2,3,4,6-tetrabromo-1H-indole

Details

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Internal ID 4376b8cd-e828-46b6-9b88-e5142ad9b55d
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Indoles
IUPAC Name 2,3,4,6-tetrabromo-1H-indole
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H3Br4N/c9-3-1-4(10)6-5(2-3)13-8(12)7(6)11/h1-2,13H
InChI Key HYJQJQUXQBDKPQ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C8H3Br4N
Molecular Weight 432.73 g/mol
Exact Mass 432.69580 g/mol
Topological Polar Surface Area (TPSA) 15.80 Ų
XlogP 5.10
Atomic LogP (AlogP) 5.22
H-Bond Acceptor 0
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2,3,4,6-tetrabromo-1H-indole

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 + 0.6194 61.94%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Lysosomes 0.7514 75.14%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9251 92.51%
OATP1B3 inhibitior + 0.9556 95.56%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.6673 66.73%
P-glycoprotein inhibitior - 0.9671 96.71%
P-glycoprotein substrate - 0.9527 95.27%
CYP3A4 substrate - 0.6599 65.99%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.6910 69.10%
CYP3A4 inhibition - 0.7006 70.06%
CYP2C9 inhibition + 0.7460 74.60%
CYP2C19 inhibition + 0.8374 83.74%
CYP2D6 inhibition - 0.8925 89.25%
CYP1A2 inhibition + 0.9626 96.26%
CYP2C8 inhibition - 0.8697 86.97%
CYP inhibitory promiscuity + 0.6981 69.81%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7042 70.42%
Carcinogenicity (trinary) Non-required 0.6454 64.54%
Eye corrosion - 0.9169 91.69%
Eye irritation + 0.9355 93.55%
Skin irritation - 0.5199 51.99%
Skin corrosion - 0.9544 95.44%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6295 62.95%
Micronuclear + 0.8400 84.00%
Hepatotoxicity + 0.7427 74.27%
skin sensitisation - 0.7136 71.36%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity - 0.8072 80.72%
Nephrotoxicity - 0.7862 78.62%
Acute Oral Toxicity (c) III 0.6001 60.01%
Estrogen receptor binding + 0.5861 58.61%
Androgen receptor binding + 0.5621 56.21%
Thyroid receptor binding + 0.5374 53.74%
Glucocorticoid receptor binding + 0.6793 67.93%
Aromatase binding + 0.5276 52.76%
PPAR gamma + 0.7333 73.33%
Honey bee toxicity - 0.8794 87.94%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.6900 69.00%
Fish aquatic toxicity + 0.9366 93.66%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.72% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.19% 91.11%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 90.94% 85.30%
CHEMBL241 Q14432 Phosphodiesterase 3A 87.64% 92.94%
CHEMBL1075162 Q13304 Uracil nucleotide/cysteinyl leukotriene receptor 87.05% 80.33%
CHEMBL2292 Q13627 Dual-specificity tyrosine-phosphorylation regulated kinase 1A 86.41% 93.24%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 84.11% 97.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.75% 95.56%
CHEMBL2708 Q16584 Mitogen-activated protein kinase kinase kinase 11 80.61% 81.14%

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 14503991
LOTUS LTS0041309
wikiData Q105035339