2-(4,7-dimethyl-3,4,4a,5,6,8a-hexahydro-2H-naphthalen-1-ylidene)propanal

Details

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Internal ID 641b9bae-3814-4e6c-905d-1be178ced1e6
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 2-(4,7-dimethyl-3,4,4a,5,6,8a-hexahydro-2H-naphthalen-1-ylidene)propanal
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H22O/c1-10-4-6-13-11(2)5-7-14(12(3)9-16)15(13)8-10/h8-9,11,13,15H,4-7H2,1-3H3
InChI Key HKDGBQGANZMYAA-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 3.20
Atomic LogP (AlogP) 3.90
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(4,7-dimethyl-3,4,4a,5,6,8a-hexahydro-2H-naphthalen-1-ylidene)propanal

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 + 0.9478 94.78%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Lysosomes 0.4312 43.12%
OATP2B1 inhibitior - 0.8502 85.02%
OATP1B1 inhibitior + 0.9389 93.89%
OATP1B3 inhibitior + 0.9337 93.37%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.7814 78.14%
P-glycoprotein inhibitior - 0.9136 91.36%
P-glycoprotein substrate - 0.8287 82.87%
CYP3A4 substrate + 0.5107 51.07%
CYP2C9 substrate - 0.8062 80.62%
CYP2D6 substrate - 0.8279 82.79%
CYP3A4 inhibition - 0.8937 89.37%
CYP2C9 inhibition - 0.7908 79.08%
CYP2C19 inhibition - 0.6576 65.76%
CYP2D6 inhibition - 0.9391 93.91%
CYP1A2 inhibition - 0.6207 62.07%
CYP2C8 inhibition - 0.8192 81.92%
CYP inhibitory promiscuity - 0.6047 60.47%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8000 80.00%
Carcinogenicity (trinary) Non-required 0.5234 52.34%
Eye corrosion - 0.8484 84.84%
Eye irritation - 0.8375 83.75%
Skin irritation - 0.5457 54.57%
Skin corrosion - 0.9448 94.48%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7360 73.60%
Micronuclear - 0.9500 95.00%
Hepatotoxicity + 0.6804 68.04%
skin sensitisation + 0.8937 89.37%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity - 0.7849 78.49%
Acute Oral Toxicity (c) III 0.7520 75.20%
Estrogen receptor binding - 0.8991 89.91%
Androgen receptor binding + 0.5302 53.02%
Thyroid receptor binding - 0.6563 65.63%
Glucocorticoid receptor binding - 0.8236 82.36%
Aromatase binding - 0.8290 82.90%
PPAR gamma - 0.6689 66.89%
Honey bee toxicity - 0.8946 89.46%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9962 99.62%

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 92.79% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.20% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.13% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.10% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.08% 89.00%
CHEMBL2581 P07339 Cathepsin D 80.34% 98.95%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 80.18% 94.80%

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.
Artemisia annua

Cross-Links

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PubChem 163004791
LOTUS LTS0119584
wikiData Q105029589