MiMeDB: Showing metabocard for 4'-(4,5-dimethyl-1,3-dioxolan-2-yl)methyl-phenol (MMDBc0008298)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2021-05-15 01:11:43 UTC

Update Date

2025-10-07 16:05:26 UTC

Metabolite ID

MMDBc0008298

Metabolite Identification

Common Name

4'-(4,5-dimethyl-1,3-dioxolan-2-yl)methyl-phenol

Description

4'-(4,5-dimethyl-1,3-dioxolan-2-yl)methyl-phenol is a phenolic compound classified as a metabolite, which has been identified in the context of marine-derived fungi. This compound was isolated alongside two other novel substances from the marine-derived fungus Trichoderma atroviride G 20-12, highlighting its potential significance in natural product chemistry and pharmacology. The presence of the dioxolane ring suggests interesting chemical properties that may contribute to its biological activity. Phenolic compounds are known for their antioxidant properties and potential therapeutic applications, which may extend to this compound as well. Further studies could elucidate its specific biological effects and mechanisms of action, as well as its potential utility in drug development or as a biochemical tool. The isolation of 4'-(4,5-dimethyl-1,3-dioxolan-2-yl)methyl-phenol from a marine source underscores the rich biodiversity of marine organisms and their capacity to produce unique metabolites with possible health benefits (PMID:22582864 ).

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152103112D          

 17 18  0  0  1  0            999 V2000
    0.7376    3.2361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    4.2911    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7613    0.1080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4559    0.6892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4257   -0.6457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1203   -0.0645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6119    1.5291    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0470    2.9812    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7145    3.4661    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2763    0.7754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6052   -0.7319    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1270    2.1965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2697   -1.4856    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3020    2.1965    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3819    2.9812    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0820    3.7960    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4496    3.8406    0.0000 H   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  1  1  6  0  0  0
  9  2  1  1  0  0  0
  9  8  1  0  0  0  0
 10  3  2  0  0  0  0
 10  4  1  0  0  0  0
 10  7  1  0  0  0  0
 11  5  2  0  0  0  0
 11  6  1  0  0  0  0
 12  7  1  0  0  0  0
 13 11  1  0  0  0  0
 14  8  1  0  0  0  0
 14 12  1  0  0  0  0
 15  9  1  0  0  0  0
 15 12  1  0  0  0  0
  8 16  1  1  0  0  0
  9 17  1  6  0  0  0
M  END
> <DATABASE_ID>
MMDBc0008298

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@@]1(C)OC(CC2=CC=C(O)C=C2)O[C@@]1([H])C

> <INCHI_IDENTIFIER>
InChI=1S/C12H16O3/c1-8-9(2)15-12(14-8)7-10-3-5-11(13)6-4-10/h3-6,8-9,12-13H,7H2,1-2H3/t8-,9-/m0/s1

> <INCHI_KEY>
LZNLGTWGIXTYMF-IUCAKERBSA-N

> <FORMULA>
C12H16O3

> <MOLECULAR_WEIGHT>
208.257

> <EXACT_MASS>
208.109944375

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
31

> <JCHEM_AVERAGE_POLARIZABILITY>
22.600304829124525

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-{[(4S,5S)-4,5-dimethyl-1,3-dioxolan-2-yl]methyl}phenol

> <ALOGPS_LOGP>
1.78

> <JCHEM_LOGP>
2.5459446376666666

> <ALOGPS_LOGS>
-2.24

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.077678214163033

> <JCHEM_PKA_STRONGEST_BASIC>
-4.056355693994267

> <JCHEM_POLAR_SURFACE_AREA>
38.69

> <JCHEM_REFRACTIVITY>
57.121100000000006

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.20e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-{[(4S,5S)-4,5-dimethyl-1,3-dioxolan-2-yl]methyl}phenol

