1,2-Epoxy-7-octene

Details

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Internal ID cbf068d2-c126-4dc5-93c1-2a3e790ae399
Taxonomy Organoheterocyclic compounds > Epoxides
IUPAC Name 2-hex-5-enyloxirane
SMILES (Canonical) C=CCCCCC1CO1
SMILES (Isomeric) C=CCCCCC1CO1
InChI InChI=1S/C8H14O/c1-2-3-4-5-6-8-7-9-8/h2,8H,1,3-7H2
InChI Key UKTHULMXFLCNAV-UHFFFAOYSA-N
Popularity 20 references in papers

Physical and Chemical Properties

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Molecular Formula C8H14O
Molecular Weight 126.20 g/mol
Exact Mass 126.104465066 g/mol
Topological Polar Surface Area (TPSA) 12.50 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.13
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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19600-63-6
2-hex-5-enyloxirane
Oxirane, 5-hexenyl-
5-Hexenyloxirane
7,8-Epoxyoctene
CCRIS 3749
EINECS 243-178-7
BRN 1305290
2-(hex-5-en-1-yl)oxirane
5-17-01-00231 (Beilstein Handbook Reference)
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 1,2-Epoxy-7-octene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9891 98.91%
Caco-2 + 0.8491 84.91%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Mitochondria 0.4104 41.04%
OATP2B1 inhibitior - 0.8550 85.50%
OATP1B1 inhibitior + 0.9543 95.43%
OATP1B3 inhibitior + 0.9550 95.50%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.9402 94.02%
P-glycoprotein inhibitior - 0.9880 98.80%
P-glycoprotein substrate - 0.9367 93.67%
CYP3A4 substrate - 0.6201 62.01%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7077 70.77%
CYP3A4 inhibition - 0.9624 96.24%
CYP2C9 inhibition - 0.7600 76.00%
CYP2C19 inhibition - 0.6509 65.09%
CYP2D6 inhibition - 0.9369 93.69%
CYP1A2 inhibition - 0.5545 55.45%
CYP2C8 inhibition - 0.8809 88.09%
CYP inhibitory promiscuity - 0.7127 71.27%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7228 72.28%
Carcinogenicity (trinary) Non-required 0.5403 54.03%
Eye corrosion + 0.9169 91.69%
Eye irritation + 0.9753 97.53%
Skin irritation + 0.8275 82.75%
Skin corrosion + 0.6490 64.90%
Ames mutagenesis + 0.9900 99.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4894 48.94%
Micronuclear - 0.8400 84.00%
Hepatotoxicity - 0.7250 72.50%
skin sensitisation + 0.7316 73.16%
Respiratory toxicity - 0.8444 84.44%
Reproductive toxicity - 0.8889 88.89%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity - 0.7164 71.64%
Acute Oral Toxicity (c) III 0.8683 86.83%
Estrogen receptor binding - 0.9006 90.06%
Androgen receptor binding - 0.9404 94.04%
Thyroid receptor binding - 0.8489 84.89%
Glucocorticoid receptor binding - 0.6816 68.16%
Aromatase binding - 0.8335 83.35%
PPAR gamma - 0.8157 81.57%
Honey bee toxicity - 0.7040 70.40%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity - 0.5160 51.60%

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 91.36% 91.11%
CHEMBL2730 P21980 Protein-glutamine gamma-glutamyltransferase 87.72% 92.38%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 82.32% 90.24%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.37% 97.09%
CHEMBL4246 P42680 Tyrosine-protein kinase TEC 80.07% 82.05%

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 capillaris

Cross-Links

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PubChem 29678
NPASS NPC46405
LOTUS LTS0038680
wikiData Q82918192