(3S)-2,2-dimethyl-3-[(2E)-3-methylpenta-2,4-dienyl]oxirane

Details

Top
Internal ID dfc0d4f0-e338-4571-a2a0-278a38941ea1
Taxonomy Organoheterocyclic compounds > Epoxides
IUPAC Name (3S)-2,2-dimethyl-3-[(2E)-3-methylpenta-2,4-dienyl]oxirane
SMILES (Canonical) CC(=CCC1C(O1)(C)C)C=C
SMILES (Isomeric) C/C(=C\C[C@H]1C(O1)(C)C)/C=C
InChI InChI=1S/C10H16O/c1-5-8(2)6-7-9-10(3,4)11-9/h5-6,9H,1,7H2,2-4H3/b8-6+/t9-/m0/s1
InChI Key LIMXJCIGROLRED-ORZBULNSSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C10H16O
Molecular Weight 152.23 g/mol
Exact Mass 152.120115130 g/mol
Topological Polar Surface Area (TPSA) 12.50 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.69
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (3S)-2,2-dimethyl-3-[(2E)-3-methylpenta-2,4-dienyl]oxirane

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9877 98.77%
Caco-2 + 0.6668 66.68%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Lysosomes 0.4498 44.98%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9085 90.85%
OATP1B3 inhibitior + 0.9308 93.08%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.7853 78.53%
P-glycoprotein inhibitior - 0.9771 97.71%
P-glycoprotein substrate - 0.9350 93.50%
CYP3A4 substrate - 0.5475 54.75%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate - 0.7659 76.59%
CYP3A4 inhibition - 0.8511 85.11%
CYP2C9 inhibition - 0.5973 59.73%
CYP2C19 inhibition + 0.6187 61.87%
CYP2D6 inhibition - 0.9346 93.46%
CYP1A2 inhibition - 0.5210 52.10%
CYP2C8 inhibition - 0.8670 86.70%
CYP inhibitory promiscuity - 0.5597 55.97%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5344 53.44%
Carcinogenicity (trinary) Non-required 0.4930 49.30%
Eye corrosion - 0.7843 78.43%
Eye irritation + 0.8544 85.44%
Skin irritation + 0.6842 68.42%
Skin corrosion - 0.9055 90.55%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5752 57.52%
Micronuclear - 0.7600 76.00%
Hepatotoxicity - 0.5571 55.71%
skin sensitisation + 0.9332 93.32%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity - 0.8778 87.78%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity + 0.6499 64.99%
Acute Oral Toxicity (c) III 0.7644 76.44%
Estrogen receptor binding - 0.8619 86.19%
Androgen receptor binding - 0.7850 78.50%
Thyroid receptor binding - 0.8631 86.31%
Glucocorticoid receptor binding - 0.8087 80.87%
Aromatase binding - 0.8939 89.39%
PPAR gamma - 0.7102 71.02%
Honey bee toxicity - 0.7329 73.29%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.7942 79.42%

Targets

Top

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 92.18% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.45% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.46% 85.14%
CHEMBL233 P35372 Mu opioid receptor 85.07% 97.93%
CHEMBL3401 O75469 Pregnane X receptor 83.49% 94.73%

Plants that contains it

Top
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.
Hesperis matronalis

Cross-Links

Top
PubChem 10898884
LOTUS LTS0052651
wikiData Q105128167