NP-MRD: Showing NP-Card for Stearaldehyde (NP0086965)

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Record Information

Version

2.0

Created at

2022-05-11 16:35:55 UTC

Updated at

2022-05-11 16:35:55 UTC

NP-MRD ID

NP0086965

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Stearaldehyde

Description

Stearaldehyde, also known as 1-octadecanal, belongs to the class of organic compounds known as fatty aldehydes. These are long chain aldehydes with a chain of at least 12 carbon atoms. Thus, stearaldehyde is considered to be a fatty aldehyde lipid molecule. Stearaldehyde is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral. Stearaldehyde is an oily tasting compound. Outside of the human body, Stearaldehyde has been detected, but not quantified in, evergreen blackberries. Stearaldehyde is found in Amphimedon compressa, Aplysina fistularis, Chrysanthemum indicum, Commiphora rostrata, Daphne odora, Mangifera indica, Mikania cordifolia, Pelargonium endlicherianum, Plumeria rubra, Stichodactyla helianthus and Tripneustes ventricosus. Stearaldehyde was first documented in 1967 (PMID: 14564703). This could make stearaldehyde a potential biomarker for the consumption of these foods.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 55 54  0  0  0  0  0  0  0  0999 V2000
   -7.3394    1.5163   -0.9633 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6863    0.0534   -0.9100 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8831   -0.5863    0.2000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4137   -0.3904   -0.1324 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5683   -1.0060    0.9359 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0808   -0.8381    0.6422 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7733    0.6141    0.5690 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2876    0.8119    0.2579 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4704    0.1886    1.3400 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9972    0.4238    1.0615 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3784   -0.1916   -0.2364 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8518    0.0052   -0.5563 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7071   -0.6175    0.4889 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1884   -0.4075    0.1452 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5844   -1.0086   -1.1455 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0105   -0.8938   -1.5485 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5668    0.4804   -1.6884 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6002    1.2723   -0.4440 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7299    2.4844   -0.5060 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5946    1.6425   -1.8010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8736    1.9185   -0.0616 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2410    2.1416   -1.1601 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3808   -0.4719   -1.8570 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7729   -0.1217   -0.7612 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1449   -1.6523    0.3451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1581   -0.0565    1.1334 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1474   -0.8731   -1.0933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2679    0.6840   -0.2596 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7284   -0.5468    1.9372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7719   -2.0879    1.0153 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7626   -1.4321   -0.2171 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5762   -1.2268    1.5761 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9840    1.0752    1.5509 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2967    1.1442   -0.2598 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1418    1.9127    0.1866 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1296    0.3272   -0.7314 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7668    0.5301    2.3470 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6472   -0.9145    1.3220 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0988    1.5450    0.9587 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6302    0.1023    1.9089 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1919   -1.2843   -0.2525 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7879    0.2259   -1.1033 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1148    1.0805   -0.6214 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9749   -0.4069   -1.5804 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5600   -0.0359    1.4333 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5055   -1.6849    0.6163 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7665   -0.7125    1.0109 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2560    0.7221    0.0446 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8945   -0.6708   -1.9763 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3712   -2.1210   -1.0724 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2081   -1.4253   -2.5279 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6440   -1.4432   -0.8139 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6504    0.3442   -1.9921 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1041    1.0493   -2.5330 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5159    0.8125    0.5186 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
 17 18  1  0
 18 19  2  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
  2 23  1  0
  2 24  1  0
  3 25  1  0
  3 26  1  0
  4 27  1  0
  4 28  1  0
  5 29  1  0
  5 30  1  0
  6 31  1  0
  6 32  1  0
  7 33  1  0
  7 34  1  0
  8 35  1  0
  8 36  1  0
  9 37  1  0
  9 38  1  0
 10 39  1  0
 10 40  1  0
 11 41  1  0
 11 42  1  0
 12 43  1  0
 12 44  1  0
 13 45  1  0
 13 46  1  0
 14 47  1  0
 14 48  1  0
 15 49  1  0
 15 50  1  0
 16 51  1  0
 16 52  1  0
 17 53  1  0
 17 54  1  0
 18 55  1  0
M  END

