MiMeDB: Showing metabocard for Hitoyol B (MMDBc0023774)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2021-05-15 13:41:58 UTC

Update Date

2025-10-07 16:07:22 UTC

Metabolite ID

MMDBc0023774

Metabolite Identification

Common Name

Hitoyol B

Description

Hitoyol B is a norsesquiterpenoid, a class of organic compounds characterized by a specific arrangement of carbon atoms and functional groups. Its chemical structure features a unique 4-cyclopentene-1,3-dione moiety, which distinguishes it from other metabolites. Hitoyol B is involved in the biosynthetic pathways of fungi, particularly within the Basidiomycete Coprinopsis cinerea, where it is produced alongside other metabolites such as hitoyol A. The investigation of the lagopodin-hitoyol biosynthetic pathway has revealed intricate details about the mechanisms involved in the synthesis of these compounds, suggesting a complex interplay of enzymatic reactions that contribute to their formation (PMID:32759961 ). This pathway not only enhances our understanding of fungal metabolite production but also provides insights into the potential for synthesizing related compounds, such as lagopodin C, which may share structural similarities and biosynthetic origins (PMID:32759961 ). Overall, Hitoyol B exemplifies the diversity of natural products arising from fungal metabolism and highlights the importance of understanding these biochemical pathways in the context of natural product chemistry.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152115412D          

 18 19  0  0  1  0            999 V2000
    3.0983    0.2646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4715    4.5289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3579    3.8706    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5530    3.2480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7883    0.9320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7242    3.7162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1234    2.4424    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6133    0.9320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4610    2.9343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5334    1.7167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8683    1.7167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5491    3.7076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7958    2.9203    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2008    2.2016    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3262    2.6876    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7488    1.9716    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6529    1.9716    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6058    2.9203    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  8  1  1  0  0  0  0
  8  5  2  0  0  0  0
  9  6  1  0  0  0  0
  9  7  1  0  0  0  0
 10  5  1  0  0  0  0
 11  8  1  0  0  0  0
 12  2  1  0  0  0  0
 12  3  1  0  0  0  0
 12  6  1  0  0  0  0
 13  4  1  6  0  0  0
 13  7  1  0  0  0  0
 13 12  1  0  0  0  0
 14 10  1  6  0  0  0
 14 11  1  0  0  0  0
 13 14  1  1  0  0  0
 15  9  2  0  0  0  0
 16 10  2  0  0  0  0
 17 11  2  0  0  0  0
 14 18  1  6  0  0  0
M  END
> <DATABASE_ID>
MMDBc0023774

> <DATABASE_NAME>
MIME

> <SMILES>
CC1=CC(=O)[C@](O)(C1=O)[C@@]1(C)CC(=O)CC1(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C14H18O4/c1-8-5-10(16)14(18,11(8)17)13(4)7-9(15)6-12(13,2)3/h5,18H,6-7H2,1-4H3/t13-,14-/m0/s1

> <INCHI_KEY>
USNQVQSHCJPDPF-KBPBESRZSA-N

> <FORMULA>
C14H18O4

> <MOLECULAR_WEIGHT>
250.294

> <EXACT_MASS>
250.12050906

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
36

> <JCHEM_AVERAGE_POLARIZABILITY>
25.75619380988902

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S)-2-hydroxy-4-methyl-2-[(1S)-1,2,2-trimethyl-4-oxocyclopentyl]cyclopent-4-ene-1,3-dione

> <ALOGPS_LOGP>
1.55

> <JCHEM_LOGP>
1.9458247786666665

> <ALOGPS_LOGS>
-1.91

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
17.896838607633136

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.999485183099369

> <JCHEM_PKA_STRONGEST_BASIC>
-4.548625047054684

> <JCHEM_POLAR_SURFACE_AREA>
71.44

> <JCHEM_REFRACTIVITY>
66.27680000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.11e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-2-hydroxy-4-methyl-2-[(1S)-1,2,2-trimethyl-4-oxocyclopentyl]cyclopent-4-ene-1,3-dione

