NP-MRD: Showing NP-Card for (8z)-1,6,10,10-tetramethyl-5,13-dioxatricyclo[10.1.0.0⁴,⁶]tridec-8-ene (NP0220612)

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Record Information

Version

2.0

Created at

2022-09-05 21:58:46 UTC

Updated at

2022-09-05 21:58:46 UTC

NP-MRD ID

NP0220612

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(8z)-1,6,10,10-tetramethyl-5,13-dioxatricyclo[10.1.0.0⁴,⁶]tridec-8-ene

Description

Humulene diepoxide A belongs to the class of organic compounds known as epoxides. Epoxides are compounds containing a cyclic ether with three ring atoms(one oxygen and two carbon atoms). Humulene diepoxide A is an extremely weak basic (essentially neutral) compound (based on its pKa). Outside of the human body, humulene diepoxide a has been detected, but not quantified in, alcoholic beverages and herbs and spices. (8z)-1,6,10,10-tetramethyl-5,13-dioxatricyclo[10.1.0.0⁴,⁶]tridec-8-ene is found in Humulus lupulus. This could make humulene diepoxide a a potential biomarker for the consumption of these foods.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 41 43  0  0  0  0  0  0  0  0999 V2000
   -2.5428   -0.9535   -0.9007 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1593   -0.1447    0.3089 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5001    0.1287    1.0283 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3458   -0.8596    1.2926 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2069   -1.4323    0.9643 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3627   -1.4243   -0.3715 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8454   -1.6608   -0.3014 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4343   -2.6372   -1.3306 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3951   -1.9755    1.0025 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7011   -0.7293    0.2557 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2558    0.4447    1.0469 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0181    1.6800    0.2266 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6121    2.0922    0.0549 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2686    2.5814   -1.3630 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0431    2.8832    0.9895 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4261    1.5690    0.8331 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6307    1.2299   -0.0457 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4348   -2.0484   -0.6787 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6419   -0.8530   -1.1562 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0343   -0.6502   -1.8324 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0473   -0.8433    1.0382 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3348    0.4218    2.0662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0867    0.8458    0.4404 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6365   -0.9579    2.3557 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3486   -1.9519    1.7555 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0682   -2.3115   -0.9256 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2018   -0.5710   -1.0047 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9642   -2.5311   -2.3062 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5129   -2.5135   -1.4093 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1837   -3.6538   -0.9314 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7747   -0.6817   -0.0678 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1194    0.7033    1.7379 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4343    0.2130    1.7545 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4970    1.4766   -0.7733 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5908    2.5746    0.6098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6728    3.1254   -1.4134 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3848    1.7885   -2.1055 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0775    3.3362   -1.5910 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4323    1.0174    1.7685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3645    1.2314   -1.1161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3742    2.0414    0.0947 H   0  0  0  0  0  0  0  0  0  0  0  0
 13 14  1  6
 13 12  1  0
 12 11  1  0
 11 10  1  0
 10  9  1  0
  9  7  1  0
  7  8  1  6
  7  6  1  0
  6  5  1  0
  5  4  2  0
  4  2  1  0
  2  1  1  0
  2  3  1  0
  2 17  1  0
 17 16  1  0
 16 15  1  0
 16 13  1  0
 15 13  1  0
  7 10  1  0
 14 36  1  0
 14 37  1  0
 14 38  1  0
 12 34  1  0
 12 35  1  0
 11 32  1  0
 11 33  1  0
 10 31  1  6
  8 28  1  0
  8 29  1  0
  8 30  1  0
  6 26  1  0
  6 27  1  0
  5 25  1  0
  4 24  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  3 21  1  0
  3 22  1  0
  3 23  1  0
 17 40  1  0
 17 41  1  0
 16 39  1  1
M  END


  Mrv0541 05061312042D          

 17 19  0  0  0  0            999 V2000
    3.4855    2.8984    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0634    1.9254    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6418    1.4436    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0514   -0.7270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2738    2.3234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8845    0.2072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5170    2.6517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4157    1.4318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1366   -0.2984    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9483    1.3408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7057    0.1288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2856    0.8495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8542    2.1604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0340    0.8857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3797    0.0299    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5254    0.2230    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6228    0.3582    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  7  5  2  0  0  0  0
  8  5  1  0  0  0  0
  9  6  1  0  0  0  0
 11  6  1  0  0  0  0
 12 10  1  0  0  0  0
 13  1  1  0  0  0  0
 13  2  1  0  0  0  0
 13  7  1  0  0  0  0
 13 10  1  0  0  0  0
 14  3  1  0  0  0  0
 14  8  1  0  0  0  0
 14 11  1  0  0  0  0
 15  4  1  0  0  0  0
 15  9  1  0  0  0  0
 15 12  1  0  0  0  0
 16 11  1  0  0  0  0
 16 14  1  0  0  0  0
 17 12  1  0  0  0  0
 17 15  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0220612

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC12CCC3OC3(C)C\C=C/C(C)(C)CC1O2

> <INCHI_IDENTIFIER>
InChI=1S/C15H24O2/c1-13(2)7-5-8-14(3)11(16-14)6-9-15(4)12(10-13)17-15/h5,7,11-12H,6,8-10H2,1-4H3/b7-5-

> <INCHI_KEY>
UFBUQKAQYQDEOE-ALCCZGGFSA-N

> <FORMULA>
C15H24O2

> <MOLECULAR_WEIGHT>
236.3499

> <EXACT_MASS>
236.177630012

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_AVERAGE_POLARIZABILITY>
27.380394960504717

