(4S)-4-hentriacontyloxolan-2-one

Details

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Internal ID 0137b7fd-adb1-4c71-a248-15acee2a0c13
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name (4S)-4-hentriacontyloxolan-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C35H68O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-25-26-27-28-29-30-31-34-32-35(36)37-33-34/h34H,2-33H2,1H3/t34-/m0/s1
InChI Key FWWALRYBHKRLHD-UMSFTDKQSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C35H68O2
Molecular Weight 520.90 g/mol
Exact Mass 520.52193141 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 16.70
Atomic LogP (AlogP) 12.27
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 30

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (4S)-4-hentriacontyloxolan-2-one

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 - 0.6986 69.86%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.4468 44.68%
OATP2B1 inhibitior - 0.8525 85.25%
OATP1B1 inhibitior + 0.9321 93.21%
OATP1B3 inhibitior + 0.9399 93.99%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.7210 72.10%
P-glycoprotein inhibitior - 0.5854 58.54%
P-glycoprotein substrate - 0.7152 71.52%
CYP3A4 substrate - 0.6120 61.20%
CYP2C9 substrate + 0.6168 61.68%
CYP2D6 substrate - 0.8637 86.37%
CYP3A4 inhibition - 0.9316 93.16%
CYP2C9 inhibition - 0.8283 82.83%
CYP2C19 inhibition - 0.7274 72.74%
CYP2D6 inhibition - 0.9184 91.84%
CYP1A2 inhibition - 0.6423 64.23%
CYP2C8 inhibition - 0.9490 94.90%
CYP inhibitory promiscuity - 0.9301 93.01%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.6933 69.33%
Eye corrosion + 0.7182 71.82%
Eye irritation + 0.8503 85.03%
Skin irritation + 0.6750 67.50%
Skin corrosion - 0.9528 95.28%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4121 41.21%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5500 55.00%
skin sensitisation - 0.7392 73.92%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity - 0.9098 90.98%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity + 0.6435 64.35%
Acute Oral Toxicity (c) III 0.7286 72.86%
Estrogen receptor binding - 0.5107 51.07%
Androgen receptor binding - 0.7782 77.82%
Thyroid receptor binding + 0.5198 51.98%
Glucocorticoid receptor binding - 0.4787 47.87%
Aromatase binding - 0.7378 73.78%
PPAR gamma - 0.5516 55.16%
Honey bee toxicity - 0.9561 95.61%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity + 0.7482 74.82%
Fish aquatic toxicity + 0.9114 91.14%

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 95.86% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.16% 97.25%
CHEMBL230 P35354 Cyclooxygenase-2 93.10% 89.63%
CHEMBL4462 Q8IXJ6 NAD-dependent deacetylase sirtuin 2 89.95% 90.24%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.65% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.00% 97.09%
CHEMBL299 P17252 Protein kinase C alpha 86.00% 98.03%
CHEMBL2996 Q05655 Protein kinase C delta 85.94% 97.79%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 85.36% 92.08%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.73% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.17% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.66% 95.56%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 81.58% 100.00%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 81.31% 91.81%

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 129881925
LOTUS LTS0027489
wikiData Q105105692