NP-MRD: Showing NP-Card for (3e)-6-[(1s,3as,8ar)-3a,6-dimethyl-2,3,4,7,8,8a-hexahydro-1h-azulen-1-yl]-2-methylhept-3-ene-2,6-diol (NP0287893)

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Record Information

Version

2.0

Created at

2022-09-09 17:22:24 UTC

Updated at

2022-09-09 17:22:24 UTC

NP-MRD ID

NP0287893

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3e)-6-[(1s,3as,8ar)-3a,6-dimethyl-2,3,4,7,8,8a-hexahydro-1h-azulen-1-yl]-2-methylhept-3-ene-2,6-diol

Description

Polasol C belongs to the class of organic compounds known as sphenolobane diterpenoids. These are diterpenoids with a structure characterized by a sphenolobane skeleton. They possess a trans-fused hydroazulenoid skeleton as a common structural motif, but differ in configuration at C(9), where a prenyl group is attached. Sphenolobane is also considered an 'extended' daucane skeleton, with a carbon side chain appended onto the cyclopentane ring. Based on a literature review very few articles have been published on Polasol C.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 56 57  0  0  0  0  0  0  0  0999 V2000
    5.4080   -1.6212   -1.5579 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2651   -0.9748   -0.8511 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4893   -0.8514    0.4570 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5662   -0.2558    1.4517 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7158    0.7617    0.7812 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4312    1.7586   -0.0495 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9747    1.5512    1.8752 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9808    2.2992    0.9793 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5236    1.1945    0.0533 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8668    0.7158    0.4159 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8833    1.8114    0.3314 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8882    0.2220    1.7242 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3227   -0.4047   -0.4897 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7102   -0.8192   -0.0652 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7427   -0.7436   -0.8993 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1064   -1.1616   -0.4505 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7928   -2.0443   -1.4453 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9075    0.1379   -0.3016 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0848   -1.7966    0.7692 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5532    0.0868    0.1310 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7987   -0.6535   -1.0979 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1502   -0.6133   -1.7230 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3759   -1.4257   -1.0498 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2715   -2.7007   -1.7002 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4909   -1.1140   -2.5606 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4266   -1.2113    0.8621 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8863   -1.0810    1.8060 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0832    0.1030    2.3669 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7339    2.1315   -0.8446 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4088    1.4468   -0.4436 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6530    2.6865    0.5593 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4369    0.8539    2.5452 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6534    2.2399    2.3980 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1743    2.7489    1.5594 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5271    3.1081    0.4722 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4851    1.5802   -0.9870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8164    2.5490    1.1608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9074    2.2991   -0.6710 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8902    1.3337    0.4435 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8318   -0.7574    1.7390 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3098   -0.1558   -1.5500 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6830   -1.2941   -0.2666 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9011   -1.1860    0.9208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6194   -0.3828   -1.9074 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3520   -2.0029   -2.4623 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8174   -3.1059   -1.0614 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8615   -1.7351   -1.5014 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8507    0.6457   -1.3045 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9501   -0.0588   -0.0370 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3667    0.7661    0.4378 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2506   -1.1460    1.4729 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1416   -0.6246    0.9109 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0756   -0.2947   -1.8834 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5425   -1.7512   -0.9900 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3625    0.3317   -2.2911 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1277   -1.3951   -2.5445 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  1  6
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 20  1  0
 20 21  1  0
 21 22  1  0
  9 10  1  0
 10 11  1  0
 10 12  1  1
 10 13  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 16 18  1  0
 16 19  1  0
 22  2  1  0
 20  5  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  3 26  1  0
  4 27  1  0
  4 28  1  0
  6 29  1  0
  6 30  1  0
  6 31  1  0
  7 32  1  0
  7 33  1  0
  8 34  1  0
  8 35  1  0
  9 36  1  6
 20 52  1  1
 21 53  1  0
 21 54  1  0
 22 55  1  0
 22 56  1  0
 11 37  1  0
 11 38  1  0
 11 39  1  0
 12 40  1  0
 13 41  1  0
 13 42  1  0
 14 43  1  0
 15 44  1  0
 17 45  1  0
 17 46  1  0
 17 47  1  0
 18 48  1  0
 18 49  1  0
 18 50  1  0
 19 51  1  0
M  END


  Mrv1652309092219222D          

 22 23  0  0  1  0            999 V2000
    4.3735    1.8011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5485    1.8011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1906    1.0578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3863    0.8742    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7413    1.3886    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5940    0.5769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9566    1.1337    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4717    1.8011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9566    2.4686    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7017    3.2532    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4863    3.5081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0829    2.9982    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4468    4.0378    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3602    4.2093    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6151    4.9939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4221    5.1655    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2291    5.3370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2506    5.9724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5936    4.3585    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7413    2.2136    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3863    2.7280    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1906    2.5444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  1  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  6  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 10 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 16 19  1  0  0  0  0
  9 20  1  0  0  0  0
  5 20  1  0  0  0  0
 20 21  1  1  0  0  0
 21 22  1  0  0  0  0
  2 22  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0287893

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=CC[C@]2(C)CC[C@@H]([C@H]2CC1)C(C)(O)C\C=C\C(C)(C)O

> <INCHI_IDENTIFIER>
InChI=1S/C20H34O2/c1-15-7-8-16-17(10-14-19(16,4)13-9-15)20(5,22)12-6-11-18(2,3)21/h6,9,11,16-17,21-22H,7-8,10,12-14H2,1-5H3/b11-6+/t16-,17+,19-,20?/m1/s1

