NP-MRD: Showing NP-Card for 4-bromo-2-methyl-5-(1,2,2-trimethylcyclopent-3-en-1-yl)phenol (NP0297062)

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Record Information

Version

2.0

Created at

2022-09-10 07:03:34 UTC

Updated at

2022-09-10 07:03:35 UTC

NP-MRD ID

NP0297062

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-bromo-2-methyl-5-(1,2,2-trimethylcyclopent-3-en-1-yl)phenol

Description

Cupalaurenol belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. 4-bromo-2-methyl-5-(1,2,2-trimethylcyclopent-3-en-1-yl)phenol is found in Aplysia dactylomela. Cupalaurenol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 36 37  0  0  0  0  0  0  0  0999 V2000
    4.6655    0.2283   -0.2843 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1929    0.2138   -0.1567 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5267    1.4090    0.0117 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1543    1.4442    0.1353 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3872    3.1809    0.3851 Br  0  0  0  0  0  0  0  0  0  0  0  0
    0.3774    0.2784    0.0956 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0574    0.4972    0.2142 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4529    1.1913    1.4621 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5238    1.1812   -1.0833 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5602   -0.0178   -2.0183 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7883   -1.1075   -1.3131 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9228   -0.7398    0.1070 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6470   -1.7954    1.1019 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3673   -0.2035    0.2375 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0343   -0.8975   -0.0704 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4283   -0.9144   -0.1937 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0350   -2.1382   -0.3593 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0466   -0.5117   -1.0174 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1306    0.1267    0.7098 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9800    1.2290   -0.6717 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1288    2.3193    0.0427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9982    2.1320    1.3451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0588    0.5517    2.1711 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5028    1.3601    2.0549 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5212    1.6030   -0.9925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7538    1.8483   -1.5046 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4126    0.0938   -3.0964 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8543   -2.0997   -1.7812 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5711   -1.8878    1.7551 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5073   -2.8213    0.7139 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8618   -1.4770    1.8267 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8494   -0.1182   -0.7544 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9819   -0.9137    0.8263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3900    0.8141    0.6710 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4663   -1.7995   -0.1122 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0292   -2.2593   -0.4573 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  4  6  2  0
  6 15  1  0
 15 16  2  0
 16 17  1  0
  6  7  1  0
  7  8  1  1
  7  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 16  2  1  0
 12  7  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  3 21  1  0
 15 35  1  0
 17 36  1  0
  8 22  1  0
  8 23  1  0
  8 24  1  0
  9 25  1  0
  9 26  1  0
 10 27  1  0
 11 28  1  0
 13 29  1  0
 13 30  1  0
 13 31  1  0
 14 32  1  0
 14 33  1  0
 14 34  1  0
M  END


  Mrv1533004161522042D          

 17 18  0  0  0  0            999 V2000
    2.4530    5.7382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9010    5.1251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1559    4.3405    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6039    3.7274    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8588    2.9428    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    0.7969    3.8989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5420    4.6835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0940    5.2966    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8391    6.0812    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2449    3.2858    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3071    3.8989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9123    2.8009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6574    2.0163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1676    2.0163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4226    2.8009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2313    2.6378    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9810    3.4082    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  1  0  0  0  0
  4  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  2  8  1  0  0  0  0
  8  9  1  0  0  0  0
  6 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 10 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0297062

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=CC(Br)=C(C=C1O)C1(C)CC=CC1(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C15H19BrO/c1-10-8-12(16)11(9-13(10)17)15(4)7-5-6-14(15,2)3/h5-6,8-9,17H,7H2,1-4H3

> <INCHI_KEY>
XLEYZFIMXAGEKY-UHFFFAOYSA-N

> <FORMULA>
C15H19BrO

> <MOLECULAR_WEIGHT>
295.22

> <EXACT_MASS>
294.061928

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
36

> <JCHEM_AVERAGE_POLARIZABILITY>
28.57976534468881

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-bromo-2-methyl-5-(1,2,2-trimethylcyclopent-3-en-1-yl)phenol

> <ALOGPS_LOGP>
5.94

> <JCHEM_LOGP>
5.147466766666668

> <ALOGPS_LOGS>
-5.45

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.465948858051213

> <JCHEM_PKA_STRONGEST_BASIC>
-6.2550667413399585

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
76.90889999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.05e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-bromo-2-methyl-5-(1,2,2-trimethylcyclopent-3-en-1-yl)phenol

