(S)-2-Hydroxypentan-3-one

Details

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Internal ID bc592950-e851-4ff4-b719-1a165cd34831
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Acyloins
IUPAC Name (2S)-2-hydroxypentan-3-one
SMILES (Canonical) CCC(=O)C(C)O
SMILES (Isomeric) CCC(=O)[C@H](C)O
InChI InChI=1S/C5H10O2/c1-3-5(7)4(2)6/h4,6H,3H2,1-2H3/t4-/m0/s1
InChI Key QMXCHEVUAIPIRM-BYPYZUCNSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C5H10O2
Molecular Weight 102.13 g/mol
Exact Mass 102.068079557 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 0.20
Atomic LogP (AlogP) 0.35
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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(S)-2-Hydroxypentan-3-one
125948-63-2
SCHEMBL1820421

2D Structure

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2D Structure of (S)-2-Hydroxypentan-3-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9951 99.51%
Caco-2 - 0.6198 61.98%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.7476 74.76%
OATP2B1 inhibitior - 0.8594 85.94%
OATP1B1 inhibitior + 0.9491 94.91%
OATP1B3 inhibitior + 0.9374 93.74%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9356 93.56%
P-glycoprotein inhibitior - 0.9855 98.55%
P-glycoprotein substrate - 0.9773 97.73%
CYP3A4 substrate - 0.7824 78.24%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7417 74.17%
CYP3A4 inhibition - 0.9494 94.94%
CYP2C9 inhibition - 0.8892 88.92%
CYP2C19 inhibition - 0.8945 89.45%
CYP2D6 inhibition - 0.9131 91.31%
CYP1A2 inhibition - 0.7883 78.83%
CYP2C8 inhibition - 0.9945 99.45%
CYP inhibitory promiscuity - 0.9416 94.16%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.5200 52.00%
Carcinogenicity (trinary) Non-required 0.7600 76.00%
Eye corrosion + 0.9699 96.99%
Eye irritation + 0.9651 96.51%
Skin irritation + 0.8175 81.75%
Skin corrosion + 0.6575 65.75%
Ames mutagenesis - 0.8678 86.78%
Human Ether-a-go-go-Related Gene inhibition - 0.8022 80.22%
Micronuclear - 0.9200 92.00%
Hepatotoxicity - 0.6801 68.01%
skin sensitisation + 0.7668 76.68%
Respiratory toxicity - 0.9556 95.56%
Reproductive toxicity - 0.7000 70.00%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity - 0.7049 70.49%
Acute Oral Toxicity (c) III 0.8106 81.06%
Estrogen receptor binding - 0.8978 89.78%
Androgen receptor binding - 0.8982 89.82%
Thyroid receptor binding - 0.8812 88.12%
Glucocorticoid receptor binding - 0.8862 88.62%
Aromatase binding - 0.9011 90.11%
PPAR gamma - 0.8914 89.14%
Honey bee toxicity - 0.9729 97.29%
Biodegradation + 0.8500 85.00%
Crustacea aquatic toxicity - 0.9600 96.00%
Fish aquatic toxicity - 0.8190 81.90%

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 95.19% 96.09%
CHEMBL2581 P07339 Cathepsin D 91.84% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.60% 97.25%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 84.56% 100.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.09% 85.14%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 81.89% 96.47%
CHEMBL221 P23219 Cyclooxygenase-1 80.52% 90.17%

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.
Isodon lophanthoides
Salvia deserta

Cross-Links

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PubChem 12384811
LOTUS LTS0021969
wikiData Q105287347