NP-MRD: Showing NP-Card for 6,10-dihydroxy-7-isopropyl-1,1,4a-trimethyl-3,4,10,10a-tetrahydro-2h-phenanthren-9-one (NP0306311)

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Record Information

Version

2.0

Created at

2022-09-10 22:42:36 UTC

Updated at

2022-09-10 22:42:36 UTC

NP-MRD ID

NP0306311

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6,10-dihydroxy-7-isopropyl-1,1,4a-trimethyl-3,4,10,10a-tetrahydro-2h-phenanthren-9-one

Description

6,10-Dihydroxy-1,1,4a-trimethyl-7-(propan-2-yl)-1,2,3,4,4a,9,10,10a-octahydrophenanthren-9-one belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. 6,10-dihydroxy-7-isopropyl-1,1,4a-trimethyl-3,4,10,10a-tetrahydro-2h-phenanthren-9-one is found in Calocedrus formosana, Cryptomeria japonica, Juniperus chinensis, Salvia yunnanensis, Sequoia sempervirens and Taiwania cryptomerioides. 6,10-Dihydroxy-1,1,4a-trimethyl-7-(propan-2-yl)-1,2,3,4,4a,9,10,10a-octahydrophenanthren-9-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 51 53  0  0  0  0  0  0  0  0999 V2000
    4.9225   -1.0564   -1.1661 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6028   -0.4495    0.1797 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6167    0.4772    0.6441 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1997   -0.0999    0.1710 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2241   -1.0729    0.0278 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8643   -0.7651    0.1284 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4474    0.4842    0.3643 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4367    1.4798    0.5210 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7879    1.1888    0.4280 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7698    2.1476    0.5696 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9940    0.9065    0.3179 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1428    2.0721    1.2477 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2027    1.4155   -1.0988 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1431    0.6638   -1.9544 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3774    0.1356   -1.3381 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3260    0.0298    0.1578 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2434   -1.0491    0.6845 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9815    1.3083    0.7023 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9263   -0.1952    0.6642 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5080   -1.5869    0.2548 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1241   -2.0886   -0.8666 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0904   -1.8473    0.1148 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3087   -3.0239   -0.0033 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9017   -2.1231   -1.2316 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9179   -0.6827   -1.5200 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2205   -0.5606   -1.9212 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6828   -1.3679    0.9173 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8830    1.3399    0.0068 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5994   -0.1159    0.7239 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4849    0.7823    1.7373 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4987   -2.1087   -0.1601 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2086    2.5144    0.7205 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4582    3.0897    0.7239 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2573    2.1793    1.9367 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9858    2.0228    1.9476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1770    3.0446    0.6941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2255    1.4666   -1.6587 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5269    2.5016   -1.1016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4818    1.3606   -2.7860 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5391   -0.0828   -2.5417 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2621    0.8178   -1.5812 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6858   -0.8162   -1.8028 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2765   -0.8417    0.2633 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9911   -2.0709    0.4285 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3673   -0.9012    1.7987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1716    1.2858    1.7690 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0389    1.2350    0.2556 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5977    2.2189    0.2525 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0387   -0.2087    1.7791 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8752   -2.2816    1.0912 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4783   -2.5362   -1.4921 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
  7 11  1  0
 11 12  1  1
 11 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 16 18  1  0
 16 19  1  0
 19 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  2  0
  9  4  1  0
 19 11  1  0
 22  6  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  2 27  1  0
  3 28  1  0
  3 29  1  0
  3 30  1  0
  5 31  1  0
  8 32  1  0
 10 33  1  0
 12 34  1  0
 12 35  1  0
 12 36  1  0
 13 37  1  0
 13 38  1  0
 14 39  1  0
 14 40  1  0
 15 41  1  0
 15 42  1  0
 17 43  1  0
 17 44  1  0
 17 45  1  0
 18 46  1  0
 18 47  1  0
 18 48  1  0
 19 49  1  1
 20 50  1  1
 21 51  1  0
M  END


