3,9-Oxy-mentha-1,8(10)-diene

Details

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Internal ID d3b46744-6799-4a7f-80c2-b9b609024b26
Taxonomy Organoheterocyclic compounds > Benzofurans
IUPAC Name 6-methyl-3-methylidene-3a,4,5,7a-tetrahydro-1-benzofuran
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H14O/c1-7-3-4-9-8(2)6-11-10(9)5-7/h5,9-10H,2-4,6H2,1H3
InChI Key FQRAKZWEBJPGTM-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C10H14O
Molecular Weight 150.22 g/mol
Exact Mass 150.104465066 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 1.20
Atomic LogP (AlogP) 2.30
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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3,9-Oxy-mentha-1,8(10)-diene

2D Structure

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2D Structure of 3,9-Oxy-mentha-1,8(10)-diene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.5000 50.00%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Lysosomes 0.4756 47.56%
OATP2B1 inhibitior - 0.8505 85.05%
OATP1B1 inhibitior + 0.9264 92.64%
OATP1B3 inhibitior + 0.9521 95.21%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.9759 97.59%
P-glycoprotein inhibitior - 0.9701 97.01%
P-glycoprotein substrate - 0.9403 94.03%
CYP3A4 substrate - 0.5350 53.50%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7040 70.40%
CYP3A4 inhibition - 0.9063 90.63%
CYP2C9 inhibition - 0.7972 79.72%
CYP2C19 inhibition + 0.5218 52.18%
CYP2D6 inhibition - 0.8805 88.05%
CYP1A2 inhibition + 0.6987 69.87%
CYP2C8 inhibition - 0.8551 85.51%
CYP inhibitory promiscuity + 0.5000 50.00%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.4885 48.85%
Eye corrosion - 0.6495 64.95%
Eye irritation + 0.8500 85.00%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.9467 94.67%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.9300 93.00%
Hepatotoxicity + 0.7875 78.75%
skin sensitisation + 0.6490 64.90%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity - 0.5778 57.78%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity - 0.6861 68.61%
Acute Oral Toxicity (c) III 0.7894 78.94%
Estrogen receptor binding - 0.9499 94.99%
Androgen receptor binding - 0.6917 69.17%
Thyroid receptor binding - 0.8670 86.70%
Glucocorticoid receptor binding - 0.8307 83.07%
Aromatase binding - 0.8339 83.39%
PPAR gamma - 0.8772 87.72%
Honey bee toxicity - 0.9122 91.22%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.9802 98.02%

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
CHEMBL3137262 O60341 LSD1/CoREST complex 87.46% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.75% 100.00%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 84.33% 86.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.07% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.42% 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.
Rhododendron groenlandicum

Cross-Links

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PubChem 22216621
LOTUS LTS0223114
wikiData Q104999814