(3S)-8-hydroxy-3-(4-methoxyphenyl)-3,4-dihydroisochromen-1-one

Details

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Internal ID 483d7c32-f053-4480-b150-1036275a9a38
Taxonomy Organoheterocyclic compounds > Benzopyrans > 2-benzopyrans
IUPAC Name (3S)-8-hydroxy-3-(4-methoxyphenyl)-3,4-dihydroisochromen-1-one
SMILES (Canonical) COC1=CC=C(C=C1)C2CC3=C(C(=CC=C3)O)C(=O)O2
SMILES (Isomeric) COC1=CC=C(C=C1)[C@@H]2CC3=C(C(=CC=C3)O)C(=O)O2
InChI InChI=1S/C16H14O4/c1-19-12-7-5-10(6-8-12)14-9-11-3-2-4-13(17)15(11)16(18)20-14/h2-8,14,17H,9H2,1H3/t14-/m0/s1
InChI Key DEFIJGJJJKEYGS-AWEZNQCLSA-N
Popularity 0 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) 55.80 Ų
XlogP 3.50
Atomic LogP (AlogP) 2.86
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3S)-8-hydroxy-3-(4-methoxyphenyl)-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 + 0.9778 97.78%
Caco-2 + 0.6644 66.44%
Blood Brain Barrier - 0.9000 90.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.7774 77.74%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9185 91.85%
OATP1B3 inhibitior + 0.9906 99.06%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.7184 71.84%
P-glycoprotein inhibitior - 0.7908 79.08%
P-glycoprotein substrate - 0.9370 93.70%
CYP3A4 substrate + 0.5793 57.93%
CYP2C9 substrate - 0.5444 54.44%
CYP2D6 substrate - 0.7993 79.93%
CYP3A4 inhibition - 0.6498 64.98%
CYP2C9 inhibition + 0.8802 88.02%
CYP2C19 inhibition + 0.7144 71.44%
CYP2D6 inhibition - 0.7918 79.18%
CYP1A2 inhibition + 0.7873 78.73%
CYP2C8 inhibition - 0.8970 89.70%
CYP inhibitory promiscuity - 0.5338 53.38%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9413 94.13%
Carcinogenicity (trinary) Non-required 0.4757 47.57%
Eye corrosion - 0.9756 97.56%
Eye irritation + 0.6125 61.25%
Skin irritation - 0.6691 66.91%
Skin corrosion - 0.9751 97.51%
Ames mutagenesis + 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4790 47.90%
Micronuclear + 0.7959 79.59%
Hepatotoxicity - 0.6343 63.43%
skin sensitisation - 0.9606 96.06%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.9778 97.78%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity + 0.6346 63.46%
Acute Oral Toxicity (c) III 0.3467 34.67%
Estrogen receptor binding + 0.7415 74.15%
Androgen receptor binding + 0.7503 75.03%
Thyroid receptor binding + 0.6777 67.77%
Glucocorticoid receptor binding - 0.5413 54.13%
Aromatase binding + 0.6426 64.26%
PPAR gamma + 0.7772 77.72%
Honey bee toxicity - 0.9377 93.77%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.8138 81.38%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.19% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.80% 91.11%
CHEMBL3192 Q9BY41 Histone deacetylase 8 95.18% 93.99%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.58% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.60% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.33% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 92.79% 99.23%
CHEMBL2581 P07339 Cathepsin D 91.97% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.13% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.49% 94.45%
CHEMBL1951 P21397 Monoamine oxidase A 87.05% 91.49%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.98% 95.89%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.64% 99.15%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.97% 86.33%
CHEMBL2535 P11166 Glucose transporter 81.22% 98.75%
CHEMBL3401 O75469 Pregnane X receptor 80.13% 94.73%

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.
Hydrangea serrata

Cross-Links

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PubChem 101165437
LOTUS LTS0015051
wikiData Q104977142