(3R)-8-hydroxy-6-methoxy-3-(7-oxoundecyl)-3,4-dihydroisochromen-1-one

Details

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Internal ID b6e7925c-7ec7-4e2a-8c3e-43e06bbeb8c3
Taxonomy Organoheterocyclic compounds > Benzopyrans > 2-benzopyrans
IUPAC Name (3R)-8-hydroxy-6-methoxy-3-(7-oxoundecyl)-3,4-dihydroisochromen-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H30O5/c1-3-4-9-16(22)10-7-5-6-8-11-17-12-15-13-18(25-2)14-19(23)20(15)21(24)26-17/h13-14,17,23H,3-12H2,1-2H3/t17-/m1/s1
InChI Key BLTFKHOIKPIAEJ-QGZVFWFLSA-N
Popularity 2 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 (3R)-8-hydroxy-6-methoxy-3-(7-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 + 0.9699 96.99%
Caco-2 + 0.7400 74.00%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.6539 65.39%
OATP2B1 inhibitior - 0.8547 85.47%
OATP1B1 inhibitior + 0.8570 85.70%
OATP1B3 inhibitior + 0.9382 93.82%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.7802 78.02%
P-glycoprotein inhibitior - 0.5169 51.69%
P-glycoprotein substrate - 0.6707 67.07%
CYP3A4 substrate + 0.5698 56.98%
CYP2C9 substrate + 0.8190 81.90%
CYP2D6 substrate - 0.8367 83.67%
CYP3A4 inhibition - 0.7473 74.73%
CYP2C9 inhibition - 0.7722 77.22%
CYP2C19 inhibition - 0.5739 57.39%
CYP2D6 inhibition - 0.8600 86.00%
CYP1A2 inhibition + 0.6060 60.60%
CYP2C8 inhibition + 0.5177 51.77%
CYP inhibitory promiscuity - 0.7579 75.79%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.7611 76.11%
Eye corrosion - 0.9829 98.29%
Eye irritation - 0.7947 79.47%
Skin irritation - 0.8187 81.87%
Skin corrosion - 0.9362 93.62%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4171 41.71%
Micronuclear - 0.8400 84.00%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation - 0.9073 90.73%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity + 0.5535 55.35%
Acute Oral Toxicity (c) III 0.5127 51.27%
Estrogen receptor binding + 0.7325 73.25%
Androgen receptor binding + 0.7339 73.39%
Thyroid receptor binding + 0.5943 59.43%
Glucocorticoid receptor binding + 0.6664 66.64%
Aromatase binding - 0.6970 69.70%
PPAR gamma + 0.7424 74.24%
Honey bee toxicity - 0.9263 92.63%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.6624 66.24%
Fish aquatic toxicity + 0.9831 98.31%

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 98.67% 91.11%
CHEMBL2581 P07339 Cathepsin D 97.66% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 96.80% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.14% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.43% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 92.88% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.11% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.70% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.41% 94.45%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.29% 96.95%
CHEMBL3192 Q9BY41 Histone deacetylase 8 84.64% 93.99%
CHEMBL340 P08684 Cytochrome P450 3A4 84.20% 91.19%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 83.61% 92.08%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.58% 85.14%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 82.40% 95.89%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.21% 95.89%
CHEMBL3401 O75469 Pregnane X receptor 81.73% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.38% 89.00%
CHEMBL2964 P36507 Dual specificity mitogen-activated protein kinase kinase 2 81.18% 80.00%
CHEMBL5255 O00206 Toll-like receptor 4 80.92% 92.50%

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 viscosa

Cross-Links

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PubChem 101664474
LOTUS LTS0155712
wikiData Q104938149