  Mrv1652310101710192D          

 23 25  0  0  0  0            999 V2000
    6.6809    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6809   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9557   -0.5841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8742   -1.1144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3809    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7309    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3184    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5559    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0309   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2059    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2684    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4434    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2059   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7934    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0309    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7934   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9684   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5559   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7309   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9684    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4434    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2059   -1.7309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5559   -1.7309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  7  6  1  0  0  0  0
  8  6  1  0  0  0  0
 11  1  1  0  0  0  0
 11  2  1  0  0  0  0
 12  9  2  0  0  0  0
 12 11  1  0  0  0  0
 13  9  1  0  0  0  0
 14 10  1  0  0  0  0
 14 13  2  0  0  0  0
 15 10  2  0  0  0  0
 15 12  1  0  0  0  0
 16 13  1  0  0  0  0
 17 16  1  0  0  0  0
 18 17  1  0  0  0  0
 19  3  1  0  0  0  0
 19  4  1  0  0  0  0
 19  7  1  0  0  0  0
 19 18  1  0  0  0  0
 20  5  1  0  0  0  0
 20  8  1  0  0  0  0
 20 14  1  0  0  0  0
 20 18  1  0  0  0  0
 21 15  1  0  0  0  0
 22 16  2  0  0  0  0
 23 17  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0306311

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C1=CC2=C(C=C1O)C1(C)CCCC(C)(C)C1C(O)C2=O

> <INCHI_IDENTIFIER>
InChI=1S/C20H28O3/c1-11(2)12-9-13-14(10-15(12)21)20(5)8-6-7-19(3,4)18(20)17(23)16(13)22/h9-11,17-18,21,23H,6-8H2,1-5H3

> <INCHI_KEY>
VQGOEQIXFUUUQP-UHFFFAOYSA-N

> <FORMULA>
C20H28O3

> <MOLECULAR_WEIGHT>
316.441

> <EXACT_MASS>
316.203844762

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
51

> <JCHEM_AVERAGE_POLARIZABILITY>
36.575078242055774

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
6,10-dihydroxy-1,1,4a-trimethyl-7-(propan-2-yl)-1,2,3,4,4a,9,10,10a-octahydrophenanthren-9-one

> <ALOGPS_LOGP>
4.37

> <JCHEM_LOGP>
4.316019262999999

> <ALOGPS_LOGS>
-4.05

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.104133997826704

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.098710023862676

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6469615295087676

> <JCHEM_POLAR_SURFACE_AREA>
57.53

> <JCHEM_REFRACTIVITY>
91.90939999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.81e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6,10-dihydroxy-7-isopropyl-1,1,4a-trimethyl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-OCT-17   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-OCT-17         0                                  
HETATM    1  C   UNK     0      12.471   2.104   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.471  -0.564   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.784  -1.090   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.498  -2.080   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.311   2.104   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.231   2.104   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.461   0.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.771   2.104   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.391  -0.564   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.851   2.104   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      11.701   0.770   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.161   0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.851  -0.564   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.081   0.770   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.391   2.104   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.081  -1.897   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.541  -1.897   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.771  -0.564   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.231  -0.564   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.541   0.770   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      10.161   3.437   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       7.851  -3.231   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       4.771  -3.231   0.000  0.00  0.00           O+0
CONECT    1   11                                                            
CONECT    2   11                                                            
CONECT    3   19                                                            
CONECT    4   19                                                            
CONECT    5   20                                                            
CONECT    6    7    8                                                       
CONECT    7    6   19                                                       
CONECT    8    6   20                                                       
CONECT    9   12   13                                                       
CONECT   10   14   15                                                       
CONECT   11    1    2   12                                                  
CONECT   12    9   11   15                                                  
CONECT   13    9   14   16                                                  
CONECT   14   10   13   20                                                  
CONECT   15   10   12   21                                                  
CONECT   16   13   17   22                                                  
CONECT   17   16   18   23                                                  
CONECT   18   17   19   20                                                  
CONECT   19    3    4    7   18                                             
CONECT   20    5    8   14   18                                             
CONECT   21   15                                                            
CONECT   22   16                                                            
CONECT   23   17                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   50    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₈O₃

