1-(4-Hydroxyoxan-2-yl)pent-3-en-2-one

Details

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Internal ID 1b09b812-6012-49e0-9be7-ea5644d41545
Taxonomy Organoheterocyclic compounds > Oxanes
IUPAC Name 1-(4-hydroxyoxan-2-yl)pent-3-en-2-one
SMILES (Canonical) CC=CC(=O)CC1CC(CCO1)O
SMILES (Isomeric) CC=CC(=O)CC1CC(CCO1)O
InChI InChI=1S/C10H16O3/c1-2-3-8(11)6-10-7-9(12)4-5-13-10/h2-3,9-10,12H,4-7H2,1H3
InChI Key XAUNHJUQNVIPMK-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16O3
Molecular Weight 184.23 g/mol
Exact Mass 184.109944368 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 0.50
Atomic LogP (AlogP) 1.06
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-(4-Hydroxyoxan-2-yl)pent-3-en-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9794 97.94%
Caco-2 + 0.6999 69.99%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.8579 85.79%
OATP2B1 inhibitior - 0.8544 85.44%
OATP1B1 inhibitior + 0.9080 90.80%
OATP1B3 inhibitior + 0.9585 95.85%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.9093 90.93%
P-glycoprotein inhibitior - 0.9893 98.93%
P-glycoprotein substrate - 0.8418 84.18%
CYP3A4 substrate + 0.5053 50.53%
CYP2C9 substrate - 0.8027 80.27%
CYP2D6 substrate - 0.8594 85.94%
CYP3A4 inhibition - 0.8941 89.41%
CYP2C9 inhibition - 0.9441 94.41%
CYP2C19 inhibition - 0.7370 73.70%
CYP2D6 inhibition - 0.9352 93.52%
CYP1A2 inhibition - 0.8757 87.57%
CYP2C8 inhibition - 0.8626 86.26%
CYP inhibitory promiscuity - 0.9493 94.93%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9328 93.28%
Carcinogenicity (trinary) Non-required 0.6829 68.29%
Eye corrosion - 0.8688 86.88%
Eye irritation + 0.8280 82.80%
Skin irritation - 0.6524 65.24%
Skin corrosion - 0.9431 94.31%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6829 68.29%
Micronuclear - 0.9400 94.00%
Hepatotoxicity - 0.5625 56.25%
skin sensitisation - 0.7909 79.09%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.5778 57.78%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity + 0.4869 48.69%
Acute Oral Toxicity (c) III 0.6398 63.98%
Estrogen receptor binding - 0.8340 83.40%
Androgen receptor binding - 0.8381 83.81%
Thyroid receptor binding - 0.7870 78.70%
Glucocorticoid receptor binding + 0.6046 60.46%
Aromatase binding - 0.9038 90.38%
PPAR gamma - 0.7362 73.62%
Honey bee toxicity - 0.8998 89.98%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity - 0.7035 70.35%

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
CHEMBL4040 P28482 MAP kinase ERK2 95.75% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.66% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.76% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.24% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.79% 89.00%
CHEMBL226 P30542 Adenosine A1 receptor 82.10% 95.93%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.81% 99.17%

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 163050909
LOTUS LTS0051599
wikiData Q104200807