4-Methyl-5-oxo-2-(14-oxopentadecyl)oxolane-3-carboxylic acid

Details

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Internal ID 211d49e0-e197-4a0a-bd6a-a322815c501b
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name 4-methyl-5-oxo-2-(14-oxopentadecyl)oxolane-3-carboxylic acid
SMILES (Canonical) CC1C(C(OC1=O)CCCCCCCCCCCCCC(=O)C)C(=O)O
SMILES (Isomeric) CC1C(C(OC1=O)CCCCCCCCCCCCCC(=O)C)C(=O)O
InChI InChI=1S/C21H36O5/c1-16(22)14-12-10-8-6-4-3-5-7-9-11-13-15-18-19(20(23)24)17(2)21(25)26-18/h17-19H,3-15H2,1-2H3,(H,23,24)
InChI Key SPGPUDJMXMJNCU-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H36O5
Molecular Weight 368.50 g/mol
Exact Mass 368.25627424 g/mol
Topological Polar Surface Area (TPSA) 80.70 Ų
XlogP 5.60
Atomic LogP (AlogP) 4.91
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 15

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-Methyl-5-oxo-2-(14-oxopentadecyl)oxolane-3-carboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8867 88.67%
Caco-2 - 0.5722 57.22%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.7955 79.55%
OATP2B1 inhibitior - 0.8536 85.36%
OATP1B1 inhibitior + 0.9184 91.84%
OATP1B3 inhibitior + 0.9403 94.03%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.5354 53.54%
P-glycoprotein inhibitior - 0.5465 54.65%
P-glycoprotein substrate - 0.8409 84.09%
CYP3A4 substrate - 0.5655 56.55%
CYP2C9 substrate + 0.6198 61.98%
CYP2D6 substrate - 0.8799 87.99%
CYP3A4 inhibition - 0.7945 79.45%
CYP2C9 inhibition - 0.8980 89.80%
CYP2C19 inhibition - 0.8959 89.59%
CYP2D6 inhibition - 0.9375 93.75%
CYP1A2 inhibition - 0.8401 84.01%
CYP2C8 inhibition - 0.9649 96.49%
CYP inhibitory promiscuity - 0.9746 97.46%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.7592 75.92%
Eye corrosion - 0.9458 94.58%
Eye irritation - 0.6325 63.25%
Skin irritation + 0.5344 53.44%
Skin corrosion - 0.8438 84.38%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4927 49.27%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.7658 76.58%
skin sensitisation - 0.9213 92.13%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity - 0.7111 71.11%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity + 0.6036 60.36%
Acute Oral Toxicity (c) III 0.5893 58.93%
Estrogen receptor binding - 0.5845 58.45%
Androgen receptor binding - 0.6565 65.65%
Thyroid receptor binding - 0.5306 53.06%
Glucocorticoid receptor binding + 0.5824 58.24%
Aromatase binding - 0.7075 70.75%
PPAR gamma + 0.5864 58.64%
Honey bee toxicity - 0.9561 95.61%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.5224 52.24%
Fish aquatic toxicity + 0.9417 94.17%

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
CHEMBL4040 P28482 MAP kinase ERK2 99.67% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.50% 96.09%
CHEMBL2581 P07339 Cathepsin D 90.88% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.74% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.96% 99.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.43% 99.23%

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 85207719
LOTUS LTS0094647
wikiData Q105257402