Indole-4-carboxaldehyde

Details

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Internal ID 75f87b22-9444-45a9-8c1e-346def6352ab
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Indoles
IUPAC Name 1H-indole-4-carbaldehyde
SMILES (Canonical) C1=CC(=C2C=CNC2=C1)C=O
SMILES (Isomeric) C1=CC(=C2C=CNC2=C1)C=O
InChI InChI=1S/C9H7NO/c11-6-7-2-1-3-9-8(7)4-5-10-9/h1-6,10H
InChI Key JFDDFGLNZWNJTK-UHFFFAOYSA-N
Popularity 13 references in papers

Physical and Chemical Properties

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Molecular Formula C9H7NO
Molecular Weight 145.16 g/mol
Exact Mass 145.052763847 g/mol
Topological Polar Surface Area (TPSA) 32.90 Ų
XlogP 2.20
Atomic LogP (AlogP) 1.98
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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1074-86-8
1H-Indole-4-carbaldehyde
indole-4-carbaldehyde
CHEBI:143235
DTXSID40318838
RefChem:148200
DTXCID30269961
625-162-5
JFDDFGLNZWNJTK-UHFFFAOYSA-N
4-Formylindole
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Indole-4-carboxaldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.9314 93.14%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Lysosomes 0.5725 57.25%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8914 89.14%
OATP1B3 inhibitior + 0.9636 96.36%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8143 81.43%
P-glycoprotein inhibitior - 0.9808 98.08%
P-glycoprotein substrate - 0.9188 91.88%
CYP3A4 substrate - 0.6674 66.74%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7443 74.43%
CYP3A4 inhibition - 0.9298 92.98%
CYP2C9 inhibition - 0.8288 82.88%
CYP2C19 inhibition + 0.6623 66.23%
CYP2D6 inhibition - 0.6626 66.26%
CYP1A2 inhibition + 0.8296 82.96%
CYP2C8 inhibition - 0.8750 87.50%
CYP inhibitory promiscuity - 0.7274 72.74%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7700 77.00%
Carcinogenicity (trinary) Non-required 0.6643 66.43%
Eye corrosion - 0.8072 80.72%
Eye irritation + 0.9964 99.64%
Skin irritation + 0.7533 75.33%
Skin corrosion - 0.9308 93.08%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6812 68.12%
Micronuclear + 0.7959 79.59%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation - 0.7276 72.76%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity - 0.5642 56.42%
Acute Oral Toxicity (c) III 0.8195 81.95%
Estrogen receptor binding - 0.8289 82.89%
Androgen receptor binding - 0.7684 76.84%
Thyroid receptor binding - 0.6446 64.46%
Glucocorticoid receptor binding - 0.7875 78.75%
Aromatase binding - 0.5619 56.19%
PPAR gamma - 0.7257 72.57%
Honey bee toxicity - 0.9070 90.70%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity - 0.5689 56.89%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.34% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.04% 94.45%
CHEMBL3830 Q2M2I8 Adaptor-associated kinase 91.45% 83.10%
CHEMBL3310 Q96DB2 Histone deacetylase 11 89.95% 88.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.67% 91.11%
CHEMBL2581 P07339 Cathepsin D 86.50% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 83.20% 94.73%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 82.95% 98.11%
CHEMBL1829 O15379 Histone deacetylase 3 82.64% 95.00%
CHEMBL2996 Q05655 Protein kinase C delta 81.63% 97.79%

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 333703
LOTUS LTS0195443
wikiData Q72482968