methyl (2Z,4E)-5-methylsulfanyldeca-2,4-dien-6,8-diynoate

Details

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Internal ID 64c54864-33c2-4e09-a9c2-1f03ca6265db
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters
IUPAC Name methyl (2Z,4E)-5-methylsulfanyldeca-2,4-dien-6,8-diynoate
SMILES (Canonical) CC#CC#CC(=CC=CC(=O)OC)SC
SMILES (Isomeric) CC#CC#C/C(=C\C=C/C(=O)OC)/SC
InChI InChI=1S/C12H12O2S/c1-4-5-6-8-11(15-3)9-7-10-12(13)14-2/h7,9-10H,1-3H3/b10-7-,11-9+
InChI Key WADRMWXNCVHUHQ-PWMCPNNSSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C12H12O2S
Molecular Weight 220.29 g/mol
Exact Mass 220.05580079 g/mol
Topological Polar Surface Area (TPSA) 51.60 Ų
XlogP 2.70
Atomic LogP (AlogP) 1.99
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of methyl (2Z,4E)-5-methylsulfanyldeca-2,4-dien-6,8-diynoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9933 99.33%
Caco-2 + 0.7408 74.08%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.5734 57.34%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9297 92.97%
OATP1B3 inhibitior + 0.9536 95.36%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.8841 88.41%
P-glycoprotein inhibitior - 0.9628 96.28%
P-glycoprotein substrate - 0.8416 84.16%
CYP3A4 substrate + 0.5351 53.51%
CYP2C9 substrate - 0.5983 59.83%
CYP2D6 substrate - 0.8950 89.50%
CYP3A4 inhibition - 0.9315 93.15%
CYP2C9 inhibition - 0.8014 80.14%
CYP2C19 inhibition - 0.8478 84.78%
CYP2D6 inhibition - 0.9521 95.21%
CYP1A2 inhibition - 0.8137 81.37%
CYP2C8 inhibition - 0.8660 86.60%
CYP inhibitory promiscuity - 0.6412 64.12%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6147 61.47%
Carcinogenicity (trinary) Non-required 0.5923 59.23%
Eye corrosion + 0.7840 78.40%
Eye irritation - 0.4812 48.12%
Skin irritation + 0.5960 59.60%
Skin corrosion - 0.8179 81.79%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4856 48.56%
Micronuclear - 0.9000 90.00%
Hepatotoxicity - 0.5223 52.23%
skin sensitisation + 0.8341 83.41%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity - 0.9222 92.22%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity + 0.8676 86.76%
Acute Oral Toxicity (c) III 0.5710 57.10%
Estrogen receptor binding - 0.7519 75.19%
Androgen receptor binding - 0.6459 64.59%
Thyroid receptor binding - 0.5681 56.81%
Glucocorticoid receptor binding + 0.5384 53.84%
Aromatase binding + 0.6196 61.96%
PPAR gamma - 0.6415 64.15%
Honey bee toxicity - 0.6318 63.18%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.9016 90.16%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.67% 96.09%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 85.08% 94.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.56% 99.17%

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.
Anthemis cretica subsp. carpatica
Cota triumfetti

Cross-Links

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PubChem 92339750
LOTUS LTS0269363
wikiData Q105300158