(5E,7E,13E)-pentadeca-5,7,13-trien-9,11-diynal

Details

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Internal ID 2f5c81fb-7a31-4338-83d7-2f52009e1731
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty aldehydes
IUPAC Name (5E,7E,13E)-pentadeca-5,7,13-trien-9,11-diynal
SMILES (Canonical) CC=CC#CC#CC=CC=CCCCC=O
SMILES (Isomeric) C/C=C/C#CC#C/C=C/C=C/CCCC=O
InChI InChI=1S/C15H16O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16/h2-3,8-11,15H,12-14H2,1H3/b3-2+,9-8+,11-10+
InChI Key CWBXCZXHOHBSLY-MMOYHAHMSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H16O
Molecular Weight 212.29 g/mol
Exact Mass 212.120115130 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.40
Atomic LogP (AlogP) 3.05
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (5E,7E,13E)-pentadeca-5,7,13-trien-9,11-diynal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9893 98.93%
Caco-2 + 0.7107 71.07%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Plasma membrane 0.3956 39.56%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7899 78.99%
OATP1B3 inhibitior + 0.9483 94.83%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.7789 77.89%
P-glycoprotein inhibitior - 0.9478 94.78%
P-glycoprotein substrate - 0.8087 80.87%
CYP3A4 substrate - 0.5125 51.25%
CYP2C9 substrate - 0.7914 79.14%
CYP2D6 substrate - 0.8191 81.91%
CYP3A4 inhibition - 0.9352 93.52%
CYP2C9 inhibition - 0.8943 89.43%
CYP2C19 inhibition - 0.9131 91.31%
CYP2D6 inhibition - 0.9725 97.25%
CYP1A2 inhibition + 0.5119 51.19%
CYP2C8 inhibition - 0.9206 92.06%
CYP inhibitory promiscuity - 0.7485 74.85%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5200 52.00%
Carcinogenicity (trinary) Non-required 0.5337 53.37%
Eye corrosion + 0.9936 99.36%
Eye irritation - 0.4942 49.42%
Skin irritation + 0.8571 85.71%
Skin corrosion + 0.6570 65.70%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6238 62.38%
Micronuclear - 0.8700 87.00%
Hepatotoxicity - 0.5662 56.62%
skin sensitisation + 0.8403 84.03%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity - 0.9000 90.00%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity + 0.8098 80.98%
Acute Oral Toxicity (c) III 0.8425 84.25%
Estrogen receptor binding + 0.6680 66.80%
Androgen receptor binding - 0.6295 62.95%
Thyroid receptor binding - 0.5171 51.71%
Glucocorticoid receptor binding - 0.5566 55.66%
Aromatase binding + 0.6293 62.93%
PPAR gamma + 0.5296 52.96%
Honey bee toxicity - 0.8664 86.64%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity - 0.7145 71.45%

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 85.53% 96.09%
CHEMBL2581 P07339 Cathepsin D 83.86% 98.95%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 83.69% 98.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.89% 96.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.68% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 81.44% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.74% 95.56%
CHEMBL4040 P28482 MAP kinase ERK2 80.12% 83.82%

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
Volutaria muricata

Cross-Links

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PubChem 14412232
LOTUS LTS0258807
wikiData Q104971147