> <INCHI_KEY>
VBDZHBHIMYSJBO-DLNAGQPESA-N

> <FORMULA>
C20H34O2

> <MOLECULAR_WEIGHT>
306.49

> <EXACT_MASS>
306.255880335

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
37.87165798246335

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3E)-6-[(1S,3aS,8aR)-3a,6-dimethyl-1,2,3,3a,4,7,8,8a-octahydroazulen-1-yl]-2-methylhept-3-ene-2,6-diol

> <JCHEM_LOGP>
3.9399128523333338

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
17.781260840317277

> <JCHEM_PKA_STRONGEST_BASIC>
-0.4433427900844559

> <JCHEM_POLAR_SURFACE_AREA>
40.46

> <JCHEM_REFRACTIVITY>
95.10829999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(3E)-6-[(1S,3aS,8aR)-3a,6-dimethyl-2,3,4,7,8,8a-hexahydro-1H-azulen-1-yl]-2-methylhept-3-ene-2,6-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0       8.164   3.362   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.624   3.362   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.956   1.975   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.454   1.632   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.250   2.592   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.975   1.077   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.786   2.116   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.881   3.362   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.786   4.608   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.310   6.073   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.774   6.548   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -0.155   5.597   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       0.834   7.537   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.672   7.857   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.148   9.322   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.655   9.642   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -4.161   9.962   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -2.334  11.149   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -2.975   8.136   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       3.250   4.132   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.454   5.092   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.956   4.750   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   22                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7   20                                             
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   20                                                  
CONECT   10    9   11   12   13                                             
CONECT   11   10                                                            
CONECT   12   10                                                            
CONECT   13   10   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18   19                                             
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19   16                                                            
CONECT   20    9    5   21                                                  
CONECT   21   20   22                                                       
CONECT   22   21    2                                                       
MASTER        0    0    0    0    0    0    0    0   22    0   46    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₃₄O₂

Average Mass

306.4900 Da

Monoisotopic Mass

306.25588 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC1=CC[C@]2(C)CC[C@@H]([C@H]2CC1)C(C)(O)C\C=C\C(C)(C)O

InChI Identifier

InChI=1S/C20H34O2/c1-15-7-8-16-17(10-14-19(16,4)13-9-15)20(5,22)12-6-11-18(2,3)21/h6,9,11,16-17,21-22H,7-8,10,12-14H2,1-5H3/b11-6+/t16-,17+,19-,20?/m1/s1

InChI Key

VBDZHBHIMYSJBO-DLNAGQPESA-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 sphenolobane diterpenoids. These are diterpenoids with a structure characterized by a sphenolobane skeleton. They possess a trans-fused hydroazulenoid skeleton as a common structural motif, but differ in configuration at C(9), where a prenyl group is attached. Sphenolobane is also considered an 'extended' daucane skeleton, with a carbon side chain appended onto the cyclopentane ring.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Sphenolobane diterpenoids

Alternative Parents

Substituents

Prenyldaucane diterpenoid
Tertiary alcohol
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic 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

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00050200

Chemspider ID

8670301

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10494900

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3e)-6-[(1s,3as,8ar)-3a,6-dimethyl-2,3,4,7,8,8a-hexahydro-1h-azulen-1-yl]-2-methylhept-3-ene-2,6-diol (NP0287893)

MOL for NP0287893 ((3e)-6-[(1s,3as,8ar)-3a,6-dimethyl-2,3,4,7,8,8a-hexahydro-1h-azulen-1-yl]-2-methylhept-3-ene-2,6-diol)

3D MOL for NP0287893 ((3e)-6-[(1s,3as,8ar)-3a,6-dimethyl-2,3,4,7,8,8a-hexahydro-1h-azulen-1-yl]-2-methylhept-3-ene-2,6-diol)

3D SDF for NP0287893 ((3e)-6-[(1s,3as,8ar)-3a,6-dimethyl-2,3,4,7,8,8a-hexahydro-1h-azulen-1-yl]-2-methylhept-3-ene-2,6-diol)

3D-SDF for NP0287893 ((3e)-6-[(1s,3as,8ar)-3a,6-dimethyl-2,3,4,7,8,8a-hexahydro-1h-azulen-1-yl]-2-methylhept-3-ene-2,6-diol)

PDB for NP0287893 ((3e)-6-[(1s,3as,8ar)-3a,6-dimethyl-2,3,4,7,8,8a-hexahydro-1h-azulen-1-yl]-2-methylhept-3-ene-2,6-diol)

3D PDB for NP0287893 ((3e)-6-[(1s,3as,8ar)-3a,6-dimethyl-2,3,4,7,8,8a-hexahydro-1h-azulen-1-yl]-2-methylhept-3-ene-2,6-diol)

SMILES for NP0287893 ((3e)-6-[(1s,3as,8ar)-3a,6-dimethyl-2,3,4,7,8,8a-hexahydro-1h-azulen-1-yl]-2-methylhept-3-ene-2,6-diol)

INCHI for NP0287893 ((3e)-6-[(1s,3as,8ar)-3a,6-dimethyl-2,3,4,7,8,8a-hexahydro-1h-azulen-1-yl]-2-methylhept-3-ene-2,6-diol)

Structure for NP0287893 ((3e)-6-[(1s,3as,8ar)-3a,6-dimethyl-2,3,4,7,8,8a-hexahydro-1h-azulen-1-yl]-2-methylhept-3-ene-2,6-diol)

3D Structure for NP0287893 ((3e)-6-[(1s,3as,8ar)-3a,6-dimethyl-2,3,4,7,8,8a-hexahydro-1h-azulen-1-yl]-2-methylhept-3-ene-2,6-diol)