3-Farnesylindole

Details

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Internal ID b6a53c4c-4114-45ec-a4ff-c22fa5886af9
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 3-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl]-2,3-dihydro-1H-indole
SMILES (Canonical) CC(=CCCC(=CCCC(=CCC1CNC2=CC=CC=C12)C)C)C
SMILES (Isomeric) CC(=CCC/C(=C/CC/C(=C/CC1CNC2=CC=CC=C12)/C)/C)C
InChI InChI=1S/C23H33N/c1-18(2)9-7-10-19(3)11-8-12-20(4)15-16-21-17-24-23-14-6-5-13-22(21)23/h5-6,9,11,13-15,21,24H,7-8,10,12,16-17H2,1-4H3/b19-11+,20-15+
InChI Key ZZFPPZXXZGMWBZ-NKFKFSAASA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C23H33N
Molecular Weight 323.50 g/mol
Exact Mass 323.261300057 g/mol
Topological Polar Surface Area (TPSA) 12.00 Ų
XlogP 7.40
Atomic LogP (AlogP) 7.01
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 8

Synonyms

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3-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl]indoline

2D Structure

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2D Structure of 3-Farnesylindole

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9964 99.64%
Caco-2 + 0.7656 76.56%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Lysosomes 0.4040 40.40%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9139 91.39%
OATP1B3 inhibitior + 0.9420 94.20%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior + 0.6000 60.00%
BSEP inhibitior + 0.9185 91.85%
P-glycoprotein inhibitior + 0.7321 73.21%
P-glycoprotein substrate - 0.7455 74.55%
CYP3A4 substrate + 0.5419 54.19%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.5791 57.91%
CYP3A4 inhibition - 0.7774 77.74%
CYP2C9 inhibition - 0.5309 53.09%
CYP2C19 inhibition - 0.5000 50.00%
CYP2D6 inhibition + 0.5117 51.17%
CYP1A2 inhibition + 0.8028 80.28%
CYP2C8 inhibition - 0.7353 73.53%
CYP inhibitory promiscuity + 0.6423 64.23%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.6582 65.82%
Eye corrosion - 0.9791 97.91%
Eye irritation - 0.9538 95.38%
Skin irritation - 0.6837 68.37%
Skin corrosion - 0.7943 79.43%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9439 94.39%
Micronuclear - 0.7400 74.00%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation - 0.6686 66.86%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.6428 64.28%
Acute Oral Toxicity (c) III 0.7140 71.40%
Estrogen receptor binding + 0.7627 76.27%
Androgen receptor binding - 0.6378 63.78%
Thyroid receptor binding + 0.6683 66.83%
Glucocorticoid receptor binding - 0.4826 48.26%
Aromatase binding + 0.5558 55.58%
PPAR gamma + 0.7976 79.76%
Honey bee toxicity - 0.9127 91.27%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity + 0.9938 99.38%

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 97.48% 91.11%
CHEMBL2581 P07339 Cathepsin D 95.63% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.83% 96.09%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 91.07% 92.08%
CHEMBL221 P23219 Cyclooxygenase-1 87.21% 90.17%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.71% 97.25%
CHEMBL3401 O75469 Pregnane X receptor 86.01% 94.73%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.36% 85.14%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 82.83% 85.49%
CHEMBL2716 Q8WUI4 Histone deacetylase 7 81.53% 89.44%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.19% 97.09%

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.
Uvaria pandensis
Uvaria scheffleri

Cross-Links

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PubChem 49768248
LOTUS LTS0116937
wikiData Q104396446