  Mrv0541 02231219312D          

 19 18  0  0  0  0            999 V2000
   22.8663  -12.4780    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   29.2967  -11.2404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.5822  -11.6529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.0112  -11.6529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.8677  -11.2404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.7257  -11.2404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.1532  -11.6529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.4401  -11.6529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.4388  -11.2404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.1547  -11.2404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.7242  -11.6529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.8691  -11.6529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.0098  -11.2404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   33.5836  -11.2404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.2953  -11.6529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   34.2981  -11.6529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.5808  -11.2404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   35.0126  -11.2404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.8663  -11.6529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1 19  2  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  3  5  1  0  0  0  0
  4  6  1  0  0  0  0
  5  7  1  0  0  0  0
  6  8  1  0  0  0  0
  7  9  1  0  0  0  0
  8 10  1  0  0  0  0
  9 11  1  0  0  0  0
 10 12  1  0  0  0  0
 11 13  1  0  0  0  0
 12 14  1  0  0  0  0
 13 15  1  0  0  0  0
 14 16  1  0  0  0  0
 15 17  1  0  0  0  0
 16 18  1  0  0  0  0
 17 19  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0086965

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCCCCCCCC=O

> <INCHI_IDENTIFIER>
InChI=1S/C18H36O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19/h18H,2-17H2,1H3

> <INCHI_KEY>
FWWQKRXKHIRPJY-UHFFFAOYSA-N

> <FORMULA>
C18H36O

> <MOLECULAR_WEIGHT>
268.4778

> <EXACT_MASS>
268.276615774

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_AVERAGE_POLARIZABILITY>
37.6525245745386

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
octadecanal

> <ALOGPS_LOGP>
8.39

> <JCHEM_LOGP>
6.987103855333334

> <ALOGPS_LOGS>
-7.08

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.55551402037299

> <JCHEM_PKA_STRONGEST_BASIC>
-6.944305999531455

> <JCHEM_POLAR_SURFACE_AREA>
17.07

> <JCHEM_REFRACTIVITY>
85.36019999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
16

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.22e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
octadecanal

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 23-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-FEB-12         0                                  
HETATM    1  O   UNK     0      42.684 -23.292   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      54.687 -20.982   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      53.353 -21.752   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      56.021 -21.752   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      52.020 -20.982   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      57.355 -20.982   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      50.686 -21.752   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      58.688 -21.752   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      49.352 -20.982   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      60.022 -20.982   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      48.019 -21.752   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      61.356 -21.752   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      46.685 -20.982   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      62.689 -20.982   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      45.351 -21.752   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      64.023 -21.752   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      44.017 -20.982   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      65.357 -20.982   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      42.684 -21.752   0.000  0.00  0.00           C+0
CONECT    1   19                                                            
CONECT    2    3    4                                                       
CONECT    3    2    5                                                       
CONECT    4    2    6                                                       
CONECT    5    3    7                                                       
CONECT    6    4    8                                                       
CONECT    7    5    9                                                       
CONECT    8    6   10                                                       
CONECT    9    7   11                                                       
CONECT   10    8   12                                                       
CONECT   11    9   13                                                       
CONECT   12   10   14                                                       
CONECT   13   11   15                                                       
CONECT   14   12   16                                                       
CONECT   15   13   17                                                       
CONECT   16   14   18                                                       
CONECT   17   15   19                                                       
CONECT   18   16                                                            
CONECT   19    1   17                                                       
MASTER        0    0    0    0    0    0    0    0   19    0   36    0
END

View in JSmol

Synonyms

Value	Source
1-Octadecanal	HMDB
N-Octadecanal	HMDB
Octadecanal	HMDB
Octadecyl aldehyde	HMDB
Stearyl aldehyde	HMDB

Chemical Formula

C₁₈H₃₆O

Average Mass

268.4778 Da

Monoisotopic Mass

268.27662 Da

IUPAC Name

octadecanal

Traditional Name

octadecanal

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCCCCCCCC=O

InChI Identifier

InChI=1S/C18H36O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19/h18H,2-17H2,1H3

