1-(3-Hydroxy-6-methyloxan-2-yl)propan-2-one

Details

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Internal ID 1e394ec3-c88e-4ef3-8544-457d22a8f34c
Taxonomy Organoheterocyclic compounds > Oxanes
IUPAC Name 1-(3-hydroxy-6-methyloxan-2-yl)propan-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H16O3/c1-6(10)5-9-8(11)4-3-7(2)12-9/h7-9,11H,3-5H2,1-2H3
InChI Key GDXDHEIQIIZPSF-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C9H16O3
Molecular Weight 172.22 g/mol
Exact Mass 172.109944368 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 0.10
Atomic LogP (AlogP) 0.89
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-(3-Hydroxy-6-methyloxan-2-yl)propan-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 + 0.9797 97.97%
Caco-2 + 0.4919 49.19%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.7975 79.75%
OATP2B1 inhibitior - 0.8443 84.43%
OATP1B1 inhibitior + 0.9068 90.68%
OATP1B3 inhibitior + 0.9552 95.52%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.9735 97.35%
P-glycoprotein inhibitior - 0.9582 95.82%
P-glycoprotein substrate - 0.8871 88.71%
CYP3A4 substrate - 0.5502 55.02%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7563 75.63%
CYP3A4 inhibition - 0.8874 88.74%
CYP2C9 inhibition - 0.9557 95.57%
CYP2C19 inhibition - 0.8905 89.05%
CYP2D6 inhibition - 0.9427 94.27%
CYP1A2 inhibition - 0.8758 87.58%
CYP2C8 inhibition - 0.9902 99.02%
CYP inhibitory promiscuity - 0.9848 98.48%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.7238 72.38%
Eye corrosion - 0.9176 91.76%
Eye irritation + 0.6503 65.03%
Skin irritation + 0.5231 52.31%
Skin corrosion - 0.8630 86.30%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7540 75.40%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.6004 60.04%
skin sensitisation - 0.7072 70.72%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity - 0.6189 61.89%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity - 0.6201 62.01%
Acute Oral Toxicity (c) III 0.7556 75.56%
Estrogen receptor binding - 0.8998 89.98%
Androgen receptor binding - 0.8440 84.40%
Thyroid receptor binding - 0.7726 77.26%
Glucocorticoid receptor binding - 0.7816 78.16%
Aromatase binding - 0.9238 92.38%
PPAR gamma - 0.8646 86.46%
Honey bee toxicity - 0.9471 94.71%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity - 0.8700 87.00%
Fish aquatic toxicity - 0.3935 39.35%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.73% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 96.43% 83.82%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.09% 85.14%
CHEMBL2581 P07339 Cathepsin D 86.30% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.07% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.56% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.08% 97.09%

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 85099644
LOTUS LTS0118266
wikiData Q104167080