(2R,3R)-2-hept-6-enyl-3-penta-2,4-diynyloxirane

Details

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Internal ID d4844283-55fc-4efa-aa3c-7724c50597b4
Taxonomy Organoheterocyclic compounds > Epoxides
IUPAC Name (2R,3R)-2-hept-6-enyl-3-penta-2,4-diynyloxirane
SMILES (Canonical) C=CCCCCCC1C(O1)CC#CC#C
SMILES (Isomeric) C=CCCCCC[C@@H]1[C@H](O1)CC#CC#C
InChI InChI=1S/C14H18O/c1-3-5-7-8-10-12-14-13(15-14)11-9-6-4-2/h2-3,13-14H,1,5,7-8,10-12H2/t13-,14-/m1/s1
InChI Key TVKDYKYMRUCXKP-ZIAGYGMSSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H18O
Molecular Weight 202.29 g/mol
Exact Mass 202.135765193 g/mol
Topological Polar Surface Area (TPSA) 12.50 Ų
XlogP 3.90
Atomic LogP (AlogP) 2.92
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2R,3R)-2-hept-6-enyl-3-penta-2,4-diynyloxirane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9824 98.24%
Caco-2 + 0.6482 64.82%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Plasma membrane 0.4484 44.84%
OATP2B1 inhibitior - 0.8566 85.66%
OATP1B1 inhibitior + 0.9048 90.48%
OATP1B3 inhibitior + 0.9481 94.81%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.8812 88.12%
P-glycoprotein inhibitior - 0.9522 95.22%
P-glycoprotein substrate - 0.8968 89.68%
CYP3A4 substrate + 0.5000 50.00%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7387 73.87%
CYP3A4 inhibition - 0.9014 90.14%
CYP2C9 inhibition - 0.6683 66.83%
CYP2C19 inhibition - 0.5585 55.85%
CYP2D6 inhibition - 0.9407 94.07%
CYP1A2 inhibition + 0.5226 52.26%
CYP2C8 inhibition - 0.6855 68.55%
CYP inhibitory promiscuity - 0.5891 58.91%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6728 67.28%
Carcinogenicity (trinary) Non-required 0.5081 50.81%
Eye corrosion + 0.6986 69.86%
Eye irritation - 0.8846 88.46%
Skin irritation + 0.6865 68.65%
Skin corrosion - 0.6159 61.59%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.8300 83.00%
Hepatotoxicity - 0.5143 51.43%
skin sensitisation + 0.6981 69.81%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity - 0.8222 82.22%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity + 0.7152 71.52%
Acute Oral Toxicity (c) III 0.8366 83.66%
Estrogen receptor binding - 0.5000 50.00%
Androgen receptor binding - 0.8422 84.22%
Thyroid receptor binding - 0.6060 60.60%
Glucocorticoid receptor binding + 0.6557 65.57%
Aromatase binding - 0.6828 68.28%
PPAR gamma - 0.5922 59.22%
Honey bee toxicity - 0.6925 69.25%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.6600 66.00%
Fish aquatic toxicity + 0.7444 74.44%

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 91.76% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 89.38% 90.17%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 87.52% 89.34%
CHEMBL226 P30542 Adenosine A1 receptor 87.15% 95.93%
CHEMBL203 P00533 Epidermal growth factor receptor erbB1 86.75% 97.34%
CHEMBL5251 Q06187 Tyrosine-protein kinase BTK 85.18% 98.51%
CHEMBL1829 O15379 Histone deacetylase 3 84.55% 95.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.43% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 82.77% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.73% 99.17%
CHEMBL2730 P21980 Protein-glutamine gamma-glutamyltransferase 82.11% 92.38%

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.
Panax ginseng

Cross-Links

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PubChem 162875475
LOTUS LTS0238522
wikiData Q105265359