NP-MRD: Showing NP-Card for Tetraisoquinene (NP0341974)

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Record Information

Version

2.0

Created at

2024-11-18 01:45:14 UTC

Updated at

2025-03-26 19:37:00 UTC

NP-MRD ID

NP0341974

Natural Product DOI

https://doi.org/10.57994/3464

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Tetraisoquinene

Description

Based on a literature review very few articles have been published on Tetraisoquibebe.

Structure

MOL SDF PDB SMILES InChI


  Mrv2104 02152301552D          

 21 24  0  0  1  0            999 V2000
    0.6733   -2.4950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3378   -1.7413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4827   -1.6551    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8227   -1.0739    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5678   -0.2893    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0997    0.1956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1553    0.9803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9803    0.9803    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6477    1.4652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6477    2.2902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3151    0.9803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0602    0.1956    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8448    0.4506    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7276   -0.2893    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7276   -1.1143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3951    0.1956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1401    0.9803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0997   -0.7742    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2352    0.1956    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9026   -0.2893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6477   -1.0739    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
  4  2  1  1  0  0  0
  5  4  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  8  7  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
 12 11  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 11 17  1  0  0  0  0
  5 18  1  1  0  0  0
 19  5  1  0  0  0  0
 19  8  1  0  0  0  0
 19 12  1  0  0  0  0
 19 20  1  6  0  0  0
 20 21  1  0  0  0  0
  4 21  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0341974

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@]12[C@@H](C)CCC1=C(C)[C@@H]1CC[C@@]3(C)[C@@H](CC[C@@]213)C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C20H32/c1-12(2)16-9-11-20-17(8-10-19(16,20)5)14(4)15-7-6-13(3)18(15)20/h12-13,16-18H,6-11H2,1-5H3/t13-,16-,17-,18-,19-,20-/m0/s1

> <INCHI_KEY>
OLBQWUIACGAWRB-VWTPSIDOSA-N

> <FORMULA>
C20H32

> <MOLECULAR_WEIGHT>
272.476

> <EXACT_MASS>
272.25040103

> <JCHEM_ACCEPTOR_COUNT>
0

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
34.77583992017453

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2S,3S,8S,11S,12S)-3,7,11-trimethyl-12-(propan-2-yl)tetracyclo[6.6.0.0^{1,11}.0^{2,6}]tetradec-6-ene

> <JCHEM_LOGP>
5.343969078

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_POLAR_SURFACE_AREA>
0.0

> <JCHEM_REFRACTIVITY>
86.4734

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,3S,8S,11S,12S)-12-isopropyl-3,7,11-trimethyltetracyclo[6.6.0.0^{1,11}.0^{2,6}]tetradec-6-ene

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 15-FEB-23   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   15-FEB-23         0                                  
HETATM    1  C   UNK     0       1.257  -4.657   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.631  -3.251   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.901  -3.090   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.536  -2.005   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.060  -0.540   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.186   0.365   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.290   1.830   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.830   1.830   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.076   2.735   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.076   4.275   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.322   1.830   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.846   0.365   0.000  0.00  0.00           C+0
HETATM   13  H   UNK     0       5.310   0.841   0.000  0.00  0.00           H+0
HETATM   14  C   UNK     0       5.092  -0.540   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.092  -2.080   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.337   0.365   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.862   1.830   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.186  -1.445   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.306   0.365   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.552  -0.540   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.076  -2.005   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   21                                                  
CONECT    5    4    6   18   19                                             
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   19                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   17                                                  
CONECT   12   11   13   14   19                                             
CONECT   13   12                                                            
CONECT   14   12   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   11                                                       
CONECT   18    5                                                            
CONECT   19    5    8   12   20                                             
CONECT   20   19   21                                                       
CONECT   21   20    4                                                       
MASTER        0    0    0    0    0    0    0    0   21    0   48    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₃₂

Average Mass

272.4760 Da

Monoisotopic Mass

272.25040 Da

IUPAC Name

(1S,2S,3S,8S,11S,12S)-3,7,11-trimethyl-12-(propan-2-yl)tetracyclo[6.6.0.0^{1,11}.0^{2,6}]tetradec-6-ene

Traditional Name

(1S,2S,3S,8S,11S,12S)-12-isopropyl-3,7,11-trimethyltetracyclo[6.6.0.0^{1,11}.0^{2,6}]tetradec-6-ene

CAS Registry Number

Not Available

SMILES

[H][C@]12[C@@H](C)CCC1=C(C)[C@@H]1CC[C@@]3(C)[C@@H](CC[C@@]213)C(C)C

InChI Identifier

InChI=1S/C20H32/c1-12(2)16-9-11-20-17(8-10-19(16,20)5)14(4)15-7-6-13(3)18(15)20/h12-13,16-18H,6-11H2,1-5H3/t13-,16-,17-,18-,19-,20-/m0/s1

InChI Key

OLBQWUIACGAWRB-VWTPSIDOSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
HMBC NMR	[¹H, ¹³C] NMR Spectrum (2D, 600 MHz, C6D6, experimental)	weixiuting@ufl.edu	University of Florida	Xiuting Wei	2024-11-18	View Spectrum
COSY NMR	[¹H, ¹H] NMR Spectrum (2D, 600 MHz, C6D6, experimental)	weixiuting@ufl.edu	University of Florida	Xiuting Wei	2024-11-18	View Spectrum
HSQC NMR	[¹H, ¹³C] NMR Spectrum (2D, 600 MHz, C6D6, experimental)	weixiuting@ufl.edu	University of Florida	Xiuting Wei	2024-11-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, C6D6, experimental)	weixiuting@ufl.edu	University of Florida	Xiuting Wei	2024-11-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, C6D6, experimental)	weixiuting@ufl.edu	University of Florida	Xiuting Wei	2024-11-18	View Spectrum
NOESY NMR	[¹H, ¹H] NMR Spectrum (2D, 600 MHz, C6D6, experimental)	weixiuting@ufl.edu	University of Florida	Xiuting Wei	2024-11-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, C6D6, experimental)	weixiuting@ufl.edu	University of Florida	Xiuting Wei	2024-11-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, C6D6, experimental)	weixiuting@ufl.edu	University of Florida	Xiuting Wei	2024-11-18	View Spectrum

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Melittangium boletus		Not Available

Chemical Taxonomy

Classification

Not classified

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	5.34	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	0	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	0 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	86.47 m³·mol⁻¹	ChemAxon
Polarizability	34.78 Å³	ChemAxon
Number of Rings	4	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Tetraisoquinene (NP0341974)

MOL for NP0341974 (Tetraisoquinene)

3D MOL for NP0341974 (Tetraisoquinene)

3D SDF for NP0341974 (Tetraisoquinene)

3D-SDF for NP0341974 (Tetraisoquinene)

PDB for NP0341974 (Tetraisoquinene)

3D PDB for NP0341974 (Tetraisoquinene)

SMILES for NP0341974 (Tetraisoquinene)

INCHI for NP0341974 (Tetraisoquinene)

Structure for NP0341974 (Tetraisoquinene)

3D Structure for NP0341974 (Tetraisoquinene)