Sclerotiorin C

Details

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Internal ID e3f5bcb2-ff22-4174-8367-466cdbd7fb10
Taxonomy Organic oxygen compounds > Organooxygen compounds > Ethers > Acetals > Ketals
IUPAC Name (6aR,8R,9aR)-3-[(5S)-3,5-dimethylhepta-1,3-dienyl]-8-methoxy-6a,8-dimethyl-9,9a-dihydrofuro[2,3-h]isochromen-6-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H30O4/c1-7-15(2)10-16(3)8-9-18-11-17-12-21(24)23(5)20(19(17)14-26-18)13-22(4,25-6)27-23/h8-12,14-15,20H,7,13H2,1-6H3/t15-,20+,22+,23+/m0/s1
InChI Key KRMNXAJBNOFESN-APQCTARYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C23H30O4
Molecular Weight 370.50 g/mol
Exact Mass 370.21440943 g/mol
Topological Polar Surface Area (TPSA) 44.80 Ų
XlogP 4.10
Atomic LogP (AlogP) 5.00
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Sclerotiorin C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9947 99.47%
Caco-2 + 0.7245 72.45%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.5898 58.98%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7982 79.82%
OATP1B3 inhibitior + 0.9085 90.85%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.9427 94.27%
P-glycoprotein inhibitior + 0.7405 74.05%
P-glycoprotein substrate - 0.5450 54.50%
CYP3A4 substrate + 0.6684 66.84%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8798 87.98%
CYP3A4 inhibition - 0.5061 50.61%
CYP2C9 inhibition - 0.8884 88.84%
CYP2C19 inhibition - 0.7981 79.81%
CYP2D6 inhibition - 0.9046 90.46%
CYP1A2 inhibition - 0.7871 78.71%
CYP2C8 inhibition + 0.5169 51.69%
CYP inhibitory promiscuity + 0.5250 52.50%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.4371 43.71%
Eye corrosion - 0.9866 98.66%
Eye irritation - 0.9329 93.29%
Skin irritation - 0.6135 61.35%
Skin corrosion - 0.9286 92.86%
Ames mutagenesis + 0.5209 52.09%
Human Ether-a-go-go-Related Gene inhibition + 0.9151 91.51%
Micronuclear - 0.6600 66.00%
Hepatotoxicity - 0.5573 55.73%
skin sensitisation - 0.7292 72.92%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.9444 94.44%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity - 0.6242 62.42%
Acute Oral Toxicity (c) III 0.6426 64.26%
Estrogen receptor binding + 0.8711 87.11%
Androgen receptor binding + 0.6370 63.70%
Thyroid receptor binding + 0.7901 79.01%
Glucocorticoid receptor binding + 0.6771 67.71%
Aromatase binding + 0.7668 76.68%
PPAR gamma + 0.6276 62.76%
Honey bee toxicity - 0.8039 80.39%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5045 50.45%
Fish aquatic toxicity + 0.9498 94.98%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.55% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.37% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.87% 96.09%
CHEMBL1937 Q92769 Histone deacetylase 2 95.54% 94.75%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.31% 85.14%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 92.48% 96.09%
CHEMBL2581 P07339 Cathepsin D 92.43% 98.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 90.94% 96.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.98% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.73% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.67% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 89.38% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.97% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.95% 99.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.52% 95.89%
CHEMBL3401 O75469 Pregnane X receptor 84.74% 94.73%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.69% 92.62%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 82.99% 100.00%
CHEMBL1871 P10275 Androgen Receptor 82.14% 96.43%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.73% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.71% 95.56%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 81.03% 95.71%
CHEMBL3922 P50579 Methionine aminopeptidase 2 81.00% 97.28%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.17% 97.14%

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 146682947
LOTUS LTS0213088
wikiData Q105145118