Isojacareubin

Details

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Internal ID a422cd24-cee7-41e6-9b74-8133e9584e7a
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > Pyranoxanthones
IUPAC Name 6,10,11-trihydroxy-3,3-dimethylpyrano[2,3-c]xanthen-7-one
SMILES (Canonical) CC1(C=CC2=C(O1)C=C(C3=C2OC4=C(C3=O)C=CC(=C4O)O)O)C
SMILES (Isomeric) CC1(C=CC2=C(O1)C=C(C3=C2OC4=C(C3=O)C=CC(=C4O)O)O)C
InChI InChI=1S/C18H14O6/c1-18(2)6-5-8-12(24-18)7-11(20)13-14(21)9-3-4-10(19)15(22)17(9)23-16(8)13/h3-7,19-20,22H,1-2H3
InChI Key FSTNFJKGRSHPBO-UHFFFAOYSA-N
Popularity 7 references in papers

Physical and Chemical Properties

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Molecular Formula C18H14O6
Molecular Weight 326.30 g/mol
Exact Mass 326.07903816 g/mol
Topological Polar Surface Area (TPSA) 96.20 Ų
XlogP 3.40
Atomic LogP (AlogP) 3.25
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 0

Synonyms

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50597-93-8
6,10,11-trihydroxy-3,3-dimethylpyrano[2,3-c]xanthen-7-one
DTXSID901045703
AKOS032949139

2D Structure

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2D Structure of Isojacareubin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9684 96.84%
Caco-2 - 0.6588 65.88%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.7763 77.63%
OATP2B1 inhibitior - 0.5605 56.05%
OATP1B1 inhibitior + 0.9209 92.09%
OATP1B3 inhibitior + 0.9898 98.98%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.5833 58.33%
P-glycoprotein inhibitior - 0.6179 61.79%
P-glycoprotein substrate - 0.6595 65.95%
CYP3A4 substrate + 0.5618 56.18%
CYP2C9 substrate - 0.6270 62.70%
CYP2D6 substrate - 0.8433 84.33%
CYP3A4 inhibition - 0.6037 60.37%
CYP2C9 inhibition - 0.5694 56.94%
CYP2C19 inhibition - 0.5540 55.40%
CYP2D6 inhibition - 0.8144 81.44%
CYP1A2 inhibition + 0.5966 59.66%
CYP2C8 inhibition - 0.6072 60.72%
CYP inhibitory promiscuity - 0.5948 59.48%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5790 57.90%
Eye corrosion - 0.9894 98.94%
Eye irritation + 0.8218 82.18%
Skin irritation - 0.6470 64.70%
Skin corrosion - 0.8850 88.50%
Ames mutagenesis + 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7526 75.26%
Micronuclear + 0.7400 74.00%
Hepatotoxicity + 0.6408 64.08%
skin sensitisation - 0.6517 65.17%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.7169 71.69%
Acute Oral Toxicity (c) III 0.6702 67.02%
Estrogen receptor binding + 0.8846 88.46%
Androgen receptor binding + 0.7790 77.90%
Thyroid receptor binding + 0.7509 75.09%
Glucocorticoid receptor binding + 0.9620 96.20%
Aromatase binding + 0.8084 80.84%
PPAR gamma + 0.8650 86.50%
Honey bee toxicity - 0.8849 88.49%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9749 97.49%

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 99.67% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.55% 94.45%
CHEMBL1951 P21397 Monoamine oxidase A 97.24% 91.49%
CHEMBL1806 P11388 DNA topoisomerase II alpha 95.04% 89.00%
CHEMBL2581 P07339 Cathepsin D 93.84% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.79% 95.56%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 91.36% 85.30%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.78% 99.15%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.89% 94.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.79% 93.99%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 85.31% 93.65%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.37% 99.23%
CHEMBL3401 O75469 Pregnane X receptor 83.37% 94.73%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 83.12% 94.42%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.35% 86.33%

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.
Garcinia xipshuanbannaensis
Hypericum japonicum
Hypericum roeperianum

Cross-Links

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PubChem 9996463
NPASS NPC275122
LOTUS LTS0275949
wikiData Q105000861