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Showing NP-Card for Butylcyclohexane (NP0049844)

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Record Information
Version2.0
Created at2022-03-17 21:19:02 UTC
Updated at2022-03-17 21:19:02 UTC
NP-MRD IDNP0049844
Secondary Accession NumbersNone
Natural Product Identification
Common NameButylcyclohexane
DescriptionButylcyclohexane, also known as 1-cyclohexyl-butane, belongs to the class of organic compounds known as cycloalkanes. These are saturated monocyclic hydrocarbons (with or without side chains). Thus, butylcyclohexane is considered to be a hydrocarbon lipid molecule. Butylcyclohexane is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral. Outside of the human body, Butylcyclohexane has been detected, but not quantified in, corns and fruits. Butylcyclohexane is found in Carica papaya . Butylcyclohexane was first documented in 1966 (PMID: 5950799). This could make butylcyclohexane a potential biomarker for the consumption of these foods (PMID: 22824734) (PMID: 16355992) (PMID: 16942233) (PMID: 10659953) (PMID: 13680096) (PMID: 12878040).
Structure
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MOLSDFPDBSMILESInChI

MOL for NP0049844 (Butylcyclohexane)


  Mrv0541 05061312392D          

 10 10  0  0  0  0            999 V2000
   -0.7145    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    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
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    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
  2  1  1  0  0  0  0
  3  2  1  0  0  0  0
  5  4  1  0  0  0  0
  6  4  1  0  0  0  0
  7  3  1  0  0  0  0
  8  5  1  0  0  0  0
  9  6  1  0  0  0  0
 10  7  1  0  0  0  0
 10  8  1  0  0  0  0
 10  9  1  0  0  0  0
M  END
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3D MOL for NP0049844 (Butylcyclohexane)

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3D SDF for NP0049844 (Butylcyclohexane)

  Mrv0541 05061312392D          

 10 10  0  0  0  0            999 V2000
   -0.7145    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    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
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    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
  2  1  1  0  0  0  0
  3  2  1  0  0  0  0
  5  4  1  0  0  0  0
  6  4  1  0  0  0  0
  7  3  1  0  0  0  0
  8  5  1  0  0  0  0
  9  6  1  0  0  0  0
 10  7  1  0  0  0  0
 10  8  1  0  0  0  0
 10  9  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0049844

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCC1CCCCC1

> <INCHI_IDENTIFIER>
InChI=1S/C10H20/c1-2-3-7-10-8-5-4-6-9-10/h10H,2-9H2,1H3

> <INCHI_KEY>
GGBJHURWWWLEQH-UHFFFAOYSA-N

> <FORMULA>
C10H20

> <MOLECULAR_WEIGHT>
140.2658

> <EXACT_MASS>
140.15650064

> <JCHEM_ACCEPTOR_COUNT>
0

> <JCHEM_AVERAGE_POLARIZABILITY>
19.161184960680444

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
butylcyclohexane

> <ALOGPS_LOGP>
5.58

> <JCHEM_LOGP>
4.288137081333333

> <ALOGPS_LOGS>
-5.32

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_POLAR_SURFACE_AREA>
0

> <JCHEM_REFRACTIVITY>
45.9576

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.74e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
butylcyclohexane

> <JCHEM_VEBER_RULE>
1

$$$$

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3D-SDF for NP0049844 (Butylcyclohexane)
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PDB for NP0049844 (Butylcyclohexane)
HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0      -1.334   6.930   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.000   6.160   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    7                                                       
CONECT    4    5    6                                                       
CONECT    5    4    8                                                       
CONECT    6    4    9                                                       
CONECT    7    3   10                                                       
CONECT    8    5   10                                                       
CONECT    9    6   10                                                       
CONECT   10    7    8    9                                                  
MASTER        0    0    0    0    0    0    0    0   10    0   20    0
END

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3D PDB for NP0049844 (Butylcyclohexane)
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SMILES for NP0049844 (Butylcyclohexane)
CCCCC1CCCCC1
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INCHI for NP0049844 (Butylcyclohexane)
InChI=1S/C10H20/c1-2-3-7-10-8-5-4-6-9-10/h10H,2-9H2,1H3
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Synonyms
ValueSource
Butyl-cyclohexaneHMDB
1-Cyclohexyl-butaneHMDB
1-CyclohexylbutaneHMDB
N-Butyl-cyclohexaneHMDB
N-ButylcyclohexaneHMDB
Chemical FormulaC10H20
Average Mass140.2658 Da
Monoisotopic Mass140.15650 Da
IUPAC Namebutylcyclohexane
Traditional Namebutylcyclohexane
CAS Registry Number1678-93-9
SMILES
CCCCC1CCCCC1
InChI Identifier
InChI=1S/C10H20/c1-2-3-7-10-8-5-4-6-9-10/h10H,2-9H2,1H3
InChI KeyGGBJHURWWWLEQH-UHFFFAOYSA-N
Experimental Spectra
Not Available
Predicted Spectra
Not Available
Chemical Shift Submissions
Not Available
Species
Species of Origin
Species NameSourceReference
Carica papaya L.Plant
Zea mays L.FooDB
    • Carlos Macku, and Takayuki Shibamoto. Headspace volatile compounds formed from heated corn oil an...
Chemical Taxonomy
Description Belongs to the class of organic compounds known as cycloalkanes. These are saturated monocyclic hydrocarbons (with or without side chains).
KingdomOrganic compounds  
Super ClassHydrocarbons  
ClassSaturated hydrocarbons  
Sub ClassCycloalkanes  
Direct ParentCycloalkanes  
Alternative ParentsNot Available
Substituents
  • Cycloalkane
    • 

