Sescandelin B

Details

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Internal ID 1231b560-3662-4cda-838f-52b4c003c32e
Taxonomy Phenylpropanoids and polyketides > Isocoumarins and derivatives
IUPAC Name 6,8-dihydroxy-4-(hydroxymethyl)-3-methylisochromen-1-one
SMILES (Canonical) CC1=C(C2=C(C(=CC(=C2)O)O)C(=O)O1)CO
SMILES (Isomeric) CC1=C(C2=C(C(=CC(=C2)O)O)C(=O)O1)CO
InChI InChI=1S/C11H10O5/c1-5-8(4-12)7-2-6(13)3-9(14)10(7)11(15)16-5/h2-3,12-14H,4H2,1H3
InChI Key SIGBMSMENCGPQO-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H10O5
Molecular Weight 222.19 g/mol
Exact Mass 222.05282342 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP 0.80
Atomic LogP (AlogP) 1.00
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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136440-67-0
6,8-Dihydroxy-4-(hydroxymethyl)-3-methyl-1H-2-benzopyran-1-one
AKOS040735936

2D Structure

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2D Structure of Sescandelin B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9474 94.74%
Caco-2 + 0.5867 58.67%
Blood Brain Barrier - 0.9250 92.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.6387 63.87%
OATP2B1 inhibitior - 0.7129 71.29%
OATP1B1 inhibitior + 0.8692 86.92%
OATP1B3 inhibitior + 0.8403 84.03%
MATE1 inhibitior - 0.5600 56.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8856 88.56%
P-glycoprotein inhibitior - 0.9338 93.38%
P-glycoprotein substrate - 0.8993 89.93%
CYP3A4 substrate - 0.5677 56.77%
CYP2C9 substrate + 0.6440 64.40%
CYP2D6 substrate - 0.8792 87.92%
CYP3A4 inhibition - 0.7288 72.88%
CYP2C9 inhibition - 0.7753 77.53%
CYP2C19 inhibition - 0.7989 79.89%
CYP2D6 inhibition - 0.9476 94.76%
CYP1A2 inhibition - 0.5484 54.84%
CYP2C8 inhibition - 0.7461 74.61%
CYP inhibitory promiscuity - 0.5130 51.30%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.7731 77.31%
Eye corrosion - 0.9867 98.67%
Eye irritation + 0.9729 97.29%
Skin irritation - 0.6458 64.58%
Skin corrosion - 0.9525 95.25%
Ames mutagenesis + 0.5536 55.36%
Human Ether-a-go-go-Related Gene inhibition - 0.7457 74.57%
Micronuclear + 0.5574 55.74%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation - 0.8655 86.55%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity - 0.8136 81.36%
Acute Oral Toxicity (c) III 0.6032 60.32%
Estrogen receptor binding + 0.5926 59.26%
Androgen receptor binding + 0.5578 55.78%
Thyroid receptor binding - 0.7165 71.65%
Glucocorticoid receptor binding + 0.8502 85.02%
Aromatase binding - 0.5078 50.78%
PPAR gamma + 0.5455 54.55%
Honey bee toxicity - 0.9545 95.45%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.9392 93.92%

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 97.98% 91.11%
CHEMBL2581 P07339 Cathepsin D 93.19% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.96% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.51% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 91.70% 94.73%
CHEMBL3192 Q9BY41 Histone deacetylase 8 90.18% 93.99%
CHEMBL1951 P21397 Monoamine oxidase A 89.30% 91.49%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.70% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.61% 86.33%
CHEMBL3194 P02766 Transthyretin 83.36% 90.71%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.21% 99.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.69% 99.23%
CHEMBL1929 P47989 Xanthine dehydrogenase 81.71% 96.12%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 81.44% 99.15%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 80.70% 93.65%

Cross-Links

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PubChem 71435035
NPASS NPC76356
LOTUS LTS0200710
wikiData Q105253728