8-Hydroxy-6-methoxy-3-(6-oxoundecyl)-3,4-dihydroisochromen-1-one

Details

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Internal ID f7e9869d-df3c-4d4b-a2d2-78de16ba96fb
Taxonomy Organoheterocyclic compounds > Benzopyrans > 2-benzopyrans
IUPAC Name 8-hydroxy-6-methoxy-3-(6-oxoundecyl)-3,4-dihydroisochromen-1-one
SMILES (Canonical) CCCCCC(=O)CCCCCC1CC2=C(C(=CC(=C2)OC)O)C(=O)O1
SMILES (Isomeric) CCCCCC(=O)CCCCCC1CC2=C(C(=CC(=C2)OC)O)C(=O)O1
InChI InChI=1S/C21H30O5/c1-3-4-6-9-16(22)10-7-5-8-11-17-12-15-13-18(25-2)14-19(23)20(15)21(24)26-17/h13-14,17,23H,3-12H2,1-2H3
InChI Key WUILFSMTLRWUAQ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H30O5
Molecular Weight 362.50 g/mol
Exact Mass 362.20932405 g/mol
Topological Polar Surface Area (TPSA) 72.80 Ų
XlogP 5.20
Atomic LogP (AlogP) 4.58
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 11

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 8-Hydroxy-6-methoxy-3-(6-oxoundecyl)-3,4-dihydroisochromen-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9663 96.63%
Caco-2 + 0.7440 74.40%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.6380 63.80%
OATP2B1 inhibitior - 0.8552 85.52%
OATP1B1 inhibitior + 0.8641 86.41%
OATP1B3 inhibitior + 0.9203 92.03%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.7448 74.48%
P-glycoprotein inhibitior - 0.4322 43.22%
P-glycoprotein substrate - 0.6540 65.40%
CYP3A4 substrate + 0.5669 56.69%
CYP2C9 substrate + 0.8190 81.90%
CYP2D6 substrate - 0.8367 83.67%
CYP3A4 inhibition - 0.7133 71.33%
CYP2C9 inhibition - 0.7933 79.33%
CYP2C19 inhibition - 0.5432 54.32%
CYP2D6 inhibition - 0.8843 88.43%
CYP1A2 inhibition + 0.5793 57.93%
CYP2C8 inhibition + 0.5271 52.71%
CYP inhibitory promiscuity - 0.7552 75.52%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.7673 76.73%
Eye corrosion - 0.9851 98.51%
Eye irritation - 0.8837 88.37%
Skin irritation - 0.8046 80.46%
Skin corrosion - 0.9332 93.32%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7523 75.23%
Micronuclear - 0.8200 82.00%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation - 0.9092 90.92%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity + 0.5479 54.79%
Acute Oral Toxicity (c) III 0.4832 48.32%
Estrogen receptor binding + 0.7742 77.42%
Androgen receptor binding + 0.7339 73.39%
Thyroid receptor binding + 0.5286 52.86%
Glucocorticoid receptor binding + 0.7112 71.12%
Aromatase binding - 0.5700 57.00%
PPAR gamma + 0.7587 75.87%
Honey bee toxicity - 0.9298 92.98%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.7059 70.59%
Fish aquatic toxicity + 0.9854 98.54%

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 98.76% 91.11%
CHEMBL2581 P07339 Cathepsin D 97.67% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 97.30% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.85% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.66% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 93.26% 99.23%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 90.08% 92.08%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.79% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.50% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.70% 97.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.33% 96.95%
CHEMBL3401 O75469 Pregnane X receptor 85.56% 94.73%
CHEMBL3192 Q9BY41 Histone deacetylase 8 85.31% 93.99%
CHEMBL340 P08684 Cytochrome P450 3A4 84.20% 91.19%
CHEMBL5255 O00206 Toll-like receptor 4 83.04% 92.50%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.74% 95.89%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 82.40% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.00% 89.00%

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.
Ononis natrix

Cross-Links

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PubChem 14539306
LOTUS LTS0138896
wikiData Q105313073