NP-MRD: Showing NP-Card for 7-bromo-4,8,16,16-tetramethyl-15-methylidene-11-oxatetracyclo[10.3.1.0¹,¹⁰.0³,⁸]hexadecan-4-ol (NP0299201)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-10 10:53:47 UTC

Updated at

2022-09-10 10:53:47 UTC

NP-MRD ID

NP0299201

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7-bromo-4,8,16,16-tetramethyl-15-methylidene-11-oxatetracyclo[10.3.1.0¹,¹⁰.0³,⁸]hexadecan-4-ol

Description

7-Bromo-4,8,16,16-tetramethyl-15-methylidene-11-oxatetracyclo[10.3.1.0¹,¹⁰.0³,⁸]Hexadecan-4-ol belongs to the class of organic compounds known as chamigranes. These are sesquiterpenoids characterized by a 1,1,5,9-tetramethylspiro[5,5]undecane skeleton, formally obtained by linking the C1-C6 and C6-C11 of farnesane together. They are predominantly isolated from algae. 7-bromo-4,8,16,16-tetramethyl-15-methylidene-11-oxatetracyclo[10.3.1.0¹,¹⁰.0³,⁸]hexadecan-4-ol is found in Laurencia majuscula. 7-Bromo-4,8,16,16-tetramethyl-15-methylidene-11-oxatetracyclo[10.3.1.0¹,¹⁰.0³,⁸]Hexadecan-4-ol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 54 57  0  0  0  0  0  0  0  0999 V2000
    1.0693   -0.4963    2.5161 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6964   -0.5051    1.3530 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0204   -1.1847    1.3430 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9246   -0.8204    0.2306 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0926   -0.4504   -0.9905 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1582   -1.4923   -1.0902 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9106   -0.9476   -0.9805 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1667   -1.8791   -0.6026 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4380   -1.1707   -0.2082 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8473   -1.6148    1.1485 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2892    0.2978   -0.4204 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0626    0.9066    0.2506 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1508    0.1126    0.1051 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3178    0.7969   -0.5627 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0050    1.5705   -1.7835 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1176    1.6351    0.4011 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5305    1.1035   -0.2028 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4021    2.0598    0.9945 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7652    1.9923   -1.2878 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7774    0.3071   -0.0201 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8548   -0.9645   -0.7803 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5677   -1.5954   -1.1640 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0893   -0.9218   -2.9345 Br  0  0  0  0  0  0  0  0  0  0  0  0
    0.1068   -0.0574    2.7270 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5483   -0.9713    3.3605 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8128   -2.2853    1.3603 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5408   -0.9738    2.3099 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6724   -0.0753    0.4880 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4886   -1.7498   -0.0741 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6868   -0.3015   -1.8891 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7375   -0.4069   -1.9424 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2020   -2.5194    0.2332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3740   -2.5583   -1.4377 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0430   -2.2626    1.6131 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9970   -0.8057    1.8905 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7370   -2.3108    1.1337 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0687    0.3959   -1.5303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2996    1.2394    1.2726 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0926    1.8821   -0.3111 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9747    1.6031   -2.1192 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6118    1.2460   -2.6807 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3183    2.6480   -1.6441 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1016    1.2770    1.4312 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1310    1.8302    0.0026 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6145    2.6466    0.4185 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3497    1.5570    1.9515 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5696    2.7547    0.7777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3321    2.6974    0.9300 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3130    2.8517   -1.1476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6508    0.9415   -0.3661 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0151    0.1787    1.0786 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4602   -0.8438   -1.7275 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4782   -1.6811   -0.1677 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6249   -2.6854   -1.2557 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 14  1  0
 14 16  1  0
 14  5  1  0
  5  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  2  3
 13  2  1  1
 13 12  1  0
 12 11  1  0
 11 17  1  0
 17 18  1  0
 17 19  1  6
 17 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 22  9  1  0
  9 10  1  1
  9  8  1  0
  8  7  1  0
  7  6  1  0
 13 14  1  0
  7 13  1  0
  6  5  1  0
  9 11  1  0
 15 40  1  0
 15 41  1  0
 15 42  1  0
 16 43  1  0
 16 44  1  0
 16 45  1  0
  5 30  1  6
  4 28  1  0
  4 29  1  0
  3 26  1  0
  3 27  1  0
  1 24  1  0
  1 25  1  0
 12 38  1  0
 12 39  1  0
 11 37  1  6
 18 46  1  0
 18 47  1  0
 18 48  1  0
 19 49  1  0
 20 50  1  0
 20 51  1  0
 21 52  1  0
 21 53  1  0
 22 54  1  6
 10 34  1  0
 10 35  1  0
 10 36  1  0
  8 32  1  0
  8 33  1  0
  7 31  1  6
M  END


