NP-MRD: Showing NP-Card for beta-Barbatene (NP0064834)

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Record Information

Version

2.0

Created at

2022-04-28 09:07:12 UTC

Updated at

2022-04-28 09:07:12 UTC

NP-MRD ID

NP0064834

Secondary Accession Numbers

None

Natural Product Identification

Common Name

beta-Barbatene

Description

Beta-Barbatene, also known as β-barbatene, belongs to the class of organic compounds known as branched unsaturated hydrocarbons. These are hydrocarbons that contains one or more unsaturated carbon atoms, and an aliphatic branch. beta-Barbatene is found in Barbilophazia floerkei, Barbilophozia attenuata, Barbilophozia barbata, Barbilophozia floerkei, Barbilophozia hatcheri, Barbilophozia lycopodioides, Bazzania pompeana, Bazzania trilobata, Bazzania trilobata L., Callitris sulcata, Chiloscyphus polyanthos, Frullania anomala, Frullania falciloba, Frullania media, Frullania monocera, Frullania scandens, Frullania squarrosula, Frullania tamarisci, Gymnomitrion obtusum, Jungermannia truncata NEES, Lejeunea aquatica, Lepidozia fauriana, Lepidozia vitrea, Lophocolea heterophylla, Marchantia polymorpha, Marsupella aquatica, Marsupella emarginata, Metacalypogeia alternifolia, Metacalypogeia cordifolia, Meum athamanticum, Neocallitropsis pancheri, Plagiochila asplenioides, Plagiochila semidecurrens, Ptilidium ciliare, Reboulia hemisphaerica, Schusterella chevalieri, Spongiporus leucomallellus (Murril), Trichocolea tomentella, Tritomaria quinquedentata, Tritomaria quinquedentata (Huds.) and Trocholejeunea sandvicensis. beta-Barbatene was first documented in 2014 (PMID: 25251011). Based on a literature review a small amount of articles have been published on beta-Barbatene (PMID: 33210234) (PMID: 31621716) (PMID: 27790999) (PMID: 30807037).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 39 41  0  0  0  0  0  0  0  0999 V2000
    2.8907   -1.4605   -0.8177 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0704   -0.5085   -0.4358 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0252    0.7636   -1.1567 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7649    1.5529   -0.9314 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0742    1.2942    0.3614 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5036    2.5820    0.9210 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0499    0.6710    1.3692 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1877   -0.7225    0.7289 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2240   -1.0458    0.2744 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8523   -2.1394    1.1019 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2753   -1.4868   -1.1678 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4935   -0.8462   -1.7572 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8759    0.3051   -0.8817 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9876    0.2406    0.3157 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7715    0.3067    1.6182 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9404   -2.4263   -0.2878 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5656   -1.3754   -1.6604 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9439    1.3704   -0.9153 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1195    0.5599   -2.2566 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0759    1.4939   -1.8249 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0814    2.6389   -0.9223 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2450    2.7479    1.9755 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0253    3.4385    0.3605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5847    2.6764    0.7059 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6109    0.5871    2.3618 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0258    1.2006    1.3528 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5530   -1.4625    1.4464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9519   -2.0696    1.0768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6082   -3.1217    0.6044 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4267   -2.2207    2.1180 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3747   -2.6102   -1.2227 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6187   -1.2399   -1.7444 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2904   -0.4540   -2.7908 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2957   -1.6114   -1.8505 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9039    1.2790   -1.3883 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9248    0.0947   -0.5177 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5148   -0.5075    2.3121 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8518    0.2521    1.3612 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6168    1.2533    2.1640 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  6  1  1
  5  7  1  0
  7  8  1  0
  8  2  1  0
  2  1  2  3
  2  3  1  0
  3  4  1  0
  8  9  1  0
  9 10  1  1
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  1
  4  5  1  0
 14  9  1  0
 14  5  1  0
  6 22  1  0
  6 23  1  0
  6 24  1  0
  7 25  1  0
  7 26  1  0
  8 27  1  1
  1 16  1  0
  1 17  1  0
  3 18  1  0
  3 19  1  0
  4 20  1  0
  4 21  1  0
 10 28  1  0
 10 29  1  0
 10 30  1  0
 11 31  1  0
 11 32  1  0
 12 33  1  0
 12 34  1  0
 13 35  1  0
 13 36  1  0
 15 37  1  0
 15 38  1  0
 15 39  1  0
M  END


