NP-MRD: Showing NP-Card for methyl (2e,6e,10s)-10,11-dihydroxy-3,7,11-trimethyldodeca-2,6-dienoate (NP0322279)

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Record Information

Version

2.0

Created at

2022-09-12 00:58:00 UTC

Updated at

2022-09-12 00:58:00 UTC

NP-MRD ID

NP0322279

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (2e,6e,10s)-10,11-dihydroxy-3,7,11-trimethyldodeca-2,6-dienoate

Description

(10S)-Juvenile hormone III diol belongs to the class of organic compounds known as sesquiterpenoids. methyl (2e,6e,10s)-10,11-dihydroxy-3,7,11-trimethyldodeca-2,6-dienoate is found in Cleistopholis glauca, Cleistopholis patens and Cleistopholis staudtii. These are terpenes with three consecutive isoprene units (10S)-Juvenile hormone III diol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 48 47  0  0  0  0  0  0  0  0999 V2000
    7.5283   -0.1016   -1.3144 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2691   -0.2278   -0.6862 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0659    0.0590   -1.3177 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1314    0.4543   -2.5260 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7717   -0.0685   -0.6787 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6776   -0.4767    0.5743 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8794   -0.8190    1.3739 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3231   -0.5956    1.2039 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2319   -0.2009    0.2393 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0806   -0.3565    0.9559 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9185    0.6556    1.1423 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4960    1.9762    0.6012 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1700    0.4166    1.8590 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4284    0.7017    1.0877 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4804   -0.1681   -0.1174 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3726    0.0948   -0.9168 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7060    0.0118   -0.9599 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6063   -0.9449   -2.1335 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9835   -0.3182   -0.2284 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8294    1.2898   -1.4751 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.2789    0.1035   -0.5153 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7483   -1.1110   -1.7667 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5660    0.6860   -2.0716 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8866    0.1754   -1.2466 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5685    0.0558    1.5086 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5321   -1.1158    2.3987 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4235   -1.6895    0.9078 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2035   -1.6702    1.4899 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2907    0.0020    2.1341 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2554   -0.8702   -0.6385 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3828    0.8478   -0.0797 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3054   -1.3532    1.3153 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3298    1.8547   -0.4866 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2356    2.7735    0.8006 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4633    2.3289    1.0610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2239   -0.6521    2.1502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2075    0.9635    2.8506 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2761    0.5115    1.7869 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5205    1.7657    0.7917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4513   -1.2335    0.2048 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9433   -0.7470   -1.2583 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5720   -1.1797   -2.4136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0597   -1.9205   -1.7929 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2017   -0.5927   -3.0093 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8132   -0.2152   -0.9591 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9738   -1.3789    0.0964 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1972    0.3895    0.5939 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0952    1.8897   -1.2462 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  2  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 17 19  1  0
 17 20  1  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
  5 24  1  0
  7 25  1  0
  7 26  1  0
  7 27  1  0
  8 28  1  0
  8 29  1  0
  9 30  1  0
  9 31  1  0
 10 32  1  0
 12 33  1  0
 12 34  1  0
 12 35  1  0
 13 36  1  0
 13 37  1  0
 14 38  1  0
 14 39  1  0
 15 40  1  1
 16 41  1  0
 18 42  1  0
 18 43  1  0
 18 44  1  0
 19 45  1  0
 19 46  1  0
 19 47  1  0
 20 48  1  0
M  END

 
  Mrv1652308181800052D          

 20 19  0  0  1  0            999 V2000
   23.0375  -19.8551    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   22.3324  -19.4404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.7426  -19.4404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.5858  -19.8551    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.3324  -18.6108    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.4892  -19.8551    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.1943  -19.4404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.8994  -19.8551    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.1943  -18.6108    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.6460  -19.4404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.3511  -19.8551    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.0562  -19.4404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.7614  -19.8551    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.0562  -18.6108    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.5079  -19.4404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.5079  -18.6108    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   30.2130  -19.8551    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   30.2130  -18.1961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.0375  -20.6801    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   21.6143  -19.0258    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  3  1  0  0  0  0
  2  4  1  0  0  0  0
  2  5  1  0  0  0  0
  3  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 16 18  1  0  0  0  0
  1 19  1  6  0  0  0
  2 20  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0322279

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)\C=C(/C)CC\C=C(/C)CC[C@H](O)C(C)(C)O

> <INCHI_IDENTIFIER>
InChI=1S/C16H28O4/c1-12(9-10-14(17)16(3,4)19)7-6-8-13(2)11-15(18)20-5/h7,11,14,17,19H,6,8-10H2,1-5H3/b12-7+,13-11+/t14-/m0/s1

> <INCHI_KEY>
MBJDYYPZJXVUHJ-RATZTOCSSA-N

> <FORMULA>
C16H28O4

> <MOLECULAR_WEIGHT>
284.396

> <EXACT_MASS>
284.198759382

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
48

> <JCHEM_AVERAGE_POLARIZABILITY>
33.50353550648566

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (2E,6E,10S)-10,11-dihydroxy-3,7,11-trimethyldodeca-2,6-dienoate

