NP-MRD: Showing NP-Card for (1R,4R,5R,9S)-4,11,11-Trimethyl-8-methylenebicyclo[7.2.0]undecane-4,5-diol (NP0331821)

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Record Information

Version

2.0

Created at

2023-09-13 16:02:39 UTC

Updated at

2024-09-03 04:17:04 UTC

NP-MRD ID

NP0331821

Natural Product DOI

https://doi.org/10.57994/0909

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1R,4R,5R,9S)-4,11,11-Trimethyl-8-methylenebicyclo[7.2.0]undecane-4,5-diol

Description

CHEMBL512948 belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. Based on a literature review very few articles have been published on CHEMBL512948.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309062206192D          

 17 18  0  0  1  0            999 V2000
    2.4366    0.8327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8491    0.1183    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6615    0.2615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3760   -0.1510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6582   -0.9262    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4832   -0.9262    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3760   -1.7015    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1996   -1.7494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5662   -2.5042    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6615   -2.1140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8491   -1.9707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3188   -1.3387    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3188   -0.5137    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4938   -0.5137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4938   -1.3387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6915   -1.5313    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3012   -2.1409    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  1  0  0  0
  5  7  1  0  0  0  0
  7  8  1  1  0  0  0
  7  9  1  6  0  0  0
  7 10  1  0  0  0  0
 10 11  1  0  0  0  0
 12 11  1  1  0  0  0
 12 13  1  0  0  0  0
  2 13  1  0  0  0  0
 13 14  1  6  0  0  0
 14 15  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
M  END
> <DATABASE_ID>
NP0331821

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)C[C@H]2[C@H]1CC[C@@](C)(O)[C@H](O)CCC2=C

> <INCHI_IDENTIFIER>
InChI=1S/C15H26O2/c1-10-5-6-13(16)15(4,17)8-7-12-11(10)9-14(12,2)3/h11-13,16-17H,1,5-9H2,2-4H3/t11-,12-,13-,15-/m1/s1

> <INCHI_KEY>
XZTGVWRBZDBQLP-RGCMKSIDSA-N

> <FORMULA>
C15H26O2

> <MOLECULAR_WEIGHT>
238.371

> <EXACT_MASS>
238.193280077

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
43

> <JCHEM_AVERAGE_POLARIZABILITY>
28.171532934428647

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,4R,5R,9S)-4,11,11-trimethyl-8-methylidenebicyclo[7.2.0]undecane-4,5-diol

> <JCHEM_LOGP>
2.456824311

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.142714658967758

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.731833425160598

> <JCHEM_PKA_STRONGEST_BASIC>
-3.20726418647566

> <JCHEM_POLAR_SURFACE_AREA>
40.46

> <JCHEM_REFRACTIVITY>
69.723

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,4R,5R,9S)-4,11,11-trimethyl-8-methylidenebicyclo[7.2.0]undecane-4,5-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0       4.548   1.554   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.318   0.221   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.835   0.488   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.169  -0.282   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.695  -1.729   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      10.235  -1.729   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       8.169  -3.176   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.706  -3.266   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       8.524  -4.675   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       6.835  -3.946   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.318  -3.679   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.328  -2.499   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.328  -0.959   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.788  -0.959   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.788  -2.499   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.291  -2.858   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.429  -3.996   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   13                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8    9   10                                             
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    7   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   15                                                  
CONECT   13   12    2   14                                                  
CONECT   14   13   15                                                       
CONECT   15   14   12   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

C₁₅H₂₆O₂

Average Mass

238.3710 Da

Monoisotopic Mass

238.19328 Da

IUPAC Name

(1R,4R,5R,9S)-4,11,11-trimethyl-8-methylidenebicyclo[7.2.0]undecane-4,5-diol

Traditional Name

(1R,4R,5R,9S)-4,11,11-trimethyl-8-methylidenebicyclo[7.2.0]undecane-4,5-diol

CAS Registry Number

Not Available

SMILES

CC1(C)C[C@H]2[C@H]1CC[C@@](C)(O)[C@H](O)CCC2=C

InChI Identifier

InChI=1S/C15H26O2/c1-10-5-6-13(16)15(4,17)8-7-12-11(10)9-14(12,2)3/h11-13,16-17H,1,5-9H2,2-4H3/t11-,12-,13-,15-/m1/s1

InChI Key

XZTGVWRBZDBQLP-RGCMKSIDSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCl3, experimental)	Not Available	Latvian Institute of Organic Synthesis	Georgijs Stakanovs	2023-09-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, CDCl3, experimental)	Not Available	Latvian Institute of Organic Synthesis	Georgijs Stakanovs	2023-09-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCl3, experimental)	Not Available	Not Available	Georgijs Stakanovs	2023-09-13	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, CDCl3, experimental)	Not Available	Not Available	Georgijs Stakanovs	2023-09-13	View Spectrum

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

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 100.578570142, CDCl₃, simulated)	st_george@inbox.lv	Latvian Institute of Organic Synthesis	Georgijs Stakanovs	2024-05-14	View Spectrum

Species

Species of Origin

Not Available

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

Caryophyllane sesquiterpenoid
Sesquiterpenoid
Tertiary alcohol
Cyclic alcohol
Secondary alcohol
1,2-diol
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Alcohol
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	2.46	ChemAxon
pKa (Strongest Acidic)	13.73	ChemAxon
pKa (Strongest Basic)	-3.2	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	0	ChemAxon
Refractivity	69.72 m³·mol⁻¹	ChemAxon
Polarizability	28.17 Å³	ChemAxon
Number of Rings	2	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

8619656

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10444237

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (1R,4R,5R,9S)-4,11,11-Trimethyl-8-methylenebicyclo[7.2.0]undecane-4,5-diol (NP0331821)

MOL for NP0331821 ((1R,4R,5R,9S)-4,11,11-Trimethyl-8-methylenebicyclo[7.2.0]undecane-4,5-diol)

3D MOL for NP0331821 ((1R,4R,5R,9S)-4,11,11-Trimethyl-8-methylenebicyclo[7.2.0]undecane-4,5-diol)

3D SDF for NP0331821 ((1R,4R,5R,9S)-4,11,11-Trimethyl-8-methylenebicyclo[7.2.0]undecane-4,5-diol)

3D-SDF for NP0331821 ((1R,4R,5R,9S)-4,11,11-Trimethyl-8-methylenebicyclo[7.2.0]undecane-4,5-diol)

PDB for NP0331821 ((1R,4R,5R,9S)-4,11,11-Trimethyl-8-methylenebicyclo[7.2.0]undecane-4,5-diol)

3D PDB for NP0331821 ((1R,4R,5R,9S)-4,11,11-Trimethyl-8-methylenebicyclo[7.2.0]undecane-4,5-diol)

SMILES for NP0331821 ((1R,4R,5R,9S)-4,11,11-Trimethyl-8-methylenebicyclo[7.2.0]undecane-4,5-diol)

INCHI for NP0331821 ((1R,4R,5R,9S)-4,11,11-Trimethyl-8-methylenebicyclo[7.2.0]undecane-4,5-diol)

Structure for NP0331821 ((1R,4R,5R,9S)-4,11,11-Trimethyl-8-methylenebicyclo[7.2.0]undecane-4,5-diol)

3D Structure for NP0331821 ((1R,4R,5R,9S)-4,11,11-Trimethyl-8-methylenebicyclo[7.2.0]undecane-4,5-diol)