  Mrv1652304282211072D          

 15 17  0  0  1  0            999 V2000
    2.1821    0.2259    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1821    1.0509    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9667    1.3058    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4517    0.6384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9667   -0.0291    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5371    1.5652    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7328    1.3817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3748    0.6384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7328   -0.1049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2184   -0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5371   -0.2885    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3054    0.6384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7207    2.3696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3294    1.8626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3294   -0.5859    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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  1  5  1  0  0  0  0
  2  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
  1 11  1  0  0  0  0
 11 12  1  6  0  0  0
  6 12  1  0  0  0  0
  6 13  1  6  0  0  0
  2 14  1  6  0  0  0
  1 15  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0064834

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@]12C[C@H](C(=C)CC1)[C@]1(C)CCC[C@]21C

> <INCHI_IDENTIFIER>
InChI=1S/C15H24/c1-11-6-9-13(2)10-12(11)14(3)7-5-8-15(13,14)4/h12H,1,5-10H2,2-4H3/t12-,13-,14+,15-/m1/s1

> <INCHI_KEY>
RTONMYLSQISFQA-APIJFGDWSA-N

> <FORMULA>
C15H24

> <MOLECULAR_WEIGHT>
204.357

> <EXACT_MASS>
204.187800773

> <JCHEM_ACCEPTOR_COUNT>
0

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
25.246239682870957

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,2R,6S,7R)-1,2,6-trimethyl-8-methylidenetricyclo[5.3.1.0^{2,6}]undecane

> <ALOGPS_LOGP>
5.34

> <JCHEM_LOGP>
4.172119880333334

> <ALOGPS_LOGS>
-5.25

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_POLAR_SURFACE_AREA>
0.0

> <JCHEM_REFRACTIVITY>
64.54839999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.14e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,6S,7R)-1,2,6-trimethyl-8-methylidenetricyclo[5.3.1.0^{2,6}]undecane

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       4.073   0.422   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.073   1.962   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.538   2.437   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.443   1.192   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.538  -0.054   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.869   2.922   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.368   2.579   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.700   1.192   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.368  -0.196   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.408  -1.400   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.869  -0.539   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.437   1.192   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.212   4.423   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.348   3.477   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.348  -1.094   0.000  0.00  0.00           C+0
CONECT    1    2    5   11   15                                             
CONECT    2    1    3    6   14                                             
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    1                                                       
CONECT    6    2    7   12   13                                             
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9    1   12                                                  
CONECT   12   11    6                                                       
CONECT   13    6                                                            
CONECT   14    2                                                            
CONECT   15    1                                                            
MASTER        0    0    0    0    0    0    0    0   15    0   34    0
END

View in JSmol

Synonyms

Value	Source
b-Barbatene	Generator
Β-barbatene	Generator

Chemical Formula

C₁₅H₂₄

Average Mass

204.3570 Da

Monoisotopic Mass

204.18780 Da

IUPAC Name

(1R,2R,6S,7R)-1,2,6-trimethyl-8-methylidenetricyclo[5.3.1.0^{2,6}]undecane

Traditional Name

(1R,2R,6S,7R)-1,2,6-trimethyl-8-methylidenetricyclo[5.3.1.0^{2,6}]undecane

CAS Registry Number

Not Available

SMILES

C[C@]12C[C@H](C(=C)CC1)[C@]1(C)CCC[C@]21C

InChI Identifier

InChI=1S/C15H24/c1-11-6-9-13(2)10-12(11)14(3)7-5-8-15(13,14)4/h12H,1,5-10H2,2-4H3/t12-,13-,14+,15-/m1/s1

