[4,5-Dimethyl-1-(6-oxooxan-2-yl)tricosan-2-yl] acetate

Details

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Internal ID aa4c5514-75f4-4bbb-b58a-de9904cfaeff
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohol esters
IUPAC Name [4,5-dimethyl-1-(6-oxooxan-2-yl)tricosan-2-yl] acetate
SMILES (Canonical) CCCCCCCCCCCCCCCCCCC(C)C(C)CC(CC1CCCC(=O)O1)OC(=O)C
SMILES (Isomeric) CCCCCCCCCCCCCCCCCCC(C)C(C)CC(CC1CCCC(=O)O1)OC(=O)C
InChI InChI=1S/C32H60O4/c1-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-22-27(2)28(3)25-31(35-29(4)33)26-30-23-21-24-32(34)36-30/h27-28,30-31H,5-26H2,1-4H3
InChI Key BWMYETQELIMXBJ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C32H60O4
Molecular Weight 508.80 g/mol
Exact Mass 508.44916039 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 12.60
Atomic LogP (AlogP) 9.72
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 23

Synonyms

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37577-42-7
[4,5-dimethyl-1-(6-oxooxan-2-yl)tricosan-2-yl] acetate
DTXSID60415772

2D Structure

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2D Structure of [4,5-Dimethyl-1-(6-oxooxan-2-yl)tricosan-2-yl] acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9681 96.81%
Caco-2 - 0.7041 70.41%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.7149 71.49%
OATP2B1 inhibitior - 0.5712 57.12%
OATP1B1 inhibitior + 0.8927 89.27%
OATP1B3 inhibitior + 0.9525 95.25%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.8479 84.79%
P-glycoprotein inhibitior + 0.6435 64.35%
P-glycoprotein substrate - 0.6085 60.85%
CYP3A4 substrate + 0.5917 59.17%
CYP2C9 substrate - 0.5862 58.62%
CYP2D6 substrate - 0.8777 87.77%
CYP3A4 inhibition - 0.8029 80.29%
CYP2C9 inhibition - 0.8643 86.43%
CYP2C19 inhibition - 0.6264 62.64%
CYP2D6 inhibition - 0.9110 91.10%
CYP1A2 inhibition - 0.8635 86.35%
CYP2C8 inhibition - 0.7936 79.36%
CYP inhibitory promiscuity - 0.9248 92.48%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.7132 71.32%
Eye corrosion - 0.8818 88.18%
Eye irritation - 0.6523 65.23%
Skin irritation - 0.7691 76.91%
Skin corrosion - 0.9341 93.41%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5288 52.88%
Micronuclear - 0.9100 91.00%
Hepatotoxicity - 0.5271 52.71%
skin sensitisation - 0.9404 94.04%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity - 0.7556 75.56%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity + 0.6047 60.47%
Acute Oral Toxicity (c) III 0.8413 84.13%
Estrogen receptor binding + 0.6421 64.21%
Androgen receptor binding - 0.7128 71.28%
Thyroid receptor binding - 0.7267 72.67%
Glucocorticoid receptor binding + 0.6071 60.71%
Aromatase binding - 0.6246 62.46%
PPAR gamma + 0.5653 56.53%
Honey bee toxicity - 0.9581 95.81%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.6619 66.19%
Fish aquatic toxicity + 0.9367 93.67%

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 99.09% 98.95%
CHEMBL3359 P21462 Formyl peptide receptor 1 96.36% 93.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 95.44% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.53% 96.09%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 92.60% 100.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.66% 97.25%
CHEMBL5255 O00206 Toll-like receptor 4 89.71% 92.50%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.58% 91.11%
CHEMBL2996 Q05655 Protein kinase C delta 87.93% 97.79%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 87.42% 96.47%
CHEMBL5103 Q969S8 Histone deacetylase 10 86.94% 90.08%
CHEMBL3401 O75469 Pregnane X receptor 86.19% 94.73%
CHEMBL4462 Q8IXJ6 NAD-dependent deacetylase sirtuin 2 86.05% 90.24%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 86.00% 98.75%
CHEMBL3837 P07711 Cathepsin L 85.98% 96.61%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 85.72% 94.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.47% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.93% 95.56%
CHEMBL4588 P22894 Matrix metalloproteinase 8 83.45% 94.66%
CHEMBL4227 P25090 Lipoxin A4 receptor 83.40% 100.00%
CHEMBL1293316 Q9HBX9 Relaxin receptor 1 83.30% 82.50%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 82.51% 91.81%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.47% 92.62%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.77% 95.89%
CHEMBL340 P08684 Cytochrome P450 3A4 81.69% 91.19%
CHEMBL4005 P42336 PI3-kinase p110-alpha subunit 80.96% 97.47%
CHEMBL2514 O95665 Neurotensin receptor 2 80.50% 100.00%

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.
Cassia javanica subsp. agnes

Cross-Links

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PubChem 5320184
NPASS NPC86491