NP-MRD: Showing NP-Card for 2-aminooctadecane-1,3-diol (NP0270577)

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Record Information

Version

2.0

Created at

2022-09-08 16:34:20 UTC

Updated at

2022-09-08 16:34:20 UTC

NP-MRD ID

NP0270577

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-aminooctadecane-1,3-diol

Description

2-Aminooctadecane-1,3-diol belongs to the class of organic compounds known as 1,2-aminoalcohols. These are organic compounds containing an alkyl chain with an amine group bound to the C1 atom and an alcohol group bound to the C2 atom. 2-Aminooctadecane-1,3-diol is a very strong basic compound (based on its pKa). 2-aminooctadecane-1,3-diol is found in Caulerpa racemosa. An aminodiol that is octadecane bearing two hydroxy substituents at positions 1 and 3 as well as an amino substituent at position 2.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 60 59  0  0  0  0  0  0  0  0999 V2000
    8.6582    2.0403    1.1015 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5348    1.2582    0.4380 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9192    0.3071    1.4387 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8249   -0.4542    0.7698 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7048    0.4010    0.2227 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7110   -0.6008   -0.4045 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5384    0.0978   -0.9930 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5959   -0.8965   -1.6105 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1102   -1.8520   -0.5771 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1394   -2.8750   -1.1303 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0846   -2.2548   -1.7201 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8176   -1.4592   -0.6743 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0708   -0.8250   -1.2803 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7728   -0.0275   -0.1624 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9876    0.5788   -0.7776 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8301    1.4232    0.1056 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.2045    2.5247    0.6595 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6097    0.6334    1.1257 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.7755    0.1841    2.1773 N   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7748    1.4792    1.6001 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2913    2.5930    2.2533 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.0962    1.4043    1.8766 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.4328    2.2195    0.3336 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2214    2.9847    1.5024 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9214    0.6772   -0.4185 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7529    1.9496    0.0393 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6231    0.7995    2.3666 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7312   -0.4469    1.6618 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1785   -1.0833   -0.0700 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3218   -1.1811    1.4731 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0074    1.1191   -0.5404 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2376    0.9221    1.0786 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3156   -1.1644   -1.1430 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3824   -1.2261    0.4614 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8237    0.9034   -1.7037 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9927    0.6096   -0.1657 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7760   -0.3126   -2.0802 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1725   -1.4167   -2.4285 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9971   -2.4699   -0.2441 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7437   -1.3330    0.3074 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1832   -3.5081   -0.2749 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6486   -3.5511   -1.8418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7590   -3.0789   -2.0322 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8799   -1.6648   -2.6365 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1879   -0.7000   -0.1981 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1437   -2.1963    0.1115 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7819   -1.5823   -1.6110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7377   -0.1121   -2.0362 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0097   -0.8247    0.5933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0883    0.6944    0.2986 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6151   -0.2600   -1.2056 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6812    1.1464   -1.7062 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6445    1.8833   -0.5691 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7568    3.3446    0.6559 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0720   -0.2702    0.6284 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8499    0.6255    2.2590 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6853   -0.8405    2.2605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2857    1.8431    0.6642 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5206    0.9042    2.1668 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0117    2.9170    2.8555 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  2 25  1  0
  2 26  1  0
  3 27  1  0
  3 28  1  0
  4 29  1  0
  4 30  1  0
  5 31  1  0
  5 32  1  0
  6 33  1  0
  6 34  1  0
  7 35  1  0
  7 36  1  0
  8 37  1  0
  8 38  1  0
  9 39  1  0
  9 40  1  0
 10 41  1  0
 10 42  1  0
 11 43  1  0
 11 44  1  0
 12 45  1  0
 12 46  1  0
 13 47  1  0
 13 48  1  0
 14 49  1  0
 14 50  1  0
 15 51  1  0
 15 52  1  0
 16 53  1  6
 17 54  1  0
 18 55  1  6
 19 56  1  0
 19 57  1  0
 20 58  1  0
 20 59  1  0
 21 60  1  0
M  END


  Mrv1533004161513452D          

 21 20  0  0  0  0            999 V2000
    9.1855    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9000    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6145    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3289    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0434    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.7579    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4724    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.1868    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.9013    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6158    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.3302    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.0447    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.7592    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.4737    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.1881    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.9026    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.9026    4.8908    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   20.6171    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.6171    6.9533    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   21.3315    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.0460    6.1283    0.0000 O   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
  3  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  1  0  0  0  0
  8  9  1  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
 13 14  1  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
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0270577

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCCCCCC(O)C(N)CO

> <INCHI_IDENTIFIER>
InChI=1S/C18H39NO2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-18(21)17(19)16-20/h17-18,20-21H,2-16,19H2,1H3