  Mrv1533004151518342D          

 23 26  0  0  0  0            999 V2000
    4.1959    2.6366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7893    1.9188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1530    2.4440    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5668    1.6430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7167    0.8317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0890    0.2963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2389   -0.5150    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    3.3115    0.5721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4675   -0.2380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6911    0.0264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9090    0.2974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2237   -0.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5012    0.2519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0553    0.9296    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2134    1.7467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0761    1.8271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3847    2.5923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6654    1.1432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3651    1.6580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1616    1.3834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0400    0.7469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8226    1.5427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3280    1.1637    0.0000 C   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
  6  8  1  0  0  0  0
  8  9  1  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  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
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 11 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
  2 20  1  0  0  0  0
  8 20  1  0  0  0  0
 18 21  1  0  0  0  0
 13 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0299201

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)C2CCC(=C)C11CC3C(C)(O)CCC(Br)C3(C)CC1O2

> <INCHI_IDENTIFIER>
InChI=1S/C20H31BrO2/c1-12-6-7-15-17(2,3)20(12)10-13-18(4,11-16(20)23-15)14(21)8-9-19(13,5)22/h13-16,22H,1,6-11H2,2-5H3

> <INCHI_KEY>
BEXLYUHLQNOFOD-UHFFFAOYSA-N

> <FORMULA>
C20H31BrO2

> <MOLECULAR_WEIGHT>
383.37

> <EXACT_MASS>
382.150743

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
39.137650825207146

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
7-bromo-4,8,16,16-tetramethyl-15-methylidene-11-oxatetracyclo[10.3.1.0¹,¹⁰.0³,⁸]hexadecan-4-ol

> <ALOGPS_LOGP>
4.75

> <JCHEM_LOGP>
3.9315639016666672

> <ALOGPS_LOGS>
-5.94

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.76805480075614

> <JCHEM_PKA_STRONGEST_BASIC>
-2.900252830149263

> <JCHEM_POLAR_SURFACE_AREA>
29.46

> <JCHEM_REFRACTIVITY>
96.25399999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.36e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
7-bromo-4,8,16,16-tetramethyl-15-methylidene-11-oxatetracyclo[10.3.1.0¹,¹⁰.0³,⁸]hexadecan-4-ol

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 15-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   15-APR-15         0                                  
HETATM    1  C   UNK     0       7.832   4.922   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.073   3.582   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       5.886   4.562   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       8.525   3.067   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.804   1.553   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.633   0.553   0.000  0.00  0.00           C+0
HETATM    7 Br   UNK     0       7.913  -0.961   0.000  0.00  0.00          Br+0
HETATM    8  C   UNK     0       6.181   1.068   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.473  -0.444   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.023   0.049   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.563   0.555   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       2.284  -0.443   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       0.936   0.470   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.103   1.735   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.398   3.260   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.009   3.411   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.585   4.839   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.109   2.134   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.415   3.095   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.902   2.582   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.941   1.394   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.536   2.880   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.612   2.172   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4   20                                             
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   10   20                                             
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   18                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   21                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   11   19   21                                             
CONECT   19   18   20                                                       
CONECT   20   19    2    8                                                  
CONECT   21   18   13   22   23                                             
CONECT   22   21                                                            
CONECT   23   21                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   52    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₃₁BrO₂

Average Mass

383.3700 Da

Monoisotopic Mass

382.15074 Da

IUPAC Name

7-bromo-4,8,16,16-tetramethyl-15-methylidene-11-oxatetracyclo[10.3.1.0¹,¹⁰.0³,⁸]hexadecan-4-ol

