NP-MRD: Showing NP-Card for (4bs)-4-hydroxy-2-isopropyl-4b,8,8-trimethyl-6,7-dihydro-5h-phenanthren-3-one (NP0156754)

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Record Information

Version

2.0

Created at

2022-09-02 14:00:27 UTC

Updated at

2022-09-02 14:00:28 UTC

NP-MRD ID

NP0156754

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(4bs)-4-hydroxy-2-isopropyl-4b,8,8-trimethyl-6,7-dihydro-5h-phenanthren-3-one

Description

15-Deoxyfuerstione belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. (4bs)-4-hydroxy-2-isopropyl-4b,8,8-trimethyl-6,7-dihydro-5h-phenanthren-3-one is found in Caryopteris clandonensis and Salvia moorcroftiana. (4bs)-4-hydroxy-2-isopropyl-4b,8,8-trimethyl-6,7-dihydro-5h-phenanthren-3-one was first documented in 2002 (PMID: 12385879). Based on a literature review a small amount of articles have been published on 15-Deoxyfuerstione (PMID: 33841524) (PMID: 34289771) (PMID: 20522992) (PMID: 22204139).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 48 50  0  0  0  0  0  0  0  0999 V2000
    5.1706   -0.2160   -1.7296 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6446   -0.5118   -0.3428 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4423    0.2340    0.7000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1984   -0.2159   -0.2618 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3683   -1.2061   -0.0354 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9151   -0.9769    0.0566 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1899   -2.0603    0.2730 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2556   -1.8745    0.3679 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8089   -0.6847    0.2445 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2896   -0.6560    0.3624 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8703   -1.9718   -0.1630 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6249   -0.6011    1.8364 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9124    0.5100   -0.3067 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1121    1.1288   -1.3992 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6788    1.3592   -1.1338 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1047    0.5798    0.0184 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2905    1.4127    1.3023 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3402    0.3489   -0.0973 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2082    1.3319   -0.3274 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7495    2.6149   -0.4868 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6421    1.1099   -0.4192 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4595    2.0525   -0.6379 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7165    0.6993   -2.1362 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8644   -1.0511   -2.3865 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2670   -0.0974   -1.7396 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8069   -1.5899   -0.1591 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4735   -0.1879    0.6731 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5490    1.3133    0.4714 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0314    0.0265    1.6884 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7624   -2.2201    0.0875 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6546   -3.0298    0.3729 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8426   -2.7864    0.5474 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3201   -2.2774   -1.0616 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9156   -1.7325   -0.4802 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8810   -2.7537    0.6174 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5856   -1.1173    2.0429 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8609   -1.1440    2.4265 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7016    0.4635    2.1924 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8721    0.1422   -0.7817 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2799    1.2914    0.4220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6395    2.0954   -1.6599 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2688    0.4993   -2.3257 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5488    2.4512   -0.8746 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0951    1.0852   -2.0398 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3148    0.6626    2.1372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1670    2.0530    1.2562 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4058    2.0582    1.4112 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1926    3.4388   -0.1088 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
 10 11  1  0
 10 12  1  0
 10 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  1
 16 18  1  0
 18 19  2  0
 19 20  1  0
 19 21  1  0
 21 22  2  0
 21  4  1  0
 18  6  1  0
 16  9  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  2 26  1  0
  3 27  1  0
  3 28  1  0
  3 29  1  0
  5 30  1  0
  7 31  1  0
  8 32  1  0
 11 33  1  0
 11 34  1  0
 11 35  1  0
 12 36  1  0
 12 37  1  0
 12 38  1  0
 13 39  1  0
 13 40  1  0
 14 41  1  0
 14 42  1  0
 15 43  1  0
 15 44  1  0
 17 45  1  0
 17 46  1  0
 17 47  1  0
 20 48  1  0
M  END


