NP-MRD: Showing NP-Card for 10-Bromo-2,7-chamigradiene (NP0064584)

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Record Information

Version

2.0

Created at

2022-04-28 08:47:07 UTC

Updated at

2022-04-28 08:47:07 UTC

NP-MRD ID

NP0064584

Secondary Accession Numbers

None

Natural Product Identification

Common Name

10-Bromo-2,7-chamigradiene

Description

CHEMBL458128 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. 10-Bromo-2,7-chamigradiene is found in Laurencia glandulifera, Laurencia pacifica and Laurencia rigida. Based on a literature review very few articles have been published on CHEMBL458128.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 39 40  0  0  0  0  0  0  0  0999 V2000
    3.8334   -1.0590    0.0856 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6259   -0.2530   -0.2053 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8803   -0.4555   -1.2980 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6924    0.4538   -1.4326 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1736    0.3966   -0.1697 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6733    0.7137    1.0031 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1522    0.8350    0.6870 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1810    1.4886   -0.3237 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7278    2.8845   -0.6892 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4807    1.3223   -0.1593 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1190    0.0244    0.2017 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0365   -0.8008    0.8632 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7449   -2.4915    1.3728 Br  0  0  0  0  0  0  0  0  0  0  0  0
   -0.8809   -0.9156   -0.1256 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0533   -2.0965    0.1958 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4974   -1.2013   -1.4807 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8135   -2.0187   -0.4422 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9162   -1.2221    1.1842 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7312   -0.4707   -0.2460 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1327   -1.2112   -2.0029 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1421    0.1533   -2.3226 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0369    1.5002   -1.5697 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4036    1.7068    1.4751 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5937   -0.0038    1.8429 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3809    1.7953    0.1701 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7009    0.8598    1.6491 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3225    3.0507   -0.4530 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8842    3.0485   -1.7760 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4008    3.6377   -0.1826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1674    2.1705   -0.2881 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5730   -0.4817   -0.6613 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9122    0.2198    0.9615 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6574   -0.1957    1.7188 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6550   -1.9882    1.0247 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5409   -2.4756   -0.6793 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7305   -2.9392    0.4644 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9719   -0.3276   -1.9371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2958   -1.9700   -1.3200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7394   -1.6837   -2.1391 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
  5  4  1  6
  5  6  1  0
  6  7  1  0
  5  8  1  0
  8  9  1  0
  8 10  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  1
 14 16  1  0
  7  2  1  0
 14  5  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  3 20  1  0
  4 21  1  0
  4 22  1  0
  6 23  1  0
  6 24  1  0
  7 25  1  0
  7 26  1  0
  9 27  1  0
  9 28  1  0
  9 29  1  0
 10 30  1  0
 11 31  1  0
 11 32  1  0
 12 33  1  1
 15 34  1  0
 15 35  1  0
 15 36  1  0
 16 37  1  0
 16 38  1  0
 16 39  1  0
M  END


  Mrv1652304282210472D          

 16 17  0  0  1  0            999 V2000
    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  1  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
    0.3020    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  2  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
    2.7770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1895    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
    1.9520   -0.3020    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
    1.5395    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105   -1.0164    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    1.1558   -1.1265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8266   -0.7392    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
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  6  5  1  1  0  0  0
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  6 11  1  0  0  0  0
  9 12  1  0  0  0  0
  5 13  1  0  0  0  0
  2 14  1  6  0  0  0
  1 15  1  0  0  0  0
  1 16  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0064584

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=CC[C@@]2(CC1)C(C)=CC[C@@H](Br)C2(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C15H23Br/c1-11-7-9-15(10-8-11)12(2)5-6-13(16)14(15,3)4/h5,7,13H,6,8-10H2,1-4H3/t13-,15-/m1/s1

