2(S)-3'-hydroxybutan-2'-yl 2-hydroxypropanoate

Details

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Internal ID 8f776d68-ee32-40cb-ab7f-e5e4eebe6ccd
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Carboxylic acid derivatives > Carboxylic acid esters
IUPAC Name 3-hydroxybutan-2-yl (2S)-2-hydroxypropanoate
SMILES (Canonical) CC(C(C)OC(=O)C(C)O)O
SMILES (Isomeric) C[C@@H](C(=O)OC(C)C(C)O)O
InChI InChI=1S/C7H14O4/c1-4(8)6(3)11-7(10)5(2)9/h4-6,8-9H,1-3H3/t4?,5-,6?/m0/s1
InChI Key IYGRJVIQVSHNEI-XRVVJQKQSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C7H14O4
Molecular Weight 162.18 g/mol
Exact Mass 162.08920892 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 0.00
Atomic LogP (AlogP) -0.32
H-Bond Acceptor 4
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(S)-3'-hydroxybutan-2'-yl 2-hydroxypropanoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9093 90.93%
Caco-2 - 0.7815 78.15%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.8357 83.57%
OATP2B1 inhibitior - 0.8551 85.51%
OATP1B1 inhibitior + 0.9515 95.15%
OATP1B3 inhibitior + 0.9456 94.56%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9744 97.44%
P-glycoprotein inhibitior - 0.9677 96.77%
P-glycoprotein substrate - 0.9854 98.54%
CYP3A4 substrate - 0.6625 66.25%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8589 85.89%
CYP3A4 inhibition - 0.9411 94.11%
CYP2C9 inhibition - 0.9208 92.08%
CYP2C19 inhibition - 0.9662 96.62%
CYP2D6 inhibition - 0.9604 96.04%
CYP1A2 inhibition - 0.9733 97.33%
CYP2C8 inhibition - 0.9885 98.85%
CYP inhibitory promiscuity - 0.9501 95.01%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) + 0.5045 50.45%
Carcinogenicity (trinary) Non-required 0.7491 74.91%
Eye corrosion + 0.8676 86.76%
Eye irritation + 0.6021 60.21%
Skin irritation - 0.7672 76.72%
Skin corrosion - 0.8345 83.45%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8391 83.91%
Micronuclear - 0.8400 84.00%
Hepatotoxicity - 0.5093 50.93%
skin sensitisation - 0.7016 70.16%
Respiratory toxicity - 0.9556 95.56%
Reproductive toxicity - 0.8444 84.44%
Mitochondrial toxicity - 0.8250 82.50%
Nephrotoxicity + 0.6326 63.26%
Acute Oral Toxicity (c) III 0.6796 67.96%
Estrogen receptor binding - 0.8216 82.16%
Androgen receptor binding - 0.8363 83.63%
Thyroid receptor binding - 0.7524 75.24%
Glucocorticoid receptor binding - 0.8013 80.13%
Aromatase binding - 0.8659 86.59%
PPAR gamma - 0.8820 88.20%
Honey bee toxicity - 0.8376 83.76%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.8000 80.00%
Fish aquatic toxicity - 0.5803 58.03%

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 90.83% 96.09%
CHEMBL2581 P07339 Cathepsin D 85.99% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.19% 94.45%

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 131231313
LOTUS LTS0185452
wikiData Q105122723