5-Dodec-10-enoyl-2,4-dimethyl-2,3-dihydropyran-6-one

Details

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Internal ID e811aa08-2cc5-4889-a02e-a4b72688f0a5
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives > Dihydropyranones
IUPAC Name 5-dodec-10-enoyl-2,4-dimethyl-2,3-dihydropyran-6-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H30O3/c1-4-5-6-7-8-9-10-11-12-13-17(20)18-15(2)14-16(3)22-19(18)21/h4-5,16H,6-14H2,1-3H3
InChI Key LDTOSUNDGREUIH-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C19H30O3
Molecular Weight 306.40 g/mol
Exact Mass 306.21949481 g/mol
Topological Polar Surface Area (TPSA) 43.40 Ų
XlogP 5.30
Atomic LogP (AlogP) 4.90
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-Dodec-10-enoyl-2,4-dimethyl-2,3-dihydropyran-6-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9830 98.30%
Caco-2 + 0.6865 68.65%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.7568 75.68%
OATP2B1 inhibitior - 0.8522 85.22%
OATP1B1 inhibitior + 0.7739 77.39%
OATP1B3 inhibitior + 0.9523 95.23%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior + 0.8208 82.08%
P-glycoprotein inhibitior - 0.5801 58.01%
P-glycoprotein substrate - 0.8214 82.14%
CYP3A4 substrate + 0.5200 52.00%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8981 89.81%
CYP3A4 inhibition - 0.7359 73.59%
CYP2C9 inhibition - 0.9258 92.58%
CYP2C19 inhibition - 0.6907 69.07%
CYP2D6 inhibition - 0.9351 93.51%
CYP1A2 inhibition - 0.6947 69.47%
CYP2C8 inhibition - 0.9405 94.05%
CYP inhibitory promiscuity - 0.9066 90.66%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8628 86.28%
Carcinogenicity (trinary) Non-required 0.6570 65.70%
Eye corrosion - 0.9521 95.21%
Eye irritation - 0.6424 64.24%
Skin irritation + 0.5523 55.23%
Skin corrosion - 0.9446 94.46%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8174 81.74%
Micronuclear - 0.9100 91.00%
Hepatotoxicity + 0.6178 61.78%
skin sensitisation - 0.7476 74.76%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity - 0.7164 71.64%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity - 0.6874 68.74%
Acute Oral Toxicity (c) III 0.5506 55.06%
Estrogen receptor binding - 0.6539 65.39%
Androgen receptor binding - 0.6476 64.76%
Thyroid receptor binding + 0.6618 66.18%
Glucocorticoid receptor binding + 0.7137 71.37%
Aromatase binding - 0.7375 73.75%
PPAR gamma + 0.6916 69.16%
Honey bee toxicity - 0.9537 95.37%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity + 0.5924 59.24%
Fish aquatic toxicity + 0.9741 97.41%

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
CHEMBL3060 Q9Y345 Glycine transporter 2 94.69% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.90% 91.11%
CHEMBL2581 P07339 Cathepsin D 91.82% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.74% 95.56%
CHEMBL325 Q13547 Histone deacetylase 1 91.33% 95.92%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.44% 96.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.93% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.35% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 82.74% 94.73%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 82.23% 96.47%
CHEMBL1829 O15379 Histone deacetylase 3 81.97% 95.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 85108162
LOTUS LTS0101731
wikiData Q104170851