FR-198248

Details

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Internal ID c0b8f4dd-736b-48b7-a4c7-c60e64c414b3
Taxonomy Organoheterocyclic compounds > Isocoumarans
IUPAC Name 4-methyl-1,3-dihydro-2-benzofuran-1,5,6,7-tetrol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H10O5/c1-3-4-2-14-9(13)5(4)7(11)8(12)6(3)10/h9-13H,2H2,1H3
InChI Key GSKYCPXSDLXGEW-UHFFFAOYSA-N
Popularity 7 references in papers

Physical and Chemical Properties

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Molecular Formula C9H10O5
Molecular Weight 198.17 g/mol
Exact Mass 198.05282342 g/mol
Topological Polar Surface Area (TPSA) 90.20 Ų
XlogP -0.10
Atomic LogP (AlogP) 0.63
H-Bond Acceptor 5
H-Bond Donor 4
Rotatable Bonds 0

Synonyms

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4-Methyl-1,3-dihydroisobenzofuran-1,5,6,7-tetraol
1,3-Dihydro-4-methyl-1,5,6,7-isobenzofurantetraol
AKOS040748402
HY-119728
CS-0077871
4-Methyl-1,3-dihydro-2-benzofuran-1,5,6,7-tetrol

2D Structure

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2D Structure of FR-198248

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9005 90.05%
Caco-2 - 0.9173 91.73%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.5658 56.58%
OATP2B1 inhibitior - 0.8517 85.17%
OATP1B1 inhibitior + 0.9093 90.93%
OATP1B3 inhibitior + 0.9669 96.69%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9398 93.98%
P-glycoprotein inhibitior - 0.9632 96.32%
P-glycoprotein substrate - 0.8962 89.62%
CYP3A4 substrate - 0.5475 54.75%
CYP2C9 substrate - 0.7958 79.58%
CYP2D6 substrate - 0.7395 73.95%
CYP3A4 inhibition - 0.9396 93.96%
CYP2C9 inhibition - 0.8190 81.90%
CYP2C19 inhibition - 0.8413 84.13%
CYP2D6 inhibition - 0.9312 93.12%
CYP1A2 inhibition + 0.5940 59.40%
CYP2C8 inhibition - 0.9042 90.42%
CYP inhibitory promiscuity - 0.7560 75.60%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5565 55.65%
Eye corrosion - 0.9799 97.99%
Eye irritation - 0.5217 52.17%
Skin irritation - 0.6095 60.95%
Skin corrosion - 0.8772 87.72%
Ames mutagenesis + 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6118 61.18%
Micronuclear + 0.5481 54.81%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation - 0.7239 72.39%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.6411 64.11%
Acute Oral Toxicity (c) III 0.5239 52.39%
Estrogen receptor binding - 0.6265 62.65%
Androgen receptor binding - 0.6109 61.09%
Thyroid receptor binding - 0.6477 64.77%
Glucocorticoid receptor binding - 0.6364 63.64%
Aromatase binding - 0.8174 81.74%
PPAR gamma - 0.5972 59.72%
Honey bee toxicity - 0.9367 93.67%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9260 92.60%

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 95.37% 91.49%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.47% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.21% 100.00%

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 9815565
LOTUS LTS0099159
wikiData Q77372205