Verbenene

Details

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Internal ID 31b2c62e-adbe-4691-90a1-cb1476030258
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Bicyclic monoterpenoids
IUPAC Name 6,6-dimethyl-4-methylidenebicyclo[3.1.1]hept-2-ene
SMILES (Canonical) CC1(C2CC1C(=C)C=C2)C
SMILES (Isomeric) CC1(C2CC1C(=C)C=C2)C
InChI InChI=1S/C10H14/c1-7-4-5-8-6-9(7)10(8,2)3/h4-5,8-9H,1,6H2,2-3H3
InChI Key YOQFOABVDRBYCG-UHFFFAOYSA-N
Popularity 10 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 2.90
Atomic LogP (AlogP) 2.77
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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4080-46-0
6,6-dimethyl-4-methylidenebicyclo[3.1.1]hept-2-ene
DTXSID50423806
4-methylene-6,6-dimethylbicyclo[3.1.1]hept-2-ene
Q67880188

2D Structure

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2D Structure of Verbenene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9921 99.21%
Caco-2 + 0.7508 75.08%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.8857 88.57%
Subcellular localzation Lysosomes 0.7431 74.31%
OATP2B1 inhibitior - 0.8656 86.56%
OATP1B1 inhibitior + 0.9229 92.29%
OATP1B3 inhibitior + 0.9197 91.97%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9298 92.98%
P-glycoprotein inhibitior - 0.9741 97.41%
P-glycoprotein substrate - 0.8824 88.24%
CYP3A4 substrate - 0.5395 53.95%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8098 80.98%
CYP3A4 inhibition - 0.6448 64.48%
CYP2C9 inhibition - 0.7595 75.95%
CYP2C19 inhibition - 0.6021 60.21%
CYP2D6 inhibition - 0.8683 86.83%
CYP1A2 inhibition - 0.7865 78.65%
CYP2C8 inhibition - 0.9660 96.60%
CYP inhibitory promiscuity - 0.5368 53.68%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5500 55.00%
Carcinogenicity (trinary) Non-required 0.5019 50.19%
Eye corrosion - 0.6865 68.65%
Eye irritation + 0.9010 90.10%
Skin irritation + 0.5577 55.77%
Skin corrosion - 0.9343 93.43%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5681 56.81%
Micronuclear - 0.9533 95.33%
Hepatotoxicity + 0.7375 73.75%
skin sensitisation + 0.8939 89.39%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity - 0.5814 58.14%
Nephrotoxicity - 0.5765 57.65%
Acute Oral Toxicity (c) III 0.7748 77.48%
Estrogen receptor binding - 0.9557 95.57%
Androgen receptor binding - 0.6697 66.97%
Thyroid receptor binding - 0.8703 87.03%
Glucocorticoid receptor binding - 0.8272 82.72%
Aromatase binding - 0.9141 91.41%
PPAR gamma - 0.9189 91.89%
Honey bee toxicity - 0.7962 79.62%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.7600 76.00%
Fish aquatic toxicity + 0.9940 99.40%

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 92.13% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.83% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.60% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.35% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.13% 100.00%

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.
Elsholtzia fruticosa
Elsholtzia pilosa
Lavandula stoechas
Liquidambar orientalis
Zea mays

Cross-Links

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PubChem 6427476
NPASS NPC134114
LOTUS LTS0256331
wikiData Q67880188