Heterocornol C

Details

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Internal ID 81682ee4-53b8-405a-8bc0-8a27b62acb50
Taxonomy Organoheterocyclic compounds > Benzoxepines
IUPAC Name 3-(1-hydroxyethyl)-1,3-dihydro-2-benzoxepin-9-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H14O3/c1-8(13)12-6-5-9-3-2-4-11(14)10(9)7-15-12/h2-6,8,12-14H,7H2,1H3
InChI Key NRRHMJWLACUEDG-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C12H14O3
Molecular Weight 206.24 g/mol
Exact Mass 206.094294304 g/mol
Topological Polar Surface Area (TPSA) 49.70 Ų
XlogP 1.40
Atomic LogP (AlogP) 1.68
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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3-(1-hydroxyethyl)-1,3-dihydro-2-benzoxepin-9-ol
RefChem:145845
CHEBI:215001

2D Structure

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2D Structure of Heterocornol C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9899 98.99%
Caco-2 + 0.7250 72.50%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.6461 64.61%
OATP2B1 inhibitior - 0.8655 86.55%
OATP1B1 inhibitior + 0.9516 95.16%
OATP1B3 inhibitior + 0.9683 96.83%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9343 93.43%
P-glycoprotein inhibitior - 0.9813 98.13%
P-glycoprotein substrate - 0.7280 72.80%
CYP3A4 substrate - 0.5453 54.53%
CYP2C9 substrate - 0.6117 61.17%
CYP2D6 substrate - 0.7062 70.62%
CYP3A4 inhibition - 0.9363 93.63%
CYP2C9 inhibition - 0.7062 70.62%
CYP2C19 inhibition - 0.6118 61.18%
CYP2D6 inhibition - 0.8993 89.93%
CYP1A2 inhibition + 0.7280 72.80%
CYP2C8 inhibition - 0.8825 88.25%
CYP inhibitory promiscuity - 0.5374 53.74%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.5113 51.13%
Eye corrosion - 0.9480 94.80%
Eye irritation - 0.4825 48.25%
Skin irritation - 0.5142 51.42%
Skin corrosion - 0.8514 85.14%
Ames mutagenesis + 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6986 69.86%
Micronuclear - 0.5119 51.19%
Hepatotoxicity + 0.6750 67.50%
skin sensitisation - 0.5639 56.39%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity - 0.7377 73.77%
Acute Oral Toxicity (c) III 0.4939 49.39%
Estrogen receptor binding - 0.6637 66.37%
Androgen receptor binding - 0.6998 69.98%
Thyroid receptor binding - 0.6093 60.93%
Glucocorticoid receptor binding - 0.8464 84.64%
Aromatase binding - 0.8426 84.26%
PPAR gamma - 0.6119 61.19%
Honey bee toxicity - 0.9466 94.66%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity + 0.7927 79.27%

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 97.30% 91.11%
CHEMBL2581 P07339 Cathepsin D 95.48% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.89% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.89% 95.56%
CHEMBL1951 P21397 Monoamine oxidase A 88.37% 91.49%
CHEMBL3359 P21462 Formyl peptide receptor 1 86.94% 93.56%
CHEMBL3401 O75469 Pregnane X receptor 83.46% 94.73%
CHEMBL2535 P11166 Glucose transporter 82.83% 98.75%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.48% 97.09%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 81.37% 99.15%
CHEMBL2996 Q05655 Protein kinase C delta 80.85% 97.79%

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 139590846
LOTUS LTS0261332
wikiData Q104179942