(6S)-2-ethenylbicyclo[4.2.0]oct-1-ene

Details

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Internal ID 705d0acc-8430-4238-b9b3-af776813561a
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name (6S)-2-ethenylbicyclo[4.2.0]oct-1-ene
SMILES (Canonical) C=CC1=C2CCC2CCC1
SMILES (Isomeric) C=CC1=C2CC[C@@H]2CCC1
InChI InChI=1S/C10H14/c1-2-8-4-3-5-9-6-7-10(8)9/h2,9H,1,3-7H2/t9-/m0/s1
InChI Key CCJGZHPMTLFOLZ-VIFPVBQESA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H14
Molecular Weight 134.22 g/mol
Exact Mass 134.109550447 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 2.70
Atomic LogP (AlogP) 3.06
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (6S)-2-ethenylbicyclo[4.2.0]oct-1-ene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9904 99.04%
Caco-2 + 0.8590 85.90%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Lysosomes 0.6317 63.17%
OATP2B1 inhibitior - 0.8465 84.65%
OATP1B1 inhibitior + 0.9530 95.30%
OATP1B3 inhibitior + 0.9554 95.54%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.9311 93.11%
P-glycoprotein inhibitior - 0.9880 98.80%
P-glycoprotein substrate - 0.9620 96.20%
CYP3A4 substrate - 0.6704 67.04%
CYP2C9 substrate - 0.8012 80.12%
CYP2D6 substrate - 0.6838 68.38%
CYP3A4 inhibition - 0.8830 88.30%
CYP2C9 inhibition - 0.8435 84.35%
CYP2C19 inhibition - 0.7993 79.93%
CYP2D6 inhibition - 0.9093 90.93%
CYP1A2 inhibition - 0.6339 63.39%
CYP2C8 inhibition - 0.8982 89.82%
CYP inhibitory promiscuity - 0.6086 60.86%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Warning 0.5064 50.64%
Eye corrosion + 0.7025 70.25%
Eye irritation + 0.9782 97.82%
Skin irritation + 0.6158 61.58%
Skin corrosion - 0.8776 87.76%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5672 56.72%
Micronuclear - 0.9758 97.58%
Hepatotoxicity + 0.7085 70.85%
skin sensitisation + 0.8305 83.05%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.6778 67.78%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity - 0.6475 64.75%
Acute Oral Toxicity (c) III 0.7738 77.38%
Estrogen receptor binding - 0.9399 93.99%
Androgen receptor binding - 0.7850 78.50%
Thyroid receptor binding - 0.8723 87.23%
Glucocorticoid receptor binding - 0.6824 68.24%
Aromatase binding - 0.7949 79.49%
PPAR gamma - 0.7781 77.81%
Honey bee toxicity - 0.7586 75.86%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9877 98.77%

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
CHEMBL3137262 O60341 LSD1/CoREST complex 84.63% 97.09%
CHEMBL240 Q12809 HERG 84.56% 89.76%
CHEMBL3438 Q05513 Protein kinase C zeta 84.25% 88.48%
CHEMBL1902 P62942 FK506-binding protein 1A 82.20% 97.05%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.54% 91.11%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.48% 95.89%
CHEMBL4246 P42680 Tyrosine-protein kinase TEC 80.79% 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.
Mosla chinensis

Cross-Links

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PubChem 163077299
LOTUS LTS0140959
wikiData Q104953385