2-Oxo-3-hydroxyindoline-3alpha-acetic acid

Details

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Internal ID 82438785-f58e-4386-8600-69559620e1d0
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Indolyl carboxylic acids and derivatives
IUPAC Name 2-[(3S)-3-hydroxy-2-oxo-1H-indol-3-yl]acetic acid
SMILES (Canonical) C1=CC=C2C(=C1)C(C(=O)N2)(CC(=O)O)O
SMILES (Isomeric) C1=CC=C2C(=C1)[C@](C(=O)N2)(CC(=O)O)O
InChI InChI=1S/C10H9NO4/c12-8(13)5-10(15)6-3-1-2-4-7(6)11-9(10)14/h1-4,15H,5H2,(H,11,14)(H,12,13)/t10-/m0/s1
InChI Key MHLHEINWUCSPTL-JTQLQIEISA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H9NO4
Molecular Weight 207.18 g/mol
Exact Mass 207.05315777 g/mol
Topological Polar Surface Area (TPSA) 86.60 Ų
XlogP 0.10
Atomic LogP (AlogP) 0.30
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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J3.667.402D

2D Structure

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2D Structure of 2-Oxo-3-hydroxyindoline-3alpha-acetic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6704 67.04%
Caco-2 + 0.4903 49.03%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.7857 78.57%
Subcellular localzation Mitochondria 0.5822 58.22%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9303 93.03%
OATP1B3 inhibitior + 0.9433 94.33%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9409 94.09%
P-glycoprotein inhibitior - 0.9908 99.08%
P-glycoprotein substrate - 0.9406 94.06%
CYP3A4 substrate - 0.6154 61.54%
CYP2C9 substrate - 0.8062 80.62%
CYP2D6 substrate - 0.7970 79.70%
CYP3A4 inhibition - 0.9724 97.24%
CYP2C9 inhibition - 0.9577 95.77%
CYP2C19 inhibition - 0.9527 95.27%
CYP2D6 inhibition - 0.9561 95.61%
CYP1A2 inhibition - 0.9126 91.26%
CYP2C8 inhibition - 0.9176 91.76%
CYP inhibitory promiscuity - 0.9585 95.85%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6290 62.90%
Eye corrosion - 0.9926 99.26%
Eye irritation + 0.7443 74.43%
Skin irritation - 0.7852 78.52%
Skin corrosion - 0.9438 94.38%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.9387 93.87%
Micronuclear + 0.8459 84.59%
Hepatotoxicity - 0.5375 53.75%
skin sensitisation - 0.8573 85.73%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity + 0.4599 45.99%
Acute Oral Toxicity (c) III 0.5603 56.03%
Estrogen receptor binding - 0.8318 83.18%
Androgen receptor binding - 0.5075 50.75%
Thyroid receptor binding - 0.6196 61.96%
Glucocorticoid receptor binding - 0.5179 51.79%
Aromatase binding - 0.6211 62.11%
PPAR gamma + 0.7668 76.68%
Honey bee toxicity - 0.9892 98.92%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity - 0.6160 61.60%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.48% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.93% 95.56%
CHEMBL2581 P07339 Cathepsin D 93.79% 98.95%
CHEMBL4208 P20618 Proteasome component C5 93.66% 90.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.39% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 89.18% 90.17%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 88.60% 94.62%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.47% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.12% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.81% 99.23%

Cross-Links

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PubChem 92449351
NPASS NPC14725
LOTUS LTS0184813
wikiData Q105163856