Isobellidifolin

Details

Top
Internal ID 78c3374e-264a-4667-be03-a0e10db4e1b6
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 1,3,8-trihydroxy-5-methoxyxanthen-9-one
SMILES (Canonical) COC1=C2C(=C(C=C1)O)C(=O)C3=C(C=C(C=C3O2)O)O
SMILES (Isomeric) COC1=C2C(=C(C=C1)O)C(=O)C3=C(C=C(C=C3O2)O)O
InChI InChI=1S/C14H10O6/c1-19-9-3-2-7(16)12-13(18)11-8(17)4-6(15)5-10(11)20-14(9)12/h2-5,15-17H,1H3
InChI Key QNJCJDZKEAVOBJ-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

Top
Molecular Formula C14H10O6
Molecular Weight 274.22 g/mol
Exact Mass 274.04773803 g/mol
Topological Polar Surface Area (TPSA) 96.20 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.07
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

Top
1,3,8-trihydroxy-5-methoxyxanthen-9-one
HY-N9370
1,3,8-trihydroxy-5-methoxyxanthone
5-Methoxy-1,3,8-trihyroxyxanthen-9-one
1,3,8-trihydroxy-5-methoxy-xanthen-9-one
CS-0159552
E89029
552-00-1

2D Structure

Top
2D Structure of Isobellidifolin

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9404 94.04%
Caco-2 + 0.5945 59.45%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.5738 57.38%
OATP2B1 inhibitior - 0.6918 69.18%
OATP1B1 inhibitior + 0.9106 91.06%
OATP1B3 inhibitior + 0.9861 98.61%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7592 75.92%
P-glycoprotein inhibitior - 0.7771 77.71%
P-glycoprotein substrate - 0.8603 86.03%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.6401 64.01%
CYP2D6 substrate - 0.8296 82.96%
CYP3A4 inhibition + 0.7957 79.57%
CYP2C9 inhibition - 0.5790 57.90%
CYP2C19 inhibition + 0.6217 62.17%
CYP2D6 inhibition - 0.6187 61.87%
CYP1A2 inhibition + 0.9450 94.50%
CYP2C8 inhibition + 0.6965 69.65%
CYP inhibitory promiscuity + 0.6664 66.64%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5499 54.99%
Eye corrosion - 0.9486 94.86%
Eye irritation + 0.9101 91.01%
Skin irritation - 0.5968 59.68%
Skin corrosion - 0.9577 95.77%
Ames mutagenesis + 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7599 75.99%
Micronuclear + 0.8000 80.00%
Hepatotoxicity - 0.6178 61.78%
skin sensitisation - 0.9129 91.29%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity + 0.5689 56.89%
Acute Oral Toxicity (c) III 0.8993 89.93%
Estrogen receptor binding + 0.9215 92.15%
Androgen receptor binding + 0.8819 88.19%
Thyroid receptor binding + 0.5698 56.98%
Glucocorticoid receptor binding + 0.9527 95.27%
Aromatase binding + 0.7042 70.42%
PPAR gamma + 0.8113 81.13%
Honey bee toxicity - 0.9046 90.46%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5849 58.49%
Fish aquatic toxicity - 0.3970 39.70%

Targets

Top

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 96.03% 91.11%
CHEMBL3194 P02766 Transthyretin 94.75% 90.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.38% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.71% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.95% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.73% 89.00%
CHEMBL2581 P07339 Cathepsin D 87.88% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.91% 94.45%
CHEMBL2535 P11166 Glucose transporter 86.03% 98.75%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.43% 99.17%
CHEMBL4208 P20618 Proteasome component C5 85.38% 90.00%
CHEMBL1255126 O15151 Protein Mdm4 84.64% 90.20%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.44% 99.23%
CHEMBL3401 O75469 Pregnane X receptor 83.12% 94.73%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 82.70% 80.78%
CHEMBL1929 P47989 Xanthine dehydrogenase 82.55% 96.12%
CHEMBL3192 Q9BY41 Histone deacetylase 8 82.37% 93.99%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 81.78% 93.65%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 81.16% 99.15%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 80.54% 98.11%
CHEMBL1951 P21397 Monoamine oxidase A 80.11% 91.49%

Plants that contains it

Top
Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Gentiana algida
Gentianella florida
Gentianopsis crinita
Swertia hookeri

Cross-Links

Top
PubChem 5322042
LOTUS LTS0058451
wikiData Q104395937