NP-MRD: Showing NP-Card for (2e,6s,8e)-10-hydroxy-2-[(4z)-6-hydroxy-4-methylhex-4-en-1-ylidene]-6,10-dimethyl-7-oxoundec-8-enal (NP0198835)

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Record Information

Version

2.0

Created at

2022-09-04 17:21:13 UTC

Updated at

2022-09-04 17:21:13 UTC

NP-MRD ID

NP0198835

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2e,6s,8e)-10-hydroxy-2-[(4z)-6-hydroxy-4-methylhex-4-en-1-ylidene]-6,10-dimethyl-7-oxoundec-8-enal

Description

(2E,6S,8E)-10-hydroxy-2-[(4Z)-6-hydroxy-4-methylhex-4-en-1-ylidene]-6,10-dimethyl-7-oxoundec-8-enal belongs to the class of organic compounds known as acyclic diterpenoids. These are diterpenoids (compounds made of four consecutive isoprene units) that do not contain a cycle. (2e,6s,8e)-10-hydroxy-2-[(4z)-6-hydroxy-4-methylhex-4-en-1-ylidene]-6,10-dimethyl-7-oxoundec-8-enal is found in Milleria quinqueflora. Based on a literature review very few articles have been published on (2E,6S,8E)-10-hydroxy-2-[(4Z)-6-hydroxy-4-methylhex-4-en-1-ylidene]-6,10-dimethyl-7-oxoundec-8-enal.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 56 55  0  0  0  0  0  0  0  0999 V2000
   -3.5051   -1.2411   -0.3015 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3972   -0.1136    0.1023 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8879    0.6156   -0.8650 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8030    1.7380   -0.6917 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1431    2.8739   -1.2325 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7176    0.1175    1.4998 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5181    0.4804    2.3538 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5395   -0.5835    2.3200 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2679   -0.4297    1.9849 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4206   -1.6158    2.0531 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8724   -2.7607    2.3980 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7166    0.8560    1.6124 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2086    1.0010    0.2134 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8593    0.0525   -0.1929 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3267    0.3545   -1.6437 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1097    0.1902   -2.5504 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3187   -0.6671   -2.0518 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9997   -1.5818   -2.8914 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6826   -0.7398   -1.5657 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2344    0.1106   -0.7210 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6509   -0.0165   -0.2514 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6207   -0.6929    1.0981 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2156    1.3804   -0.1237 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3831   -0.7620   -1.1824 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8830   -1.6865   -1.2795 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5225   -2.0932    0.3978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4996   -0.8729   -0.5647 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6016    0.3848   -1.9178 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0941    2.0259    0.3047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6692    1.5881   -1.3849 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9098    2.7193   -2.1866 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5343    0.8219    1.7133 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1355   -0.8755    1.9002 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9075    0.5308    3.4112 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2024    1.4756    2.0008 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8734   -1.5808    2.5999 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6048   -1.5807    1.8232 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2788    1.7530    1.9557 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2458    0.9505    2.2509 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0478    0.9891   -0.5228 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2691    2.0354    0.1638 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3550   -0.9624   -0.3405 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7405   -0.0167    0.4186 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7564    1.3530   -1.7186 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4576    1.1367   -2.4749 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4452   -0.0198   -3.5849 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4536   -0.6809   -2.1310 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3637   -1.5450   -1.8888 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6833    0.9455   -0.3463 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3594   -1.7694    0.9541 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8305   -0.2256    1.7081 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6154   -0.5881    1.5937 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8420    1.8026    0.8371 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3345    1.3612   -0.1028 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8372    2.0381   -0.9313 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3844   -0.2603   -2.0283 H   0  0  0  0  0  0  0  0  0  0  0  0
 16 15  1  0
 15 14  1  0
 14 13  1  0
 13 12  1  0
 12  9  1  0
  9 10  1  0
 10 11  2  0
  9  8  2  0
  8  7  1  0
  7  6  1  0
  6  2  1  0
  2  1  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
 15 17  1  0
 17 18  2  0
 17 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  1  0
 21 23  1  0
 21 24  1  0
 16 45  1  0
 16 46  1  0
 16 47  1  0
 15 44  1  1
 14 42  1  0
 14 43  1  0
 13 40  1  0
 13 41  1  0
 12 38  1  0
 12 39  1  0
 10 37  1  0
  8 36  1  0
  7 34  1  0
  7 35  1  0
  6 32  1  0
  6 33  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  3 28  1  0
  4 29  1  0
  4 30  1  0
  5 31  1  0
 19 48  1  0
 20 49  1  0
 22 50  1  0
 22 51  1  0
 22 52  1  0
 23 53  1  0
 23 54  1  0
 23 55  1  0
 24 56  1  0
M  END


