1,3,5-Trioxepane

Details

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Internal ID ac002ed5-425f-4e78-9bc1-78efd7a4abd4
Taxonomy Organic oxygen compounds > Organooxygen compounds > Ethers > Acetals
IUPAC Name 1,3,5-trioxepane
SMILES (Canonical) C1COCOCO1
SMILES (Isomeric) C1COCOCO1
InChI InChI=1S/C4H8O3/c1-2-6-4-7-3-5-1/h1-4H2
InChI Key ULAGGPJVDRGWTI-UHFFFAOYSA-N
Popularity 23 references in papers

Physical and Chemical Properties

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Molecular Formula C4H8O3
Molecular Weight 104.10 g/mol
Exact Mass 104.047344113 g/mol
Topological Polar Surface Area (TPSA) 27.70 Ų
XlogP -0.40
Atomic LogP (AlogP) -0.04
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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1,3,5-TRIOXACYCLOHEPTANE
5981-06-6
038R511H1R
NSC-511991
1,5-Trioxepane
NSC511991
1,3,5-trioxepan
1,5-Trioxacycloheptane
SCHEMBL1246546
UNII-038R511H1R
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 1,3,5-Trioxepane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9425 94.25%
Caco-2 + 0.7470 74.70%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.5613 56.13%
OATP2B1 inhibitior - 0.8594 85.94%
OATP1B1 inhibitior + 0.9826 98.26%
OATP1B3 inhibitior + 0.9520 95.20%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9638 96.38%
P-glycoprotein inhibitior - 0.9876 98.76%
P-glycoprotein substrate - 0.9948 99.48%
CYP3A4 substrate - 0.7904 79.04%
CYP2C9 substrate - 0.8046 80.46%
CYP2D6 substrate - 0.8050 80.50%
CYP3A4 inhibition - 0.9327 93.27%
CYP2C9 inhibition - 0.8824 88.24%
CYP2C19 inhibition - 0.8323 83.23%
CYP2D6 inhibition - 0.9178 91.78%
CYP1A2 inhibition - 0.8482 84.82%
CYP2C8 inhibition - 0.9894 98.94%
CYP inhibitory promiscuity - 0.9524 95.24%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7500 75.00%
Carcinogenicity (trinary) Non-required 0.4668 46.68%
Eye corrosion + 0.7461 74.61%
Eye irritation + 0.9952 99.52%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.8761 87.61%
Ames mutagenesis - 0.9500 95.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7338 73.38%
Micronuclear - 0.9500 95.00%
Hepatotoxicity + 0.8875 88.75%
skin sensitisation - 0.8851 88.51%
Respiratory toxicity - 0.9333 93.33%
Reproductive toxicity - 0.7333 73.33%
Mitochondrial toxicity - 0.9500 95.00%
Nephrotoxicity + 0.8002 80.02%
Acute Oral Toxicity (c) III 0.7171 71.71%
Estrogen receptor binding - 0.9124 91.24%
Androgen receptor binding - 0.9401 94.01%
Thyroid receptor binding - 0.8780 87.80%
Glucocorticoid receptor binding - 0.8637 86.37%
Aromatase binding - 0.8652 86.52%
PPAR gamma - 0.9029 90.29%
Honey bee toxicity - 0.7886 78.86%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.8800 88.00%
Fish aquatic toxicity - 0.8054 80.54%

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
No predicted targets yet!

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.
Citrus maxima

Cross-Links

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PubChem 22294
NPASS NPC25717