NP-MRD: Showing NP-Card for α-bergamotene (NP0296450)

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Record Information

Version

1.0

Created at

2022-09-10 06:02:04 UTC

Updated at

2022-09-10 06:02:04 UTC

NP-MRD ID

NP0296450

Secondary Accession Numbers

None

Natural Product Identification

Common Name

α-bergamotene

Description

Alpha-bergamotene belongs to the class of organic compounds known as bicyclic monoterpenoids. These are monoterpenoids containing exactly 2 rings, which are fused to each other. α-bergamotene is found in Ageratum conyzoides, Alpinia chinensis, Alpinia conchigera, Alpinia galanga, Aristolochia gigantea, Asarum fauriei, Asarum megacalyx, Asarum trigynum, Cannabis sativa, Castanopsis cuspidata, Citrus aurantium, Citrus bergamia, Citrus hystrix, Citrus medica, Commiphora kataf, Curcuma longa, Daucus carota, Dumortiera hirsuta, Elsholtzia blanda, Elsholtzia ciliata, Encelia canescens, Erigeron canadensis, Eupatorium cannabinum, Gossypium hirsutum, Heterotheca subaxillaris, Humulus lupulus, Mesosphaerum suaveolens, Isocoma tenuisecta, Juglans regia, Phyla nodiflora, Micromeria sinaica, Ocimum basilicum, Pectis brevipedunculata, Pelargonium endlicherianum, Perilla frutescens, Pimpinella anisum, Polygala senega, Polyscias fruticosa, Populus alba, Pulicaria arabica, Rhanterium epapposum, Salvia aurea, Santalum spicatum, Sideritis athoa, Smallanthus uvedalia, Stevia rebaudiana, Swertia japonica, Thymus longicaulis and Zanthoxylum zanthoxyloides. It was first documented in 2002 (PMID: 12562082). Alpha-bergamotene is possibly neutral (PMID: 22474938) (PMID: 23786100).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 39 40  0  0  0  0  0  0  0  0999 V2000
    4.3220   -0.1379    0.5149 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1372   -0.1732   -0.4067 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9186   -1.3656   -1.2333 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3405    0.8847   -0.4351 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1529    0.9742   -1.2898 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1498    1.1955   -0.5976 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5290    0.1291    0.3476 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4232   -0.1071    1.4848 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9531   -1.1960   -0.2385 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7918   -1.0555   -1.4671 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0094   -0.2375   -1.1914 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9162    0.6096   -0.1512 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7416    1.8494   -0.0793 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9454    0.2301    0.9097 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9253   -1.2841    0.9509 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1036   -0.7522    1.4237 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6133    0.8943    0.7622 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2028   -0.6093    0.0177 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3003   -1.1448   -2.2542 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4698   -2.2381   -0.7949 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8640   -1.6785   -1.3363 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5596    1.7527    0.1949 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0293    0.0709   -1.9463 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3729    1.8016   -2.0315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2042    2.2232   -0.1239 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9286    1.2679   -1.4091 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0450    0.7758    1.7238 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0244   -1.0378    1.3355 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1218   -0.3178    2.4586 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2245   -2.0019   -0.2336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1566   -2.0686   -1.7407 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2323   -0.6844   -2.3482 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9161   -0.3187   -1.7913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6444    1.7187    0.5557 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0810    2.6348    0.3673 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0494    2.1506   -1.0899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0386    0.7409    1.8635 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8973   -1.7516    0.6759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4230   -1.7436    1.8031 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  7  6  1  6
  7  8  1  0
  7  9  1  0
  9 15  1  0
 15 14  1  0
 14 12  1  0
 12 13  1  0
 12 11  2  0
 11 10  1  0
 14  7  1  0
 10  9  1  0
  1 16  1  0
  1 17  1  0
  1 18  1  0
  3 19  1  0
  3 20  1  0
  3 21  1  0
  4 22  1  0
  5 23  1  0
  5 24  1  0
  6 25  1  0
  6 26  1  0
  8 27  1  0
  8 28  1  0
  8 29  1  0
  9 30  1  6
 15 38  1  0
 15 39  1  0
 14 37  1  1
 13 34  1  0
 13 35  1  0
 13 36  1  0
 11 33  1  0
 10 31  1  0
 10 32  1  0
M  END


