3-Butanoyl-4-(hydroxymethyl)oxolan-2-one

Details

Top
Internal ID 19f3e0a3-3110-41ee-b60f-e9784a7814f8
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name 3-butanoyl-4-(hydroxymethyl)oxolan-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H14O4/c1-2-3-7(11)8-6(4-10)5-13-9(8)12/h6,8,10H,2-5H2,1H3
InChI Key FTLILBHSSONTBQ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C9H14O4
Molecular Weight 186.20 g/mol
Exact Mass 186.08920892 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 0.20
Atomic LogP (AlogP) 0.14
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 3-Butanoyl-4-(hydroxymethyl)oxolan-2-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9494 94.94%
Caco-2 - 0.7084 70.84%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.7811 78.11%
OATP2B1 inhibitior - 0.8494 84.94%
OATP1B1 inhibitior + 0.9301 93.01%
OATP1B3 inhibitior + 0.9547 95.47%
MATE1 inhibitior - 0.9612 96.12%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.8612 86.12%
P-glycoprotein inhibitior - 0.9616 96.16%
P-glycoprotein substrate - 0.8238 82.38%
CYP3A4 substrate - 0.6371 63.71%
CYP2C9 substrate - 0.5624 56.24%
CYP2D6 substrate - 0.8630 86.30%
CYP3A4 inhibition - 0.9506 95.06%
CYP2C9 inhibition - 0.9191 91.91%
CYP2C19 inhibition - 0.8789 87.89%
CYP2D6 inhibition - 0.9467 94.67%
CYP1A2 inhibition - 0.8521 85.21%
CYP2C8 inhibition - 0.9737 97.37%
CYP inhibitory promiscuity - 0.9802 98.02%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9243 92.43%
Carcinogenicity (trinary) Non-required 0.6534 65.34%
Eye corrosion - 0.9424 94.24%
Eye irritation + 0.8506 85.06%
Skin irritation - 0.6598 65.98%
Skin corrosion - 0.9168 91.68%
Ames mutagenesis + 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7887 78.87%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation - 0.9487 94.87%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity - 0.7222 72.22%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity + 0.5944 59.44%
Acute Oral Toxicity (c) III 0.7804 78.04%
Estrogen receptor binding - 0.7178 71.78%
Androgen receptor binding - 0.7447 74.47%
Thyroid receptor binding - 0.7811 78.11%
Glucocorticoid receptor binding - 0.6719 67.19%
Aromatase binding - 0.8907 89.07%
PPAR gamma - 0.7698 76.98%
Honey bee toxicity - 0.9771 97.71%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6632 66.32%
Fish aquatic toxicity - 0.4490 44.90%

Targets

Top

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.24% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.67% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.98% 96.09%
CHEMBL2581 P07339 Cathepsin D 89.98% 98.95%
CHEMBL4040 P28482 MAP kinase ERK2 88.49% 83.82%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.27% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.51% 97.09%
CHEMBL218 P21554 Cannabinoid CB1 receptor 87.26% 96.61%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.22% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.37% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.08% 99.23%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.05% 100.00%

Plants that contains it

Top
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.
There are no matching plants.

Cross-Links

Top
PubChem 10877826
LOTUS LTS0149248
wikiData Q104166762