NP-MRD: Showing NP-Card for (+)-5-epi-aristolochene (NP0155095)

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Record Information

Version

2.0

Created at

2022-09-02 12:06:05 UTC

Updated at

2022-09-02 12:06:05 UTC

NP-MRD ID

NP0155095

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-5-epi-aristolochene

Description

(+)-5-Epi-aristolochene belongs to the class of organic compounds known as eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids. These are sesquiterpenoids with a structure based either on the eremophilane skeleton, its 8,9-seco derivative, or the furoeremophilane skeleton. Eremophilanes have been shown to be derived from eudesmanes by migration of the methyl group at C-10 to C-5. Thus, (+)-5-epi-aristolochene is considered to be an isoprenoid. (+)-5-epi-aristolochene is found in Nicotiana tabacum. (+)-5-epi-aristolochene was first documented in 2016 (PMID: 27328867). Based on a literature review a significant number of articles have been published on (+)-5-epi-aristolochene (PMID: 34264250) (PMID: 32694584) (PMID: 31864296) (PMID: 31534022) (PMID: 31294452) (PMID: 30919065).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 39 40  0  0  0  0  0  0  0  0999 V2000
    2.6987    1.7560    2.4705 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3351    1.3391    1.2714 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9843    1.9013    0.0591 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2840    0.3156    1.1485 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8940   -0.9920    0.6294 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7555   -1.9541    0.6504 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3678   -1.5906    0.0525 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5123   -2.5426    0.0670 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8433   -1.8778    0.0043 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7862   -0.3811   -0.0015 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8287    0.0662   -1.0487 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9135    1.5163   -1.3978 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4152   -0.2650   -0.5957 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4446   -0.2068   -1.8575 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0984    0.7691    0.3745 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4633    2.5022    2.5891 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2324    1.3530    3.3559 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4878    1.0782   -0.4974 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2171    2.3825   -0.5982 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7396    2.6338    0.3523 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9163    0.0377    2.1821 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3912   -0.8900   -0.3311 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5901   -1.3191    1.4457 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8321   -2.9305    1.1395 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4929   -3.2032    0.9591 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3766   -3.2343   -0.8155 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5019   -2.1800    0.8647 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4164   -2.1953   -0.9082 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5602    0.0404    0.9991 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8082   -0.0137   -0.2825 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0055   -0.5306   -1.9647 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7192    1.6386   -2.1797 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9849    1.9452   -1.7822 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2470    2.1225   -0.5387 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2101    0.5693   -1.8060 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1704    0.0530   -2.7691 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8384   -1.2300   -2.1123 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2978    1.7257   -0.1915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7608    1.0017    1.0634 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 11  1  0
 11 10  1  0
 10  9  1  0
  9  8  1  0
  8  7  1  0
  7  6  2  0
  6  5  1  0
  5  4  1  0
  4 15  1  0
 15 13  1  0
 13 14  1  6
  4  2  1  0
  2  3  1  0
  2  1  2  3
 13 11  1  0
 13  7  1  0
 12 32  1  0
 12 33  1  0
 12 34  1  0
 11 31  1  6
 10 29  1  0
 10 30  1  0
  9 27  1  0
  9 28  1  0
  8 25  1  0
  8 26  1  0
  6 24  1  0
  5 22  1  0
  5 23  1  0
  4 21  1  1
 15 38  1  0
 15 39  1  0
 14 35  1  0
 14 36  1  0
 14 37  1  0
  3 18  1  0
  3 19  1  0
  3 20  1  0
  1 16  1  0
  1 17  1  0
M  END


  Mrv1652309022214062D          

 15 16  0  0  1  0            999 V2000
    0.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    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
    0.7145   -1.2375    0.0000 C   0  0  2  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
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1434   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  4  2  1  6  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  1  0  0  0
 11 13  1  0  0  0  0
  7 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  0  0  0  0
  4 15  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0155095

