MiMeDB: Showing metabocard for Ficiolide K (MMDBc0006204)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-14 23:31:16 UTC

Update Date

2022-08-31 06:25:03 UTC

Metabolite ID

MMDBc0006204

Metabolite Identification

Common Name

Ficiolide K

Description

Ficiolide K belongs to the class of organic compounds known as fatty alcohols. These are aliphatic alcohols consisting of a chain of a least six carbon atoms. Based on a literature review very few articles have been published on Ficiolide K.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152101312D          

 27 28  0  0  1  0            999 V2000
    4.0520    5.8483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1941    5.8483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9086    5.4358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4796    5.4358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6230    5.8483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2348    5.8483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1497    4.8893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3375    5.4358    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.8482    5.6573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9493    5.4358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0599    5.9005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3166    4.6131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3783    5.4358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9214    4.0519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3375    4.6108    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9493    4.6108    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9369    6.7163    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5486    4.3117    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7372    4.1749    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1841    4.9705    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6638    5.8483    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3375    6.2608    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4094    6.2621    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3037    6.2304    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6528    5.1030    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2027    5.4666    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6782    3.2636    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  3  2  1  0  0  0  0
  4  2  1  0  0  0  0
  5  3  1  0  0  0  0
  6  4  2  0  0  0  0
  8  1  1  0  0  0  0
  8  5  1  0  0  0  0
  9  7  1  0  0  0  0
  6 10  1  4  0  0  0
 11  9  1  0  0  0  0
 13 11  1  0  0  0  0
 13 12  1  0  0  0  0
 14 12  1  0  0  0  0
  8 15  1  6  0  0  0
 16 10  2  0  0  0  0
 17 11  1  0  0  0  0
 18 12  1  0  0  0  0
 19  7  1  0  0  0  0
 19 14  1  0  0  0  0
 20  9  1  0  0  0  0
 20 14  1  0  0  0  0
 21 10  1  0  0  0  0
 21 13  1  0  0  0  0
  8 22  1  6  0  0  0
 23  9  1  0  0  0  0
 24 11  1  0  0  0  0
 25 12  1  0  0  0  0
 26 13  1  0  0  0  0
 27 14  1  0  0  0  0
M  END


  Mrv1652305152101312D          

 27 28  0  0  1  0            999 V2000
    4.0520    5.8483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1941    5.8483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9086    5.4358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4796    5.4358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6230    5.8483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2348    5.8483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1497    4.8893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3375    5.4358    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.8482    5.6573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9493    5.4358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0599    5.9005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3166    4.6131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3783    5.4358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9214    4.0519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3375    4.6108    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9493    4.6108    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9369    6.7163    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5486    4.3117    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7372    4.1749    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1841    4.9705    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6638    5.8483    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3375    6.2608    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4094    6.2621    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3037    6.2304    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6528    5.1030    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2027    5.4666    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6782    3.2636    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  3  2  1  0  0  0  0
  4  2  1  0  0  0  0
  5  3  1  0  0  0  0
  6  4  2  0  0  0  0
  8  1  1  0  0  0  0
  8  5  1  0  0  0  0
  9  7  1  0  0  0  0
  6 10  1  4  0  0  0
 11  9  1  0  0  0  0
 13 11  1  0  0  0  0
 13 12  1  0  0  0  0
 14 12  1  0  0  0  0
  8 15  1  6  0  0  0
 16 10  2  0  0  0  0
 17 11  1  0  0  0  0
 18 12  1  0  0  0  0
 19  7  1  0  0  0  0
 19 14  1  0  0  0  0
 20  9  1  0  0  0  0
 20 14  1  0  0  0  0
 21 10  1  0  0  0  0
 21 13  1  0  0  0  0
  8 22  1  6  0  0  0
 23  9  1  0  0  0  0
 24 11  1  0  0  0  0
 25 12  1  0  0  0  0
 26 13  1  0  0  0  0
 27 14  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0006204

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@](C)(O)CCCC=CC(=O)OC1([H])C([H])(O)C2([H])COC([H])(O2)C1([H])O

> <INCHI_IDENTIFIER>
InChI=1S/C14H22O7/c1-8(15)5-3-2-4-6-10(16)21-13-11(17)9-7-19-14(20-9)12(13)18/h4,6,8-9,11-15,17-18H,2-3,5,7H2,1H3/t8-,9?,11?,12?,13?,14?/m1/s1

> <INCHI_KEY>
VHYHVKOVKKLPQI-LLSZIJKQSA-N

> <FORMULA>
C14H22O7

> <MOLECULAR_WEIGHT>
302.323

> <EXACT_MASS>
302.136553048

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
43

> <JCHEM_AVERAGE_POLARIZABILITY>
30.210854550407845

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2,4-dihydroxy-6,8-dioxabicyclo[3.2.1]octan-3-yl (7R)-7-hydroxyoct-2-enoate