> <ALOGPS_LOGP>
2.91

> <JCHEM_LOGP>
2.721160687666667

> <ALOGPS_LOGS>
-3.19

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.321398023513435

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.842453158603472

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0892666139021854

> <JCHEM_POLAR_SURFACE_AREA>
66.76

> <JCHEM_REFRACTIVITY>
81.96879999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.85e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl (2E,6E,10S)-10,11-dihydroxy-3,7,11-trimethyldodeca-2,6-dienoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 18-AUG-18   NONE
TITLE     NULL                                                        
COMPND    MOLECULE:                                                   
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   18-AUG-18         0                                  
HETATM    1  C   UNK     0      43.003 -37.063   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      41.687 -36.289   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      44.320 -36.289   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      40.294 -37.063   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      41.687 -34.740   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      45.713 -37.063   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      47.029 -36.289   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      48.346 -37.063   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      47.029 -34.740   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      49.739 -36.289   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      51.055 -37.063   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      52.372 -36.289   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      53.688 -37.063   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      52.372 -34.740   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      55.081 -36.289   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      55.081 -34.740   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0      56.398 -37.063   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      56.398 -33.966   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      43.003 -38.603   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      40.347 -35.515   0.000  0.00  0.00           O+0
CONECT    1    2    3   19                                                  
CONECT    2    1    4    5   20                                             
CONECT    3    1    6                                                       
CONECT    4    2                                                            
CONECT    5    2                                                            
CONECT    6    3    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7   10                                                       
CONECT    9    7                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12   15                                                       
CONECT   14   12                                                            
CONECT   15   13   16   17                                                  
CONECT   16   15   18                                                       
CONECT   17   15                                                            
CONECT   18   16                                                            
CONECT   19    1                                                            
CONECT   20    2                                                            
MASTER        0    0    0    0    0    0    0    0   20    0   38    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₆H₂₈O₄

Average Mass

284.3960 Da

Monoisotopic Mass

284.19876 Da

IUPAC Name

methyl (2E,6E,10S)-10,11-dihydroxy-3,7,11-trimethyldodeca-2,6-dienoate

Traditional Name

methyl (2E,6E,10S)-10,11-dihydroxy-3,7,11-trimethyldodeca-2,6-dienoate

CAS Registry Number

Not Available

SMILES

COC(=O)\C=C(/C)CC\C=C(/C)CC[C@H](O)C(C)(C)O

InChI Identifier

InChI=1S/C16H28O4/c1-12(9-10-14(17)16(3,4)19)7-6-8-13(2)11-15(18)20-5/h7,11,14,17,19H,6,8-10H2,1-5H3/b12-7+,13-11+/t14-/m0/s1

InChI Key

MBJDYYPZJXVUHJ-RATZTOCSSA-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
Cleistopholis glauca	LOTUS Database	35616633
Cleistopholis patens	LOTUS Database	35616633
Cleistopholis staudtii	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Sesquiterpenoids

Alternative Parents

Substituents

Sesquiterpenoid
Farsesane sesquiterpenoid
Fatty alcohol
Fatty acid ester
Fatty acyl
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Methyl ester
Tertiary alcohol
1,2-diol
Carboxylic acid ester
Secondary alcohol
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxide
Organic oxygen compound
Alcohol
Carbonyl group
Organooxygen compound
Hydrocarbon derivative
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

tertiary alcohol (CHEBI:80537 )
secondary alcohol (CHEBI:80537 )
methyl ester (CHEBI:80537 )
diol (CHEBI:80537 )
enoate ester (CHEBI:80537 )
sesquiterpenoid (CHEBI:80537 )

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	2.91	ALOGPS
logP	2.72	ChemAxon
logS	-3.2	ALOGPS
pKa (Strongest Acidic)	13.84	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	66.76 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	81.97 m³·mol⁻¹	ChemAxon
Polarizability	33.5 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	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

Not Available

KEGG Compound ID

C16505

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10859043

PDB ID

Not Available

ChEBI ID

80537

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (2e,6e,10s)-10,11-dihydroxy-3,7,11-trimethyldodeca-2,6-dienoate (NP0322279)

MOL for NP0322279 (methyl (2e,6e,10s)-10,11-dihydroxy-3,7,11-trimethyldodeca-2,6-dienoate)

3D MOL for NP0322279 (methyl (2e,6e,10s)-10,11-dihydroxy-3,7,11-trimethyldodeca-2,6-dienoate)

3D SDF for NP0322279 (methyl (2e,6e,10s)-10,11-dihydroxy-3,7,11-trimethyldodeca-2,6-dienoate)

3D-SDF for NP0322279 (methyl (2e,6e,10s)-10,11-dihydroxy-3,7,11-trimethyldodeca-2,6-dienoate)

PDB for NP0322279 (methyl (2e,6e,10s)-10,11-dihydroxy-3,7,11-trimethyldodeca-2,6-dienoate)

3D PDB for NP0322279 (methyl (2e,6e,10s)-10,11-dihydroxy-3,7,11-trimethyldodeca-2,6-dienoate)

SMILES for NP0322279 (methyl (2e,6e,10s)-10,11-dihydroxy-3,7,11-trimethyldodeca-2,6-dienoate)

INCHI for NP0322279 (methyl (2e,6e,10s)-10,11-dihydroxy-3,7,11-trimethyldodeca-2,6-dienoate)

Structure for NP0322279 (methyl (2e,6e,10s)-10,11-dihydroxy-3,7,11-trimethyldodeca-2,6-dienoate)

3D Structure for NP0322279 (methyl (2e,6e,10s)-10,11-dihydroxy-3,7,11-trimethyldodeca-2,6-dienoate)