2-Methyl-5-(fur-3-yl)-pent-3-en-2-ol

Details

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Internal ID b420fff4-b6f0-4e7d-80a5-2fe9086c0662
Taxonomy Organoheterocyclic compounds > Heteroaromatic compounds
IUPAC Name (E)-5-(furan-3-yl)-2-methylpent-3-en-2-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H14O2/c1-10(2,11)6-3-4-9-5-7-12-8-9/h3,5-8,11H,4H2,1-2H3/b6-3+
InChI Key XAZOEZDWXXKFEO-ZZXKWVIFSA-N
Popularity 3 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) 33.40 Ų
XlogP 1.60
Atomic LogP (AlogP) 2.15
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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XAZOEZDWXXKFEO-ZZXKWVIFSA-N
139528-07-7
(3E)-5-(3-Furyl)-2-methyl-3-penten-2-ol #

2D Structure

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2D Structure of 2-Methyl-5-(fur-3-yl)-pent-3-en-2-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9811 98.11%
Caco-2 + 0.9645 96.45%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.5782 57.82%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7757 77.57%
OATP1B3 inhibitior + 0.9447 94.47%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8490 84.90%
P-glycoprotein inhibitior - 0.9769 97.69%
P-glycoprotein substrate - 0.9436 94.36%
CYP3A4 substrate - 0.6372 63.72%
CYP2C9 substrate - 0.6104 61.04%
CYP2D6 substrate - 0.7369 73.69%
CYP3A4 inhibition - 0.9005 90.05%
CYP2C9 inhibition - 0.6706 67.06%
CYP2C19 inhibition - 0.5695 56.95%
CYP2D6 inhibition - 0.8923 89.23%
CYP1A2 inhibition - 0.7073 70.73%
CYP2C8 inhibition - 0.7938 79.38%
CYP inhibitory promiscuity + 0.6063 60.63%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.6744 67.44%
Carcinogenicity (trinary) Non-required 0.3561 35.61%
Eye corrosion - 0.6604 66.04%
Eye irritation + 0.8581 85.81%
Skin irritation + 0.6006 60.06%
Skin corrosion - 0.6231 62.31%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6415 64.15%
Micronuclear - 0.8100 81.00%
Hepatotoxicity + 0.5199 51.99%
skin sensitisation + 0.7921 79.21%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity - 0.6615 66.15%
Acute Oral Toxicity (c) III 0.7913 79.13%
Estrogen receptor binding - 0.7562 75.62%
Androgen receptor binding - 0.9170 91.70%
Thyroid receptor binding - 0.7950 79.50%
Glucocorticoid receptor binding - 0.7373 73.73%
Aromatase binding - 0.7625 76.25%
PPAR gamma - 0.8638 86.38%
Honey bee toxicity - 0.9500 95.00%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity - 0.4191 41.91%

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
CHEMBL3401 O75469 Pregnane X receptor 92.34% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.54% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.03% 91.11%
CHEMBL2581 P07339 Cathepsin D 84.63% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.21% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.20% 99.17%

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 salsoloides

Cross-Links

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PubChem 5363576
LOTUS LTS0262581
wikiData Q105324255