NP-MRD: Showing NP-Card for (2s,4s)-2,4-dihydroxyheptadec-16-yn-1-yl acetate (NP0286597)

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Record Information

Version

2.0

Created at

2022-09-09 15:14:15 UTC

Updated at

2022-09-09 15:14:15 UTC

NP-MRD ID

NP0286597

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s,4s)-2,4-dihydroxyheptadec-16-yn-1-yl acetate

Description

16-Heptadecyne-1,2,4-triol, 1-acetate, (2S,4S)- belongs to the class of organic compounds known as long-chain fatty alcohols. These are fatty alcohols that have an aliphatic tail of 13 to 21 carbon atoms. (2s,4s)-2,4-dihydroxyheptadec-16-yn-1-yl acetate is found in Persea americana. Based on a literature review very few articles have been published on 16-Heptadecyne-1,2,4-triol, 1-acetate, (2S,4S)-.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 57 56  0  0  0  0  0  0  0  0999 V2000
    5.6948    3.0772    3.5194 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0532    2.3331    2.6196 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4774    1.4481    1.5576 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4426    1.4691    0.4180 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1572    1.0052    1.0248 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0720    0.9953    0.0098 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3530    0.0930   -1.1475 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5449   -1.3254   -0.7298 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3332   -1.8425   -0.0432 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1103   -1.8035   -0.9161 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0943   -2.3594   -0.1452 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3445   -2.3505   -0.9617 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7138   -0.9681   -1.3982 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9840   -0.9752   -2.2215 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.2309    0.2561   -2.7552 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1569   -1.5106   -1.4998 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6641   -0.7276   -0.3368 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.8310   -1.3656    0.1875 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1150    0.6749   -0.6611 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6233    1.3420    0.4791 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8645    1.5898    1.5831 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4049    2.2968    2.7999 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6782    1.2325    1.6207 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3804    3.7070    4.3033 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5018    0.3976    1.9314 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4507    1.7727    1.1445 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3446    2.4772   -0.0159 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7435    0.7006   -0.3535 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3392   -0.0001    1.4584 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8930    1.6703    1.8837 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9190    2.0282   -0.4053 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1173    0.7546    0.5233 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2562    0.5023   -1.6856 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5420    0.1281   -1.9060 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4134   -1.4695   -0.0518 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7491   -1.9621   -1.6165 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5307   -2.9062    0.2660 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0978   -1.3144    0.9065 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2281   -2.3783   -1.8484 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8800   -0.7337   -1.1735 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1997   -1.8621    0.8324 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1792   -3.4296    0.0791 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2566   -2.9954   -1.8455 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1541   -2.7794   -0.3373 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9138   -0.6226   -2.1183 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7259   -0.2304   -0.5844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7800   -1.6698   -3.0810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8328    0.2102   -3.5521 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0073   -1.5289   -2.2503 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0472   -2.6072   -1.2443 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9209   -0.7325    0.4691 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5940   -2.2823    0.5052 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9105    0.5889   -1.4335 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2795    1.3069   -1.0649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2625    2.9389    2.5137 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5961    2.9821    3.1294 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6182    1.6005    3.6186 H   0  0  0  0  0  0  0  0  0  0  0  0
 22 21  1  0
 21 23  2  0
 21 20  1  0
 20 19  1  0
 19 17  1  0
 17 18  1  0
 17 16  1  0
 16 14  1  0
 14 15  1  0
 14 13  1  0
 13 12  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  3  0
 22 55  1  0
 22 56  1  0
 22 57  1  0
 19 53  1  0
 19 54  1  0
 17 51  1  1
 18 52  1  0
 16 49  1  0
 16 50  1  0
 14 47  1  6
 15 48  1  0
 13 45  1  0
 13 46  1  0
 12 43  1  0
 12 44  1  0
 11 41  1  0
 11 42  1  0
 10 39  1  0
 10 40  1  0
  9 37  1  0
  9 38  1  0
  8 35  1  0
  8 36  1  0
  7 33  1  0
  7 34  1  0
  6 31  1  0
  6 32  1  0
  5 29  1  0
  5 30  1  0
  4 27  1  0
  4 28  1  0
  3 25  1  0
  3 26  1  0
  1 24  1  0
M  END


  Mrv1652309092217142D          

 23 22  0  0  1  0            999 V2000
    8.4711    6.5408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    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  2  0  0  0  0  0  0  0  0  0
   17.7592    6.9533    0.0000 O   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  2  0  0  0  0  0  0  0  0  0
   19.1881    6.9533    0.0000 O   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
   20.6171    6.1283    0.0000 O   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 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.3315    4.8908    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  3  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  6  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0286597

