Bisdethiodi(methylthio)-1-demethylhyalodendrin

Details

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Internal ID 00333907-55e1-4b80-a04a-3655e1a0e6a5
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives
IUPAC Name (3S,6S)-6-benzyl-3-(hydroxymethyl)-1-methyl-3,6-bis(methylsulfanyl)piperazine-2,5-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H20N2O3S2/c1-17-13(20)14(10-18,21-2)16-12(19)15(17,22-3)9-11-7-5-4-6-8-11/h4-8,18H,9-10H2,1-3H3,(H,16,19)/t14-,15-/m0/s1
InChI Key UHSDUNORVAKCRV-GJZGRUSLSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C15H20N2O3S2
Molecular Weight 340.50 g/mol
Exact Mass 340.09153485 g/mol
Topological Polar Surface Area (TPSA) 120.00 Ų
XlogP 1.90
Atomic LogP (AlogP) 0.93
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Bisdethiodi(methylthio)-1-demethylhyalodendrin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.4856 48.56%
Caco-2 - 0.5606 56.06%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.5150 51.50%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8673 86.73%
OATP1B3 inhibitior + 0.9350 93.50%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9649 96.49%
BSEP inhibitior - 0.5473 54.73%
P-glycoprotein inhibitior - 0.8667 86.67%
P-glycoprotein substrate - 0.7899 78.99%
CYP3A4 substrate - 0.5191 51.91%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8276 82.76%
CYP3A4 inhibition - 0.7596 75.96%
CYP2C9 inhibition - 0.8450 84.50%
CYP2C19 inhibition - 0.8142 81.42%
CYP2D6 inhibition - 0.8863 88.63%
CYP1A2 inhibition - 0.8095 80.95%
CYP2C8 inhibition - 0.8295 82.95%
CYP inhibitory promiscuity - 0.9701 97.01%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7300 73.00%
Carcinogenicity (trinary) Non-required 0.6330 63.30%
Eye corrosion - 0.9879 98.79%
Eye irritation - 0.9947 99.47%
Skin irritation - 0.7629 76.29%
Skin corrosion - 0.9316 93.16%
Ames mutagenesis - 0.5554 55.54%
Human Ether-a-go-go-Related Gene inhibition - 0.4044 40.44%
Micronuclear + 0.8200 82.00%
Hepatotoxicity + 0.7141 71.41%
skin sensitisation - 0.8418 84.18%
Respiratory toxicity + 0.8111 81.11%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.9500 95.00%
Nephrotoxicity + 0.5343 53.43%
Acute Oral Toxicity (c) III 0.6283 62.83%
Estrogen receptor binding - 0.5266 52.66%
Androgen receptor binding + 0.6015 60.15%
Thyroid receptor binding - 0.5097 50.97%
Glucocorticoid receptor binding - 0.5786 57.86%
Aromatase binding + 0.6299 62.99%
PPAR gamma + 0.5755 57.55%
Honey bee toxicity - 0.9239 92.39%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity - 0.4578 45.78%

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
CHEMBL2581 P07339 Cathepsin D 99.28% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.10% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.53% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.58% 86.33%
CHEMBL4208 P20618 Proteasome component C5 89.54% 90.00%
CHEMBL221 P23219 Cyclooxygenase-1 84.43% 90.17%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.32% 85.14%
CHEMBL5805 Q9NR97 Toll-like receptor 8 80.14% 96.25%

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 11035217
LOTUS LTS0157515
wikiData Q77483445