(2R,3S)-2-nonadecyl-3-octyloxirane

Details

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Internal ID e7011daa-2fbf-41e5-ab42-f357fc92272f
Taxonomy Organoheterocyclic compounds > Epoxides
IUPAC Name (2R,3S)-2-nonadecyl-3-octyloxirane
SMILES (Canonical) CCCCCCCCCCCCCCCCCCCC1C(O1)CCCCCCCC
SMILES (Isomeric) CCCCCCCCCCCCCCCCCCC[C@@H]1[C@@H](O1)CCCCCCCC
InChI InChI=1S/C29H58O/c1-3-5-7-9-11-12-13-14-15-16-17-18-19-20-21-23-25-27-29-28(30-29)26-24-22-10-8-6-4-2/h28-29H,3-27H2,1-2H3/t28-,29+/m0/s1
InChI Key MVKMNJAUWSPNPL-URLMMPGGSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C29H58O
Molecular Weight 422.80 g/mol
Exact Mass 422.448766469 g/mol
Topological Polar Surface Area (TPSA) 12.50 Ų
XlogP 13.90
Atomic LogP (AlogP) 10.55
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 25

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2R,3S)-2-nonadecyl-3-octyloxirane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9920 99.20%
Caco-2 - 0.5407 54.07%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.3696 36.96%
OATP2B1 inhibitior - 0.8511 85.11%
OATP1B1 inhibitior + 0.9305 93.05%
OATP1B3 inhibitior + 0.9492 94.92%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.5792 57.92%
P-glycoprotein inhibitior - 0.7159 71.59%
P-glycoprotein substrate - 0.9267 92.67%
CYP3A4 substrate - 0.6663 66.63%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7350 73.50%
CYP3A4 inhibition - 0.8988 89.88%
CYP2C9 inhibition - 0.7540 75.40%
CYP2C19 inhibition - 0.7239 72.39%
CYP2D6 inhibition - 0.9253 92.53%
CYP1A2 inhibition + 0.5606 56.06%
CYP2C8 inhibition - 0.9273 92.73%
CYP inhibitory promiscuity - 0.8154 81.54%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7400 74.00%
Carcinogenicity (trinary) Non-required 0.5881 58.81%
Eye corrosion + 0.7209 72.09%
Eye irritation + 0.8501 85.01%
Skin irritation + 0.6942 69.42%
Skin corrosion - 0.9169 91.69%
Ames mutagenesis - 0.9800 98.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6457 64.57%
Micronuclear - 0.8100 81.00%
Hepatotoxicity + 0.6405 64.05%
skin sensitisation + 0.7761 77.61%
Respiratory toxicity - 0.8778 87.78%
Reproductive toxicity - 0.8533 85.33%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity + 0.6841 68.41%
Acute Oral Toxicity (c) IV 0.4829 48.29%
Estrogen receptor binding - 0.6874 68.74%
Androgen receptor binding - 0.7290 72.90%
Thyroid receptor binding - 0.5083 50.83%
Glucocorticoid receptor binding - 0.6575 65.75%
Aromatase binding - 0.6403 64.03%
PPAR gamma - 0.5826 58.26%
Honey bee toxicity - 0.9799 97.99%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.7856 78.56%
Fish aquatic toxicity + 0.8304 83.04%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.34% 97.25%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 92.08% 92.08%
CHEMBL4462 Q8IXJ6 NAD-dependent deacetylase sirtuin 2 91.21% 90.24%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.26% 96.09%
CHEMBL2996 Q05655 Protein kinase C delta 90.01% 97.79%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 88.55% 92.86%
CHEMBL230 P35354 Cyclooxygenase-2 87.99% 89.63%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 87.90% 97.29%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 85.66% 91.81%
CHEMBL2581 P07339 Cathepsin D 85.60% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 84.59% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.91% 99.17%

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.
Rubus thibetanus

Cross-Links

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PubChem 11144321
LOTUS LTS0100074
wikiData Q105173112