NP-MRD: Showing NP-Card for 7-bromo-1-(hydroxymethyl)-2,4b,8,8,10a-pentamethyl-decahydrophenanthren-2-ol (NP0157603)

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Record Information

Version

2.0

Created at

2022-09-02 15:01:25 UTC

Updated at

2022-09-02 15:01:25 UTC

NP-MRD ID

NP0157603

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7-bromo-1-(hydroxymethyl)-2,4b,8,8,10a-pentamethyl-decahydrophenanthren-2-ol

Description

7-Bromo-1-(hydroxymethyl)-2,4b,8,8,10a-pentamethyl-tetradecahydrophenanthren-2-ol belongs to the class of organic compounds known as isocopalane and spongiane diterpenoids. These are diterpenoids with a structure based on the isocopalane (Tetradecahydro-1,1,4a,7,8,8a-hexamethylphenanthrene) or the 15,16-epoxyisocopalane skeleton. 7-bromo-1-(hydroxymethyl)-2,4b,8,8,10a-pentamethyl-decahydrophenanthren-2-ol is found in Aplysia kurodai. 7-Bromo-1-(hydroxymethyl)-2,4b,8,8,10a-pentamethyl-tetradecahydrophenanthren-2-ol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 58 60  0  0  0  0  0  0  0  0999 V2000
   -3.8473   -1.1401   -0.0007 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9690   -0.0439    0.4935 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2515    0.0555    2.0063 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3402    1.3138   -0.0619 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4089    2.6395    1.0300 Br  0  0  0  0  0  0  0  0  0  0  0  0
   -2.8748    1.3698   -1.4655 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3861    1.1588   -1.6511 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9395   -0.1678   -1.0223 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5759   -1.2090   -1.9596 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5216   -0.2253    0.3385 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0950   -1.5070    0.9790 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3388   -1.3252    1.3554 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2180   -0.7505    0.2751 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2046   -1.8936   -0.0557 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0607    0.2840    0.9988 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8544   -0.2677    2.1278 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7659   -1.2402    1.8523 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8305    1.2388    0.1858 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0821    0.8107   -0.4462 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1878    2.2799    1.0934 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8279    1.8965   -0.7373 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2776    0.8667   -1.6396 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5602   -0.2959   -0.9586 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.0747   -1.1204   -1.0694 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8451   -1.0115    0.5172 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4571   -2.0973    0.3811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5215   -0.9451    2.4062 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1333    0.7037    2.1886 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3762    0.4571    2.5123 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4045    1.5304   -0.0242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0610    2.4219   -1.8354 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4997    0.7290   -2.0861 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8943    2.0303   -1.2529 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2978    1.0469   -2.7756 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9215   -2.0990   -1.4584 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3017   -0.8129   -2.6555 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7021   -1.5442   -2.6005 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0303    0.6115    0.9216 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6718   -1.6695    1.9286 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1952   -2.4136    0.4016 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3121   -0.6883    2.2923 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6713   -2.3181    1.7345 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7703   -2.4548   -0.9390 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2757   -2.6313    0.7377 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1774   -1.5649   -0.3692 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2696    0.9313    1.5088 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4069    0.6014    2.5950 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2217   -0.6465    2.9863 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8803   -1.8730    2.6055 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7102    1.7430   -0.6055 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0239    0.3795   -1.4638 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6691    0.2043    0.2527 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8758    2.8318    0.6081 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4031    2.6090   -1.3609 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1481    2.4612   -0.1092 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6526    1.3675   -2.3937 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1617    0.5047   -2.2558 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7589   -1.1222   -1.7264 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  1  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  6
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  6
 13 15  1  0
 15 16  1  0
 16 17  1  0
 15 18  1  0
 18 19  1  0
 18 20  1  1
 18 21  1  0
 21 22  1  0
 22 23  1  0
 10  2  1  0
 23 13  1  0
 23  8  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  3 27  1  0
  3 28  1  0
  3 29  1  0
  4 30  1  6
  6 31  1  0
  6 32  1  0
  7 33  1  0
  7 34  1  0
  9 35  1  0
  9 36  1  0
  9 37  1  0
 10 38  1  1
 11 39  1  0
 11 40  1  0
 12 41  1  0
 12 42  1  0
 14 43  1  0
 14 44  1  0
 14 45  1  0
 15 46  1  1
 16 47  1  0
 16 48  1  0
 17 49  1  0
 19 50  1  0
 19 51  1  0
 19 52  1  0
 20 53  1  0
 21 54  1  0
 21 55  1  0
 22 56  1  0
 22 57  1  0
 23 58  1  6
M  END


  Mrv1533004161520202D          

 23 25  0  0  0  0            999 V2000
    4.6465    0.9428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6465   -0.1178    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1895   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4452   -1.1144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4733   -0.5841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355    0.4125    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    0.3020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395   -1.0164    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  1  0  0  0  0
  5  6  1  0  0  0  0
  6  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
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 12 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
  6 19  1  0  0  0  0
 11 19  1  0  0  0  0
 19 20  1  0  0  0  0
  7 21  1  0  0  0  0
  2 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0157603

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)C(Br)CCC2(C)C1CCC1(C)C(CO)C(C)(O)CCC21

> <INCHI_IDENTIFIER>
InChI=1S/C20H35BrO2/c1-17(2)13-6-9-19(4)14(18(13,3)10-8-16(17)21)7-11-20(5,23)15(19)12-22/h13-16,22-23H,6-12H2,1-5H3

