NP-MRD: Showing NP-Card for 3,3',4,4'-Tetradehydro-1,1',2,2'-tetrahydro-1,1'-dimethoxy-psi,psi-carotene (NP0065704)

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Record Information

Version

2.0

Created at

2022-04-28 09:54:14 UTC

Updated at

2022-04-28 09:54:14 UTC

NP-MRD ID

NP0065704

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3,3',4,4'-Tetradehydro-1,1',2,2'-tetrahydro-1,1'-dimethoxy-psi,psi-carotene

Description

3,3',4,4'-Tetradehydro-1,1',2,2'-tetrahydro-1,1'-dimethoxy-psi,psi-carotene is found in Rhodomicrobium vannielii, Rhodopseudomonas acidophila and Rhodospirillum rubrum.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282211542D          

 44 43  0  0  0  0            999 V2000
   12.3750   -1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9625   -2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   11.9625   -3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3750   -4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9625   -5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   11.9625   -6.4302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2480   -6.0177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.5500   -7.1447    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.9625   -7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6770   -6.8427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1375   -3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   12.3750   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
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 14 44  1  0  0  0  0
M  END

     RDKit          3D

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  1 47  1  0
M  END


  Mrv1652304282211542D          

 44 43  0  0  0  0            999 V2000
   12.3750   -1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9625   -2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3750   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9625   -3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3750   -4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9625   -5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3750   -5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9625   -6.4302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2480   -6.0177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.5500   -7.1447    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.9625   -7.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6770   -6.8427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1375   -3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9625   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1375   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7250   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4875    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6625    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2500    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4250    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0125    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1875    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7750    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9500    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7125    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000    1.4289    0.0000 C   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
    2.0625    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    0.0000    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
   -0.4125   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2375   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2375    0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0625   -0.7145    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
   -1.2375   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7750    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9000    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3750   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  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
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
  8 12  1  0  0  0  0
  4 13  1  0  0  0  0
  1 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 35 37  1  0  0  0  0
 37 38  1  0  0  0  0
 35 39  1  0  0  0  0
 31 40  1  0  0  0  0
 27 41  1  0  0  0  0
 23 42  1  0  0  0  0
 18 43  1  0  0  0  0
 14 44  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0065704

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(C)(C)C\C=C\C(\C)=C\C=C\C(\C)=C\C=C\C(\C)=C\C=C\C=C(/C)\C=C/C=C(\C)/C=C/C=C(\C)/C=C/CC(C)(C)OC

> <INCHI_IDENTIFIER>
InChI=1S/C42H60O2/c1-35(23-15-25-37(3)27-17-29-39(5)31-19-33-41(7,8)43-11)21-13-14-22-36(2)24-16-26-38(4)28-18-30-40(6)32-20-34-42(9,10)44-12/h13-32H,33-34H2,1-12H3/b14-13+,23-15-,24-16+,27-17+,28-18+,31-19+,32-20+,35-21+,36-22+,37-25+,38-26+,39-29+,40-30+

> <INCHI_KEY>
VAZQBTJCYODOSV-TWUHMXIZSA-N

> <FORMULA>
C42H60O2

> <MOLECULAR_WEIGHT>
596.94

> <EXACT_MASS>
596.459331172

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
104

> <JCHEM_AVERAGE_POLARIZABILITY>
76.74126376149943

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(4E,6E,8E,10E,12Z,14E,16E,18E,20E,22E,24E,26E,28E)-2,31-dimethoxy-2,6,10,14,19,23,27,31-octamethyldotriaconta-4,6,8,10,12,14,16,18,20,22,24,26,28-tridecaene

> <ALOGPS_LOGP>
9.24

> <JCHEM_LOGP>
10.363171106

> <ALOGPS_LOGS>
-6.27

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-3.8416154578584245

> <JCHEM_POLAR_SURFACE_AREA>
18.46

> <JCHEM_REFRACTIVITY>
211.51380000000012

> <JCHEM_ROTATABLE_BOND_COUNT>
18

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.21e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(4E,6E,8E,10E,12Z,14E,16E,18E,20E,22E,24E,26E,28E)-2,31-dimethoxy-2,6,10,14,19,23,27,31-octamethyldotriaconta-4,6,8,10,12,14,16,18,20,22,24,26,28-tridecaene