> <INCHI_KEY>
FATUEZUBMFMGFR-UKRRQHHQSA-N

> <FORMULA>
C15H23Br

> <MOLECULAR_WEIGHT>
283.253

> <EXACT_MASS>
282.098314

> <JCHEM_ACCEPTOR_COUNT>
0

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
28.79303218770199

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(4R,6S)-4-bromo-1,5,5,9-tetramethylspiro[5.5]undeca-1,8-diene

> <ALOGPS_LOGP>
6.38

> <JCHEM_LOGP>
4.783679796666666

> <ALOGPS_LOGS>
-5.29

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_POLAR_SURFACE_AREA>
0.0

> <JCHEM_REFRACTIVITY>
76.00139999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.45e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(4R,6S)-4-bromo-1,5,5,9-tetramethylspiro[5.5]undeca-1,8-diene

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       2.104  -0.564   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.564  -0.564   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.206   0.770   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.564   2.104   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.104   2.104   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.874   0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.644   2.104   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.184   2.104   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.954   0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.184  -0.564   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.644  -0.564   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.494   0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.874   3.437   0.000  0.00  0.00           C+0
HETATM   14 Br   UNK     0      -0.206  -1.897   0.000  0.00  0.00          Br+0
HETATM   15  C   UNK     0       2.157  -2.103   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.410  -1.380   0.000  0.00  0.00           C+0
CONECT    1    2    6   15   16                                             
CONECT    2    1    3   14                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   13                                                  
CONECT    6    5    1    7   11                                             
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   12                                                  
CONECT   10    9   11                                                       
CONECT   11   10    6                                                       
CONECT   12    9                                                            
CONECT   13    5                                                            
CONECT   14    2                                                            
CONECT   15    1                                                            
CONECT   16    1                                                            
MASTER        0    0    0    0    0    0    0    0   16    0   34    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₂₃Br

Average Mass

283.2530 Da

Monoisotopic Mass

282.09831 Da

IUPAC Name

(4R,6S)-4-bromo-1,5,5,9-tetramethylspiro[5.5]undeca-1,8-diene

Traditional Name

(4R,6S)-4-bromo-1,5,5,9-tetramethylspiro[5.5]undeca-1,8-diene

CAS Registry Number

Not Available

SMILES

CC1=CC[C@@]2(CC1)C(C)=CC[C@@H](Br)C2(C)C

InChI Identifier

InChI=1S/C15H23Br/c1-11-7-9-15(10-8-11)12(2)5-6-13(16)14(15,3)4/h5,7,13H,6,8-10H2,1-4H3/t13-,15-/m1/s1

InChI Key

FATUEZUBMFMGFR-UKRRQHHQSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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 glandulifera	-	KNApSAcK
Laurencia pacifica	-	KNApSAcK
Laurencia rigida	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
Hydrocarbon derivative
Organobromide
Organohalogen 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	6.38	ALOGPS
logP	4.78	ChemAxon
logS	-5.3	ALOGPS
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	0	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	0 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	76 m³·mol⁻¹	ChemAxon
Polarizability	28.79 Å³	ChemAxon
Number of Rings	2	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

10288072

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

21675021

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 10-Bromo-2,7-chamigradiene (NP0064584)

MOL for NP0064584 (10-Bromo-2,7-chamigradiene)

3D MOL for NP0064584 (10-Bromo-2,7-chamigradiene)

3D SDF for NP0064584 (10-Bromo-2,7-chamigradiene)

3D-SDF for NP0064584 (10-Bromo-2,7-chamigradiene)

PDB for NP0064584 (10-Bromo-2,7-chamigradiene)

3D PDB for NP0064584 (10-Bromo-2,7-chamigradiene)

SMILES for NP0064584 (10-Bromo-2,7-chamigradiene)

INCHI for NP0064584 (10-Bromo-2,7-chamigradiene)

Structure for NP0064584 (10-Bromo-2,7-chamigradiene)

3D Structure for NP0064584 (10-Bromo-2,7-chamigradiene)