CID 85114443

Details

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Internal ID 41e9a646-fca7-4044-98c2-c82974e8efb9
Taxonomy Benzenoids > Tetralins
IUPAC Name 14-hydroxy-4-methoxy-14-methyl-19,20-dioxahexacyclo[8.8.1.12,9.01,10.03,8.011,16]icosa-3(8),4,6,11(16),17-pentaen-12-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H18O5/c1-18(22)8-10-6-7-19-17-14-11(4-3-5-13(14)23-2)16(24-17)20(19,25-19)15(10)12(21)9-18/h3-7,16-17,22H,8-9H2,1-2H3
InChI Key BOYWLALFDCIWJG-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H18O5
Molecular Weight 338.40 g/mol
Exact Mass 338.11542367 g/mol
Topological Polar Surface Area (TPSA) 68.30 Ų
XlogP -0.10
Atomic LogP (AlogP) 2.31
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 85114443

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9954 99.54%
Caco-2 + 0.7696 76.96%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.7058 70.58%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9319 93.19%
OATP1B3 inhibitior + 0.9446 94.46%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.8798 87.98%
P-glycoprotein inhibitior - 0.5758 57.58%
P-glycoprotein substrate - 0.5692 56.92%
CYP3A4 substrate + 0.6931 69.31%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8358 83.58%
CYP3A4 inhibition + 0.6380 63.80%
CYP2C9 inhibition - 0.7777 77.77%
CYP2C19 inhibition - 0.5226 52.26%
CYP2D6 inhibition - 0.7281 72.81%
CYP1A2 inhibition - 0.7060 70.60%
CYP2C8 inhibition + 0.5315 53.15%
CYP inhibitory promiscuity - 0.6484 64.84%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.4567 45.67%
Eye corrosion - 0.9831 98.31%
Eye irritation - 0.9396 93.96%
Skin irritation - 0.7227 72.27%
Skin corrosion - 0.9402 94.02%
Ames mutagenesis + 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3629 36.29%
Micronuclear + 0.6100 61.00%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation - 0.6909 69.09%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity + 0.8000 80.00%
Nephrotoxicity + 0.7249 72.49%
Acute Oral Toxicity (c) II 0.3511 35.11%
Estrogen receptor binding + 0.9074 90.74%
Androgen receptor binding + 0.6834 68.34%
Thyroid receptor binding + 0.6523 65.23%
Glucocorticoid receptor binding + 0.7709 77.09%
Aromatase binding + 0.7988 79.88%
PPAR gamma + 0.7729 77.29%
Honey bee toxicity - 0.8457 84.57%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9140 91.40%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.44% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.97% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.83% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.64% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.54% 95.56%
CHEMBL2581 P07339 Cathepsin D 93.13% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.30% 99.23%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 89.49% 97.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.22% 89.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 84.64% 97.25%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.37% 95.89%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.99% 94.45%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 82.84% 96.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 81.90% 93.99%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.69% 94.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.36% 92.62%

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 85114443
LOTUS LTS0111540
wikiData Q77520470