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1CCCC2=CC[C@H](C[C@]12C)C(C)=C

> <INCHI_IDENTIFIER>
InChI=1S/C15H24/c1-11(2)13-8-9-14-7-5-6-12(3)15(14,4)10-13/h9,12-13H,1,5-8,10H2,2-4H3/t12-,13-,15-/m1/s1

> <INCHI_KEY>
YONHOSLUBQJXPR-UMVBOHGHSA-N

> <FORMULA>
C15H24

> <MOLECULAR_WEIGHT>
204.357

> <EXACT_MASS>
204.187800773

> <JCHEM_ACCEPTOR_COUNT>
0

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
25.896680655176084

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(4R,4aR,6R)-4,4a-dimethyl-6-(prop-1-en-2-yl)-1,2,3,4,4a,5,6,7-octahydronaphthalene

> <ALOGPS_LOGP>
5.85

> <JCHEM_LOGP>
4.519309391666669

> <ALOGPS_LOGS>
-4.87

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_POLAR_SURFACE_AREA>
0.0

> <JCHEM_REFRACTIVITY>
67.4524

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.74e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(+)-5-epi-aristolochene

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.001  -3.850   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   15                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   13                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11    7   14   15                                             
CONECT   14   13                                                            
CONECT   15   13    4                                                       
MASTER        0    0    0    0    0    0    0    0   15    0   32    0
END

View in JSmol

Synonyms

Value	Source
Epi-aristolochene	ChEBI
(+)-5-Epiaristolochene	Kegg
5-Epi-aristolochene	Kegg

Chemical Formula

C₁₅H₂₄

Average Mass

204.3570 Da

Monoisotopic Mass

204.18780 Da

IUPAC Name

(4R,4aR,6R)-4,4a-dimethyl-6-(prop-1-en-2-yl)-1,2,3,4,4a,5,6,7-octahydronaphthalene

Traditional Name

(+)-5-epi-aristolochene

CAS Registry Number

Not Available

SMILES

C[C@@H]1CCCC2=CC[C@H](C[C@]12C)C(C)=C

InChI Identifier

InChI=1S/C15H24/c1-11(2)13-8-9-14-7-5-6-12(3)15(14,4)10-13/h9,12-13H,1,5-8,10H2,2-4H3/t12-,13-,15-/m1/s1

InChI Key

YONHOSLUBQJXPR-UMVBOHGHSA-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
Nicotiana tabacum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids. These are sesquiterpenoids with a structure based either on the eremophilane skeleton, its 8,9-seco derivative, or the furoeremophilane skeleton. Eremophilanes have been shown to be derived from eudesmanes by migration of the methyl group at C-10 to C-5.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids

Alternative Parents

Substituents

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

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

carbobicyclic compound (CHEBI:23925 )
sesquiterpene (CHEBI:23925 )
Aristolane sesquiterpenoids (LMPR0103270004 )

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	5.85	ALOGPS
logP	4.52	ChemAxon
logS	-4.9	ALOGPS
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	0	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	0 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	67.45 m³·mol⁻¹	ChemAxon
Polarizability	25.9 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

