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Showing chemical card for Palmitic Acid (CFc000322583)
Record Information
Version
1.0
Creation Date
2022-09-06 19:45:53 UTC
Update Date
2022-09-14 04:52:45 UTC
Chemfont ID
CFc000322583
Molecule Identification
Common Name
Palmitic Acid
Definition
A common saturated fatty acid found in fats and waxes including olive oil, palm oil, and body lipids.
Structure
MOL
SDF
PDB
SMILES
InChI
×
MOL for CFc000322583 (Palmitic Acid)
Not Available
×
3D MOL for CFc000322583 (Palmitic Acid)
Not Available
×
3D SDF for CFc000322583 (Palmitic Acid)
Not Available
×
3D-SDF for CFc000322583 (Palmitic Acid)
Not Available
×
PDB for CFc000322583 (Palmitic Acid)
Not Available
×
3D PDB for CFc000322583 (Palmitic Acid)
Not Available
×
SMILES for CFc000322583 (Palmitic Acid)
Not Available
×
INCHI for CFc000322583 (Palmitic Acid)
Not Available
×
Structure for CFc000322583 (Palmitic Acid)
×
3D Structure for CFc000322583 (Palmitic Acid)
Not Available
Synonyms
Not Available
Chemical Formula
Average Molecular Weight
Monoisotopic Molecular Weight
IUPAC Name
Traditional Name
CAS Registry Number
1957-10-03
SMILES
Not Available
InChI Identifier
InChI Key
Chemical Taxonomy
Classification
Not classified
Functional Ontology
Physiological effect
Not Available
Disposition
Biological location
Cellular substructure
Cytoplasm
(HMDB:
HMDB0000220
)
Membrane
(HMDB:
HMDB0000220
)
Extracellular
(HMDB:
HMDB0000220
)
Organelle
Peroxisome
(HMDB:
HMDB0000220
)
Endoplasmic reticulum
(HMDB:
HMDB0000220
)
Tissue
Connective tissue
Adipose tissue
(HMDB:
HMDB0000220
)
Muscle tissue
Skeletal muscle
(HMDB:
HMDB0000220
)
Epithelium
Epidermis
(HMDB:
HMDB0000220
)
Cell
Fibroblasts
(HMDB:
HMDB0000220
)
Hematocyte
Platelet
(HMDB:
HMDB0000220
)
Stratum Corneum
(HMDB:
HMDB0000220
)
Organ
Prostate
(HMDB:
HMDB0000220
)
Bladder
(HMDB:
HMDB0000220
)
Kidney
(HMDB:
HMDB0000220
)
Source
Exogenous
Exogenous
(HMDB:
HMDB0000220
)
Process
Naturally occurring process
Biological process
Biochemical pathway
Metabolic pathway
Fatty Acid Metabolism
(HMDB:
HMDB0000220
)
Glycerolipid Metabolism
(HMDB:
HMDB0000220
)
Fatty Acid Biosynthesis
(HMDB:
HMDB0000220
)
Fatty Acid Elongation In Mitochondria
(HMDB:
HMDB0000220
)
Steroid Biosynthesis
(HMDB:
HMDB0000220
)
Bile Acid Biosynthesis
(HMDB:
HMDB0000220
)
Drug action pathway
Ibandronate Action Pathway
(HMDB:
HMDB0000220
)
Simvastatin Action Pathway
(HMDB:
HMDB0000220
)
Pravastatin Action Pathway
(HMDB:
HMDB0000220
)
Rosuvastatin Action Pathway
(HMDB:
HMDB0000220
)
Alendronate Action Pathway
(HMDB:
HMDB0000220
)
Lovastatin Action Pathway
(HMDB:
HMDB0000220
)
Zoledronate Action Pathway
(HMDB:
HMDB0000220
)
Cerivastatin Action Pathway
(HMDB:
HMDB0000220
)
Risedronate Action Pathway
(HMDB:
HMDB0000220
)
Pamidronate Action Pathway
(HMDB:
HMDB0000220
)
Fluvastatin Action Pathway
(HMDB:
HMDB0000220
)
Atorvastatin Action Pathway
(HMDB:
HMDB0000220
)
Disease pathway
Trifunctional Protein Deficiency
(HMDB:
HMDB0000220
)
Cerebrotendinous Xanthomatosis (CTX)
(HMDB:
HMDB0000220
)
Short-Chain Acyl-CoA Dehydrogenase Deficiency (SCAD Deficiency)
(HMDB:
HMDB0000220
)
Hypercholesterolemia
(HMDB:
HMDB0000220
)
Glutaric Aciduria Type I
(HMDB:
HMDB0000220
)
Mevalonic Aciduria
(HMDB:
HMDB0000220
)
Cholesteryl Ester Storage Disease
(HMDB:
HMDB0000220
)
Carnitine Palmitoyl Transferase Deficiency II
(HMDB:
HMDB0000220
)
D-Glyceric Acidura
(HMDB:
HMDB0000220
)
Long Chain Acyl-CoA Dehydrogenase Deficiency (LCAD)
(HMDB:
HMDB0000220
)
Wolman Disease
(HMDB:
HMDB0000220
)
Glycerol Kinase Deficiency
(HMDB:
HMDB0000220
)
Familial Hypercholanemia (FHCA)
(HMDB:
HMDB0000220
)
Chondrodysplasia Punctata II, X-Linked Dominant (CDPX2)
(HMDB:
HMDB0000220
)
CHILD Syndrome
(HMDB:
HMDB0000220
)
Smith-Lemli-Opitz Syndrome (SLOS)
(HMDB:
HMDB0000220
)
27-Hydroxylase Deficiency
(HMDB:
HMDB0000220
)
Congenital Bile Acid Synthesis Defect Type III
(HMDB:
HMDB0000220
)
Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD)
(HMDB:
HMDB0000220
)
Long-Chain-3-Hydroxyacyl-CoA Dehydrogenase Deficiency (LCHAD)
(HMDB:
HMDB0000220
)
Desmosterolosis
(HMDB:
HMDB0000220
)
Hyper-IgD Syndrome
(HMDB:
HMDB0000220
)
Lysosomal Acid Lipase Deficiency (Wolman Disease)
(HMDB:
HMDB0000220
)
Ethylmalonic Encephalopathy
(HMDB:
HMDB0000220
)
Zellweger Syndrome
(HMDB:
HMDB0000220
)
Congenital Bile Acid Synthesis Defect Type II
(HMDB:
HMDB0000220
)
Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency (VLCAD)
(HMDB:
HMDB0000220
)
Carnitine Palmitoyl Transferase Deficiency I
(HMDB:
HMDB0000220
)
Role
Biological role
Plant metabolite
(HMDB:
HMDB0000220
)
Modulator
Inhibitor
EC 1.1.1.189 (prostaglandin-E2 9-reductase) inhibitor
(HMDB:
HMDB0000220
)
Physical Properties
Predicted Properties
Not Available
External Links
External Links
Not Available
References
Synthesis Reference
Not Available
