NP-MRD: Showing NP-Card for (E,E,E)-10-(2-Hydroxy-1-methylethylidene)-3,7-dimethyl-3,7-cyclodecadien-1-one (NP0058346)

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Record Information

Version

2.0

Created at

2022-04-28 03:42:38 UTC

Updated at

2022-04-28 03:42:38 UTC

NP-MRD ID

NP0058346

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(E,E,E)-10-(2-Hydroxy-1-methylethylidene)-3,7-dimethyl-3,7-cyclodecadien-1-one

Description

13-Hydroxygermacrone belongs to the class of organic compounds known as germacrane sesquiterpenoids. These are sesquiterpenoids having the germacrane skeleton, with a structure characterized by a cyclodecane ring substituted with an isopropyl and two methyl groups. (E,E,E)-10-(2-Hydroxy-1-methylethylidene)-3,7-dimethyl-3,7-cyclodecadien-1-one is found in Curcuma aromatica and Curcuma zedoaria . (E,E,E)-10-(2-Hydroxy-1-methylethylidene)-3,7-dimethyl-3,7-cyclodecadien-1-one was first documented in 2002 (PMID: 12033504). Based on a literature review a small amount of articles have been published on 13-Hydroxygermacrone (PMID: 18663560) (PMID: 33866197) (PMID: 25471012) (PMID: 16901812).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 39 39  0  0  0  0  0  0  0  0999 V2000
   -1.7076    3.3017   -0.2514 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2883    1.9889    0.3571 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0291    1.6313    0.4469 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4926    0.3689    1.0239 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3735   -0.3526    0.0705 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6788   -0.1506   -0.0070 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4820   -0.9382   -1.0103 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3879    0.8326    0.8508 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3500    0.1216    1.6063 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7631   -1.3372   -0.8434 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4152   -2.3498   -1.2091 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6508   -1.1376   -1.3488 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6548   -1.7877   -0.5065 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4512   -3.2536   -0.1928 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7006   -1.1665   -0.0253 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9944    0.2640   -0.2702 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4020    1.1407    0.8440 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1696    3.1363   -1.2525 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4454    3.7435    0.4749 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8792    4.0067   -0.3265 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7718    2.3034    0.0682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3500   -0.2981    1.3675 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0087    0.6272    1.9777 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0177   -0.8656   -2.0179 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6501   -1.9542   -0.6558 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4601   -0.4289   -1.1015 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7752    1.3851    1.5451 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9669    1.4844    0.1478 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4956    0.5748    2.4835 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6890   -1.6712   -2.3451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8147   -0.0924   -1.5876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6970   -3.4005    0.8984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4298   -3.5623   -0.3941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1798   -3.8136   -0.7888 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4523   -1.6823    0.6128 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6102    0.6407   -1.2304 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1088    0.4159   -0.3236 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2492    1.7722    1.2042 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1355    0.5031    1.7088 H   0  0  0  0  0  0  0  0  0  0  0  0
  7  6  1  0
  6  8  1  0
  8  9  1  0
  6  5  2  0
  5  4  1  0
  4  3  1  0
  3  2  2  0
  2  1  1  0
  2 17  1  0
 17 16  1  0
 16 15  1  0
 15 13  2  0
 13 14  1  0
 13 12  1  0
 12 10  1  0
 10 11  2  0
 10  5  1  0
  7 24  1  0
  7 25  1  0
  7 26  1  0
  8 27  1  0
  8 28  1  0
  9 29  1  0
  4 22  1  0
  4 23  1  0
  3 21  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
 17 38  1  0
 17 39  1  0
 16 36  1  0
 16 37  1  0
 15 35  1  0
 14 32  1  0
 14 33  1  0
 14 34  1  0
 12 30  1  0
 12 31  1  0
M  END


