Methyl 3-hydroxy-2-methylbutanoate

Details

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Internal ID b02e381d-cafc-40c7-9102-c0cbeeb31a63
Taxonomy Organic acids and derivatives > Hydroxy acids and derivatives > Beta hydroxy acids and derivatives
IUPAC Name methyl 3-hydroxy-2-methylbutanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H12O3/c1-4(5(2)7)6(8)9-3/h4-5,7H,1-3H3
InChI Key FFJMPYODEQVBEX-UHFFFAOYSA-N
Popularity 9 references in papers

Physical and Chemical Properties

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Molecular Formula C6H12O3
Molecular Weight 132.16 g/mol
Exact Mass 132.078644241 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 0.40
Atomic LogP (AlogP) 0.18
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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34293-67-9
methyl 3-hydroxy-2-methylbutyrate
SCHEMBL6907462
methyl3-hydroxy-2-methylbutanoate
FFJMPYODEQVBEX-UHFFFAOYSA-N
AKOS011681302
EN300-115257

2D Structure

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2D Structure of Methyl 3-hydroxy-2-methylbutanoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9750 97.50%
Caco-2 - 0.6497 64.97%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.8459 84.59%
OATP2B1 inhibitior - 0.8601 86.01%
OATP1B1 inhibitior + 0.9685 96.85%
OATP1B3 inhibitior + 0.9626 96.26%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9529 95.29%
P-glycoprotein inhibitior - 0.9790 97.90%
P-glycoprotein substrate - 0.9729 97.29%
CYP3A4 substrate - 0.6714 67.14%
CYP2C9 substrate - 0.8008 80.08%
CYP2D6 substrate - 0.8650 86.50%
CYP3A4 inhibition - 0.9761 97.61%
CYP2C9 inhibition - 0.9788 97.88%
CYP2C19 inhibition - 0.9680 96.80%
CYP2D6 inhibition - 0.9654 96.54%
CYP1A2 inhibition - 0.9661 96.61%
CYP2C8 inhibition - 0.9911 99.11%
CYP inhibitory promiscuity - 0.9652 96.52%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) + 0.6036 60.36%
Carcinogenicity (trinary) Non-required 0.6925 69.25%
Eye corrosion + 0.9635 96.35%
Eye irritation + 0.9051 90.51%
Skin irritation + 0.5542 55.42%
Skin corrosion - 0.7378 73.78%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7672 76.72%
Micronuclear - 0.9000 90.00%
Hepatotoxicity - 0.5602 56.02%
skin sensitisation - 0.8336 83.36%
Respiratory toxicity - 0.9111 91.11%
Reproductive toxicity - 0.8222 82.22%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity + 0.6452 64.52%
Acute Oral Toxicity (c) III 0.7396 73.96%
Estrogen receptor binding - 0.9287 92.87%
Androgen receptor binding - 0.8557 85.57%
Thyroid receptor binding - 0.8688 86.88%
Glucocorticoid receptor binding - 0.8755 87.55%
Aromatase binding - 0.8086 80.86%
PPAR gamma - 0.9206 92.06%
Honey bee toxicity - 0.8343 83.43%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity - 0.8900 89.00%
Fish aquatic toxicity - 0.7846 78.46%

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 94.01% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.01% 85.14%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 86.04% 100.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.36% 94.45%
CHEMBL2581 P07339 Cathepsin D 82.89% 98.95%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 80.73% 94.33%
CHEMBL340 P08684 Cytochrome P450 3A4 80.41% 91.19%

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.
Ipomoea capillacea

Cross-Links

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PubChem 12815182
LOTUS LTS0141848
wikiData Q104994483