(2E,8Z)-deca-2,8-dien-4,6-diyn-1-ol

Details

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Internal ID 0c1d45a7-0ded-4ecf-a03f-c529089c88a8
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name (2E,8Z)-deca-2,8-dien-4,6-diyn-1-ol
SMILES (Canonical) CC=CC#CC#CC=CCO
SMILES (Isomeric) C/C=C\C#CC#C/C=C/CO
InChI InChI=1S/C10H10O/c1-2-3-4-5-6-7-8-9-10-11/h2-3,8-9,11H,10H2,1H3/b3-2-,9-8+
InChI Key ONZYQGMNWZGRPO-MIZUJWOHSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H10O
Molecular Weight 146.19 g/mol
Exact Mass 146.073164938 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 1.80
Atomic LogP (AlogP) 1.12
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2E,8Z)-deca-2,8-dien-4,6-diyn-1-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9863 98.63%
Caco-2 - 0.5780 57.80%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Lysosomes 0.5183 51.83%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8427 84.27%
OATP1B3 inhibitior + 0.9566 95.66%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8825 88.25%
P-glycoprotein inhibitior - 0.9769 97.69%
P-glycoprotein substrate - 0.9484 94.84%
CYP3A4 substrate - 0.6554 65.54%
CYP2C9 substrate - 0.6050 60.50%
CYP2D6 substrate - 0.8110 81.10%
CYP3A4 inhibition - 0.9385 93.85%
CYP2C9 inhibition - 0.8955 89.55%
CYP2C19 inhibition - 0.8810 88.10%
CYP2D6 inhibition - 0.9698 96.98%
CYP1A2 inhibition - 0.6367 63.67%
CYP2C8 inhibition - 0.9653 96.53%
CYP inhibitory promiscuity - 0.8203 82.03%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) + 0.5783 57.83%
Carcinogenicity (trinary) Non-required 0.5562 55.62%
Eye corrosion + 0.9670 96.70%
Eye irritation + 0.5446 54.46%
Skin irritation + 0.8375 83.75%
Skin corrosion + 0.9366 93.66%
Ames mutagenesis - 0.6137 61.37%
Human Ether-a-go-go-Related Gene inhibition - 0.6677 66.77%
Micronuclear - 0.8741 87.41%
Hepatotoxicity - 0.5072 50.72%
skin sensitisation - 0.5742 57.42%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.7889 78.89%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity + 0.6048 60.48%
Acute Oral Toxicity (c) I 0.5449 54.49%
Estrogen receptor binding - 0.8356 83.56%
Androgen receptor binding - 0.8048 80.48%
Thyroid receptor binding - 0.6911 69.11%
Glucocorticoid receptor binding - 0.6301 63.01%
Aromatase binding - 0.6545 65.45%
PPAR gamma - 0.6850 68.50%
Honey bee toxicity - 0.9137 91.37%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.8500 85.00%
Fish aquatic toxicity - 0.7026 70.26%

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 86.73% 96.09%

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.
Grindelia hirsutula
Pellacalyx axillaris

Cross-Links

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PubChem 92449063
LOTUS LTS0017479
wikiData Q105214857