4,5,6-Trihydroxy-3-methylphthalide

Details

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Internal ID 1445f3ef-fbf9-44bc-9903-2801e89c85eb
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Hydroxybenzoic acid derivatives > Gallic acid and derivatives
IUPAC Name 4,5,6-trihydroxy-3-methyl-3H-2-benzofuran-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H8O5/c1-3-6-4(9(13)14-3)2-5(10)7(11)8(6)12/h2-3,10-12H,1H3
InChI Key AGUVVAYMPQDJDX-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C9H8O5
Molecular Weight 196.16 g/mol
Exact Mass 196.03717335 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP 0.70
Atomic LogP (AlogP) 1.03
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 0

Synonyms

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4,5,6-trihydroxy-3-methylphthalide
AGUVVAYMPQDJDX-UHFFFAOYSA-
BDBM50242174
3-methyl-4,5,6-trihydroxy-phthalide
PD181935
InChI=1/C9H8O5/c1-3-6-4(9(13)14-3)2-5(10)7(11)8(6)12/h2-3,10-12H,1H3

2D Structure

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2D Structure of 4,5,6-Trihydroxy-3-methylphthalide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9399 93.99%
Caco-2 - 0.8339 83.39%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.6191 61.91%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7813 78.13%
OATP1B3 inhibitior + 0.9524 95.24%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9707 97.07%
P-glycoprotein inhibitior - 0.9590 95.90%
P-glycoprotein substrate - 0.9678 96.78%
CYP3A4 substrate - 0.5969 59.69%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8586 85.86%
CYP3A4 inhibition - 0.8072 80.72%
CYP2C9 inhibition - 0.9167 91.67%
CYP2C19 inhibition - 0.8926 89.26%
CYP2D6 inhibition - 0.9639 96.39%
CYP1A2 inhibition + 0.7093 70.93%
CYP2C8 inhibition - 0.9591 95.91%
CYP inhibitory promiscuity - 0.7473 74.73%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5624 56.24%
Eye corrosion - 0.9384 93.84%
Eye irritation + 0.8610 86.10%
Skin irritation + 0.6007 60.07%
Skin corrosion - 0.8694 86.94%
Ames mutagenesis - 0.5818 58.18%
Human Ether-a-go-go-Related Gene inhibition - 0.7971 79.71%
Micronuclear + 0.9000 90.00%
Hepatotoxicity + 0.6750 67.50%
skin sensitisation - 0.5728 57.28%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity - 0.6996 69.96%
Acute Oral Toxicity (c) IV 0.4014 40.14%
Estrogen receptor binding - 0.5407 54.07%
Androgen receptor binding + 0.6117 61.17%
Thyroid receptor binding - 0.6994 69.94%
Glucocorticoid receptor binding + 0.5763 57.63%
Aromatase binding - 0.8212 82.12%
PPAR gamma - 0.8298 82.98%
Honey bee toxicity - 0.9531 95.31%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9006 90.06%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.72% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 92.69% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.10% 95.56%
CHEMBL2581 P07339 Cathepsin D 89.59% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.05% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.13% 94.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.96% 85.14%
CHEMBL3401 O75469 Pregnane X receptor 83.90% 94.73%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.56% 99.23%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 80.56% 99.15%

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 11424128
LOTUS LTS0112977
wikiData Q103816103