Heptadeca-2,8,10,16-tetraen-4,6-diynal

Details

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Internal ID ac97b087-cdee-44b1-85f2-6e4ed36ae960
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty aldehydes
IUPAC Name heptadeca-2,8,10,16-tetraen-4,6-diynal
SMILES (Canonical) C=CCCCCC=CC=CC#CC#CC=CC=O
SMILES (Isomeric) C=CCCCCC=CC=CC#CC#CC=CC=O
InChI InChI=1S/C17H18O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18/h2,7-10,15-17H,1,3-6H2
InChI Key GTUMMNFTYXVUQK-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H18O
Molecular Weight 238.32 g/mol
Exact Mass 238.135765193 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 4.70
Atomic LogP (AlogP) 3.61
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 Heptadeca-2,8,10,16-tetraen-4,6-diynal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9820 98.20%
Caco-2 + 0.6692 66.92%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Plasma membrane 0.4423 44.23%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8809 88.09%
OATP1B3 inhibitior + 0.9452 94.52%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.7754 77.54%
P-glycoprotein inhibitior - 0.9065 90.65%
P-glycoprotein substrate - 0.8948 89.48%
CYP3A4 substrate - 0.5201 52.01%
CYP2C9 substrate - 0.6114 61.14%
CYP2D6 substrate - 0.8186 81.86%
CYP3A4 inhibition - 0.9372 93.72%
CYP2C9 inhibition - 0.8327 83.27%
CYP2C19 inhibition - 0.8721 87.21%
CYP2D6 inhibition - 0.9669 96.69%
CYP1A2 inhibition - 0.5186 51.86%
CYP2C8 inhibition - 0.8529 85.29%
CYP inhibitory promiscuity - 0.6529 65.29%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5600 56.00%
Carcinogenicity (trinary) Non-required 0.4927 49.27%
Eye corrosion + 0.9936 99.36%
Eye irritation - 0.4914 49.14%
Skin irritation + 0.7948 79.48%
Skin corrosion + 0.5280 52.80%
Ames mutagenesis + 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3868 38.68%
Micronuclear - 0.9000 90.00%
Hepatotoxicity - 0.5625 56.25%
skin sensitisation + 0.8869 88.69%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity - 0.9000 90.00%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity + 0.7605 76.05%
Acute Oral Toxicity (c) III 0.5805 58.05%
Estrogen receptor binding + 0.6642 66.42%
Androgen receptor binding - 0.5221 52.21%
Thyroid receptor binding + 0.5476 54.76%
Glucocorticoid receptor binding - 0.4796 47.96%
Aromatase binding + 0.6733 67.33%
PPAR gamma + 0.6284 62.84%
Honey bee toxicity - 0.6559 65.59%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.8487 84.87%

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
CHEMBL3060 Q9Y345 Glycine transporter 2 83.90% 99.17%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 82.60% 89.34%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.60% 96.00%

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 napifolia
Jacobaea erucifolia
Tridax trilobata

Cross-Links

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PubChem 162965407
LOTUS LTS0093337
wikiData Q105019497