MiMeDB: Showing metabocard for Coruscol A (MMDBc0015217)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2021-05-15 06:05:56 UTC

Update Date

2025-10-07 16:06:22 UTC

Metabolite ID

MMDBc0015217

Metabolite Identification

Common Name

Coruscol A

Description

Coruscol A is a novel metabolite belonging to the chemical class of compounds featuring a 1,3-dioxane ring. This compound was isolated from the mycelium of the marine-derived fungus Penicillium sp., which was obtained from the Okinawan marine bivalve Mytilus coruscus. The structure of coruscol A was elucidated using various spectroscopic techniques, confirming its unique chemical architecture. The discovery of coruscol A highlights the potential of marine fungi as a source of bioactive metabolites, which may have implications in pharmacology and natural product chemistry. The exploration of such metabolites is significant as they may exhibit various biological activities, contributing to the understanding of marine biodiversity and its applications in medicine. The isolation and characterization of coruscol A underscore the importance of marine ecosystems as reservoirs of novel chemical entities that could lead to the development of new therapeutic agents. Further research into the biological properties of coruscol A and its derivatives may reveal additional insights into its potential uses in biomedical applications. (PMID:10869231 )

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152108052D          

 15 15  0  0  1  0            999 V2000
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    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
   -0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  2  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
    0.7145    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    1.6500    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    0.4125    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -0.8250    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0  0  0  0
  3  2  1  0  0  0  0
  6  5  1  0  0  0  0
  7  4  1  6  0  0  0
  7  6  1  0  0  0  0
  8  3  1  1  0  0  0
  9  4  1  0  0  0  0
  6 10  1  6  0  0  0
 11  5  1  0  0  0  0
 11  8  1  0  0  0  0
 12  7  1  0  0  0  0
 12  8  1  0  0  0  0
  6 13  1  1  0  0  0
  7 14  1  6  0  0  0
  8 15  1  6  0  0  0
M  END
> <DATABASE_ID>
MMDBc0015217

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@@]1(O)CO[C@@]([H])(CCC)O[C@@]1([H])CO

> <INCHI_IDENTIFIER>
InChI=1S/C8H16O4/c1-2-3-8-11-5-6(10)7(4-9)12-8/h6-10H,2-5H2,1H3/t6-,7+,8-/m1/s1

> <INCHI_KEY>
RYJRBBKILQAOIA-GJMOJQLCSA-N

> <FORMULA>
C8H16O4

> <MOLECULAR_WEIGHT>
176.212

> <EXACT_MASS>
176.104858995

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
28

> <JCHEM_AVERAGE_POLARIZABILITY>
18.332810858622967

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R,4S,5R)-4-(hydroxymethyl)-2-propyl-1,3-dioxan-5-ol

> <ALOGPS_LOGP>
-0.34

> <JCHEM_LOGP>
0.06645471833333304

> <ALOGPS_LOGS>
0.42

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.707884434356885

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.315529321354816

> <JCHEM_PKA_STRONGEST_BASIC>
-2.980701969601344

> <JCHEM_POLAR_SURFACE_AREA>
58.92

> <JCHEM_REFRACTIVITY>
42.7336

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.65e+02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R,4S,5R)-4-(hydroxymethyl)-2-propyl-1,3-dioxan-5-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       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.667  -3.080   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      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -2.667   1.540   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0       1.334   3.850   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0       2.667  -0.000   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   13  H   UNK     0       0.000   3.080   0.000  0.00  0.00           H+0
HETATM   14  H   UNK     0       1.334   0.770   0.000  0.00  0.00           H+0
HETATM   15  H   UNK     0      -0.000  -1.540   0.000  0.00  0.00           H+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    8                                                       
CONECT    4    7    9                                                       
CONECT    5    6   11                                                       
CONECT    6    5    7   10   13                                             
CONECT    7    4    6   12   14                                             
CONECT    8    3   11   12   15                                             
CONECT    9    4                                                            
CONECT   10    6                                                            
CONECT   11    5    8                                                       
CONECT   12    7    8                                                       
CONECT   13    6                                                            
CONECT   14    7                                                            
CONECT   15    8                                                            
MASTER        0    0    0    0    0    0    0    0   15    0   30    0
END

Synonyms

Not Available

Molecular Formula

C₈H₁₆O₄

Average Mass

176.212

Monoisotopic Mass

176.104858995

IUPAC Name

(2R,4S,5R)-4-(hydroxymethyl)-2-propyl-1,3-dioxan-5-ol

Traditional Name

(2R,4S,5R)-4-(hydroxymethyl)-2-propyl-1,3-dioxan-5-ol

CAS Registry Number

Not Available

SMILES

[H][C@@]1(O)CO[C@@]([H])(CCC)O[C@@]1([H])CO

InChI Identifier

InChI=1S/C8H16O4/c1-2-3-8-11-5-6(10)7(4-9)12-8/h6-10H,2-5H2,1H3/t6-,7+,8-/m1/s1

InChI Key

RYJRBBKILQAOIA-GJMOJQLCSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 1,3-dioxanes. These are organic compounds containing 1,3-dioxane, an aliphatic six-member ring with two oxygen atoms in ring positions 1 and 3.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Dioxanes

Sub Class

1,3-dioxanes

Direct Parent

1,3-dioxanes

Alternative Parents

Substituents

Meta-dioxane
Secondary alcohol
Oxacycle
Acetal
Organic oxygen compound
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Alcohol
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	465 g/L	ALOGPS
logP	-0.34	ALOGPS
logP	0.066	ChemAxon
logS	0.42	ALOGPS
pKa (Strongest Acidic)	13.32	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	58.92 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	42.73 m³·mol⁻¹	ChemAxon
Polarizability	18.33 Å³	ChemAxon
Number of Rings	1	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

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
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

10242572

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

21606535

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

CMMC Knowledgebase

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 Coruscol A (MMDBc0015217)

MOL for #<Metabolite:0x00007f8dc8bcd308>

3D MOL for #<Metabolite:0x00007f8dc8bcd308>

3D SDF for #<Metabolite:0x00007f8dc8bcd308>

3D-SDF for #<Metabolite:0x00007f8dc8bcd308>

PDB for #<Metabolite:0x00007f8dc8bcd308>

3D PDB for #<Metabolite:0x00007f8dc8bcd308>

SMILES for #<Metabolite:0x00007f8dc8bcd308>

INCHI for #<Metabolite:0x00007f8dc8bcd308>

Structure for #<Metabolite:0x00007f8dc8bcd308>

3D Structure for #<Metabolite:0x00007f8dc8bcd308>