> <JCHEM_VEBER_RULE>
1

$$$$

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       4.579  10.711   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.548   9.567   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.024   8.102   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.994   6.958   0.000  0.00  0.00           C+0
HETATM    5 Br   UNK     0       3.470   5.493   0.000  0.00  0.00          Br+0
HETATM    6  C   UNK     0       1.488   7.278   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.012   8.743   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.042   9.887   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       1.566  11.352   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       0.457   6.134   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.573   7.278   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.703   5.228   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.227   3.764   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.313   3.764   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.789   5.228   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.298   4.924   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.831   6.362   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    8                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7   10                                                  
CONECT    7    6    8                                                       
CONECT    8    7    2    9                                                  
CONECT    9    8                                                            
CONECT   10    6   11   12   15                                             
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   10   16   17                                             
CONECT   16   15                                                            
CONECT   17   15                                                            
MASTER        0    0    0    0    0    0    0    0   17    0   36    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₁₉BrO

Average Mass

295.2200 Da

Monoisotopic Mass

294.06193 Da

IUPAC Name

4-bromo-2-methyl-5-(1,2,2-trimethylcyclopent-3-en-1-yl)phenol

Traditional Name

4-bromo-2-methyl-5-(1,2,2-trimethylcyclopent-3-en-1-yl)phenol

CAS Registry Number

Not Available

SMILES

CC1=CC(Br)=C(C=C1O)C1(C)CC=CC1(C)C

InChI Identifier

InChI=1S/C15H19BrO/c1-10-8-12(16)11(9-13(10)17)15(4)7-5-6-14(15,2)3/h5-6,8-9,17H,7H2,1-4H3

InChI Key

XLEYZFIMXAGEKY-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 dactylomela	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Sesquiterpenoids

Alternative Parents

Substituents

Sesquiterpenoid
Cuparane sesquiterpenoid
4-halophenol
O-cresol
4-bromophenol
Bromobenzene
Halobenzene
1-hydroxy-2-unsubstituted benzenoid
Phenol
Toluene
Aryl halide
Aryl bromide
Monocyclic benzene moiety
Benzenoid
Organooxygen compound
Organobromide
Organohalogen compound
Organic oxygen compound
Hydrocarbon derivative
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic 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	5.94	ALOGPS
logP	5.15	ChemAxon
logS	-5.4	ALOGPS
pKa (Strongest Acidic)	9.47	ChemAxon
pKa (Strongest Basic)	-6.3	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	76.91 m³·mol⁻¹	ChemAxon
Polarizability	28.58 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	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

599711

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4-bromo-2-methyl-5-(1,2,2-trimethylcyclopent-3-en-1-yl)phenol (NP0297062)

MOL for NP0297062 (4-bromo-2-methyl-5-(1,2,2-trimethylcyclopent-3-en-1-yl)phenol)

3D MOL for NP0297062 (4-bromo-2-methyl-5-(1,2,2-trimethylcyclopent-3-en-1-yl)phenol)

3D SDF for NP0297062 (4-bromo-2-methyl-5-(1,2,2-trimethylcyclopent-3-en-1-yl)phenol)

3D-SDF for NP0297062 (4-bromo-2-methyl-5-(1,2,2-trimethylcyclopent-3-en-1-yl)phenol)

PDB for NP0297062 (4-bromo-2-methyl-5-(1,2,2-trimethylcyclopent-3-en-1-yl)phenol)

3D PDB for NP0297062 (4-bromo-2-methyl-5-(1,2,2-trimethylcyclopent-3-en-1-yl)phenol)

SMILES for NP0297062 (4-bromo-2-methyl-5-(1,2,2-trimethylcyclopent-3-en-1-yl)phenol)

INCHI for NP0297062 (4-bromo-2-methyl-5-(1,2,2-trimethylcyclopent-3-en-1-yl)phenol)

Structure for NP0297062 (4-bromo-2-methyl-5-(1,2,2-trimethylcyclopent-3-en-1-yl)phenol)

3D Structure for NP0297062 (4-bromo-2-methyl-5-(1,2,2-trimethylcyclopent-3-en-1-yl)phenol)