1-Pent-2-enylcyclohexa-1,3-diene

Details

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Internal ID 111f65f4-d3a4-416d-ba7c-ded710ee3f66
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name 1-pent-2-enylcyclohexa-1,3-diene
SMILES (Canonical) CCC=CCC1=CC=CCC1
SMILES (Isomeric) CCC=CCC1=CC=CCC1
InChI InChI=1S/C11H16/c1-2-3-5-8-11-9-6-4-7-10-11/h3-6,9H,2,7-8,10H2,1H3
InChI Key AIELHXXAVIMENK-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C11H16
Molecular Weight 148.24 g/mol
Exact Mass 148.125200510 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.50
Atomic LogP (AlogP) 3.62
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-Pent-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 + 0.9684 96.84%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Lysosomes 0.4515 45.15%
OATP2B1 inhibitior - 0.8663 86.63%
OATP1B1 inhibitior + 0.9174 91.74%
OATP1B3 inhibitior + 0.9421 94.21%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8981 89.81%
P-glycoprotein inhibitior - 0.9898 98.98%
P-glycoprotein substrate - 0.9074 90.74%
CYP3A4 substrate - 0.6780 67.80%
CYP2C9 substrate - 0.8164 81.64%
CYP2D6 substrate - 0.7603 76.03%
CYP3A4 inhibition - 0.9246 92.46%
CYP2C9 inhibition - 0.9045 90.45%
CYP2C19 inhibition - 0.8913 89.13%
CYP2D6 inhibition - 0.9180 91.80%
CYP1A2 inhibition - 0.5908 59.08%
CYP2C8 inhibition - 0.9104 91.04%
CYP inhibitory promiscuity + 0.7290 72.90%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5800 58.00%
Carcinogenicity (trinary) Warning 0.5285 52.85%
Eye corrosion + 0.9130 91.30%
Eye irritation + 0.9814 98.14%
Skin irritation + 0.7548 75.48%
Skin corrosion - 0.9700 97.00%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5478 54.78%
Micronuclear - 0.9400 94.00%
Hepatotoxicity - 0.5625 56.25%
skin sensitisation + 0.9692 96.92%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity - 0.6556 65.56%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity - 0.7342 73.42%
Acute Oral Toxicity (c) III 0.8634 86.34%
Estrogen receptor binding - 0.8911 89.11%
Androgen receptor binding - 0.8749 87.49%
Thyroid receptor binding - 0.8220 82.20%
Glucocorticoid receptor binding - 0.8059 80.59%
Aromatase binding - 0.8829 88.29%
PPAR gamma - 0.6556 65.56%
Honey bee toxicity - 0.9332 93.32%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9641 96.41%

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 88.97% 96.09%
CHEMBL4208 P20618 Proteasome component C5 84.82% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.81% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.12% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 80.74% 90.17%

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 86022408
LOTUS LTS0014042
wikiData Q104912685