3,8-Dimethyl-1-propan-2-ylcyclodeca-1,3,7-triene

Details

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Internal ID cf7cd5bd-39ea-4beb-9c16-145738c08a72
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name 3,8-dimethyl-1-propan-2-ylcyclodeca-1,3,7-triene
SMILES (Canonical) CC1=CCCC=C(C=C(CC1)C(C)C)C
SMILES (Isomeric) CC1=CCCC=C(C=C(CC1)C(C)C)C
InChI InChI=1S/C15H24/c1-12(2)15-10-9-13(3)7-5-6-8-14(4)11-15/h7-8,11-12H,5-6,9-10H2,1-4H3
InChI Key QHXWKDFSZKIWAT-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 4.10
Atomic LogP (AlogP) 5.04
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 3,8-Dimethyl-1-propan-2-ylcyclodeca-1,3,7-triene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9933 99.33%
Caco-2 + 0.9118 91.18%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Lysosomes 0.4255 42.55%
OATP2B1 inhibitior - 0.8550 85.50%
OATP1B1 inhibitior + 0.9513 95.13%
OATP1B3 inhibitior + 0.9557 95.57%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.4726 47.26%
P-glycoprotein inhibitior - 0.9494 94.94%
P-glycoprotein substrate - 0.9403 94.03%
CYP3A4 substrate - 0.6635 66.35%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7650 76.50%
CYP3A4 inhibition - 0.9515 95.15%
CYP2C9 inhibition - 0.8556 85.56%
CYP2C19 inhibition - 0.8447 84.47%
CYP2D6 inhibition - 0.9427 94.27%
CYP1A2 inhibition - 0.7131 71.31%
CYP2C8 inhibition - 0.9537 95.37%
CYP inhibitory promiscuity - 0.7471 74.71%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6800 68.00%
Carcinogenicity (trinary) Warning 0.4922 49.22%
Eye corrosion + 0.5247 52.47%
Eye irritation + 0.6090 60.90%
Skin irritation + 0.7729 77.29%
Skin corrosion - 0.9586 95.86%
Ames mutagenesis - 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7315 73.15%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation + 0.9263 92.63%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity - 0.7444 74.44%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity + 0.5867 58.67%
Acute Oral Toxicity (c) III 0.7428 74.28%
Estrogen receptor binding - 0.9512 95.12%
Androgen receptor binding - 0.7686 76.86%
Thyroid receptor binding - 0.5209 52.09%
Glucocorticoid receptor binding - 0.6881 68.81%
Aromatase binding - 0.8240 82.40%
PPAR gamma - 0.6819 68.19%
Honey bee toxicity - 0.9484 94.84%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.9944 99.44%

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
CHEMBL2581 P07339 Cathepsin D 88.93% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.86% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.54% 96.09%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.34% 90.71%
CHEMBL3401 O75469 Pregnane X receptor 80.87% 94.73%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 80.71% 86.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.04% 94.45%

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.
Cupressus macrocarpa

Cross-Links

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PubChem 162943353
LOTUS LTS0188297
wikiData Q105221198