NP-MRD: Showing NP-Card for (2r,4r)-heptadec-16-ene-1,2,4-triol (NP0305530)

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Record Information

Version

2.0

Created at

2022-09-10 21:26:24 UTC

Updated at

2022-09-10 21:26:24 UTC

NP-MRD ID

NP0305530

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,4r)-heptadec-16-ene-1,2,4-triol

Description

Avocadene 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. Thus, avocadene is considered to be a fatty alcohol. (2r,4r)-heptadec-16-ene-1,2,4-triol is found in Persea americana. (2r,4r)-heptadec-16-ene-1,2,4-triol was first documented in 2019 (PMID: 31647231). Based on a literature review a small amount of articles have been published on Avocadene (PMID: 35966924) (PMID: 35201599) (PMID: 34397122) (PMID: 32221368).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 54 53  0  0  0  0  0  0  0  0999 V2000
   -8.0125    1.6456   -1.6928 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6182    0.4273   -1.3618 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9259    0.1871   -0.0724 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5490   -0.3886   -0.4239 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8291   -0.6398    0.8706 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4503   -1.2164    0.6452 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5728   -0.3127   -0.1595 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1895   -0.8707   -0.3962 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4998   -1.0995    0.9212 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8777   -1.6545    0.6850 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7431   -0.7170   -0.1369 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9251    0.6140    0.5262 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7669    1.4988   -0.3398 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1149    0.9185   -0.6101 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.8095    1.6965   -1.5530 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8598    0.7070    0.6621 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1542    0.0037    0.6002 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.0740   -1.3501    0.3212 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1708    0.6859   -0.2579 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9238    0.4715   -1.5843 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8228    2.4562   -1.0125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5269    1.8471   -2.6423 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8138   -0.3784   -2.0523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4364   -0.5849    0.5367 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7289    1.1132    0.4844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7444   -1.3196   -0.9731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9732    0.3191   -1.0264 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3698   -1.3716    1.5119 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7040    0.2659    1.4788 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0562   -1.4586    1.6370 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5124   -2.1890    0.0909 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0088   -0.1479   -1.1738 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4236    0.6850    0.3285 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2280   -1.8080   -1.0107 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6561   -0.1308   -1.0276 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0617   -1.7809    1.5805 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4756   -0.1236    1.4491 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3782   -1.9614    1.6224 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7723   -2.5828    0.0781 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3034   -0.6391   -1.1314 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7417   -1.2263   -0.1776 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9230    1.1274    0.6672 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3071    0.4639    1.5474 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2469    1.6795   -1.3324 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8265    2.5255    0.0994 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0469   -0.0894   -1.1134 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6462    2.6484   -1.4576 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9418    1.7145    1.1635 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2085    0.1343    1.3989 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5721   -0.0160    1.6979 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1901   -1.5523   -0.6460 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1298    1.8075   -0.1048 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2005    0.3429    0.0460 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3348   -0.3763   -1.8619 H   0  0  0  0  0  0  0  0  0  0  0  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  2  3
 20 54  1  0
 19 52  1  0
 19 53  1  0
 17 50  1  1
 18 51  1  0
 16 48  1  0
 16 49  1  0
 14 46  1  6
 15 47  1  0
 13 44  1  0
 13 45  1  0
 12 42  1  0
 12 43  1  0
 11 40  1  0
 11 41  1  0
 10 38  1  0
 10 39  1  0
  9 36  1  0
  9 37  1  0
  8 34  1  0
  8 35  1  0
  7 32  1  0
  7 33  1  0
  6 30  1  0
  6 31  1  0
  5 28  1  0
  5 29  1  0
  4 26  1  0
  4 27  1  0
  3 24  1  0
  3 25  1  0
  2 23  1  0
  1 21  1  0
  1 22  1  0
M  END


  Mrv1652309102223262D          

 20 19  0  0  1  0            999 V2000
    7.2336    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9480    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6625    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3770    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0914    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8059    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.5204    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2349    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9493    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6638    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.3783    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0927    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.8072    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.5217    5.4138    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   16.5217    6.2388    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.2362    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.9506    5.4138    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   17.9506    6.2388    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.6651    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.3796    5.4138    0.0000 O   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  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  1  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  1  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0305530

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C17H34O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-16(19)14-17(20)15-18/h2,16-20H,1,3-15H2/t16-,17-/m1/s1

