(7S)-1-hydroxy-3-p-menthen-9-oic acid

Details

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Internal ID da56c1d7-8feb-421e-b62b-fb75c275d301
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Menthane monoterpenoids
IUPAC Name (2S)-2-(4-hydroxy-4-methylcyclohexen-1-yl)propanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H16O3/c1-7(9(11)12)8-3-5-10(2,13)6-4-8/h3,7,13H,4-6H2,1-2H3,(H,11,12)/t7-,10?/m0/s1
InChI Key LHTQNNMXYABMAX-BYDSUWOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16O3
Molecular Weight 184.23 g/mol
Exact Mass 184.109944368 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 0.90
Atomic LogP (AlogP) 1.57
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (7S)-1-hydroxy-3-p-menthen-9-oic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9929 99.29%
Caco-2 + 0.6646 66.46%
Blood Brain Barrier - 0.5645 56.45%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.8774 87.74%
OATP2B1 inhibitior - 0.8415 84.15%
OATP1B1 inhibitior + 0.9311 93.11%
OATP1B3 inhibitior + 0.9548 95.48%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6069 60.69%
BSEP inhibitior - 0.9083 90.83%
P-glycoprotein inhibitior - 0.9769 97.69%
P-glycoprotein substrate - 0.9621 96.21%
CYP3A4 substrate - 0.6065 60.65%
CYP2C9 substrate + 0.6346 63.46%
CYP2D6 substrate - 0.8921 89.21%
CYP3A4 inhibition - 0.9220 92.20%
CYP2C9 inhibition - 0.8390 83.90%
CYP2C19 inhibition - 0.9165 91.65%
CYP2D6 inhibition - 0.9317 93.17%
CYP1A2 inhibition - 0.9051 90.51%
CYP2C8 inhibition - 0.9820 98.20%
CYP inhibitory promiscuity - 0.9643 96.43%
UGT catelyzed - 0.5638 56.38%
Carcinogenicity (binary) - 0.8843 88.43%
Carcinogenicity (trinary) Non-required 0.5647 56.47%
Eye corrosion - 0.9770 97.70%
Eye irritation + 0.7991 79.91%
Skin irritation + 0.5612 56.12%
Skin corrosion - 0.9683 96.83%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7887 78.87%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.7397 73.97%
skin sensitisation + 0.6946 69.46%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.5723 57.23%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.8135 81.35%
Acute Oral Toxicity (c) III 0.7304 73.04%
Estrogen receptor binding - 0.9384 93.84%
Androgen receptor binding - 0.7845 78.45%
Thyroid receptor binding - 0.7314 73.14%
Glucocorticoid receptor binding - 0.7972 79.72%
Aromatase binding - 0.8325 83.25%
PPAR gamma - 0.5994 59.94%
Honey bee toxicity - 0.9562 95.62%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity + 0.9726 97.26%

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 95.74% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.31% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.96% 97.25%
CHEMBL221 P23219 Cyclooxygenase-1 90.42% 90.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.97% 94.45%
CHEMBL2581 P07339 Cathepsin D 88.53% 98.95%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.95% 93.56%
CHEMBL4227 P25090 Lipoxin A4 receptor 82.16% 100.00%
CHEMBL5028 O14672 ADAM10 81.03% 97.50%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.71% 95.56%

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 139590699
LOTUS LTS0232563
wikiData Q105151950