> <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       5.783   0.494   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.747   8.454   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.401   7.225   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.766   6.063   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.338   1.740   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.352   6.937   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.097   4.559   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.878   1.740   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.861   5.477   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.862   3.204   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.354   3.204   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.892   6.921   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.352   5.451   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.108   4.110   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -0.609   5.017   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0       1.398   3.680   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       6.819   3.680   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0       4.864   5.451   0.000  0.00  0.00           O+0
CONECT    1    8                                                            
CONECT    2   12                                                            
CONECT    3   12                                                            
CONECT    4   13                                                            
CONECT    5    8   10                                                       
CONECT    6    9   12                                                       
CONECT    7    9   13                                                       
CONECT    8    1    5   11                                                  
CONECT    9    6    7   15                                                  
CONECT   10    5   14   16                                                  
CONECT   11    8   14   17                                                  
CONECT   12    2    3    6   13                                             
CONECT   13    4    7   12   14                                             
CONECT   14   10   11   13   18                                             
CONECT   15    9                                                            
CONECT   16   10                                                            
CONECT   17   11                                                            
CONECT   18   14                                                            
MASTER        0    0    0    0    0    0    0    0   18    0   38    0
END

Synonyms

Not Available

Molecular Formula

C₁₄H₁₈O₄

Average Mass

250.294

Monoisotopic Mass

250.12050906

IUPAC Name

(2S)-2-hydroxy-4-methyl-2-[(1S)-1,2,2-trimethyl-4-oxocyclopentyl]cyclopent-4-ene-1,3-dione

Traditional Name

(2S)-2-hydroxy-4-methyl-2-[(1S)-1,2,2-trimethyl-4-oxocyclopentyl]cyclopent-4-ene-1,3-dione

CAS Registry Number

Not Available

SMILES

CC1=CC(=O)[C@](O)(C1=O)[C@@]1(C)CC(=O)CC1(C)C

InChI Identifier

InChI=1S/C14H18O4/c1-8-5-10(16)14(18,11(8)17)13(4)7-9(15)6-12(13,2)3/h5,18H,6-7H2,1-4H3/t13-,14-/m0/s1

InChI Key

USNQVQSHCJPDPF-KBPBESRZSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as iridoids and derivatives. These are monoterpenes containing a skeleton structurally characterized by the presence of a cylopentane fused to a pyran ( forming a 4,7-dimethylcyclopenta[c]pyran), or a derivative where the pentane moiety is open.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Monoterpenoids

Direct Parent

Iridoids and derivatives

Alternative Parents

Substituents

Monocyclic monoterpenoid
11-noriridane monoterpenoid
Acyloin
Tertiary alcohol
Cyclic ketone
Ketone
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic homomonocyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	3.11 g/L	ALOGPS
logP	1.55	ALOGPS
logP	1.95	ChemAxon
logS	-1.9	ALOGPS
pKa (Strongest Acidic)	11	ChemAxon
pKa (Strongest Basic)	-4.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	71.44 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	66.28 m³·mol⁻¹	ChemAxon
Polarizability	25.76 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

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
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

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	Basidiomycota	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

78439320

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139591065

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 Hitoyol B (MMDBc0023774)

MOL for #<Metabolite:0x00007f8de9a30f10>

3D MOL for #<Metabolite:0x00007f8de9a30f10>

3D SDF for #<Metabolite:0x00007f8de9a30f10>

3D-SDF for #<Metabolite:0x00007f8de9a30f10>

PDB for #<Metabolite:0x00007f8de9a30f10>

3D PDB for #<Metabolite:0x00007f8de9a30f10>

SMILES for #<Metabolite:0x00007f8de9a30f10>

INCHI for #<Metabolite:0x00007f8de9a30f10>

Structure for #<Metabolite:0x00007f8de9a30f10>

3D Structure for #<Metabolite:0x00007f8de9a30f10>