Azulene

Details

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Internal ID deca3aaa-bb0d-4a2c-8442-84b15ea07f1a
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Olefins > Cyclic olefins > Azulenes
IUPAC Name azulene
SMILES (Canonical) C1=CC=C2C=CC=C2C=C1
SMILES (Isomeric) C1=CC=C2C=CC=C2C=C1
InChI InChI=1S/C10H8/c1-2-5-9-7-4-8-10(9)6-3-1/h1-8H
InChI Key CUFNKYGDVFVPHO-UHFFFAOYSA-N
Popularity 2,256 references in papers

Physical and Chemical Properties

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Molecular Formula C10H8
Molecular Weight 128.17 g/mol
Exact Mass 128.062600255 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.20
Atomic LogP (AlogP) 2.79
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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275-51-4
Cyclopentacycloheptene
Azunamic
Bicyclo[5.3.0]decapentaene
azulen
Bicyclo(5.3.0)decapentaene
EINECS 205-993-6
Bicyclo(5.3.0)-1,3,5,7,9-decapentaene
Bicyclo(5.3.0)-deca-2,4,6,8,10-pentaene
NSC 89248
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Azulene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9949 99.49%
Caco-2 + 0.9771 97.71%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.9286 92.86%
Subcellular localzation Lysosomes 0.8833 88.33%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9855 98.55%
OATP1B3 inhibitior + 0.9678 96.78%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.8293 82.93%
P-glycoprotein inhibitior - 0.9824 98.24%
P-glycoprotein substrate - 0.9930 99.30%
CYP3A4 substrate - 0.8623 86.23%
CYP2C9 substrate - 0.8036 80.36%
CYP2D6 substrate + 0.3525 35.25%
CYP3A4 inhibition - 0.9479 94.79%
CYP2C9 inhibition - 0.9421 94.21%
CYP2C19 inhibition - 0.9206 92.06%
CYP2D6 inhibition - 0.9128 91.28%
CYP1A2 inhibition - 0.6815 68.15%
CYP2C8 inhibition - 0.8612 86.12%
CYP inhibitory promiscuity - 0.8490 84.90%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6217 62.17%
Carcinogenicity (trinary) Warning 0.4807 48.07%
Eye corrosion + 0.9148 91.48%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.9335 93.35%
Skin corrosion - 0.7241 72.41%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7644 76.44%
Micronuclear - 0.7449 74.49%
Hepatotoxicity + 0.9500 95.00%
skin sensitisation + 0.8149 81.49%
Respiratory toxicity - 0.9778 97.78%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity + 0.5975 59.75%
Acute Oral Toxicity (c) III 0.8232 82.32%
Estrogen receptor binding - 0.6484 64.84%
Androgen receptor binding - 0.5883 58.83%
Thyroid receptor binding - 0.8039 80.39%
Glucocorticoid receptor binding - 0.8727 87.27%
Aromatase binding - 0.7175 71.75%
PPAR gamma - 0.8126 81.26%
Honey bee toxicity - 0.9427 94.27%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.9900 99.00%
Fish aquatic toxicity + 0.8182 81.82%

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
CHEMBL221 P23219 Cyclooxygenase-1 90.37% 90.17%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 89.07% 94.62%
CHEMBL2581 P07339 Cathepsin D 87.92% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.05% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.62% 86.33%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 85.14% 92.08%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 83.60% 94.23%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.62% 95.50%

Cross-Links

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PubChem 9231
NPASS NPC264470
LOTUS LTS0131168
wikiData Q144362