NP-MRD: Showing NP-Card for 3-{1-methyl-2-[(3-methylfuran-2-yl)methyl]-3-methylidene-6-(prop-1-en-2-yl)cyclohexyl}propanoic acid (NP0302641)

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Record Information

Version

2.0

Created at

2022-09-10 16:21:45 UTC

Updated at

2022-09-10 16:21:45 UTC

NP-MRD ID

NP0302641

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-{1-methyl-2-[(3-methylfuran-2-yl)methyl]-3-methylidene-6-(prop-1-en-2-yl)cyclohexyl}propanoic acid

Description

3-{1-Methyl-2-[(3-methylfuran-2-yl)methyl]-3-methylidene-6-(prop-1-en-2-yl)cyclohexyl}propanoic acid belongs to the class of organic compounds known as aromatic monoterpenoids. These are monoterpenoids containing at least one aromatic ring. 3-{1-methyl-2-[(3-methylfuran-2-yl)methyl]-3-methylidene-6-(prop-1-en-2-yl)cyclohexyl}propanoic acid is found in Croton skutchii. 3-{1-Methyl-2-[(3-methylfuran-2-yl)methyl]-3-methylidene-6-(prop-1-en-2-yl)cyclohexyl}propanoic acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 51 52  0  0  0  0  0  0  0  0999 V2000
   -2.1404   -3.3060   -0.8455 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3437   -2.0944   -0.3273 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7551   -1.6232   -0.2951 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1848   -1.3321    0.1673 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2175   -1.1248    1.6598 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1504   -0.6691    2.1137 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7375    0.3352    1.1971 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4880    1.3051    1.7433 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5316    0.3476   -0.2588 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4598   -0.4578   -1.0856 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8949   -0.0377   -0.9284 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5318    0.7946   -1.7452 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7602    0.9894   -1.3754 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9924    0.2553   -0.2433 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8006   -0.3993    0.0385 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5443   -1.3497    1.1520 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9392   -0.0185   -0.5005 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2331   -0.0347   -1.9790 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7645    1.0768    0.1193 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6027    2.4276   -0.5005 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5133    3.4013    0.2170 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2482    3.0573    1.1608 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5242    4.7253   -0.1984 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1243   -3.7354   -0.9096 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9218   -3.9401   -1.2293 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9294   -0.8982   -1.0997 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4686   -2.4972   -0.3796 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0387   -1.1467    0.6613 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2666   -1.9635   -0.0096 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3655   -2.1174    2.1904 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0339   -0.4996    2.0274 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8066   -1.5321    2.1837 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0070   -0.2086    3.1356 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6510    1.3421    2.8037 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9295    2.0533    1.1011 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6281    1.4075   -0.6488 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2433   -0.3814   -2.1713 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4522   -1.5482   -0.8621 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5061    1.6254   -1.8639 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8763    0.1438    0.3707 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7064   -2.0078    0.8707 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4396   -1.9932    1.3109 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3239   -0.8345    2.0831 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4876    0.6649   -2.4595 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2230    0.4191   -2.1744 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0799   -1.0112   -2.4480 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4085    1.2109    1.1918 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8598    0.8493    0.1272 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6141    2.8747   -0.4625 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9583    2.4029   -1.5468 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2008    5.0528   -1.0786 H   0  0  0  0  0  0  0  0  0  0  0  0
  3  2  1  0
  2  1  2  3
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  2  3
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 15  2  0
 15 16  1  0
 15 14  1  0
 14 13  2  0
 13 12  1  0
  9 17  1  0
 17 18  1  6
 17 19  1  0
 19 20  1  0
 20 21  1  0
 21 23  1  0
 21 22  2  0
 17  4  1  0
 12 11  1  0
  3 26  1  0
  3 27  1  0
  3 28  1  0
  1 24  1  0
  1 25  1  0
  4 29  1  1
  5 30  1  0
  5 31  1  0
  6 32  1  0
  6 33  1  0
  8 34  1  0
  8 35  1  0
  9 36  1  6
 10 37  1  0
 10 38  1  0
 16 41  1  0
 16 42  1  0
 16 43  1  0
 14 40  1  0
 13 39  1  0
 18 44  1  0
 18 45  1  0
 18 46  1  0
 19 47  1  0
 19 48  1  0
 20 49  1  0
 20 50  1  0
 23 51  1  0
M  END


  Mrv1533004251506412D          

 23 24  0  0  0  0            999 V2000
    2.8579    7.1786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    6.7661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    7.1786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    5.9411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    5.5286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    4.7036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    4.2911    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    3.4661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    4.7036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    4.2911    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    3.4661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8109    2.9812    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5559    2.1965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7309    2.1965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4760    2.9812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6914    3.2361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    5.5286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0334    5.5574    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4207    6.2282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5962    6.1994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1590    6.8991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3345    6.8703    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5463    7.6275    0.0000 O   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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 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
 11 15  2  0  0  0  0
 15 16  1  0  0  0  0
  9 17  1  0  0  0  0
  4 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0302641

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=C)C1CCC(=C)C(CC2=C(C)C=CO2)C1(C)CCC(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C20H28O3/c1-13(2)16-7-6-14(3)17(12-18-15(4)9-11-23-18)20(16,5)10-8-19(21)22/h9,11,16-17H,1,3,6-8,10,12H2,2,4-5H3,(H,21,22)

> <INCHI_KEY>
MISLDQYVNNBESZ-UHFFFAOYSA-N

> <FORMULA>
C20H28O3

> <MOLECULAR_WEIGHT>
316.441

> <EXACT_MASS>
316.203844762

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
51

> <JCHEM_AVERAGE_POLARIZABILITY>
36.12238840973728

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-{1-methyl-2-[(3-methylfuran-2-yl)methyl]-3-methylidene-6-(prop-1-en-2-yl)cyclohexyl}propanoic acid

