Nonadecanal

Details

Top
Internal ID 78f92f2e-faae-41ff-b3a9-8f12ee211895
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty aldehydes
IUPAC Name nonadecanal
SMILES (Canonical) CCCCCCCCCCCCCCCCCCC=O
SMILES (Isomeric) CCCCCCCCCCCCCCCCCCC=O
InChI InChI=1S/C19H38O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20/h19H,2-18H2,1H3
InChI Key SXIYYZWCMUFWBW-UHFFFAOYSA-N
Popularity 14 references in papers

Physical and Chemical Properties

Top
Molecular Formula C19H38O
Molecular Weight 282.50 g/mol
Exact Mass 282.292265831 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 8.70
Atomic LogP (AlogP) 6.84
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 17

Synonyms

Top
17352-32-8
SCHEMBL120789
AMY5934
DTXSID10938401
CHEBI:179288
SXIYYZWCMUFWBW-UHFFFAOYSA-N
LMFA06000247
AKOS032950019
LS-96796
H11226
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of Nonadecanal

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9948 99.48%
Caco-2 + 0.7254 72.54%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.3433 34.33%
OATP2B1 inhibitior - 0.8524 85.24%
OATP1B1 inhibitior + 0.9024 90.24%
OATP1B3 inhibitior + 0.9214 92.14%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.6433 64.33%
P-glycoprotein inhibitior - 0.9027 90.27%
P-glycoprotein substrate - 0.9337 93.37%
CYP3A4 substrate - 0.7002 70.02%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7756 77.56%
CYP3A4 inhibition - 0.9876 98.76%
CYP2C9 inhibition - 0.9372 93.72%
CYP2C19 inhibition - 0.9645 96.45%
CYP2D6 inhibition - 0.9645 96.45%
CYP1A2 inhibition + 0.7096 70.96%
CYP2C8 inhibition - 0.9715 97.15%
CYP inhibitory promiscuity - 0.9015 90.15%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5900 59.00%
Carcinogenicity (trinary) Non-required 0.7426 74.26%
Eye corrosion + 0.9967 99.67%
Eye irritation + 0.9817 98.17%
Skin irritation + 0.8808 88.08%
Skin corrosion - 0.8416 84.16%
Ames mutagenesis - 0.9900 99.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4422 44.22%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6691 66.91%
skin sensitisation + 0.8238 82.38%
Respiratory toxicity - 1.0000 100.00%
Reproductive toxicity - 0.9584 95.84%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity + 0.6700 67.00%
Acute Oral Toxicity (c) III 0.8649 86.49%
Estrogen receptor binding - 0.6792 67.92%
Androgen receptor binding - 0.8204 82.04%
Thyroid receptor binding + 0.6349 63.49%
Glucocorticoid receptor binding - 0.8119 81.19%
Aromatase binding - 0.6934 69.34%
PPAR gamma + 0.5940 59.40%
Honey bee toxicity - 0.9862 98.62%
Biodegradation + 0.8750 87.50%
Crustacea aquatic toxicity + 0.8784 87.84%
Fish aquatic toxicity + 0.8971 89.71%

Targets

Top

Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL230 P35354 Cyclooxygenase-2 96.51% 89.63%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 95.17% 92.08%
CHEMBL2581 P07339 Cathepsin D 93.42% 98.95%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 91.30% 97.29%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 91.25% 85.94%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 89.79% 92.86%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.28% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.57% 96.09%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 85.14% 89.34%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 83.61% 91.81%
CHEMBL2664 P23526 Adenosylhomocysteinase 82.42% 86.67%
CHEMBL3401 O75469 Pregnane X receptor 81.91% 94.73%
CHEMBL221 P23219 Cyclooxygenase-1 81.76% 90.17%

Plants that contains it

Top
Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Glehnia littoralis
Hamamelis virginiana

Cross-Links

Top
PubChem 176926
NPASS NPC173949
LOTUS LTS0054212
wikiData Q67880027