3-Methyl-4-methylenebicyclo(3.2.1)oct-2-ene

Details

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Internal ID 2f2d987f-3284-4a20-b0f4-09325b2c2443
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name 3-methyl-4-methylidenebicyclo[3.2.1]oct-2-ene
SMILES (Canonical) CC1=CC2CCC(C2)C1=C
SMILES (Isomeric) CC1=CC2CCC(C2)C1=C
InChI InChI=1S/C10H14/c1-7-5-9-3-4-10(6-9)8(7)2/h5,9-10H,2-4,6H2,1H3
InChI Key AUDQUDMLUZNYFA-UHFFFAOYSA-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) 2.92
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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3-methyl-4-methylidenebicyclo[3.2.1]oct-2-ene
3-METHYL-4-METHYLENEBICYCLO(3.2.1)OCT-2-ENE
Bicyclo[3.2.1]oct-2-ene, 3-methyl-4-methylene-
DTXSID60866144
AUDQUDMLUZNYFA-UHFFFAOYSA-N
3-Methyl-4-methylenebicyclo[3.2.1]oct-2-ene #

2D Structure

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2D Structure of 3-Methyl-4-methylenebicyclo(3.2.1)oct-2-ene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9888 98.88%
Caco-2 + 0.7750 77.50%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Lysosomes 0.7490 74.90%
OATP2B1 inhibitior - 0.8462 84.62%
OATP1B1 inhibitior + 0.9472 94.72%
OATP1B3 inhibitior + 0.9352 93.52%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8988 89.88%
P-glycoprotein inhibitior - 0.9832 98.32%
P-glycoprotein substrate - 0.8984 89.84%
CYP3A4 substrate - 0.5924 59.24%
CYP2C9 substrate - 0.8092 80.92%
CYP2D6 substrate - 0.7875 78.75%
CYP3A4 inhibition - 0.8929 89.29%
CYP2C9 inhibition - 0.8906 89.06%
CYP2C19 inhibition - 0.7773 77.73%
CYP2D6 inhibition - 0.9149 91.49%
CYP1A2 inhibition - 0.5597 55.97%
CYP2C8 inhibition - 0.9271 92.71%
CYP inhibitory promiscuity - 0.5541 55.41%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7100 71.00%
Carcinogenicity (trinary) Warning 0.4274 42.74%
Eye corrosion + 0.5406 54.06%
Eye irritation + 0.9751 97.51%
Skin irritation + 0.6253 62.53%
Skin corrosion - 0.9648 96.48%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6895 68.95%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.7875 78.75%
skin sensitisation + 0.8833 88.33%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity + 0.5111 51.11%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity + 0.6129 61.29%
Acute Oral Toxicity (c) III 0.8013 80.13%
Estrogen receptor binding - 0.9291 92.91%
Androgen receptor binding - 0.7351 73.51%
Thyroid receptor binding - 0.8834 88.34%
Glucocorticoid receptor binding - 0.7397 73.97%
Aromatase binding - 0.8435 84.35%
PPAR gamma - 0.8238 82.38%
Honey bee toxicity - 0.9246 92.46%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.8300 83.00%
Fish aquatic toxicity + 0.9895 98.95%

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 88.04% 97.09%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 82.70% 97.23%
CHEMBL1907589 P17787 Neuronal acetylcholine receptor; alpha4/beta2 81.71% 94.55%

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.
Juniperus monticola

Cross-Links

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PubChem 39540
LOTUS LTS0191579
wikiData Q104918860