Average Mass

316.4410 Da

Monoisotopic Mass

316.20384 Da

IUPAC Name

6,10-dihydroxy-1,1,4a-trimethyl-7-(propan-2-yl)-1,2,3,4,4a,9,10,10a-octahydrophenanthren-9-one

Traditional Name

6,10-dihydroxy-7-isopropyl-1,1,4a-trimethyl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one

CAS Registry Number

Not Available

SMILES

CC(C)C1=CC2=C(C=C1O)C1(C)CCCC(C)(C)C1C(O)C2=O

InChI Identifier

InChI=1S/C20H28O3/c1-11(2)12-9-13-14(10-15(12)21)20(5)8-6-7-19(3,4)18(20)17(23)16(13)22/h9-11,17-18,21,23H,6-8H2,1-5H3

InChI Key

VQGOEQIXFUUUQP-UHFFFAOYSA-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
Calocedrus formosana	LOTUS Database	35616633
Cryptomeria japonica	LOTUS Database	35616633
Juniperus chinensis	LOTUS Database	35616633
Salvia Yunnanensis	LOTUS Database	35616633
Sequoia sempervirens	LOTUS Database	35616633
Taiwania cryptomerioides	LOTUS Database	35616633

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

Abietane diterpenoid
Diterpenoid
Hydrophenanthrene
Phenanthrene
Tetralin
Aryl alkyl ketone
Aryl ketone
1-hydroxy-2-unsubstituted benzenoid
Benzenoid
Secondary alcohol
Ketone
Alcohol
Hydrocarbon derivative
Organooxygen compound
Organic oxide
Organic oxygen compound
Aromatic homopolycyclic compound

Molecular Framework

Aromatic 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
logP	4.37	ALOGPS
logP	4.32	ChemAxon
logS	-4	ALOGPS
pKa (Strongest Acidic)	8.1	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	57.53 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	91.91 m³·mol⁻¹	ChemAxon
Polarizability	36.58 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

HMDB0179080

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

73095180

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 6,10-dihydroxy-7-isopropyl-1,1,4a-trimethyl-3,4,10,10a-tetrahydro-2h-phenanthren-9-one (NP0306311)

MOL for NP0306311 (6,10-dihydroxy-7-isopropyl-1,1,4a-trimethyl-3,4,10,10a-tetrahydro-2h-phenanthren-9-one)

3D MOL for NP0306311 (6,10-dihydroxy-7-isopropyl-1,1,4a-trimethyl-3,4,10,10a-tetrahydro-2h-phenanthren-9-one)

3D SDF for NP0306311 (6,10-dihydroxy-7-isopropyl-1,1,4a-trimethyl-3,4,10,10a-tetrahydro-2h-phenanthren-9-one)

3D-SDF for NP0306311 (6,10-dihydroxy-7-isopropyl-1,1,4a-trimethyl-3,4,10,10a-tetrahydro-2h-phenanthren-9-one)

PDB for NP0306311 (6,10-dihydroxy-7-isopropyl-1,1,4a-trimethyl-3,4,10,10a-tetrahydro-2h-phenanthren-9-one)

3D PDB for NP0306311 (6,10-dihydroxy-7-isopropyl-1,1,4a-trimethyl-3,4,10,10a-tetrahydro-2h-phenanthren-9-one)

SMILES for NP0306311 (6,10-dihydroxy-7-isopropyl-1,1,4a-trimethyl-3,4,10,10a-tetrahydro-2h-phenanthren-9-one)

INCHI for NP0306311 (6,10-dihydroxy-7-isopropyl-1,1,4a-trimethyl-3,4,10,10a-tetrahydro-2h-phenanthren-9-one)

Structure for NP0306311 (6,10-dihydroxy-7-isopropyl-1,1,4a-trimethyl-3,4,10,10a-tetrahydro-2h-phenanthren-9-one)

3D Structure for NP0306311 (6,10-dihydroxy-7-isopropyl-1,1,4a-trimethyl-3,4,10,10a-tetrahydro-2h-phenanthren-9-one)