NP-MRD: Showing NP-Card for (2s)-2-amino-6-[(1-hydroxydodecylidene)amino]hexanoic acid (NP0170916)

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Record Information

Version

2.0

Created at

2022-09-03 07:12:53 UTC

Updated at

2022-09-03 07:12:53 UTC

NP-MRD ID

NP0170916

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s)-2-amino-6-[(1-hydroxydodecylidene)amino]hexanoic acid

Description

N6-lauroyl lysine belongs to the class of organic compounds known as l-alpha-amino acids. These are alpha amino acids which have the L-configuration of the alpha-carbon atom. Thus, N6-lauroyl lysine is considered to be a fatty amide lipid molecule. N6-lauroyl lysine is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 59 58  0  0  0  0  0  0  0  0999 V2000
   -6.9838    2.0662   -0.1797 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4593    1.2153   -1.3295 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5199   -0.2459   -0.9403 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1716   -0.7787   -0.5173 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1495   -0.6626   -1.6231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8057   -1.1841   -1.2302 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2140   -0.4578   -0.0461 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8485   -1.0882    0.2474 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3081   -0.3282    1.4313 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0247   -0.8506    1.8622 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0212   -0.7192    0.7429 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3206   -1.2217    1.2343 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4152   -2.5288    1.6610 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3415   -0.4614    1.2649 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4179    0.9072    0.8636 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6150    1.0303   -0.6327 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8721    0.3594   -1.1044 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0655    0.9752   -0.4466 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2886    0.2427   -0.9854 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.2656   -1.1585   -0.7036 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.4745    0.8623   -0.3761 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2745    0.1643    0.2710 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.7239    2.2289   -0.5093 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8870    2.2595   -0.3072 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0588    1.5310    0.8057 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5623    3.0037   -0.1279 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5056    1.5382   -1.5554 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8705    1.4169   -2.2226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1828   -0.3096   -0.0541 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9009   -0.8753   -1.7439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8724   -0.2294    0.3938 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3271   -1.8369   -0.2204 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5120   -1.2677   -2.4795 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1306    0.3876   -1.9673 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8385   -2.2523   -1.0062 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1319   -1.0587   -2.1079 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0283    0.6032   -0.2342 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8440   -0.6669    0.8377 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1770   -0.9328   -0.6290 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9058   -2.1674    0.4355 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9891   -0.4217    2.3169 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2895    0.7654    1.2135 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1170   -1.9292    2.1450 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3524   -0.2899    2.7732 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0140    0.3141    0.4029 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6449   -1.3770   -0.1001 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9721   -3.2401    1.1936 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2345    1.4160    1.4131 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4874    1.4641    1.1832 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7772    0.5708   -1.1954 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6016    2.1193   -0.8788 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7794   -0.7208   -0.8403 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9076    0.4879   -2.2131 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1419    2.0239   -0.7861 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0351    0.9689    0.6416 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2561    0.3767   -2.0902 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5269   -1.3576   -0.0003 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1700   -1.4720   -0.2865 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5697    2.7922    0.3217 H   0  0  0  0  0  0  0  0  0  0  0  0
 19 20  1  0
 19 18  1  0
 18 17  1  0
 17 16  1  0
 16 15  1  0
 15 14  1  0
 14 12  2  0
 12 13  1  0
 12 11  1  0
 11 10  1  0
 10  9  1  0
  9  8  1  0
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  1  0
 19 21  1  0
 21 23  1  0
 21 22  2  0
 19 56  1  6
 20 57  1  0
 20 58  1  0
 18 54  1  0
 18 55  1  0
 17 52  1  0
 17 53  1  0
 16 50  1  0
 16 51  1  0
 15 48  1  0
 15 49  1  0
 13 47  1  0
 11 45  1  0
 11 46  1  0
 10 43  1  0
 10 44  1  0
  9 41  1  0
  9 42  1  0
  8 39  1  0
  8 40  1  0
  7 37  1  0
  7 38  1  0
  6 35  1  0
  6 36  1  0
  5 33  1  0
  5 34  1  0
  4 31  1  0
  4 32  1  0
  3 29  1  0
  3 30  1  0
  2 27  1  0
  2 28  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
 23 59  1  0
M  END


  Mrv1572004251602322D          

 24 23  0  0  1  0            999 V2000
    3.5211    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2355    3.2704    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
    5.6645    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3789    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0934    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8079    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5224    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2368    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9513    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2381    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5237    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.9526    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6658    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8092    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6671    3.2704    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.3802    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.3815    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6671    4.0954    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   12.0947    2.8579    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   11.3802    4.0954    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.0960    3.2704    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.3815    2.0329    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.6671    2.4454    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0  0  0  0
  3  2  1  0  0  0  0
  4  3  1  0  0  0  0
  5  4  1  0  0  0  0
  6  5  1  0  0  0  0
  7  6  1  0  0  0  0
  8  7  1  0  0  0  0
  9  8  1  0  0  0  0
 10  9  1  0  0  0  0
 12 11  1  0  0  0  0
 13 11  1  0  0  0  0
 14 10  1  0  0  0  0
 15 12  1  0  0  0  0
 16 13  1  0  0  0  0
 17 14  1  0  0  0  0
 18 16  1  0  0  0  0
 16 19  1  1  0  0  0
 20 15  1  4  0  0  0
 20 17  2  0  0  0  0
 21 17  1  0  0  0  0
 22 18  2  0  0  0  0
 23 18  1  0  0  0  0
 16 24  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0170916

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@](N)(CCCCN=C(O)CCCCCCCCCCC)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C18H36N2O3/c1-2-3-4-5-6-7-8-9-10-14-17(21)20-15-12-11-13-16(19)18(22)23/h16H,2-15,19H2,1H3,(H,20,21)(H,22,23)/t16-/m0/s1

