2-(5-Formyl-4-hydroxy-1,2,4a-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)acetic acid

Details

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Internal ID 3dc9f53d-b195-4d05-88e6-fc941564fa42
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Cyclic alcohols and derivatives
IUPAC Name 2-(5-formyl-4-hydroxy-1,2,4a-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)acetic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H24O4/c1-10-7-13(18)16(3)11(9-17)5-4-6-12(16)15(10,2)8-14(19)20/h5,9-10,12-13,18H,4,6-8H2,1-3H3,(H,19,20)
InChI Key FUPWOGMZEYIFOH-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C16H24O4
Molecular Weight 280.36 g/mol
Exact Mass 280.16745924 g/mol
Topological Polar Surface Area (TPSA) 74.60 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.41
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(5-Formyl-4-hydroxy-1,2,4a-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)acetic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9837 98.37%
Caco-2 + 0.7569 75.69%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.8082 80.82%
OATP2B1 inhibitior - 0.8543 85.43%
OATP1B1 inhibitior + 0.8409 84.09%
OATP1B3 inhibitior + 0.8866 88.66%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7021 70.21%
BSEP inhibitior - 0.6643 66.43%
P-glycoprotein inhibitior - 0.9134 91.34%
P-glycoprotein substrate - 0.7837 78.37%
CYP3A4 substrate + 0.5531 55.31%
CYP2C9 substrate - 0.7939 79.39%
CYP2D6 substrate - 0.8997 89.97%
CYP3A4 inhibition - 0.6393 63.93%
CYP2C9 inhibition - 0.9663 96.63%
CYP2C19 inhibition - 0.9724 97.24%
CYP2D6 inhibition - 0.9422 94.22%
CYP1A2 inhibition - 0.9268 92.68%
CYP2C8 inhibition - 0.7061 70.61%
CYP inhibitory promiscuity - 0.9236 92.36%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.7033 70.33%
Eye corrosion - 0.9961 99.61%
Eye irritation - 0.9290 92.90%
Skin irritation + 0.7299 72.99%
Skin corrosion - 0.9612 96.12%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5171 51.71%
Micronuclear - 0.7800 78.00%
Hepatotoxicity + 0.5267 52.67%
skin sensitisation - 0.6242 62.42%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.8625 86.25%
Nephrotoxicity - 0.7672 76.72%
Acute Oral Toxicity (c) III 0.8438 84.38%
Estrogen receptor binding - 0.5764 57.64%
Androgen receptor binding - 0.6080 60.80%
Thyroid receptor binding - 0.6032 60.32%
Glucocorticoid receptor binding - 0.7623 76.23%
Aromatase binding - 0.5079 50.79%
PPAR gamma - 0.6417 64.17%
Honey bee toxicity - 0.9325 93.25%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity + 0.9957 99.57%

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 96.67% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 93.81% 90.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.21% 91.11%
CHEMBL2581 P07339 Cathepsin D 91.15% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.90% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.36% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.18% 100.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.55% 97.25%
CHEMBL340 P08684 Cytochrome P450 3A4 85.01% 91.19%
CHEMBL5028 O14672 ADAM10 84.01% 97.50%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 80.62% 93.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.40% 86.33%

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.
Dicranopteris linearis

Cross-Links

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PubChem 163081710
LOTUS LTS0240531
wikiData Q105001935