NP-MRD: Showing NP-Card for ent-9alpha,13R-Epoxy-18-hydroxy-14-labden-7-one (NP0065176)

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Record Information

Version

2.0

Created at

2022-04-28 09:26:04 UTC

Updated at

2022-04-28 09:26:04 UTC

NP-MRD ID

NP0065176

Secondary Accession Numbers

None

Natural Product Identification

Common Name

ent-9alpha,13R-Epoxy-18-hydroxy-14-labden-7-one

Description

(1S,2S,4aR,5S,5'S,8aR)-5'-ethenyl-5-(hydroxymethyl)-2,5,5',8a-tetramethyl-octahydro-2H-spiro[naphthalene-1,2'-oxolane]-3-one belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. ent-9alpha,13R-Epoxy-18-hydroxy-14-labden-7-one is found in Austrobrickellia patens. Based on a literature review very few articles have been published on (1S,2S,4aR,5S,5'S,8aR)-5'-ethenyl-5-(hydroxymethyl)-2,5,5',8a-tetramethyl-octahydro-2H-spiro[naphthalene-1,2'-oxolane]-3-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 55 57  0  0  0  0  0  0  0  0999 V2000
    2.8899    3.0163    1.4874 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7079    2.3631    0.3425 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6220    0.8547    0.3496 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6509    0.3973    1.3624 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0059    0.3764   -1.0023 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9829   -0.6793   -1.3016 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9742   -0.5876   -0.1891 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3524    0.4242    0.6539 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8422   -1.8999    0.5025 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9749   -2.8433    0.3219 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3992   -2.6442    0.1338 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4006   -3.7805   -0.2959 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7325   -1.9787    0.2916 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4193   -0.4885    0.3067 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6805    0.2927    0.2446 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.9089   -0.6228    0.3490 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7939    1.2350    1.4418 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7802    0.4650    2.5958 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8631    1.1082   -0.9930 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6602    1.8681   -1.4345 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3575    1.3053   -0.9414 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4097   -0.1905   -0.7362 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6241   -0.8860   -2.0417 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9753    2.4420    2.4262 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9615    4.0750    1.5726 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6277    2.9462   -0.5588 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2090   -0.4456    0.9135 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1742   -0.0022    2.2803 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3967    1.1830    1.5763 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0570   -0.0376   -0.9911 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0333    1.1786   -1.7739 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5494   -0.4471   -2.2939 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4895   -1.6384   -1.3819 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7586   -1.6842    1.6064 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9730   -2.4394    0.4296 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8373   -3.4218   -0.6388 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8699   -3.6405    1.1178 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3344   -2.2750   -0.5724 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2020   -2.3120    1.2462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9331   -0.3062    1.3098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7778    0.0974    0.4086 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9062   -1.1971    1.2955 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0714   -1.2103   -0.5508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7858    1.7424    1.3830 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9994    1.9781    1.4731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7616    0.9899    3.4128 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6651    1.8716   -0.7615 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3190    0.5022   -1.8309 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6901    2.9411   -1.0815 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6814    1.9495   -2.5530 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1042    1.7577    0.0232 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4094    1.5081   -1.7153 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0252   -1.8033   -2.1583 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6623   -1.2447   -2.1989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4268   -0.1625   -2.8618 H   0  0  0  0  0  0  0  0  0  0  0  0
 10  9  1  0
  9 11  1  0
 11 12  2  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  1
 15 17  1  0
 17 18  1  0
 15 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  6
 22  7  1  0
  7  6  1  0
  6  5  1  0
  5  3  1  0
  3  4  1  1
  3  8  1  0
  3  2  1  0
  2  1  2  3
  7  9  1  0
  7  8  1  1
 22 14  1  0
 10 35  1  0
 10 36  1  0
 10 37  1  0
  9 34  1  1
 13 38  1  0
 13 39  1  0
 14 40  1  1
 16 41  1  0
 16 42  1  0
 16 43  1  0
 17 44  1  0
 17 45  1  0
 18 46  1  0
 19 47  1  0
 19 48  1  0
 20 49  1  0
 20 50  1  0
 21 51  1  0
 21 52  1  0
 23 53  1  0
 23 54  1  0
 23 55  1  0
  6 32  1  0
  6 33  1  0
  5 30  1  0
  5 31  1  0
  4 27  1  0
  4 28  1  0
  4 29  1  0
  2 26  1  0
  1 24  1  0
  1 25  1  0
M  END


  Mrv1652304282211262D          

 23 25  0  0  1  0            999 V2000
    1.6704    0.3724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2728    0.9361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0857    1.7396    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2964    1.9794    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6940    1.4157    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8811    0.6122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0954    1.6554    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2824    2.4590    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3199    3.0227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1329    3.8262    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1093    2.7829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0718    2.6987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0066    0.8368    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7404    0.4868    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3042    1.0891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9055    1.8114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2740   -0.1425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0857    0.0050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4786   -0.2956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2953    0.6934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3529    2.5202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8822    1.9546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4667    1.3723    0.0000 O   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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  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  2  0  0  0  0
  9 11  1  0  0  0  0
  4 11  1  6  0  0  0
  8 12  1  6  0  0  0
  7 13  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
  7 16  1  0  0  0  0
 14 17  1  6  0  0  0
 17 18  2  0  0  0  0
 14 19  1  1  0  0  0
  5 20  1  6  0  0  0
  3 21  1  6  0  0  0
  3 22  1  1  0  0  0
 22 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0065176

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1C(=O)C[C@@H]2[C@@](C)(CO)CCC[C@@]2(C)[C@]11CC[C@](C)(O1)C=C

