NP-MRD: Showing NP-Card for methyl (2z,4e)-5-[(1r,3s,5r,8s)-3,8-dihydroxy-1,5-dimethyl-6-oxabicyclo[3.2.1]octan-8-yl]-3-methylpenta-2,4-dienoate (NP0329622)

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Record Information

Version

2.0

Created at

2022-09-12 14:10:31 UTC

Updated at

2022-09-12 14:10:31 UTC

NP-MRD ID

NP0329622

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (2z,4e)-5-[(1r,3s,5r,8s)-3,8-dihydroxy-1,5-dimethyl-6-oxabicyclo[3.2.1]octan-8-yl]-3-methylpenta-2,4-dienoate

Description

Methyl (2Z,4E)-5-[(1R,3S,5R,8S)-3,8-dihydroxy-1,5-dimethyl-6-oxabicyclo[3.2.1]Octan-8-yl]-3-methylpenta-2,4-dienoate belongs to the class of organic compounds known as abscisic acids and derivatives. These are terpene compounds containing the abscisic acid moiety, which is characterized by a 3-methylpenta-2,4-dienoic acid attached to the C1 carbon of a 4-oxocyclohex-2-ene moiety. Based on a literature review very few articles have been published on methyl (2Z,4E)-5-[(1R,3S,5R,8S)-3,8-dihydroxy-1,5-dimethyl-6-oxabicyclo[3.2.1]Octan-8-yl]-3-methylpenta-2,4-dienoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 45 46  0  0  0  0  0  0  0  0999 V2000
    5.5007   -2.1136    1.0023 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0551   -1.1972    0.0374 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7582   -0.6700    0.0163 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0079   -1.0628    0.9129 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4282    0.2625   -1.0289 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2555    0.8060   -1.1350 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0879    1.7658   -2.2991 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1639    0.5439   -0.2339 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0320    1.1470   -0.4053 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1898    0.9570    0.4359 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2981    2.0084    1.3770 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3208   -0.3116    1.1960 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4976   -0.4214    2.4334 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7988   -0.1551    1.6132 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4232    0.5527    0.6253 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5025    0.9481   -0.3141 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8045    2.2437   -0.9875 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4573   -0.1596   -1.3762 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5103   -1.4706   -0.6196 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4817   -2.5592   -1.5022 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3074   -1.5438    0.3257 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6910   -2.5667    1.5964 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2439   -1.6831    1.7082 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0714   -2.9097    0.4392 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2190    0.5346   -1.7891 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1489    1.3961   -2.8071 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9774    2.7698   -1.8832 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8808    1.6620   -3.0397 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1450   -0.1044    0.6192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0934    1.8195   -1.2486 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1126    2.8782    0.9525 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0373    0.5314    2.6397 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1640   -1.3117    2.4323 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1616   -0.5524    3.3400 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2477   -1.1067    1.8907 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7493    0.4543    2.5630 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7184    3.1024   -0.3156 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1336    2.3325   -1.8697 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8342    2.1877   -1.3899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5033   -0.0290   -1.9316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3442   -0.0369   -2.0015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4642   -1.5137   -0.0944 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9128   -3.3583   -1.1042 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4296   -1.6568   -0.3012 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5074   -2.4094    0.9975 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  2  0
  9 10  1  0
 10 11  1  1
 10 12  1  0
 12 13  1  1
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  6
 16 18  1  0
 18 19  1  0
 19 20  1  0
 19 21  1  0
 16 10  1  0
 21 12  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  5 25  1  0
  7 26  1  0
  7 27  1  0
  7 28  1  0
  8 29  1  0
  9 30  1  0
 11 31  1  0
 13 32  1  0
 13 33  1  0
 13 34  1  0
 14 35  1  0
 14 36  1  0
 17 37  1  0
 17 38  1  0
 17 39  1  0
 18 40  1  0
 18 41  1  0
 19 42  1  1
 20 43  1  0
 21 44  1  0
 21 45  1  0
M  END


