NP-MRD: Showing NP-Card for (4r,7r,8r,9s,12r)-9-[(2r)-6-methylhept-5-en-2-yl]-3-oxatricyclo[5.4.1.0⁴,¹²]dodeca-1(11),5-dien-8-ol (NP0162880)

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Record Information

Version

2.0

Created at

2022-09-02 21:22:41 UTC

Updated at

2022-09-02 21:22:41 UTC

NP-MRD ID

NP0162880

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(4r,7r,8r,9s,12r)-9-[(2r)-6-methylhept-5-en-2-yl]-3-oxatricyclo[5.4.1.0⁴,¹²]dodeca-1(11),5-dien-8-ol

Description

Dictyol A belongs to the class of organic compounds known as oxolanes. These are organic compounds containing an oxolane (tetrahydrofuran) ring, which is a saturated aliphatic five-member ring containing one oxygen and five carbon atoms. (4r,7r,8r,9s,12r)-9-[(2r)-6-methylhept-5-en-2-yl]-3-oxatricyclo[5.4.1.0⁴,¹²]dodeca-1(11),5-dien-8-ol is found in Dictyota dichotoma. Based on a literature review very few articles have been published on Dictyol A.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 49 51  0  0  0  0  0  0  0  0999 V2000
    4.5383    1.2359   -0.6479 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5738    0.0672    0.2645 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5427   -1.0216   -0.0094 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7371    0.0338    1.2966 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7904    1.1290    1.5387 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3492    0.7381    1.5030 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8365    0.2040    0.2057 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5151   -1.0395   -0.2063 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7012    0.1052    0.2170 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0680   -0.9784    1.1425 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5354   -1.1280    1.4067 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5569   -0.5154    0.8373 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0036   -0.5904    1.0193 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4499   -0.4289   -0.3301 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7410    0.6272   -0.8279 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4717    0.6289   -2.2760 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2823    0.1228   -2.5611 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6239   -0.2767   -1.3441 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1783    0.0994   -1.1753 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3795   -0.5747   -2.0946 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3684    0.4918   -0.2554 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5169    1.3826   -1.0689 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8554    2.1567   -0.1138 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2154    1.1144   -1.5063 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5021   -0.7365    0.4457 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1653   -1.9952    0.3727 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6978   -1.0674   -1.1069 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8016   -0.8438    1.9649 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9321    1.9671    0.7970 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0281    1.6279    2.5307 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2168   -0.0289    2.3373 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7754    1.6679    1.8179 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0487    1.0002   -0.5839 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2074   -0.8401   -1.0463 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0923   -1.5741    0.5741 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8104   -1.8200   -0.6101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9878    1.0856    0.7398 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6210   -1.9738    0.8539 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6319   -0.7567    2.1389 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8333   -1.8296    2.1671 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3935    0.2318    1.6420 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3830   -1.5477    1.4042 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1418    1.6186   -0.5284 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1686    1.0023   -3.0235 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8812    0.0312   -3.5687 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7377   -1.3865   -1.1744 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1156    1.1832   -1.5292 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3878   -0.0052   -2.3824 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8809    1.4061    0.0553 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  2  2  3
  2  1  1  0
  2  3  1  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 21  1  0
 18 19  1  0
 19 20  1  0
 19  9  1  0
 21 12  1  0
 21 15  1  0
  8 34  1  0
  8 35  1  0
  8 36  1  0
  7 33  1  6
  6 31  1  0
  6 32  1  0
  5 29  1  0
  5 30  1  0
  4 28  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  3 25  1  0
  3 26  1  0
  3 27  1  0
  9 37  1  1
 10 38  1  0
 10 39  1  0
 11 40  1  0
 13 41  1  0
 13 42  1  0
 15 43  1  1
 16 44  1  0
 17 45  1  0
 18 46  1  1
 21 49  1  1
 19 47  1  6
 20 48  1  0
M  END


  Mrv1652309022223222D          

 21 23  0  0  1  0            999 V2000
    7.3766    2.4240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0438    1.6691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5312    1.0035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2237    1.5799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8909    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0708    0.7357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7380   -0.0192    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2254   -0.6849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9178   -0.1085    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6424   -0.8862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8627   -1.1557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1658   -0.7141    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1291   -0.8343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7573   -0.0978    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3429    0.4834    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4750    1.2977    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2903    1.4237    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6621    0.6872    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4816    0.5917    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9231    1.2886    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0765    0.1060    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  9  7  1  6  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 15 14  1  6  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 18 17  1  1  0  0  0
 18 19  1  0  0  0  0
  9 19  1  0  0  0  0
 19 20  1  6  0  0  0
 18 21  1  0  0  0  0
 21 12  1  6  0  0  0
 15 21  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0162880

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H](CCC=C(C)C)[C@@H]1CC=C2CO[C@@H]3C=C[C@H]([C@H]23)[C@@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C19H28O2/c1-12(2)5-4-6-13(3)15-8-7-14-11-21-17-10-9-16(18(14)17)19(15)20/h5,7,9-10,13,15-20H,4,6,8,11H2,1-3H3/t13-,15+,16-,17-,18+,19-/m1/s1

> <INCHI_KEY>
CCQZRSHKJKLNRK-PUNHEFHTSA-N

> <FORMULA>
C19H28O2

> <MOLECULAR_WEIGHT>
288.431

> <EXACT_MASS>
288.208930142

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
49

> <JCHEM_AVERAGE_POLARIZABILITY>
34.55473174751776

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(4R,7R,8R,9S,12R)-9-[(2R)-6-methylhept-5-en-2-yl]-3-oxatricyclo[5.4.1.0^{4,12}]dodeca-1(11),5-dien-8-ol