InChI Key

FWWQKRXKHIRPJY-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Amphimedon compressa	LOTUS Database	35616633
Anas platyrhynchos	FooDB	FooDB
Anatidae	FooDB	FooDB
Anser anser	FooDB	FooDB
Aplysina fistularis	LOTUS Database	35616633
Bison bison	FooDB	FooDB
Bos taurus	FooDB	FooDB
Bos taurus X Bison bison	FooDB	FooDB
Bubalus bubalis	FooDB	FooDB
Capra aegagrus hircus	FooDB	FooDB
Cervidae	FooDB	FooDB
Cervus canadensis	FooDB	FooDB
Chrysanthemum indicum	LOTUS Database	35616633
Columba	FooDB	FooDB
Columbidae	FooDB	FooDB
Commiphora rostrata	LOTUS Database	35616633
Daphne odora	LOTUS Database	35616633
Dromaius novaehollandiae	FooDB	FooDB
Equus caballus	FooDB	FooDB
Gallus gallus	FooDB	FooDB
Lagopus muta	FooDB	FooDB
Leporidae	FooDB	FooDB
Lepus timidus	FooDB	FooDB
Mangifera indica	LOTUS Database	35616633
Melanitta fusca	FooDB	FooDB
Meleagris gallopavo	FooDB	FooDB
Mikania cordifolia	LOTUS Database	35616633
Numida meleagris	FooDB	FooDB
Odocoileus	FooDB	FooDB
Oryctolagus	FooDB	FooDB
Ovis aries	FooDB	FooDB
Pelargonium endlicherianum	LOTUS Database	35616633
Phasianidae	FooDB	FooDB
Phasianus colchicus	FooDB	FooDB
Plumeria rubra	LOTUS Database	35616633
Stichodactyla helianthus	LOTUS Database	35616633
Struthio camelus	FooDB	FooDB
Sus scrofa	FooDB	FooDB
Sus scrofa domestica	FooDB	FooDB
Tripneustes ventricosus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as fatty aldehydes. These are long chain aldehydes with a chain of at least 12 carbon atoms.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty aldehydes

Direct Parent

Fatty aldehydes

Alternative Parents

Substituents

Fatty aldehyde
Alpha-hydrogen aldehyde
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aldehyde
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

alpha-CH2-containing aldehyde (CHEBI:17034 )
Fatty aldehydes (C01838 )
Fatty aldehydes (LMFA06000098 )
a small molecule (CPD-55 )

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	8.39	ALOGPS
logP	6.99	ChemAxon
logS	-7.1	ALOGPS
pKa (Strongest Acidic)	15.56	ChemAxon
pKa (Strongest Basic)	-6.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	17.07 Å²	ChemAxon
Rotatable Bond Count	16	ChemAxon
Refractivity	85.36 m³·mol⁻¹	ChemAxon
Polarizability	37.65 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

HMDB0002384

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB022988

KNApSAcK ID

Not Available

Chemspider ID

12016

KEGG Compound ID

C01838

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

12533

PDB ID

Not Available

ChEBI ID

17034

Good Scents ID

Not Available

References

General References

Gilbertson JR, Ferrell WJ, Gelman RA: Isolation and analysis of free fatty aldehydes from rat, dog, and bovine heart muscle. J Lipid Res. 1967 Jan;8(1):38-45. [PubMed:14564703 ]

Showing NP-Card for Stearaldehyde (NP0086965)

MOL for NP0086965 (Stearaldehyde)

3D MOL for NP0086965 (Stearaldehyde)

3D SDF for NP0086965 (Stearaldehyde)

3D-SDF for NP0086965 (Stearaldehyde)

PDB for NP0086965 (Stearaldehyde)

3D PDB for NP0086965 (Stearaldehyde)

SMILES for NP0086965 (Stearaldehyde)

INCHI for NP0086965 (Stearaldehyde)

Structure for NP0086965 (Stearaldehyde)

3D Structure for NP0086965 (Stearaldehyde)