> <ALOGPS_LOGP>
0.01

> <JCHEM_LOGP>
0.3601535026666668

> <ALOGPS_LOGS>
-1.17

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.204530305316514

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.257826411958504

> <JCHEM_PKA_STRONGEST_BASIC>
-1.590516293347123

> <JCHEM_POLAR_SURFACE_AREA>
105.45000000000002

> <JCHEM_REFRACTIVITY>
72.0365

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.03e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2,4-dihydroxy-6,8-dioxabicyclo[3.2.1]octan-3-yl (7R)-7-hydroxyoct-2-enoate

> <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       7.564  10.917   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.229  10.917   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.563  10.147   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.895  10.147   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.896  10.917   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.438  10.917   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -7.746   9.127   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.230  10.147   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -7.183  10.560   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.772  10.147   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -5.712  11.014   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -4.324   8.611   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -4.439  10.147   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -5.453   7.564   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       6.230   8.607   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0      -1.772   8.607   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0      -5.482  12.537   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0      -2.891   8.048   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0      -6.976   7.793   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      -5.944   9.278   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      -3.106  10.917   0.000  0.00  0.00           O+0
HETATM   22  H   UNK     0       6.230  11.687   0.000  0.00  0.00           H+0
HETATM   23  H   UNK     0      -8.231  11.689   0.000  0.00  0.00           H+0
HETATM   24  H   UNK     0      -4.300  11.630   0.000  0.00  0.00           H+0
HETATM   25  H   UNK     0      -3.085   9.526   0.000  0.00  0.00           H+0
HETATM   26  H   UNK     0      -5.978  10.204   0.000  0.00  0.00           H+0
HETATM   27  H   UNK     0      -4.999   6.092   0.000  0.00  0.00           H+0
CONECT    1    8                                                            
CONECT    2    3    4                                                       
CONECT    3    2    5                                                       
CONECT    4    2    6                                                       
CONECT    5    3    8                                                       
CONECT    6    4   10                                                       
CONECT    7    9   19                                                       
CONECT    8    1    5   15   22                                             
CONECT    9    7   11   20   23                                             
CONECT   10    6   16   21                                                  
CONECT   11    9   13   17   24                                             
CONECT   12   13   14   18   25                                             
CONECT   13   11   12   21   26                                             
CONECT   14   12   19   20   27                                             
CONECT   15    8                                                            
CONECT   16   10                                                            
CONECT   17   11                                                            
CONECT   18   12                                                            
CONECT   19    7   14                                                       
CONECT   20    9   14                                                       
CONECT   21   10   13                                                       
CONECT   22    8                                                            
CONECT   23    9                                                            
CONECT   24   11                                                            
CONECT   25   12                                                            
CONECT   26   13                                                            
CONECT   27   14                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   56    0
END

Synonyms

Not Available

Molecular Formula

C₁₄H₂₂O₇

Average Mass

302.323

Monoisotopic Mass

302.136553048

IUPAC Name

2,4-dihydroxy-6,8-dioxabicyclo[3.2.1]octan-3-yl (7R)-7-hydroxyoct-2-enoate

Traditional Name

2,4-dihydroxy-6,8-dioxabicyclo[3.2.1]octan-3-yl (7R)-7-hydroxyoct-2-enoate

CAS Registry Number

Not Available

SMILES

[H][C@](C)(O)CCCC=CC(=O)OC1([H])C([H])(O)C2([H])COC([H])(O2)C1([H])O

InChI Identifier

InChI=1S/C14H22O7/c1-8(15)5-3-2-4-6-10(16)21-13-11(17)9-7-19-14(20-9)12(13)18/h4,6,8-9,11-15,17-18H,2-3,5,7H2,1H3/t8-,9?,11?,12?,13?,14?/m1/s1

InChI Key

VHYHVKOVKKLPQI-LLSZIJKQSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as fatty alcohols. These are aliphatic alcohols consisting of a chain of a least six carbon atoms.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty alcohols

Direct Parent

Fatty alcohols

Alternative Parents

Substituents

Fatty alcohol
Oxepane
Fatty acid ester
Oxane
Monosaccharide
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Meta-dioxolane
Secondary alcohol
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Acetal
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	20.3 g/L	ALOGPS
logP	0.01	ALOGPS
logP	0.36	ChemAxon
logS	-1.2	ALOGPS
pKa (Strongest Acidic)	12.26	ChemAxon
pKa (Strongest Basic)	-1.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	105.45 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	72.04 m³·mol⁻¹	ChemAxon
Polarizability	30.21 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

Metabolic Reactions

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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139584647

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 Ficiolide K (MMDBc0006204)

MOL for #<Metabolite:0x00007f923eae0e98>

3D MOL for #<Metabolite:0x00007f923eae0e98>

3D SDF for #<Metabolite:0x00007f923eae0e98>

3D-SDF for #<Metabolite:0x00007f923eae0e98>

PDB for #<Metabolite:0x00007f923eae0e98>

3D PDB for #<Metabolite:0x00007f923eae0e98>

SMILES for #<Metabolite:0x00007f923eae0e98>

INCHI for #<Metabolite:0x00007f923eae0e98>

Structure for #<Metabolite:0x00007f923eae0e98>

3D Structure for #<Metabolite:0x00007f923eae0e98>