Octadeca-9,11,13,15-tetraenal

Details

Top
Internal ID d632fb0c-d2fd-4065-a15e-ad78e447e8d3
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty aldehydes
IUPAC Name octadeca-9,11,13,15-tetraenal
SMILES (Canonical) CCC=CC=CC=CC=CCCCCCCCC=O
SMILES (Isomeric) CCC=CC=CC=CC=CCCCCCCCC=O
InChI InChI=1S/C18H28O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19/h3-10,18H,2,11-17H2,1H3
InChI Key RETRRXAPSLSKSS-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C18H28O
Molecular Weight 260.40 g/mol
Exact Mass 260.214015512 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 5.90
Atomic LogP (AlogP) 5.55
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 12

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Octadeca-9,11,13,15-tetraenal

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9947 99.47%
Caco-2 + 0.8453 84.53%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Plasma membrane 0.6783 67.83%
OATP2B1 inhibitior - 0.8593 85.93%
OATP1B1 inhibitior + 0.8803 88.03%
OATP1B3 inhibitior + 0.9337 93.37%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.5589 55.89%
P-glycoprotein inhibitior - 0.7840 78.40%
P-glycoprotein substrate - 0.8932 89.32%
CYP3A4 substrate - 0.6155 61.55%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate - 0.8090 80.90%
CYP3A4 inhibition - 0.9752 97.52%
CYP2C9 inhibition - 0.9030 90.30%
CYP2C19 inhibition - 0.9406 94.06%
CYP2D6 inhibition - 0.9708 97.08%
CYP1A2 inhibition + 0.6041 60.41%
CYP2C8 inhibition - 0.9535 95.35%
CYP inhibitory promiscuity - 0.7596 75.96%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5400 54.00%
Carcinogenicity (trinary) Non-required 0.6509 65.09%
Eye corrosion + 0.9942 99.42%
Eye irritation + 0.8876 88.76%
Skin irritation + 0.7457 74.57%
Skin corrosion - 0.9663 96.63%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6983 69.83%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5875 58.75%
skin sensitisation + 0.9175 91.75%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity - 0.9177 91.77%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity + 0.5714 57.14%
Acute Oral Toxicity (c) III 0.9289 92.89%
Estrogen receptor binding + 0.6829 68.29%
Androgen receptor binding - 0.6443 64.43%
Thyroid receptor binding + 0.6032 60.32%
Glucocorticoid receptor binding - 0.6998 69.98%
Aromatase binding + 0.5470 54.70%
PPAR gamma + 0.5766 57.66%
Honey bee toxicity - 0.9417 94.17%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.6900 69.00%
Fish aquatic toxicity + 0.7443 74.43%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.58% 96.09%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 87.93% 89.34%
CHEMBL2581 P07339 Cathepsin D 87.52% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.01% 99.17%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 84.34% 97.29%
CHEMBL2664 P23526 Adenosylhomocysteinase 82.42% 86.67%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.61% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 80.30% 94.73%

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.
Centaurea cineraria subsp. cineraria
Centaurea deusta

Cross-Links

Top
PubChem 3035814
LOTUS LTS0215818
wikiData Q105235095