  Mrv1652304282205422D          

 17 17  0  0  0  0            999 V2000
    1.4289    1.5039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6990    0.7243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5091    0.5684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7792   -0.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5893   -0.3671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8593   -1.1466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1294    0.2566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9395    0.1007    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2391   -0.8348    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5091   -1.6143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.6789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1589    0.1007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3488    0.2566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0787    1.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6188    1.6598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2293    0.9227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9690    2.1275    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
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  4  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
  1 15  1  0  0  0  0
 12 16  1  0  0  0  0
  1 17  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0058346

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C(CO)=C1\C\C=C(C)\CC\C=C(C)\CC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C15H22O2/c1-11-5-4-6-12(2)9-15(17)14(8-7-11)13(3)10-16/h6-7,16H,4-5,8-10H2,1-3H3/b11-7+,12-6+,14-13+

> <INCHI_KEY>
OYONKNQJEXRUQZ-UPXYLJBOSA-N

> <FORMULA>
C15H22O2

> <MOLECULAR_WEIGHT>
234.339

> <EXACT_MASS>
234.161979948

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
26.884324317071858

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3E,7E,10E)-10-(1-hydroxypropan-2-ylidene)-3,7-dimethylcyclodeca-3,7-dien-1-one

> <ALOGPS_LOGP>
3.01

> <JCHEM_LOGP>
2.829880913666667

> <ALOGPS_LOGS>
-3.13

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
16.27559648431211

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.061424189045628

> <JCHEM_PKA_STRONGEST_BASIC>
-2.7527381815689447

> <JCHEM_POLAR_SURFACE_AREA>
37.3

> <JCHEM_REFRACTIVITY>
73.5567

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.75e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3E,7E,10E)-10-(1-hydroxypropan-2-ylidene)-3,7-dimethylcyclodeca-3,7-dien-1-one

> <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       2.667   2.807   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.171   1.352   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.684   1.061   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.188  -0.394   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.700  -0.685   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.204  -2.140   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.708   0.479   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       9.220   0.188   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       4.180  -1.558   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       4.684  -3.013   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       2.667  -1.267   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.163   0.188   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.651   0.479   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.147   1.934   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.155   3.098   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.295   1.722   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.676   3.971   0.000  0.00  0.00           C+0
CONECT    1    2   15   17                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    9                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7                                                            
CONECT    9    4   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   16                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14    1                                                       
CONECT   16   12                                                            
CONECT   17    1                                                            
MASTER        0    0    0    0    0    0    0    0   17    0   34    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₂₂O₂

Average Mass

234.3390 Da

Monoisotopic Mass

234.16198 Da

IUPAC Name

(3E,7E,10E)-10-(1-hydroxypropan-2-ylidene)-3,7-dimethylcyclodeca-3,7-dien-1-one

Traditional Name

(3E,7E,10E)-10-(1-hydroxypropan-2-ylidene)-3,7-dimethylcyclodeca-3,7-dien-1-one

CAS Registry Number

Not Available

SMILES

C\C(CO)=C1\C\C=C(C)\CC\C=C(C)\CC1=O

InChI Identifier

InChI=1S/C15H22O2/c1-11-5-4-6-12(2)9-15(17)14(8-7-11)13(3)10-16/h6-7,16H,4-5,8-10H2,1-3H3/b11-7+,12-6+,14-13+

InChI Key

OYONKNQJEXRUQZ-UPXYLJBOSA-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
Curcuma aromatica	LOTUS Database	35616633
Curcuma zedoaria	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as germacrane sesquiterpenoids. These are sesquiterpenoids having the germacrane skeleton, with a structure characterized by a cyclodecane ring substituted with an isopropyl and two methyl groups.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Germacrane sesquiterpenoids

Alternative Parents

Substituents

Germacrane sesquiterpenoid
Cyclic ketone
Ketone
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic homomonocyclic 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	3.01	ALOGPS
logP	2.83	ChemAxon
logS	-3.1	ALOGPS
pKa (Strongest Acidic)	15.06	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	37.3 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	73.56 m³·mol⁻¹	ChemAxon
Polarizability	26.88 Å³	ChemAxon
Number of Rings	1	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