  Mrv1652309022216002D          

 22 24  0  0  1  0            999 V2000
    0.7954   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2079   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7954   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0329   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4454   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6021    0.7019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5206    0.1716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1579   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7454   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9204   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5079   -0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0954   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2704   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829   -2.2539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4454   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0329   -2.2539    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
  2  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  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  1  0  0  0  0
 15 16  1  0  0  0  0
  9 16  1  0  0  0  0
 16 17  1  1  0  0  0
 16 18  1  0  0  0  0
  6 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
  4 21  1  0  0  0  0
 21 22  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0156754

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C1=CC2=CC=C3C(C)(C)CCC[C@]3(C)C2=C(O)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C20H26O2/c1-12(2)14-11-13-7-8-15-19(3,4)9-6-10-20(15,5)16(13)18(22)17(14)21/h7-8,11-12,22H,6,9-10H2,1-5H3/t20-/m0/s1

> <INCHI_KEY>
RRCPSCYNWVOUBD-FQEVSTJZSA-N

> <FORMULA>
C20H26O2

> <MOLECULAR_WEIGHT>
298.426

> <EXACT_MASS>
298.193280077

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
48

> <JCHEM_AVERAGE_POLARIZABILITY>
35.14616770668015

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(4bS)-4-hydroxy-4b,8,8-trimethyl-2-(propan-2-yl)-3,4b,5,6,7,8-hexahydrophenanthren-3-one

> <ALOGPS_LOGP>
4.94

> <JCHEM_LOGP>
4.123517602333331

> <ALOGPS_LOGS>
-4.13

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.791790569428034

> <JCHEM_PKA_STRONGEST_BASIC>
-3.445330804932177

> <JCHEM_POLAR_SURFACE_AREA>
37.3

> <JCHEM_REFRACTIVITY>
93.83429999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.19e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(4bS)-4-hydroxy-2-isopropyl-4b,8,8-trimethyl-6,7-dihydro-5H-phenanthren-3-one

> <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       1.485  -2.874   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.255  -1.540   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.485  -0.206   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.795  -1.540   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.565  -0.206   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.105  -0.206   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.875   1.127   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.415   1.127   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.185  -0.206   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.725  -0.206   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.457   1.310   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      12.172   0.320   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      11.495  -1.540   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.725  -2.874   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.185  -2.874   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.415  -1.540   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.645  -2.874   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.875  -1.540   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.105  -2.874   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       6.875  -4.207   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       4.565  -2.874   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       3.795  -4.207   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   21                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   18                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   16                                                  
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    9   17   18                                             
CONECT   17   16                                                            
CONECT   18   16    6   19                                                  
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19    4   22                                                  
CONECT   22   21                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   48    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₆O₂

Average Mass

298.4260 Da

Monoisotopic Mass

298.19328 Da

IUPAC Name

(4bS)-4-hydroxy-4b,8,8-trimethyl-2-(propan-2-yl)-3,4b,5,6,7,8-hexahydrophenanthren-3-one

Traditional Name

(4bS)-4-hydroxy-2-isopropyl-4b,8,8-trimethyl-6,7-dihydro-5H-phenanthren-3-one

CAS Registry Number

Not Available

SMILES

CC(C)C1=CC2=CC=C3C(C)(C)CCC[C@]3(C)C2=C(O)C1=O

InChI Identifier

InChI=1S/C20H26O2/c1-12(2)14-11-13-7-8-15-19(3,4)9-6-10-20(15,5)16(13)18(22)17(14)21/h7-8,11-12,22H,6,9-10H2,1-5H3/t20-/m0/s1

InChI Key

RRCPSCYNWVOUBD-FQEVSTJZSA-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
Caryopteris x clandonensis	LOTUS Database	35616633
Salvia moorcroftiana	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

Diterpenoid
Abietane diterpenoid
Phenanthrene
Hydrophenanthrene
Cyclic ketone
Ketone
Enol
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
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
logP	4.94	ALOGPS
logP	4.12	ChemAxon
logS	-4.1	ALOGPS
pKa (Strongest Acidic)	9.79	ChemAxon
pKa (Strongest Basic)	-3.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	37.3 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	93.83 m³·mol⁻¹	ChemAxon
Polarizability	35.15 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	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

