MiMeDB: Showing metabocard for Hynapene C (MMDBc0004266)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-14 22:19:40 UTC

Update Date

2025-10-07 16:04:51 UTC

Metabolite ID

MMDBc0004266

Metabolite Identification

Common Name

Hynapene C

Description

Hynapene C is a metabolite classified within the chemical class of alkaloids. There is limited literature available on Hynapene C, and further research is needed to fully understand its properties and potential biological significance.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152100192D          

 25 26  0  0  0  0            999 V2000
    4.2868    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0980    1.3808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6623   -0.4563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3802    0.3190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4748   -0.5995    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4323    0.4623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7570   -1.3748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    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  0  0  0  0  0  0  0  0  0  0
   -1.2267   -2.0067    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5694   -1.5180    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
   -0.1320   -1.0882    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9105    0.9510    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0051    0.0325    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9626   -0.1697    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  4  1  0  0  0  0
  6  4  2  0  0  0  0
  8  5  2  0  0  0  0
  9  7  2  0  0  0  0
 12  1  1  0  0  0  0
 12 10  1  0  0  0  0
 12 11  1  0  0  0  0
 13  2  1  0  0  0  0
 13 10  1  0  0  0  0
 14  7  1  0  0  0  0
 14 11  1  0  0  0  0
 15  6  1  0  0  0  0
 16 13  1  0  0  0  0
 16 14  1  0  0  0  0
 17 16  1  0  0  0  0
 18  3  1  0  0  0  0
 18  8  1  0  0  0  0
 18  9  1  0  0  0  0
 18 17  1  0  0  0  0
 19 15  2  0  0  0  0
 20 15  1  0  0  0  0
 21 17  2  0  0  0  0
 22  4  1  0  0  0  0
 23  5  1  0  0  0  0
 24  6  1  0  0  0  0
 25  8  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0004266

> <DATABASE_NAME>
MIME

> <SMILES>
[H]\C(\C(\[H])=C(/[H])C1(C)C=CC2CC(C)CC(C)C2C1=O)=C(\[H])C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C18H24O3/c1-12-10-13(2)16-14(11-12)7-9-18(3,17(16)21)8-5-4-6-15(19)20/h4-9,12-14,16H,10-11H2,1-3H3,(H,19,20)/b6-4+,8-5+

> <INCHI_KEY>
NUIMPRVESYOKAD-HLQBBKRNSA-N

> <FORMULA>
C18H24O3

> <MOLECULAR_WEIGHT>
288.387

> <EXACT_MASS>
288.172544633

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
33.23945954131513

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2E,4E)-5-(2,6,8-trimethyl-1-oxo-1,2,4a,5,6,7,8,8a-octahydronaphthalen-2-yl)penta-2,4-dienoic acid

> <ALOGPS_LOGP>
4.49

> <JCHEM_LOGP>
4.148662911000001

> <ALOGPS_LOGS>
-4.59

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.386928206336064

> <JCHEM_PKA_STRONGEST_BASIC>
-7.706475496937642

> <JCHEM_POLAR_SURFACE_AREA>
54.370000000000005

> <JCHEM_REFRACTIVITY>
86.3389

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.43e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2E,4E)-5-(2,6,8-trimethyl-1-oxo-4a,5,6,7,8,8a-hexahydronaphthalen-2-yl)penta-2,4-dienoic acid

