(3E,4R,5R)-3-dodeca-9,11-diynylidene-4-hydroxy-5-methyloxolan-2-one

Details

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Internal ID 5df06977-7c20-4e10-b337-ef552830378b
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name (3E,4R,5R)-3-dodeca-9,11-diynylidene-4-hydroxy-5-methyloxolan-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H22O3/c1-3-4-5-6-7-8-9-10-11-12-13-15-16(18)14(2)20-17(15)19/h1,13-14,16,18H,6-12H2,2H3/b15-13+/t14-,16+/m1/s1
InChI Key YGTBCEMCUXZJFM-AHZXUYQPSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C17H22O3
Molecular Weight 274.35 g/mol
Exact Mass 274.15689456 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 3.90
Atomic LogP (AlogP) 2.59
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3E,4R,5R)-3-dodeca-9,11-diynylidene-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 + 0.9626 96.26%
Caco-2 + 0.5155 51.55%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.7564 75.64%
OATP2B1 inhibitior - 0.8553 85.53%
OATP1B1 inhibitior + 0.8667 86.67%
OATP1B3 inhibitior + 0.9589 95.89%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.8539 85.39%
P-glycoprotein inhibitior - 0.8967 89.67%
P-glycoprotein substrate - 0.8473 84.73%
CYP3A4 substrate + 0.5283 52.83%
CYP2C9 substrate - 0.6109 61.09%
CYP2D6 substrate - 0.8666 86.66%
CYP3A4 inhibition - 0.8617 86.17%
CYP2C9 inhibition - 0.7860 78.60%
CYP2C19 inhibition - 0.6803 68.03%
CYP2D6 inhibition - 0.9285 92.85%
CYP1A2 inhibition - 0.6130 61.30%
CYP2C8 inhibition - 0.8425 84.25%
CYP inhibitory promiscuity - 0.6399 63.99%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8528 85.28%
Carcinogenicity (trinary) Non-required 0.4893 48.93%
Eye corrosion - 0.7873 78.73%
Eye irritation - 0.9287 92.87%
Skin irritation - 0.5380 53.80%
Skin corrosion - 0.8664 86.64%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4926 49.26%
Micronuclear - 0.8000 80.00%
Hepatotoxicity + 0.5679 56.79%
skin sensitisation - 0.7358 73.58%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity - 0.5111 51.11%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity - 0.5860 58.60%
Acute Oral Toxicity (c) III 0.5804 58.04%
Estrogen receptor binding + 0.6399 63.99%
Androgen receptor binding - 0.6574 65.74%
Thyroid receptor binding + 0.5584 55.84%
Glucocorticoid receptor binding + 0.6165 61.65%
Aromatase binding + 0.5729 57.29%
PPAR gamma - 0.5069 50.69%
Honey bee toxicity - 0.9178 91.78%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity + 0.7224 72.24%
Fish aquatic toxicity + 0.9040 90.40%

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 93.29% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.49% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 91.62% 90.17%
CHEMBL230 P35354 Cyclooxygenase-2 89.97% 89.63%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.25% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.33% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.89% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.49% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 81.92% 94.73%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 81.56% 96.47%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.01% 96.00%

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.
Hortonia floribunda

Cross-Links

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PubChem 163003544
LOTUS LTS0111630
wikiData Q105348256