14104679

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Hadavand Mirzaei H, Firuzi O, Jassbi AR: Diterpenoids from Roots of Salvia lachnocalyx; In-silico and In-vitro Toxicity against Human Cancer Cell Lines. Iran J Pharm Res. 2020 Fall;19(4):85-94. doi: 10.22037/ijpr.2019.15429.13095. [PubMed:33841524 ]
Jassbi AR, Hadavand Mirzaei H, Firuzi O, Pirhadi S, Asadollahi M, Chandran JN, Schneider B: Cytotoxic abietane-type diterpenoids from roots of Salvia spinosa and their in Silico pharmacophore modeling. Nat Prod Res. 2021 Jul 22:1-6. doi: 10.1080/14786419.2021.1952202. [PubMed:34289771 ]
Hannedouche S, Souchard JP, Jacquemond-Collet I, Moulis C: Molluscicidal and radical scavenging activity of quinones from the root bark of Caryopteris x clandonensis. Fitoterapia. 2002 Oct;73(6):520-2. doi: 10.1016/s0367-326x(02)00163-6. [PubMed:12385879 ]
Tada M, Kurabe J, Yoshida T, Ohkanda T, Matsumoto Y: Syntheses and antibacterial activities of diterpene catechol derivatives with abietane, totarane and podocarpane skeletons against methicillin-resistant Staphylococcus aureus and Propionibacterium acnes. Chem Pharm Bull (Tokyo). 2010 Jun;58(6):818-24. doi: 10.1248/cpb.58.818. [PubMed:20522992 ]
Kuzma L, Kisiel W, Krolicka A, Wysokinska H: Genetic transformation of Salvia austriaca by Agrobacterium rhizogenes and diterpenoid isolation. Pharmazie. 2011 Nov;66(11):904-7. [PubMed:22204139 ]
LOTUS database [Link]

Showing NP-Card for (4bs)-4-hydroxy-2-isopropyl-4b,8,8-trimethyl-6,7-dihydro-5h-phenanthren-3-one (NP0156754)

MOL for NP0156754 ((4bs)-4-hydroxy-2-isopropyl-4b,8,8-trimethyl-6,7-dihydro-5h-phenanthren-3-one)

3D MOL for NP0156754 ((4bs)-4-hydroxy-2-isopropyl-4b,8,8-trimethyl-6,7-dihydro-5h-phenanthren-3-one)

3D SDF for NP0156754 ((4bs)-4-hydroxy-2-isopropyl-4b,8,8-trimethyl-6,7-dihydro-5h-phenanthren-3-one)

3D-SDF for NP0156754 ((4bs)-4-hydroxy-2-isopropyl-4b,8,8-trimethyl-6,7-dihydro-5h-phenanthren-3-one)

PDB for NP0156754 ((4bs)-4-hydroxy-2-isopropyl-4b,8,8-trimethyl-6,7-dihydro-5h-phenanthren-3-one)

3D PDB for NP0156754 ((4bs)-4-hydroxy-2-isopropyl-4b,8,8-trimethyl-6,7-dihydro-5h-phenanthren-3-one)

SMILES for NP0156754 ((4bs)-4-hydroxy-2-isopropyl-4b,8,8-trimethyl-6,7-dihydro-5h-phenanthren-3-one)

INCHI for NP0156754 ((4bs)-4-hydroxy-2-isopropyl-4b,8,8-trimethyl-6,7-dihydro-5h-phenanthren-3-one)

Structure for NP0156754 ((4bs)-4-hydroxy-2-isopropyl-4b,8,8-trimethyl-6,7-dihydro-5h-phenanthren-3-one)

3D Structure for NP0156754 ((4bs)-4-hydroxy-2-isopropyl-4b,8,8-trimethyl-6,7-dihydro-5h-phenanthren-3-one)