1,5-Dimethyl-8-propan-2-ylazulene

Details

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Internal ID 82baa9e5-d368-4a4c-8c50-97b67d129956
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Olefins > Cyclic olefins > Azulenes
IUPAC Name 1,5-dimethyl-8-propan-2-ylazulene
SMILES (Canonical) CC1=CC2=CC=C(C2=C(C=C1)C(C)C)C
SMILES (Isomeric) CC1=CC2=CC=C(C2=C(C=C1)C(C)C)C
InChI InChI=1S/C15H18/c1-10(2)14-8-5-11(3)9-13-7-6-12(4)15(13)14/h5-10H,1-4H3
InChI Key DBZHHRPNWDNKNX-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H18
Molecular Weight 198.30 g/mol
Exact Mass 198.140850574 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.80
Atomic LogP (AlogP) 4.53
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 1,5-Dimethyl-8-propan-2-ylazulene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9962 99.62%
Caco-2 + 0.9359 93.59%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Lysosomes 0.7827 78.27%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9646 96.46%
OATP1B3 inhibitior + 0.9642 96.42%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.7304 73.04%
P-glycoprotein inhibitior - 0.9349 93.49%
P-glycoprotein substrate - 0.9031 90.31%
CYP3A4 substrate - 0.7072 70.72%
CYP2C9 substrate - 0.7802 78.02%
CYP2D6 substrate + 0.3462 34.62%
CYP3A4 inhibition - 0.9298 92.98%
CYP2C9 inhibition - 0.9051 90.51%
CYP2C19 inhibition - 0.8945 89.45%
CYP2D6 inhibition - 0.8698 86.98%
CYP1A2 inhibition - 0.6173 61.73%
CYP2C8 inhibition - 0.7288 72.88%
CYP inhibitory promiscuity - 0.8212 82.12%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6200 62.00%
Carcinogenicity (trinary) Warning 0.4146 41.46%
Eye corrosion + 0.6733 67.33%
Eye irritation + 0.9517 95.17%
Skin irritation + 0.7366 73.66%
Skin corrosion - 0.9481 94.81%
Ames mutagenesis - 0.5354 53.54%
Human Ether-a-go-go-Related Gene inhibition + 0.7165 71.65%
Micronuclear - 0.8875 88.75%
Hepatotoxicity + 0.7875 78.75%
skin sensitisation + 0.6918 69.18%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity - 0.5222 52.22%
Mitochondrial toxicity - 0.6500 65.00%
Nephrotoxicity - 0.7246 72.46%
Acute Oral Toxicity (c) III 0.7976 79.76%
Estrogen receptor binding - 0.6442 64.42%
Androgen receptor binding - 0.7067 70.67%
Thyroid receptor binding - 0.5165 51.65%
Glucocorticoid receptor binding - 0.7293 72.93%
Aromatase binding - 0.5585 55.85%
PPAR gamma - 0.6936 69.36%
Honey bee toxicity - 0.8847 88.47%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.7500 75.00%
Fish aquatic toxicity + 0.9266 92.66%

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 94.71% 98.95%
CHEMBL260 Q16539 MAP kinase p38 alpha 91.97% 97.78%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 90.47% 97.23%
CHEMBL4581 P52732 Kinesin-like protein 1 90.41% 93.18%
CHEMBL1907 P15144 Aminopeptidase N 89.81% 93.31%
CHEMBL3401 O75469 Pregnane X receptor 88.91% 94.73%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 88.48% 99.15%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.73% 95.56%
CHEMBL3961 Q15759 MAP kinase p38 beta 85.77% 94.75%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 85.29% 93.65%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.99% 96.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.69% 96.09%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 84.61% 96.21%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.91% 91.11%
CHEMBL284 P27487 Dipeptidyl peptidase IV 82.71% 95.69%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.66% 90.71%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.34% 93.56%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 80.93% 100.00%

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.
Achillea alpina

Cross-Links

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PubChem 163035097
LOTUS LTS0240230
wikiData Q104975044