NP-MRD: Showing NP-Card for 2-isopropyl-4,6b-dimethyl-1h,1ah,2h,3h,3ah,6h,6ah-cyclopropa[e]indene (NP0190527)

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Record Information

Version

2.0

Created at

2022-09-04 07:13:20 UTC

Updated at

2022-09-04 07:13:20 UTC

NP-MRD ID

NP0190527

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-isopropyl-4,6b-dimethyl-1h,1ah,2h,3h,3ah,6h,6ah-cyclopropa[e]indene

Description

1A,4-dimethyl-6-(propan-2-yl)-1H,1aH,1bH,2H,4aH,5H,6H,6aH-cyclopropa[e]indene belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. 2-isopropyl-4,6b-dimethyl-1h,1ah,2h,3h,3ah,6h,6ah-cyclopropa[e]indene is found in Baccharis dracunculifolia, Bazzania trilobata, Calypogeia granulata, Helichrysum italicum, Helichrysum odoratissimum, Lavandula stoechas, Rhododendron tomentosum, Lepechinia floribunda, Lepidozia vitrea, Melaleuca leucadendra, Origanum acutidens, Origanum adanense, Pelargonium endlicherianum and Syzygium nervosum. Based on a literature review very few articles have been published on 1a,4-dimethyl-6-(propan-2-yl)-1H,1aH,1bH,2H,4aH,5H,6H,6aH-cyclopropa[e]indene.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 39 41  0  0  0  0  0  0  0  0999 V2000
    2.7738    2.7449    0.6524 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3801    1.3543    0.2784 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0253    0.6233   -0.6044 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3801   -0.7014   -0.7436 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5528   -0.8229    0.4980 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2198    0.6018    0.8391 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0261    1.0861    0.1897 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2022    0.2288    0.5934 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2990    0.5056   -0.4308 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4885   -0.3432   -0.0463 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6660    1.9713   -0.4551 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9351   -1.2216    0.5672 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4997   -1.7358   -0.8269 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3889   -1.7307    0.3963 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6465   -3.1536    0.9185 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3835    2.7349    1.5694 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8471    3.3299    0.7293 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3956    3.2156   -0.1418 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9191    0.9578   -1.1577 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7897   -0.7819   -1.6851 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1806   -1.4949   -0.7656 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2313   -1.1875    1.3067 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1415    0.7013    1.9245 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0246    1.0654   -0.9135 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2221    2.1178    0.5277 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5634    0.5938    1.5697 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9006    0.1570   -1.4058 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5924   -1.2357   -0.7110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4371   -0.7146    0.9876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3922    0.2965   -0.1151 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5303    2.0766   -1.1337 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8291    2.5572   -0.8371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9282    2.2547    0.5944 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6939   -1.8396    1.1084 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0156   -2.6733   -1.1319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2301   -0.9995   -1.5851 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0472   -3.7878    0.0866 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2770   -3.6294    1.2680 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4010   -3.1213    1.7215 H   0  0  0  0  0  0  0  0  0  0  0  0
 10  9  1  0
  9 11  1  0
  9  8  1  0
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  3  1  0
  3  2  2  0
  2  1  1  0
  5 14  1  0
 14 15  1  1
 14 13  1  0
 13 12  1  0
 12  8  1  0
  2  6  1  0
 12 14  1  0
 10 28  1  0
 10 29  1  0
 10 30  1  0
  9 27  1  0
 11 31  1  0
 11 32  1  0
 11 33  1  0
  8 26  1  1
  7 24  1  0
  7 25  1  0
  6 23  1  1
  5 22  1  1
  4 20  1  0
  4 21  1  0
  3 19  1  0
  1 16  1  0
  1 17  1  0
  1 18  1  0
 15 37  1  0
 15 38  1  0
 15 39  1  0
 13 35  1  0
 13 36  1  0
 12 34  1  1
M  END


  Mrv1652309042209132D          

 15 17  0  0  0  0            999 V2000
    4.6534   -0.7017    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0894   -0.0996    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2449    0.7106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5224    1.1089    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9203    0.5448    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2707   -0.2021    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7991   -0.8790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9771   -0.8090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5055   -1.4859    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8558   -2.2328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6834   -1.4159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6267   -0.0621    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2763    0.6848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0983    0.6148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1683    1.4368    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
  5  6  1  0  0  0  0
  2  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
  8 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
  5 14  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0190527

