(2R)-3-methyl-2-(3-methylbut-3-enyl)-2,5-dihydrofuran

Details

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Internal ID d12dea73-1cd6-4715-b614-c39ecf3b5fad
Taxonomy Organoheterocyclic compounds > Dihydrofurans
IUPAC Name (2R)-3-methyl-2-(3-methylbut-3-enyl)-2,5-dihydrofuran
SMILES (Canonical) CC1=CCOC1CCC(=C)C
SMILES (Isomeric) CC1=CCO[C@@H]1CCC(=C)C
InChI InChI=1S/C10H16O/c1-8(2)4-5-10-9(3)6-7-11-10/h6,10H,1,4-5,7H2,2-3H3/t10-/m1/s1
InChI Key YCDULPVXDZNTND-SNVBAGLBSA-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 2.30
Atomic LogP (AlogP) 2.69
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2R)-3-methyl-2-(3-methylbut-3-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 + 0.9927 99.27%
Caco-2 + 0.6469 64.69%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Lysosomes 0.4591 45.91%
OATP2B1 inhibitior - 0.8507 85.07%
OATP1B1 inhibitior + 0.9400 94.00%
OATP1B3 inhibitior + 0.9280 92.80%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.9116 91.16%
P-glycoprotein inhibitior - 0.9834 98.34%
P-glycoprotein substrate - 0.9107 91.07%
CYP3A4 substrate - 0.5948 59.48%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7269 72.69%
CYP3A4 inhibition - 0.8575 85.75%
CYP2C9 inhibition - 0.8793 87.93%
CYP2C19 inhibition - 0.7428 74.28%
CYP2D6 inhibition - 0.9226 92.26%
CYP1A2 inhibition + 0.5088 50.88%
CYP2C8 inhibition - 0.8448 84.48%
CYP inhibitory promiscuity - 0.5967 59.67%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8228 82.28%
Carcinogenicity (trinary) Non-required 0.5197 51.97%
Eye corrosion - 0.7651 76.51%
Eye irritation + 0.7826 78.26%
Skin irritation + 0.5296 52.96%
Skin corrosion - 0.9403 94.03%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6139 61.39%
Micronuclear - 0.9500 95.00%
Hepatotoxicity + 0.6426 64.26%
skin sensitisation + 0.6532 65.32%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity - 0.6778 67.78%
Mitochondrial toxicity - 0.8250 82.50%
Nephrotoxicity - 0.7327 73.27%
Acute Oral Toxicity (c) III 0.8528 85.28%
Estrogen receptor binding - 0.9226 92.26%
Androgen receptor binding - 0.9021 90.21%
Thyroid receptor binding - 0.8485 84.85%
Glucocorticoid receptor binding - 0.9049 90.49%
Aromatase binding - 0.8291 82.91%
PPAR gamma - 0.8567 85.67%
Honey bee toxicity - 0.9092 90.92%
Biodegradation + 0.8250 82.50%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.9633 96.33%

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 93.11% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.78% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 84.62% 97.25%
CHEMBL2581 P07339 Cathepsin D 83.76% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 83.44% 94.73%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 81.63% 97.21%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.83% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.53% 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.
Baccharis aliena

Cross-Links

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PubChem 163015296
LOTUS LTS0248772
wikiData Q105346219