(2E,4R)-4-ethenyl-2,5-dimethylhexa-2,5-dien-1-ol

Details

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Internal ID de7e3e8f-d9fd-4cb6-bbdd-0a97ddea383e
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name (2E,4R)-4-ethenyl-2,5-dimethylhexa-2,5-dien-1-ol
SMILES (Canonical) CC(=C)C(C=C)C=C(C)CO
SMILES (Isomeric) CC(=C)[C@H](C=C)/C=C(\C)/CO
InChI InChI=1S/C10H16O/c1-5-10(8(2)3)6-9(4)7-11/h5-6,10-11H,1-2,7H2,3-4H3/b9-6+/t10-/m1/s1
InChI Key NHJXCMQPMLBAMK-OLKPEBQYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16O
Molecular Weight 152.23 g/mol
Exact Mass 152.120115130 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.30
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 (2E,4R)-4-ethenyl-2,5-dimethylhexa-2,5-dien-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 + 0.9845 98.45%
Caco-2 + 0.7989 79.89%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Lysosomes 0.6266 62.66%
OATP2B1 inhibitior - 0.8630 86.30%
OATP1B1 inhibitior + 0.9470 94.70%
OATP1B3 inhibitior + 0.9543 95.43%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9394 93.94%
P-glycoprotein inhibitior - 0.9695 96.95%
P-glycoprotein substrate - 0.9455 94.55%
CYP3A4 substrate - 0.6316 63.16%
CYP2C9 substrate - 0.6463 64.63%
CYP2D6 substrate - 0.7907 79.07%
CYP3A4 inhibition - 0.8095 80.95%
CYP2C9 inhibition - 0.9290 92.90%
CYP2C19 inhibition - 0.8279 82.79%
CYP2D6 inhibition - 0.9335 93.35%
CYP1A2 inhibition - 0.8103 81.03%
CYP2C8 inhibition - 0.9593 95.93%
CYP inhibitory promiscuity - 0.8549 85.49%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) + 0.5883 58.83%
Carcinogenicity (trinary) Non-required 0.6331 63.31%
Eye corrosion + 0.9083 90.83%
Eye irritation + 0.9394 93.94%
Skin irritation + 0.5979 59.79%
Skin corrosion - 0.7616 76.16%
Ames mutagenesis - 0.6883 68.83%
Human Ether-a-go-go-Related Gene inhibition - 0.7193 71.93%
Micronuclear - 0.9741 97.41%
Hepatotoxicity + 0.5534 55.34%
skin sensitisation + 0.6374 63.74%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity - 0.9778 97.78%
Mitochondrial toxicity - 0.8250 82.50%
Nephrotoxicity + 0.6034 60.34%
Acute Oral Toxicity (c) III 0.6968 69.68%
Estrogen receptor binding - 0.9161 91.61%
Androgen receptor binding - 0.8856 88.56%
Thyroid receptor binding - 0.7816 78.16%
Glucocorticoid receptor binding - 0.8920 89.20%
Aromatase binding - 0.8344 83.44%
PPAR gamma - 0.8447 84.47%
Honey bee toxicity - 0.8249 82.49%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.9200 92.00%
Fish aquatic toxicity + 0.7409 74.09%

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 90.54% 96.09%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 88.97% 97.29%
CHEMBL2581 P07339 Cathepsin D 88.78% 98.95%
CHEMBL203 P00533 Epidermal growth factor receptor erbB1 88.74% 97.34%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.20% 91.11%

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.
Artemisia tridentata
Glebionis coronaria
Tanacetum vulgare

Cross-Links

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PubChem 162933896
LOTUS LTS0113747
wikiData Q105179431