> <INCHI_IDENTIFIER>
InChI=1S/C20H32O3/c1-6-18(4)10-11-20(23-18)14(2)15(22)12-16-17(3,13-21)8-7-9-19(16,20)5/h6,14,16,21H,1,7-13H2,2-5H3/t14-,16-,17-,18-,19-,20+/m1/s1

> <INCHI_KEY>
SVFACCMCEHBXFZ-PJACHSRJSA-N

> <FORMULA>
C20H32O3

> <MOLECULAR_WEIGHT>
320.473

> <EXACT_MASS>
320.23514489

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
36.89022285674962

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2S,4aR,5S,5'S,8aR)-5'-ethenyl-5-(hydroxymethyl)-2,5,5',8a-tetramethyl-octahydro-2H-spiro[naphthalene-1,2'-oxolane]-3-one

> <ALOGPS_LOGP>
3.21

> <JCHEM_LOGP>
3.6063549813333338

> <ALOGPS_LOGS>
-5.31

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
18.79391051470562

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.651955363523342

> <JCHEM_PKA_STRONGEST_BASIC>
-1.2010410495213617

> <JCHEM_POLAR_SURFACE_AREA>
46.53

> <JCHEM_REFRACTIVITY>
91.6068

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.57e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,4aR,5S,5'S,8aR)-5'-ethenyl-5-(hydroxymethyl)-2,5,5',8a-tetramethyl-hexahydrospiro[naphthalene-1,2'-oxolane]-3-one

> <JCHEM_VEBER_RULE>
0

$$$$

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       3.118   0.695   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.243   1.747   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.893   3.247   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.420   3.695   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.295   2.643   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.645   1.143   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.178   3.090   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.527   4.590   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.597   5.642   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       0.248   7.142   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       2.071   5.195   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.001   5.038   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       0.012   1.562   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -1.382   0.909   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.434   2.033   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.690   3.381   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -2.378  -0.266   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -3.893   0.009   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.893  -0.552   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.551   1.294   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.392   4.704   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.380   3.649   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       6.471   2.562   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4   21   22                                             
CONECT    4    3    5   11                                                  
CONECT    5    4    6    7   20                                             
CONECT    6    5    1                                                       
CONECT    7    5    8   13   16                                             
CONECT    8    7    9   12                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9    4                                                       
CONECT   12    8                                                            
CONECT   13    7   14                                                       
CONECT   14   13   15   17   19                                             
CONECT   15   14   16                                                       
CONECT   16   15    7                                                       
CONECT   17   14   18                                                       
CONECT   18   17                                                            
CONECT   19   14                                                            
CONECT   20    5                                                            
CONECT   21    3                                                            
CONECT   22    3   23                                                       
CONECT   23   22                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   50    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₃₂O₃

Average Mass

320.4730 Da

Monoisotopic Mass

320.23514 Da

IUPAC Name

(1S,2S,4aR,5S,5'S,8aR)-5'-ethenyl-5-(hydroxymethyl)-2,5,5',8a-tetramethyl-octahydro-2H-spiro[naphthalene-1,2'-oxolane]-3-one

Traditional Name

(1S,2S,4aR,5S,5'S,8aR)-5'-ethenyl-5-(hydroxymethyl)-2,5,5',8a-tetramethyl-hexahydrospiro[naphthalene-1,2'-oxolane]-3-one

CAS Registry Number

Not Available

SMILES

C[C@@H]1C(=O)C[C@@H]2[C@@](C)(CO)CCC[C@@]2(C)[C@]11CC[C@](C)(O1)C=C

InChI Identifier

InChI=1S/C20H32O3/c1-6-18(4)10-11-20(23-18)14(2)15(22)12-16-17(3,13-21)8-7-9-19(16,20)5/h6,14,16,21H,1,7-13H2,2-5H3/t14-,16-,17-,18-,19-,20+/m1/s1

InChI Key

SVFACCMCEHBXFZ-PJACHSRJSA-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
Austrobrickellia patens	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Diterpenoids

Alternative Parents

Substituents

Diterpenoid
Grindelane diterpenoid
Tetrahydrofuran
Ketone
Cyclic ketone
Dialkyl ether
Ether
Oxacycle
Organoheterocyclic compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Organooxygen compound
Primary alcohol
Carbonyl group
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	3.21	ALOGPS
logP	3.61	ChemAxon
logS	-5.3	ALOGPS
pKa (Strongest Acidic)	18.65	ChemAxon
pKa (Strongest Basic)	-1.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	46.53 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	91.61 m³·mol⁻¹	ChemAxon
Polarizability	36.89 Å³	ChemAxon
Number of Rings	3	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

162883257

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for ent-9alpha,13R-Epoxy-18-hydroxy-14-labden-7-one (NP0065176)

MOL for NP0065176 (ent-9alpha,13R-Epoxy-18-hydroxy-14-labden-7-one)

3D MOL for NP0065176 (ent-9alpha,13R-Epoxy-18-hydroxy-14-labden-7-one)

3D SDF for NP0065176 (ent-9alpha,13R-Epoxy-18-hydroxy-14-labden-7-one)

3D-SDF for NP0065176 (ent-9alpha,13R-Epoxy-18-hydroxy-14-labden-7-one)

PDB for NP0065176 (ent-9alpha,13R-Epoxy-18-hydroxy-14-labden-7-one)

3D PDB for NP0065176 (ent-9alpha,13R-Epoxy-18-hydroxy-14-labden-7-one)

SMILES for NP0065176 (ent-9alpha,13R-Epoxy-18-hydroxy-14-labden-7-one)

INCHI for NP0065176 (ent-9alpha,13R-Epoxy-18-hydroxy-14-labden-7-one)

Structure for NP0065176 (ent-9alpha,13R-Epoxy-18-hydroxy-14-labden-7-one)

3D Structure for NP0065176 (ent-9alpha,13R-Epoxy-18-hydroxy-14-labden-7-one)