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC[C@@H](O)C[C@@H](O)CCCCCCCCCCCC#C

> <INCHI_IDENTIFIER>
InChI=1S/C19H34O4/c1-3-4-5-6-7-8-9-10-11-12-13-14-18(21)15-19(22)16-23-17(2)20/h1,18-19,21-22H,4-16H2,2H3/t18-,19-/m0/s1

> <INCHI_KEY>
JAKAZHIACKJNNB-OALUTQOASA-N

> <FORMULA>
C19H34O4

> <MOLECULAR_WEIGHT>
326.477

> <EXACT_MASS>
326.245709575

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
57

> <JCHEM_AVERAGE_POLARIZABILITY>
40.347241090583054

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S,4S)-2,4-dihydroxyheptadec-16-yn-1-yl acetate

> <JCHEM_LOGP>
3.6842690976666654

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.336743501337324

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.29766549997698

> <JCHEM_PKA_STRONGEST_BASIC>
-2.722735692963231

> <JCHEM_POLAR_SURFACE_AREA>
66.75999999999999

> <JCHEM_REFRACTIVITY>
92.54839999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
16

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2S,4S)-2,4-dihydroxyheptadec-16-yn-1-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0      15.813  12.209   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      17.146  11.439   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      18.480  10.669   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      19.814  11.439   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      21.147  10.669   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      22.481  11.439   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      23.815  10.669   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      25.148  11.439   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      26.482  10.669   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      27.816  11.439   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      29.149  10.669   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      30.483  11.439   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      31.817  10.669   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      33.150  11.439   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      33.150  12.979   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      34.484  10.669   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      35.818  11.439   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      35.818  12.979   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      37.152  10.669   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      38.485  11.439   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      39.819  10.669   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      41.153  11.439   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      39.819   9.129   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   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   44    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₃₄O₄

Average Mass

326.4770 Da

Monoisotopic Mass

326.24571 Da

IUPAC Name

(2S,4S)-2,4-dihydroxyheptadec-16-yn-1-yl acetate

Traditional Name

(2S,4S)-2,4-dihydroxyheptadec-16-yn-1-yl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)OC[C@@H](O)C[C@@H](O)CCCCCCCCCCCC#C

InChI Identifier

InChI=1S/C19H34O4/c1-3-4-5-6-7-8-9-10-11-12-13-14-18(21)15-19(22)16-23-17(2)20/h1,18-19,21-22H,4-16H2,2H3/t18-,19-/m0/s1

InChI Key

JAKAZHIACKJNNB-OALUTQOASA-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
Persea americana	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as long-chain fatty alcohols. These are fatty alcohols that have an aliphatic tail of 13 to 21 carbon atoms.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty alcohols

Direct Parent

Long-chain fatty alcohols

Alternative Parents

Substituents

Long chain fatty alcohol
Fatty alcohol ester
Secondary alcohol
Carboxylic acid ester
Acetylide
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
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	3.68	ChemAxon
pKa (Strongest Acidic)	14.3	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	66.76 Å²	ChemAxon
Rotatable Bond Count	16	ChemAxon
Refractivity	92.55 m³·mol⁻¹	ChemAxon
Polarizability	40.35 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

156180

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

179422

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2s,4s)-2,4-dihydroxyheptadec-16-yn-1-yl acetate (NP0286597)

MOL for NP0286597 ((2s,4s)-2,4-dihydroxyheptadec-16-yn-1-yl acetate)

3D MOL for NP0286597 ((2s,4s)-2,4-dihydroxyheptadec-16-yn-1-yl acetate)

3D SDF for NP0286597 ((2s,4s)-2,4-dihydroxyheptadec-16-yn-1-yl acetate)

3D-SDF for NP0286597 ((2s,4s)-2,4-dihydroxyheptadec-16-yn-1-yl acetate)

PDB for NP0286597 ((2s,4s)-2,4-dihydroxyheptadec-16-yn-1-yl acetate)

3D PDB for NP0286597 ((2s,4s)-2,4-dihydroxyheptadec-16-yn-1-yl acetate)

SMILES for NP0286597 ((2s,4s)-2,4-dihydroxyheptadec-16-yn-1-yl acetate)

INCHI for NP0286597 ((2s,4s)-2,4-dihydroxyheptadec-16-yn-1-yl acetate)

Structure for NP0286597 ((2s,4s)-2,4-dihydroxyheptadec-16-yn-1-yl acetate)

3D Structure for NP0286597 ((2s,4s)-2,4-dihydroxyheptadec-16-yn-1-yl acetate)