> <INCHI_KEY>
OTKJDMGTUTTYMP-UHFFFAOYSA-N

> <FORMULA>
C18H39NO2

> <MOLECULAR_WEIGHT>
301.515

> <EXACT_MASS>
301.2980795

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
40.4711287664863

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-aminooctadecane-1,3-diol

> <ALOGPS_LOGP>
5.20

> <JCHEM_LOGP>
4.772594245333334

> <ALOGPS_LOGS>
-4.82

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
15.262227395125855

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.419876288941946

> <JCHEM_PKA_STRONGEST_BASIC>
9.287692505029561

> <JCHEM_POLAR_SURFACE_AREA>
66.48

> <JCHEM_REFRACTIVITY>
90.92939999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
16

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.53e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-aminooctadecane-1,3-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0      17.146  11.439   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      18.480  10.669   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      19.814  11.439   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      21.147  10.669   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      22.481  11.439   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      23.815  10.669   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      25.148  11.439   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      26.482  10.669   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      27.816  11.439   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      29.149  10.669   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      30.483  11.439   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      31.817  10.669   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      33.150  11.439   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      34.484  10.669   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      35.818  11.439   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      37.152  10.669   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      37.152   9.129   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      38.485  11.439   0.000  0.00  0.00           C+0
HETATM   19  N   UNK     0      38.485  12.979   0.000  0.00  0.00           N+0
HETATM   20  C   UNK     0      39.819  10.669   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      41.153  11.439   0.000  0.00  0.00           O+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   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   40    0
END

View in JSmol

Synonyms

Value	Source
2-Amino-1,3-octadecanediol	ChEBI
Dihydrosphingosine	MeSH
erythro-D-Sphinganine	MeSH
Safingol	MeSH
Safingol hydrochloride	MeSH
Safingol, ((r,s)-(+-))-isomer	MeSH
Safingol, (R-(r,r))-isomer	MeSH
Safingol, (S-(r,s))-isomer	MeSH
Saginfol	MeSH
Sphinganine	MeSH
threo-Dihydrosphingosine	MeSH

Chemical Formula

C₁₈H₃₉NO₂

Average Mass

301.5150 Da

Monoisotopic Mass

301.29808 Da

IUPAC Name

2-aminooctadecane-1,3-diol

Traditional Name

2-aminooctadecane-1,3-diol

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCCCCCC(O)C(N)CO

InChI Identifier

InChI=1S/C18H39NO2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-18(21)17(19)16-20/h17-18,20-21H,2-16,19H2,1H3

InChI Key

OTKJDMGTUTTYMP-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
Caulerpa racemosa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 1,2-aminoalcohols. These are organic compounds containing an alkyl chain with an amine group bound to the C1 atom and an alcohol group bound to the C2 atom.

Kingdom

Organic compounds

Super Class

Organic nitrogen compounds

Class

Organonitrogen compounds

Sub Class

Amines

Direct Parent

1,2-aminoalcohols

Alternative Parents

Substituents

Secondary alcohol
1,2-aminoalcohol
Organic oxygen compound
Organopnictogen compound
Hydrocarbon derivative
Primary amine
Primary alcohol
Organooxygen compound
Primary aliphatic amine
Alcohol
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

sphingoid (CHEBI:46968 )
aminodiol (CHEBI:46968 )
a sphinganine C18 (CPD-13613 )

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	5.2	ALOGPS
logP	4.77	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	14.42	ChemAxon
pKa (Strongest Basic)	9.29	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	66.48 Å²	ChemAxon
Rotatable Bond Count	16	ChemAxon
Refractivity	90.93 m³·mol⁻¹	ChemAxon
Polarizability	40.47 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

Not Available

PDB ID

Not Available

ChEBI ID

46968

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-aminooctadecane-1,3-diol (NP0270577)

MOL for NP0270577 (2-aminooctadecane-1,3-diol)

3D MOL for NP0270577 (2-aminooctadecane-1,3-diol)

3D SDF for NP0270577 (2-aminooctadecane-1,3-diol)

3D-SDF for NP0270577 (2-aminooctadecane-1,3-diol)

PDB for NP0270577 (2-aminooctadecane-1,3-diol)

3D PDB for NP0270577 (2-aminooctadecane-1,3-diol)

SMILES for NP0270577 (2-aminooctadecane-1,3-diol)

INCHI for NP0270577 (2-aminooctadecane-1,3-diol)

Structure for NP0270577 (2-aminooctadecane-1,3-diol)

3D Structure for NP0270577 (2-aminooctadecane-1,3-diol)