> <ALOGPS_LOGP>
4.74

> <JCHEM_LOGP>
4.716860410666667

> <ALOGPS_LOGS>
-4.28

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.200568034822938

> <JCHEM_PKA_STRONGEST_BASIC>
-2.7262452872076697

> <JCHEM_POLAR_SURFACE_AREA>
50.44

> <JCHEM_REFRACTIVITY>
92.1296

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.68e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-{1-methyl-2-[(3-methylfuran-2-yl)methyl]-3-methylidene-6-(prop-1-en-2-yl)cyclohexyl}propanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0       5.335  13.400   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.668  12.630   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.002  13.400   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.668  11.090   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.002  10.320   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.002   8.780   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.668   8.010   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.668   6.470   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.335   8.780   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.001   8.010   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.001   6.470   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       5.247   5.565   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       4.771   4.100   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.231   4.100   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.755   5.565   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.291   6.041   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.335  10.320   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.796  10.374   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.519  11.626   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.980  11.572   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.164  12.878   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       0.624  12.825   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       2.886  14.238   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   17                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   17                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   15                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   11   16                                                  
CONECT   16   15                                                            
CONECT   17    9    4   18   19                                             
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   48    0
END

View in JSmol

Synonyms

Value	Source
3-{1-methyl-2-[(3-methylfuran-2-yl)methyl]-3-methylidene-6-(prop-1-en-2-yl)cyclohexyl}propanoate	Generator

Chemical Formula

C₂₀H₂₈O₃

Average Mass

316.4410 Da

Monoisotopic Mass

316.20384 Da

IUPAC Name

3-{1-methyl-2-[(3-methylfuran-2-yl)methyl]-3-methylidene-6-(prop-1-en-2-yl)cyclohexyl}propanoic acid

Traditional Name

3-{1-methyl-2-[(3-methylfuran-2-yl)methyl]-3-methylidene-6-(prop-1-en-2-yl)cyclohexyl}propanoic acid

CAS Registry Number

Not Available

SMILES

CC(=C)C1CCC(=C)C(CC2=C(C)C=CO2)C1(C)CCC(O)=O

InChI Identifier

InChI=1S/C20H28O3/c1-13(2)16-7-6-14(3)17(12-18-15(4)9-11-23-18)20(16,5)10-8-19(21)22/h9,11,16-17H,1,3,6-8,10,12H2,2,4-5H3,(H,21,22)

InChI Key

MISLDQYVNNBESZ-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
Croton skutchii	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as aromatic monoterpenoids. These are monoterpenoids containing at least one aromatic ring.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Monoterpenoids

Direct Parent

Aromatic monoterpenoids

Alternative Parents

Substituents

Aromatic monoterpenoid
Monocyclic monoterpenoid
P-menthane monoterpenoid
Carbocyclic fatty acid
Fatty acyl
Furan
Heteroaromatic compound
Carboxylic acid derivative
Carboxylic acid
Monocarboxylic acid or derivatives
Oxacycle
Organoheterocyclic compound
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
Carbonyl group
Organooxygen compound
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic 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	4.74	ALOGPS
logP	4.72	ChemAxon
logS	-4.3	ALOGPS
pKa (Strongest Acidic)	5.2	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	50.44 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	92.13 m³·mol⁻¹	ChemAxon
Polarizability	36.12 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

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

102204498

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-{1-methyl-2-[(3-methylfuran-2-yl)methyl]-3-methylidene-6-(prop-1-en-2-yl)cyclohexyl}propanoic acid (NP0302641)

MOL for NP0302641 (3-{1-methyl-2-[(3-methylfuran-2-yl)methyl]-3-methylidene-6-(prop-1-en-2-yl)cyclohexyl}propanoic acid)

3D MOL for NP0302641 (3-{1-methyl-2-[(3-methylfuran-2-yl)methyl]-3-methylidene-6-(prop-1-en-2-yl)cyclohexyl}propanoic acid)

3D SDF for NP0302641 (3-{1-methyl-2-[(3-methylfuran-2-yl)methyl]-3-methylidene-6-(prop-1-en-2-yl)cyclohexyl}propanoic acid)

3D-SDF for NP0302641 (3-{1-methyl-2-[(3-methylfuran-2-yl)methyl]-3-methylidene-6-(prop-1-en-2-yl)cyclohexyl}propanoic acid)

PDB for NP0302641 (3-{1-methyl-2-[(3-methylfuran-2-yl)methyl]-3-methylidene-6-(prop-1-en-2-yl)cyclohexyl}propanoic acid)

3D PDB for NP0302641 (3-{1-methyl-2-[(3-methylfuran-2-yl)methyl]-3-methylidene-6-(prop-1-en-2-yl)cyclohexyl}propanoic acid)

SMILES for NP0302641 (3-{1-methyl-2-[(3-methylfuran-2-yl)methyl]-3-methylidene-6-(prop-1-en-2-yl)cyclohexyl}propanoic acid)

INCHI for NP0302641 (3-{1-methyl-2-[(3-methylfuran-2-yl)methyl]-3-methylidene-6-(prop-1-en-2-yl)cyclohexyl}propanoic acid)

Structure for NP0302641 (3-{1-methyl-2-[(3-methylfuran-2-yl)methyl]-3-methylidene-6-(prop-1-en-2-yl)cyclohexyl}propanoic acid)

3D Structure for NP0302641 (3-{1-methyl-2-[(3-methylfuran-2-yl)methyl]-3-methylidene-6-(prop-1-en-2-yl)cyclohexyl}propanoic acid)