MiMeDB: Showing metabocard for 10-Oxodehydrodihydrobotrydial (MMDBc0007004)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2021-05-15 00:21:10 UTC

Update Date

2025-10-07 16:05:16 UTC

Metabolite ID

MMDBc0007004

Metabolite Identification

Common Name

10-Oxodehydrodihydrobotrydial

Description

10-Oxodehydrodihydrobotrydial is a botryane-type metabolite characterized by its unique structural features and is classified within the chemical class of terpenoids. This compound has been identified as part of a complex mixture of heterodimeric botryane ethers, including other related compounds, isolated from the solid cultures of the insect-associated fungus Hypocrea sp. (PMID:27328173 ). The biosynthetic pathways leading to 10-oxodehydrodihydrobotrydial suggest a mixed-biogenetic origin, potentially involving precursors akin to coumarin and dihydrobotrydiol, indicating its intricate relationship with other metabolites in fungal metabolism (PMID:24490837 ). The presence of this compound in fungal cultures highlights its possible ecological role and underscores the diverse chemical arsenal produced by fungi, which may have implications for biological activity and interactions within their environments.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152102212D          

 17 19  0  0  1  0            999 V2000
    1.4326   -0.4748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0325    3.5918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1393    2.9428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6393    2.5387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8514    0.8306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9377    1.6511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7713    2.7713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7799    1.6511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5189    0.3457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6913    1.9867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2725    0.6813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3588    1.5017    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1987    0.3457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9463    2.7713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0262    1.9867    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3141   -0.4712    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8661    0.8306    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  2  0  0  0  0
  9  1  1  0  0  0  0
  9  5  1  0  0  0  0
 10  6  1  0  0  0  0
 11  9  2  0  0  0  0
 12 10  2  0  0  0  0
 12 11  1  0  0  0  0
 13 11  1  0  0  0  0
 14  2  1  0  0  0  0
 14  3  1  0  0  0  0
 14  7  1  0  0  0  0
 14 10  1  0  0  0  0
 15  4  1  1  0  0  0
 15  7  1  0  0  0  0
 15  8  1  0  0  0  0
 15 12  1  0  0  0  0
 16 13  2  0  0  0  0
 17  8  1  0  0  0  0
 17 13  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0007004

> <DATABASE_NAME>
MIME

> <SMILES>
CC1=C2C3=C(C=C1)C(C)(C)C[C@]3(C)COC2=O

> <INCHI_IDENTIFIER>
InChI=1S/C15H18O2/c1-9-5-6-10-12-11(9)13(16)17-8-15(12,4)7-14(10,2)3/h5-6H,7-8H2,1-4H3/t15-/m1/s1

> <INCHI_KEY>
CAMCSBCRRUTMEK-OAHLLOKOSA-N

> <FORMULA>
C15H18O2

> <MOLECULAR_WEIGHT>
230.307

> <EXACT_MASS>
230.13067982

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
35

> <JCHEM_AVERAGE_POLARIZABILITY>
25.75428652498718

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(4S)-2,2,4,9-tetramethyl-6-oxatricyclo[6.3.1.0^{4,12}]dodeca-1(12),8,10-trien-7-one

> <ALOGPS_LOGP>
4.07

> <JCHEM_LOGP>
3.7097680549999996

> <ALOGPS_LOGS>
-4.49

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-6.91109954423277

> <JCHEM_POLAR_SURFACE_AREA>
26.3

> <JCHEM_REFRACTIVITY>
67.5665

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.38e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(4S)-2,2,4,9-tetramethyl-6-oxatricyclo[6.3.1.0^{4,12}]dodeca-1(12),8,10-trien-7-one

> <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       2.674  -0.886   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.794   6.705   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.127   5.493   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.793   4.739   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.589   1.550   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.750   3.082   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.173   5.173   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.056   3.082   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.835   0.645   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.157   3.708   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.242   1.272   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.403   2.803   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.971   0.645   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.633   5.173   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.649   3.708   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       6.186  -0.880   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       7.217   1.550   0.000  0.00  0.00           O+0
CONECT    1    9                                                            
CONECT    2   14                                                            
CONECT    3   14                                                            
CONECT    4   15                                                            
CONECT    5    6    9                                                       
CONECT    6    5   10                                                       
CONECT    7   14   15                                                       
CONECT    8   15   17                                                       
CONECT    9    1    5   11                                                  
CONECT   10    6   12   14                                                  
CONECT   11    9   12   13                                                  
CONECT   12   10   11   15                                                  
CONECT   13   11   16   17                                                  
CONECT   14    2    3    7   10                                             
CONECT   15    4    7    8   12                                             
CONECT   16   13                                                            
CONECT   17    8   13                                                       
MASTER        0    0    0    0    0    0    0    0   17    0   38    0
END

Synonyms

Not Available

Molecular Formula

C₁₅H₁₈O₂

Average Mass

230.307

Monoisotopic Mass

230.13067982

IUPAC Name

(4S)-2,2,4,9-tetramethyl-6-oxatricyclo[6.3.1.0^{4,12}]dodeca-1(12),8,10-trien-7-one

Traditional Name

(4S)-2,2,4,9-tetramethyl-6-oxatricyclo[6.3.1.0^{4,12}]dodeca-1(12),8,10-trien-7-one

CAS Registry Number

Not Available

SMILES

CC1=C2C3=C(C=C1)C(C)(C)C[C@]3(C)COC2=O

InChI Identifier

InChI=1S/C15H18O2/c1-9-5-6-10-12-11(9)13(16)17-8-15(12,4)7-14(10,2)3/h5-6H,7-8H2,1-4H3/t15-/m1/s1

InChI Key

CAMCSBCRRUTMEK-OAHLLOKOSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 2-benzopyrans. These are organic aromatic compounds that 1-benzopyran, a bicyclic compound made up of a benzene ring fused to a pyran, so that the oxygen atom is at the 2-position.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

2-benzopyrans

Direct Parent

2-benzopyrans

Alternative Parents

Substituents

2-benzopyran
Indane
Benzenoid
Lactone
Carboxylic acid ester
Oxacycle
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen 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	0.0074 g/L	ALOGPS
logP	4.07	ALOGPS
logP	3.71	ChemAxon
logS	-4.5	ALOGPS
pKa (Strongest Basic)	-6.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	26.3 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	67.57 m³·mol⁻¹	ChemAxon
Polarizability	25.75 Å³	ChemAxon
Number of Rings	3	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 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
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-22	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	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

C00021655

Chemspider ID

9032568

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10857277

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 10-Oxodehydrodihydrobotrydial (MMDBc0007004)

MOL for #<Metabolite:0x00007f2ac537d6a0>

3D MOL for #<Metabolite:0x00007f2ac537d6a0>

3D SDF for #<Metabolite:0x00007f2ac537d6a0>

3D-SDF for #<Metabolite:0x00007f2ac537d6a0>

PDB for #<Metabolite:0x00007f2ac537d6a0>

3D PDB for #<Metabolite:0x00007f2ac537d6a0>

SMILES for #<Metabolite:0x00007f2ac537d6a0>

INCHI for #<Metabolite:0x00007f2ac537d6a0>

Structure for #<Metabolite:0x00007f2ac537d6a0>

3D Structure for #<Metabolite:0x00007f2ac537d6a0>