1-Methyl-4-(1,2,2-trimethylcyclopentyl)-1,4-cyclohexadiene

Details

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Internal ID d6077616-7680-4edf-ae9f-2c69d9604598
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 1-methyl-4-(1,2,2-trimethylcyclopentyl)cyclohexa-1,4-diene
SMILES (Canonical) CC1=CCC(=CC1)C2(CCCC2(C)C)C
SMILES (Isomeric) CC1=CCC(=CC1)C2(CCCC2(C)C)C
InChI InChI=1S/C15H24/c1-12-6-8-13(9-7-12)15(4)11-5-10-14(15,2)3/h6,9H,5,7-8,10-11H2,1-4H3
InChI Key MDJJOJZGNNCGHU-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24
Molecular Weight 204.35 g/mol
Exact Mass 204.187800766 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.80
Atomic LogP (AlogP) 4.87
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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MDJJOJZGNNCGHU-UHFFFAOYSA-N
1-Methyl-4-(1,2,2-trimethylcyclopentyl)-1,4-cyclohexadiene

2D Structure

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2D Structure of 1-Methyl-4-(1,2,2-trimethylcyclopentyl)-1,4-cyclohexadiene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9923 99.23%
Caco-2 + 0.9788 97.88%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Lysosomes 0.5307 53.07%
OATP2B1 inhibitior - 0.8501 85.01%
OATP1B1 inhibitior + 0.9450 94.50%
OATP1B3 inhibitior - 0.2206 22.06%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.6967 69.67%
P-glycoprotein inhibitior - 0.9743 97.43%
P-glycoprotein substrate - 0.9467 94.67%
CYP3A4 substrate + 0.5115 51.15%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7625 76.25%
CYP3A4 inhibition - 0.9465 94.65%
CYP2C9 inhibition - 0.8877 88.77%
CYP2C19 inhibition - 0.8640 86.40%
CYP2D6 inhibition - 0.9604 96.04%
CYP1A2 inhibition - 0.8528 85.28%
CYP2C8 inhibition - 0.8991 89.91%
CYP inhibitory promiscuity - 0.5412 54.12%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7700 77.00%
Carcinogenicity (trinary) Non-required 0.4566 45.66%
Eye corrosion - 0.9114 91.14%
Eye irritation + 0.7379 73.79%
Skin irritation + 0.4903 49.03%
Skin corrosion - 0.9865 98.65%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6468 64.68%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.7281 72.81%
skin sensitisation + 0.8372 83.72%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity + 0.4555 45.55%
Acute Oral Toxicity (c) III 0.5765 57.65%
Estrogen receptor binding - 0.8872 88.72%
Androgen receptor binding - 0.6437 64.37%
Thyroid receptor binding - 0.6666 66.66%
Glucocorticoid receptor binding - 0.8340 83.40%
Aromatase binding - 0.7835 78.35%
PPAR gamma - 0.8166 81.66%
Honey bee toxicity - 0.9608 96.08%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.6900 69.00%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 91.77% 86.00%
CHEMBL4072 P07858 Cathepsin B 88.77% 93.67%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.69% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.42% 96.09%

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.
Bazzania trilobata
Platycladus orientalis
Reboulia hemisphaerica

Cross-Links

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PubChem 14830706
NPASS NPC105220
LOTUS LTS0041503
wikiData Q104254532