1H-indole-3-carboxamide

Details

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Internal ID 3f6856f3-d076-4c21-ad7f-42125de270c8
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Indolecarboxylic acids and derivatives > Indolecarboxamides and derivatives
IUPAC Name 1H-indole-3-carboxamide
SMILES (Canonical) C1=CC=C2C(=C1)C(=CN2)C(=O)N
SMILES (Isomeric) C1=CC=C2C(=C1)C(=CN2)C(=O)N
InChI InChI=1S/C9H8N2O/c10-9(12)7-5-11-8-4-2-1-3-6(7)8/h1-5,11H,(H2,10,12)
InChI Key LSGKMZLPZFPAIN-UHFFFAOYSA-N
Popularity 60 references in papers

Physical and Chemical Properties

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Molecular Formula C9H8N2O
Molecular Weight 160.17 g/mol
Exact Mass 160.063662883 g/mol
Topological Polar Surface Area (TPSA) 58.90 Ų
XlogP 1.30

Synonyms

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1H-Indole-3-carboxylic acid amide
1670-85-5
indole-3-carboxamide
1H-Indole-3-carboxamide(9CI)
1-H-Indole-3-carboxamide
Cambridge id 5106715
MLS001048867
SCHEMBL117198
CHEMBL379099
BDBM93016
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 1H-indole-3-carboxamide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
No predicted properties yet!

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL3577 P00352 Aldehyde dehydrogenase 1A1 39810.7 nM
Potency
via CMAUP
CHEMBL3797 Q13315 Serine-protein kinase ATM 631 nM
631 nM
Potency
Potency
PMID: 20550123
via Super-PRED

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.30% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.52% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.31% 96.09%
CHEMBL3830 Q2M2I8 Adaptor-associated kinase 89.70% 83.10%
CHEMBL2535 P11166 Glucose transporter 84.66% 98.75%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.60% 94.45%
CHEMBL213 P08588 Beta-1 adrenergic receptor 83.80% 95.56%
CHEMBL2708 Q16584 Mitogen-activated protein kinase kinase kinase 11 82.46% 81.14%
CHEMBL3310 Q96DB2 Histone deacetylase 11 81.27% 88.56%
CHEMBL3902 P09211 Glutathione S-transferase Pi 80.70% 93.81%

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.
Isatis tinctoria

Cross-Links

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PubChem 2192542
NPASS NPC131718
ChEMBL CHEMBL379099
LOTUS LTS0010601
wikiData Q82152400