S-(4-methoxy-3-methylidene-1,2-dihydropyrrol-5-yl) tridecanethioate

Details

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Internal ID bc45068e-9c76-48d8-a021-bda11bc1e410
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acyl thioesters
IUPAC Name S-(4-methoxy-3-methylidene-1,2-dihydropyrrol-5-yl) tridecanethioate
SMILES (Canonical) CCCCCCCCCCCCC(=O)SC1=C(C(=C)CN1)OC
SMILES (Isomeric) CCCCCCCCCCCCC(=O)SC1=C(C(=C)CN1)OC
InChI InChI=1S/C19H33NO2S/c1-4-5-6-7-8-9-10-11-12-13-14-17(21)23-19-18(22-3)16(2)15-20-19/h20H,2,4-15H2,1,3H3
InChI Key JLIIEXZJMXLONC-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H33NO2S
Molecular Weight 339.50 g/mol
Exact Mass 339.22320047 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 6.60
Atomic LogP (AlogP) 5.53
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 13

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of S-(4-methoxy-3-methylidene-1,2-dihydropyrrol-5-yl) tridecanethioate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9690 96.90%
Caco-2 + 0.7026 70.26%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Lysosomes 0.4615 46.15%
OATP2B1 inhibitior - 0.8530 85.30%
OATP1B1 inhibitior + 0.8997 89.97%
OATP1B3 inhibitior + 0.9383 93.83%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior + 0.6485 64.85%
P-glycoprotein inhibitior - 0.5610 56.10%
P-glycoprotein substrate - 0.6819 68.19%
CYP3A4 substrate - 0.5177 51.77%
CYP2C9 substrate - 0.5820 58.20%
CYP2D6 substrate - 0.8840 88.40%
CYP3A4 inhibition - 0.8836 88.36%
CYP2C9 inhibition - 0.6466 64.66%
CYP2C19 inhibition - 0.5361 53.61%
CYP2D6 inhibition - 0.8315 83.15%
CYP1A2 inhibition + 0.5986 59.86%
CYP2C8 inhibition - 0.6771 67.71%
CYP inhibitory promiscuity + 0.6355 63.55%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8700 87.00%
Carcinogenicity (trinary) Non-required 0.5593 55.93%
Eye corrosion - 0.9716 97.16%
Eye irritation + 0.6155 61.55%
Skin irritation - 0.7430 74.30%
Skin corrosion - 0.9009 90.09%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7054 70.54%
Micronuclear - 0.7300 73.00%
Hepatotoxicity + 0.5212 52.12%
skin sensitisation - 0.7949 79.49%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.5222 52.22%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.7722 77.22%
Acute Oral Toxicity (c) III 0.5828 58.28%
Estrogen receptor binding - 0.6198 61.98%
Androgen receptor binding - 0.7435 74.35%
Thyroid receptor binding + 0.6468 64.68%
Glucocorticoid receptor binding - 0.6289 62.89%
Aromatase binding - 0.6776 67.76%
PPAR gamma + 0.6265 62.65%
Honey bee toxicity - 0.9752 97.52%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity + 0.7059 70.59%
Fish aquatic toxicity + 0.9178 91.78%

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 98.27% 96.09%
CHEMBL2581 P07339 Cathepsin D 98.08% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.99% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.85% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.09% 94.45%
CHEMBL2885 P07451 Carbonic anhydrase III 88.00% 87.45%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 87.21% 91.81%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 80.57% 92.08%

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 11759587
LOTUS LTS0055625
wikiData Q105130776