9,10-Epoxy-1,5-cyclododecadiene

Details

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Internal ID 81828f99-cab8-4f0e-a6fd-c48221af4ea5
Taxonomy Organoheterocyclic compounds > Epoxides
IUPAC Name (4Z,8Z)-13-oxabicyclo[10.1.0]trideca-4,8-diene
SMILES (Canonical) C1CC=CCCC2C(O2)CCC=C1
SMILES (Isomeric) C1/C=C\CCC2OC2CC/C=C\C1
InChI InChI=1S/C12H18O/c1-2-4-6-8-10-12-11(13-12)9-7-5-3-1/h3-6,11-12H,1-2,7-10H2/b5-3-,6-4-
InChI Key OWUVDWLTQIPNLN-GLIMQPGKSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C12H18O
Molecular Weight 178.27 g/mol
Exact Mass 178.135765193 g/mol
Topological Polar Surface Area (TPSA) 12.50 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.22
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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943-93-1
(4Z,8Z)-13-oxabicyclo[10.1.0]trideca-4,8-diene
13-Oxabicyclo[10.1.0]trideca-4,8-diene
1,2-epoxycyclododeca-5,9-diene
13-Oxabicyclo(10.1.0)trideca-4,8-diene
epoxycyclododeca-5,9-diene
SCHEMBL328857
SCHEMBL328858
AKOS025295947
CS-0458887
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 9,10-Epoxy-1,5-cyclododecadiene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9948 99.48%
Caco-2 + 0.8398 83.98%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Plasma membrane 0.5813 58.13%
OATP2B1 inhibitior - 0.8598 85.98%
OATP1B1 inhibitior + 0.9642 96.42%
OATP1B3 inhibitior + 0.9665 96.65%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.9191 91.91%
P-glycoprotein inhibitior - 0.9541 95.41%
P-glycoprotein substrate - 0.9838 98.38%
CYP3A4 substrate - 0.7174 71.74%
CYP2C9 substrate - 0.8150 81.50%
CYP2D6 substrate - 0.6990 69.90%
CYP3A4 inhibition - 0.9743 97.43%
CYP2C9 inhibition - 0.7861 78.61%
CYP2C19 inhibition - 0.6563 65.63%
CYP2D6 inhibition - 0.9547 95.47%
CYP1A2 inhibition + 0.5553 55.53%
CYP2C8 inhibition - 0.9303 93.03%
CYP inhibitory promiscuity - 0.8306 83.06%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7000 70.00%
Carcinogenicity (trinary) Non-required 0.5169 51.69%
Eye corrosion + 0.8119 81.19%
Eye irritation + 0.9474 94.74%
Skin irritation + 0.7599 75.99%
Skin corrosion - 0.7091 70.91%
Ames mutagenesis - 0.8582 85.82%
Human Ether-a-go-go-Related Gene inhibition + 0.7083 70.83%
Micronuclear - 0.7958 79.58%
Hepatotoxicity + 0.6427 64.27%
skin sensitisation + 0.6800 68.00%
Respiratory toxicity - 0.8778 87.78%
Reproductive toxicity - 0.8111 81.11%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity + 0.7027 70.27%
Acute Oral Toxicity (c) III 0.8574 85.74%
Estrogen receptor binding - 0.9084 90.84%
Androgen receptor binding - 0.8322 83.22%
Thyroid receptor binding - 0.6906 69.06%
Glucocorticoid receptor binding - 0.8431 84.31%
Aromatase binding - 0.8096 80.96%
PPAR gamma - 0.5458 54.58%
Honey bee toxicity - 0.8394 83.94%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity - 0.6599 65.99%

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 86.46% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.00% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.88% 96.09%

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.
Bupleurum chinense
Bupleurum falcatum
Bupleurum scorzonerifolium

Cross-Links

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PubChem 6025413
NPASS NPC140099