(3S,4S)-4-hydroxy-3-methyloctanoic acid

Details

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Internal ID f812a8cd-bc8f-48ba-a2e7-bad0f1abf011
Taxonomy Organic acids and derivatives > Hydroxy acids and derivatives > Medium-chain hydroxy acids and derivatives
IUPAC Name (3S,4S)-4-hydroxy-3-methyloctanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H18O3/c1-3-4-5-8(10)7(2)6-9(11)12/h7-8,10H,3-6H2,1-2H3,(H,11,12)/t7-,8-/m0/s1
InChI Key ASSMLIFISOILOS-YUMQZZPRSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C9H18O3
Molecular Weight 174.24 g/mol
Exact Mass 174.125594432 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 1.70
Atomic LogP (AlogP) 1.65
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3S,4S)-4-hydroxy-3-methyloctanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9850 98.50%
Caco-2 + 0.8389 83.89%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.7957 79.57%
OATP2B1 inhibitior - 0.8384 83.84%
OATP1B1 inhibitior + 0.9338 93.38%
OATP1B3 inhibitior + 0.9182 91.82%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9608 96.08%
P-glycoprotein inhibitior - 0.9807 98.07%
P-glycoprotein substrate - 0.9059 90.59%
CYP3A4 substrate - 0.6789 67.89%
CYP2C9 substrate + 0.6000 60.00%
CYP2D6 substrate - 0.8625 86.25%
CYP3A4 inhibition - 0.9105 91.05%
CYP2C9 inhibition - 0.8833 88.33%
CYP2C19 inhibition - 0.9509 95.09%
CYP2D6 inhibition - 0.9401 94.01%
CYP1A2 inhibition - 0.5260 52.60%
CYP2C8 inhibition - 0.9921 99.21%
CYP inhibitory promiscuity - 0.9296 92.96%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7615 76.15%
Carcinogenicity (trinary) Non-required 0.7430 74.30%
Eye corrosion + 0.6030 60.30%
Eye irritation + 0.8097 80.97%
Skin irritation - 0.8307 83.07%
Skin corrosion - 0.8888 88.88%
Ames mutagenesis - 0.9200 92.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7500 75.00%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5461 54.61%
skin sensitisation + 0.6127 61.27%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity - 0.7387 73.87%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity + 0.5195 51.95%
Acute Oral Toxicity (c) III 0.7543 75.43%
Estrogen receptor binding - 0.8799 87.99%
Androgen receptor binding - 0.8141 81.41%
Thyroid receptor binding - 0.8172 81.72%
Glucocorticoid receptor binding - 0.8144 81.44%
Aromatase binding - 0.8989 89.89%
PPAR gamma - 0.8486 84.86%
Honey bee toxicity - 0.9899 98.99%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity + 0.9142 91.42%

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
CHEMBL2581 P07339 Cathepsin D 98.24% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.82% 96.09%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 91.73% 97.29%
CHEMBL221 P23219 Cyclooxygenase-1 91.23% 90.17%
CHEMBL3359 P21462 Formyl peptide receptor 1 90.13% 93.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.92% 99.17%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 87.23% 100.00%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 86.61% 96.47%
CHEMBL1907 P15144 Aminopeptidase N 85.76% 93.31%
CHEMBL268 P43235 Cathepsin K 84.89% 96.85%
CHEMBL3776 Q14790 Caspase-8 83.27% 97.06%
CHEMBL4227 P25090 Lipoxin A4 receptor 81.30% 100.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.02% 96.95%

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.
Platycarya strobilacea

Cross-Links

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PubChem 88423886
LOTUS LTS0001706
wikiData Q104918038