> <JCHEM_VEBER_RULE>
1

$$$$

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       1.377   6.041   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.334   8.010   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.288   0.202   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.851   1.286   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.661  -1.205   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.225  -0.120   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -3.009   2.854   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.088   5.565   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.334   6.470   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.382   1.447   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.130  -1.366   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.104   4.100   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -0.503  -2.773   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0      -0.564   4.100   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0      -2.580   5.565   0.000  0.00  0.00           O+0
HETATM   16  H   UNK     0       0.153   7.086   0.000  0.00  0.00           H+0
HETATM   17  H   UNK     0      -2.706   7.169   0.000  0.00  0.00           H+0
CONECT    1    8                                                            
CONECT    2    9                                                            
CONECT    3    5   10                                                       
CONECT    4    6   10                                                       
CONECT    5    3   11                                                       
CONECT    6    4   11                                                       
CONECT    7   10   12                                                       
CONECT    8    1    9   14   16                                             
CONECT    9    2    8   15   17                                             
CONECT   10    3    4    7                                                  
CONECT   11    5    6   13                                                  
CONECT   12    7   14   15                                                  
CONECT   13   11                                                            
CONECT   14    8   12                                                       
CONECT   15    9   12                                                       
CONECT   16    8                                                            
CONECT   17    9                                                            
MASTER        0    0    0    0    0    0    0    0   17    0   36    0
END

Synonyms

Not Available

Molecular Formula

C₁₂H₁₆O₃

Average Mass

208.257

Monoisotopic Mass

208.109944375

IUPAC Name

4-{[(4S,5S)-4,5-dimethyl-1,3-dioxolan-2-yl]methyl}phenol

Traditional Name

4-{[(4S,5S)-4,5-dimethyl-1,3-dioxolan-2-yl]methyl}phenol

CAS Registry Number

Not Available

SMILES

[H][C@@]1(C)OC(CC2=CC=C(O)C=C2)O[C@@]1([H])C

InChI Identifier

InChI=1S/C12H16O3/c1-8-9(2)15-12(14-8)7-10-3-5-11(13)6-4-10/h3-6,8-9,12-13H,7H2,1-2H3/t8-,9-/m0/s1

InChI Key

LZNLGTWGIXTYMF-IUCAKERBSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 1-hydroxy-2-unsubstituted benzenoids. These are phenols that are unsubstituted at the 2-position.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Phenols

Sub Class

1-hydroxy-2-unsubstituted benzenoids

Direct Parent

1-hydroxy-2-unsubstituted benzenoids

Alternative Parents

Substituents

1-hydroxy-2-unsubstituted benzenoid
Monocyclic benzene moiety
Meta-dioxolane
Oxacycle
Organoheterocyclic compound
Acetal
Organic oxygen compound
Hydrocarbon derivative
Organooxygen 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	1.2 g/L	ALOGPS
logP	1.78	ALOGPS
logP	2.55	ChemAxon
logS	-2.2	ALOGPS
pKa (Strongest Acidic)	10.08	ChemAxon
pKa (Strongest Basic)	-4.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	38.69 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	57.12 m³·mol⁻¹	ChemAxon
Polarizability	22.6 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	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	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	Not Available	2022-08-10	View Spectrum
MS	Mass Spectrum (Electron Ionization)	Not Available	2022-08-06	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-21	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-21	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	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	2	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

78441004

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139585257

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

CMMC Knowledgebase

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 4'-(4,5-dimethyl-1,3-dioxolan-2-yl)methyl-phenol (MMDBc0008298)

MOL for #<Metabolite:0x00007f2a98d25e00>

3D MOL for #<Metabolite:0x00007f2a98d25e00>

3D SDF for #<Metabolite:0x00007f2a98d25e00>

3D-SDF for #<Metabolite:0x00007f2a98d25e00>

PDB for #<Metabolite:0x00007f2a98d25e00>

3D PDB for #<Metabolite:0x00007f2a98d25e00>

SMILES for #<Metabolite:0x00007f2a98d25e00>

INCHI for #<Metabolite:0x00007f2a98d25e00>

Structure for #<Metabolite:0x00007f2a98d25e00>

3D Structure for #<Metabolite:0x00007f2a98d25e00>