Irisxanthone

Details

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Internal ID 37db7be0-4f70-4913-abf6-9adce68b08f0
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 1,3,6-trihydroxy-5-methoxy-2-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]xanthen-9-one
SMILES (Canonical) COC1=C(C=CC2=C1OC3=C(C2=O)C(=C(C(=C3)O)C4C(C(C(C(O4)CO)O)O)O)O)O
SMILES (Isomeric) COC1=C(C=CC2=C1OC3=C(C2=O)C(=C(C(=C3)O)[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O)O)O
InChI InChI=1S/C20H20O11/c1-29-19-7(22)3-2-6-13(24)12-9(30-18(6)19)4-8(23)11(15(12)26)20-17(28)16(27)14(25)10(5-21)31-20/h2-4,10,14,16-17,20-23,25-28H,5H2,1H3/t10-,14-,16+,17-,20+/m1/s1
InChI Key MTQVPZUZBBTLNO-HSLVGEKZSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C20H20O11
Molecular Weight 436.40 g/mol
Exact Mass 436.10056145 g/mol
Topological Polar Surface Area (TPSA) 186.00 Ų
XlogP 0.00
Atomic LogP (AlogP) -0.41
H-Bond Acceptor 11
H-Bond Donor 7
Rotatable Bonds 3

Synonyms

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51419-56-8
1,3,6-trihydroxy-5-methoxy-2-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]xanthen-9-one
CHEBI:5973
DTXSID70415162
1,3,6-trihydroxy-5-methoxy-2-((2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)xanthen-9-one
1,3,6-trihydroxy-5-methoxy-2-((2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl)xanthen-9-one
1,3,6-trihydroxy-5-methoxy-2-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]xanthen-9-one
RefChem:1062407
DTXCID60366013
2-beta-D-Glucopyranosyl-1,3,6-trihydroxy-5-methoxy-9H-xanthen-9-one
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Irisxanthone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6545 65.45%
Caco-2 - 0.9013 90.13%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.6233 62.33%
OATP2B1 inhibitior + 0.5864 58.64%
OATP1B1 inhibitior + 0.8654 86.54%
OATP1B3 inhibitior + 0.9830 98.30%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.7635 76.35%
P-glycoprotein inhibitior - 0.7480 74.80%
P-glycoprotein substrate - 0.7293 72.93%
CYP3A4 substrate + 0.6014 60.14%
CYP2C9 substrate - 0.8087 80.87%
CYP2D6 substrate - 0.8299 82.99%
CYP3A4 inhibition - 0.7983 79.83%
CYP2C9 inhibition - 0.8483 84.83%
CYP2C19 inhibition - 0.8386 83.86%
CYP2D6 inhibition - 0.9339 93.39%
CYP1A2 inhibition - 0.8015 80.15%
CYP2C8 inhibition + 0.5086 50.86%
CYP inhibitory promiscuity - 0.6314 63.14%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6988 69.88%
Eye corrosion - 0.9896 98.96%
Eye irritation - 0.8308 83.08%
Skin irritation - 0.8040 80.40%
Skin corrosion - 0.9556 95.56%
Ames mutagenesis + 0.6963 69.63%
Human Ether-a-go-go-Related Gene inhibition - 0.4480 44.80%
Micronuclear + 0.6359 63.59%
Hepatotoxicity - 0.5500 55.00%
skin sensitisation - 0.9200 92.00%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.9074 90.74%
Acute Oral Toxicity (c) III 0.6599 65.99%
Estrogen receptor binding + 0.7355 73.55%
Androgen receptor binding + 0.6480 64.80%
Thyroid receptor binding - 0.4920 49.20%
Glucocorticoid receptor binding + 0.7925 79.25%
Aromatase binding - 0.5170 51.70%
PPAR gamma - 0.5115 51.15%
Honey bee toxicity - 0.7975 79.75%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity - 0.4258 42.58%

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 99.72% 91.11%
CHEMBL4040 P28482 MAP kinase ERK2 96.09% 83.82%
CHEMBL2581 P07339 Cathepsin D 95.99% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 95.00% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.56% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.63% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.12% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.14% 86.33%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 87.72% 99.15%
CHEMBL3401 O75469 Pregnane X receptor 86.76% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.49% 99.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.41% 99.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.46% 96.09%
CHEMBL3192 Q9BY41 Histone deacetylase 8 80.65% 93.99%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.40% 96.00%

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.
Iris florentina

Cross-Links

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PubChem 5281637
LOTUS LTS0178745
wikiData Q27106955