Roseobacticide E

Details

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Internal ID 951aa592-7d44-4445-8e4d-16873d915080
Taxonomy Organoheterocyclic compounds > Cycloheptafurans
IUPAC Name 7-(methyldisulfanyl)-3-phenylcyclohepta[b]furan-2-one
SMILES (Canonical) CSSC1=CC=CC2=C(C(=O)OC2=C1)C3=CC=CC=C3
SMILES (Isomeric) CSSC1=CC=CC2=C(C(=O)OC2=C1)C3=CC=CC=C3
InChI InChI=1S/C16H12O2S2/c1-19-20-12-8-5-9-13-14(10-12)18-16(17)15(13)11-6-3-2-4-7-11/h2-10H,1H3
InChI Key FAJBPAJIEYOYNL-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C16H12O2S2
Molecular Weight 300.40 g/mol
Exact Mass 300.02787197 g/mol
Topological Polar Surface Area (TPSA) 76.90 Ų
XlogP 3.50
Atomic LogP (AlogP) 4.78
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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SCHEMBL469716

2D Structure

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2D Structure of Roseobacticide E

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9972 99.72%
Caco-2 + 0.7489 74.89%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.4651 46.51%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9356 93.56%
OATP1B3 inhibitior + 0.9550 95.50%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.7246 72.46%
P-glycoprotein inhibitior - 0.6099 60.99%
P-glycoprotein substrate - 0.7977 79.77%
CYP3A4 substrate - 0.5301 53.01%
CYP2C9 substrate - 0.8331 83.31%
CYP2D6 substrate - 0.8451 84.51%
CYP3A4 inhibition + 0.6236 62.36%
CYP2C9 inhibition + 0.5668 56.68%
CYP2C19 inhibition + 0.5644 56.44%
CYP2D6 inhibition - 0.8830 88.30%
CYP1A2 inhibition + 0.7448 74.48%
CYP2C8 inhibition + 0.5200 52.00%
CYP inhibitory promiscuity + 0.6489 64.89%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7818 78.18%
Carcinogenicity (trinary) Non-required 0.5082 50.82%
Eye corrosion - 0.9208 92.08%
Eye irritation + 0.6469 64.69%
Skin irritation - 0.6217 62.17%
Skin corrosion - 0.8919 89.19%
Ames mutagenesis + 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5621 56.21%
Micronuclear + 0.6240 62.40%
Hepatotoxicity + 0.6875 68.75%
skin sensitisation - 0.6847 68.47%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity - 0.6196 61.96%
Nephrotoxicity + 0.6568 65.68%
Acute Oral Toxicity (c) III 0.5383 53.83%
Estrogen receptor binding + 0.9290 92.90%
Androgen receptor binding + 0.8738 87.38%
Thyroid receptor binding + 0.6643 66.43%
Glucocorticoid receptor binding + 0.9052 90.52%
Aromatase binding + 0.9431 94.31%
PPAR gamma + 0.8564 85.64%
Honey bee toxicity - 0.8684 86.84%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.7000 70.00%
Fish aquatic toxicity + 0.9666 96.66%

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 98.58% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.96% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.31% 95.56%
CHEMBL262 P49841 Glycogen synthase kinase-3 beta 93.17% 95.72%
CHEMBL1907 P15144 Aminopeptidase N 90.90% 93.31%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 85.87% 96.67%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.53% 99.23%
CHEMBL3401 O75469 Pregnane X receptor 85.46% 94.73%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 84.87% 94.03%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.40% 91.11%
CHEMBL2083 P15090 Fatty acid binding protein adipocyte 84.19% 95.71%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.66% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.97% 94.00%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 82.57% 96.09%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.93% 95.50%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 81.78% 87.67%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 81.58% 81.11%
CHEMBL5805 Q9NR97 Toll-like receptor 8 80.34% 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 87112909
LOTUS LTS0179681
wikiData Q75058544