> <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       8.002   4.620   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.183   2.577   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.236  -0.852   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.710   0.595   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.753  -1.119   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.807   0.863   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.335   4.620   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.668   3.850   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -3.280  -2.566   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -2.290  -3.746   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      -4.796  -2.834   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       2.667   0.000   0.000  0.00  0.00           O+0
HETATM   22  H   UNK     0      -0.246  -2.031   0.000  0.00  0.00           H+0
HETATM   23  H   UNK     0      -1.700   1.775   0.000  0.00  0.00           H+0
HETATM   24  H   UNK     0      -3.743   0.061   0.000  0.00  0.00           H+0
HETATM   25  H   UNK     0       1.797  -0.317   0.000  0.00  0.00           H+0
CONECT    1   12                                                            
CONECT    2   13                                                            
CONECT    3   18                                                            
CONECT    4    5    6   22                                                  
CONECT    5    4    8   23                                                  
CONECT    6    4   15   24                                                  
CONECT    7    9   14                                                       
CONECT    8    5   18   25                                                  
CONECT    9    7   18                                                       
CONECT   10   12   13                                                       
CONECT   11   12   14                                                       
CONECT   12    1   10   11                                                  
CONECT   13    2   10   16                                                  
CONECT   14    7   11   16                                                  
CONECT   15    6   19   20                                                  
CONECT   16   13   14   17                                                  
CONECT   17   16   18   21                                                  
CONECT   18    3    8    9   17                                             
CONECT   19   15                                                            
CONECT   20   15                                                            
CONECT   21   17                                                            
CONECT   22    4                                                            
CONECT   23    5                                                            
CONECT   24    6                                                            
CONECT   25    8                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   52    0
END

Synonyms

Value	Source
5-(3-Ene-1-oxo-2,6,8-trimethyldecalin-2-yl)-2,4-pentadienoic acid	MeSH

Molecular Formula

C₁₈H₂₄O₃

Average Mass

288.387

Monoisotopic Mass

288.172544633

IUPAC Name

(2E,4E)-5-(2,6,8-trimethyl-1-oxo-1,2,4a,5,6,7,8,8a-octahydronaphthalen-2-yl)penta-2,4-dienoic acid

Traditional Name

(2E,4E)-5-(2,6,8-trimethyl-1-oxo-4a,5,6,7,8,8a-hexahydronaphthalen-2-yl)penta-2,4-dienoic acid

CAS Registry Number

Not Available

SMILES

[H]\C(\C(\[H])=C(/[H])C1(C)C=CC2CC(C)CC(C)C2C1=O)=C(\[H])C(O)=O

InChI Identifier

InChI=1S/C18H24O3/c1-12-10-13(2)16-14(11-12)7-9-18(3,17(16)21)8-5-4-6-15(19)20/h4-9,12-14,16H,10-11H2,1-3H3,(H,19,20)/b6-4+,8-5+

InChI Key

NUIMPRVESYOKAD-HLQBBKRNSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as medium-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 4 and 12 carbon atoms.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acids and conjugates

Direct Parent

Medium-chain fatty acids

Alternative Parents

Substituents

Medium-chain fatty acid
Cyclohexenone
Unsaturated fatty acid
Ketone
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic 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	4.49	ALOGPS
logP	4.15	ChemAxon
logS	-4.6	ALOGPS
pKa (Strongest Acidic)	4.39	ChemAxon
pKa (Strongest Basic)	-7.7	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	54.37 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	86.34 m³·mol⁻¹	ChemAxon
Polarizability	33.24 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

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 sputum; Human ; 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

C00016921

Chemspider ID

4947684

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

6443715

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 Hynapene C (MMDBc0004266)

MOL for #<Metabolite:0x00007fb4ccbbafe8>

3D MOL for #<Metabolite:0x00007fb4ccbbafe8>

3D SDF for #<Metabolite:0x00007fb4ccbbafe8>

3D-SDF for #<Metabolite:0x00007fb4ccbbafe8>

PDB for #<Metabolite:0x00007fb4ccbbafe8>

3D PDB for #<Metabolite:0x00007fb4ccbbafe8>

SMILES for #<Metabolite:0x00007fb4ccbbafe8>

INCHI for #<Metabolite:0x00007fb4ccbbafe8>

Structure for #<Metabolite:0x00007fb4ccbbafe8>

3D Structure for #<Metabolite:0x00007fb4ccbbafe8>