7-(2-Hydroxypropan-2-yl)-4-methylazulene-1-carbaldehyde

Details

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Internal ID c2f17c4c-1f45-4572-9edf-900257e700c6
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Guaianes
IUPAC Name 7-(2-hydroxypropan-2-yl)-4-methylazulene-1-carbaldehyde
SMILES (Canonical) CC1=C2C=CC(=C2C=C(C=C1)C(C)(C)O)C=O
SMILES (Isomeric) CC1=C2C=CC(=C2C=C(C=C1)C(C)(C)O)C=O
InChI InChI=1S/C15H16O2/c1-10-4-6-12(15(2,3)17)8-14-11(9-16)5-7-13(10)14/h4-9,17H,1-3H3
InChI Key KFKGAXNLWYAHMT-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H16O2
Molecular Weight 228.29 g/mol
Exact Mass 228.115029749 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 2.40
Atomic LogP (AlogP) 3.14
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-(2-Hydroxypropan-2-yl)-4-methylazulene-1-carbaldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9963 99.63%
Caco-2 + 0.9015 90.15%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.6134 61.34%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8373 83.73%
OATP1B3 inhibitior + 0.9590 95.90%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.4939 49.39%
P-glycoprotein inhibitior - 0.9409 94.09%
P-glycoprotein substrate - 0.8098 80.98%
CYP3A4 substrate - 0.5208 52.08%
CYP2C9 substrate - 0.8060 80.60%
CYP2D6 substrate - 0.7571 75.71%
CYP3A4 inhibition - 0.9040 90.40%
CYP2C9 inhibition - 0.8805 88.05%
CYP2C19 inhibition - 0.8636 86.36%
CYP2D6 inhibition - 0.8607 86.07%
CYP1A2 inhibition - 0.5663 56.63%
CYP2C8 inhibition + 0.4734 47.34%
CYP inhibitory promiscuity - 0.8995 89.95%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.6200 62.00%
Carcinogenicity (trinary) Non-required 0.6009 60.09%
Eye corrosion - 0.6217 62.17%
Eye irritation + 0.9909 99.09%
Skin irritation + 0.6670 66.70%
Skin corrosion - 0.7355 73.55%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7118 71.18%
Micronuclear - 0.7723 77.23%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation - 0.5526 55.26%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.5556 55.56%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity + 0.5277 52.77%
Acute Oral Toxicity (c) III 0.8245 82.45%
Estrogen receptor binding + 0.5711 57.11%
Androgen receptor binding + 0.7561 75.61%
Thyroid receptor binding - 0.4901 49.01%
Glucocorticoid receptor binding + 0.6730 67.30%
Aromatase binding - 0.6152 61.52%
PPAR gamma - 0.4903 49.03%
Honey bee toxicity - 0.9808 98.08%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.7215 72.15%

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
CHEMBL1951 P21397 Monoamine oxidase A 97.67% 91.49%
CHEMBL2581 P07339 Cathepsin D 96.76% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.33% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.53% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 92.49% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.97% 91.11%
CHEMBL3492 P49721 Proteasome Macropain subunit 88.26% 90.24%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.81% 96.00%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 85.74% 93.65%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 84.95% 90.93%
CHEMBL1841 P06241 Tyrosine-protein kinase FYN 82.22% 81.29%
CHEMBL1907 P15144 Aminopeptidase N 82.18% 93.31%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 81.72% 98.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.57% 89.00%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 80.83% 100.00%
CHEMBL4208 P20618 Proteasome component C5 80.04% 90.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 101408066
LOTUS LTS0050911
wikiData Q105140429