(13S)-8,19-dihydroxy-6,17-dimethoxy-14,14-dimethyl-3,15-dioxapentacyclo[11.6.1.02,11.04,9.016,20]icosa-1(20),2(11),4,6,8,16,18-heptaen-10-one

Details

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Internal ID 7ae5263b-b147-4eaf-958b-263a2239e92a
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name (13S)-8,19-dihydroxy-6,17-dimethoxy-14,14-dimethyl-3,15-dioxapentacyclo[11.6.1.02,11.04,9.016,20]icosa-1(20),2(11),4,6,8,16,18-heptaen-10-one
SMILES (Canonical) CC1(C2CC3=C(C4=C2C(=C(C=C4O)OC)O1)OC5=CC(=CC(=C5C3=O)O)OC)C
SMILES (Isomeric) CC1([C@H]2CC3=C(C4=C2C(=C(C=C4O)OC)O1)OC5=CC(=CC(=C5C3=O)O)OC)C
InChI InChI=1S/C22H20O7/c1-22(2)11-7-10-19(25)17-12(23)5-9(26-3)6-14(17)28-20(10)18-13(24)8-15(27-4)21(29-22)16(11)18/h5-6,8,11,23-24H,7H2,1-4H3/t11-/m0/s1
InChI Key VAAPHFWVXAMOLR-NSHDSACASA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H20O7
Molecular Weight 396.40 g/mol
Exact Mass 396.12090297 g/mol
Topological Polar Surface Area (TPSA) 94.40 Ų
XlogP 3.40
Atomic LogP (AlogP) 3.70
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (13S)-8,19-dihydroxy-6,17-dimethoxy-14,14-dimethyl-3,15-dioxapentacyclo[11.6.1.02,11.04,9.016,20]icosa-1(20),2(11),4,6,8,16,18-heptaen-10-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9864 98.64%
Caco-2 + 0.5994 59.94%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.7782 77.82%
OATP2B1 inhibitior - 0.7101 71.01%
OATP1B1 inhibitior + 0.8653 86.53%
OATP1B3 inhibitior + 0.9333 93.33%
MATE1 inhibitior - 0.7400 74.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.7042 70.42%
P-glycoprotein inhibitior + 0.6986 69.86%
P-glycoprotein substrate - 0.6324 63.24%
CYP3A4 substrate + 0.6566 65.66%
CYP2C9 substrate - 0.5598 55.98%
CYP2D6 substrate - 0.8049 80.49%
CYP3A4 inhibition - 0.7522 75.22%
CYP2C9 inhibition - 0.7493 74.93%
CYP2C19 inhibition + 0.5919 59.19%
CYP2D6 inhibition + 0.5000 50.00%
CYP1A2 inhibition + 0.5994 59.94%
CYP2C8 inhibition + 0.6875 68.75%
CYP inhibitory promiscuity + 0.5000 50.00%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.4642 46.42%
Eye corrosion - 0.9869 98.69%
Eye irritation + 0.5280 52.80%
Skin irritation - 0.7722 77.22%
Skin corrosion - 0.9619 96.19%
Ames mutagenesis + 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7106 71.06%
Micronuclear + 0.5900 59.00%
Hepatotoxicity - 0.8000 80.00%
skin sensitisation - 0.8381 83.81%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity - 0.5967 59.67%
Acute Oral Toxicity (c) III 0.6143 61.43%
Estrogen receptor binding + 0.8853 88.53%
Androgen receptor binding + 0.7631 76.31%
Thyroid receptor binding + 0.6521 65.21%
Glucocorticoid receptor binding + 0.8603 86.03%
Aromatase binding + 0.5779 57.79%
PPAR gamma + 0.8139 81.39%
Honey bee toxicity - 0.7706 77.06%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.6151 61.51%
Fish aquatic toxicity + 0.9218 92.18%

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 99.65% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.97% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.02% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.25% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.29% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.76% 89.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.55% 96.09%
CHEMBL4208 P20618 Proteasome component C5 89.33% 90.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.12% 97.09%
CHEMBL2581 P07339 Cathepsin D 88.42% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.84% 99.23%
CHEMBL241 Q14432 Phosphodiesterase 3A 86.21% 92.94%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.11% 95.89%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 85.86% 97.14%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.54% 99.15%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.57% 93.99%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.40% 92.62%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.12% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.54% 86.33%
CHEMBL340 P08684 Cytochrome P450 3A4 81.55% 91.19%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 81.22% 95.71%

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.
Artocarpus integer

Cross-Links

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PubChem 162967042
LOTUS LTS0010836
wikiData Q105282580