1-methyl-2-oxo-7-prop-1-en-2-yl-5,6,7,8-tetrahydro-3H-azulene-4-carbaldehyde

Details

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Internal ID ef60c191-b3ac-423b-9e54-9bd18aa3de65
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 1-methyl-2-oxo-7-prop-1-en-2-yl-5,6,7,8-tetrahydro-3H-azulene-4-carbaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H18O2/c1-9(2)11-4-5-12(8-16)14-7-15(17)10(3)13(14)6-11/h8,11H,1,4-7H2,2-3H3
InChI Key HIQKUIKVCRGNBQ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H18O2
Molecular Weight 230.30 g/mol
Exact Mass 230.130679813 g/mol
Topological Polar Surface Area (TPSA) 34.10 Ų
XlogP 2.00
Atomic LogP (AlogP) 3.15
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-methyl-2-oxo-7-prop-1-en-2-yl-5,6,7,8-tetrahydro-3H-azulene-4-carbaldehyde

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 + 0.8051 80.51%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.5999 59.99%
OATP2B1 inhibitior - 0.8538 85.38%
OATP1B1 inhibitior + 0.8965 89.65%
OATP1B3 inhibitior + 0.9381 93.81%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior - 0.5809 58.09%
P-glycoprotein inhibitior - 0.9367 93.67%
P-glycoprotein substrate - 0.8593 85.93%
CYP3A4 substrate - 0.5121 51.21%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8570 85.70%
CYP3A4 inhibition - 0.9230 92.30%
CYP2C9 inhibition - 0.8832 88.32%
CYP2C19 inhibition - 0.7992 79.92%
CYP2D6 inhibition - 0.9032 90.32%
CYP1A2 inhibition - 0.6428 64.28%
CYP2C8 inhibition - 0.8699 86.99%
CYP inhibitory promiscuity - 0.9041 90.41%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5901 59.01%
Eye corrosion - 0.9301 93.01%
Eye irritation + 0.7141 71.41%
Skin irritation - 0.5183 51.83%
Skin corrosion - 0.9477 94.77%
Ames mutagenesis - 0.6554 65.54%
Human Ether-a-go-go-Related Gene inhibition - 0.4340 43.40%
Micronuclear - 0.8700 87.00%
Hepatotoxicity + 0.6199 61.99%
skin sensitisation + 0.6854 68.54%
Respiratory toxicity - 0.7667 76.67%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity + 0.5219 52.19%
Acute Oral Toxicity (c) III 0.7168 71.68%
Estrogen receptor binding - 0.6889 68.89%
Androgen receptor binding - 0.6441 64.41%
Thyroid receptor binding - 0.6682 66.82%
Glucocorticoid receptor binding - 0.5090 50.90%
Aromatase binding - 0.7854 78.54%
PPAR gamma - 0.5441 54.41%
Honey bee toxicity - 0.8876 88.76%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.9750 97.50%

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
CHEMBL4040 P28482 MAP kinase ERK2 97.92% 83.82%
CHEMBL1951 P21397 Monoamine oxidase A 95.26% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.57% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.79% 91.11%
CHEMBL2581 P07339 Cathepsin D 89.06% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.49% 100.00%
CHEMBL1902 P62942 FK506-binding protein 1A 84.16% 97.05%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.02% 99.23%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.84% 95.89%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 80.66% 93.00%

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.
Daphne oleoides

Cross-Links

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PubChem 15478916
NPASS NPC3130
LOTUS LTS0154000
wikiData Q105028968