Hexadeca-7,14-dien-10,12-diynal

Details

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Internal ID 6a4b6367-0059-4251-9d08-f445f3f06bbc
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty aldehydes
IUPAC Name hexadeca-7,14-dien-10,12-diynal
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H20O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17/h2-3,9-10,16H,8,11-15H2,1H3
InChI Key BDXVAPVXTZVJHO-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C16H20O
Molecular Weight 228.33 g/mol
Exact Mass 228.151415257 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 4.20
Atomic LogP (AlogP) 3.67
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Hexadeca-7,14-dien-10,12-diynal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9902 99.02%
Caco-2 + 0.6510 65.10%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Plasma membrane 0.5460 54.60%
OATP2B1 inhibitior - 0.8593 85.93%
OATP1B1 inhibitior + 0.8111 81.11%
OATP1B3 inhibitior + 0.9411 94.11%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7581 75.81%
P-glycoprotein inhibitior - 0.9011 90.11%
P-glycoprotein substrate - 0.7869 78.69%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.7914 79.14%
CYP2D6 substrate - 0.8191 81.91%
CYP3A4 inhibition - 0.9477 94.77%
CYP2C9 inhibition - 0.8419 84.19%
CYP2C19 inhibition - 0.9206 92.06%
CYP2D6 inhibition - 0.9733 97.33%
CYP1A2 inhibition + 0.5740 57.40%
CYP2C8 inhibition - 0.8498 84.98%
CYP inhibitory promiscuity - 0.7305 73.05%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5000 50.00%
Carcinogenicity (trinary) Non-required 0.5921 59.21%
Eye corrosion + 0.9893 98.93%
Eye irritation + 0.5778 57.78%
Skin irritation + 0.7424 74.24%
Skin corrosion - 0.8209 82.09%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6030 60.30%
Micronuclear - 0.9500 95.00%
Hepatotoxicity - 0.6592 65.92%
skin sensitisation + 0.8862 88.62%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity - 0.9288 92.88%
Mitochondrial toxicity - 0.8250 82.50%
Nephrotoxicity + 0.7184 71.84%
Acute Oral Toxicity (c) III 0.8288 82.88%
Estrogen receptor binding - 0.5000 50.00%
Androgen receptor binding - 0.7236 72.36%
Thyroid receptor binding + 0.5343 53.43%
Glucocorticoid receptor binding - 0.5571 55.71%
Aromatase binding + 0.5212 52.12%
PPAR gamma + 0.7608 76.08%
Honey bee toxicity - 0.8789 87.89%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.7200 72.00%
Fish aquatic toxicity + 0.7241 72.41%

Targets

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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 89.90% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.47% 99.17%
CHEMBL2581 P07339 Cathepsin D 88.44% 98.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.78% 96.00%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 81.34% 89.34%

Plants that contains it

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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 macrocephala

Cross-Links

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PubChem 85546031
LOTUS LTS0253795
wikiData Q104932399