NP-MRD: Showing NP-Card for 3-[1-methyl-2-(3-methyl-4-oxobut-2-en-1-yl)-3-methylidene-6-(prop-1-en-2-yl)cyclohexyl]propanoic acid (NP0203708)

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Record Information

Version

2.0

Created at

2022-09-04 23:13:54 UTC

Updated at

2022-09-04 23:13:54 UTC

NP-MRD ID

NP0203708

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-[1-methyl-2-(3-methyl-4-oxobut-2-en-1-yl)-3-methylidene-6-(prop-1-en-2-yl)cyclohexyl]propanoic acid

Description

3-[1-Methyl-2-(3-methyl-4-oxobut-2-en-1-yl)-3-methylidene-6-(prop-1-en-2-yl)cyclohexyl]propanoic acid belongs to the class of organic compounds known as menthane monoterpenoids. These are monoterpenoids with a structure based on the o-, m-, or p-menthane backbone. P-menthane consists of the cyclohexane ring with a methyl group and a (2-methyl)-propyl group at the 1 and 4 ring position, respectively. The o- and m- menthanes are much rarer, and presumably arise by alkyl migration of p-menthanes. 3-[1-methyl-2-(3-methyl-4-oxobut-2-en-1-yl)-3-methylidene-6-(prop-1-en-2-yl)cyclohexyl]propanoic acid is found in Croton skutchii. 3-[1-Methyl-2-(3-methyl-4-oxobut-2-en-1-yl)-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

 50 50  0  0  0  0  0  0  0  0999 V2000
    1.1135   -0.2622   -2.5027 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7725   -0.5726   -1.2844 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4583   -2.0236   -0.9857 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8284   -2.1521   -0.2832 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3101   -1.0414    0.6019 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7724   -1.3105    0.7958 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8115   -0.5970    0.6017 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0323   -2.7172    1.3617 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9134    0.2981    0.1630 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5703    0.6626   -1.1342 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2068    1.3279    1.2221 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8296    2.7265    0.9741 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4159    3.4474   -0.1502 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7874    3.6373   -1.2117 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7120    3.9519   -0.0696 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6198    0.3178   -0.1029 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3804   -0.1569    1.0746 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8232   -0.2824    1.0503 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8021    0.1142    0.3166 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2335   -0.3253    0.7436 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7651    0.9791   -0.8205 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8874    1.2258   -1.4198 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1805   -0.9972   -3.3035 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3466    0.7487   -2.8006 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3118   -2.4130   -0.3883 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4288   -2.6111   -1.9241 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6705   -2.4575   -0.9700 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7398   -3.0712    0.3841 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8945   -1.2517    1.6454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8057   -1.0365    0.8532 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8600    0.3780    0.2057 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3519   -3.3907    0.5418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1479   -3.1173    1.8489 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8972   -2.6037    2.0605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3349    1.4471   -1.0703 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9908   -0.2597   -1.6435 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8214    1.0338   -1.8637 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2939    1.3123    1.4304 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7595    0.9842    2.2221 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2855    2.8707    0.8712 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0531    3.3786    1.8892 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3309    3.8584   -0.8563 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9194    1.3296   -0.3680 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9400   -1.2045    1.2994 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1459    0.4792    1.9965 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1839   -0.9291    1.9665 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6117   -0.9398   -0.0724 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8175    0.6044    0.8383 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1708   -0.8440    1.7099 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9437    1.4545   -1.2464 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  6  1  0
  6  7  2  3
  6  5  1  0
  5  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  2  3
  2 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 19 21  1  0
 21 22  2  0
 16  9  1  0
  9 10  1  6
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 15  1  0
 13 14  2  0
  9  5  1  0
  8 32  1  0
  8 33  1  0
  8 34  1  0
  7 30  1  0
  7 31  1  0
  5 29  1  1
  4 27  1  0
  4 28  1  0
  3 25  1  0
  3 26  1  0
  1 23  1  0
  1 24  1  0
 16 43  1  6
 17 44  1  0
 17 45  1  0
 18 46  1  0
 20 47  1  0
 20 48  1  0
 20 49  1  0
 21 50  1  0
 10 35  1  0
 10 36  1  0
 10 37  1  0
 11 38  1  0
 11 39  1  0
 12 40  1  0
 12 41  1  0
 15 42  1  0
M  END


  Mrv1533004251506122D          

 22 22  0  0  0  0            999 V2000
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3272    1.9659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1018    1.9659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6646    2.6656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0519    3.3940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6147    4.0936    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8764    3.4228    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
 11 10  1  4  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
  9 16  1  0  0  0  0
  4 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0203708

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C19H28O3/c1-13(2)16-9-7-15(4)17(8-6-14(3)12-20)19(16,5)11-10-18(21)22/h6,12,16-17H,1,4,7-11H2,2-3,5H3,(H,21,22)

> <INCHI_KEY>
HMGDRTLMZZMEPT-UHFFFAOYSA-N

> <FORMULA>
C19H28O3

> <MOLECULAR_WEIGHT>
304.43

> <EXACT_MASS>
304.203844762

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
50

> <JCHEM_AVERAGE_POLARIZABILITY>
34.72162169631919

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-[1-methyl-2-(3-methyl-4-oxobut-2-en-1-yl)-3-methylidene-6-(prop-1-en-2-yl)cyclohexyl]propanoic acid

