(3Z,4S,5S)-4-hydroxy-5-methyl-3-tetradecylideneoxolan-2-one

Details

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Internal ID 9af7a48b-e214-4483-afc3-c543535ac547
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name (3Z,4S,5S)-4-hydroxy-5-methyl-3-tetradecylideneoxolan-2-one
SMILES (Canonical) CCCCCCCCCCCCCC=C1C(C(OC1=O)C)O
SMILES (Isomeric) CCCCCCCCCCCCC/C=C\1/[C@@H]([C@@H](OC1=O)C)O
InChI InChI=1S/C19H34O3/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-17-18(20)16(2)22-19(17)21/h15-16,18,20H,3-14H2,1-2H3/b17-15-/t16-,18+/m0/s1
InChI Key KBHLNNQHHPFDSG-TUEARFBRSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C19H34O3
Molecular Weight 310.50 g/mol
Exact Mass 310.25079494 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 6.70
Atomic LogP (AlogP) 4.92
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 12

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3Z,4S,5S)-4-hydroxy-5-methyl-3-tetradecylideneoxolan-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 + 0.9832 98.32%
Caco-2 + 0.7015 70.15%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.6151 61.51%
OATP2B1 inhibitior - 0.8524 85.24%
OATP1B1 inhibitior + 0.8513 85.13%
OATP1B3 inhibitior + 0.9516 95.16%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.5500 55.00%
BSEP inhibitior - 0.5194 51.94%
P-glycoprotein inhibitior - 0.7727 77.27%
P-glycoprotein substrate - 0.8921 89.21%
CYP3A4 substrate - 0.5771 57.71%
CYP2C9 substrate - 0.6133 61.33%
CYP2D6 substrate - 0.8705 87.05%
CYP3A4 inhibition - 0.6973 69.73%
CYP2C9 inhibition - 0.7918 79.18%
CYP2C19 inhibition - 0.5474 54.74%
CYP2D6 inhibition - 0.8593 85.93%
CYP1A2 inhibition + 0.5261 52.61%
CYP2C8 inhibition - 0.9228 92.28%
CYP inhibitory promiscuity - 0.6306 63.06%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5838 58.38%
Eye corrosion - 0.9426 94.26%
Eye irritation + 0.6098 60.98%
Skin irritation + 0.6097 60.97%
Skin corrosion - 0.9078 90.78%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4408 44.08%
Micronuclear - 0.9500 95.00%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation - 0.6341 63.41%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity - 0.6333 63.33%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity - 0.5743 57.43%
Acute Oral Toxicity (c) III 0.5376 53.76%
Estrogen receptor binding - 0.6478 64.78%
Androgen receptor binding - 0.6617 66.17%
Thyroid receptor binding + 0.6651 66.51%
Glucocorticoid receptor binding + 0.5682 56.82%
Aromatase binding - 0.7348 73.48%
PPAR gamma + 0.5698 56.98%
Honey bee toxicity - 0.9813 98.13%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity + 0.7806 78.06%
Fish aquatic toxicity + 0.9867 98.67%

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 96.41% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 92.81% 92.08%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.08% 99.17%
CHEMBL230 P35354 Cyclooxygenase-2 89.76% 89.63%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.72% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.27% 89.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.00% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 85.08% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.07% 86.33%
CHEMBL299 P17252 Protein kinase C alpha 83.43% 98.03%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.27% 97.25%
CHEMBL221 P23219 Cyclooxygenase-1 80.27% 90.17%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 80.17% 96.47%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.01% 99.23%

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.
Aiouea trinervis
Microcos paniculata

Cross-Links

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PubChem 11681139
NPASS NPC202543
LOTUS LTS0007565
wikiData Q105138215