9-Hydroxy-8-(1,3,8,10-tetrahydroxy-6-methyl-9-oxoanthracen-2-ylidene)xanthene-1,7-dione

Details

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Internal ID a79e9d49-f0e1-4d85-8359-ec1e90742c7c
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthenes
IUPAC Name 9-hydroxy-8-(1,3,8,10-tetrahydroxy-6-methyl-9-oxoanthracen-2-ylidene)xanthene-1,7-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C28H16O9/c1-10-7-11-19(15(31)8-10)26(34)20-12(25(11)33)9-16(32)23(27(20)35)22-14(30)5-6-18-24(22)28(36)21-13(29)3-2-4-17(21)37-18/h2-9,31-33,35-36H,1H3
InChI Key WLIKTAAWSFUHIZ-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C28H16O9
Molecular Weight 496.40 g/mol
Exact Mass 496.07943208 g/mol
Topological Polar Surface Area (TPSA) 162.00 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.70
H-Bond Acceptor 9
H-Bond Donor 5
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 9-Hydroxy-8-(1,3,8,10-tetrahydroxy-6-methyl-9-oxoanthracen-2-ylidene)xanthene-1,7-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9844 98.44%
Caco-2 - 0.8301 83.01%
Blood Brain Barrier - 0.7879 78.79%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.7909 79.09%
OATP2B1 inhibitior + 0.5771 57.71%
OATP1B1 inhibitior + 0.8878 88.78%
OATP1B3 inhibitior + 0.9363 93.63%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.6892 68.92%
P-glycoprotein inhibitior - 0.6028 60.28%
P-glycoprotein substrate - 0.7381 73.81%
CYP3A4 substrate + 0.5973 59.73%
CYP2C9 substrate - 0.6107 61.07%
CYP2D6 substrate - 0.8689 86.89%
CYP3A4 inhibition + 0.5830 58.30%
CYP2C9 inhibition + 0.9455 94.55%
CYP2C19 inhibition + 0.8052 80.52%
CYP2D6 inhibition - 0.8767 87.67%
CYP1A2 inhibition + 0.8384 83.84%
CYP2C8 inhibition + 0.5156 51.56%
CYP inhibitory promiscuity + 0.9181 91.81%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.4577 45.77%
Eye corrosion - 0.9910 99.10%
Eye irritation - 0.7100 71.00%
Skin irritation - 0.5681 56.81%
Skin corrosion - 0.9086 90.86%
Ames mutagenesis + 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4565 45.65%
Micronuclear + 0.9000 90.00%
Hepatotoxicity + 0.7125 71.25%
skin sensitisation - 0.7909 79.09%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity + 0.5515 55.15%
Acute Oral Toxicity (c) III 0.3959 39.59%
Estrogen receptor binding + 0.8423 84.23%
Androgen receptor binding + 0.7702 77.02%
Thyroid receptor binding - 0.5995 59.95%
Glucocorticoid receptor binding + 0.6876 68.76%
Aromatase binding - 0.5164 51.64%
PPAR gamma + 0.7551 75.51%
Honey bee toxicity - 0.8926 89.26%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.9870 98.70%

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
CHEMBL2581 P07339 Cathepsin D 98.65% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.11% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.75% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 95.99% 99.23%
CHEMBL3401 O75469 Pregnane X receptor 95.98% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 95.44% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.67% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.69% 86.33%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 88.20% 96.21%
CHEMBL1951 P21397 Monoamine oxidase A 87.70% 91.49%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 86.85% 93.65%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 82.59% 99.15%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.21% 93.56%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 82.15% 96.67%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.18% 90.71%
CHEMBL3192 Q9BY41 Histone deacetylase 8 80.99% 93.99%

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 136747556
LOTUS LTS0237091
wikiData Q104398606