Thiomarinol E

Details

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Internal ID 210369bb-3da9-4c45-9bc4-da1f049b6d1a
Taxonomy Organic nitrogen compounds > Organonitrogen compounds > N-arylamides
IUPAC Name [10-oxo-10-[(5-oxo-4H-dithiolo[4,3-b]pyrrol-6-yl)amino]decyl] (E)-4-[3,4-dihydroxy-5-[(E)-5-hydroxy-4-methylhex-2-enyl]oxan-2-yl]-4-hydroxy-3-methylbut-2-enoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C32H48N2O9S2/c1-19(21(3)35)12-11-13-22-17-43-30(29(40)28(22)39)27(38)20(2)16-25(37)42-15-10-8-6-4-5-7-9-14-24(36)34-26-31-23(18-44-45-31)33-32(26)41/h11-12,16,18-19,21-22,27-30,35,38-40H,4-10,13-15,17H2,1-3H3,(H,33,41)(H,34,36)/b12-11+,20-16+
InChI Key DIZXGLMCRBSVBM-PBBJMKGWSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C32H48N2O9S2
Molecular Weight 668.90 g/mol
Exact Mass 668.28012346 g/mol
Topological Polar Surface Area (TPSA) 225.00 Ų
XlogP 3.10
Atomic LogP (AlogP) 4.21
H-Bond Acceptor 11
H-Bond Donor 6
Rotatable Bonds 18

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Thiomarinol E

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6561 65.61%
Caco-2 - 0.8487 84.87%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.8571 85.71%
Subcellular localzation Nucleus 0.4734 47.34%
OATP2B1 inhibitior - 0.7166 71.66%
OATP1B1 inhibitior + 0.8495 84.95%
OATP1B3 inhibitior + 0.9246 92.46%
MATE1 inhibitior - 0.8846 88.46%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.6830 68.30%
P-glycoprotein inhibitior + 0.7238 72.38%
P-glycoprotein substrate + 0.6949 69.49%
CYP3A4 substrate + 0.7074 70.74%
CYP2C9 substrate - 0.8087 80.87%
CYP2D6 substrate - 0.8677 86.77%
CYP3A4 inhibition - 0.5939 59.39%
CYP2C9 inhibition - 0.6941 69.41%
CYP2C19 inhibition - 0.6301 63.01%
CYP2D6 inhibition - 0.8955 89.55%
CYP1A2 inhibition - 0.7290 72.90%
CYP2C8 inhibition + 0.5561 55.61%
CYP inhibitory promiscuity - 0.6956 69.56%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.5997 59.97%
Eye corrosion - 0.9833 98.33%
Eye irritation - 0.9216 92.16%
Skin irritation - 0.7589 75.89%
Skin corrosion - 0.9237 92.37%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6594 65.94%
Micronuclear + 0.8100 81.00%
Hepatotoxicity - 0.6375 63.75%
skin sensitisation - 0.8421 84.21%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.9778 97.78%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity - 0.8632 86.32%
Acute Oral Toxicity (c) III 0.6229 62.29%
Estrogen receptor binding + 0.8108 81.08%
Androgen receptor binding + 0.6968 69.68%
Thyroid receptor binding - 0.5544 55.44%
Glucocorticoid receptor binding + 0.6384 63.84%
Aromatase binding + 0.6118 61.18%
PPAR gamma + 0.6457 64.57%
Honey bee toxicity - 0.7401 74.01%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5076 50.76%
Fish aquatic toxicity + 0.9487 94.87%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.14% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.14% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.56% 96.09%
CHEMBL2581 P07339 Cathepsin D 97.43% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 96.14% 99.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 95.87% 99.23%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 95.50% 89.34%
CHEMBL4040 P28482 MAP kinase ERK2 94.99% 83.82%
CHEMBL4302 P08183 P-glycoprotein 1 92.85% 92.98%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 92.84% 97.21%
CHEMBL3267 P48736 PI3-kinase p110-gamma subunit 91.79% 95.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.73% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.42% 89.00%
CHEMBL325 Q13547 Histone deacetylase 1 90.32% 95.92%
CHEMBL3401 O75469 Pregnane X receptor 89.99% 94.73%
CHEMBL2563 Q9UQL6 Histone deacetylase 5 89.46% 89.67%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 88.96% 82.69%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 87.88% 90.71%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 87.84% 91.07%
CHEMBL1937 Q92769 Histone deacetylase 2 87.64% 94.75%
CHEMBL255 P29275 Adenosine A2b receptor 87.21% 98.59%
CHEMBL1829 O15379 Histone deacetylase 3 85.45% 95.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 85.40% 93.56%
CHEMBL2716 Q8WUI4 Histone deacetylase 7 84.46% 89.44%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 82.88% 95.17%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 82.23% 93.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.44% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.38% 86.33%
CHEMBL2535 P11166 Glucose transporter 81.17% 98.75%

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 9964038
LOTUS LTS0224394
wikiData Q77377231