4-(3-Methylsulfanylprop-2-enoylamino)butyl 3-methylsulfanylprop-2-enoate

Details

Top
Internal ID ba32bc25-8e63-4d13-94e6-4bc2e5011435
Taxonomy Organic acids and derivatives > Vinylogous thioesters
IUPAC Name 4-(3-methylsulfanylprop-2-enoylamino)butyl 3-methylsulfanylprop-2-enoate
SMILES (Canonical) CSC=CC(=O)NCCCCOC(=O)C=CSC
SMILES (Isomeric) CSC=CC(=O)NCCCCOC(=O)C=CSC
InChI InChI=1S/C12H19NO3S2/c1-17-9-5-11(14)13-7-3-4-8-16-12(15)6-10-18-2/h5-6,9-10H,3-4,7-8H2,1-2H3,(H,13,14)
InChI Key GVFWUEUUBBYYPB-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C12H19NO3S2
Molecular Weight 289.40 g/mol
Exact Mass 289.08063582 g/mol
Topological Polar Surface Area (TPSA) 106.00 Ų
XlogP 1.60
Atomic LogP (AlogP) 2.18
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 9

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 4-(3-Methylsulfanylprop-2-enoylamino)butyl 3-methylsulfanylprop-2-enoate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9342 93.42%
Caco-2 + 0.5559 55.59%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.8043 80.43%
OATP2B1 inhibitior - 0.8558 85.58%
OATP1B1 inhibitior + 0.9351 93.51%
OATP1B3 inhibitior + 0.9460 94.60%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.7657 76.57%
P-glycoprotein inhibitior - 0.8913 89.13%
P-glycoprotein substrate - 0.7079 70.79%
CYP3A4 substrate + 0.5279 52.79%
CYP2C9 substrate - 0.6039 60.39%
CYP2D6 substrate - 0.8508 85.08%
CYP3A4 inhibition - 0.8598 85.98%
CYP2C9 inhibition - 0.8540 85.40%
CYP2C19 inhibition - 0.7968 79.68%
CYP2D6 inhibition - 0.9140 91.40%
CYP1A2 inhibition - 0.5994 59.94%
CYP2C8 inhibition - 0.8846 88.46%
CYP inhibitory promiscuity - 0.6995 69.95%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7800 78.00%
Carcinogenicity (trinary) Non-required 0.6705 67.05%
Eye corrosion - 0.9314 93.14%
Eye irritation - 0.7780 77.80%
Skin irritation - 0.7976 79.76%
Skin corrosion - 0.9317 93.17%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4799 47.99%
Micronuclear - 0.6300 63.00%
Hepatotoxicity + 0.5125 51.25%
skin sensitisation - 0.8747 87.47%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity - 0.7830 78.30%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity + 0.4903 49.03%
Acute Oral Toxicity (c) III 0.6058 60.58%
Estrogen receptor binding - 0.5116 51.16%
Androgen receptor binding - 0.5741 57.41%
Thyroid receptor binding + 0.5961 59.61%
Glucocorticoid receptor binding - 0.7171 71.71%
Aromatase binding - 0.6814 68.14%
PPAR gamma - 0.6080 60.80%
Honey bee toxicity - 0.8733 87.33%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity - 0.7054 70.54%

Targets

Top

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 94.07% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.01% 99.17%
CHEMBL2581 P07339 Cathepsin D 91.07% 98.95%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 84.52% 97.29%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 84.04% 94.33%
CHEMBL2001 Q9H244 Purinergic receptor P2Y12 82.28% 96.00%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 82.06% 89.34%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.65% 96.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.34% 91.11%

Plants that contains it

Top
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.
Aglaia tenuicaulis

Cross-Links

Top
PubChem 162931975
LOTUS LTS0117282
wikiData Q105021129