(2R,3R)-2-hex-5-enyl-3-[(1E,7E)-nona-1,7-dien-3,5-diynyl]oxirane

Details

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Internal ID 51d9da1b-17d8-4160-9365-e30bd17ecd35
Taxonomy Organoheterocyclic compounds > Epoxides
IUPAC Name (2R,3R)-2-hex-5-enyl-3-[(1E,7E)-nona-1,7-dien-3,5-diynyl]oxirane
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H20O/c1-3-5-7-9-10-11-13-15-17-16(18-17)14-12-8-6-4-2/h3-5,13,15-17H,2,6,8,12,14H2,1H3/b5-3+,15-13+/t16-,17-/m1/s1
InChI Key GRIRFVRSWUHHTQ-YZDWNGRYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C17H20O
Molecular Weight 240.34 g/mol
Exact Mass 240.151415257 g/mol
Topological Polar Surface Area (TPSA) 12.50 Ų
XlogP 4.60
Atomic LogP (AlogP) 3.64
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2R,3R)-2-hex-5-enyl-3-[(1E,7E)-nona-1,7-dien-3,5-diynyl]oxirane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9822 98.22%
Caco-2 + 0.5941 59.41%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.3778 37.78%
OATP2B1 inhibitior - 0.8588 85.88%
OATP1B1 inhibitior + 0.8673 86.73%
OATP1B3 inhibitior + 0.9523 95.23%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8740 87.40%
P-glycoprotein inhibitior - 0.8745 87.45%
P-glycoprotein substrate - 0.7697 76.97%
CYP3A4 substrate + 0.5398 53.98%
CYP2C9 substrate + 0.6085 60.85%
CYP2D6 substrate - 0.7869 78.69%
CYP3A4 inhibition - 0.8356 83.56%
CYP2C9 inhibition - 0.7184 71.84%
CYP2C19 inhibition - 0.5294 52.94%
CYP2D6 inhibition - 0.9412 94.12%
CYP1A2 inhibition + 0.5655 56.55%
CYP2C8 inhibition - 0.7724 77.24%
CYP inhibitory promiscuity - 0.5519 55.19%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6628 66.28%
Carcinogenicity (trinary) Non-required 0.4015 40.15%
Eye corrosion + 0.6886 68.86%
Eye irritation - 0.8973 89.73%
Skin irritation + 0.6799 67.99%
Skin corrosion - 0.7017 70.17%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7279 72.79%
Micronuclear - 0.8000 80.00%
Hepatotoxicity - 0.5321 53.21%
skin sensitisation + 0.7248 72.48%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity - 0.8222 82.22%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity + 0.6668 66.68%
Acute Oral Toxicity (c) III 0.7694 76.94%
Estrogen receptor binding + 0.6502 65.02%
Androgen receptor binding - 0.8143 81.43%
Thyroid receptor binding + 0.5473 54.73%
Glucocorticoid receptor binding + 0.6458 64.58%
Aromatase binding + 0.6529 65.29%
PPAR gamma - 0.5109 51.09%
Honey bee toxicity - 0.7242 72.42%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity - 0.3962 39.62%

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
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 88.16% 96.42%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.30% 96.09%
CHEMBL2730 P21980 Protein-glutamine gamma-glutamyltransferase 85.98% 92.38%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.80% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 83.53% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.58% 99.17%
CHEMBL2581 P07339 Cathepsin D 81.03% 98.95%
CHEMBL2996 Q05655 Protein kinase C delta 80.16% 97.79%

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.
Coreopsis venusta

Cross-Links

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PubChem 163189087
LOTUS LTS0001418
wikiData Q105016049