Isogentisin

Details

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Internal ID 6f4fe1de-c81f-4ebc-b085-9fd98ddbebd1
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 1,3-dihydroxy-7-methoxyxanthen-9-one
SMILES (Canonical) COC1=CC2=C(C=C1)OC3=CC(=CC(=C3C2=O)O)O
SMILES (Isomeric) COC1=CC2=C(C=C1)OC3=CC(=CC(=C3C2=O)O)O
InChI InChI=1S/C14H10O5/c1-18-8-2-3-11-9(6-8)14(17)13-10(16)4-7(15)5-12(13)19-11/h2-6,15-16H,1H3
InChI Key FVIYCYAHKMJVJK-UHFFFAOYSA-N
Popularity 40 references in papers

Physical and Chemical Properties

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Molecular Formula C14H10O5
Molecular Weight 258.23 g/mol
Exact Mass 258.05282342 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.37
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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1,3-Dihydroxy-7-methoxy-9H-xanthen-9-one
491-64-5
Isogentisine
1,3-Dihydroxy-7-methoxyxanthen-9-one
CCRIS 3969
1,3-dihydroxy-7-methoxyxanthone
1,3-Dihydroxy--7-methoxyxanthone
JPC53Q6QYC
BRN 0258402
9H-Xanthen-9-one, 1,3-dihydroxy-7-methoxy-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Isogentisin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9597 95.97%
Caco-2 + 0.7804 78.04%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.6472 64.72%
OATP2B1 inhibitior - 0.7014 70.14%
OATP1B1 inhibitior + 0.8878 88.78%
OATP1B3 inhibitior + 0.9919 99.19%
MATE1 inhibitior + 0.5400 54.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8165 81.65%
P-glycoprotein inhibitior - 0.6837 68.37%
P-glycoprotein substrate - 0.8414 84.14%
CYP3A4 substrate + 0.5265 52.65%
CYP2C9 substrate - 0.6401 64.01%
CYP2D6 substrate - 0.8296 82.96%
CYP3A4 inhibition + 0.8731 87.31%
CYP2C9 inhibition + 0.6350 63.50%
CYP2C19 inhibition + 0.7814 78.14%
CYP2D6 inhibition - 0.6470 64.70%
CYP1A2 inhibition + 0.9706 97.06%
CYP2C8 inhibition + 0.5151 51.51%
CYP inhibitory promiscuity + 0.7193 71.93%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.5520 55.20%
Eye corrosion - 0.9464 94.64%
Eye irritation + 0.9530 95.30%
Skin irritation - 0.6045 60.45%
Skin corrosion - 0.9640 96.40%
Ames mutagenesis + 0.9800 98.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5488 54.88%
Micronuclear + 0.8100 81.00%
Hepatotoxicity - 0.6060 60.60%
skin sensitisation - 0.9436 94.36%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.7290 72.90%
Acute Oral Toxicity (c) III 0.8871 88.71%
Estrogen receptor binding + 0.8530 85.30%
Androgen receptor binding + 0.8628 86.28%
Thyroid receptor binding + 0.7212 72.12%
Glucocorticoid receptor binding + 0.9517 95.17%
Aromatase binding + 0.8679 86.79%
PPAR gamma + 0.8158 81.58%
Honey bee toxicity - 0.8976 89.76%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.6705 67.05%

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 98.52% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.80% 95.56%
CHEMBL1951 P21397 Monoamine oxidase A 94.72% 91.49%
CHEMBL3192 Q9BY41 Histone deacetylase 8 94.46% 93.99%
CHEMBL1929 P47989 Xanthine dehydrogenase 94.37% 96.12%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.24% 94.00%
CHEMBL2581 P07339 Cathepsin D 90.97% 98.95%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.98% 99.15%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.57% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.47% 89.00%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 88.74% 93.65%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.06% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.83% 99.17%
CHEMBL2535 P11166 Glucose transporter 86.81% 98.75%
CHEMBL3401 O75469 Pregnane X receptor 85.55% 94.73%
CHEMBL4208 P20618 Proteasome component C5 85.24% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.71% 86.33%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.61% 92.94%
CHEMBL3194 P02766 Transthyretin 80.47% 90.71%

Plants that contains it

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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 asclepiadea
Gentiana lutea
Gentianopsis thermalis
Polygala cyparissias
Swertia petiolata

Cross-Links

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PubChem 5281640
NPASS NPC14786
LOTUS LTS0023614
wikiData Q27106981