5-Formyl-8-hydroxy-3-methyl-3,4-dihydroisocoumarin

Details

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Internal ID 8d465a1e-d171-4b0c-a264-93187c04517b
Taxonomy Organoheterocyclic compounds > Benzopyrans > 2-benzopyrans
IUPAC Name 8-hydroxy-3-methyl-1-oxo-3,4-dihydroisochromene-5-carbaldehyde
SMILES (Canonical) CC1CC2=C(C=CC(=C2C(=O)O1)O)C=O
SMILES (Isomeric) CC1CC2=C(C=CC(=C2C(=O)O1)O)C=O
InChI InChI=1S/C11H10O4/c1-6-4-8-7(5-12)2-3-9(13)10(8)11(14)15-6/h2-3,5-6,13H,4H2,1H3
InChI Key PTNGWSBREHHWFF-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C11H10O4
Molecular Weight 206.19 g/mol
Exact Mass 206.05790880 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 1.90
Atomic LogP (AlogP) 1.31
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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5-formyl-8-hydroxy-3-methyl-3,4-dihydroisocoumarin
BDBM50208246

2D Structure

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2D Structure of 5-Formyl-8-hydroxy-3-methyl-3,4-dihydroisocoumarin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9636 96.36%
Caco-2 + 0.6151 61.51%
Blood Brain Barrier - 0.8500 85.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.6883 68.83%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8557 85.57%
OATP1B3 inhibitior + 0.9906 99.06%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9242 92.42%
P-glycoprotein inhibitior - 0.9694 96.94%
P-glycoprotein substrate - 0.9150 91.50%
CYP3A4 substrate - 0.5594 55.94%
CYP2C9 substrate + 0.6383 63.83%
CYP2D6 substrate - 0.8476 84.76%
CYP3A4 inhibition - 0.8515 85.15%
CYP2C9 inhibition + 0.5973 59.73%
CYP2C19 inhibition - 0.9001 90.01%
CYP2D6 inhibition - 0.9036 90.36%
CYP1A2 inhibition + 0.5679 56.79%
CYP2C8 inhibition - 0.9067 90.67%
CYP inhibitory promiscuity - 0.9415 94.15%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9413 94.13%
Carcinogenicity (trinary) Non-required 0.5510 55.10%
Eye corrosion - 0.9670 96.70%
Eye irritation + 0.9737 97.37%
Skin irritation - 0.5401 54.01%
Skin corrosion - 0.9121 91.21%
Ames mutagenesis + 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7972 79.72%
Micronuclear + 0.7059 70.59%
Hepatotoxicity + 0.7566 75.66%
skin sensitisation - 0.8672 86.72%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.8000 80.00%
Nephrotoxicity + 0.6874 68.74%
Acute Oral Toxicity (c) I 0.5455 54.55%
Estrogen receptor binding + 0.6815 68.15%
Androgen receptor binding + 0.5435 54.35%
Thyroid receptor binding - 0.6722 67.22%
Glucocorticoid receptor binding - 0.6350 63.50%
Aromatase binding - 0.8792 87.92%
PPAR gamma - 0.6114 61.14%
Honey bee toxicity - 0.9383 93.83%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.8894 88.94%

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
CHEMBL1951 P21397 Monoamine oxidase A 99.35% 91.49%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.80% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.53% 95.56%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 95.92% 98.11%
CHEMBL2581 P07339 Cathepsin D 92.75% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.24% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.58% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.78% 99.23%
CHEMBL4208 P20618 Proteasome component C5 84.22% 90.00%
CHEMBL3401 O75469 Pregnane X receptor 83.73% 94.73%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 80.27% 85.11%

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.
Brucea javanica
Picea glauca

Cross-Links

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PubChem 44423672
LOTUS LTS0110990
wikiData Q105214771