2,3,4,5-Tetrahydro-1-benzoxepin-3-ol

Details

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Internal ID 10eded71-1d6a-4e7b-bc60-94855aeb5159
Taxonomy Organoheterocyclic compounds > Benzoxepines
IUPAC Name 2,3,4,5-tetrahydro-1-benzoxepin-3-ol
SMILES (Canonical) C1CC2=CC=CC=C2OCC1O
SMILES (Isomeric) C1CC2=CC=CC=C2OCC1O
InChI InChI=1S/C10H12O2/c11-9-6-5-8-3-1-2-4-10(8)12-7-9/h1-4,9,11H,5-7H2
InChI Key DEOPESDQXGFICL-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H12O2
Molecular Weight 164.20 g/mol
Exact Mass 164.083729621 g/mol
Topological Polar Surface Area (TPSA) 29.50 Ų
XlogP 1.90
Atomic LogP (AlogP) 1.37
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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38824-30-5
1-Benzoxepin-3-ol, 2,3,4,5-tetrahydro-
DTXSID70344367
DEOPESDQXGFICL-UHFFFAOYSA-N
2,3,4,5-Tetrahydro-1-benzoxepin-3-ol #

2D Structure

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2D Structure of 2,3,4,5-Tetrahydro-1-benzoxepin-3-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.9565 95.65%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.6976 69.76%
OATP2B1 inhibitior - 0.8609 86.09%
OATP1B1 inhibitior + 0.9698 96.98%
OATP1B3 inhibitior + 0.9445 94.45%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.9366 93.66%
P-glycoprotein inhibitior - 0.9896 98.96%
P-glycoprotein substrate - 0.9234 92.34%
CYP3A4 substrate - 0.6475 64.75%
CYP2C9 substrate - 0.8037 80.37%
CYP2D6 substrate + 0.5761 57.61%
CYP3A4 inhibition - 0.9550 95.50%
CYP2C9 inhibition - 0.8735 87.35%
CYP2C19 inhibition - 0.6939 69.39%
CYP2D6 inhibition - 0.9313 93.13%
CYP1A2 inhibition + 0.5384 53.84%
CYP2C8 inhibition - 0.8876 88.76%
CYP inhibitory promiscuity - 0.9332 93.32%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.8100 81.00%
Carcinogenicity (trinary) Non-required 0.5624 56.24%
Eye corrosion - 0.8679 86.79%
Eye irritation + 0.9589 95.89%
Skin irritation + 0.5171 51.71%
Skin corrosion - 0.9116 91.16%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4634 46.34%
Micronuclear - 0.8741 87.41%
Hepatotoxicity - 0.5550 55.50%
skin sensitisation + 0.4869 48.69%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity - 0.8084 80.84%
Acute Oral Toxicity (c) III 0.7967 79.67%
Estrogen receptor binding - 0.6594 65.94%
Androgen receptor binding - 0.7611 76.11%
Thyroid receptor binding - 0.7935 79.35%
Glucocorticoid receptor binding - 0.7124 71.24%
Aromatase binding - 0.8557 85.57%
PPAR gamma - 0.6823 68.23%
Honey bee toxicity - 0.8879 88.79%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity - 0.6186 61.86%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.69% 91.11%
CHEMBL4040 P28482 MAP kinase ERK2 96.08% 83.82%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.58% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.09% 100.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.10% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.76% 97.09%
CHEMBL2581 P07339 Cathepsin D 81.69% 98.95%
CHEMBL3192 Q9BY41 Histone deacetylase 8 80.71% 93.99%

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.
Inula japonica
Pentanema britannicum

Cross-Links

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PubChem 596274
NPASS NPC298084