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C1CC2C(CC=C2C)C2(C)CC12

> <INCHI_IDENTIFIER>
InChI=1S/C15H24/c1-9(2)11-7-12-10(3)5-6-13(12)15(4)8-14(11)15/h5,9,11-14H,6-8H2,1-4H3

> <INCHI_KEY>
QTZAETFGONVPST-UHFFFAOYSA-N

> <FORMULA>
C15H24

> <MOLECULAR_WEIGHT>
204.357

> <EXACT_MASS>
204.187800773

> <JCHEM_ACCEPTOR_COUNT>
0

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
26.26438709746694

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1a,4-dimethyl-6-(propan-2-yl)-1H,1aH,1bH,2H,4aH,5H,6H,6aH-cyclopropa[e]indene

> <JCHEM_LOGP>
4.0881301626666655

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_POLAR_SURFACE_AREA>
0.0

> <JCHEM_REFRACTIVITY>
65.7679

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
6-isopropyl-1a,4-dimethyl-1H,1bH,2H,4aH,5H,6H,6aH-cyclopropa[e]indene

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       8.686  -1.310   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.633  -0.186   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.924   1.326   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.575   2.070   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.451   1.017   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.105  -0.377   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.225  -1.641   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.691  -1.510   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.810  -2.774   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.464  -4.168   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.276  -2.643   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.036  -0.116   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.382   1.278   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.917   1.148   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.048   2.682   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    6                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   14                                                  
CONECT    6    5    2    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   12                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    8   13   14                                                  
CONECT   13   12   14                                                       
CONECT   14   13    5   12   15                                             
CONECT   15   14                                                            
MASTER        0    0    0    0    0    0    0    0   15    0   34    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₂₄

Average Mass

204.3570 Da

Monoisotopic Mass

204.18780 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(C)C1CC2C(CC=C2C)C2(C)CC12

InChI Identifier

InChI=1S/C15H24/c1-9(2)11-7-12-10(3)5-6-13(12)15(4)8-14(11)15/h5,9,11-14H,6-8H2,1-4H3

InChI Key

QTZAETFGONVPST-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
Baccharis dracunculifolia	LOTUS Database	35616633
Bazzania trilobata	LOTUS Database	35616633
Calypogeia granulata	LOTUS Database	35616633
Helichrysum italicum	LOTUS Database	35616633
Helichrysum odoratissimum	LOTUS Database	35616633
Lavandula stoechas	LOTUS Database	35616633
Ledum palustre	LOTUS Database	35616633
Lepechinia floribunda	LOTUS Database	35616633
Lepidozia vitrea	LOTUS Database	35616633
Melaleuca leucadendra	LOTUS Database	35616633
Origanum acutidens	LOTUS Database	35616633
Origanum adanense	LOTUS Database	35616633
Pelargonium endlicherianum	LOTUS Database	35616633
Syzygium nervosum	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
Branched unsaturated hydrocarbon
Polycyclic hydrocarbon
Cyclic olefin
Unsaturated aliphatic hydrocarbon
Unsaturated hydrocarbon
Olefin
Hydrocarbon
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

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

459467

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

527107

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-isopropyl-4,6b-dimethyl-1h,1ah,2h,3h,3ah,6h,6ah-cyclopropa[e]indene (NP0190527)

MOL for NP0190527 (2-isopropyl-4,6b-dimethyl-1h,1ah,2h,3h,3ah,6h,6ah-cyclopropa[e]indene)

3D MOL for NP0190527 (2-isopropyl-4,6b-dimethyl-1h,1ah,2h,3h,3ah,6h,6ah-cyclopropa[e]indene)

3D SDF for NP0190527 (2-isopropyl-4,6b-dimethyl-1h,1ah,2h,3h,3ah,6h,6ah-cyclopropa[e]indene)

3D-SDF for NP0190527 (2-isopropyl-4,6b-dimethyl-1h,1ah,2h,3h,3ah,6h,6ah-cyclopropa[e]indene)

PDB for NP0190527 (2-isopropyl-4,6b-dimethyl-1h,1ah,2h,3h,3ah,6h,6ah-cyclopropa[e]indene)

3D PDB for NP0190527 (2-isopropyl-4,6b-dimethyl-1h,1ah,2h,3h,3ah,6h,6ah-cyclopropa[e]indene)

SMILES for NP0190527 (2-isopropyl-4,6b-dimethyl-1h,1ah,2h,3h,3ah,6h,6ah-cyclopropa[e]indene)

INCHI for NP0190527 (2-isopropyl-4,6b-dimethyl-1h,1ah,2h,3h,3ah,6h,6ah-cyclopropa[e]indene)

Structure for NP0190527 (2-isopropyl-4,6b-dimethyl-1h,1ah,2h,3h,3ah,6h,6ah-cyclopropa[e]indene)

3D Structure for NP0190527 (2-isopropyl-4,6b-dimethyl-1h,1ah,2h,3h,3ah,6h,6ah-cyclopropa[e]indene)