(3S)-7,8-dihydroxy-3-methyl-3,4-dihydroisochromen-1-one

Details

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Internal ID b4319943-ca4c-4bf6-b3b6-2803a051e9be
Taxonomy Organoheterocyclic compounds > Benzopyrans > 2-benzopyrans
IUPAC Name (3S)-7,8-dihydroxy-3-methyl-3,4-dihydroisochromen-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H10O4/c1-5-4-6-2-3-7(11)9(12)8(6)10(13)14-5/h2-3,5,11-12H,4H2,1H3/t5-/m0/s1
InChI Key NNADFONXCWKMRA-YFKPBYRVSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C10H10O4
Molecular Weight 194.18 g/mol
Exact Mass 194.05790880 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 2.10
Atomic LogP (AlogP) 1.20
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3S)-7,8-dihydroxy-3-methyl-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 + 0.8635 86.35%
Caco-2 - 0.6028 60.28%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.6737 67.37%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9083 90.83%
OATP1B3 inhibitior + 0.9879 98.79%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9657 96.57%
P-glycoprotein inhibitior - 0.9754 97.54%
P-glycoprotein substrate - 0.9452 94.52%
CYP3A4 substrate - 0.5712 57.12%
CYP2C9 substrate - 0.5555 55.55%
CYP2D6 substrate - 0.8498 84.98%
CYP3A4 inhibition - 0.9034 90.34%
CYP2C9 inhibition - 0.7656 76.56%
CYP2C19 inhibition - 0.8851 88.51%
CYP2D6 inhibition - 0.8687 86.87%
CYP1A2 inhibition + 0.8185 81.85%
CYP2C8 inhibition - 0.9643 96.43%
CYP inhibitory promiscuity - 0.9052 90.52%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5585 55.85%
Eye corrosion - 0.9818 98.18%
Eye irritation + 0.8247 82.47%
Skin irritation - 0.5229 52.29%
Skin corrosion - 0.8963 89.63%
Ames mutagenesis + 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7768 77.68%
Micronuclear + 0.7359 73.59%
Hepatotoxicity + 0.6750 67.50%
skin sensitisation - 0.7640 76.40%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.8000 80.00%
Nephrotoxicity - 0.6269 62.69%
Acute Oral Toxicity (c) I 0.3638 36.38%
Estrogen receptor binding - 0.6530 65.30%
Androgen receptor binding + 0.6875 68.75%
Thyroid receptor binding - 0.6669 66.69%
Glucocorticoid receptor binding - 0.6577 65.77%
Aromatase binding - 0.8557 85.57%
PPAR gamma - 0.6351 63.51%
Honey bee toxicity - 0.9638 96.38%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9016 90.16%

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 99.12% 91.49%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.62% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.64% 95.56%
CHEMBL2581 P07339 Cathepsin D 89.69% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.40% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.78% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 83.95% 94.73%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.98% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.71% 86.33%

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 130776091
LOTUS LTS0134257
wikiData Q105182036