MiMeDB: Showing metabocard for Chrysogine (MMDBc0009966)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2021-05-15 02:18:53 UTC

Update Date

2025-10-07 16:05:40 UTC

Metabolite ID

MMDBc0009966

Metabolite Identification

Common Name

Chrysogine

Description

Chrysogine is a nonribosomal peptide belonging to the chemical class of metabolites. This compound has garnered attention in biomedical literature due to its association with various biological functions and its presence in different fungal species. Phylogenetic analysis has revealed that chrysogine is part of a group of distinct nonribosomal peptide synthetases (NRPSs) linked to diverse biological activities (PMID:40974433 ). It has been isolated alongside other metabolites from fungal extracts, indicating its significance in the metabolic profiles of these organisms (PMID:40812239 ). In Aspergillus flavus, chrysogine is one of several compounds identified, suggesting its potential role in the fungal metabolic landscape (PMID:39130166 ). Additionally, studies on coculture methods have shown enhanced levels of chrysogine relative to monocultures, highlighting its biosynthetic potential (PMID:37630296 ). Investigations into the chrysogine biosynthetic pathway have unveiled unique assembly mechanisms involving nonribosomal peptide synthases, further emphasizing its biochemical importance (PMID:32796640 ). Overall, chrysogine represents a notable example of fungal metabolites with potential implications in both chemistry and biology, warranting further exploration of its biosynthetic pathways and biological activities.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152104182D          

 15 16  0  0  1  0            999 V2000
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.8250    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  3  2  2  0  0  0  0
  4  2  1  0  0  0  0
  5  3  1  0  0  0  0
  6  1  1  0  0  0  0
  7  4  2  0  0  0  0
  8  5  2  0  0  0  0
  8  7  1  0  0  0  0
  9  6  1  0  0  0  0
 10  7  1  0  0  0  0
 11  8  1  0  0  0  0
 11  9  2  0  0  0  0
 12  9  1  0  0  0  0
 12 10  2  0  0  0  0
  6 13  1  1  0  0  0
 14 10  1  0  0  0  0
  6 15  1  1  0  0  0
M  END
> <DATABASE_ID>
MMDBc0009966

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@@](C)(O)C1=NC2=CC=CC=C2C(O)=N1

> <INCHI_IDENTIFIER>
InChI=1S/C10H10N2O2/c1-6(13)9-11-8-5-3-2-4-7(8)10(14)12-9/h2-6,13H,1H3,(H,11,12,14)/t6-/m0/s1

> <INCHI_KEY>
BMBSGGZMJQTQSO-LURJTMIESA-N

> <FORMULA>
C10H10N2O2

> <MOLECULAR_WEIGHT>
190.202

> <EXACT_MASS>
190.07422757

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
24

> <JCHEM_AVERAGE_POLARIZABILITY>
19.341146768133047

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-[(1S)-1-hydroxyethyl]quinazolin-4-ol

> <ALOGPS_LOGP>
1.22

> <JCHEM_LOGP>
2.0116771673333336

> <ALOGPS_LOGS>
-1.38

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.523403053787092

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.99163076919998

> <JCHEM_PKA_STRONGEST_BASIC>
0.2954896449375224

> <JCHEM_POLAR_SURFACE_AREA>
66.24000000000001

> <JCHEM_REFRACTIVITY>
51.9154

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.00e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-[(1S)-1-hydroxyethyl]quinazolin-4-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       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0       2.667  -3.080   0.000  0.00  0.00           N+0
HETATM   12  N   UNK     0       4.001  -0.770   0.000  0.00  0.00           N+0
HETATM   13  O   UNK     0       5.335  -4.620   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0       2.667   1.540   0.000  0.00  0.00           O+0
HETATM   15  H   UNK     0       5.335  -1.540   0.000  0.00  0.00           H+0
CONECT    1    6                                                            
CONECT    2    3    4                                                       
CONECT    3    2    5                                                       
CONECT    4    2    7                                                       
CONECT    5    3    8                                                       
CONECT    6    1    9   13   15                                             
CONECT    7    4    8   10                                                  
CONECT    8    5    7   11                                                  
CONECT    9    6   11   12                                                  
CONECT   10    7   12   14                                                  
CONECT   11    8    9                                                       
CONECT   12    9   10                                                       
CONECT   13    6                                                            
CONECT   14   10                                                            
CONECT   15    6                                                            
MASTER        0    0    0    0    0    0    0    0   15    0   32    0
END

Synonyms

Not Available

Molecular Formula

C₁₀H₁₀N₂O₂

Average Mass

190.202

Monoisotopic Mass

190.07422757

IUPAC Name

2-[(1S)-1-hydroxyethyl]quinazolin-4-ol

Traditional Name

2-[(1S)-1-hydroxyethyl]quinazolin-4-ol

CAS Registry Number

Not Available

SMILES

[H][C@@](C)(O)C1=NC2=CC=CC=C2C(O)=N1

InChI Identifier

InChI=1S/C10H10N2O2/c1-6(13)9-11-8-5-3-2-4-7(8)10(14)12-9/h2-6,13H,1H3,(H,11,12,14)/t6-/m0/s1

InChI Key

BMBSGGZMJQTQSO-LURJTMIESA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as quinazolines. Quinazolines are compounds containing a quinazoline moiety, which is made up of two fused six-member aromatic rings, a benzene ring and a pyrimidine ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Diazanaphthalenes

Sub Class

Benzodiazines

Direct Parent

Quinazolines

Alternative Parents

Substituents

Quinazoline
Pyrimidone
Pyrimidine
Benzenoid
Vinylogous amide
Heteroaromatic compound
Secondary alcohol
Azacycle
Alcohol
Hydrocarbon derivative
Aromatic alcohol
Organic oxide
Organic oxygen compound
Organic nitrogen compound
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	8 g/L	ALOGPS
logP	1.22	ALOGPS
logP	2.01	ChemAxon
logS	-1.4	ALOGPS
pKa (Strongest Acidic)	11.99	ChemAxon
pKa (Strongest Basic)	0.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	66.24 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	51.92 m³·mol⁻¹	ChemAxon
Polarizability	19.34 Å³	ChemAxon
Number of Rings	2	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

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	Species

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	7	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

9291957

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11116825

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

CMMC Knowledgebase

BMBSGGZMJQTQSO-LURJTMIESA-N

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 Chrysogine (MMDBc0009966)

MOL for #<Metabolite:0x00007f2abaa36ce0>

3D MOL for #<Metabolite:0x00007f2abaa36ce0>

3D SDF for #<Metabolite:0x00007f2abaa36ce0>

3D-SDF for #<Metabolite:0x00007f2abaa36ce0>

PDB for #<Metabolite:0x00007f2abaa36ce0>

3D PDB for #<Metabolite:0x00007f2abaa36ce0>

SMILES for #<Metabolite:0x00007f2abaa36ce0>

INCHI for #<Metabolite:0x00007f2abaa36ce0>

Structure for #<Metabolite:0x00007f2abaa36ce0>

3D Structure for #<Metabolite:0x00007f2abaa36ce0>