Azulenalkohol

Details

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Internal ID 380c7dec-a0f1-4305-8bd1-8b7986248410
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Olefins > Cyclic olefins > Azulenes
IUPAC Name azulen-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H8O/c11-10-7-6-8-4-2-1-3-5-9(8)10/h1-7,11H
InChI Key VETGQECQXHDROF-UHFFFAOYSA-N
Popularity 21 references in papers

Physical and Chemical Properties

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Molecular Formula C10H8O
Molecular Weight 144.17 g/mol
Exact Mass 144.057514874 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.50
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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SCHEMBL219224

2D Structure

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2D Structure of Azulenalkohol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.9678 96.78%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.4402 44.02%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9622 96.22%
OATP1B3 inhibitior + 0.9623 96.23%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.8559 85.59%
P-glycoprotein inhibitior - 0.9783 97.83%
P-glycoprotein substrate - 0.9893 98.93%
CYP3A4 substrate - 0.7745 77.45%
CYP2C9 substrate - 0.8333 83.33%
CYP2D6 substrate + 0.3949 39.49%
CYP3A4 inhibition - 0.9576 95.76%
CYP2C9 inhibition - 0.8139 81.39%
CYP2C19 inhibition - 0.7547 75.47%
CYP2D6 inhibition - 0.8482 84.82%
CYP1A2 inhibition + 0.7549 75.49%
CYP2C8 inhibition - 0.6529 65.29%
CYP inhibitory promiscuity - 0.8784 87.84%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7108 71.08%
Carcinogenicity (trinary) Non-required 0.4623 46.23%
Eye corrosion + 0.7654 76.54%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.8697 86.97%
Skin corrosion + 0.7874 78.74%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8322 83.22%
Micronuclear - 0.7070 70.70%
Hepatotoxicity + 0.6750 67.50%
skin sensitisation + 0.8384 83.84%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity + 0.5111 51.11%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity + 0.6446 64.46%
Acute Oral Toxicity (c) II 0.5694 56.94%
Estrogen receptor binding - 0.4894 48.94%
Androgen receptor binding + 0.5402 54.02%
Thyroid receptor binding - 0.6532 65.32%
Glucocorticoid receptor binding - 0.7946 79.46%
Aromatase binding - 0.7050 70.50%
PPAR gamma + 0.5362 53.62%
Honey bee toxicity - 0.9632 96.32%
Biodegradation + 0.7750 77.50%
Crustacea aquatic toxicity + 0.6600 66.00%
Fish aquatic toxicity + 0.6496 64.96%

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 93.62% 98.95%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 92.76% 99.15%
CHEMBL1951 P21397 Monoamine oxidase A 92.19% 91.49%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.87% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.47% 95.56%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 86.05% 94.62%
CHEMBL5284 Q96RR4 CaM-kinase kinase beta 85.69% 89.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.38% 86.33%
CHEMBL242 Q92731 Estrogen receptor beta 84.69% 98.35%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 84.63% 95.50%
CHEMBL221 P23219 Cyclooxygenase-1 84.45% 90.17%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 81.51% 91.71%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 80.86% 94.08%

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.
Micromeria sinaica

Cross-Links

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PubChem 14446361
LOTUS LTS0096021
wikiData Q105284845