NP-MRD: Showing NP-Card for {4-[(3-aminopropyl)dimethylammonio]butyl}(3-{[(2z,6e,10e)-1-hydroxy-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraen-1-ylidene]amino}propyl)dimethylazanium (NP0200949)

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Record Information

Version

2.0

Created at

2022-09-04 19:54:06 UTC

Updated at

2022-09-04 19:54:07 UTC

NP-MRD ID

NP0200949

Secondary Accession Numbers

None

Natural Product Identification

Common Name

{4-[(3-aminopropyl)dimethylammonio]butyl}(3-{[(2z,6e,10e)-1-hydroxy-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraen-1-ylidene]amino}propyl)dimethylazanium

Description

(2Z,6E,10E)-N-[3-[[4-[(3-Aminopropyl)dimethylaminio]butyl]dimethylaminio]propyl]-3,7,11,15-tetramethyl-2,6,10,14-hexadecatetrenamide 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. Based on a literature review very few articles have been published on (2Z,6E,10E)-N-[3-[[4-[(3-Aminopropyl)dimethylaminio]butyl]dimethylaminio]propyl]-3,7,11,15-tetramethyl-2,6,10,14-hexadecatetrenamide.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042221542D          

 39 38  0  0  0  0            999 V2000
    9.9000    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4875    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    8.6625    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2500    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4250    2.8579    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
    7.4250    1.4289    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    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.5375    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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 38 39  1  0  0  0  0
M  CHG  2  26   1  33   1
M  END

     RDKit          3D

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M  CHG  2  26   1  33   1
M  END


  Mrv1652309042221542D          

 39 38  0  0  0  0            999 V2000
    9.9000    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4875    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9000    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6625    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2500    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4250    2.8579    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
    7.4250    1.4289    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    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9500    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9500    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7125    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4750    0.0000    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
    2.4750    1.4289    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
    1.2375   -0.7145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 N   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
   -1.6500   -1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4750   -1.4289    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
   -2.4750   -0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4750   -2.2539    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
   -3.7125   -2.1434    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
   -4.9500   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7750   -2.8579    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
   -5.7750   -2.0329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7750   -3.6829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6000   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0125   -3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8375   -3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2500   -4.2868    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  2  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  1  0  0  0  0
  7  9  2  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
 12 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  2  0  0  0  0
 22 23  1  4  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 26 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
 33 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
M  CHG  2  26   1  33   1
M  END
> <DATABASE_ID>
NP0200949

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCC\C(C)=C\CC\C(C)=C\CC\C(C)=C/C(O)=NCCC[N+](C)(C)CCCC[N+](C)(C)CCCN

> <INCHI_IDENTIFIER>
InChI=1S/C34H65N4O/c1-30(2)17-12-18-31(3)19-13-20-32(4)21-14-22-33(5)29-34(39)36-24-16-28-38(8,9)26-11-10-25-37(6,7)27-15-23-35/h17,19,21,29H,10-16,18,20,22-28,35H2,1-9H3/q+1/p+1/b31-19+,32-21+,33-29-

> <INCHI_KEY>
CENDAKYLVBQITO-NRGYNBSRSA-O

> <FORMULA>
C34H66N4O

> <MOLECULAR_WEIGHT>
546.928

> <EXACT_MASS>
546.522565601

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
105

> <JCHEM_AVERAGE_POLARIZABILITY>
70.55020525370027

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
2

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
{4-[(3-aminopropyl)dimethylazaniumyl]butyl}(3-{[(2Z,6E,10E)-1-hydroxy-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraen-1-ylidene]amino}propyl)dimethylazanium

> <JCHEM_LOGP>
-3.249626802211811

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
3

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.930178449582937

> <JCHEM_PKA_STRONGEST_BASIC>
10.015511353201164

> <JCHEM_POLAR_SURFACE_AREA>
58.61

> <JCHEM_REFRACTIVITY>
200.95129999999995

> <JCHEM_ROTATABLE_BOND_COUNT>
22

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
{4-[(3-aminopropyl)dimethylammonio]butyl}(3-{[(2Z,6E,10E)-1-hydroxy-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraen-1-ylidene]amino}propyl)dimethylazanium

> <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      18.480   8.002   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      17.710   6.668   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      18.480   5.335   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      16.170   6.668   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      15.400   5.335   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      13.860   5.335   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      13.090   4.001   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      13.860   2.667   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      11.550   4.001   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.780   2.667   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.240   2.667   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.470   1.334   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.240   0.000   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.930   1.334   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.160   0.000   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.620   0.000   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.850   1.334   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.620   2.667   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.310   1.334   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.540   0.000   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       2.310  -1.334   0.000  0.00  0.00           O+0
HETATM   22  N   UNK     0       0.000   0.000   0.000  0.00  0.00           N+0
HETATM   23  C   UNK     0      -0.770  -1.334   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -2.310  -1.334   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -3.080  -2.667   0.000  0.00  0.00           C+0
HETATM   26  N   UNK     0      -4.620  -2.667   0.000  0.00  0.00           N+1
HETATM   27  C   UNK     0      -4.620  -1.127   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -4.620  -4.207   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -6.160  -2.667   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -6.930  -4.001   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -8.470  -4.001   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -9.240  -5.335   0.000  0.00  0.00           C+0
HETATM   33  N   UNK     0     -10.780  -5.335   0.000  0.00  0.00           N+1
HETATM   34  C   UNK     0     -10.780  -3.795   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0     -10.780  -6.875   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0     -12.320  -5.335   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0     -13.090  -6.668   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0     -14.630  -6.668   0.000  0.00  0.00           C+0
HETATM   39  N   UNK     0     -15.400  -8.002   0.000  0.00  0.00           N+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   28   29                                             
CONECT   27   26                                                            
CONECT   28   26                                                            
CONECT   29   26   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34   35   36                                             
CONECT   34   33                                                            
CONECT   35   33                                                            
CONECT   36   33   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38                                                            
MASTER        0    0    0    0    0    0    0    0   39    0   76    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₄H₆₆N₄O

