4-(Hydroxymethyl)-6-methoxy-2-methyl-3-benzoxepine-5-carbaldehyde

Details

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Internal ID 9ffab894-1e13-4065-93b8-9c7de5a33c77
Taxonomy Organoheterocyclic compounds > Benzoxepines
IUPAC Name 4-(hydroxymethyl)-6-methoxy-2-methyl-3-benzoxepine-5-carbaldehyde
SMILES (Canonical) CC1=CC2=C(C(=CC=C2)OC)C(=C(O1)CO)C=O
SMILES (Isomeric) CC1=CC2=C(C(=CC=C2)OC)C(=C(O1)CO)C=O
InChI InChI=1S/C14H14O4/c1-9-6-10-4-3-5-12(17-2)14(10)11(7-15)13(8-16)18-9/h3-7,16H,8H2,1-2H3
InChI Key CREMPVZYABCSKM-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C14H14O4
Molecular Weight 246.26 g/mol
Exact Mass 246.08920892 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 1.20
Atomic LogP (AlogP) 1.99
H-Bond Acceptor 4
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 4-(Hydroxymethyl)-6-methoxy-2-methyl-3-benzoxepine-5-carbaldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9908 99.08%
Caco-2 + 0.7919 79.19%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.6621 66.21%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8385 83.85%
OATP1B3 inhibitior + 0.9573 95.73%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.7963 79.63%
P-glycoprotein inhibitior - 0.9386 93.86%
P-glycoprotein substrate - 0.8191 81.91%
CYP3A4 substrate + 0.5664 56.64%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8203 82.03%
CYP3A4 inhibition - 0.5252 52.52%
CYP2C9 inhibition - 0.7900 79.00%
CYP2C19 inhibition + 0.5510 55.10%
CYP2D6 inhibition - 0.8913 89.13%
CYP1A2 inhibition + 0.5473 54.73%
CYP2C8 inhibition + 0.5337 53.37%
CYP inhibitory promiscuity + 0.5941 59.41%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9018 90.18%
Carcinogenicity (trinary) Non-required 0.7180 71.80%
Eye corrosion - 0.9718 97.18%
Eye irritation + 0.7608 76.08%
Skin irritation - 0.7285 72.85%
Skin corrosion - 0.9647 96.47%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4357 43.57%
Micronuclear + 0.5240 52.40%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation - 0.5310 53.10%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity + 0.5952 59.52%
Acute Oral Toxicity (c) II 0.4511 45.11%
Estrogen receptor binding + 0.7011 70.11%
Androgen receptor binding - 0.5113 51.13%
Thyroid receptor binding - 0.5580 55.80%
Glucocorticoid receptor binding + 0.6458 64.58%
Aromatase binding + 0.5852 58.52%
PPAR gamma + 0.6219 62.19%
Honey bee toxicity - 0.8908 89.08%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6255 62.55%
Fish aquatic toxicity + 0.7133 71.33%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.58% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.21% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.87% 96.09%
CHEMBL2581 P07339 Cathepsin D 91.13% 98.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 90.39% 96.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.52% 99.17%
CHEMBL3492 P49721 Proteasome Macropain subunit 86.17% 90.24%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.19% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 84.17% 94.73%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 83.50% 95.50%
CHEMBL2535 P11166 Glucose transporter 82.61% 98.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.32% 99.23%

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.
Asphodeline tenuior

Cross-Links

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PubChem 14258969
LOTUS LTS0117997
wikiData Q104968495