1,2-Dideuterio-3-methylindole

Details

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Internal ID 979c17ea-1080-414d-b517-59e47ac4fa4a
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Indoles > 3-alkylindoles > 3-methylindoles
IUPAC Name 1,2-dideuterio-3-methylindole
SMILES (Canonical) CC1=CNC2=CC=CC=C12
SMILES (Isomeric) [2H]C1=C(C2=CC=CC=C2N1[2H])C
InChI InChI=1S/C9H9N/c1-7-6-10-9-5-3-2-4-8(7)9/h2-6,10H,1H3/i6D/hD
InChI Key ZFRKQXVRDFCRJG-MOEATMQCSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C9H9N
Molecular Weight 133.19 g/mol
Exact Mass 133.086052783 g/mol
Topological Polar Surface Area (TPSA) 15.80 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.48
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 1,2-Dideuterio-3-methylindole

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9973 99.73%
Caco-2 + 0.9710 97.10%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Lysosomes 0.5697 56.97%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9431 94.31%
OATP1B3 inhibitior + 0.9591 95.91%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8414 84.14%
P-glycoprotein inhibitior - 0.9778 97.78%
P-glycoprotein substrate - 0.9275 92.75%
CYP3A4 substrate - 0.5782 57.82%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate - 0.7001 70.01%
CYP3A4 inhibition - 0.8474 84.74%
CYP2C9 inhibition - 0.5820 58.20%
CYP2C19 inhibition + 0.8241 82.41%
CYP2D6 inhibition - 0.6493 64.93%
CYP1A2 inhibition + 0.8656 86.56%
CYP2C8 inhibition - 0.8464 84.64%
CYP inhibitory promiscuity + 0.7088 70.88%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8000 80.00%
Carcinogenicity (trinary) Non-required 0.5069 50.69%
Eye corrosion - 0.9369 93.69%
Eye irritation + 0.9946 99.46%
Skin irritation + 0.6460 64.60%
Skin corrosion - 0.9254 92.54%
Ames mutagenesis + 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6936 69.36%
Micronuclear + 0.7659 76.59%
Hepatotoxicity + 0.8198 81.98%
skin sensitisation - 0.7260 72.60%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity - 0.6323 63.23%
Nephrotoxicity - 0.6075 60.75%
Acute Oral Toxicity (c) III 0.8131 81.31%
Estrogen receptor binding - 0.8017 80.17%
Androgen receptor binding - 0.8823 88.23%
Thyroid receptor binding - 0.6280 62.80%
Glucocorticoid receptor binding - 0.7864 78.64%
Aromatase binding - 0.8417 84.17%
PPAR gamma - 0.6986 69.86%
Honey bee toxicity - 0.9700 97.00%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.7800 78.00%
Fish aquatic toxicity + 0.8504 85.04%

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 92.91% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.13% 91.11%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 87.44% 92.67%
CHEMBL2581 P07339 Cathepsin D 86.15% 98.95%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 85.06% 94.62%
CHEMBL3155 P34969 Serotonin 7 (5-HT7) receptor 84.55% 90.71%
CHEMBL3310 Q96DB2 Histone deacetylase 11 84.00% 88.56%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 83.21% 93.65%
CHEMBL2996 Q05655 Protein kinase C delta 83.01% 97.79%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 82.37% 89.62%
CHEMBL5805 Q9NR97 Toll-like receptor 8 80.98% 96.25%
CHEMBL3401 O75469 Pregnane X receptor 80.93% 94.73%
CHEMBL3192 Q9BY41 Histone deacetylase 8 80.78% 93.99%

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.
Catharanthus roseus

Cross-Links

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PubChem 11819121
NPASS NPC78498