3,7-Diprenyl indole

Details

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Internal ID a0c5b46d-89ea-467c-8cb4-3f7ee6cdbc3e
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Indoles > 3-alkylindoles
IUPAC Name 3,7-bis(3-methylbut-2-enyl)-1H-indole
SMILES (Canonical) CC(=CCC1=C2C(=CC=C1)C(=CN2)CC=C(C)C)C
SMILES (Isomeric) CC(=CCC1=C2C(=CC=C1)C(=CN2)CC=C(C)C)C
InChI InChI=1S/C18H23N/c1-13(2)8-10-15-6-5-7-17-16(11-9-14(3)4)12-19-18(15)17/h5-9,12,19H,10-11H2,1-4H3
InChI Key HTOGKHXNDXIBKM-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H23N
Molecular Weight 253.40 g/mol
Exact Mass 253.183049738 g/mol
Topological Polar Surface Area (TPSA) 15.80 Ų
XlogP 5.90
Atomic LogP (AlogP) 5.19
H-Bond Acceptor 0
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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3,7-Diprenyl indole
NSC-712180

2D Structure

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2D Structure of 3,7-Diprenyl 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 + 0.9481 94.81%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Lysosomes 0.5234 52.34%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9374 93.74%
OATP1B3 inhibitior + 0.9482 94.82%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.8051 80.51%
P-glycoprotein inhibitior - 0.7894 78.94%
P-glycoprotein substrate - 0.8145 81.45%
CYP3A4 substrate - 0.5764 57.64%
CYP2C9 substrate - 0.8037 80.37%
CYP2D6 substrate + 0.3835 38.35%
CYP3A4 inhibition - 0.5981 59.81%
CYP2C9 inhibition + 0.5677 56.77%
CYP2C19 inhibition + 0.6910 69.10%
CYP2D6 inhibition + 0.5767 57.67%
CYP1A2 inhibition + 0.7952 79.52%
CYP2C8 inhibition - 0.8904 89.04%
CYP inhibitory promiscuity + 0.8432 84.32%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8400 84.00%
Carcinogenicity (trinary) Non-required 0.5718 57.18%
Eye corrosion - 0.9783 97.83%
Eye irritation + 0.5963 59.63%
Skin irritation - 0.5996 59.96%
Skin corrosion - 0.8218 82.18%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8805 88.05%
Micronuclear + 0.5559 55.59%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation - 0.5744 57.44%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.6810 68.10%
Acute Oral Toxicity (c) III 0.6929 69.29%
Estrogen receptor binding + 0.8914 89.14%
Androgen receptor binding - 0.7715 77.15%
Thyroid receptor binding + 0.6849 68.49%
Glucocorticoid receptor binding + 0.6066 60.66%
Aromatase binding + 0.8154 81.54%
PPAR gamma + 0.9032 90.32%
Honey bee toxicity - 0.9336 93.36%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9707 97.07%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.56% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 93.27% 94.73%
CHEMBL2581 P07339 Cathepsin D 91.65% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.48% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.80% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.22% 86.33%
CHEMBL1951 P21397 Monoamine oxidase A 83.94% 91.49%
CHEMBL213 P08588 Beta-1 adrenergic receptor 82.70% 95.56%
CHEMBL2535 P11166 Glucose transporter 82.38% 98.75%
CHEMBL3830 Q2M2I8 Adaptor-associated kinase 81.50% 83.10%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.51% 94.45%

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.
Glycosmis trichanthera

Cross-Links

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PubChem 400448
LOTUS LTS0242808
wikiData Q105033537