Trideca-1,5-dien-7,9-diyn-4-ol

Details

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Internal ID 8b739215-88c9-4a85-9a35-9b2bee0cfffe
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name trideca-1,5-dien-7,9-diyn-4-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H16O/c1-3-5-6-7-8-9-10-12-13(14)11-4-2/h4,10,12-14H,2-3,5,11H2,1H3
InChI Key AAOBYDYOAZKODR-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H16O
Molecular Weight 188.26 g/mol
Exact Mass 188.120115130 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.30
Atomic LogP (AlogP) 2.29
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Trideca-1,5-dien-7,9-diyn-4-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9870 98.70%
Caco-2 - 0.6672 66.72%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Plasma membrane 0.4036 40.36%
OATP2B1 inhibitior - 0.8612 86.12%
OATP1B1 inhibitior + 0.8911 89.11%
OATP1B3 inhibitior + 0.9354 93.54%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9101 91.01%
P-glycoprotein inhibitior - 0.9699 96.99%
P-glycoprotein substrate - 0.8478 84.78%
CYP3A4 substrate - 0.5659 56.59%
CYP2C9 substrate - 0.7982 79.82%
CYP2D6 substrate - 0.7649 76.49%
CYP3A4 inhibition - 0.8721 87.21%
CYP2C9 inhibition - 0.8812 88.12%
CYP2C19 inhibition - 0.7688 76.88%
CYP2D6 inhibition - 0.9451 94.51%
CYP1A2 inhibition + 0.5464 54.64%
CYP2C8 inhibition - 0.8622 86.22%
CYP inhibitory promiscuity - 0.7765 77.65%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.5200 52.00%
Carcinogenicity (trinary) Non-required 0.6317 63.17%
Eye corrosion + 0.5494 54.94%
Eye irritation - 0.5671 56.71%
Skin irritation + 0.7307 73.07%
Skin corrosion - 0.7628 76.28%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5825 58.25%
Micronuclear - 0.9500 95.00%
Hepatotoxicity + 0.5051 50.51%
skin sensitisation + 0.8571 85.71%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity - 0.9556 95.56%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity - 0.5555 55.55%
Acute Oral Toxicity (c) II 0.6260 62.60%
Estrogen receptor binding - 0.7377 73.77%
Androgen receptor binding - 0.8049 80.49%
Thyroid receptor binding + 0.5551 55.51%
Glucocorticoid receptor binding - 0.7144 71.44%
Aromatase binding - 0.5781 57.81%
PPAR gamma - 0.5483 54.83%
Honey bee toxicity - 0.7672 76.72%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity - 0.5485 54.85%

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 93.40% 96.09%
CHEMBL2581 P07339 Cathepsin D 93.08% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.51% 99.17%
CHEMBL221 P23219 Cyclooxygenase-1 87.46% 90.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.95% 94.45%
CHEMBL203 P00533 Epidermal growth factor receptor erbB1 85.59% 97.34%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 84.73% 92.86%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.17% 93.56%

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.
Cineraria saxifraga

Cross-Links

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PubChem 162905881
LOTUS LTS0075768
wikiData Q104908246