> <INCHI_KEY>
DFEHQWFIOMAGBM-IAGOWNOFSA-N

> <FORMULA>
C17H34O3

> <MOLECULAR_WEIGHT>
286.456

> <EXACT_MASS>
286.250794955

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
36.7359830988141

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R,4R)-heptadec-16-ene-1,2,4-triol

> <JCHEM_LOGP>
3.7463104646666663

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.172085921145062

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.168676430764624

> <JCHEM_PKA_STRONGEST_BASIC>
-2.7227167368545206

> <JCHEM_POLAR_SURFACE_AREA>
60.69

> <JCHEM_REFRACTIVITY>
84.9794

> <JCHEM_ROTATABLE_BOND_COUNT>
15

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2R,4R)-heptadec-16-ene-1,2,4-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0      13.503   9.336   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      14.836  10.106   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      16.170   9.336   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      17.504  10.106   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      18.837   9.336   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      20.171  10.106   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      21.505   9.336   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      22.838  10.106   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      24.172   9.336   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      25.506  10.106   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      26.839   9.336   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      28.173  10.106   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      29.507   9.336   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      30.840  10.106   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      30.840  11.646   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      32.174   9.336   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      33.508  10.106   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      33.508  11.646   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      34.842   9.336   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      36.175  10.106   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                                                            
MASTER        0    0    0    0    0    0    0    0   20    0   38    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₇H₃₄O₃

Average Mass

286.4560 Da

Monoisotopic Mass

286.25079 Da

IUPAC Name

(2R,4R)-heptadec-16-ene-1,2,4-triol

Traditional Name

(2R,4R)-heptadec-16-ene-1,2,4-triol

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C17H34O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-16(19)14-17(20)15-18/h2,16-20H,1,3-15H2/t16-,17-/m1/s1

InChI Key

DFEHQWFIOMAGBM-IAGOWNOFSA-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
Secondary alcohol
1,2-diol
Polyol
Organic oxygen compound
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
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	3.75	ChemAxon
pKa (Strongest Acidic)	14.17	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	60.69 Å²	ChemAxon
Rotatable Bond Count	15	ChemAxon
Refractivity	84.98 m³·mol⁻¹	ChemAxon
Polarizability	36.74 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

C00054700

Chemspider ID

10269464

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

21635755

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Zhao M, Liu X, Bu X, Li Y, Wang M, Zhang B, Sun W, Li C: Application of plasma metabolome for monitoring the effect of rivaroxaban in patients with nonvalvular atrial fibrillation. PeerJ. 2022 Aug 9;10:e13853. doi: 10.7717/peerj.13853. eCollection 2022. [PubMed:35966924 ]
Louis MRLM, Rani VP, Krishnan P, Reegan AD, Balakrishna K, Ignacimuthu S, Packiam SM, Maheswaran R, Shirota O: Mosquito Larvicidal Activity of Compounds from Unripe Fruit Peel of Avocado (Persea americana Mill.). Appl Biochem Biotechnol. 2022 Feb 24. doi: 10.1007/s12010-022-03831-w. [PubMed:35201599 ]
Tcheng M, Minden MD, Spagnuolo PA: Avocado-derived avocadyne is a potent inhibitor of fatty acid oxidation. J Food Biochem. 2022 Mar;46(3):e13895. doi: 10.1111/jfbc.13895. Epub 2021 Aug 16. [PubMed:34397122 ]
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LOTUS database [Link]

Showing NP-Card for (2r,4r)-heptadec-16-ene-1,2,4-triol (NP0305530)

MOL for NP0305530 ((2r,4r)-heptadec-16-ene-1,2,4-triol)

3D MOL for NP0305530 ((2r,4r)-heptadec-16-ene-1,2,4-triol)

3D SDF for NP0305530 ((2r,4r)-heptadec-16-ene-1,2,4-triol)

3D-SDF for NP0305530 ((2r,4r)-heptadec-16-ene-1,2,4-triol)

PDB for NP0305530 ((2r,4r)-heptadec-16-ene-1,2,4-triol)

3D PDB for NP0305530 ((2r,4r)-heptadec-16-ene-1,2,4-triol)

SMILES for NP0305530 ((2r,4r)-heptadec-16-ene-1,2,4-triol)

INCHI for NP0305530 ((2r,4r)-heptadec-16-ene-1,2,4-triol)

Structure for NP0305530 ((2r,4r)-heptadec-16-ene-1,2,4-triol)

3D Structure for NP0305530 ((2r,4r)-heptadec-16-ene-1,2,4-triol)