(1S,4aS,8aS)-2,5,5,8a-tetramethyl-1,4,4a,6,7,8-hexahydronaphthalene-1-carbaldehyde

Details

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Internal ID cc415804-06c4-49bf-ae54-126b06222acb
Taxonomy Organic oxygen compounds > Organic oxides
IUPAC Name (1S,4aS,8aS)-2,5,5,8a-tetramethyl-1,4,4a,6,7,8-hexahydronaphthalene-1-carbaldehyde
SMILES (Canonical) CC1=CCC2C(CCCC2(C1C=O)C)(C)C
SMILES (Isomeric) CC1=CC[C@@H]2[C@@]([C@H]1C=O)(CCCC2(C)C)C
InChI InChI=1S/C15H24O/c1-11-6-7-13-14(2,3)8-5-9-15(13,4)12(11)10-16/h6,10,12-13H,5,7-9H2,1-4H3/t12-,13-,15+/m0/s1
InChI Key TUWKAEMGKORGLZ-KCQAQPDRSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C15H24O
Molecular Weight 220.35 g/mol
Exact Mass 220.182715385 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 4.00
Atomic LogP (AlogP) 3.98
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 (1S,4aS,8aS)-2,5,5,8a-tetramethyl-1,4,4a,6,7,8-hexahydronaphthalene-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 + 0.9969 99.69%
Caco-2 + 0.8379 83.79%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Lysosomes 0.4686 46.86%
OATP2B1 inhibitior - 0.8506 85.06%
OATP1B1 inhibitior + 0.8587 85.87%
OATP1B3 inhibitior + 0.8172 81.72%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.8611 86.11%
P-glycoprotein inhibitior - 0.9509 95.09%
P-glycoprotein substrate - 0.9518 95.18%
CYP3A4 substrate + 0.5285 52.85%
CYP2C9 substrate - 0.6147 61.47%
CYP2D6 substrate - 0.7806 78.06%
CYP3A4 inhibition - 0.8822 88.22%
CYP2C9 inhibition - 0.7553 75.53%
CYP2C19 inhibition - 0.5239 52.39%
CYP2D6 inhibition - 0.9473 94.73%
CYP1A2 inhibition - 0.8383 83.83%
CYP2C8 inhibition - 0.8579 85.79%
CYP inhibitory promiscuity - 0.5705 57.05%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7900 79.00%
Carcinogenicity (trinary) Non-required 0.5546 55.46%
Eye corrosion - 0.9706 97.06%
Eye irritation - 0.5561 55.61%
Skin irritation - 0.5608 56.08%
Skin corrosion - 0.9756 97.56%
Ames mutagenesis - 0.9300 93.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4580 45.80%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.5334 53.34%
skin sensitisation + 0.8693 86.93%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity - 0.6268 62.68%
Acute Oral Toxicity (c) III 0.6993 69.93%
Estrogen receptor binding - 0.7825 78.25%
Androgen receptor binding - 0.5645 56.45%
Thyroid receptor binding - 0.6179 61.79%
Glucocorticoid receptor binding - 0.8468 84.68%
Aromatase binding - 0.8182 81.82%
PPAR gamma - 0.8423 84.23%
Honey bee toxicity - 0.9126 91.26%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.31% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.31% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.15% 91.11%
CHEMBL1937 Q92769 Histone deacetylase 2 87.71% 94.75%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.10% 100.00%
CHEMBL1871 P10275 Androgen Receptor 84.36% 96.43%
CHEMBL3401 O75469 Pregnane X receptor 83.66% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.97% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.76% 86.33%
CHEMBL6007 O75762 Transient receptor potential cation channel subfamily A member 1 81.35% 92.17%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 80.55% 86.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.24% 97.09%

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.
Bazzania trilobata

Cross-Links

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PubChem 11031395
LOTUS LTS0149615
wikiData Q105265081