NP-MRD: Showing NP-Card for (1s,13s)-13-hydroxy-3-isopropyl-1,8,13-trimethyltricyclo[7.4.1.0⁵,¹⁴]tetradeca-3,5,7,9(14)-tetraene-2,10-dione (NP0287491)

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Record Information

Version

2.0

Created at

2022-09-09 16:36:08 UTC

Updated at

2022-09-09 16:36:08 UTC

NP-MRD ID

NP0287491

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,13s)-13-hydroxy-3-isopropyl-1,8,13-trimethyltricyclo[7.4.1.0⁵,¹⁴]tetradeca-3,5,7,9(14)-tetraene-2,10-dione

Description

1-Oxosalvibretol belongs to the class of organic compounds known as naphthalenes. Naphthalenes are compounds containing a naphthalene moiety, which consists of two fused benzene rings. (1s,13s)-13-hydroxy-3-isopropyl-1,8,13-trimethyltricyclo[7.4.1.0⁵,¹⁴]tetradeca-3,5,7,9(14)-tetraene-2,10-dione is found in Salvia candidissima, Salvia kronenburgii, Salvia montbretii and Salvia staminea. (1s,13s)-13-hydroxy-3-isopropyl-1,8,13-trimethyltricyclo[7.4.1.0⁵,¹⁴]tetradeca-3,5,7,9(14)-tetraene-2,10-dione was first documented in 2013 (PMID: 23122169). Based on a literature review very few articles have been published on 1-Oxosalvibretol.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 47 49  0  0  0  0  0  0  0  0999 V2000
   -3.2430    3.3338    0.0231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9276    2.6965    0.2536 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8300    3.3838    0.7236 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3777    2.7762    0.9321 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5620    1.4087    0.6769 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5123    0.6799    0.2125 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7425    1.3400    0.0033 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9960    0.7982   -0.5359 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0027    1.2621   -0.0101 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1614   -0.2229   -1.6225 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8254   -0.9371   -1.8259 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3549   -1.5511   -0.5562 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9328   -3.0066   -0.7486 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4855   -1.6058    0.2990 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2845   -0.8026    0.1520 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3529   -1.2008    1.6631 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0620   -1.1215   -0.2528 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4023   -2.0039   -1.0818 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1651   -0.3453    0.3558 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5316   -0.9111    0.4322 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4568    0.0851    1.0530 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0497   -1.3174   -0.9307 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9341    0.8859    0.7607 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6474    3.2550   -0.9993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9710    4.4440    0.0023 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9388    3.3498    0.8564 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9455    4.4577    0.9334 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2332    3.3371    1.3035 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3743    0.3149   -2.5605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9768   -0.9005   -1.3907 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0160   -1.7423   -2.5649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0845   -0.2545   -2.2604 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8154   -3.6504   -0.5807 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2165   -3.2391    0.0547 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5013   -3.1454   -1.7631 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5318   -2.4490    0.7900 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2758   -0.4526    2.1835 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0105   -2.2255    1.8119 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3813   -1.1099    2.0387 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5465   -1.8333    1.0559 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5596    1.0122    0.4690 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4646   -0.3819    1.1430 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0837    0.3390    2.0772 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1547   -1.2070   -0.8943 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6385   -0.6661   -1.7224 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8497   -2.3911   -1.1076 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7153    1.5146    1.1482 H   0  0  0  0  0  0  0  0  0  0  0  0
 21 20  1  0
 20 22  1  0
 20 19  1  0
 19 23  2  0
 23  5  1  0
  5  4  2  0
  4  3  1  0
  3  2  2  0
  2  1  1  0
  2  7  1  0
  7  6  2  0
  6 15  1  0
 15 16  1  1
 15 17  1  0
 17 18  2  0
 15 12  1  0
 12 13  1  0
 12 14  1  1
 12 11  1  0
 11 10  1  0
 10  8  1  0
  8  9  2  0
 17 19  1  0
  6  5  1  0
  8  7  1  0
 21 41  1  0
 21 42  1  0
 21 43  1  0
 20 40  1  0
 22 44  1  0
 22 45  1  0
 22 46  1  0
 23 47  1  0
  4 28  1  0
  3 27  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
 16 37  1  0
 16 38  1  0
 16 39  1  0
 13 33  1  0
 13 34  1  0
 13 35  1  0
 14 36  1  0
 11 31  1  0
 11 32  1  0
 10 29  1  0
 10 30  1  0
M  END


