5,6-Dihydro-1,4-dimethyl-7-ethylazulene

Details

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Internal ID 299321c0-2289-4682-815f-bd7c2775d165
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name 7-ethyl-1,4-dimethyl-5,6-dihydroazulene
SMILES (Canonical) CCC1=CC2=C(C=CC2=C(CC1)C)C
SMILES (Isomeric) CCC1=CC2=C(C=CC2=C(CC1)C)C
InChI InChI=1S/C14H18/c1-4-12-7-5-10(2)13-8-6-11(3)14(13)9-12/h6,8-9H,4-5,7H2,1-3H3
InChI Key GMAWSFXIELFLDC-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H18
Molecular Weight 186.29 g/mol
Exact Mass 186.140850574 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 2.70
Atomic LogP (AlogP) 4.32
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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5,6-Dihydro-1,4-dimethyl-7-ethylazulene
18454-89-2

2D Structure

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2D Structure of 5,6-Dihydro-1,4-dimethyl-7-ethylazulene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9950 99.50%
Caco-2 + 0.9847 98.47%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Lysosomes 0.5094 50.94%
OATP2B1 inhibitior - 0.8569 85.69%
OATP1B1 inhibitior + 0.9498 94.98%
OATP1B3 inhibitior + 0.9677 96.77%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.7914 79.14%
P-glycoprotein inhibitior - 0.9739 97.39%
P-glycoprotein substrate - 0.8646 86.46%
CYP3A4 substrate - 0.6197 61.97%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7358 73.58%
CYP3A4 inhibition - 0.9385 93.85%
CYP2C9 inhibition - 0.7999 79.99%
CYP2C19 inhibition - 0.7785 77.85%
CYP2D6 inhibition - 0.8892 88.92%
CYP1A2 inhibition - 0.5147 51.47%
CYP2C8 inhibition - 0.9618 96.18%
CYP inhibitory promiscuity + 0.5000 50.00%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7900 79.00%
Carcinogenicity (trinary) Non-required 0.4382 43.82%
Eye corrosion - 0.8442 84.42%
Eye irritation + 0.9420 94.20%
Skin irritation + 0.5957 59.57%
Skin corrosion - 0.9445 94.45%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6995 69.95%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.7375 73.75%
skin sensitisation + 0.8306 83.06%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity - 0.6889 68.89%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.7387 73.87%
Acute Oral Toxicity (c) III 0.7858 78.58%
Estrogen receptor binding - 0.8999 89.99%
Androgen receptor binding - 0.6656 66.56%
Thyroid receptor binding - 0.7992 79.92%
Glucocorticoid receptor binding - 0.8045 80.45%
Aromatase binding - 0.8107 81.07%
PPAR gamma - 0.8563 85.63%
Honey bee toxicity - 0.9565 95.65%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9921 99.21%

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 94.79% 89.63%
CHEMBL2581 P07339 Cathepsin D 92.44% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.68% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.93% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.95% 91.11%

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.
Catha edulis
Tanacetum annuum

Cross-Links

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PubChem 85705095
NPASS NPC167213
LOTUS LTS0037350
wikiData Q105011553