4-Hydroxy-3-icos-19-en-11-ynyl-5-methyloxolan-2-one

Details

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Internal ID a00a2278-af31-40ed-8162-ddb574a5a603
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name 4-hydroxy-3-icos-19-en-11-ynyl-5-methyloxolan-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C25H42O3/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-23-24(26)22(2)28-25(23)27/h3,22-24,26H,1,4-9,12-21H2,2H3
InChI Key JFAPEZBOYBDCPU-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C25H42O3
Molecular Weight 390.60 g/mol
Exact Mass 390.31339520 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 8.60
Atomic LogP (AlogP) 6.34
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 16

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-Hydroxy-3-icos-19-en-11-ynyl-5-methyloxolan-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9419 94.19%
Caco-2 - 0.7191 71.91%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.7112 71.12%
OATP2B1 inhibitior - 0.8544 85.44%
OATP1B1 inhibitior + 0.8621 86.21%
OATP1B3 inhibitior + 0.9397 93.97%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior - 0.5135 51.35%
P-glycoprotein inhibitior - 0.6024 60.24%
P-glycoprotein substrate - 0.8328 83.28%
CYP3A4 substrate + 0.5439 54.39%
CYP2C9 substrate - 0.8032 80.32%
CYP2D6 substrate - 0.8640 86.40%
CYP3A4 inhibition - 0.7004 70.04%
CYP2C9 inhibition - 0.8042 80.42%
CYP2C19 inhibition - 0.6448 64.48%
CYP2D6 inhibition - 0.9418 94.18%
CYP1A2 inhibition - 0.6958 69.58%
CYP2C8 inhibition - 0.8639 86.39%
CYP inhibitory promiscuity - 0.8173 81.73%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8728 87.28%
Carcinogenicity (trinary) Non-required 0.5697 56.97%
Eye corrosion - 0.8406 84.06%
Eye irritation - 0.7523 75.23%
Skin irritation - 0.5385 53.85%
Skin corrosion - 0.8091 80.91%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4854 48.54%
Micronuclear - 0.8600 86.00%
Hepatotoxicity - 0.5375 53.75%
skin sensitisation - 0.7333 73.33%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity + 0.6464 64.64%
Acute Oral Toxicity (c) III 0.6220 62.20%
Estrogen receptor binding + 0.7014 70.14%
Androgen receptor binding - 0.4819 48.19%
Thyroid receptor binding - 0.4946 49.46%
Glucocorticoid receptor binding + 0.6112 61.12%
Aromatase binding - 0.6147 61.47%
PPAR gamma + 0.5456 54.56%
Honey bee toxicity - 0.8244 82.44%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.6062 60.62%
Fish aquatic toxicity + 0.9503 95.03%

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 94.19% 91.11%
CHEMBL2581 P07339 Cathepsin D 89.84% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.17% 96.09%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 86.22% 89.34%
CHEMBL3975 P09467 Fructose-1,6-bisphosphatase 86.20% 92.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.59% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.31% 99.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.10% 89.00%
CHEMBL221 P23219 Cyclooxygenase-1 83.66% 90.17%
CHEMBL3401 O75469 Pregnane X receptor 82.31% 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.
Porcelia macrocarpa

Cross-Links

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PubChem 499694
LOTUS LTS0025902
wikiData Q105126564