MiMeDB: Showing metabocard for african-1-ene (MMDBc0055690)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2022-06-17 20:02:21 UTC

Update Date

2025-10-07 16:09:17 UTC

Metabolite ID

MMDBc0055690

Metabolite Identification

Common Name

african-1-ene

Description

african-1-ene is a sesquiterpene, a class of terpenes composed of three isoprene units. Its chemical structure features a characteristic bicyclic arrangement, which is typical of many sesquiterpenes, contributing to its unique reactivity and potential biological activities. African-1-ene has been isolated from the soft coral Sinularia dissecta, indicating its presence in marine ecosystems and suggesting a role in the chemical ecology of these organisms. In terms of biochemical pathways, sesquiterpenes like african-1-ene are often involved in the biosynthesis of various secondary metabolites, which can serve functions such as defense mechanisms against predators or pathogens. The isolation of african-1-ene alongside other known sesquiterpenes and diterpenoids highlights its potential significance in the study of marine natural products and their applications in pharmacology. The reference for its isolation is documented in the literature, specifically in PMID:12141876 , which provides insights into the diversity of terpenoid compounds found in marine organisms and their potential roles in ecological interactions.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652306172222022D          

 18 20  0  0  1  0            999 V2000
    4.2604    0.3140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2034    1.6466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2266    1.7534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7059   -1.5937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6715   -1.0330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9033   -1.3339    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0798    0.6253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7606   -0.9888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5584    0.7796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6227   -0.2095    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9807   -0.1937    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8244   -0.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3798   -0.6962    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7819    1.0585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5592   -0.7818    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4458    0.5963    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1713   -0.0336    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0663   -1.4594    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  1  0  0  0  0
 10  1  1  6  0  0  0
 10  5  1  0  0  0  0
 11  7  1  0  0  0  0
 11  8  1  0  0  0  0
 12  9  2  0  0  0  0
 12 10  1  0  0  0  0
 13  6  1  0  0  0  0
 13 12  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  9  1  0  0  0  0
 15  4  1  1  0  0  0
 15  8  1  0  0  0  0
 15 11  1  0  0  0  0
 15 13  1  0  0  0  0
 10 16  1  1  0  0  0
 11 17  1  1  0  0  0
 13 18  1  6  0  0  0
M  END
> <DATABASE_ID>
MMDBc0055690

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@]12C[C@@]1(C)[C@]1([H])CC[C@@]([H])(C)C1=CC(C)(C)C2

> <INCHI_IDENTIFIER>
InChI=1S/C15H24/c1-10-5-6-13-12(10)9-14(2,3)7-11-8-15(11,13)4/h9-11,13H,5-8H2,1-4H3/t10-,11+,13-,15-/m1/s1

> <INCHI_KEY>
FCQGZOYPTSMOOM-NDPMZMCLSA-N

> <FORMULA>
C15H24

> <MOLECULAR_WEIGHT>
204.357

> <EXACT_MASS>
204.187800773

> <JCHEM_ACCEPTOR_COUNT>
0

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
25.995280068233384

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1aR,5R,7aS,7bR)-3,3,5,7b-tetramethyl-1H,1aH,2H,3H,5H,6H,7H,7aH,7bH-cyclopropa[e]azulene

> <JCHEM_LOGP>
4.101158186333333

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_POLAR_SURFACE_AREA>
0.0

> <JCHEM_REFRACTIVITY>
65.6944

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1aR,5R,7aS,7bR)-3,3,5,7b-tetramethyl-1H,1aH,2H,5H,6H,7H,7aH-cyclopropa[e]azulene

