3-Hexadeca-11,15-dien-7,9-diynyl-4-hydroxy-5-methyloxolan-2-one

Details

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Internal ID 6adb91e5-5f93-438a-a7b9-f1addabc7c35
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name 3-hexadeca-11,15-dien-7,9-diynyl-4-hydroxy-5-methyloxolan-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H28O3/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-19-20(22)18(2)24-21(19)23/h3,6-7,18-20,22H,1,4-5,12-17H2,2H3
InChI Key BWHZURYINQNHCL-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H28O3
Molecular Weight 328.40 g/mol
Exact Mass 328.20384475 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 5.30
Atomic LogP (AlogP) 3.78
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-Hexadeca-11,15-dien-7,9-diynyl-4-hydroxy-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 - 0.6610 66.10%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.7112 71.12%
OATP2B1 inhibitior - 0.8543 85.43%
OATP1B1 inhibitior + 0.8313 83.13%
OATP1B3 inhibitior + 0.9397 93.97%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior - 0.5000 50.00%
P-glycoprotein inhibitior - 0.6725 67.25%
P-glycoprotein substrate - 0.6903 69.03%
CYP3A4 substrate + 0.6084 60.84%
CYP2C9 substrate - 0.8487 84.87%
CYP2D6 substrate - 0.8740 87.40%
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 - 0.7792 77.92%
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 - 0.9397 93.97%
Skin irritation - 0.5385 53.85%
Skin corrosion - 0.8091 80.91%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6988 69.88%
Micronuclear - 0.8600 86.00%
Hepatotoxicity - 0.5625 56.25%
skin sensitisation - 0.7333 73.33%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity + 0.6645 66.45%
Acute Oral Toxicity (c) III 0.6220 62.20%
Estrogen receptor binding + 0.5433 54.33%
Androgen receptor binding + 0.5749 57.49%
Thyroid receptor binding + 0.5741 57.41%
Glucocorticoid receptor binding + 0.5690 56.90%
Aromatase binding - 0.6188 61.88%
PPAR gamma + 0.6734 67.34%
Honey bee toxicity - 0.7870 78.70%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.6362 63.62%
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 89.92% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.11% 96.09%
CHEMBL2581 P07339 Cathepsin D 86.95% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.85% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.92% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.02% 94.45%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 84.96% 89.34%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.13% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 80.18% 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.
Sapranthus palanga

Cross-Links

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PubChem 85382743
LOTUS LTS0050703
wikiData Q104947254