Tetracosanoic acid tryptamide, analytical standard

Details

Top
Internal ID 02d00ec8-8d0e-4318-919b-94d450981882
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > N-alkylindoles
IUPAC Name N-(2-indol-1-ylethyl)tetracosanamide
SMILES (Canonical) CCCCCCCCCCCCCCCCCCCCCCCC(=O)NCCN1C=CC2=CC=CC=C21
SMILES (Isomeric) CCCCCCCCCCCCCCCCCCCCCCCC(=O)NCCN1C=CC2=CC=CC=C21
InChI InChI=1S/C34H58N2O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-27-34(37)35-29-31-36-30-28-32-25-23-24-26-33(32)36/h23-26,28,30H,2-22,27,29,31H2,1H3,(H,35,37)
InChI Key KRRKABAFWRIPGX-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C34H58N2O
Molecular Weight 510.80 g/mol
Exact Mass 510.454914478 g/mol
Topological Polar Surface Area (TPSA) 34.00 Ų
XlogP 12.90
Atomic LogP (AlogP) 10.36
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 25

Synonyms

Top
Tetracosanoic acid tryptamide, analytical standard

2D Structure

Top
2D Structure of Tetracosanoic acid tryptamide, analytical standard

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 - 0.7834 78.34%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Lysosomes 0.7464 74.64%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9129 91.29%
OATP1B3 inhibitior + 0.9419 94.19%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior + 0.5990 59.90%
P-glycoprotein inhibitior - 0.4378 43.78%
P-glycoprotein substrate + 0.5841 58.41%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.8046 80.46%
CYP2D6 substrate - 0.8221 82.21%
CYP3A4 inhibition - 0.6527 65.27%
CYP2C9 inhibition - 0.8972 89.72%
CYP2C19 inhibition + 0.8459 84.59%
CYP2D6 inhibition + 0.5985 59.85%
CYP1A2 inhibition + 0.7760 77.60%
CYP2C8 inhibition - 0.6612 66.12%
CYP inhibitory promiscuity + 0.6259 62.59%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.7280 72.80%
Eye corrosion - 0.9836 98.36%
Eye irritation - 0.8868 88.68%
Skin irritation - 0.7882 78.82%
Skin corrosion - 0.8857 88.57%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6963 69.63%
Micronuclear - 0.5500 55.00%
Hepatotoxicity + 0.5326 53.26%
skin sensitisation - 0.9262 92.62%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.8625 86.25%
Nephrotoxicity - 0.5994 59.94%
Acute Oral Toxicity (c) III 0.7007 70.07%
Estrogen receptor binding + 0.6165 61.65%
Androgen receptor binding + 0.7181 71.81%
Thyroid receptor binding + 0.5283 52.83%
Glucocorticoid receptor binding - 0.5139 51.39%
Aromatase binding + 0.5237 52.37%
PPAR gamma + 0.6235 62.35%
Honey bee toxicity - 0.9896 98.96%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.7850 78.50%
Fish aquatic toxicity + 0.7890 78.90%

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 98.49% 98.95%
CHEMBL230 P35354 Cyclooxygenase-2 97.67% 89.63%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.19% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 95.03% 99.17%
CHEMBL240 Q12809 HERG 94.65% 89.76%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 92.84% 92.08%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.72% 99.23%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 90.62% 85.94%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 89.17% 82.69%
CHEMBL221 P23219 Cyclooxygenase-1 88.87% 90.17%
CHEMBL3401 O75469 Pregnane X receptor 87.24% 94.73%
CHEMBL4179 P45984 c-Jun N-terminal kinase 2 84.47% 90.75%
CHEMBL1781 P11387 DNA topoisomerase I 82.68% 97.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.53% 86.33%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 82.50% 97.29%
CHEMBL5261 Q7L7X3 Serine/threonine-protein kinase TAO1 81.53% 89.33%
CHEMBL1936 P10721 Stem cell growth factor receptor 80.48% 84.17%
CHEMBL3891 P07384 Calpain 1 80.44% 93.04%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.40% 95.56%

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.
Annona mucosa

Cross-Links

Top
PubChem 16211114
LOTUS LTS0101228
wikiData Q82474931