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 17-JUN-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-JUN-22         0                                  
HETATM    1  C   UNK     0       7.953   0.586   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.246   3.074   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.156   3.273   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.184  -2.975   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.853  -1.928   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.419  -2.490   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.016   1.167   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.420  -1.846   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.776   1.455   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.762  -0.391   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.831  -0.362   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.272  -0.002   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.442  -1.300   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.326   1.976   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.911  -1.459   0.000  0.00  0.00           C+0
HETATM   16  H   UNK     0       6.432   1.113   0.000  0.00  0.00           H+0
HETATM   17  H   UNK     0       0.320  -0.063   0.000  0.00  0.00           H+0
HETATM   18  H   UNK     0       3.857  -2.724   0.000  0.00  0.00           H+0
CONECT    1   10                                                            
CONECT    2   14                                                            
CONECT    3   14                                                            
CONECT    4   15                                                            
CONECT    5    6   10                                                       
CONECT    6    5   13                                                       
CONECT    7   11   14                                                       
CONECT    8   11   15                                                       
CONECT    9   12   14                                                       
CONECT   10    1    5   12   16                                             
CONECT   11    7    8   15   17                                             
CONECT   12    9   10   13                                                  
CONECT   13    6   12   15   18                                             
CONECT   14    2    3    7    9                                             
CONECT   15    4    8   11   13                                             
CONECT   16   10                                                            
CONECT   17   11                                                            
CONECT   18   13                                                            
MASTER        0    0    0    0    0    0    0    0   18    0   40    0
END

Synonyms

Not Available

Molecular Formula

C₁₅H₂₄

Average Mass

204.357

Monoisotopic Mass

204.187800773

IUPAC Name

(1aR,5R,7aS,7bR)-3,3,5,7b-tetramethyl-1H,1aH,2H,3H,5H,6H,7H,7aH,7bH-cyclopropa[e]azulene

Traditional Name

(1aR,5R,7aS,7bR)-3,3,5,7b-tetramethyl-1H,1aH,2H,5H,6H,7H,7aH-cyclopropa[e]azulene

CAS Registry Number

Not Available

SMILES

[H][C@]12C[C@@]1(C)[C@]1([H])CC[C@@]([H])(C)C1=CC(C)(C)C2

InChI Identifier

InChI=1S/C15H24/c1-10-5-6-13-12(10)9-14(2,3)7-11-8-15(11,13)4/h9-11,13H,5-8H2,1-4H3/t10-,11+,13-,15-/m1/s1

InChI Key

FCQGZOYPTSMOOM-NDPMZMCLSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as polycyclic hydrocarbons. These are polycyclic organic compounds made up only of carbon and hydrogen atoms.

Kingdom

Organic compounds

Super Class

Hydrocarbons

Class

Polycyclic hydrocarbons

Sub Class

Not Available

Direct Parent

Polycyclic hydrocarbons

Alternative Parents

Substituents

Polycyclic hydrocarbon
Cyclic olefin
Unsaturated aliphatic hydrocarbon
Unsaturated hydrocarbon
Olefin
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
logP	4.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	0	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	0 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	65.69 m³·mol⁻¹	ChemAxon
Polarizability	26 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
MS	Mass Spectrum (Electron Ionization)	Not Available	2022-08-06	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

Chromatographic Retention Times and Retention Indices

Retention Times

Not Available

Retention Indices

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

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	Ascomycota	1	Human feces

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

8926061

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10750737

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

CMMC Knowledgebase

Not Available

General References

Bansal P, Morgat A, Axelsen KB, Muthukrishnan V, Coudert E, Aimo L, Hyka-Nouspikel N, Gasteiger E, Kerhornou A, Neto TB, Pozzato M, Blatter MC, Ignatchenko A, Redaschi N, Bridge A: Rhea, the reaction knowledgebase in 2022. Nucleic Acids Res. 2022 Jan 7;50(D1):D693-D700. doi: 10.1093/nar/gkab1016. [PubMed:34755880 ]

Showing metabocard for african-1-ene (MMDBc0055690)

MOL for #<Metabolite:0x00007faddc99e3c8>

3D MOL for #<Metabolite:0x00007faddc99e3c8>

3D SDF for #<Metabolite:0x00007faddc99e3c8>

3D-SDF for #<Metabolite:0x00007faddc99e3c8>

PDB for #<Metabolite:0x00007faddc99e3c8>

3D PDB for #<Metabolite:0x00007faddc99e3c8>

SMILES for #<Metabolite:0x00007faddc99e3c8>

INCHI for #<Metabolite:0x00007faddc99e3c8>

Structure for #<Metabolite:0x00007faddc99e3c8>

3D Structure for #<Metabolite:0x00007faddc99e3c8>