2-(1H-indol-3-yl)ethyl octadeca-9,14-dien-12-ynoate

Details

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Internal ID a885f5e6-19b5-4d4a-9311-45fe5cb3b096
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Indoles > 3-alkylindoles
IUPAC Name 2-(1H-indol-3-yl)ethyl octadeca-9,14-dien-12-ynoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C28H37NO2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-21-28(30)31-23-22-25-24-29-27-20-18-17-19-26(25)27/h4-5,9-10,17-20,24,29H,2-3,8,11-16,21-23H2,1H3
InChI Key YTTXOFYGAUPLSL-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C28H37NO2
Molecular Weight 419.60 g/mol
Exact Mass 419.282429423 g/mol
Topological Polar Surface Area (TPSA) 42.10 Ų
XlogP 8.40
Atomic LogP (AlogP) 7.29
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 14

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(1H-indol-3-yl)ethyl octadeca-9,14-dien-12-ynoate

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 - 0.6599 65.99%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Plasma membrane 0.5787 57.87%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8368 83.68%
OATP1B3 inhibitior + 0.9434 94.34%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.7276 72.76%
P-glycoprotein inhibitior + 0.7389 73.89%
P-glycoprotein substrate - 0.5941 59.41%
CYP3A4 substrate + 0.6686 66.86%
CYP2C9 substrate - 0.8063 80.63%
CYP2D6 substrate - 0.8412 84.12%
CYP3A4 inhibition - 0.5698 56.98%
CYP2C9 inhibition + 0.8350 83.50%
CYP2C19 inhibition + 0.8625 86.25%
CYP2D6 inhibition - 0.8724 87.24%
CYP1A2 inhibition + 0.8709 87.09%
CYP2C8 inhibition + 0.7794 77.94%
CYP inhibitory promiscuity + 0.8852 88.52%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.5907 59.07%
Eye corrosion - 0.9787 97.87%
Eye irritation - 0.9323 93.23%
Skin irritation - 0.8033 80.33%
Skin corrosion - 0.9529 95.29%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8377 83.77%
Micronuclear - 0.5800 58.00%
Hepatotoxicity - 0.7164 71.64%
skin sensitisation - 0.7797 77.97%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.7299 72.99%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.8562 85.62%
Acute Oral Toxicity (c) III 0.6676 66.76%
Estrogen receptor binding + 0.7798 77.98%
Androgen receptor binding - 0.7253 72.53%
Thyroid receptor binding + 0.5178 51.78%
Glucocorticoid receptor binding + 0.5518 55.18%
Aromatase binding - 0.5713 57.13%
PPAR gamma + 0.5412 54.12%
Honey bee toxicity - 0.8535 85.35%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.9847 98.47%

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 98.16% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 97.11% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.10% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 96.45% 99.17%
CHEMBL2581 P07339 Cathepsin D 95.95% 98.95%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 94.17% 94.62%
CHEMBL230 P35354 Cyclooxygenase-2 93.07% 89.63%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 92.38% 92.08%
CHEMBL1781 P11387 DNA topoisomerase I 91.76% 97.00%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 89.62% 91.81%
CHEMBL2535 P11166 Glucose transporter 88.32% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.54% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.41% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.17% 89.00%
CHEMBL1937 Q92769 Histone deacetylase 2 85.17% 94.75%
CHEMBL2996 Q05655 Protein kinase C delta 83.88% 97.79%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.74% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 82.90% 94.73%
CHEMBL3004 P33527 Multidrug resistance-associated protein 1 82.42% 96.37%
CHEMBL255 P29275 Adenosine A2b receptor 82.16% 98.59%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 82.09% 89.62%
CHEMBL3310 Q96DB2 Histone deacetylase 11 81.40% 88.56%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.31% 92.62%

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 162849704
LOTUS LTS0182565
wikiData Q105362039