  Mrv1652309122216102D          

 21 22  0  0  1  0            999 V2000
    0.4439   -3.9945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2530   -3.8331    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5177   -3.0517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9734   -2.4318    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3267   -2.8903    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5915   -2.1089    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4005   -1.9475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0471   -1.4890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3540   -0.5832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3941   -0.0001    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3430    0.4923    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1624    0.9268    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8377    1.7174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5174    0.4124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5174   -0.4126    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1624   -0.9270    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8073   -1.7084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9667   -0.7434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3247   -0.0001    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2302    0.0765    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9667    0.7432    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  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  6  0  0  0
 10 12  1  0  0  0  0
 12 13  1  6  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 10 16  1  0  0  0  0
 16 17  1  6  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  6  0  0  0
 19 21  1  0  0  0  0
 12 21  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0329622

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)\C=C(\C)/C=C/[C@]1(O)[C@@]2(C)CO[C@]1(C)C[C@@H](O)C2

> <INCHI_IDENTIFIER>
InChI=1S/C16H24O5/c1-11(7-13(18)20-4)5-6-16(19)14(2)8-12(17)9-15(16,3)21-10-14/h5-7,12,17,19H,8-10H2,1-4H3/b6-5+,11-7-/t12-,14+,15+,16-/m0/s1

> <INCHI_KEY>
QNMHUZMKLBWTQM-PCXCFBAQSA-N

> <FORMULA>
C16H24O5

> <MOLECULAR_WEIGHT>
296.363

> <EXACT_MASS>
296.162373873

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
31.437567683096177

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl (2Z,4E)-5-[(1R,3S,5R,8S)-3,8-dihydroxy-1,5-dimethyl-6-oxabicyclo[3.2.1]octan-8-yl]-3-methylpenta-2,4-dienoate

> <JCHEM_LOGP>
0.881721330666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.15046660811451

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.890714828183388

> <JCHEM_PKA_STRONGEST_BASIC>
-2.7397165799455063

> <JCHEM_POLAR_SURFACE_AREA>
75.99000000000001

> <JCHEM_REFRACTIVITY>
79.77299999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
methyl (2Z,4E)-5-[(1R,3S,5R,8S)-3,8-dihydroxy-1,5-dimethyl-6-oxabicyclo[3.2.1]octan-8-yl]-3-methylpenta-2,4-dienoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0       0.829  -7.456   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       2.339  -7.155   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       2.833  -5.697   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       1.817  -4.539   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       4.343  -5.395   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.837  -3.937   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.348  -3.635   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.821  -2.779   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.394  -1.089   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.602  -0.000   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       4.374   0.919   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       2.170   1.730   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.564   3.206   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.966   0.770   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       0.966  -0.770   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       2.170  -1.730   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.507  -3.189   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.671  -1.388   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.339  -0.000   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       6.030   0.143   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       3.671   1.387   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12   16                                             
CONECT   11   10                                                            
CONECT   12   10   13   14   21                                             
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   10   17   18                                             
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   12                                                       
MASTER        0    0    0    0    0    0    0    0   21    0   44    0
END

View in JSmol

Synonyms

Value	Source
Methyl (2Z,4E)-5-[(1R,3S,5R,8S)-3,8-dihydroxy-1,5-dimethyl-6-oxabicyclo[3.2.1]octan-8-yl]-3-methylpenta-2,4-dienoic acid	Generator

Chemical Formula

C₁₆H₂₄O₅

Average Mass

296.3630 Da

Monoisotopic Mass

296.16237 Da

IUPAC Name

methyl (2Z,4E)-5-[(1R,3S,5R,8S)-3,8-dihydroxy-1,5-dimethyl-6-oxabicyclo[3.2.1]octan-8-yl]-3-methylpenta-2,4-dienoate

Traditional Name

methyl (2Z,4E)-5-[(1R,3S,5R,8S)-3,8-dihydroxy-1,5-dimethyl-6-oxabicyclo[3.2.1]octan-8-yl]-3-methylpenta-2,4-dienoate

CAS Registry Number

Not Available

SMILES

COC(=O)\C=C(\C)/C=C/[C@]1(O)[C@@]2(C)CO[C@]1(C)C[C@@H](O)C2

InChI Identifier

InChI=1S/C16H24O5/c1-11(7-13(18)20-4)5-6-16(19)14(2)8-12(17)9-15(16,3)21-10-14/h5-7,12,17,19H,8-10H2,1-4H3/b6-5+,11-7-/t12-,14+,15+,16-/m0/s1