Average Mass

546.9280 Da

Monoisotopic Mass

546.52257 Da

IUPAC Name

{4-[(3-aminopropyl)dimethylazaniumyl]butyl}(3-{[(2Z,6E,10E)-1-hydroxy-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraen-1-ylidene]amino}propyl)dimethylazanium

Traditional Name

{4-[(3-aminopropyl)dimethylammonio]butyl}(3-{[(2Z,6E,10E)-1-hydroxy-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraen-1-ylidene]amino}propyl)dimethylazanium

CAS Registry Number

Not Available

SMILES

CC(C)=CCC\C(C)=C\CC\C(C)=C\CC\C(C)=C/C(O)=NCCC[N+](C)(C)CCCC[N+](C)(C)CCCN

InChI Identifier

InChI=1S/C34H65N4O/c1-30(2)17-12-18-31(3)19-13-20-32(4)21-14-22-33(5)29-34(39)36-24-16-28-38(8,9)26-11-10-25-37(6,7)27-15-23-35/h17,19,21,29H,10-16,18,20,22-28,35H2,1-9H3/q+1/p+1/b31-19+,32-21+,33-29-

InChI Key

CENDAKYLVBQITO-NRGYNBSRSA-O

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

Not Available

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
N-acyl-amine
Tetraalkylammonium salt
Quaternary ammonium salt
Amino acid or derivatives
Carboxamide group
Secondary carboxylic acid amide
Carboxylic acid derivative
Organic nitrogen compound
Amine
Primary amine
Organooxygen compound
Organonitrogen compound
Primary aliphatic amine
Hydrocarbon derivative
Organic oxide
Carbonyl group
Organic oxygen compound
Organic cation
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	-3.2	ChemAxon
pKa (Strongest Acidic)	6.93	ChemAxon
pKa (Strongest Basic)	10.02	ChemAxon
Physiological Charge	3	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	58.61 Å²	ChemAxon
Rotatable Bond Count	22	ChemAxon
Refractivity	200.95 m³·mol⁻¹	ChemAxon
Polarizability	70.55 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

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

8803438

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10628075

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for {4-[(3-aminopropyl)dimethylammonio]butyl}(3-{[(2z,6e,10e)-1-hydroxy-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraen-1-ylidene]amino}propyl)dimethylazanium (NP0200949)

MOL for NP0200949 ({4-[(3-aminopropyl)dimethylammonio]butyl}(3-{[(2z,6e,10e)-1-hydroxy-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraen-1-ylidene]amino}propyl)dimethylazanium)

3D MOL for NP0200949 ({4-[(3-aminopropyl)dimethylammonio]butyl}(3-{[(2z,6e,10e)-1-hydroxy-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraen-1-ylidene]amino}propyl)dimethylazanium)

3D SDF for NP0200949 ({4-[(3-aminopropyl)dimethylammonio]butyl}(3-{[(2z,6e,10e)-1-hydroxy-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraen-1-ylidene]amino}propyl)dimethylazanium)

3D-SDF for NP0200949 ({4-[(3-aminopropyl)dimethylammonio]butyl}(3-{[(2z,6e,10e)-1-hydroxy-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraen-1-ylidene]amino}propyl)dimethylazanium)

PDB for NP0200949 ({4-[(3-aminopropyl)dimethylammonio]butyl}(3-{[(2z,6e,10e)-1-hydroxy-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraen-1-ylidene]amino}propyl)dimethylazanium)

3D PDB for NP0200949 ({4-[(3-aminopropyl)dimethylammonio]butyl}(3-{[(2z,6e,10e)-1-hydroxy-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraen-1-ylidene]amino}propyl)dimethylazanium)

SMILES for NP0200949 ({4-[(3-aminopropyl)dimethylammonio]butyl}(3-{[(2z,6e,10e)-1-hydroxy-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraen-1-ylidene]amino}propyl)dimethylazanium)

INCHI for NP0200949 ({4-[(3-aminopropyl)dimethylammonio]butyl}(3-{[(2z,6e,10e)-1-hydroxy-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraen-1-ylidene]amino}propyl)dimethylazanium)

Structure for NP0200949 ({4-[(3-aminopropyl)dimethylammonio]butyl}(3-{[(2z,6e,10e)-1-hydroxy-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraen-1-ylidene]amino}propyl)dimethylazanium)

3D Structure for NP0200949 ({4-[(3-aminopropyl)dimethylammonio]butyl}(3-{[(2z,6e,10e)-1-hydroxy-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraen-1-ylidene]amino}propyl)dimethylazanium)