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Showing NP-Card for camphene hydrate (NP0190494)

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Record Information
Version2.0
Created at2022-09-04 07:10:40 UTC
Updated at2022-09-04 07:10:40 UTC
NP-MRD IDNP0190494
Secondary Accession NumbersNone
Natural Product Identification
Common Namecamphene hydrate
DescriptionCamphene-hydrate belongs to the class of organic compounds known as bicyclic monoterpenoids. These are monoterpenoids containing exactly 2 rings, which are fused to each other. camphene hydrate is found in Alpinia latilabris, Artemisia annua, Cannabis sativa, Juniperus jaliscana, Juniperus monticola, Pistacia vera, Zingiber officinale and Zingiber zerumbet. Camphene-hydrate is an extremely weak basic (essentially neutral) compound (based on its pKa).
Structure
Thumb
MOL3D MOLSDFPDBSMILESInChI

MOL for NP0190494 (camphene hydrate)


  Mrv0541 02241220422D          

 11 12  0  0  0  0            999 V2000
    0.2522   -2.8768    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1351   -2.0602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6764   -1.9114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9106   -1.6699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6411   -2.0402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9362   -1.4148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1407   -0.9495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9807   -0.1341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5004   -1.3997    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1641   -0.6464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2847   -1.1463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  4  8  1  0  0  0  0
  7  9  1  0  0  0  0
  2  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
M  END
Download

3D MOL for NP0190494 (camphene hydrate)

     RDKit          3D

 29 30  0  0  0  0  0  0  0  0999 V2000
    1.5098    0.0438   -1.4348 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8220   -0.0009   -0.0848 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8617    0.3416    0.9553 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2637   -1.3502    0.2354 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6164   -1.7887   -0.9139 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8453   -0.8700   -0.8231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5521    0.0025    0.3387 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8145   -0.9789    1.2663 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3779    0.9102   -0.0206 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2882    1.9649    1.0190 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5999    1.4101   -1.3082 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7480    0.2185   -2.1927 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1065   -0.8819   -1.5809 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2603    0.8759   -1.4158 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6565   -0.4477    0.8647 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5004    0.2981    1.9813 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3797    1.2990    0.7350 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9579   -2.0884    0.5903 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8888   -2.8410   -0.7976 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1518   -1.6081   -1.8933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7598   -1.4720   -0.6413 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0038   -0.3276   -1.7768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3729    0.5043    0.8118 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4280   -1.8355    1.5321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4156   -0.3936    2.0905 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7055    2.3645    1.2110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7691    1.6557    1.9918 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9273    2.8307    0.6748 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0394    2.1647   -1.4142 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
  9 11  1  6
  9  2  1  0
  8  4  1  0
  1 12  1  0
  1 13  1  0
  1 14  1  0
  3 15  1  0
  3 16  1  0
  3 17  1  0
  4 18  1  1
  5 19  1  0
  5 20  1  0
  6 21  1  0
  6 22  1  0
  7 23  1  1
  8 24  1  0
  8 25  1  0
 10 26  1  0
 10 27  1  0
 10 28  1  0
 11 29  1  0
M  END
Download

3D SDF for NP0190494 (camphene hydrate)


  Mrv0541 02241220422D          

 11 12  0  0  0  0            999 V2000
    0.2522   -2.8768    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1351   -2.0602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6764   -1.9114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9106   -1.6699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6411   -2.0402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9362   -1.4148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1407   -0.9495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9807   -0.1341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5004   -1.3997    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1641   -0.6464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2847   -1.1463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  4  8  1  0  0  0  0
  7  9  1  0  0  0  0
  2  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0190494

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)C2CCC(C2)C1(C)O

> <INCHI_IDENTIFIER>
InChI=1S/C10H18O/c1-9(2)7-4-5-8(6-7)10(9,3)11/h7-8,11H,4-6H2,1-3H3

> <INCHI_KEY>
PXRCIOIWVGAZEP-UHFFFAOYSA-N

> <FORMULA>
C10H18O

> <MOLECULAR_WEIGHT>
154.2493

> <EXACT_MASS>
154.135765198

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_AVERAGE_POLARIZABILITY>
18.311503056754084

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2,3,3-trimethylbicyclo[2.2.1]heptan-2-ol

> <ALOGPS_LOGP>
2.87

> <JCHEM_LOGP>
2.0479411626666666

> <ALOGPS_LOGS>
-2.29

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-0.40065289958004324

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
45.40039999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.86e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2,3,3-trimethylbicyclo[2.2.1]heptan-2-ol