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(8Z)-1,6,10,10-tetramethyl-5,13-dioxatricyclo[10.1.0.0⁴,⁶]tridec-8-ene

> <ALOGPS_LOGP>
3.51

> <JCHEM_LOGP>
3.0767160879999995

> <ALOGPS_LOGS>
-4.49

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-3.9245950614628193

> <JCHEM_POLAR_SURFACE_AREA>
25.06

> <JCHEM_REFRACTIVITY>
69.06950000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.60e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(8Z)-1,6,10,10-tetramethyl-5,13-dioxatricyclo[10.1.0.0⁴,⁶]tridec-8-ene

> <JCHEM_VEBER_RULE>
1

$$$$

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       6.506   5.410   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.718   3.594   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      12.398   2.695   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.696  -1.357   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.844   4.337   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.118   0.387   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.432   4.950   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      10.109   2.673   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.722  -0.557   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.370   2.503   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.651   0.240   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.133   1.586   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.195   4.033   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      11.263   1.653   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.309   0.056   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      12.181   0.416   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       4.896   0.669   0.000  0.00  0.00           O+0
CONECT    1   13                                                            
CONECT    2   13                                                            
CONECT    3   14                                                            
CONECT    4   15                                                            
CONECT    5    7    8                                                       
CONECT    6    9   11                                                       
CONECT    7    5   13                                                       
CONECT    8    5   14                                                       
CONECT    9    6   15                                                       
CONECT   10   12   13                                                       
CONECT   11    6   14   16                                                  
CONECT   12   10   15   17                                                  
CONECT   13    1    2    7   10                                             
CONECT   14    3    8   11   16                                             
CONECT   15    4    9   12   17                                             
CONECT   16   11   14                                                       
CONECT   17   12   15                                                       
MASTER        0    0    0    0    0    0    0    0   17    0   38    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₂₄O₂

Average Mass

236.3499 Da

Monoisotopic Mass

236.17763 Da

IUPAC Name

(8Z)-1,6,10,10-tetramethyl-5,13-dioxatricyclo[10.1.0.0⁴,⁶]tridec-8-ene

Traditional Name

(8Z)-1,6,10,10-tetramethyl-5,13-dioxatricyclo[10.1.0.0⁴,⁶]tridec-8-ene

CAS Registry Number

Not Available

SMILES

CC12CCC3OC3(C)C\C=C/C(C)(C)CC1O2

InChI Identifier

InChI=1S/C15H24O2/c1-13(2)7-5-8-14(3)11(16-14)6-9-15(4)12(10-13)17-15/h5,7,11-12H,6,8-10H2,1-4H3/b7-5-

InChI Key

UFBUQKAQYQDEOE-ALCCZGGFSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Humulus lupulus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as epoxides. Epoxides are compounds containing a cyclic ether with three ring atoms(one oxygen and two carbon atoms).

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Epoxides

Sub Class

Not Available

Direct Parent

Epoxides

Alternative Parents

Substituents

Oxacycle
Ether
Oxirane
Dialkyl ether
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	3.51	ALOGPS
logP	3.08	ChemAxon
logS	-4.5	ALOGPS
pKa (Strongest Basic)	-3.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	25.06 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	69.07 m³·mol⁻¹	ChemAxon
Polarizability	27.38 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

External Links

HMDB ID

HMDB0040712

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB020517

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

101215174

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (8z)-1,6,10,10-tetramethyl-5,13-dioxatricyclo[10.1.0.0⁴,⁶]tridec-8-ene (NP0220612)

MOL for NP0220612 ((8z)-1,6,10,10-tetramethyl-5,13-dioxatricyclo[10.1.0.0⁴,⁶]tridec-8-ene)

3D MOL for NP0220612 ((8z)-1,6,10,10-tetramethyl-5,13-dioxatricyclo[10.1.0.0⁴,⁶]tridec-8-ene)

3D SDF for NP0220612 ((8z)-1,6,10,10-tetramethyl-5,13-dioxatricyclo[10.1.0.0⁴,⁶]tridec-8-ene)

3D-SDF for NP0220612 ((8z)-1,6,10,10-tetramethyl-5,13-dioxatricyclo[10.1.0.0⁴,⁶]tridec-8-ene)

PDB for NP0220612 ((8z)-1,6,10,10-tetramethyl-5,13-dioxatricyclo[10.1.0.0⁴,⁶]tridec-8-ene)

3D PDB for NP0220612 ((8z)-1,6,10,10-tetramethyl-5,13-dioxatricyclo[10.1.0.0⁴,⁶]tridec-8-ene)

SMILES for NP0220612 ((8z)-1,6,10,10-tetramethyl-5,13-dioxatricyclo[10.1.0.0⁴,⁶]tridec-8-ene)

INCHI for NP0220612 ((8z)-1,6,10,10-tetramethyl-5,13-dioxatricyclo[10.1.0.0⁴,⁶]tridec-8-ene)

Structure for NP0220612 ((8z)-1,6,10,10-tetramethyl-5,13-dioxatricyclo[10.1.0.0⁴,⁶]tridec-8-ene)

3D Structure for NP0220612 ((8z)-1,6,10,10-tetramethyl-5,13-dioxatricyclo[10.1.0.0⁴,⁶]tridec-8-ene)