2-octadecyl-1H-indol-3-ol

Details

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Internal ID 0e8e9317-f185-4bba-bb45-28e85d3aae92
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Hydroxyindoles
IUPAC Name 2-octadecyl-1H-indol-3-ol
SMILES (Canonical) CCCCCCCCCCCCCCCCCCC1=C(C2=CC=CC=C2N1)O
SMILES (Isomeric) CCCCCCCCCCCCCCCCCCC1=C(C2=CC=CC=C2N1)O
InChI InChI=1S/C26H43NO/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-22-25-26(28)23-20-18-19-21-24(23)27-25/h18-21,27-28H,2-17,22H2,1H3
InChI Key AYPYUZXAFNVUEC-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C26H43NO
Molecular Weight 385.60 g/mol
Exact Mass 385.334464995 g/mol
Topological Polar Surface Area (TPSA) 36.00 Ų
XlogP 11.00
Atomic LogP (AlogP) 8.68
H-Bond Acceptor 1
H-Bond Donor 2
Rotatable Bonds 17

Synonyms

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Fistulosin
octadecyl 3-hydroxyindole
CHEBI:185477
1,2-Dihydro-2-octadecyl-3H-indol-3-one

2D Structure

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2D Structure of 2-octadecyl-1H-indol-3-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9961 99.61%
Caco-2 - 0.5578 55.78%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Mitochondria 0.4527 45.27%
OATP2B1 inhibitior - 0.8581 85.81%
OATP1B1 inhibitior + 0.7638 76.38%
OATP1B3 inhibitior + 0.9451 94.51%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior + 0.6982 69.82%
P-glycoprotein inhibitior - 0.5457 54.57%
P-glycoprotein substrate - 0.6004 60.04%
CYP3A4 substrate + 0.5360 53.60%
CYP2C9 substrate - 0.8129 81.29%
CYP2D6 substrate - 0.6870 68.70%
CYP3A4 inhibition - 0.7716 77.16%
CYP2C9 inhibition - 0.6877 68.77%
CYP2C19 inhibition + 0.6200 62.00%
CYP2D6 inhibition - 0.6685 66.85%
CYP1A2 inhibition + 0.7057 70.57%
CYP2C8 inhibition + 0.6364 63.64%
CYP inhibitory promiscuity + 0.7769 77.69%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.6569 65.69%
Eye corrosion - 0.9791 97.91%
Eye irritation - 0.5103 51.03%
Skin irritation - 0.7301 73.01%
Skin corrosion - 0.8396 83.96%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8053 80.53%
Micronuclear - 0.6300 63.00%
Hepatotoxicity + 0.5509 55.09%
skin sensitisation - 0.7621 76.21%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity - 0.7325 73.25%
Acute Oral Toxicity (c) III 0.6387 63.87%
Estrogen receptor binding + 0.7585 75.85%
Androgen receptor binding + 0.6526 65.26%
Thyroid receptor binding + 0.6242 62.42%
Glucocorticoid receptor binding - 0.5830 58.30%
Aromatase binding - 0.5842 58.42%
PPAR gamma + 0.6810 68.10%
Honey bee toxicity - 0.9904 99.04%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.8065 80.65%
Fish aquatic toxicity + 0.9452 94.52%

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
CHEMBL2581 P07339 Cathepsin D 98.26% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.84% 91.11%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 96.24% 92.08%
CHEMBL2885 P07451 Carbonic anhydrase III 93.35% 87.45%
CHEMBL1951 P21397 Monoamine oxidase A 92.94% 91.49%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.70% 96.09%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 92.05% 91.71%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 89.87% 91.81%
CHEMBL3192 Q9BY41 Histone deacetylase 8 88.59% 93.99%
CHEMBL1781 P11387 DNA topoisomerase I 87.88% 97.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.40% 95.56%
CHEMBL2996 Q05655 Protein kinase C delta 85.12% 97.79%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.43% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 84.03% 94.73%
CHEMBL5805 Q9NR97 Toll-like receptor 8 83.55% 96.25%
CHEMBL230 P35354 Cyclooxygenase-2 82.89% 89.63%
CHEMBL1907 P15144 Aminopeptidase N 82.69% 93.31%
CHEMBL3004 P33527 Multidrug resistance-associated protein 1 82.14% 96.37%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.58% 99.23%
CHEMBL5979 P05186 Alkaline phosphatase, tissue-nonspecific isozyme 81.49% 85.40%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 80.61% 85.94%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 80.52% 94.62%

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.
Allium fistulosum

Cross-Links

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PubChem 11574561
LOTUS LTS0066696
wikiData Q104921317