Traditional Name

7-bromo-4,8,16,16-tetramethyl-15-methylidene-11-oxatetracyclo[10.3.1.0¹,¹⁰.0³,⁸]hexadecan-4-ol

CAS Registry Number

Not Available

SMILES

CC1(C)C2CCC(=C)C11CC3C(C)(O)CCC(Br)C3(C)CC1O2

InChI Identifier

InChI=1S/C20H31BrO2/c1-12-6-7-15-17(2,3)20(12)10-13-18(4,11-16(20)23-15)14(21)8-9-19(13,5)22/h13-16,22H,1,6-11H2,2-5H3

InChI Key

BEXLYUHLQNOFOD-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
Laurencia majuscula	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as chamigranes. These are sesquiterpenoids characterized by a 1,1,5,9-tetramethylspiro[5,5]undecane skeleton, formally obtained by linking the C1-C6 and C6-C11 of farnesane together. They are predominantly isolated from algae.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Chamigranes

Alternative Parents

Substituents

Chamigrane sesquiterpenoid
Naphthofuran
Oxepane
Cyclic alcohol
Tertiary alcohol
Tetrahydrofuran
Oxacycle
Ether
Dialkyl ether
Organoheterocyclic compound
Organooxygen compound
Organobromide
Organohalogen compound
Hydrocarbon derivative
Alcohol
Organic oxygen compound
Alkyl halide
Alkyl bromide
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic 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	4.75	ALOGPS
logP	3.93	ChemAxon
logS	-5.9	ALOGPS
pKa (Strongest Acidic)	14.77	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	29.46 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	96.25 m³·mol⁻¹	ChemAxon
Polarizability	39.14 Å³	ChemAxon
Number of Rings	4	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

23427436

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-4,8,16,16-tetramethyl-15-methylidene-11-oxatetracyclo[10.3.1.0¹,¹⁰.0³,⁸]hexadecan-4-ol (NP0299201)

MOL for NP0299201 (7-bromo-4,8,16,16-tetramethyl-15-methylidene-11-oxatetracyclo[10.3.1.0¹,¹⁰.0³,⁸]hexadecan-4-ol)

3D MOL for NP0299201 (7-bromo-4,8,16,16-tetramethyl-15-methylidene-11-oxatetracyclo[10.3.1.0¹,¹⁰.0³,⁸]hexadecan-4-ol)

3D SDF for NP0299201 (7-bromo-4,8,16,16-tetramethyl-15-methylidene-11-oxatetracyclo[10.3.1.0¹,¹⁰.0³,⁸]hexadecan-4-ol)

3D-SDF for NP0299201 (7-bromo-4,8,16,16-tetramethyl-15-methylidene-11-oxatetracyclo[10.3.1.0¹,¹⁰.0³,⁸]hexadecan-4-ol)

PDB for NP0299201 (7-bromo-4,8,16,16-tetramethyl-15-methylidene-11-oxatetracyclo[10.3.1.0¹,¹⁰.0³,⁸]hexadecan-4-ol)

3D PDB for NP0299201 (7-bromo-4,8,16,16-tetramethyl-15-methylidene-11-oxatetracyclo[10.3.1.0¹,¹⁰.0³,⁸]hexadecan-4-ol)

SMILES for NP0299201 (7-bromo-4,8,16,16-tetramethyl-15-methylidene-11-oxatetracyclo[10.3.1.0¹,¹⁰.0³,⁸]hexadecan-4-ol)

INCHI for NP0299201 (7-bromo-4,8,16,16-tetramethyl-15-methylidene-11-oxatetracyclo[10.3.1.0¹,¹⁰.0³,⁸]hexadecan-4-ol)

Structure for NP0299201 (7-bromo-4,8,16,16-tetramethyl-15-methylidene-11-oxatetracyclo[10.3.1.0¹,¹⁰.0³,⁸]hexadecan-4-ol)

3D Structure for NP0299201 (7-bromo-4,8,16,16-tetramethyl-15-methylidene-11-oxatetracyclo[10.3.1.0¹,¹⁰.0³,⁸]hexadecan-4-ol)