  Mrv1652309092218362D          

 23 25  0  0  1  0            999 V2000
    2.8768    2.4403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0740    1.3394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8783    1.1558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3926    1.8008    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2362    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8783   -0.3308    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0740   -0.5144    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4319   -1.2577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.0288    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1161   -0.7634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    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  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  2  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  6  0  0  0
 12 15  1  0  0  0  0
  6 15  1  0  0  0  0
 15 16  1  6  0  0  0
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 19 23  2  0  0  0  0
  5 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0287491

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C1=CC2=CC=C(C)C3=C2[C@](C)(C1=O)[C@@](C)(O)CCC3=O

> <INCHI_IDENTIFIER>
InChI=1S/C20H24O3/c1-11(2)14-10-13-7-6-12(3)16-15(21)8-9-19(4,23)20(5,17(13)16)18(14)22/h6-7,10-11,23H,8-9H2,1-5H3/t19-,20+/m0/s1

> <INCHI_KEY>
CZDMJFHCCVCECP-VQTJNVASSA-N

> <FORMULA>
C20H24O3

> <MOLECULAR_WEIGHT>
312.409

> <EXACT_MASS>
312.172544633

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
34.85915207948908

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,13S)-13-hydroxy-1,8,13-trimethyl-3-(propan-2-yl)tricyclo[7.4.1.0^{5,14}]tetradeca-3,5,7,9(14)-tetraene-2,10-dione

> <JCHEM_LOGP>
3.9105890709999995

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.779701004682828

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.157380883257623

> <JCHEM_PKA_STRONGEST_BASIC>
-3.1402767979410777

> <JCHEM_POLAR_SURFACE_AREA>
54.37

> <JCHEM_REFRACTIVITY>
92.27949999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,13S)-13-hydroxy-3-isopropyl-1,8,13-trimethyltricyclo[7.4.1.0^{5,14}]tetradeca-3,5,7,9(14)-tetraene-2,10-dione

> <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       5.370   4.555   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.871   2.500   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.373   2.157   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       6.333   3.362   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       6.041   0.770   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.373  -0.617   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.871  -0.960   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.540  -2.348   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       2.667  -1.920   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.083  -1.425   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       1.334  -2.310   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   23                                                  
CONECT    6    5    7   15                                                  
CONECT    7    6    2    8                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14   15                                             
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15   12    6   16   17                                             
CONECT   16   15                                                            
CONECT   17   15   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   23                                                  
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   19    5                                                       
MASTER        0    0    0    0    0    0    0    0   23    0   50    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₄O₃

Average Mass

312.4090 Da

Monoisotopic Mass

312.17254 Da

IUPAC Name

(1S,13S)-13-hydroxy-1,8,13-trimethyl-3-(propan-2-yl)tricyclo[7.4.1.0^{5,14}]tetradeca-3,5,7,9(14)-tetraene-2,10-dione

Traditional Name

(1S,13S)-13-hydroxy-3-isopropyl-1,8,13-trimethyltricyclo[7.4.1.0^{5,14}]tetradeca-3,5,7,9(14)-tetraene-2,10-dione

CAS Registry Number

Not Available

SMILES

CC(C)C1=CC2=CC=C(C)C3=C2[C@](C)(C1=O)[C@@](C)(O)CCC3=O

InChI Identifier

InChI=1S/C20H24O3/c1-11(2)14-10-13-7-6-12(3)16-15(21)8-9-19(4,23)20(5,17(13)16)18(14)22/h6-7,10-11,23H,8-9H2,1-5H3/t19-,20+/m0/s1

