4-Methyl-1,3-dioxane

Details

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Internal ID 55283d1e-f32e-4106-b396-22a44e424133
Taxonomy Organoheterocyclic compounds > Dioxanes > 1,3-dioxanes
IUPAC Name 4-methyl-1,3-dioxane
SMILES (Canonical) CC1CCOCO1
SMILES (Isomeric) CC1CCOCO1
InChI InChI=1S/C5H10O2/c1-5-2-3-6-4-7-5/h5H,2-4H2,1H3
InChI Key INCCMBMMWVKEGJ-UHFFFAOYSA-N
Popularity 25 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) 18.50 Ų
XlogP 0.60
Atomic LogP (AlogP) 0.77
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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1120-97-4
4-Methyl-m-dioxane
1,3-Dioxane, 4-methyl-
m-Dioxane, 4-methyl-
4-METHYLDIOXANE
1,3-Butanediol formal
NSC 292
EINECS 214-323-1
XCM6KK2C4N
BRN 0102735
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 4-Methyl-1,3-dioxane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9771 97.71%
Caco-2 + 0.8108 81.08%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.4821 48.21%
OATP2B1 inhibitior - 0.8589 85.89%
OATP1B1 inhibitior + 0.9561 95.61%
OATP1B3 inhibitior + 0.9450 94.50%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.9729 97.29%
P-glycoprotein inhibitior - 0.9891 98.91%
P-glycoprotein substrate - 0.9644 96.44%
CYP3A4 substrate - 0.6323 63.23%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate - 0.7842 78.42%
CYP3A4 inhibition - 0.8883 88.83%
CYP2C9 inhibition - 0.8952 89.52%
CYP2C19 inhibition - 0.7788 77.88%
CYP2D6 inhibition - 0.9161 91.61%
CYP1A2 inhibition - 0.7263 72.63%
CYP2C8 inhibition - 0.9781 97.81%
CYP inhibitory promiscuity - 0.9570 95.70%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.4654 46.54%
Eye corrosion + 0.6059 60.59%
Eye irritation + 0.9949 99.49%
Skin irritation + 0.5704 57.04%
Skin corrosion - 0.8968 89.68%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7630 76.30%
Micronuclear - 0.9000 90.00%
Hepatotoxicity + 0.7750 77.50%
skin sensitisation - 0.8397 83.97%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity - 0.8667 86.67%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity + 0.6464 64.64%
Acute Oral Toxicity (c) III 0.7903 79.03%
Estrogen receptor binding - 0.9328 93.28%
Androgen receptor binding - 0.9236 92.36%
Thyroid receptor binding - 0.8899 88.99%
Glucocorticoid receptor binding - 0.9134 91.34%
Aromatase binding - 0.9012 90.12%
PPAR gamma - 0.8918 89.18%
Honey bee toxicity - 0.8325 83.25%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity - 0.6994 69.94%

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
CHEMBL3137262 O60341 LSD1/CoREST complex 88.40% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.82% 96.09%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 83.30% 86.00%
CHEMBL1163125 O60885 Bromodomain-containing protein 4 82.12% 97.31%
CHEMBL2581 P07339 Cathepsin D 81.80% 98.95%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 81.52% 94.80%
CHEMBL1907601 P11802 Cyclin-dependent kinase 4/cyclin D1 80.43% 98.99%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.32% 91.11%

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.
Pterocarpus indicus

Cross-Links

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PubChem 14269
NPASS NPC168422