C00011729

Chemspider ID

8574578

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10399140

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Qu Y, Xu F, Nakamura S, Matsuda H, Pongpiriyadacha Y, Wu L, Yoshikawa M: Sesquiterpenes from Curcuma comosa. J Nat Med. 2009 Jan;63(1):102-4. doi: 10.1007/s11418-008-0282-8. Epub 2008 Jul 29. [PubMed:18663560 ]
Tong H, Yu M, Fei C, Ji, Dong J, Su L, Gu W, Mao C, Li L, Bian Z, Lu T, Hao M, Zeng B: Bioactive constituents and the molecular mechanism of Curcumae Rhizoma in the treatment of primary dysmenorrhea based on network pharmacology and molecular docking. Phytomedicine. 2021 Jun;86:153558. doi: 10.1016/j.phymed.2021.153558. Epub 2021 Mar 27. [PubMed:33866197 ]
Park JH, Mohamed MA, Jung YJ, Shrestha S, Lee TH, Lee CH, Han D, Kim J, Baek NI: Germacrane sesquiterpenes isolated from the rhizome of Curcuma xanthorrhiza Roxb. inhibit UVB-induced upregulation of MMP-1, -2, and -3 expression in human keratinocytes. Arch Pharm Res. 2015 Oct;38(10):1752-60. doi: 10.1007/s12272-014-0525-z. Epub 2014 Dec 4. [PubMed:25471012 ]
Makabe H, Maru N, Kuwabara A, Kamo T, Hirota M: Anti-inflammatory sesquiterpenes from Curcuma zedoaria. Nat Prod Res. 2006 Jun;20(7):680-5. doi: 10.1080/14786410500462900. [PubMed:16901812 ]
Morikawa T, Matsuda H, Ninomiya K, Yoshikawa M: Medicinal foodstuffs. XXIX. Potent protective effects of sesquiterpenes and curcumin from Zedoariae Rhizoma on liver injury induced by D-galactosamine/lipopolysaccharide or tumor necrosis factor-alpha. Biol Pharm Bull. 2002 May;25(5):627-31. doi: 10.1248/bpb.25.627. [PubMed:12033504 ]

Showing NP-Card for (E,E,E)-10-(2-Hydroxy-1-methylethylidene)-3,7-dimethyl-3,7-cyclodecadien-1-one (NP0058346)

MOL for NP0058346 ((E,E,E)-10-(2-Hydroxy-1-methylethylidene)-3,7-dimethyl-3,7-cyclodecadien-1-one)

3D MOL for NP0058346 ((E,E,E)-10-(2-Hydroxy-1-methylethylidene)-3,7-dimethyl-3,7-cyclodecadien-1-one)

3D SDF for NP0058346 ((E,E,E)-10-(2-Hydroxy-1-methylethylidene)-3,7-dimethyl-3,7-cyclodecadien-1-one)

3D-SDF for NP0058346 ((E,E,E)-10-(2-Hydroxy-1-methylethylidene)-3,7-dimethyl-3,7-cyclodecadien-1-one)

PDB for NP0058346 ((E,E,E)-10-(2-Hydroxy-1-methylethylidene)-3,7-dimethyl-3,7-cyclodecadien-1-one)

3D PDB for NP0058346 ((E,E,E)-10-(2-Hydroxy-1-methylethylidene)-3,7-dimethyl-3,7-cyclodecadien-1-one)

SMILES for NP0058346 ((E,E,E)-10-(2-Hydroxy-1-methylethylidene)-3,7-dimethyl-3,7-cyclodecadien-1-one)

INCHI for NP0058346 ((E,E,E)-10-(2-Hydroxy-1-methylethylidene)-3,7-dimethyl-3,7-cyclodecadien-1-one)

Structure for NP0058346 ((E,E,E)-10-(2-Hydroxy-1-methylethylidene)-3,7-dimethyl-3,7-cyclodecadien-1-one)

3D Structure for NP0058346 ((E,E,E)-10-(2-Hydroxy-1-methylethylidene)-3,7-dimethyl-3,7-cyclodecadien-1-one)