NP-MRD: Showing NP-Card for (11e)-4-bromo-8-isopropyl-1,4a-dimethyl-7-methylidene-3,4,5,6,8,9,10,12a-octahydro-2h-benzo[10]annulen-1-ol (NP0315758)

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Record Information

Version

2.0

Created at

2022-09-11 14:32:57 UTC

Updated at

2022-09-11 14:32:58 UTC

NP-MRD ID

NP0315758

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(11e)-4-bromo-8-isopropyl-1,4a-dimethyl-7-methylidene-3,4,5,6,8,9,10,12a-octahydro-2h-benzo[10]annulen-1-ol

Description

(11e)-4-bromo-8-isopropyl-1,4a-dimethyl-7-methylidene-3,4,5,6,8,9,10,12a-octahydro-2h-benzo[10]annulen-1-ol is found in Sphaerococcus coronopifolius.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 55 56  0  0  0  0  0  0  0  0999 V2000
    3.1457   -2.4577   -0.8055 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2944   -1.4707   -0.5149 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9917   -1.6171   -1.2968 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0171   -0.9177   -0.4847 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4203   -0.7423   -0.7112 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1516   -2.0381   -0.6940 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7219    0.1384   -1.8769 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0822   -0.5553   -3.5369 Br  0  0  0  0  0  0  0  0  0  0  0  0
   -3.2085    0.3612   -1.9636 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7891    0.9478   -0.7281 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2414    0.4249    0.5501 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4926    1.4525    1.6308 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9842   -0.7183    0.9245 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8139    0.0717    0.5570 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8922    1.2092    0.8174 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1838    1.3198    1.5203 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9326    0.3708    2.3449 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0125   -0.4560    1.7990 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5997   -0.3678    0.4603 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8560    0.9528   -0.1334 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4794    0.8007   -1.5359 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9395    1.6633    0.6915 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9890   -3.2583   -1.4799 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1067   -2.3969   -0.2629 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1417   -1.2928   -2.3325 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7061   -2.7057   -1.3483 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0301   -1.5144    0.4415 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3912    0.1049   -0.4805 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7273   -2.6755   -1.5108 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9394   -2.5399    0.2720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2323   -1.9631   -0.9054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2359    1.1204   -1.6986 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6820   -0.5619   -2.3178 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3596    1.1144   -2.7919 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8955    0.7263   -0.7395 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7279    2.0617   -0.7399 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6140    2.4835    1.1924 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6951    1.4294    2.3970 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4607    1.2522    2.1451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6354   -1.0954    1.7649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6333   -0.6517    1.3825 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2570    2.1092    0.2720 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6600    2.3274    1.5211 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1573    0.8890    3.3311 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1390   -0.3677    2.7088 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8244   -0.3465    2.6157 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8485   -1.5787    1.9727 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7080   -0.6473    0.6685 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0852    1.6858   -0.2695 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7255    0.5248   -2.2757 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2836    0.0406   -1.4140 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9905    1.7586   -1.7771 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6279    2.2372    0.0369 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5636    0.9378    1.2457 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4626    2.4204    1.3623 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 18  1  0
 18 17  1  0
 17 16  1  0
 16 15  2  0
 15 14  1  0
 14 11  1  0
 11 12  1  0
 11 13  1  1
 11 10  1  0
 10  9  1  0
  9  7  1  0
  7  8  1  0
  7  5  1  0
  5  6  1  6
  5  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  2  3
  2 19  1  0
  5 14  1  0
 21 50  1  0
 21 51  1  0
 21 52  1  0
 20 49  1  0
 22 53  1  0
 22 54  1  0
 22 55  1  0
 19 48  1  1
 18 46  1  0
 18 47  1  0
 17 44  1  0
 17 45  1  0
 16 43  1  0
 15 42  1  0
 14 41  1  1
 12 37  1  0
 12 38  1  0
 12 39  1  0
 13 40  1  0
 10 35  1  0
 10 36  1  0
  9 33  1  0
  9 34  1  0
  7 32  1  1
  6 29  1  0
  6 30  1  0
  6 31  1  0
  4 27  1  0
  4 28  1  0
  3 25  1  0
  3 26  1  0
  1 23  1  0
  1 24  1  0
M  END


  Mrv1652309112216322D          

 22 23  0  0  0  0            999 V2000
    2.0900    2.1602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1604    1.3382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8903    0.5586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0802    0.4027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5401    1.0264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2700    0.2468    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2700    0.8704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5401    0.0909    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
   -0.8101    1.4941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5401    2.2736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2700    2.4296    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0242    3.2003    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9780    2.8531    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8101    1.8059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6203    1.9618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8903    2.7414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7004    2.8973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2405    2.2736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9705    1.4941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5106    0.8704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3207    1.0264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2405    0.0909    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 11 14  1  0  0  0  0
  5 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
  2 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
M  END
> <DATABASE_ID>
NP0315758

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C1CC\C=C\C2C(C)(O)CCC(Br)C2(C)CCC1=C

> <INCHI_IDENTIFIER>
InChI=1S/C20H33BrO/c1-14(2)16-8-6-7-9-17-19(4,12-10-15(16)3)18(21)11-13-20(17,5)22/h7,9,14,16-18,22H,3,6,8,10-13H2,1-2,4-5H3/b9-7+

