Methyl dioxindole-3-acetate

Details

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Internal ID 89a03439-4736-4c2b-bd77-55ae27710497
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Indolyl carboxylic acids and derivatives
IUPAC Name methyl 2-(3-hydroxy-2-oxo-1H-indol-3-yl)acetate
SMILES (Canonical) COC(=O)CC1(C2=CC=CC=C2NC1=O)O
SMILES (Isomeric) COC(=O)CC1(C2=CC=CC=C2NC1=O)O
InChI InChI=1S/C11H11NO4/c1-16-9(13)6-11(15)7-4-2-3-5-8(7)12-10(11)14/h2-5,15H,6H2,1H3,(H,12,14)
InChI Key BHWUWPHGCCRYBU-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C11H11NO4
Molecular Weight 221.21 g/mol
Exact Mass 221.06880783 g/mol
Topological Polar Surface Area (TPSA) 75.60 Ų
XlogP 0.40
Atomic LogP (AlogP) 0.39
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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57061-18-4
METHYL 2-(3-HYDROXY-2-OXO-1H-INDOL-3-YL)ACETATE
1H-Indole-3-acetic acid, 2,3-dihydro-3-hydroxy-2-oxo-, methyl ester
DTXSID00554755
CHEBI:174124
NCGC00385588-01
2-Oxo-3-hydroxyindoline-3-acetic acid methyl ester
Methyl (3-hydroxy-2-oxo-2,3-dihydro-1H-indol-3-yl)acetate
methyl 2-(3-hydroxy-2-oxo-2,3-dihydro-1H-indol-3-yl)acetate

2D Structure

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2D Structure of Methyl dioxindole-3-acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7312 73.12%
Caco-2 + 0.5565 55.65%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.5631 56.31%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9314 93.14%
OATP1B3 inhibitior + 0.9449 94.49%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8042 80.42%
P-glycoprotein inhibitior - 0.9763 97.63%
P-glycoprotein substrate - 0.8722 87.22%
CYP3A4 substrate - 0.5065 50.65%
CYP2C9 substrate - 0.7907 79.07%
CYP2D6 substrate - 0.7733 77.33%
CYP3A4 inhibition - 0.9206 92.06%
CYP2C9 inhibition - 0.9036 90.36%
CYP2C19 inhibition - 0.9341 93.41%
CYP2D6 inhibition - 0.9540 95.40%
CYP1A2 inhibition - 0.8125 81.25%
CYP2C8 inhibition - 0.8397 83.97%
CYP inhibitory promiscuity - 0.9147 91.47%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6129 61.29%
Eye corrosion - 0.9920 99.20%
Eye irritation - 0.5959 59.59%
Skin irritation - 0.8000 80.00%
Skin corrosion - 0.9441 94.41%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8108 81.08%
Micronuclear + 0.8259 82.59%
Hepatotoxicity - 0.6097 60.97%
skin sensitisation - 0.8810 88.10%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.9444 94.44%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity + 0.6149 61.49%
Acute Oral Toxicity (c) III 0.6244 62.44%
Estrogen receptor binding - 0.6962 69.62%
Androgen receptor binding + 0.5336 53.36%
Thyroid receptor binding - 0.5303 53.03%
Glucocorticoid receptor binding - 0.4917 49.17%
Aromatase binding - 0.6055 60.55%
PPAR gamma + 0.5932 59.32%
Honey bee toxicity - 0.9648 96.48%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity - 0.5399 53.99%

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 97.56% 91.11%
CHEMBL4208 P20618 Proteasome component C5 94.72% 90.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.03% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.23% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.01% 95.56%
CHEMBL2581 P07339 Cathepsin D 89.20% 98.95%
CHEMBL4040 P28482 MAP kinase ERK2 88.58% 83.82%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.33% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.33% 99.23%

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.
Rubus chingii
Rubus coreanus
Rubus idaeus

Cross-Links

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PubChem 14033762
NPASS NPC46324