InChI Key

QNMHUZMKLBWTQM-PCXCFBAQSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as abscisic acids and derivatives. These are terpene compounds containing the abscisic acid moiety, which is characterized by a 3-methylpenta-2,4-dienoic acid attached to the C1 carbon of a 4-oxocyclohex-2-ene moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Abscisic acids and derivatives

Alternative Parents

Substituents

Abscisic acid
Fatty acid ester
Oxepane
Fatty acyl
Cyclic alcohol
Tertiary alcohol
Tetrahydrofuran
Methyl ester
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Secondary alcohol
Carboxylic acid ester
Monocarboxylic acid or derivatives
Ether
Dialkyl ether
Carboxylic acid derivative
Organoheterocyclic compound
Oxacycle
Alcohol
Hydrocarbon derivative
Organooxygen compound
Organic oxide
Organic oxygen compound
Carbonyl group
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic 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	0.88	ChemAxon
pKa (Strongest Acidic)	12.89	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	75.99 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	79.77 m³·mol⁻¹	ChemAxon
Polarizability	31.44 Å³	ChemAxon
Number of Rings	2	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

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

163003230

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (2z,4e)-5-[(1r,3s,5r,8s)-3,8-dihydroxy-1,5-dimethyl-6-oxabicyclo[3.2.1]octan-8-yl]-3-methylpenta-2,4-dienoate (NP0329622)

MOL for NP0329622 (methyl (2z,4e)-5-[(1r,3s,5r,8s)-3,8-dihydroxy-1,5-dimethyl-6-oxabicyclo[3.2.1]octan-8-yl]-3-methylpenta-2,4-dienoate)

3D MOL for NP0329622 (methyl (2z,4e)-5-[(1r,3s,5r,8s)-3,8-dihydroxy-1,5-dimethyl-6-oxabicyclo[3.2.1]octan-8-yl]-3-methylpenta-2,4-dienoate)

3D SDF for NP0329622 (methyl (2z,4e)-5-[(1r,3s,5r,8s)-3,8-dihydroxy-1,5-dimethyl-6-oxabicyclo[3.2.1]octan-8-yl]-3-methylpenta-2,4-dienoate)

3D-SDF for NP0329622 (methyl (2z,4e)-5-[(1r,3s,5r,8s)-3,8-dihydroxy-1,5-dimethyl-6-oxabicyclo[3.2.1]octan-8-yl]-3-methylpenta-2,4-dienoate)

PDB for NP0329622 (methyl (2z,4e)-5-[(1r,3s,5r,8s)-3,8-dihydroxy-1,5-dimethyl-6-oxabicyclo[3.2.1]octan-8-yl]-3-methylpenta-2,4-dienoate)

3D PDB for NP0329622 (methyl (2z,4e)-5-[(1r,3s,5r,8s)-3,8-dihydroxy-1,5-dimethyl-6-oxabicyclo[3.2.1]octan-8-yl]-3-methylpenta-2,4-dienoate)

SMILES for NP0329622 (methyl (2z,4e)-5-[(1r,3s,5r,8s)-3,8-dihydroxy-1,5-dimethyl-6-oxabicyclo[3.2.1]octan-8-yl]-3-methylpenta-2,4-dienoate)

INCHI for NP0329622 (methyl (2z,4e)-5-[(1r,3s,5r,8s)-3,8-dihydroxy-1,5-dimethyl-6-oxabicyclo[3.2.1]octan-8-yl]-3-methylpenta-2,4-dienoate)

Structure for NP0329622 (methyl (2z,4e)-5-[(1r,3s,5r,8s)-3,8-dihydroxy-1,5-dimethyl-6-oxabicyclo[3.2.1]octan-8-yl]-3-methylpenta-2,4-dienoate)

3D Structure for NP0329622 (methyl (2z,4e)-5-[(1r,3s,5r,8s)-3,8-dihydroxy-1,5-dimethyl-6-oxabicyclo[3.2.1]octan-8-yl]-3-methylpenta-2,4-dienoate)