(3E)-3-(3-oxo-1H-indol-2-ylidene)-1H-indol-2-one

Details

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Internal ID 830c16a1-efb9-4ff1-8b51-ad74471997b8
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Indolines
IUPAC Name (3E)-3-(3-oxo-1H-indol-2-ylidene)-1H-indol-2-one
SMILES (Canonical) C1=CC=C2C(=C1)C(=C3C(=O)C4=CC=CC=C4N3)C(=O)N2
SMILES (Isomeric) C1=CC=C2C(=C1)/C(=C\3/C(=O)C4=CC=CC=C4N3)/C(=O)N2
InChI InChI=1S/C16H10N2O2/c19-15-10-6-2-4-8-12(10)17-14(15)13-9-5-1-3-7-11(9)18-16(13)20/h1-8,17H,(H,18,20)/b14-13+
InChI Key CRDNMYFJWFXOCH-BUHFOSPRSA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C16H10N2O2
Molecular Weight 262.26 g/mol
Exact Mass 262.074227566 g/mol
Topological Polar Surface Area (TPSA) 58.20 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.66
H-Bond Acceptor 3
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 (3E)-3-(3-oxo-1H-indol-2-ylidene)-1H-indol-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9958 99.58%
Caco-2 + 0.7622 76.22%
Blood Brain Barrier + 0.7379 73.79%
Human oral bioavailability + 0.8714 87.14%
Subcellular localzation Plasma membrane 0.5536 55.36%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9443 94.43%
OATP1B3 inhibitior + 0.9361 93.61%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.6521 65.21%
P-glycoprotein inhibitior - 0.8857 88.57%
P-glycoprotein substrate - 0.9438 94.38%
CYP3A4 substrate - 0.5588 55.88%
CYP2C9 substrate - 0.8038 80.38%
CYP2D6 substrate - 0.8482 84.82%
CYP3A4 inhibition - 0.7701 77.01%
CYP2C9 inhibition + 0.7922 79.22%
CYP2C19 inhibition + 0.7526 75.26%
CYP2D6 inhibition - 0.6903 69.03%
CYP1A2 inhibition + 0.8837 88.37%
CYP2C8 inhibition - 0.9532 95.32%
CYP inhibitory promiscuity + 0.9517 95.17%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8643 86.43%
Carcinogenicity (trinary) Non-required 0.4943 49.43%
Eye corrosion - 0.9896 98.96%
Eye irritation + 0.7760 77.60%
Skin irritation - 0.8398 83.98%
Skin corrosion - 0.9622 96.22%
Ames mutagenesis + 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7080 70.80%
Micronuclear + 0.9400 94.00%
Hepatotoxicity + 0.8125 81.25%
skin sensitisation - 0.9176 91.76%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity + 0.7890 78.90%
Acute Oral Toxicity (c) III 0.5903 59.03%
Estrogen receptor binding + 0.8465 84.65%
Androgen receptor binding + 0.8689 86.89%
Thyroid receptor binding + 0.5666 56.66%
Glucocorticoid receptor binding + 0.8459 84.59%
Aromatase binding + 0.8674 86.74%
PPAR gamma + 0.6449 64.49%
Honey bee toxicity - 0.7865 78.65%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity + 0.8819 88.19%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL262 P49841 Glycogen synthase kinase-3 beta 4 nM
IC50
via Super-PRED
CHEMBL1293224 P10636 Microtubule-associated protein tau 89.1 nM
Potency
via Super-PRED

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.26% 95.56%
CHEMBL2581 P07339 Cathepsin D 93.27% 98.95%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 89.53% 82.69%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 88.80% 93.03%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 87.42% 92.88%
CHEMBL2850 P49840 Glycogen synthase kinase-3 alpha 87.41% 88.84%
CHEMBL1937 Q92769 Histone deacetylase 2 87.02% 94.75%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 87.00% 94.62%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.83% 91.11%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 85.45% 94.08%
CHEMBL299 P17252 Protein kinase C alpha 84.69% 98.03%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.15% 99.23%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 82.01% 96.67%
CHEMBL4237 O75582 Ribosomal protein S6 kinase alpha 5 81.18% 91.00%

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.
Calanthe discolor
Couroupita guianensis
Isatis tinctoria
Persicaria tinctoria
Strobilanthes cusia

Cross-Links

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PubChem 5359405
NPASS NPC72416
LOTUS LTS0210157
wikiData Q1661452