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      23.100  -2.667   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      22.330  -4.001   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      23.100  -5.335   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      22.330  -6.668   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      23.100  -8.002   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      22.330  -9.336   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      23.100 -10.669   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      22.330 -12.003   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      20.996 -11.233   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      21.560 -13.337   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      22.330 -14.670   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      23.664 -12.773   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      20.790  -6.668   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      22.330  -1.334   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      20.790  -1.334   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      20.020  -0.000   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      18.480  -0.000   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      17.710   1.334   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      16.170   1.334   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      15.400   2.667   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      13.860   2.667   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      13.090   4.001   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      11.550   4.001   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      10.780   5.335   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       9.240   5.335   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.470   4.001   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.930   4.001   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.160   2.667   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.620   2.667   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       3.850   1.334   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       2.310   1.334   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       1.540   0.000   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -0.770  -1.334   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -2.310  -1.334   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -2.310   0.206   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      -3.850  -1.334   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      -4.620  -2.667   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      -2.310  -2.874   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       1.540   2.667   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       6.160   5.335   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      10.780   2.667   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      18.480   2.667   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      23.100  -0.000   0.000  0.00  0.00           C+0
CONECT    1    2   14                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   13                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10   12                                             
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10                                                            
CONECT   12    8                                                            
CONECT   13    4                                                            
CONECT   14    1   15   44                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   43                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   42                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   41                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32   40                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36   37   39                                             
CONECT   36   35                                                            
CONECT   37   35   38                                                       
CONECT   38   37                                                            
CONECT   39   35                                                            
CONECT   40   31                                                            
CONECT   41   27                                                            
CONECT   42   23                                                            
CONECT   43   18                                                            
CONECT   44   14                                                            
MASTER        0    0    0    0    0    0    0    0   44    0   86    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₂H₆₀O₂

Average Mass

596.9400 Da

Monoisotopic Mass

596.45933 Da

IUPAC Name

(4E,6E,8E,10E,12Z,14E,16E,18E,20E,22E,24E,26E,28E)-2,31-dimethoxy-2,6,10,14,19,23,27,31-octamethyldotriaconta-4,6,8,10,12,14,16,18,20,22,24,26,28-tridecaene

Traditional Name

(4E,6E,8E,10E,12Z,14E,16E,18E,20E,22E,24E,26E,28E)-2,31-dimethoxy-2,6,10,14,19,23,27,31-octamethyldotriaconta-4,6,8,10,12,14,16,18,20,22,24,26,28-tridecaene

CAS Registry Number

Not Available

SMILES

COC(C)(C)C\C=C\C(\C)=C\C=C\C(\C)=C\C=C\C(\C)=C\C=C\C=C(/C)\C=C/C=C(\C)/C=C/C=C(\C)/C=C/CC(C)(C)OC

InChI Identifier

InChI=1S/C42H60O2/c1-35(23-15-25-37(3)27-17-29-39(5)31-19-33-41(7,8)43-11)21-13-14-22-36(2)24-16-26-38(4)28-18-30-40(6)32-20-34-42(9,10)44-12/h13-32H,33-34H2,1-12H3/b14-13+,23-15-,24-16+,27-17+,28-18+,31-19+,32-20+,35-21+,36-22+,37-25+,38-26+,39-29+,40-30+

InChI Key

VAZQBTJCYODOSV-TWUHMXIZSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Rhodomicrobium vannielii	Bacteria	KNApSAcK
Rhodopseudomonas acidophila	--	KNApSAcK
Rhodospirillum rubrum	Bacteria	KNApSAcK

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	9.24	ALOGPS
logP	10.36	ChemAxon
logS	-6.3	ALOGPS
pKa (Strongest Basic)	-3.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	18.46 Å²	ChemAxon
Rotatable Bond Count	18	ChemAxon
Refractivity	211.51 m³·mol⁻¹	ChemAxon
Polarizability	76.74 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

Not Available

References

General References

Not Available

Showing NP-Card for 3,3',4,4'-Tetradehydro-1,1',2,2'-tetrahydro-1,1'-dimethoxy-psi,psi-carotene (NP0065704)

MOL for NP0065704 (3,3',4,4'-Tetradehydro-1,1',2,2'-tetrahydro-1,1'-dimethoxy-psi,psi-carotene)

3D MOL for NP0065704 (3,3',4,4'-Tetradehydro-1,1',2,2'-tetrahydro-1,1'-dimethoxy-psi,psi-carotene)

3D SDF for NP0065704 (3,3',4,4'-Tetradehydro-1,1',2,2'-tetrahydro-1,1'-dimethoxy-psi,psi-carotene)

3D-SDF for NP0065704 (3,3',4,4'-Tetradehydro-1,1',2,2'-tetrahydro-1,1'-dimethoxy-psi,psi-carotene)

PDB for NP0065704 (3,3',4,4'-Tetradehydro-1,1',2,2'-tetrahydro-1,1'-dimethoxy-psi,psi-carotene)

3D PDB for NP0065704 (3,3',4,4'-Tetradehydro-1,1',2,2'-tetrahydro-1,1'-dimethoxy-psi,psi-carotene)

SMILES for NP0065704 (3,3',4,4'-Tetradehydro-1,1',2,2'-tetrahydro-1,1'-dimethoxy-psi,psi-carotene)

INCHI for NP0065704 (3,3',4,4'-Tetradehydro-1,1',2,2'-tetrahydro-1,1'-dimethoxy-psi,psi-carotene)

Structure for NP0065704 (3,3',4,4'-Tetradehydro-1,1',2,2'-tetrahydro-1,1'-dimethoxy-psi,psi-carotene)

3D Structure for NP0065704 (3,3',4,4'-Tetradehydro-1,1',2,2'-tetrahydro-1,1'-dimethoxy-psi,psi-carotene)