(4aS,5R,8S,8aR)-8-hydroxy-5-methyl-8-propan-2-yl-4,4a,5,6,7,8a-hexahydro-3H-naphthalene-2-carbaldehyde

Details

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Internal ID caa40f35-7382-480b-907a-0b4294d5cddc
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (4aS,5R,8S,8aR)-8-hydroxy-5-methyl-8-propan-2-yl-4,4a,5,6,7,8a-hexahydro-3H-naphthalene-2-carbaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24O2/c1-10(2)15(17)7-6-11(3)13-5-4-12(9-16)8-14(13)15/h8-11,13-14,17H,4-7H2,1-3H3/t11-,13+,14+,15+/m1/s1
InChI Key LKWJJVMGCJTHQE-UNQGMJICSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O2
Molecular Weight 236.35 g/mol
Exact Mass 236.177630004 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.95
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 (4aS,5R,8S,8aR)-8-hydroxy-5-methyl-8-propan-2-yl-4,4a,5,6,7,8a-hexahydro-3H-naphthalene-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 + 0.8613 86.13%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.7277 72.77%
OATP2B1 inhibitior - 0.8534 85.34%
OATP1B1 inhibitior + 0.9120 91.20%
OATP1B3 inhibitior + 0.9645 96.45%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior + 0.6000 60.00%
BSEP inhibitior - 0.8429 84.29%
P-glycoprotein inhibitior - 0.9383 93.83%
P-glycoprotein substrate - 0.8013 80.13%
CYP3A4 substrate + 0.5399 53.99%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8526 85.26%
CYP3A4 inhibition - 0.8349 83.49%
CYP2C9 inhibition - 0.7382 73.82%
CYP2C19 inhibition - 0.5647 56.47%
CYP2D6 inhibition - 0.9400 94.00%
CYP1A2 inhibition - 0.8665 86.65%
CYP2C8 inhibition - 0.9298 92.98%
CYP inhibitory promiscuity - 0.8924 89.24%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5459 54.59%
Eye corrosion - 0.9879 98.79%
Eye irritation - 0.9232 92.32%
Skin irritation + 0.5933 59.33%
Skin corrosion - 0.9727 97.27%
Ames mutagenesis - 0.8170 81.70%
Human Ether-a-go-go-Related Gene inhibition - 0.5446 54.46%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.7053 70.53%
skin sensitisation + 0.6858 68.58%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity - 0.7981 79.81%
Acute Oral Toxicity (c) III 0.8772 87.72%
Estrogen receptor binding - 0.6537 65.37%
Androgen receptor binding + 0.5372 53.72%
Thyroid receptor binding - 0.5513 55.13%
Glucocorticoid receptor binding - 0.5223 52.23%
Aromatase binding - 0.7651 76.51%
PPAR gamma - 0.8025 80.25%
Honey bee toxicity - 0.8950 89.50%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.9760 97.60%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.27% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.74% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.54% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.61% 95.56%
CHEMBL2581 P07339 Cathepsin D 88.75% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.31% 100.00%
CHEMBL4227 P25090 Lipoxin A4 receptor 84.69% 100.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 83.60% 94.80%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.44% 94.45%

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.
Fabiana imbricata

Cross-Links

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PubChem 163000610
LOTUS LTS0213710
wikiData Q105153320