(4aS,8aR)-5,5,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalene-2-carbaldehyde

Details

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Internal ID 9282696b-dd21-4676-b62c-c2aaac538ca6
Taxonomy Organic oxygen compounds > Organic oxides
IUPAC Name (4aS,8aR)-5,5,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalene-2-carbaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H22O/c1-13(2)7-4-8-14(3)9-11(10-15)5-6-12(13)14/h9-10,12H,4-8H2,1-3H3/t12-,14+/m0/s1
InChI Key BMCFYFMNLALBBR-GXTWGEPZSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C14H22O
Molecular Weight 206.32 g/mol
Exact Mass 206.167065321 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 4.30
Atomic LogP (AlogP) 3.74
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 (4aS,8aR)-5,5,8a-trimethyl-3,4,4a,6,7,8-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 + 0.9968 99.68%
Caco-2 + 0.8977 89.77%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Lysosomes 0.4627 46.27%
OATP2B1 inhibitior - 0.8497 84.97%
OATP1B1 inhibitior + 0.8812 88.12%
OATP1B3 inhibitior + 0.8919 89.19%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.7667 76.67%
P-glycoprotein inhibitior - 0.9627 96.27%
P-glycoprotein substrate - 0.9496 94.96%
CYP3A4 substrate + 0.5158 51.58%
CYP2C9 substrate - 0.8129 81.29%
CYP2D6 substrate - 0.8129 81.29%
CYP3A4 inhibition - 0.8953 89.53%
CYP2C9 inhibition - 0.6707 67.07%
CYP2C19 inhibition + 0.5414 54.14%
CYP2D6 inhibition - 0.9334 93.34%
CYP1A2 inhibition - 0.8504 85.04%
CYP2C8 inhibition - 0.8334 83.34%
CYP inhibitory promiscuity - 0.6511 65.11%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7800 78.00%
Carcinogenicity (trinary) Non-required 0.5440 54.40%
Eye corrosion - 0.9401 94.01%
Eye irritation - 0.5178 51.78%
Skin irritation - 0.5546 55.46%
Skin corrosion - 0.9712 97.12%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5401 54.01%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.5215 52.15%
skin sensitisation + 0.8649 86.49%
Respiratory toxicity - 0.7667 76.67%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity - 0.5835 58.35%
Acute Oral Toxicity (c) III 0.7515 75.15%
Estrogen receptor binding - 0.6858 68.58%
Androgen receptor binding - 0.6556 65.56%
Thyroid receptor binding - 0.6205 62.05%
Glucocorticoid receptor binding - 0.7471 74.71%
Aromatase binding - 0.7409 74.09%
PPAR gamma - 0.6228 62.28%
Honey bee toxicity - 0.9332 93.32%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity + 0.6600 66.00%
Fish aquatic toxicity + 0.9970 99.70%

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 91.72% 95.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.89% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.68% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 90.12% 100.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.12% 96.09%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 85.52% 93.40%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.93% 94.45%
CHEMBL2581 P07339 Cathepsin D 83.06% 98.95%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.63% 95.89%

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 101924433
LOTUS LTS0040732
wikiData Q104254577