21-(Furan-2-yl)henicosa-14,16-diynyl 19-(furan-2-yl)nonadeca-5,7-diynoate

Details

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Internal ID a2c6ddf0-936e-4a32-a980-c1b67ca43f7d
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohol esters
IUPAC Name 21-(furan-2-yl)henicosa-14,16-diynyl 19-(furan-2-yl)nonadeca-5,7-diynoate
SMILES (Canonical) C1=COC(=C1)CCCCCCCCCCCC#CC#CCCCC(=O)OCCCCCCCCCCCCCC#CC#CCCCCC2=CC=CO2
SMILES (Isomeric) C1=COC(=C1)CCCCCCCCCCCC#CC#CCCCC(=O)OCCCCCCCCCCCCCC#CC#CCCCCC2=CC=CO2
InChI InChI=1S/C48H68O4/c49-48(42-34-30-26-22-18-14-10-6-5-9-13-17-21-25-29-33-39-47-41-37-45-51-47)52-43-35-31-27-23-19-15-11-7-3-1-2-4-8-12-16-20-24-28-32-38-46-40-36-44-50-46/h36-37,40-41,44-45H,1-7,9-11,13,15,17,19,21,23-25,27-35,38-39,42-43H2
InChI Key IIMUYKPOBAQTRX-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C48H68O4
Molecular Weight 709.00 g/mol
Exact Mass 708.51176065 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 16.50
Atomic LogP (AlogP) 13.14
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 31

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 21-(Furan-2-yl)henicosa-14,16-diynyl 19-(furan-2-yl)nonadeca-5,7-diynoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9767 97.67%
Caco-2 - 0.8190 81.90%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.8617 86.17%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8904 89.04%
OATP1B3 inhibitior + 0.9484 94.84%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.9125 91.25%
P-glycoprotein inhibitior + 0.7273 72.73%
P-glycoprotein substrate - 0.8764 87.64%
CYP3A4 substrate + 0.5524 55.24%
CYP2C9 substrate - 0.6221 62.21%
CYP2D6 substrate - 0.8193 81.93%
CYP3A4 inhibition - 0.8385 83.85%
CYP2C9 inhibition - 0.6072 60.72%
CYP2C19 inhibition - 0.5786 57.86%
CYP2D6 inhibition - 0.8804 88.04%
CYP1A2 inhibition - 0.5163 51.63%
CYP2C8 inhibition + 0.6024 60.24%
CYP inhibitory promiscuity + 0.5163 51.63%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8400 84.00%
Carcinogenicity (trinary) Non-required 0.5636 56.36%
Eye corrosion - 0.7712 77.12%
Eye irritation - 0.8244 82.44%
Skin irritation - 0.7674 76.74%
Skin corrosion - 0.8660 86.60%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7283 72.83%
Micronuclear - 0.8300 83.00%
Hepatotoxicity - 0.6467 64.67%
skin sensitisation - 0.8427 84.27%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity + 0.5802 58.02%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity + 0.5525 55.25%
Acute Oral Toxicity (c) III 0.7296 72.96%
Estrogen receptor binding + 0.7956 79.56%
Androgen receptor binding + 0.5336 53.36%
Thyroid receptor binding - 0.5421 54.21%
Glucocorticoid receptor binding + 0.5806 58.06%
Aromatase binding + 0.5373 53.73%
PPAR gamma + 0.5780 57.80%
Honey bee toxicity - 0.9181 91.81%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.6274 62.74%
Fish aquatic toxicity + 0.9072 90.72%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.72% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.61% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.98% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.79% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.77% 86.33%
CHEMBL2581 P07339 Cathepsin D 83.33% 98.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.24% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 83.14% 94.73%

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.
Polyalthia evecta

Cross-Links

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PubChem 11614600
LOTUS LTS0169645
wikiData Q105113618