(2S)-2-methyl-4-(6-methylhepta-1,5-dien-3-yn-2-yl)-2H-furan-5-one

Details

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Internal ID cdcb20e6-7a55-439f-abdb-231f33f0dd27
Taxonomy Organoheterocyclic compounds > Dihydrofurans > Furanones > Butenolides
IUPAC Name (2S)-2-methyl-4-(6-methylhepta-1,5-dien-3-yn-2-yl)-2H-furan-5-one
SMILES (Canonical) CC1C=C(C(=O)O1)C(=C)C#CC=C(C)C
SMILES (Isomeric) C[C@H]1C=C(C(=O)O1)C(=C)C#CC=C(C)C
InChI InChI=1S/C13H14O2/c1-9(2)6-5-7-10(3)12-8-11(4)15-13(12)14/h6,8,11H,3H2,1-2,4H3/t11-/m0/s1
InChI Key IWINLURPOFHRBJ-NSHDSACASA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H14O2
Molecular Weight 202.25 g/mol
Exact Mass 202.099379685 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 3.70
Atomic LogP (AlogP) 2.38
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2S)-2-methyl-4-(6-methylhepta-1,5-dien-3-yn-2-yl)-2H-furan-5-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9937 99.37%
Caco-2 + 0.5260 52.60%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.6439 64.39%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8772 87.72%
OATP1B3 inhibitior + 0.9458 94.58%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8709 87.09%
P-glycoprotein inhibitior - 0.9386 93.86%
P-glycoprotein substrate - 0.9322 93.22%
CYP3A4 substrate - 0.5243 52.43%
CYP2C9 substrate + 0.5827 58.27%
CYP2D6 substrate - 0.8914 89.14%
CYP3A4 inhibition - 0.8943 89.43%
CYP2C9 inhibition - 0.9109 91.09%
CYP2C19 inhibition - 0.7497 74.97%
CYP2D6 inhibition - 0.9507 95.07%
CYP1A2 inhibition - 0.7195 71.95%
CYP2C8 inhibition - 0.9494 94.94%
CYP inhibitory promiscuity + 0.5437 54.37%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7944 79.44%
Carcinogenicity (trinary) Non-required 0.4603 46.03%
Eye corrosion - 0.5857 58.57%
Eye irritation + 0.7991 79.91%
Skin irritation + 0.4945 49.45%
Skin corrosion - 0.8980 89.80%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5208 52.08%
Micronuclear - 0.5800 58.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation + 0.6910 69.10%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity - 0.6667 66.67%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity + 0.7681 76.81%
Acute Oral Toxicity (c) III 0.6364 63.64%
Estrogen receptor binding - 0.5509 55.09%
Androgen receptor binding - 0.7316 73.16%
Thyroid receptor binding - 0.6490 64.90%
Glucocorticoid receptor binding - 0.7583 75.83%
Aromatase binding - 0.5098 50.98%
PPAR gamma - 0.6875 68.75%
Honey bee toxicity - 0.7649 76.49%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.9413 94.13%

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 94.58% 91.49%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.99% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.83% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.25% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 84.75% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.58% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.91% 99.23%
CHEMBL2581 P07339 Cathepsin D 81.64% 98.95%

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 10081567
LOTUS LTS0022449
wikiData Q105121657