3-Methyl-2-(3-methylbut-2-enyl)-2,5-dihydrofuran

Details

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Internal ID f20d9636-1d51-41dd-a8af-42eab51e5639
Taxonomy Organoheterocyclic compounds > Dihydrofurans
IUPAC Name 3-methyl-2-(3-methylbut-2-enyl)-2,5-dihydrofuran
SMILES (Canonical) CC1=CCOC1CC=C(C)C
SMILES (Isomeric) CC1=CCOC1CC=C(C)C
InChI InChI=1S/C10H16O/c1-8(2)4-5-10-9(3)6-7-11-10/h4,6,10H,5,7H2,1-3H3
InChI Key OBWLQYFNTCZMSR-UHFFFAOYSA-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) 9.20 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.69
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-Methyl-2-(3-methylbut-2-enyl)-2,5-dihydrofuran

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9947 99.47%
Caco-2 + 0.5629 56.29%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.5073 50.73%
OATP2B1 inhibitior - 0.8616 86.16%
OATP1B1 inhibitior + 0.9456 94.56%
OATP1B3 inhibitior + 0.9410 94.10%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8362 83.62%
P-glycoprotein inhibitior - 0.9832 98.32%
P-glycoprotein substrate - 0.9158 91.58%
CYP3A4 substrate - 0.6200 62.00%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7269 72.69%
CYP3A4 inhibition - 0.9295 92.95%
CYP2C9 inhibition - 0.8248 82.48%
CYP2C19 inhibition - 0.7203 72.03%
CYP2D6 inhibition - 0.9233 92.33%
CYP1A2 inhibition - 0.6437 64.37%
CYP2C8 inhibition - 0.9240 92.40%
CYP inhibitory promiscuity + 0.5535 55.35%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7144 71.44%
Carcinogenicity (trinary) Non-required 0.4895 48.95%
Eye corrosion - 0.8085 80.85%
Eye irritation + 0.7425 74.25%
Skin irritation + 0.5347 53.47%
Skin corrosion - 0.8976 89.76%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5182 51.82%
Micronuclear - 0.8600 86.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation + 0.6697 66.97%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.7444 74.44%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity - 0.7072 70.72%
Acute Oral Toxicity (c) III 0.7348 73.48%
Estrogen receptor binding - 0.9514 95.14%
Androgen receptor binding - 0.9225 92.25%
Thyroid receptor binding - 0.8883 88.83%
Glucocorticoid receptor binding - 0.9254 92.54%
Aromatase binding - 0.8864 88.64%
PPAR gamma - 0.9044 90.44%
Honey bee toxicity - 0.9343 93.43%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9130 91.30%

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 91.42% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 89.36% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.77% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.89% 100.00%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 80.52% 83.57%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.31% 97.09%

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.
Artemisia pallens

Cross-Links

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PubChem 11019056
LOTUS LTS0209191
wikiData Q105189194