(3R,4R,5S)-3-hexadeca-9,11,15-trien-7-ynyl-4-hydroxy-5-methyloxolan-2-one

Details

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Internal ID 94fa24d5-778a-468b-8815-f9077f6dc93f
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name (3R,4R,5S)-3-hexadeca-9,11,15-trien-7-ynyl-4-hydroxy-5-methyloxolan-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H30O3/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/h3,6-9,18-20,22H,1,4-5,12-17H2,2H3/t18-,19+,20-/m0/s1
InChI Key CJMUGJLGEQOFLP-ZCNNSNEGSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C21H30O3
Molecular Weight 330.50 g/mol
Exact Mass 330.21949481 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 5.60
Atomic LogP (AlogP) 4.33
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3R,4R,5S)-3-hexadeca-9,11,15-trien-7-ynyl-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 - 0.6682 66.82%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.7286 72.86%
Subcellular localzation Mitochondria 0.7112 71.12%
OATP2B1 inhibitior - 0.8557 85.57%
OATP1B1 inhibitior + 0.8425 84.25%
OATP1B3 inhibitior + 0.9397 93.97%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior + 0.6515 65.15%
P-glycoprotein inhibitior - 0.5462 54.62%
P-glycoprotein substrate - 0.7078 70.78%
CYP3A4 substrate + 0.6046 60.46%
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 - 0.7912 79.12%
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 - 0.9590 95.90%
Skin irritation - 0.5385 53.85%
Skin corrosion - 0.8091 80.91%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7391 73.91%
Micronuclear - 0.8600 86.00%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation - 0.7333 73.33%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity + 0.7623 76.23%
Acute Oral Toxicity (c) III 0.6220 62.20%
Estrogen receptor binding + 0.6059 60.59%
Androgen receptor binding + 0.5494 54.94%
Thyroid receptor binding + 0.5838 58.38%
Glucocorticoid receptor binding - 0.4792 47.92%
Aromatase binding - 0.5904 59.04%
PPAR gamma + 0.7423 74.23%
Honey bee toxicity - 0.7613 76.13%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.7000 70.00%
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 93.44% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.97% 96.09%
CHEMBL2581 P07339 Cathepsin D 87.85% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.20% 99.17%
CHEMBL3975 P09467 Fructose-1,6-bisphosphatase 85.79% 92.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.94% 95.56%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 83.23% 89.34%
CHEMBL3401 O75469 Pregnane X receptor 82.85% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.17% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.30% 89.00%

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.
Meiogyne cylindrocarpa

Cross-Links

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PubChem 163015070
LOTUS LTS0003481
wikiData Q104961404