3,7,7-Trimethylbicyclo[4.1.0]hept-1-ene

Details

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Internal ID cf80062b-795d-4453-be1a-0df955308231
Taxonomy Hydrocarbons > Polycyclic hydrocarbons
IUPAC Name 3,7,7-trimethylbicyclo[4.1.0]hept-1-ene
SMILES (Canonical) CC1CCC2C(=C1)C2(C)C
SMILES (Isomeric) CC1CCC2C(=C1)C2(C)C
InChI InChI=1S/C10H16/c1-7-4-5-8-9(6-7)10(8,2)3/h6-8H,4-5H2,1-3H3
InChI Key KALFVDDBBPRATR-UHFFFAOYSA-N
Popularity 373 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16
Molecular Weight 136.23 g/mol
Exact Mass 136.125200510 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.00
Atomic LogP (AlogP) 3.00
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3,7,7-Trimethylbicyclo[4.1.0]hept-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 + 0.9897 98.97%
Caco-2 + 0.6490 64.90%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.8286 82.86%
Subcellular localzation Lysosomes 0.6901 69.01%
OATP2B1 inhibitior - 0.8537 85.37%
OATP1B1 inhibitior + 0.9067 90.67%
OATP1B3 inhibitior + 0.9059 90.59%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.9621 96.21%
P-glycoprotein inhibitior - 0.9697 96.97%
P-glycoprotein substrate - 0.9437 94.37%
CYP3A4 substrate - 0.5984 59.84%
CYP2C9 substrate - 0.7890 78.90%
CYP2D6 substrate - 0.7441 74.41%
CYP3A4 inhibition - 0.9218 92.18%
CYP2C9 inhibition - 0.8030 80.30%
CYP2C19 inhibition - 0.7575 75.75%
CYP2D6 inhibition - 0.9010 90.10%
CYP1A2 inhibition - 0.7587 75.87%
CYP2C8 inhibition - 0.9821 98.21%
CYP inhibitory promiscuity - 0.7757 77.57%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6800 68.00%
Carcinogenicity (trinary) Warning 0.4529 45.29%
Eye corrosion - 0.8948 89.48%
Eye irritation + 0.8674 86.74%
Skin irritation + 0.7229 72.29%
Skin corrosion - 0.9318 93.18%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6658 66.58%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.7500 75.00%
skin sensitisation + 0.8239 82.39%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity + 0.5660 56.60%
Nephrotoxicity - 0.5648 56.48%
Acute Oral Toxicity (c) III 0.8435 84.35%
Estrogen receptor binding - 0.9332 93.32%
Androgen receptor binding - 0.8700 87.00%
Thyroid receptor binding - 0.8591 85.91%
Glucocorticoid receptor binding - 0.8432 84.32%
Aromatase binding - 0.8828 88.28%
PPAR gamma - 0.9154 91.54%
Honey bee toxicity - 0.9531 95.31%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity + 0.8200 82.00%
Fish aquatic toxicity + 0.9839 98.39%

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 90.29% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.52% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.20% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 84.32% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.26% 95.56%
CHEMBL2581 P07339 Cathepsin D 81.64% 98.95%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.22% 95.89%

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.
Forsythia viridissima
Zea mays

Cross-Links

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PubChem 14568304
LOTUS LTS0063902
wikiData Q105137888