  Mrv1533004161506052D          

 15 16  0  0  0  0            999 V2000
   -1.6569    3.3928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0249    2.8625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1681    2.0501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5362    1.5198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6794    0.7073    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0474    0.1770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6794   -0.3533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3651    0.8915    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1901    0.8915    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6026    0.1770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1901   -0.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6026   -1.2519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3651   -0.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5437    0.1770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2496    3.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  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
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
  6 13  1  0  0  0  0
 13 14  1  0  0  0  0
  8 14  1  0  0  0  0
  2 15  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0296450

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCCC1(C)C2CC1C(C)=CC2

> <INCHI_IDENTIFIER>
InChI=1S/C15H24/c1-11(2)6-5-9-15(4)13-8-7-12(3)14(15)10-13/h6-7,13-14H,5,8-10H2,1-4H3

> <INCHI_KEY>
YMBFCQPIMVLNIU-UHFFFAOYSA-N

> <FORMULA>
C15H24

> <MOLECULAR_WEIGHT>
204.357

> <EXACT_MASS>
204.187800773

> <JCHEM_ACCEPTOR_COUNT>
0

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
26.379436846094496

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2,6-dimethyl-6-(4-methylpent-3-en-1-yl)bicyclo[3.1.1]hept-2-ene

> <ALOGPS_LOGP>
5.91

> <JCHEM_LOGP>
4.461375721333334

> <ALOGPS_LOGS>
-4.48

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_POLAR_SURFACE_AREA>
0.0

> <JCHEM_REFRACTIVITY>
68.5249

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.82e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
α-bergamotene

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0      -3.093   6.333   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.913   5.343   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.181   3.827   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.001   2.837   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.268   1.320   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.089   0.330   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.268  -0.659   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.681   1.664   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.221   1.664   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.991   0.330   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.221  -1.003   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.991  -2.337   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.681  -1.003   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.015   0.330   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.466   5.870   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   15                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8   13                                             
CONECT    7    6                                                            
CONECT    8    6    9   14                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11    6   14                                                  
CONECT   14   13    8                                                       
CONECT   15    2                                                            
MASTER        0    0    0    0    0    0    0    0   15    0   32    0
END

View in JSmol

Synonyms

Value	Source
a-Bergamotene	Generator
Α-bergamotene	Generator
trans-alpha-Bergamotene	MeSH
cis-alpha-Bergamotene	MeSH

Chemical Formula

C₁₅H₂₄

Average Mass

204.3570 Da

Monoisotopic Mass

204.18780 Da

IUPAC Name

2,6-dimethyl-6-(4-methylpent-3-en-1-yl)bicyclo[3.1.1]hept-2-ene

Traditional Name

α-bergamotene

CAS Registry Number

Not Available

SMILES

CC(C)=CCCC1(C)C2CC1C(C)=CC2

InChI Identifier

InChI=1S/C15H24/c1-11(2)6-5-9-15(4)13-8-7-12(3)14(15)10-13/h6-7,13-14H,5,8-10H2,1-4H3

