1-But-2-enylcyclohexa-1,3-diene

Details

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Internal ID 03a0084e-a31e-4647-9ede-4a296d3d1e07
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name 1-but-2-enylcyclohexa-1,3-diene
SMILES (Canonical) CC=CCC1=CC=CCC1
SMILES (Isomeric) CC=CCC1=CC=CCC1
InChI InChI=1S/C10H14/c1-2-3-7-10-8-5-4-6-9-10/h2-5,8H,6-7,9H2,1H3
InChI Key KRIFSZAXQKBLQM-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 3.00
Atomic LogP (AlogP) 3.23
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-But-2-enylcyclohexa-1,3-diene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9914 99.14%
Caco-2 + 0.9338 93.38%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Lysosomes 0.4906 49.06%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9261 92.61%
OATP1B3 inhibitior + 0.9464 94.64%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.9054 90.54%
P-glycoprotein inhibitior - 0.9899 98.99%
P-glycoprotein substrate - 0.9096 90.96%
CYP3A4 substrate - 0.7007 70.07%
CYP2C9 substrate - 0.8164 81.64%
CYP2D6 substrate - 0.7603 76.03%
CYP3A4 inhibition - 0.9121 91.21%
CYP2C9 inhibition - 0.9261 92.61%
CYP2C19 inhibition - 0.8762 87.62%
CYP2D6 inhibition - 0.9180 91.80%
CYP1A2 inhibition - 0.6077 60.77%
CYP2C8 inhibition - 0.9339 93.39%
CYP inhibitory promiscuity + 0.5983 59.83%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6200 62.00%
Carcinogenicity (trinary) Warning 0.4695 46.95%
Eye corrosion + 0.9368 93.68%
Eye irritation + 0.9846 98.46%
Skin irritation + 0.8478 84.78%
Skin corrosion - 0.8734 87.34%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5400 54.00%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.6298 62.98%
skin sensitisation + 0.9586 95.86%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity - 0.5778 57.78%
Mitochondrial toxicity - 0.7750 77.50%
Nephrotoxicity - 0.7447 74.47%
Acute Oral Toxicity (c) III 0.7619 76.19%
Estrogen receptor binding - 0.8977 89.77%
Androgen receptor binding - 0.8605 86.05%
Thyroid receptor binding - 0.8435 84.35%
Glucocorticoid receptor binding - 0.8062 80.62%
Aromatase binding - 0.8814 88.14%
PPAR gamma - 0.8348 83.48%
Honey bee toxicity - 0.9377 93.77%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.9706 97.06%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.09% 96.09%
CHEMBL3492 P49721 Proteasome Macropain subunit 90.36% 90.24%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.20% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.92% 95.56%
CHEMBL4208 P20618 Proteasome component C5 84.95% 90.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.41% 97.09%

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.
Ligusticum grayi

Cross-Links

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PubChem 162866956
LOTUS LTS0109508
wikiData Q105145032