Pacharin

Details

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Internal ID b648975d-a095-4af3-8c10-647f54c89e40
Taxonomy Organoheterocyclic compounds > Benzoxepines > Dibenzoxepines
IUPAC Name 3-methoxy-2-methylbenzo[b][1]benzoxepine-1,7-diol
SMILES (Canonical) CC1=C(C=C2C=CC3=C(C=CC=C3OC2=C1O)O)OC
SMILES (Isomeric) CC1=C(C=C2C=CC3=C(C=CC=C3OC2=C1O)O)OC
InChI InChI=1S/C16H14O4/c1-9-14(19-2)8-10-6-7-11-12(17)4-3-5-13(11)20-16(10)15(9)18/h3-8,17-18H,1-2H3
InChI Key OZKUMALKRPIULU-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C16H14O4
Molecular Weight 270.28 g/mol
Exact Mass 270.08920892 g/mol
Topological Polar Surface Area (TPSA) 58.90 Ų
XlogP 3.60
Atomic LogP (AlogP) 3.69
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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8-methoxy-7-methyl-dibenzo[b,f]oxepine-1,6-diol
CHEMBL482048

2D Structure

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2D Structure of Pacharin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9827 98.27%
Caco-2 + 0.7188 71.88%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.4838 48.38%
OATP2B1 inhibitior - 0.8543 85.43%
OATP1B1 inhibitior + 0.8991 89.91%
OATP1B3 inhibitior + 0.9749 97.49%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.5834 58.34%
P-glycoprotein inhibitior - 0.7130 71.30%
P-glycoprotein substrate - 0.8494 84.94%
CYP3A4 substrate + 0.5450 54.50%
CYP2C9 substrate + 0.6108 61.08%
CYP2D6 substrate - 0.6908 69.08%
CYP3A4 inhibition + 0.5000 50.00%
CYP2C9 inhibition - 0.6461 64.61%
CYP2C19 inhibition + 0.7908 79.08%
CYP2D6 inhibition - 0.6578 65.78%
CYP1A2 inhibition + 0.8229 82.29%
CYP2C8 inhibition + 0.6867 68.67%
CYP inhibitory promiscuity + 0.8358 83.58%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8951 89.51%
Carcinogenicity (trinary) Non-required 0.4784 47.84%
Eye corrosion - 0.9802 98.02%
Eye irritation + 0.9212 92.12%
Skin irritation - 0.6436 64.36%
Skin corrosion - 0.9336 93.36%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7027 70.27%
Micronuclear + 0.8200 82.00%
Hepatotoxicity + 0.5125 51.25%
skin sensitisation - 0.7500 75.00%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity - 0.8687 86.87%
Acute Oral Toxicity (c) II 0.4862 48.62%
Estrogen receptor binding + 0.8321 83.21%
Androgen receptor binding + 0.7710 77.10%
Thyroid receptor binding + 0.8565 85.65%
Glucocorticoid receptor binding + 0.8888 88.88%
Aromatase binding + 0.7264 72.64%
PPAR gamma + 0.8066 80.66%
Honey bee toxicity - 0.9318 93.18%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.9629 96.29%

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
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.42% 94.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.52% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.16% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.62% 99.15%
CHEMBL2581 P07339 Cathepsin D 88.87% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.85% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.26% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 86.38% 94.73%
CHEMBL3192 Q9BY41 Histone deacetylase 8 84.95% 93.99%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.19% 89.00%
CHEMBL1951 P21397 Monoamine oxidase A 83.73% 91.49%
CHEMBL2535 P11166 Glucose transporter 82.82% 98.75%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.63% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.92% 99.17%
CHEMBL1255126 O15151 Protein Mdm4 80.74% 90.20%

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.
Alnus cordata
Aloe deltoideodonta
Bauhinia purpurea
Bauhinia racemosa
Crinum latifolium
Hemionitis aschenborniana
Leitneria floridana
Thermopsis mollis

Cross-Links

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PubChem 11851219
NPASS NPC161203
LOTUS LTS0009373
wikiData Q105203905