InChI Key

RTONMYLSQISFQA-APIJFGDWSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Barbilophazia floerkei	-	KNApSAcK
Barbilophozia attenuata	Plant	KNApSAcK
Barbilophozia barbata	Plant	KNApSAcK
Barbilophozia floerkei	Plant	KNApSAcK
Barbilophozia hatcheri	Plant	KNApSAcK
Barbilophozia lycopodioides	Plant	KNApSAcK
Bazzania pompeana	Plant	KNApSAcK
Bazzania trilobata	LOTUS Database	35616633
Bazzania trilobata L.	Plant	KNApSAcK
Callitris sulcata	Plant	KNApSAcK
Chiloscyphus polyanthos	-	KNApSAcK
Frullania anomala	Plant	KNApSAcK
Frullania falciloba	Plant	KNApSAcK
Frullania media	Plant	KNApSAcK
Frullania monocera	Plant	KNApSAcK
Frullania scandens	Plant	KNApSAcK
Frullania squarrosula	Plant	KNApSAcK
Frullania tamarisci	Plant	KNApSAcK
Gymnomitrion obtusum	-	KNApSAcK
Jungermannia truncata NEES	Plant	KNApSAcK
Lejeunea aquatica	LOTUS Database	35616633
Lepidozia fauriana	Plant	KNApSAcK
Lepidozia vitrea	Plant	KNApSAcK
Lophocolea heterophylla	LOTUS Database	35616633
Marchantia polymorpha	LOTUS Database	35616633
Marsupella aquatica	Plant	KNApSAcK
Marsupella emarginata	Plant	KNApSAcK
Metacalypogeia alternifolia	LOTUS Database	35616633
Metacalypogeia cordifolia	LOTUS Database	35616633
Meum athamanticum	LOTUS Database	35616633
Neocallitropsis pancheri	Plant	KNApSAcK
Plagiochila asplenioides	LOTUS Database	35616633
Plagiochila semidecurrens	LOTUS Database	35616633
Ptilidium ciliare	Plant	KNApSAcK
Reboulia hemisphaerica	Plant	KNApSAcK
Schusterella chevalieri	-	KNApSAcK
Spongiporus leucomallellus (Murril)	-	KNApSAcK
Trichocolea tomentella	LOTUS Database	35616633
Trilophozia quinquedentata	LOTUS Database	35616633
Tritomaria quinquedentata (Huds.)	Plant	KNApSAcK
Trocholejeunea sandvicensis	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as branched unsaturated hydrocarbons. These are hydrocarbons that contains one or more unsaturated carbon atoms, and an aliphatic branch.

Kingdom

Organic compounds

Super Class

Hydrocarbons

Class

Unsaturated hydrocarbons

Sub Class

Branched unsaturated hydrocarbons

Direct Parent

Branched unsaturated hydrocarbons

Alternative Parents

Substituents

Branched unsaturated hydrocarbon
Polycyclic hydrocarbon
Cyclic olefin
Unsaturated aliphatic hydrocarbon
Olefin
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic 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	5.34	ALOGPS
logP	4.17	ChemAxon
logS	-5.2	ALOGPS
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	64.55 m³·mol⁻¹	ChemAxon
Polarizability	25.25 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

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00021886

Chemspider ID

66738200

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

14109421

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Abdulsalam O, Wagner K, Wirth S, Kunert M, David A, Kallenbach M, Boland W, Kothe E, Krause K: Phytohormones and volatile organic compounds, like geosmin, in the ectomycorrhiza of Tricholoma vaccinum and Norway spruce (Picea abies). Mycorrhiza. 2021 Mar;31(2):173-188. doi: 10.1007/s00572-020-01005-2. Epub 2020 Nov 18. [PubMed:33210234 ]
Rinkel J, Kollner TG, Chen F, Dickschat JS: Characterisation of three terpene synthases for beta-barbatene, beta-araneosene and nephthenol from social amoebae. Chem Commun (Camb). 2019 Oct 31;55(88):13255-13258. doi: 10.1039/c9cc07681f. [PubMed:31621716 ]
Chen X, Kollner TG, Jia Q, Norris A, Santhanam B, Rabe P, Dickschat JS, Shaulsky G, Gershenzon J, Chen F: Terpene synthase genes in eukaryotes beyond plants and fungi: Occurrence in social amoebae. Proc Natl Acad Sci U S A. 2016 Oct 25;113(43):12132-12137. doi: 10.1073/pnas.1610379113. Epub 2016 Oct 7. [PubMed:27790999 ]
Yongabi KA, Novakovie M, Bukvicki D, Reeb C, Asakawa Y: Management of Diabetic Bacterial Foot Infections with Organic Extracts of Liverwort Marchantia debilis from Cameroon. Nat Prod Commun. 2016 Sep;11(9):1333-1336. [PubMed:30807037 ]
Petek M, Rotter A, Kogovsek P, Baebler S, Mithofer A, Gruden K: Potato virus Y infection hinders potato defence response and renders plants more vulnerable to Colorado potato beetle attack. Mol Ecol. 2014 Nov;23(21):5378-91. doi: 10.1111/mec.12932. Epub 2014 Oct 9. [PubMed:25251011 ]

Showing NP-Card for beta-Barbatene (NP0064834)

MOL for NP0064834 (beta-Barbatene)

3D MOL for NP0064834 (beta-Barbatene)

3D SDF for NP0064834 (beta-Barbatene)

3D-SDF for NP0064834 (beta-Barbatene)

PDB for NP0064834 (beta-Barbatene)

3D PDB for NP0064834 (beta-Barbatene)

SMILES for NP0064834 (beta-Barbatene)

INCHI for NP0064834 (beta-Barbatene)

Structure for NP0064834 (beta-Barbatene)

3D Structure for NP0064834 (beta-Barbatene)