  Mrv1652309042219212D          

 24 23  0  0  1  0            999 V2000
    3.9039    3.9039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1895    4.3164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1895    5.1414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4750    5.5539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4750    6.3789    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4750    3.9039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4750    3.0789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7605    2.6664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7605    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0461    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0461    0.6039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4750    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1895    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9039    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6184    1.8414    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6184    2.6664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3329    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3329    0.6039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0474    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7618    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4763    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1908    2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8888    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0638    2.5559    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
  3  4  1  0  0  0  0
  4  5  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  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
  9 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  6  0  0  0
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 21 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0198835

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H](CCC\C(C=O)=C/CC\C(C)=C/CO)C(=O)\C=C\C(C)(C)O

> <INCHI_IDENTIFIER>
InChI=1S/C20H32O4/c1-16(12-14-21)7-5-9-18(15-22)10-6-8-17(2)19(23)11-13-20(3,4)24/h9,11-13,15,17,21,24H,5-8,10,14H2,1-4H3/b13-11+,16-12-,18-9+/t17-/m0/s1

> <INCHI_KEY>
IJNXCNLFOIXWSL-AJKKVAPQSA-N

> <FORMULA>
C20H32O4

> <MOLECULAR_WEIGHT>
336.472

> <EXACT_MASS>
336.23005951

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
39.02706047716279

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2E,6S,8E)-10-hydroxy-2-[(4Z)-6-hydroxy-4-methylhex-4-en-1-ylidene]-6,10-dimethyl-7-oxoundec-8-enal

> <JCHEM_LOGP>
3.425412876666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
16.34925987514578

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.96676459247675

> <JCHEM_PKA_STRONGEST_BASIC>
-2.217047406799513

> <JCHEM_POLAR_SURFACE_AREA>
74.6

> <JCHEM_REFRACTIVITY>
101.32179999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2E,6S,8E)-10-hydroxy-2-[(4Z)-6-hydroxy-4-methylhex-4-en-1-ylidene]-6,10-dimethyl-7-oxoundec-8-enal

> <JCHEM_VEBER_RULE>
0

$$$$

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       7.287   7.287   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.954   8.057   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.954   9.597   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.620  10.367   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       4.620  11.907   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       4.620   7.287   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.620   5.747   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.286   4.977   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.286   3.437   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.953   2.667   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       1.953   1.127   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       4.620   2.667   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.954   3.437   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.287   2.667   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.621   3.437   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.621   4.977   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.955   2.667   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       9.955   1.127   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      11.288   3.437   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      12.622   2.667   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      13.956   3.437   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      15.289   4.207   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      14.726   2.104   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      13.186   4.771   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    6                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4                                                            
CONECT    6    2    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   12                                                  
CONECT   10    9   11                                                       
CONECT   11   10                                                            
CONECT   12    9   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23   24                                             
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   21                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   46    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₃₂O₄

Average Mass

336.4720 Da

Monoisotopic Mass

336.23006 Da

IUPAC Name

(2E,6S,8E)-10-hydroxy-2-[(4Z)-6-hydroxy-4-methylhex-4-en-1-ylidene]-6,10-dimethyl-7-oxoundec-8-enal

Traditional Name

(2E,6S,8E)-10-hydroxy-2-[(4Z)-6-hydroxy-4-methylhex-4-en-1-ylidene]-6,10-dimethyl-7-oxoundec-8-enal

