3a-methyl-1-propan-2-yl-2,3,4,7-tetrahydro-1H-azulene-6-carbaldehyde

Details

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Internal ID ae91a22a-d315-418d-900d-83311700230a
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 3a-methyl-1-propan-2-yl-2,3,4,7-tetrahydro-1H-azulene-6-carbaldehyde
SMILES (Canonical) CC(C)C1CCC2(C1=CCC(=CC2)C=O)C
SMILES (Isomeric) CC(C)C1CCC2(C1=CCC(=CC2)C=O)C
InChI InChI=1S/C15H22O/c1-11(2)13-7-9-15(3)8-6-12(10-16)4-5-14(13)15/h5-6,10-11,13H,4,7-9H2,1-3H3
InChI Key SZOHSTQGGUHULY-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O
Molecular Weight 218.33 g/mol
Exact Mass 218.167065321 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.80
Atomic LogP (AlogP) 3.90
H-Bond Acceptor 1
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 3a-methyl-1-propan-2-yl-2,3,4,7-tetrahydro-1H-azulene-6-carbaldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9948 99.48%
Caco-2 + 0.9297 92.97%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Lysosomes 0.5729 57.29%
OATP2B1 inhibitior - 0.8563 85.63%
OATP1B1 inhibitior + 0.9047 90.47%
OATP1B3 inhibitior + 0.9541 95.41%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior - 0.8202 82.02%
P-glycoprotein inhibitior - 0.9636 96.36%
P-glycoprotein substrate - 0.7937 79.37%
CYP3A4 substrate + 0.5299 52.99%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8425 84.25%
CYP3A4 inhibition - 0.9499 94.99%
CYP2C9 inhibition - 0.6713 67.13%
CYP2C19 inhibition - 0.6523 65.23%
CYP2D6 inhibition - 0.9329 93.29%
CYP1A2 inhibition - 0.7153 71.53%
CYP2C8 inhibition - 0.9041 90.41%
CYP inhibitory promiscuity - 0.8152 81.52%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7600 76.00%
Carcinogenicity (trinary) Non-required 0.5291 52.91%
Eye corrosion - 0.9016 90.16%
Eye irritation - 0.8462 84.62%
Skin irritation + 0.5882 58.82%
Skin corrosion - 0.9692 96.92%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6622 66.22%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.5556 55.56%
skin sensitisation + 0.8174 81.74%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity - 0.7111 71.11%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity + 0.6271 62.71%
Acute Oral Toxicity (c) III 0.8107 81.07%
Estrogen receptor binding - 0.7678 76.78%
Androgen receptor binding - 0.6556 65.56%
Thyroid receptor binding - 0.7802 78.02%
Glucocorticoid receptor binding - 0.7085 70.85%
Aromatase binding - 0.5828 58.28%
PPAR gamma - 0.8821 88.21%
Honey bee toxicity - 0.8761 87.61%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.9919 99.19%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.91% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.33% 95.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.44% 97.25%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.18% 94.45%
CHEMBL2581 P07339 Cathepsin D 88.40% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.77% 91.11%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.02% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.82% 100.00%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 82.60% 93.40%
CHEMBL5203 P33316 dUTP pyrophosphatase 81.62% 99.18%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 80.52% 91.03%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 80.33% 98.33%

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.
Rosa rugosa

Cross-Links

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PubChem 14543557
LOTUS LTS0234138
wikiData Q105264295