16-(1,3-benzodioxol-5-yl)-N-(2-methylpropyl)hexadecanamide

Details

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Internal ID 4a3afdae-44e3-44dd-bde2-59538039f080
Taxonomy Organoheterocyclic compounds > Benzodioxoles
IUPAC Name 16-(1,3-benzodioxol-5-yl)-N-(2-methylpropyl)hexadecanamide
SMILES (Canonical) CC(C)CNC(=O)CCCCCCCCCCCCCCCC1=CC2=C(C=C1)OCO2
SMILES (Isomeric) CC(C)CNC(=O)CCCCCCCCCCCCCCCC1=CC2=C(C=C1)OCO2
InChI InChI=1S/C27H45NO3/c1-23(2)21-28-27(29)17-15-13-11-9-7-5-3-4-6-8-10-12-14-16-24-18-19-25-26(20-24)31-22-30-25/h18-20,23H,3-17,21-22H2,1-2H3,(H,28,29)
InChI Key ADTJKMBQRHOONK-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C27H45NO3
Molecular Weight 431.70 g/mol
Exact Mass 431.33994430 g/mol
Topological Polar Surface Area (TPSA) 47.60 Ų
XlogP 9.40
Atomic LogP (AlogP) 7.19
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 18

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 16-(1,3-benzodioxol-5-yl)-N-(2-methylpropyl)hexadecanamide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9969 99.69%
Caco-2 - 0.5672 56.72%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Mitochondria 0.6797 67.97%
OATP2B1 inhibitior - 0.8583 85.83%
OATP1B1 inhibitior + 0.9387 93.87%
OATP1B3 inhibitior + 0.9399 93.99%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior + 0.9355 93.55%
P-glycoprotein inhibitior + 0.7254 72.54%
P-glycoprotein substrate - 0.6475 64.75%
CYP3A4 substrate - 0.5137 51.37%
CYP2C9 substrate - 0.7890 78.90%
CYP2D6 substrate - 0.8175 81.75%
CYP3A4 inhibition - 0.6740 67.40%
CYP2C9 inhibition - 0.6781 67.81%
CYP2C19 inhibition + 0.7592 75.92%
CYP2D6 inhibition + 0.5648 56.48%
CYP1A2 inhibition + 0.5065 50.65%
CYP2C8 inhibition - 0.8697 86.97%
CYP inhibitory promiscuity + 0.7529 75.29%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8100 81.00%
Carcinogenicity (trinary) Non-required 0.6432 64.32%
Eye corrosion - 0.9891 98.91%
Eye irritation - 0.8336 83.36%
Skin irritation - 0.7595 75.95%
Skin corrosion - 0.9136 91.36%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3922 39.22%
Micronuclear - 0.6100 61.00%
Hepatotoxicity - 0.5967 59.67%
skin sensitisation - 0.8306 83.06%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity - 0.7845 78.45%
Acute Oral Toxicity (c) III 0.6991 69.91%
Estrogen receptor binding + 0.5798 57.98%
Androgen receptor binding + 0.6719 67.19%
Thyroid receptor binding + 0.5936 59.36%
Glucocorticoid receptor binding - 0.5442 54.42%
Aromatase binding - 0.4928 49.28%
PPAR gamma + 0.5608 56.08%
Honey bee toxicity - 0.9475 94.75%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.5676 56.76%
Fish aquatic toxicity + 0.7300 73.00%

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 99.25% 98.95%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 98.36% 94.80%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.68% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.66% 91.11%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 96.60% 96.77%
CHEMBL3492 P49721 Proteasome Macropain subunit 96.40% 90.24%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 96.10% 95.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.74% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.40% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 93.57% 94.73%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 93.53% 80.96%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 92.66% 90.71%
CHEMBL5261 Q7L7X3 Serine/threonine-protein kinase TAO1 88.59% 89.33%
CHEMBL2179 P04062 Beta-glucocerebrosidase 87.00% 85.31%
CHEMBL4208 P20618 Proteasome component C5 84.68% 90.00%
CHEMBL5701 Q9H2K8 Serine/threonine-protein kinase TAO3 84.15% 96.67%
CHEMBL2535 P11166 Glucose transporter 83.58% 98.75%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 82.92% 95.89%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.86% 92.62%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.08% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.08% 95.56%

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.
Piper mullesua

Cross-Links

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PubChem 163036936
LOTUS LTS0057194
wikiData Q104909795