> <INCHI_KEY>
KKTOETZBFFCICP-VQHVLOKHSA-N

> <FORMULA>
C20H33BrO

> <MOLECULAR_WEIGHT>
369.387

> <EXACT_MASS>
368.171479

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
39.079614266528274

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4-bromo-1,4a-dimethyl-7-methylidene-8-(propan-2-yl)-1,2,3,4,4a,5,6,7,8,9,10,12a-dodecahydrobenzo[10]annulen-1-ol

> <JCHEM_LOGP>
5.6223297993333325

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.708121067737743

> <JCHEM_PKA_STRONGEST_BASIC>
-2.926467844971511

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
99.90369999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
4-bromo-8-isopropyl-1,4a-dimethyl-7-methylidene-3,4,5,6,8,9,10,12a-octahydro-2H-benzo[10]annulen-1-ol

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0       3.901   4.032   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.033   2.498   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.529   1.043   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.016   0.752   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.008   1.916   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.504   0.461   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.504   1.625   0.000  0.00  0.00           C+0
HETATM    8 Br   UNK     0      -1.008   0.170   0.000  0.00  0.00          Br+0
HETATM    9  C   UNK     0      -1.512   2.789   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.008   4.244   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.504   4.535   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.045   5.974   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       1.826   5.326   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       1.512   3.371   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.024   3.662   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.529   5.117   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.041   5.408   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.049   4.244   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.545   2.789   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.553   1.625   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.065   1.916   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.049   0.170   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   19                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7   14                                             
CONECT    6    5                                                            
CONECT    7    5    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13   14                                             
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14   11    5   15                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18    2   20                                                  
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   46    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₃₃BrO

Average Mass

369.3870 Da

Monoisotopic Mass

368.17148 Da

IUPAC Name

4-bromo-1,4a-dimethyl-7-methylidene-8-(propan-2-yl)-1,2,3,4,4a,5,6,7,8,9,10,12a-dodecahydrobenzo[10]annulen-1-ol

Traditional Name

4-bromo-8-isopropyl-1,4a-dimethyl-7-methylidene-3,4,5,6,8,9,10,12a-octahydro-2H-benzo[10]annulen-1-ol

CAS Registry Number

Not Available

SMILES

CC(C)C1CC\C=C\C2C(C)(O)CCC(Br)C2(C)CCC1=C

InChI Identifier

InChI=1S/C20H33BrO/c1-14(2)16-8-6-7-9-17-19(4,12-10-15(16)3)18(21)11-13-20(17,5)22/h7,9,14,16-18,22H,3,6,8,10-13H2,1-2,4-5H3/b9-7+

InChI Key

KKTOETZBFFCICP-VQHVLOKHSA-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
Sphaerococcus coronopifolius	LOTUS Database	35616633

Chemical Taxonomy

Classification

Not classified

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	5.62	ChemAxon
pKa (Strongest Acidic)	14.71	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	20.23 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	99.9 m³·mol⁻¹	ChemAxon
Polarizability	39.08 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (11e)-4-bromo-8-isopropyl-1,4a-dimethyl-7-methylidene-3,4,5,6,8,9,10,12a-octahydro-2h-benzo[10]annulen-1-ol (NP0315758)

MOL for NP0315758 ((11e)-4-bromo-8-isopropyl-1,4a-dimethyl-7-methylidene-3,4,5,6,8,9,10,12a-octahydro-2h-benzo[10]annulen-1-ol)

3D MOL for NP0315758 ((11e)-4-bromo-8-isopropyl-1,4a-dimethyl-7-methylidene-3,4,5,6,8,9,10,12a-octahydro-2h-benzo[10]annulen-1-ol)

3D SDF for NP0315758 ((11e)-4-bromo-8-isopropyl-1,4a-dimethyl-7-methylidene-3,4,5,6,8,9,10,12a-octahydro-2h-benzo[10]annulen-1-ol)

3D-SDF for NP0315758 ((11e)-4-bromo-8-isopropyl-1,4a-dimethyl-7-methylidene-3,4,5,6,8,9,10,12a-octahydro-2h-benzo[10]annulen-1-ol)

PDB for NP0315758 ((11e)-4-bromo-8-isopropyl-1,4a-dimethyl-7-methylidene-3,4,5,6,8,9,10,12a-octahydro-2h-benzo[10]annulen-1-ol)

3D PDB for NP0315758 ((11e)-4-bromo-8-isopropyl-1,4a-dimethyl-7-methylidene-3,4,5,6,8,9,10,12a-octahydro-2h-benzo[10]annulen-1-ol)

SMILES for NP0315758 ((11e)-4-bromo-8-isopropyl-1,4a-dimethyl-7-methylidene-3,4,5,6,8,9,10,12a-octahydro-2h-benzo[10]annulen-1-ol)

INCHI for NP0315758 ((11e)-4-bromo-8-isopropyl-1,4a-dimethyl-7-methylidene-3,4,5,6,8,9,10,12a-octahydro-2h-benzo[10]annulen-1-ol)

Structure for NP0315758 ((11e)-4-bromo-8-isopropyl-1,4a-dimethyl-7-methylidene-3,4,5,6,8,9,10,12a-octahydro-2h-benzo[10]annulen-1-ol)

3D Structure for NP0315758 ((11e)-4-bromo-8-isopropyl-1,4a-dimethyl-7-methylidene-3,4,5,6,8,9,10,12a-octahydro-2h-benzo[10]annulen-1-ol)