> <ALOGPS_LOGP>
3.92

> <JCHEM_LOGP>
3.361964712666666

> <ALOGPS_LOGS>
-3.53

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.594638951671051

> <JCHEM_PKA_STRONGEST_BASIC>
-2.976104922539082

> <JCHEM_POLAR_SURFACE_AREA>
29.46

> <JCHEM_REFRACTIVITY>
89.33760000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.45e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(4R,7R,8R,9S,12R)-9-[(2R)-6-methylhept-5-en-2-yl]-3-oxatricyclo[5.4.1.0^{4,12}]dodeca-1(11),5-dien-8-ol

> <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      13.770   4.525   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.149   3.116   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      14.058   1.873   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.618   2.949   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.996   1.540   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.465   1.373   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.844  -0.036   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.754  -1.278   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.313  -0.203   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.799  -1.654   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.344  -2.157   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.043  -1.333   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.108  -1.557   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       1.414  -0.183   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       2.507   0.902   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.753   2.422   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.275   2.658   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.969   1.283   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.499   1.105   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       7.323   2.405   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       3.876   0.198   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   19                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   21                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   21                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   21                                                  
CONECT   19   18    9   20                                                  
CONECT   20   19                                                            
CONECT   21   18   12   15                                                  
MASTER        0    0    0    0    0    0    0    0   21    0   46    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₂₈O₂

Average Mass

288.4310 Da

Monoisotopic Mass

288.20893 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

C[C@H](CCC=C(C)C)[C@@H]1CC=C2CO[C@@H]3C=C[C@H]([C@H]23)[C@@H]1O

InChI Identifier

InChI=1S/C19H28O2/c1-12(2)5-4-6-13(3)15-8-7-14-11-21-17-10-9-16(18(14)17)19(15)20/h5,7,9-10,13,15-20H,4,6,8,11H2,1-3H3/t13-,15+,16-,17-,18+,19-/m1/s1

InChI Key

CCQZRSHKJKLNRK-PUNHEFHTSA-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
Dictyota dichotoma	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oxolanes. These are organic compounds containing an oxolane (tetrahydrofuran) ring, which is a saturated aliphatic five-member ring containing one oxygen and five carbon atoms.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Oxolanes

Sub Class

Not Available

Direct Parent

Oxolanes

Alternative Parents

Substituents

Oxolane
Secondary alcohol
Oxacycle
Ether
Dialkyl ether
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Alcohol
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	3.92	ALOGPS
logS	-3.5	ALOGPS

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00035579

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

101316751

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (4r,7r,8r,9s,12r)-9-[(2r)-6-methylhept-5-en-2-yl]-3-oxatricyclo[5.4.1.0⁴,¹²]dodeca-1(11),5-dien-8-ol (NP0162880)

MOL for NP0162880 ((4r,7r,8r,9s,12r)-9-[(2r)-6-methylhept-5-en-2-yl]-3-oxatricyclo[5.4.1.0⁴,¹²]dodeca-1(11),5-dien-8-ol)

3D MOL for NP0162880 ((4r,7r,8r,9s,12r)-9-[(2r)-6-methylhept-5-en-2-yl]-3-oxatricyclo[5.4.1.0⁴,¹²]dodeca-1(11),5-dien-8-ol)

3D SDF for NP0162880 ((4r,7r,8r,9s,12r)-9-[(2r)-6-methylhept-5-en-2-yl]-3-oxatricyclo[5.4.1.0⁴,¹²]dodeca-1(11),5-dien-8-ol)

3D-SDF for NP0162880 ((4r,7r,8r,9s,12r)-9-[(2r)-6-methylhept-5-en-2-yl]-3-oxatricyclo[5.4.1.0⁴,¹²]dodeca-1(11),5-dien-8-ol)

PDB for NP0162880 ((4r,7r,8r,9s,12r)-9-[(2r)-6-methylhept-5-en-2-yl]-3-oxatricyclo[5.4.1.0⁴,¹²]dodeca-1(11),5-dien-8-ol)

3D PDB for NP0162880 ((4r,7r,8r,9s,12r)-9-[(2r)-6-methylhept-5-en-2-yl]-3-oxatricyclo[5.4.1.0⁴,¹²]dodeca-1(11),5-dien-8-ol)

SMILES for NP0162880 ((4r,7r,8r,9s,12r)-9-[(2r)-6-methylhept-5-en-2-yl]-3-oxatricyclo[5.4.1.0⁴,¹²]dodeca-1(11),5-dien-8-ol)

INCHI for NP0162880 ((4r,7r,8r,9s,12r)-9-[(2r)-6-methylhept-5-en-2-yl]-3-oxatricyclo[5.4.1.0⁴,¹²]dodeca-1(11),5-dien-8-ol)

Structure for NP0162880 ((4r,7r,8r,9s,12r)-9-[(2r)-6-methylhept-5-en-2-yl]-3-oxatricyclo[5.4.1.0⁴,¹²]dodeca-1(11),5-dien-8-ol)

3D Structure for NP0162880 ((4r,7r,8r,9s,12r)-9-[(2r)-6-methylhept-5-en-2-yl]-3-oxatricyclo[5.4.1.0⁴,¹²]dodeca-1(11),5-dien-8-ol)