InChI Key

YMBFCQPIMVLNIU-UHFFFAOYSA-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
Ageratum conyzoides	LOTUS Database	35616633
Alpinia chinensis	LOTUS Database	35616633
Alpinia conchigera	LOTUS Database	35616633
Alpinia galanga	LOTUS Database	35616633
Aristolochia gigantea	LOTUS Database	35616633
Asarum fauriei	LOTUS Database	35616633
Asarum megacalyx	LOTUS Database	35616633
Asarum trigynum	LOTUS Database	35616633
Cannabis sativa	LOTUS Database	35616633
Castanopsis cuspidata	LOTUS Database	35616633
Citrus aurantium	LOTUS Database	35616633
Citrus bergamia	LOTUS Database	35616633
Citrus hystrix	LOTUS Database	35616633
Citrus medica	LOTUS Database	35616633
Commiphora kataf	LOTUS Database	35616633
Curcuma longa	LOTUS Database	35616633
Daucus carota	LOTUS Database	35616633
Dumortiera hirsuta	LOTUS Database	35616633
Elsholtzia blanda	LOTUS Database	35616633
Elsholtzia ciliata	LOTUS Database	35616633
Encelia canescens	LOTUS Database	35616633
Erigeron canadensis	LOTUS Database	35616633
Eupatorium cannabinum	LOTUS Database	35616633
Gossypium hirsutum	LOTUS Database	35616633
Heterotheca subaxillaris	LOTUS Database	35616633
Humulus lupulus	LOTUS Database	35616633
Hyptis suaveolens	LOTUS Database	35616633
Isocoma tenuisecta	LOTUS Database	35616633
Juglans regia	LOTUS Database	35616633
Lippia nodiflora	LOTUS Database	35616633
Micromeria sinaica	LOTUS Database	35616633
Ocimum basilicum	LOTUS Database	35616633
Pectis brevipedunculata	LOTUS Database	35616633
Pelargonium endlicherianum	LOTUS Database	35616633
Perilla frutescens	LOTUS Database	35616633
Pimpinella anisum	LOTUS Database	35616633
Polygala senega	LOTUS Database	35616633
Polyscias fruticosa	LOTUS Database	35616633
Populus alba	LOTUS Database	35616633
Pulicaria arabica	LOTUS Database	35616633
Rhanterium epapposum	LOTUS Database	35616633
Salvia africana-lutea	LOTUS Database	35616633
Santalum spicatum	LOTUS Database	35616633
Sideritis athoa	LOTUS Database	35616633
Smallanthus uvedalia	LOTUS Database	35616633
Stevia rebaudiana	LOTUS Database	35616633
Swertia japonica	LOTUS Database	35616633
Thymus longicaulis	LOTUS Database	35616633
Zanthoxylum zanthoxyloides	LOTUS Database	35616633

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.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Monoterpenoids

Direct Parent

Bicyclic monoterpenoids

Alternative Parents

Substituents

Pinane monoterpenoid
Bicyclic monoterpenoid
Branched unsaturated hydrocarbon
Polycyclic hydrocarbon
Cyclic olefin
Unsaturated aliphatic hydrocarbon
Unsaturated hydrocarbon
Olefin
Hydrocarbon
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

bridged compound (CHEBI:62755 )
sesquiterpene (CHEBI:62755 )
polycyclic olefin (CHEBI:62755 )
Bisabolanes (C17088 )
a sesquiterpenoid (CPD-8849 )

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	5.91	ALOGPS
logP	4.46	ChemAxon
logS	-4.5	ALOGPS
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	0	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	0 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	68.52 m³·mol⁻¹	ChemAxon
Polarizability	26.38 Å³	ChemAxon
Number of Rings	2	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

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00048311

Chemspider ID

Not Available

KEGG Compound ID

C17088

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Bergamotene

METLIN ID

Not Available

PubChem Compound

86608

PDB ID

Not Available

ChEBI ID

62755

Good Scents ID

Not Available

References

General References

Jayaprakasha GK, Rao LJ, Sakariah KK: Chemical composition of volatile oil from Cinnamomum zeylanicum buds. Z Naturforsch C J Biosci. 2002 Nov-Dec;57(11-12):990-3. doi: 10.1515/znc-2002-11-1206. [PubMed:12562082 ]
Weston RJ, Smith GJ: Sesquiterpenes from the inner bark of the silver birch and the paper birch. Nat Prod Commun. 2012 Feb;7(2):145-8. [PubMed:22474938 ]
Chen Y: Analyzing blends of herbivore-induced volatile organic compounds with factor analysis: revisiting "cotton plant, Gossypium hirsutum L., defense in response to nitrogen fertilization". J Econ Entomol. 2013 Apr;106(2):1053-7. doi: 10.1603/ec12178. [PubMed:23786100 ]
LOTUS database [Link]

Showing NP-Card for α-bergamotene (NP0296450)

MOL for NP0296450 (α-bergamotene)

3D MOL for NP0296450 (α-bergamotene)

3D SDF for NP0296450 (α-bergamotene)

3D-SDF for NP0296450 (α-bergamotene)

PDB for NP0296450 (α-bergamotene)

3D PDB for NP0296450 (α-bergamotene)

SMILES for NP0296450 (α-bergamotene)

INCHI for NP0296450 (α-bergamotene)

Structure for NP0296450 (α-bergamotene)

3D Structure for NP0296450 (α-bergamotene)