> <JCHEM_VEBER_RULE>
1

$$$$
Download

3D-SDF for NP0190494 (camphene hydrate)

Download
PDB for NP0190494 (camphene hydrate)
HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  O   UNK     0       0.471  -5.370   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       0.252  -3.846   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.263  -3.568   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.700  -3.117   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.063  -3.808   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.614  -2.641   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.129  -1.772   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.831  -0.250   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.934  -2.613   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.306  -1.207   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.531  -2.140   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4    9                                             
CONECT    3    2                                                            
CONECT    4    2    5    8                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7    4                                                       
CONECT    9    7    2   10   11                                             
CONECT   10    9                                                            
CONECT   11    9                                                            
MASTER        0    0    0    0    0    0    0    0   11    0   24    0
END

Download
3D PDB for NP0190494 (camphene hydrate)
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SMILES for NP0190494 (camphene hydrate)
CC1(C)C2CCC(C2)C1(C)O
Download
INCHI for NP0190494 (camphene hydrate)
InChI=1S/C10H18O/c1-9(2)7-4-5-8(6-7)10(9,3)11/h7-8,11H,4-6H2,1-3H3
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View in JSmol
Synonyms
ValueSource
Camphene-hydric acidGenerator
Chemical FormulaC10H18O
Average Mass154.2493 Da
Monoisotopic Mass154.13577 Da
IUPAC Name2,3,3-trimethylbicyclo[2.2.1]heptan-2-ol
Traditional Name2,3,3-trimethylbicyclo[2.2.1]heptan-2-ol
CAS Registry NumberNot Available
SMILES
CC1(C)C2CCC(C2)C1(C)O
InChI Identifier
InChI=1S/C10H18O/c1-9(2)7-4-5-8(6-7)10(9,3)11/h7-8,11H,4-6H2,1-3H3
InChI KeyPXRCIOIWVGAZEP-UHFFFAOYSA-N
Experimental Spectra
Not Available
Predicted Spectra
Spectrum TypeDescriptionDepositor IDDepositor OrganizationDepositorDeposition DateView
1D NMR13C NMR Spectrum (1D, 25 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 100 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 252 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 1000 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 50 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 200 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 75 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 300 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 101 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 400 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 126 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 500 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 151 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 600 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 176 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 700 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 201 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 800 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 226 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR1H NMR Spectrum (1D, 900 MHz, H2O, predicted)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
Chemical Shift Submissions
Not Available
Species
Species of Origin
Species NameSourceReference
Alpinia latilabrisLOTUS Database
Artemisia annuaLOTUS Database
Cannabis sativaLOTUS Database
Juniperus jaliscanaLOTUS Database
Juniperus monticolaLOTUS Database
Pistacia veraLOTUS Database
Zingiber officinaleLOTUS Database
Zingiber zerumbetLOTUS Database
Chemical Taxonomy
Description Belongs to the class of organic compounds known as bicyclic monoterpenoids. These are monoterpenoids containing exactly 2 rings, which are fused to each other.
KingdomOrganic compounds  
Super ClassLipids and lipid-like molecules  
ClassPrenol lipids  
Sub ClassMonoterpenoids  
Direct ParentBicyclic monoterpenoids  
Alternative Parents
Substituents
  • Bicyclic monoterpenoid
    • 

  • Tertiary alcohol
    • 

  • Cyclic alcohol
    • 

  • Organic oxygen compound
    • 

  • Hydrocarbon derivative
    • 

  • Organooxygen compound
    • 

  • Alcohol
    • 

  • Aliphatic homopolycyclic compound
Molecular FrameworkAliphatic homopolycyclic compounds
External DescriptorsNot Available
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
logP2.87ALOGPS
logP2.05ChemAxon
logS-2.3ALOGPS
pKa (Strongest Basic)-0.4ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count1ChemAxon
Hydrogen Donor Count1ChemAxon
Polar Surface Area20.23 ŲChemAxon
Rotatable Bond Count0ChemAxon
Refractivity45.4 m³·mol⁻¹ChemAxon
Polarizability18.31 ųChemAxon
Number of Rings2ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleNoChemAxon
HMDB IDNot Available
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FoodDB IDFDB007782  
KNApSAcK IDNot Available
Chemspider IDNot Available
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound101680  
PDB IDNot Available
ChEBI IDNot Available
Good Scents IDNot Available
References
General References
  1. LOTUS database [Link]