> <ALOGPS_LOGP>
4.24

> <JCHEM_LOGP>
3.9689491563333332

> <ALOGPS_LOGS>
-4.76

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.926393560996859

> <JCHEM_PKA_STRONGEST_BASIC>
-4.200191826091132

> <JCHEM_POLAR_SURFACE_AREA>
54.370000000000005

> <JCHEM_REFRACTIVITY>
89.84089999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.28e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-[1-methyl-2-(3-methyl-4-oxobut-2-en-1-yl)-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       4.001   3.850   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -4.001   2.310   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -4.001   3.850   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -5.335   1.540   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -6.668   2.310   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.611   3.670   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.057   3.670   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.241   4.976   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.964   6.335   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       1.148   7.641   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       3.503   6.389   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   16                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   16                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14                                                            
CONECT   16    9    4   17   18                                             
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   44    0
END

View in JSmol

Synonyms

Value	Source
3-[1-Methyl-2-(3-methyl-4-oxobut-2-en-1-yl)-3-methylidene-6-(prop-1-en-2-yl)cyclohexyl]propanoate	Generator

Chemical Formula

C₁₉H₂₈O₃

Average Mass

304.4300 Da

Monoisotopic Mass

304.20384 Da

IUPAC Name

3-[1-methyl-2-(3-methyl-4-oxobut-2-en-1-yl)-3-methylidene-6-(prop-1-en-2-yl)cyclohexyl]propanoic acid

Traditional Name

3-[1-methyl-2-(3-methyl-4-oxobut-2-en-1-yl)-3-methylidene-6-(prop-1-en-2-yl)cyclohexyl]propanoic acid

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C19H28O3/c1-13(2)16-9-7-15(4)17(8-6-14(3)12-20)19(16,5)11-10-18(21)22/h6,12,16-17H,1,4,7-11H2,2-3,5H3,(H,21,22)

InChI Key

HMGDRTLMZZMEPT-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 menthane monoterpenoids. These are monoterpenoids with a structure based on the o-, m-, or p-menthane backbone. P-menthane consists of the cyclohexane ring with a methyl group and a (2-methyl)-propyl group at the 1 and 4 ring position, respectively. The o- and m- menthanes are much rarer, and presumably arise by alkyl migration of p-menthanes.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Monoterpenoids

Direct Parent

Menthane monoterpenoids

Alternative Parents

Substituents

P-menthane monoterpenoid
Monocyclic monoterpenoid
Carbocyclic fatty acid
Fatty acyl
Alpha,beta-unsaturated aldehyde
Enal
Carboxylic acid derivative
Carboxylic acid
Monocarboxylic acid or derivatives
Aldehyde
Carbonyl group
Organic oxide
Hydrocarbon derivative
Organic oxygen compound
Organooxygen compound
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic homomonocyclic 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	4.24	ALOGPS
logP	3.97	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	4.93	ChemAxon
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	54.37 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	89.84 m³·mol⁻¹	ChemAxon
Polarizability	34.72 Å³	ChemAxon
Number of Rings	1	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

Not Available

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-methyl-4-oxobut-2-en-1-yl)-3-methylidene-6-(prop-1-en-2-yl)cyclohexyl]propanoic acid (NP0203708)

MOL for NP0203708 (3-[1-methyl-2-(3-methyl-4-oxobut-2-en-1-yl)-3-methylidene-6-(prop-1-en-2-yl)cyclohexyl]propanoic acid)

3D MOL for NP0203708 (3-[1-methyl-2-(3-methyl-4-oxobut-2-en-1-yl)-3-methylidene-6-(prop-1-en-2-yl)cyclohexyl]propanoic acid)

3D SDF for NP0203708 (3-[1-methyl-2-(3-methyl-4-oxobut-2-en-1-yl)-3-methylidene-6-(prop-1-en-2-yl)cyclohexyl]propanoic acid)

3D-SDF for NP0203708 (3-[1-methyl-2-(3-methyl-4-oxobut-2-en-1-yl)-3-methylidene-6-(prop-1-en-2-yl)cyclohexyl]propanoic acid)

PDB for NP0203708 (3-[1-methyl-2-(3-methyl-4-oxobut-2-en-1-yl)-3-methylidene-6-(prop-1-en-2-yl)cyclohexyl]propanoic acid)

3D PDB for NP0203708 (3-[1-methyl-2-(3-methyl-4-oxobut-2-en-1-yl)-3-methylidene-6-(prop-1-en-2-yl)cyclohexyl]propanoic acid)

SMILES for NP0203708 (3-[1-methyl-2-(3-methyl-4-oxobut-2-en-1-yl)-3-methylidene-6-(prop-1-en-2-yl)cyclohexyl]propanoic acid)

INCHI for NP0203708 (3-[1-methyl-2-(3-methyl-4-oxobut-2-en-1-yl)-3-methylidene-6-(prop-1-en-2-yl)cyclohexyl]propanoic acid)

Structure for NP0203708 (3-[1-methyl-2-(3-methyl-4-oxobut-2-en-1-yl)-3-methylidene-6-(prop-1-en-2-yl)cyclohexyl]propanoic acid)

3D Structure for NP0203708 (3-[1-methyl-2-(3-methyl-4-oxobut-2-en-1-yl)-3-methylidene-6-(prop-1-en-2-yl)cyclohexyl]propanoic acid)