Cis-Bis(Methylthio)Silvatin

Details

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Internal ID e52880a2-d59f-4721-b71f-1e47c9fd362f
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives
IUPAC Name (3R,6R)-1,4-dimethyl-3-[[4-(3-methylbut-2-enoxy)phenyl]methyl]-3,6-bis(methylsulfanyl)piperazine-2,5-dione
SMILES (Canonical) CC(=CCOC1=CC=C(C=C1)CC2(C(=O)N(C(C(=O)N2C)SC)C)SC)C
SMILES (Isomeric) CC(=CCOC1=CC=C(C=C1)C[C@]2(C(=O)N([C@@H](C(=O)N2C)SC)C)SC)C
InChI InChI=1S/C20H28N2O3S2/c1-14(2)11-12-25-16-9-7-15(8-10-16)13-20(27-6)19(24)21(3)18(26-5)17(23)22(20)4/h7-11,18H,12-13H2,1-6H3/t18-,20-/m1/s1
InChI Key XBKBUMFBHNQOLC-UYAOXDASSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C20H28N2O3S2
Molecular Weight 408.60 g/mol
Exact Mass 408.15413511 g/mol
Topological Polar Surface Area (TPSA) 100.00 Ų
XlogP 3.90
Atomic LogP (AlogP) 3.25
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

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(3R,6R)-1,4-dimethyl-3-((4-(3-methylbut-2-enoxy)phenyl)methyl)-3,6-bis(methylsulfanyl)piperazine-2,5-dione
(3R,6R)-1,4-dimethyl-3-[[4-(3-methylbut-2-enoxy)phenyl]methyl]-3,6-bis(methylsulfanyl)piperazine-2,5-dione
RefChem:126434
77053-25-9
CHEMBL253544

2D Structure

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2D Structure of Cis-Bis(Methylthio)Silvatin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9010 90.10%
Caco-2 + 0.5000 50.00%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.6078 60.78%
OATP2B1 inhibitior - 0.8557 85.57%
OATP1B1 inhibitior + 0.9034 90.34%
OATP1B3 inhibitior + 0.9360 93.60%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7649 76.49%
BSEP inhibitior + 0.9513 95.13%
P-glycoprotein inhibitior + 0.6387 63.87%
P-glycoprotein substrate - 0.7322 73.22%
CYP3A4 substrate + 0.6508 65.08%
CYP2C9 substrate - 0.8052 80.52%
CYP2D6 substrate - 0.8283 82.83%
CYP3A4 inhibition - 0.6271 62.71%
CYP2C9 inhibition + 0.5000 50.00%
CYP2C19 inhibition + 0.5147 51.47%
CYP2D6 inhibition - 0.8770 87.70%
CYP1A2 inhibition - 0.5860 58.60%
CYP2C8 inhibition - 0.6619 66.19%
CYP inhibitory promiscuity + 0.8378 83.78%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8513 85.13%
Carcinogenicity (trinary) Non-required 0.6257 62.57%
Eye corrosion - 0.9856 98.56%
Eye irritation - 0.9632 96.32%
Skin irritation - 0.7674 76.74%
Skin corrosion - 0.9240 92.40%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4556 45.56%
Micronuclear + 0.6400 64.00%
Hepatotoxicity + 0.6593 65.93%
skin sensitisation - 0.8417 84.17%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.8625 86.25%
Nephrotoxicity + 0.6209 62.09%
Acute Oral Toxicity (c) III 0.6221 62.21%
Estrogen receptor binding + 0.7536 75.36%
Androgen receptor binding + 0.7366 73.66%
Thyroid receptor binding + 0.6541 65.41%
Glucocorticoid receptor binding + 0.6150 61.50%
Aromatase binding + 0.5865 58.65%
PPAR gamma + 0.6908 69.08%
Honey bee toxicity - 0.6797 67.97%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.9427 94.27%

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
CHEMBL2581 P07339 Cathepsin D 98.73% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.03% 96.09%
CHEMBL321 P14780 Matrix metalloproteinase 9 93.39% 92.12%
CHEMBL221 P23219 Cyclooxygenase-1 91.34% 90.17%
CHEMBL4208 P20618 Proteasome component C5 90.64% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.18% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.82% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.68% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.32% 94.00%
CHEMBL3492 P49721 Proteasome Macropain subunit 87.43% 90.24%
CHEMBL1937 Q92769 Histone deacetylase 2 87.34% 94.75%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 85.13% 94.42%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.86% 95.89%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 83.99% 89.34%
CHEMBL2563 Q9UQL6 Histone deacetylase 5 83.51% 89.67%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 83.32% 93.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.30% 96.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.14% 91.11%

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.
Tetradium ruticarpum

Cross-Links

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PubChem 11069575
NPASS NPC189908
LOTUS LTS0109481
wikiData Q105324538