  • Aliphatic homomonocyclic compound
Molecular FrameworkAliphatic homomonocyclic compounds
External Descriptors
Physical Properties
StateNot Available
Experimental Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Predicted Properties
PropertyValueSource
logP5.58ALOGPS
logP4.29ChemAxon
logS-5.3ALOGPS
Physiological Charge0ChemAxon
Hydrogen Acceptor Count0ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area0 ŲChemAxon
Rotatable Bond Count3ChemAxon
Refractivity45.96 m³·mol⁻¹ChemAxon
Polarizability19.16 ųChemAxon
Number of Rings1ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleNoChemAxon
HMDB IDHMDB0041402  
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FoodDB IDFDB021341  
KNApSAcK IDNot Available
Chemspider ID14753  
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound15506  
PDB IDNot Available
ChEBI IDNot Available
Good Scents IDNot Available
References
General References
  1. MacKinnon G, Duncan HJ: Phytotoxicity of branched cyclohexanes found in the volatile fraction of diesel fuel on germination of selected grass species. Chemosphere. 2013 Jan;90(3):952-7. doi: 10.1016/j.chemosphere.2012.06.038. Epub 2012 Jul 21. [PubMed:22824734  ] 
  2. Gill G, Pawar DM, Noe EA: Conformational study of cis-1,4-di-tert-butylcyclohexane by dynamic NMR spectroscopy and computational methods. Observation of chair and twist-boat conformations. J Org Chem. 2005 Dec 23;70(26):10726-31. doi: 10.1021/jo051654z. [PubMed:16355992  ] 
  3. Mandanici A, Cutroni M, Triolo A, Rodriguez-Mora V, Ramos MA: Thermodynamic study of alkyl-cyclohexanes in liquid, glassy, and crystalline states. J Chem Phys. 2006 Aug 7;125(5):054514. doi: 10.1063/1.2238863. [PubMed:16942233  ] 
  4. Juvonen RO, Gynther J, Pasanen M, Alhava E, Poso A: Pronounced differences in inhibition potency of lactone and non-lactone compounds for mouse and human coumarin 7-hydroxylases (CYP2A5 and CYP2A6). Xenobiotica. 2000 Jan;30(1):81-92. doi: 10.1080/004982500237848. [PubMed:10659953  ] 
  5. Aam BB, Myhre O, Fonnum F: Transcellular signalling pathways and TNF-alpha release involved in formation of reactive oxygen species in rat alveolar macrophages exposed to tert-butylcyclohexane. Arch Toxicol. 2003 Dec;77(12):678-84. doi: 10.1007/s00204-003-0507-2. Epub 2003 Sep 10. [PubMed:13680096  ] 
  6. Dreiem A, Myhre O, Fonnum F: Involvement of the extracellular signal regulated kinase pathway in hydrocarbon-induced reactive oxygen species formation in human neutrophil granulocytes. Toxicol Appl Pharmacol. 2003 Jul 15;190(2):102-10. doi: 10.1016/s0041-008x(03)00158-3. [PubMed:12878040  ] 
  7. Devine AB, Lack RE: Structure and biological activity of steroids. I. The hydrogen-bonding properties of halogenohydrins in the t-butylcyclohexane and steroid series. J Chem Soc Perkin 1. 1966;21:1902-7. doi: 10.1039/j39660001902. [PubMed:5950799  ] 
  8. Rivedal E, Mikalsen SO, Roseng LE, Sanner T, Eide I: Effects of hydrocarbons on transformation and intercellular communication in Syrian hamster embryo cells. Pharmacol Toxicol. 1992 Jul;71(1):57-61. doi: 10.1111/j.1600-0773.1992.tb00521.x. [PubMed:1523195  ] 
  9. Ma Y, Ramirez A, Singh KJ, Keresztes I, Collum DB: Lithium diisopropylamide solvated by hexamethylphosphoramide: substrate-dependent mechanisms for dehydrobrominations. J Am Chem Soc. 2006 Dec 6;128(48):15399-404. doi: 10.1021/ja060964b. [PubMed:17132006  ] 
  10. Henningsen GM, Yu KO, Salomon RA, Ferry MJ, Lopez I, Roberts J, Serve MP: The metabolism of t-butylcyclohexane in Fischer-344 male rats with hyaline droplet nephropathy. Toxicol Lett. 1987 Dec;39(2-3):313-8. doi: 10.1016/0378-4274(87)90247-5. [PubMed:3686558  ] 
  11. Landstetter C, Wallner G: Determination of strontium-90 in deer bones by liquid scintillation spectrometry after separation on Sr-specific ion exchange columns. J Environ Radioact. 2006;87(3):315-24. doi: 10.1016/j.jenvrad.2005.12.008. Epub 2006 Feb 20. [PubMed:16488519  ] 
  12. Dreiem A, Ring A, Fonnum F: Organic solvent-induced cell death in rat cerebellar granule cells: structure dependence of c10 hydrocarbons and relationship to reactive oxygen species formation. Neurotoxicology. 2005 Jun;26(3):321-30. doi: 10.1016/j.neuro.2005.01.006. [PubMed:15935204  ]