> <INCHI_KEY>
WVAADOIHOIZUJC-UHFFFAOYSA-N

> <FORMULA>
C20H35BrO2

> <MOLECULAR_WEIGHT>
387.402

> <EXACT_MASS>
386.182043

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
40.97638792920532

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
7-bromo-1-(hydroxymethyl)-2,4b,8,8,10a-pentamethyl-tetradecahydrophenanthren-2-ol

> <ALOGPS_LOGP>
4.85

> <JCHEM_LOGP>
4.026456815999999

> <ALOGPS_LOGS>
-5.96

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.547289566237115

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.61521615256704

> <JCHEM_PKA_STRONGEST_BASIC>
-2.6395336916260064

> <JCHEM_POLAR_SURFACE_AREA>
40.46

> <JCHEM_REFRACTIVITY>
98.7331

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.28e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
7-bromo-1-(hydroxymethyl)-2,4b,8,8,10a-pentamethyl-decahydrophenanthren-2-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0       8.673   1.760   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.494   0.770   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       8.673  -0.220   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       6.724   2.104   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.184   2.104   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.414   0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.184  -0.564   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.954  -1.897   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.414  -1.897   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.874  -1.897   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.104  -0.564   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.564  -0.564   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.831  -2.080   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.883  -1.090   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.206   0.770   0.000  0.00  0.00           C+0
HETATM   16 Br   UNK     0      -1.746   0.770   0.000  0.00  0.00          Br+0
HETATM   17  C   UNK     0       0.564   2.104   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.104   2.104   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.874   0.770   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.644   2.104   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.724  -0.564   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.494  -1.897   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       9.034  -1.897   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4   21                                             
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   19                                                  
CONECT    7    6    8    9   21                                             
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   19                                                  
CONECT   12   11   13   14   15                                             
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15   12   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18    6   11   20                                             
CONECT   20   19                                                            
CONECT   21    7    2   22                                                  
CONECT   22   21   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

C₂₀H₃₅BrO₂

Average Mass

387.4020 Da

Monoisotopic Mass

386.18204 Da

IUPAC Name

7-bromo-1-(hydroxymethyl)-2,4b,8,8,10a-pentamethyl-tetradecahydrophenanthren-2-ol

Traditional Name

7-bromo-1-(hydroxymethyl)-2,4b,8,8,10a-pentamethyl-decahydrophenanthren-2-ol

CAS Registry Number

Not Available

SMILES

CC1(C)C(Br)CCC2(C)C1CCC1(C)C(CO)C(C)(O)CCC21

InChI Identifier

InChI=1S/C20H35BrO2/c1-17(2)13-6-9-19(4)14(18(13,3)10-8-16(17)21)7-11-20(5,23)15(19)12-22/h13-16,22-23H,6-12H2,1-5H3

InChI Key

WVAADOIHOIZUJC-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
Aplysia kurodai	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as isocopalane and spongiane diterpenoids. These are diterpenoids with a structure based on the isocopalane (Tetradecahydro-1,1,4a,7,8,8a-hexamethylphenanthrene) or the 15,16-epoxyisocopalane skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Isocopalane and spongiane diterpenoids

Alternative Parents

Substituents

Isocopalane diterpenoid
13-hydroxysteroid
Hydroxysteroid
Steroid
Hydrophenanthrene
Phenanthrene
Cyclic alcohol
Tertiary alcohol
Alcohol
Organohalogen compound
Organobromide
Organooxygen compound
Primary alcohol
Hydrocarbon derivative
Organic oxygen compound
Alkyl halide
Alkyl bromide
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	4.85	ALOGPS
logP	4.03	ChemAxon
logS	-6	ALOGPS
pKa (Strongest Acidic)	14.62	ChemAxon
pKa (Strongest Basic)	-2.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	40.46 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	98.73 m³·mol⁻¹	ChemAxon
Polarizability	40.98 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

74051290

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 7-bromo-1-(hydroxymethyl)-2,4b,8,8,10a-pentamethyl-decahydrophenanthren-2-ol (NP0157603)

MOL for NP0157603 (7-bromo-1-(hydroxymethyl)-2,4b,8,8,10a-pentamethyl-decahydrophenanthren-2-ol)

3D MOL for NP0157603 (7-bromo-1-(hydroxymethyl)-2,4b,8,8,10a-pentamethyl-decahydrophenanthren-2-ol)

3D SDF for NP0157603 (7-bromo-1-(hydroxymethyl)-2,4b,8,8,10a-pentamethyl-decahydrophenanthren-2-ol)

3D-SDF for NP0157603 (7-bromo-1-(hydroxymethyl)-2,4b,8,8,10a-pentamethyl-decahydrophenanthren-2-ol)

PDB for NP0157603 (7-bromo-1-(hydroxymethyl)-2,4b,8,8,10a-pentamethyl-decahydrophenanthren-2-ol)

3D PDB for NP0157603 (7-bromo-1-(hydroxymethyl)-2,4b,8,8,10a-pentamethyl-decahydrophenanthren-2-ol)

SMILES for NP0157603 (7-bromo-1-(hydroxymethyl)-2,4b,8,8,10a-pentamethyl-decahydrophenanthren-2-ol)

INCHI for NP0157603 (7-bromo-1-(hydroxymethyl)-2,4b,8,8,10a-pentamethyl-decahydrophenanthren-2-ol)

Structure for NP0157603 (7-bromo-1-(hydroxymethyl)-2,4b,8,8,10a-pentamethyl-decahydrophenanthren-2-ol)

3D Structure for NP0157603 (7-bromo-1-(hydroxymethyl)-2,4b,8,8,10a-pentamethyl-decahydrophenanthren-2-ol)