5-Methyl-8-propan-2-yl-3,4,4a,7,8,8a-hexahydronaphthalene-2-carbaldehyde

Details

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Internal ID d141cf9c-3c02-4c96-8329-26ac9d698385
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 5-methyl-8-propan-2-yl-3,4,4a,7,8,8a-hexahydronaphthalene-2-carbaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H22O/c1-10(2)13-6-4-11(3)14-7-5-12(9-16)8-15(13)14/h4,8-10,13-15H,5-7H2,1-3H3
InChI Key XOJRZWAZKRAFFU-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 3.30
Atomic LogP (AlogP) 3.76
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 5-Methyl-8-propan-2-yl-3,4,4a,7,8,8a-hexahydronaphthalene-2-carbaldehyde

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 + 0.8358 83.58%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Lysosomes 0.4993 49.93%
OATP2B1 inhibitior - 0.8563 85.63%
OATP1B1 inhibitior + 0.8897 88.97%
OATP1B3 inhibitior + 0.9032 90.32%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.7891 78.91%
P-glycoprotein inhibitior - 0.9268 92.68%
P-glycoprotein substrate - 0.8937 89.37%
CYP3A4 substrate - 0.5139 51.39%
CYP2C9 substrate - 0.8062 80.62%
CYP2D6 substrate - 0.8279 82.79%
CYP3A4 inhibition - 0.9596 95.96%
CYP2C9 inhibition - 0.8105 81.05%
CYP2C19 inhibition - 0.6512 65.12%
CYP2D6 inhibition - 0.9210 92.10%
CYP1A2 inhibition - 0.7157 71.57%
CYP2C8 inhibition - 0.9227 92.27%
CYP inhibitory promiscuity - 0.5578 55.78%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7700 77.00%
Carcinogenicity (trinary) Non-required 0.5703 57.03%
Eye corrosion - 0.8393 83.93%
Eye irritation - 0.8476 84.76%
Skin irritation + 0.5724 57.24%
Skin corrosion - 0.8930 89.30%
Ames mutagenesis - 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3674 36.74%
Micronuclear - 0.9500 95.00%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation + 0.9096 90.96%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity + 0.4599 45.99%
Acute Oral Toxicity (c) III 0.6422 64.22%
Estrogen receptor binding - 0.9037 90.37%
Androgen receptor binding - 0.5844 58.44%
Thyroid receptor binding - 0.7344 73.44%
Glucocorticoid receptor binding - 0.6965 69.65%
Aromatase binding - 0.8395 83.95%
PPAR gamma - 0.7692 76.92%
Honey bee toxicity - 0.9116 91.16%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9829 98.29%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.33% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.22% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.01% 100.00%
CHEMBL2581 P07339 Cathepsin D 84.80% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.30% 97.09%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 83.22% 95.89%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.07% 93.56%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.77% 90.71%

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.
Juniperus oxycedrus

Cross-Links

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PubChem 526983
LOTUS LTS0272689
wikiData Q105337774