(2S,3S)-2-dec-9-en-1,3,5,7-tetraynyl-3-methyloxirane

Details

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Internal ID 75d5166a-1075-4256-b99f-5aad261cce91
Taxonomy Organoheterocyclic compounds > Epoxides
IUPAC Name (2S,3S)-2-dec-9-en-1,3,5,7-tetraynyl-3-methyloxirane
SMILES (Canonical) CC1C(O1)C#CC#CC#CC#CC=C
SMILES (Isomeric) C[C@H]1[C@@H](O1)C#CC#CC#CC#CC=C
InChI InChI=1S/C13H8O/c1-3-4-5-6-7-8-9-10-11-13-12(2)14-13/h3,12-13H,1H2,2H3/t12-,13-/m0/s1
InChI Key WFHUMVBFESKVLU-STQMWFEESA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H8O
Molecular Weight 180.20 g/mol
Exact Mass 180.057514874 g/mol
Topological Polar Surface Area (TPSA) 12.50 Ų
XlogP 2.50
Atomic LogP (AlogP) 0.97
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2S,3S)-2-dec-9-en-1,3,5,7-tetraynyl-3-methyloxirane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9876 98.76%
Caco-2 - 0.6134 61.34%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Lysosomes 0.3800 38.00%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8745 87.45%
OATP1B3 inhibitior + 0.9642 96.42%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8209 82.09%
P-glycoprotein inhibitior - 0.9400 94.00%
P-glycoprotein substrate - 0.9630 96.30%
CYP3A4 substrate - 0.5797 57.97%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate - 0.8222 82.22%
CYP3A4 inhibition - 0.9480 94.80%
CYP2C9 inhibition - 0.7334 73.34%
CYP2C19 inhibition + 0.5059 50.59%
CYP2D6 inhibition - 0.9559 95.59%
CYP1A2 inhibition - 0.5000 50.00%
CYP2C8 inhibition - 0.9247 92.47%
CYP inhibitory promiscuity - 0.6255 62.55%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5344 53.44%
Carcinogenicity (trinary) Non-required 0.4069 40.69%
Eye corrosion + 0.7975 79.75%
Eye irritation - 0.8040 80.40%
Skin irritation + 0.6936 69.36%
Skin corrosion + 0.5441 54.41%
Ames mutagenesis + 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6383 63.83%
Micronuclear - 0.6800 68.00%
Hepatotoxicity + 0.7500 75.00%
skin sensitisation + 0.6756 67.56%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity - 0.8000 80.00%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity + 0.6663 66.63%
Acute Oral Toxicity (c) II 0.5568 55.68%
Estrogen receptor binding - 0.6332 63.32%
Androgen receptor binding - 0.7116 71.16%
Thyroid receptor binding - 0.5405 54.05%
Glucocorticoid receptor binding - 0.5250 52.50%
Aromatase binding + 0.5995 59.95%
PPAR gamma - 0.5709 57.09%
Honey bee toxicity - 0.7062 70.62%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.6737 67.37%

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
CHEMBL1951 P21397 Monoamine oxidase A 91.38% 91.49%
CHEMBL5251 Q06187 Tyrosine-protein kinase BTK 84.89% 98.51%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 84.12% 95.58%
CHEMBL3401 O75469 Pregnane X receptor 83.84% 94.73%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 82.12% 94.80%
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 81.53% 96.42%

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.
Bidens andicola

Cross-Links

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PubChem 162922576
LOTUS LTS0217738
wikiData Q105303912