5-Methyl-5-prop-1-enylcyclohexa-1,3-diene

Details

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Internal ID 43f6dd8e-bdbe-4e30-95d9-14ad8e60f50a
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Olefins > Cyclic olefins
IUPAC Name 5-methyl-5-prop-1-enylcyclohexa-1,3-diene
SMILES (Canonical) CC=CC1(CC=CC=C1)C
SMILES (Isomeric) CC=CC1(CC=CC=C1)C
InChI InChI=1S/C10H14/c1-3-7-10(2)8-5-4-6-9-10/h3-8H,9H2,1-2H3
InChI Key DLBWDJSQBJZAKF-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 3.50
Atomic LogP (AlogP) 3.08
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-Methyl-5-prop-1-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 + 0.9889 98.89%
Caco-2 + 0.9464 94.64%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Lysosomes 0.6682 66.82%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9087 90.87%
OATP1B3 inhibitior + 0.9389 93.89%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.7424 74.24%
P-glycoprotein inhibitior - 0.9850 98.50%
P-glycoprotein substrate - 0.9349 93.49%
CYP3A4 substrate - 0.6001 60.01%
CYP2C9 substrate - 0.8164 81.64%
CYP2D6 substrate - 0.7848 78.48%
CYP3A4 inhibition - 0.8600 86.00%
CYP2C9 inhibition - 0.8916 89.16%
CYP2C19 inhibition - 0.9308 93.08%
CYP2D6 inhibition - 0.9429 94.29%
CYP1A2 inhibition - 0.8613 86.13%
CYP2C8 inhibition - 0.8989 89.89%
CYP inhibitory promiscuity - 0.8276 82.76%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5564 55.64%
Carcinogenicity (trinary) Warning 0.5096 50.96%
Eye corrosion + 0.9047 90.47%
Eye irritation + 0.9676 96.76%
Skin irritation + 0.8144 81.44%
Skin corrosion - 0.9188 91.88%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6914 69.14%
Micronuclear - 0.9500 95.00%
Hepatotoxicity + 0.7051 70.51%
skin sensitisation + 0.9696 96.96%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity - 0.5222 52.22%
Mitochondrial toxicity - 0.5895 58.95%
Nephrotoxicity + 0.6444 64.44%
Acute Oral Toxicity (c) III 0.8572 85.72%
Estrogen receptor binding - 0.9263 92.63%
Androgen receptor binding - 0.8419 84.19%
Thyroid receptor binding - 0.8522 85.22%
Glucocorticoid receptor binding - 0.8067 80.67%
Aromatase binding - 0.8636 86.36%
PPAR gamma - 0.8626 86.26%
Honey bee toxicity - 0.6996 69.96%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity + 0.9459 94.59%

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
CHEMBL230 P35354 Cyclooxygenase-2 95.53% 89.63%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.44% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 87.71% 90.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.37% 91.11%
CHEMBL1937 Q92769 Histone deacetylase 2 80.72% 94.75%

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.
Artemisia judaica

Cross-Links

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PubChem 86041546
LOTUS LTS0197323
wikiData Q104984091