(-)-beta-Butyrolactone

Details

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Internal ID dbcda88d-f6ee-4b47-a788-6b058ad82d9a
Taxonomy Organoheterocyclic compounds > Lactones > Beta propiolactones
IUPAC Name (4S)-4-methyloxetan-2-one
SMILES (Canonical) CC1CC(=O)O1
SMILES (Isomeric) C[C@H]1CC(=O)O1
InChI InChI=1S/C4H6O2/c1-3-2-4(5)6-3/h3H,2H2,1H3/t3-/m0/s1
InChI Key GSCLMSFRWBPUSK-VKHMYHEASA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C4H6O2
Molecular Weight 86.09 g/mol
Exact Mass 86.036779430 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 0.30
Atomic LogP (AlogP) 0.32
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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(4S)-4-methyloxetan-2-one
(S)-Butyrolactone
65058-82-4
beta-Butyrolactone, (-)-
2-Oxetanone, 4-methyl-, (4S)-
UNII-X25Z9LJI75
(-)-beta-Methylpropiolactone
X25Z9LJI75
(s)-beta-butyrolactone
beta-hydroxybutrolactone
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of (-)-beta-Butyrolactone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9915 99.15%
Caco-2 + 0.5247 52.47%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.5678 56.78%
OATP2B1 inhibitior - 0.8672 86.72%
OATP1B1 inhibitior + 0.9491 94.91%
OATP1B3 inhibitior + 0.9726 97.26%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9441 94.41%
P-glycoprotein inhibitior - 0.9833 98.33%
P-glycoprotein substrate - 0.9796 97.96%
CYP3A4 substrate - 0.7436 74.36%
CYP2C9 substrate - 0.7965 79.65%
CYP2D6 substrate - 0.8634 86.34%
CYP3A4 inhibition - 0.9710 97.10%
CYP2C9 inhibition - 0.9126 91.26%
CYP2C19 inhibition - 0.7769 77.69%
CYP2D6 inhibition - 0.9599 95.99%
CYP1A2 inhibition - 0.7458 74.58%
CYP2C8 inhibition - 0.9977 99.77%
CYP inhibitory promiscuity - 0.9831 98.31%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6800 68.00%
Carcinogenicity (trinary) Warning 0.5304 53.04%
Eye corrosion + 0.9023 90.23%
Eye irritation + 0.9884 98.84%
Skin irritation + 0.8622 86.22%
Skin corrosion - 0.5314 53.14%
Ames mutagenesis + 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8237 82.37%
Micronuclear + 0.6900 69.00%
Hepatotoxicity + 0.8875 88.75%
skin sensitisation - 0.7640 76.40%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity - 0.7111 71.11%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity + 0.7115 71.15%
Acute Oral Toxicity (c) IV 0.6249 62.49%
Estrogen receptor binding - 0.9470 94.70%
Androgen receptor binding - 0.8393 83.93%
Thyroid receptor binding - 0.9206 92.06%
Glucocorticoid receptor binding - 0.9276 92.76%
Aromatase binding - 0.8735 87.35%
PPAR gamma - 0.9143 91.43%
Honey bee toxicity - 0.9383 93.83%
Biodegradation + 0.8500 85.00%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity - 0.8214 82.14%

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 86.42% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.15% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.03% 95.56%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 81.31% 86.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 80.45% 94.80%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.42% 99.23%

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.
Angelica acutiloba
Angelica gigas
Angelica sinensis
Capsicum annuum
Lycium barbarum
Lycium chinense

Cross-Links

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PubChem 6998969
NPASS NPC217218