CAS Registry Number

Not Available

SMILES

C[C@@H](CCC\C(C=O)=C/CC\C(C)=C/CO)C(=O)\C=C\C(C)(C)O

InChI Identifier

InChI=1S/C20H32O4/c1-16(12-14-21)7-5-9-18(15-22)10-6-8-17(2)19(23)11-13-20(3,4)24/h9,11-13,15,17,21,24H,5-8,10,14H2,1-4H3/b13-11+,16-12-,18-9+/t17-/m0/s1

InChI Key

IJNXCNLFOIXWSL-AJKKVAPQSA-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
Milleria quinqueflora	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as acyclic diterpenoids. These are diterpenoids (compounds made of four consecutive isoprene units) that do not contain a cycle.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Acyclic diterpenoids

Alternative Parents

Substituents

Acyclic diterpenoid
Long chain fatty alcohol
Fatty alcohol
Medium-chain aldehyde
Fatty acyl
Acryloyl-group
Alpha,beta-unsaturated aldehyde
Enal
Enone
Alpha,beta-unsaturated ketone
Tertiary alcohol
Ketone
Organic oxide
Aldehyde
Alcohol
Carbonyl group
Hydrocarbon derivative
Organooxygen compound
Primary alcohol
Organic oxygen compound
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic 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	3.43	ChemAxon
pKa (Strongest Acidic)	14.97	ChemAxon
pKa (Strongest Basic)	-2.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	74.6 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	101.32 m³·mol⁻¹	ChemAxon
Polarizability	39.03 Å³	ChemAxon
Number of Rings	0	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

163194263

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2e,6s,8e)-10-hydroxy-2-[(4z)-6-hydroxy-4-methylhex-4-en-1-ylidene]-6,10-dimethyl-7-oxoundec-8-enal (NP0198835)

MOL for NP0198835 ((2e,6s,8e)-10-hydroxy-2-[(4z)-6-hydroxy-4-methylhex-4-en-1-ylidene]-6,10-dimethyl-7-oxoundec-8-enal)

3D MOL for NP0198835 ((2e,6s,8e)-10-hydroxy-2-[(4z)-6-hydroxy-4-methylhex-4-en-1-ylidene]-6,10-dimethyl-7-oxoundec-8-enal)

3D SDF for NP0198835 ((2e,6s,8e)-10-hydroxy-2-[(4z)-6-hydroxy-4-methylhex-4-en-1-ylidene]-6,10-dimethyl-7-oxoundec-8-enal)

3D-SDF for NP0198835 ((2e,6s,8e)-10-hydroxy-2-[(4z)-6-hydroxy-4-methylhex-4-en-1-ylidene]-6,10-dimethyl-7-oxoundec-8-enal)

PDB for NP0198835 ((2e,6s,8e)-10-hydroxy-2-[(4z)-6-hydroxy-4-methylhex-4-en-1-ylidene]-6,10-dimethyl-7-oxoundec-8-enal)

3D PDB for NP0198835 ((2e,6s,8e)-10-hydroxy-2-[(4z)-6-hydroxy-4-methylhex-4-en-1-ylidene]-6,10-dimethyl-7-oxoundec-8-enal)

SMILES for NP0198835 ((2e,6s,8e)-10-hydroxy-2-[(4z)-6-hydroxy-4-methylhex-4-en-1-ylidene]-6,10-dimethyl-7-oxoundec-8-enal)

INCHI for NP0198835 ((2e,6s,8e)-10-hydroxy-2-[(4z)-6-hydroxy-4-methylhex-4-en-1-ylidene]-6,10-dimethyl-7-oxoundec-8-enal)

Structure for NP0198835 ((2e,6s,8e)-10-hydroxy-2-[(4z)-6-hydroxy-4-methylhex-4-en-1-ylidene]-6,10-dimethyl-7-oxoundec-8-enal)

3D Structure for NP0198835 ((2e,6s,8e)-10-hydroxy-2-[(4z)-6-hydroxy-4-methylhex-4-en-1-ylidene]-6,10-dimethyl-7-oxoundec-8-enal)