4-Hydroxymethyl-3-(2,4-dimethyl-7-indolyl)-2-methylindole

Details

Top
Internal ID 6f04f61c-afc2-4982-b986-807b358bcde9
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Indoles
IUPAC Name [3-(2,4-dimethyl-1H-indol-7-yl)-2-methyl-1H-indol-4-yl]methanol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H20N2O/c1-11-7-8-15(20-16(11)9-12(2)21-20)18-13(3)22-17-6-4-5-14(10-23)19(17)18/h4-9,21-23H,10H2,1-3H3
InChI Key SBTXBKCHDDDFJM-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C20H20N2O
Molecular Weight 304.40 g/mol
Exact Mass 304.157563266 g/mol
Topological Polar Surface Area (TPSA) 51.80 Ų
XlogP 4.10
Atomic LogP (AlogP) 4.73
H-Bond Acceptor 1
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 4-Hydroxymethyl-3-(2,4-dimethyl-7-indolyl)-2-methylindole

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9936 99.36%
Caco-2 + 0.5864 58.64%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.8044 80.44%
OATP2B1 inhibitior - 0.7107 71.07%
OATP1B1 inhibitior + 0.8685 86.85%
OATP1B3 inhibitior + 0.9347 93.47%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.8090 80.90%
P-glycoprotein inhibitior - 0.7335 73.35%
P-glycoprotein substrate - 0.5810 58.10%
CYP3A4 substrate + 0.5919 59.19%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.6964 69.64%
CYP3A4 inhibition + 0.6905 69.05%
CYP2C9 inhibition + 0.7797 77.97%
CYP2C19 inhibition + 0.9066 90.66%
CYP2D6 inhibition + 0.5702 57.02%
CYP1A2 inhibition + 0.9234 92.34%
CYP2C8 inhibition + 0.6509 65.09%
CYP inhibitory promiscuity + 0.9434 94.34%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.5277 52.77%
Eye corrosion - 0.9943 99.43%
Eye irritation - 0.6286 62.86%
Skin irritation - 0.8081 80.81%
Skin corrosion - 0.9420 94.20%
Ames mutagenesis + 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4553 45.53%
Micronuclear + 0.7400 74.00%
Hepatotoxicity - 0.5268 52.68%
skin sensitisation - 0.8540 85.40%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.8642 86.42%
Acute Oral Toxicity (c) III 0.4311 43.11%
Estrogen receptor binding + 0.8533 85.33%
Androgen receptor binding + 0.7755 77.55%
Thyroid receptor binding + 0.7857 78.57%
Glucocorticoid receptor binding + 0.8380 83.80%
Aromatase binding + 0.7761 77.61%
PPAR gamma + 0.8498 84.98%
Honey bee toxicity - 0.9363 93.63%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.6982 69.82%

Targets

Top

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
CHEMBL2581 P07339 Cathepsin D 98.09% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.36% 91.11%
CHEMBL3192 Q9BY41 Histone deacetylase 8 96.82% 93.99%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.58% 95.56%
CHEMBL1907 P15144 Aminopeptidase N 92.98% 93.31%
CHEMBL3401 O75469 Pregnane X receptor 92.36% 94.73%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 91.85% 91.71%
CHEMBL4302 P08183 P-glycoprotein 1 90.45% 92.98%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 89.96% 91.79%
CHEMBL1163125 O60885 Bromodomain-containing protein 4 89.09% 97.31%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.48% 96.09%
CHEMBL260 Q16539 MAP kinase p38 alpha 87.83% 97.78%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.81% 86.33%
CHEMBL1781 P11387 DNA topoisomerase I 86.72% 97.00%
CHEMBL2535 P11166 Glucose transporter 86.64% 98.75%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.42% 96.00%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 84.95% 96.21%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.91% 89.00%
CHEMBL5805 Q9NR97 Toll-like receptor 8 82.63% 96.25%
CHEMBL1936 P10721 Stem cell growth factor receptor 81.55% 84.17%
CHEMBL3310 Q96DB2 Histone deacetylase 11 81.51% 88.56%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.45% 92.62%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 81.32% 94.80%

Plants that contains it

Top
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.
There are no matching plants.

Cross-Links

Top
PubChem 10542553
LOTUS LTS0005140
wikiData Q104197150