InChI Key

CZDMJFHCCVCECP-VQTJNVASSA-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
Salvia candidissima	LOTUS Database	35616633
Salvia kronenburgii	LOTUS Database	35616633
Salvia montbretii	LOTUS Database	35616633
Salvia staminea	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as naphthalenes. Naphthalenes are compounds containing a naphthalene moiety, which consists of two fused benzene rings.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Naphthalenes

Sub Class

Not Available

Direct Parent

Naphthalenes

Alternative Parents

Substituents

Naphthalene
Aryl alkyl ketone
Aryl ketone
Tertiary alcohol
Ketone
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
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	3.91	ChemAxon
pKa (Strongest Acidic)	14.16	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	54.37 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	92.28 m³·mol⁻¹	ChemAxon
Polarizability	34.86 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

8670723

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10495322

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Zhou W, Xie H, Wu P, Wei X: Abietane diterpenoids from Isodon lophanthoides var. graciliflorus and their cytotoxicity. Food Chem. 2013 Jan 15;136(2):1110-6. doi: 10.1016/j.foodchem.2012.08.015. Epub 2012 Aug 16. [PubMed:23122169 ]
LOTUS database [Link]

Showing NP-Card for (1s,13s)-13-hydroxy-3-isopropyl-1,8,13-trimethyltricyclo[7.4.1.0⁵,¹⁴]tetradeca-3,5,7,9(14)-tetraene-2,10-dione (NP0287491)

MOL for NP0287491 ((1s,13s)-13-hydroxy-3-isopropyl-1,8,13-trimethyltricyclo[7.4.1.0⁵,¹⁴]tetradeca-3,5,7,9(14)-tetraene-2,10-dione)

3D MOL for NP0287491 ((1s,13s)-13-hydroxy-3-isopropyl-1,8,13-trimethyltricyclo[7.4.1.0⁵,¹⁴]tetradeca-3,5,7,9(14)-tetraene-2,10-dione)

3D SDF for NP0287491 ((1s,13s)-13-hydroxy-3-isopropyl-1,8,13-trimethyltricyclo[7.4.1.0⁵,¹⁴]tetradeca-3,5,7,9(14)-tetraene-2,10-dione)

3D-SDF for NP0287491 ((1s,13s)-13-hydroxy-3-isopropyl-1,8,13-trimethyltricyclo[7.4.1.0⁵,¹⁴]tetradeca-3,5,7,9(14)-tetraene-2,10-dione)

PDB for NP0287491 ((1s,13s)-13-hydroxy-3-isopropyl-1,8,13-trimethyltricyclo[7.4.1.0⁵,¹⁴]tetradeca-3,5,7,9(14)-tetraene-2,10-dione)

3D PDB for NP0287491 ((1s,13s)-13-hydroxy-3-isopropyl-1,8,13-trimethyltricyclo[7.4.1.0⁵,¹⁴]tetradeca-3,5,7,9(14)-tetraene-2,10-dione)

SMILES for NP0287491 ((1s,13s)-13-hydroxy-3-isopropyl-1,8,13-trimethyltricyclo[7.4.1.0⁵,¹⁴]tetradeca-3,5,7,9(14)-tetraene-2,10-dione)

INCHI for NP0287491 ((1s,13s)-13-hydroxy-3-isopropyl-1,8,13-trimethyltricyclo[7.4.1.0⁵,¹⁴]tetradeca-3,5,7,9(14)-tetraene-2,10-dione)

Structure for NP0287491 ((1s,13s)-13-hydroxy-3-isopropyl-1,8,13-trimethyltricyclo[7.4.1.0⁵,¹⁴]tetradeca-3,5,7,9(14)-tetraene-2,10-dione)

3D Structure for NP0287491 ((1s,13s)-13-hydroxy-3-isopropyl-1,8,13-trimethyltricyclo[7.4.1.0⁵,¹⁴]tetradeca-3,5,7,9(14)-tetraene-2,10-dione)