
 12  4  1  0  0  0  0
 12  9  1  0  0  0  0
 13  5  2  0  0  0  0
 13  6  1  0  0  0  0
 14  7  1  0  0  0  0
 14 10  2  0  0  0  0
 15  8  1  0  0  0  0
 16 10  1  0  0  0  0
 16 15  2  0  0  0  0
 17  9  1  0  0  0  0
 18 11  1  0  0  0  0
 18 17  2  0  0  0  0
 19 11  2  0  0  0  0
 20 15  1  0  0  0  0
 20 17  1  0  0  0  0
 20 19  1  0  0  0  0
 21 13  1  0  0  0  0
 22  1  1  0  0  0  0
 22 14  1  0  0  0  0
 23  2  1  0  0  0  0
 23 16  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0001792

> <DATABASE_NAME>
MIME

> <SMILES>
COC1=CC(OC)=C(C=C1)N1N=CN=C1CC1=CC=C(O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C17H17N3O3/c1-22-14-7-8-15(16(10-14)23-2)20-17(18-11-19-20)9-12-3-5-13(21)6-4-12/h3-8,10-11,21H,9H2,1-2H3

> <INCHI_KEY>
VVAYTQZCXQEHFX-UHFFFAOYSA-N

> <FORMULA>
C17H17N3O3

> <MOLECULAR_WEIGHT>
311.341

> <EXACT_MASS>
311.126991419

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
40

> <JCHEM_AVERAGE_POLARIZABILITY>
32.20195805249759

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-{[1-(2,4-dimethoxyphenyl)-1H-1,2,4-triazol-5-yl]methyl}phenol

> <ALOGPS_LOGP>
2.80

> <JCHEM_LOGP>
2.7110413779999996

> <ALOGPS_LOGS>
-3.44

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.875569085483763

> <JCHEM_PKA_STRONGEST_BASIC>
2.1083169394197223

> <JCHEM_POLAR_SURFACE_AREA>
69.4

> <JCHEM_REFRACTIVITY>
87.6637

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.13e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-{[2-(2,4-dimethoxyphenyl)-1,2,4-triazol-3-yl]methyl}phenol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 14-MAY-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   14-MAY-21         0                                  
HETATM    1  C   UNK     0      12.560   2.390   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.206  -3.557   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.802   3.735   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.468   1.425   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.468   4.505   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.134   2.195   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.631   1.438   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.166   0.962   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.136   1.425   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.455  -1.099   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.366  -2.485   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.802   2.195   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.134   3.735   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.775   0.407   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.846  -0.544   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.990  -1.575   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.136  -0.115   0.000  0.00  0.00           C+0
HETATM   18  N   UNK     0       3.890  -1.020   0.000  0.00  0.00           N+0
HETATM   19  N   UNK     0       5.906  -2.485   0.000  0.00  0.00           N+0
HETATM   20  N   UNK     0       6.381  -1.020   0.000  0.00  0.00           N+0
HETATM   21  O   UNK     0      -0.199   4.505   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      12.240   0.883   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       8.670  -3.081   0.000  0.00  0.00           O+0
CONECT    1   22                                                            
CONECT    2   23                                                            
CONECT    3    5   12                                                       
CONECT    4    6   12                                                       
CONECT    5    3   13                                                       
CONECT    6    4   13                                                       
CONECT    7    8   14                                                       
CONECT    8    7   15                                                       
CONECT    9   12   17                                                       
CONECT   10   14   16                                                       
CONECT   11   18   19                                                       
CONECT   12    3    4    9                                                  
CONECT   13    5    6   21                                                  
CONECT   14    7   10   22                                                  
CONECT   15    8   16   20                                                  
CONECT   16   10   15   23                                                  
CONECT   17    9   18   20                                                  
CONECT   18   11   17                                                       
CONECT   19   11   20                                                       
CONECT   20   15   17   19                                                  
CONECT   21   13                                                            
CONECT   22    1   14                                                       
CONECT   23    2   16                                                       
MASTER        0    0    0    0    0    0    0    0   23    0   50    0
END

Synonyms

Not Available

Molecular Formula

C₁₇H₁₇N₃O₃

Average Mass

311.341

Monoisotopic Mass

311.126991419

IUPAC Name

4-{[1-(2,4-dimethoxyphenyl)-1H-1,2,4-triazol-5-yl]methyl}phenol

Traditional Name

4-{[2-(2,4-dimethoxyphenyl)-1,2,4-triazol-3-yl]methyl}phenol

CAS Registry Number

Not Available

SMILES

COC1=CC(OC)=C(C=C1)N1N=CN=C1CC1=CC=C(O)C=C1

InChI Identifier

InChI=1S/C17H17N3O3/c1-22-14-7-8-15(16(10-14)23-2)20-17(18-11-19-20)9-12-3-5-13(21)6-4-12/h3-8,10-11,21H,9H2,1-2H3

InChI Key

VVAYTQZCXQEHFX-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenyl-1,2,4-triazoles. These are organic compounds containing a 1,2,4-triazole substituted by a phenyl group.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Azoles

Sub Class

Triazoles

Direct Parent

Phenyl-1,2,4-triazoles

Alternative Parents

Substituents

Phenyl-1,2,4-triazole
M-dimethoxybenzene
Dimethoxybenzene
Methoxyaniline
Phenoxy compound
Anisole
Phenol ether
Methoxybenzene
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
Phenol
Monocyclic benzene moiety
Benzenoid
Heteroaromatic compound
Ether
Azacycle
Organic nitrogen compound
Organooxygen compound
Organonitrogen compound
Hydrocarbon derivative
Organic oxygen compound
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.11 g/L	ALOGPS
logP	2.8	ALOGPS
logP	2.71	ChemAxon
logS	-3.4	ALOGPS
pKa (Strongest Acidic)	9.88	ChemAxon
pKa (Strongest Basic)	2.11	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	69.4 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	87.66 m³·mol⁻¹	ChemAxon
Polarizability	32.2 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Spectrum Type	Description	Splash Key	Deposition Date	View
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2022-08-08	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	Not Available	2022-08-09	View Spectrum
MS	Mass Spectrum (Electron Ionization)	Not Available	2022-08-06	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-20	View Spectrum

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

This table shows at most 5 pathways. For the full list of associated pathways:

See All Associated Bacterial Pathways

Name	SMPDB/PathBank

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
Eukaryota/Fungi	Ascomycota	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

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

29215632

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

71605365

PDB ID

Not Available

ChEBI ID

Not Available

CMMC Knowledgebase

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 Chrysotriazole A (MMDBc0001792)

MOL for #<Metabolite:0x00005654abc3ad10>

3D MOL for #<Metabolite:0x00005654abc3ad10>

3D SDF for #<Metabolite:0x00005654abc3ad10>

3D-SDF for #<Metabolite:0x00005654abc3ad10>

PDB for #<Metabolite:0x00005654abc3ad10>

3D PDB for #<Metabolite:0x00005654abc3ad10>

SMILES for #<Metabolite:0x00005654abc3ad10>

INCHI for #<Metabolite:0x00005654abc3ad10>

Structure for #<Metabolite:0x00005654abc3ad10>

3D Structure for #<Metabolite:0x00005654abc3ad10>