Deca-2,4-dien-6-yne-1,10-diol

Details

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Internal ID f3ccd585-8475-4f00-ab82-182c8ddd7db7
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name deca-2,4-dien-6-yne-1,10-diol
SMILES (Canonical) C(CC#CC=CC=CCO)CO
SMILES (Isomeric) C(CC#CC=CC=CCO)CO
InChI InChI=1S/C10H14O2/c11-9-7-5-3-1-2-4-6-8-10-12/h1,3,5,7,11-12H,6,8-10H2
InChI Key VTYZRIHEJNGHHM-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H14O2
Molecular Weight 166.22 g/mol
Exact Mass 166.099379685 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 1.00
Atomic LogP (AlogP) 0.87
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Deca-2,4-dien-6-yne-1,10-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9643 96.43%
Caco-2 + 0.7422 74.22%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.4548 45.48%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8895 88.95%
OATP1B3 inhibitior + 0.9453 94.53%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8876 88.76%
P-glycoprotein inhibitior - 0.9858 98.58%
P-glycoprotein substrate - 0.9409 94.09%
CYP3A4 substrate - 0.5940 59.40%
CYP2C9 substrate - 0.8075 80.75%
CYP2D6 substrate - 0.7593 75.93%
CYP3A4 inhibition - 0.8779 87.79%
CYP2C9 inhibition - 0.8871 88.71%
CYP2C19 inhibition - 0.9034 90.34%
CYP2D6 inhibition - 0.9611 96.11%
CYP1A2 inhibition - 0.6709 67.09%
CYP2C8 inhibition - 0.8668 86.68%
CYP inhibitory promiscuity - 0.8630 86.30%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.6200 62.00%
Carcinogenicity (trinary) Non-required 0.5677 56.77%
Eye corrosion + 0.9547 95.47%
Eye irritation + 0.7808 78.08%
Skin irritation + 0.7463 74.63%
Skin corrosion + 0.7003 70.03%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6072 60.72%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.5649 56.49%
skin sensitisation + 0.5813 58.13%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity - 0.9667 96.67%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity + 0.7911 79.11%
Acute Oral Toxicity (c) II 0.4667 46.67%
Estrogen receptor binding - 0.7876 78.76%
Androgen receptor binding - 0.6166 61.66%
Thyroid receptor binding - 0.6060 60.60%
Glucocorticoid receptor binding - 0.5203 52.03%
Aromatase binding - 0.6598 65.98%
PPAR gamma + 0.6707 67.07%
Honey bee toxicity - 0.8494 84.94%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.7555 75.55%
Fish aquatic toxicity - 0.9399 93.99%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.58% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.44% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.41% 99.17%
CHEMBL2885 P07451 Carbonic anhydrase III 81.97% 87.45%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 80.84% 86.92%
CHEMBL1977 P11473 Vitamin D receptor 80.59% 99.43%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 162994718
LOTUS LTS0174146
wikiData Q105293101