(7E,9E,15E)-heptadeca-7,9,15-trien-11,13-diynal

Details

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Internal ID 4772e1a9-a56b-4eac-8eb9-561372b8786a
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty aldehydes
IUPAC Name (7E,9E,15E)-heptadeca-7,9,15-trien-11,13-diynal
SMILES (Canonical) CC=CC#CC#CC=CC=CCCCCCC=O
SMILES (Isomeric) C/C=C/C#CC#C/C=C/C=C/CCCCCC=O
InChI InChI=1S/C17H20O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18/h2-3,8-11,17H,12-16H2,1H3/b3-2+,9-8+,11-10+
InChI Key LTDHYWCQZMPBOF-MMOYHAHMSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H20O
Molecular Weight 240.34 g/mol
Exact Mass 240.151415257 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 4.50
Atomic LogP (AlogP) 3.83
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 (7E,9E,15E)-heptadeca-7,9,15-trien-11,13-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 + 0.7157 71.57%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Plasma membrane 0.5460 54.60%
OATP2B1 inhibitior - 0.8611 86.11%
OATP1B1 inhibitior + 0.8411 84.11%
OATP1B3 inhibitior + 0.9411 94.11%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8080 80.80%
P-glycoprotein inhibitior - 0.9082 90.82%
P-glycoprotein substrate - 0.8201 82.01%
CYP3A4 substrate - 0.5133 51.33%
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 - 0.9171 91.71%
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 - 0.5070 50.70%
Skin irritation + 0.7424 74.24%
Skin corrosion - 0.8209 82.09%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4046 40.46%
Micronuclear - 0.9500 95.00%
Hepatotoxicity - 0.5754 57.54%
skin sensitisation + 0.8862 88.62%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity - 0.9288 92.88%
Mitochondrial toxicity - 0.8250 82.50%
Nephrotoxicity + 0.7663 76.63%
Acute Oral Toxicity (c) III 0.8288 82.88%
Estrogen receptor binding + 0.5445 54.45%
Androgen receptor binding - 0.5318 53.18%
Thyroid receptor binding + 0.5209 52.09%
Glucocorticoid receptor binding - 0.6562 65.62%
Aromatase binding + 0.5600 56.00%
PPAR gamma + 0.5472 54.72%
Honey bee toxicity - 0.8712 87.12%
Biodegradation - 0.7500 75.00%
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 89.35% 96.09%
CHEMBL2581 P07339 Cathepsin D 86.36% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.33% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.42% 96.00%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 83.34% 89.34%
CHEMBL4040 P28482 MAP kinase ERK2 82.32% 83.82%
CHEMBL3401 O75469 Pregnane X receptor 81.05% 94.73%

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 pullata
Pleiotaxis rugosa
Volutaria muricata

Cross-Links

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PubChem 14412234
LOTUS LTS0064340
wikiData Q105156892