Not Available

Chemspider ID

4574150

KEGG Compound ID

C19708

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5460659

PDB ID

Not Available

ChEBI ID

23925

Good Scents ID

Not Available

References

General References

Huang JQ, Li DM, Li JX, Lin JL, Tian X, Wang LJ, Chen XY, Fang X: 1,10/1,11-Cyclization catalyzed by diverged plant sesquiterpene synthases is dependent on a single residue. Org Biomol Chem. 2021 Aug 5;19(30):6650-6656. doi: 10.1039/d1ob00827g. [PubMed:34264250 ]
Baba VY, Powell AF, Ivamoto-Suzuki ST, Pereira LFP, Vanzela ALL, Giacomin RM, Strickler SR, Mueller LA, Rodrigues R, Goncalves LSA: Capsidiol-related genes are highly expressed in response to Colletotrichum scovillei during Capsicum annuum fruit development stages. Sci Rep. 2020 Jul 21;10(1):12048. doi: 10.1038/s41598-020-68949-5. [PubMed:32694584 ]
Kojima T, Asakura N, Hasegawa S, Hirasawa T, Mizuno Y, Takemoto D, Katou S: Transcriptional induction of capsidiol synthesis genes by wounding can promote pathogen signal-induced capsidiol synthesis. BMC Plant Biol. 2019 Dec 21;19(1):576. doi: 10.1186/s12870-019-2204-1. [PubMed:31864296 ]
Nguyen TD, Kwon M, Kim SU, Fischer C, Ro DK: Catalytic Plasticity of Germacrene A Oxidase Underlies Sesquiterpene Lactone Diversification. Plant Physiol. 2019 Nov;181(3):945-960. doi: 10.1104/pp.19.00629. Epub 2019 Sep 18. [PubMed:31534022 ]
Song N, Ma L, Wang W, Sun H, Wang L, Baldwin IT, Wu J: An ERF2-like transcription factor regulates production of the defense sesquiterpene capsidiol upon Alternaria alternata infection. J Exp Bot. 2019 Oct 24;70(20):5895-5908. doi: 10.1093/jxb/erz327. [PubMed:31294452 ]
Cai Y, Whitehead P, Chappell J, Chapman KD: Mouse lipogenic proteins promote the co-accumulation of triacylglycerols and sesquiterpenes in plant cells. Planta. 2019 Jul;250(1):79-94. doi: 10.1007/s00425-019-03148-9. Epub 2019 Mar 27. [PubMed:30919065 ]
Koo HJ, Vickery CR, Xu Y, Louie GV, O'Maille PE, Bowman M, Nartey CM, Burkart MD, Noel JP: Biosynthetic potential of sesquiterpene synthases: product profiles of Egyptian Henbane premnaspirodiene synthase and related mutants. J Antibiot (Tokyo). 2016 Jul;69(7):524-33. doi: 10.1038/ja.2016.68. Epub 2016 Jun 22. [PubMed:27328867 ]
Imano S, Fushimi M, Camagna M, Tsuyama-Koike A, Mori H, Ashida A, Tanaka A, Sato I, Chiba S, Kawakita K, Ojika M, Takemoto D: AP2/ERF Transcription Factor NbERF-IX-33 Is Involved in the Regulation of Phytoalexin Production for the Resistance of Nicotiana benthamiana to Phytophthora infestans. Front Plant Sci. 2022 Jan 27;12:821574. doi: 10.3389/fpls.2021.821574. eCollection 2021. [PubMed:35154216 ]
Lee HA, Kim S, Kim S, Choi D: Expansion of sesquiterpene biosynthetic gene clusters in pepper confers nonhost resistance to the Irish potato famine pathogen. New Phytol. 2017 Aug;215(3):1132-1143. doi: 10.1111/nph.14637. Epub 2017 Jun 20. [PubMed:28631815 ]
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LOTUS database [Link]

Showing NP-Card for (+)-5-epi-aristolochene (NP0155095)

MOL for NP0155095 ((+)-5-epi-aristolochene)

3D MOL for NP0155095 ((+)-5-epi-aristolochene)

3D SDF for NP0155095 ((+)-5-epi-aristolochene)

3D-SDF for NP0155095 ((+)-5-epi-aristolochene)

PDB for NP0155095 ((+)-5-epi-aristolochene)

3D PDB for NP0155095 ((+)-5-epi-aristolochene)

SMILES for NP0155095 ((+)-5-epi-aristolochene)

INCHI for NP0155095 ((+)-5-epi-aristolochene)

Structure for NP0155095 ((+)-5-epi-aristolochene)

3D Structure for NP0155095 ((+)-5-epi-aristolochene)