5-Dec-9-ynyl-3-(2,3-dihydroxypropyl)oxolan-2-one

Details

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Internal ID 83515dbc-e43f-400c-bf90-70b0958ec397
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name 5-dec-9-ynyl-3-(2,3-dihydroxypropyl)oxolan-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H28O4/c1-2-3-4-5-6-7-8-9-10-16-12-14(17(20)21-16)11-15(19)13-18/h1,14-16,18-19H,3-13H2
InChI Key VXZFZXZSRWYUBE-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H28O4
Molecular Weight 296.40 g/mol
Exact Mass 296.19875937 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 3.30
Atomic LogP (AlogP) 2.42
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 11

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-Dec-9-ynyl-3-(2,3-dihydroxypropyl)oxolan-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 + 0.6749 67.49%
Caco-2 - 0.6886 68.86%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.8354 83.54%
OATP2B1 inhibitior - 0.8527 85.27%
OATP1B1 inhibitior + 0.9510 95.10%
OATP1B3 inhibitior + 0.9533 95.33%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7542 75.42%
BSEP inhibitior - 0.7377 73.77%
P-glycoprotein inhibitior - 0.9092 90.92%
P-glycoprotein substrate - 0.8050 80.50%
CYP3A4 substrate + 0.5167 51.67%
CYP2C9 substrate - 0.5966 59.66%
CYP2D6 substrate - 0.8382 83.82%
CYP3A4 inhibition - 0.9140 91.40%
CYP2C9 inhibition - 0.8914 89.14%
CYP2C19 inhibition - 0.8576 85.76%
CYP2D6 inhibition - 0.9514 95.14%
CYP1A2 inhibition - 0.8666 86.66%
CYP2C8 inhibition - 0.9071 90.71%
CYP inhibitory promiscuity - 0.9720 97.20%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.7522 75.22%
Eye corrosion - 0.9562 95.62%
Eye irritation - 0.9157 91.57%
Skin irritation - 0.7829 78.29%
Skin corrosion - 0.8668 86.68%
Ames mutagenesis - 0.6170 61.70%
Human Ether-a-go-go-Related Gene inhibition + 0.6574 65.74%
Micronuclear - 0.8700 87.00%
Hepatotoxicity + 0.5481 54.81%
skin sensitisation - 0.9222 92.22%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity - 0.5556 55.56%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity - 0.5715 57.15%
Acute Oral Toxicity (c) III 0.5355 53.55%
Estrogen receptor binding - 0.6775 67.75%
Androgen receptor binding - 0.7026 70.26%
Thyroid receptor binding + 0.5245 52.45%
Glucocorticoid receptor binding + 0.6991 69.91%
Aromatase binding - 0.7723 77.23%
PPAR gamma - 0.6676 66.76%
Honey bee toxicity - 0.8387 83.87%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.6683 66.83%
Fish aquatic toxicity - 0.5924 59.24%

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 95.92% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.10% 97.09%
CHEMBL230 P35354 Cyclooxygenase-2 91.82% 89.63%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.40% 96.09%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 85.52% 86.92%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 84.79% 97.29%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.62% 99.17%
CHEMBL2581 P07339 Cathepsin D 84.36% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.25% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.26% 89.00%
CHEMBL5103 Q969S8 Histone deacetylase 10 80.33% 90.08%
CHEMBL3975 P09467 Fructose-1,6-bisphosphatase 80.29% 92.95%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 80.17% 100.00%

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.
Sextonia rubra

Cross-Links

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PubChem 12315103
LOTUS LTS0144198
wikiData Q104199986