4,5,6-Trihydroxy-7-methylphthalide

Details

Top
Internal ID 65d0d6b2-bc70-4bd0-9cf1-ee1e7a99139e
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Hydroxybenzoic acid derivatives > Gallic acid and derivatives
IUPAC Name 4,5,6-trihydroxy-7-methyl-3H-2-benzofuran-1-one
SMILES (Canonical) CC1=C2C(=C(C(=C1O)O)O)COC2=O
SMILES (Isomeric) CC1=C2C(=C(C(=C1O)O)O)COC2=O
InChI InChI=1S/C9H8O5/c1-3-5-4(2-14-9(5)13)7(11)8(12)6(3)10/h10-12H,2H2,1H3
InChI Key RABLYBQDMDORFH-UHFFFAOYSA-N
Popularity 7 references in papers

Physical and Chemical Properties

Top
Molecular Formula C9H8O5
Molecular Weight 196.16 g/mol
Exact Mass 196.03717335 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP 0.60
Atomic LogP (AlogP) 0.78
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 0

Synonyms

Top
4,5,6-Trihydroxy-7-methyl-1,3-dihydroisobenzofuran-1-one

2D Structure

Top
2D Structure of 4,5,6-Trihydroxy-7-methylphthalide

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8805 88.05%
Caco-2 - 0.7881 78.81%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.6781 67.81%
OATP2B1 inhibitior - 0.8527 85.27%
OATP1B1 inhibitior + 0.9107 91.07%
OATP1B3 inhibitior + 0.9565 95.65%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9118 91.18%
P-glycoprotein inhibitior - 0.9517 95.17%
P-glycoprotein substrate - 0.9647 96.47%
CYP3A4 substrate - 0.5889 58.89%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8586 85.86%
CYP3A4 inhibition - 0.8915 89.15%
CYP2C9 inhibition - 0.8470 84.70%
CYP2C19 inhibition - 0.8715 87.15%
CYP2D6 inhibition - 0.9635 96.35%
CYP1A2 inhibition + 0.6156 61.56%
CYP2C8 inhibition - 0.9596 95.96%
CYP inhibitory promiscuity - 0.7567 75.67%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5964 59.64%
Eye corrosion - 0.9813 98.13%
Eye irritation + 0.9450 94.50%
Skin irritation - 0.6242 62.42%
Skin corrosion - 0.9068 90.68%
Ames mutagenesis + 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7488 74.88%
Micronuclear + 0.6681 66.81%
Hepatotoxicity + 0.8375 83.75%
skin sensitisation - 0.7044 70.44%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity + 0.5838 58.38%
Acute Oral Toxicity (c) III 0.4945 49.45%
Estrogen receptor binding - 0.6077 60.77%
Androgen receptor binding + 0.5570 55.70%
Thyroid receptor binding - 0.8261 82.61%
Glucocorticoid receptor binding - 0.5308 53.08%
Aromatase binding - 0.7768 77.68%
PPAR gamma - 0.7888 78.88%
Honey bee toxicity - 0.9676 96.76%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9073 90.73%

Targets

Top

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
CHEMBL2002 P12268 Inosine-5'-monophosphate dehydrogenase 2 95.46% 98.21%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.25% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.67% 95.56%
CHEMBL2581 P07339 Cathepsin D 92.24% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.38% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.92% 89.00%
CHEMBL1951 P21397 Monoamine oxidase A 84.63% 91.49%

Cross-Links

Top
PubChem 10420195
NPASS NPC76662
LOTUS LTS0002228
wikiData Q75068754