> <INCHI_KEY>
GYDYJUYZBRGMCC-INIZCTEOSA-N

> <FORMULA>
C18H36N2O3

> <MOLECULAR_WEIGHT>
328.497

> <EXACT_MASS>
328.272593027

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
40.7391285903624

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S)-2-amino-6-[(1-hydroxydodecylidene)amino]hexanoic acid

> <ALOGPS_LOGP>
1.30

> <JCHEM_LOGP>
1.6628330216607654

> <ALOGPS_LOGS>
-4.73

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
4.725868515589936

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.1156358047540746

> <JCHEM_PKA_STRONGEST_BASIC>
9.527547676654239

> <JCHEM_POLAR_SURFACE_AREA>
95.91000000000001

> <JCHEM_REFRACTIVITY>
93.81089999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
16

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.11e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-2-amino-6-[(1-hydroxydodecylidene)amino]hexanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-16   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-16         0                                  
HETATM    1  C   UNK     0       6.573   5.335   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.906   6.105   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.240   5.335   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.574   6.105   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      11.907   5.335   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      13.241   6.105   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      14.575   5.335   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      15.908   6.105   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      17.242   5.335   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      18.576   6.105   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      26.578   6.105   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      25.244   5.335   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      27.912   5.335   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      19.909   5.335   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      23.910   6.105   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      29.245   6.105   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      21.243   6.105   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      30.579   5.335   0.000  0.00  0.00           C+0
HETATM   19  N   UNK     0      29.245   7.645   0.000  0.00  0.00           N+0
HETATM   20  N   UNK     0      22.577   5.335   0.000  0.00  0.00           N+0
HETATM   21  O   UNK     0      21.243   7.645   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      31.913   6.105   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      30.579   3.795   0.000  0.00  0.00           O+0
HETATM   24  H   UNK     0      29.245   4.565   0.000  0.00  0.00           H+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   14                                                       
CONECT   11   12   13                                                       
CONECT   12   11   15                                                       
CONECT   13   11   16                                                       
CONECT   14   10   17                                                       
CONECT   15   12   20                                                       
CONECT   16   13   18   19   24                                             
CONECT   17   14   20   21                                                  
CONECT   18   16   22   23                                                  
CONECT   19   16                                                            
CONECT   20   15   17                                                       
CONECT   21   17                                                            
CONECT   22   18                                                            
CONECT   23   18                                                            
CONECT   24   16                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   46    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₃₆N₂O₃

Average Mass

328.4970 Da

Monoisotopic Mass

328.27259 Da

IUPAC Name

(2S)-2-amino-6-[(1-hydroxydodecylidene)amino]hexanoic acid

Traditional Name

(2S)-2-amino-6-[(1-hydroxydodecylidene)amino]hexanoic acid

CAS Registry Number

Not Available

SMILES

[H][C@](N)(CCCCN=C(O)CCCCCCCCCCC)C(O)=O

InChI Identifier

InChI=1S/C18H36N2O3/c1-2-3-4-5-6-7-8-9-10-14-17(21)20-15-12-11-13-16(19)18(22)23/h16H,2-15,19H2,1H3,(H,20,21)(H,22,23)/t16-/m0/s1

InChI Key

GYDYJUYZBRGMCC-INIZCTEOSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as l-alpha-amino acids. These are alpha amino acids which have the L-configuration of the alpha-carbon atom.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

L-alpha-amino acids

Alternative Parents

Substituents

L-alpha-amino acid
Medium-chain fatty acid
Amino fatty acid
Fatty amide
Fatty acyl
Fatty acid
N-acyl-amine
Carboxamide group
Amino acid
Secondary carboxylic acid amide
Carboxylic acid
Monocarboxylic acid or derivatives
Amine
Organooxygen compound
Organonitrogen compound
Primary amine
Hydrocarbon derivative
Primary aliphatic amine
Organic oxide
Organopnictogen compound
Organic oxygen compound
Carbonyl group
Organic nitrogen 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	1.3	ALOGPS
logP	1.66	ChemAxon
logS	-4.7	ALOGPS
pKa (Strongest Acidic)	2.12	ChemAxon
pKa (Strongest Basic)	9.53	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	95.91 Å²	ChemAxon
Rotatable Bond Count	16	ChemAxon
Refractivity	93.81 m³·mol⁻¹	ChemAxon
Polarizability	40.74 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

104151

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2s)-2-amino-6-[(1-hydroxydodecylidene)amino]hexanoic acid (NP0170916)

MOL for NP0170916 ((2s)-2-amino-6-[(1-hydroxydodecylidene)amino]hexanoic acid)

3D MOL for NP0170916 ((2s)-2-amino-6-[(1-hydroxydodecylidene)amino]hexanoic acid)

3D SDF for NP0170916 ((2s)-2-amino-6-[(1-hydroxydodecylidene)amino]hexanoic acid)

3D-SDF for NP0170916 ((2s)-2-amino-6-[(1-hydroxydodecylidene)amino]hexanoic acid)

PDB for NP0170916 ((2s)-2-amino-6-[(1-hydroxydodecylidene)amino]hexanoic acid)

3D PDB for NP0170916 ((2s)-2-amino-6-[(1-hydroxydodecylidene)amino]hexanoic acid)

SMILES for NP0170916 ((2s)-2-amino-6-[(1-hydroxydodecylidene)amino]hexanoic acid)

INCHI for NP0170916 ((2s)-2-amino-6-[(1-hydroxydodecylidene)amino]hexanoic acid)

Structure for NP0170916 ((2s)-2-amino-6-[(1-hydroxydodecylidene)amino]hexanoic acid)

3D Structure for NP0170916 ((2s)-2-amino-6-[(1-hydroxydodecylidene)amino]hexanoic acid)