2-[(1R,5R,10R,11R,13S)-5,11-dimethyl-6-oxo-2,4,9,12-tetraoxatricyclo[8.4.0.03,8]tetradecan-13-yl]-1,6,10-trihydroxy-8-methyltetracene-5,12-dione

Details

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Internal ID 9f34d79a-a10e-487e-97fe-e026fad53275
Taxonomy Benzenoids > Naphthacenes > Tetracenequinones
IUPAC Name 2-[(1R,5R,10R,11R,13S)-5,11-dimethyl-6-oxo-2,4,9,12-tetraoxatricyclo[8.4.0.03,8]tetradecan-13-yl]-1,6,10-trihydroxy-8-methyltetracene-5,12-dione
SMILES (Canonical) CC1C2C(CC(O1)C3=C(C4=C(C=C3)C(=O)C5=C(C4=O)C=C6C(=CC(=CC6=C5O)C)O)O)OC7C(O2)CC(=O)C(O7)C
SMILES (Isomeric) C[C@@H]1[C@@H]2[C@@H](C[C@H](O1)C3=C(C4=C(C=C3)C(=O)C5=C(C4=O)C=C6C(=CC(=CC6=C5O)C)O)O)OC7C(O2)CC(=O)[C@H](O7)C
InChI InChI=1S/C31H28O10/c1-11-6-17-16(20(33)7-11)8-18-25(28(17)36)27(35)15-5-4-14(26(34)24(15)29(18)37)21-10-22-30(13(3)38-21)40-23-9-19(32)12(2)39-31(23)41-22/h4-8,12-13,21-23,30-31,33-34,36H,9-10H2,1-3H3/t12-,13-,21+,22-,23?,30-,31?/m1/s1
InChI Key FNLPBRGKEZDCNF-MEAGLVDUSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C31H28O10
Molecular Weight 560.50 g/mol
Exact Mass 560.16824709 g/mol
Topological Polar Surface Area (TPSA) 149.00 Ų
XlogP 4.40
Atomic LogP (AlogP) 3.75
H-Bond Acceptor 10
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-[(1R,5R,10R,11R,13S)-5,11-dimethyl-6-oxo-2,4,9,12-tetraoxatricyclo[8.4.0.03,8]tetradecan-13-yl]-1,6,10-trihydroxy-8-methyltetracene-5,12-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8910 89.10%
Caco-2 - 0.8283 82.83%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.7665 76.65%
OATP2B1 inhibitior - 0.5721 57.21%
OATP1B1 inhibitior + 0.8448 84.48%
OATP1B3 inhibitior + 0.8626 86.26%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.9320 93.20%
P-glycoprotein inhibitior + 0.7350 73.50%
P-glycoprotein substrate + 0.5645 56.45%
CYP3A4 substrate + 0.6866 68.66%
CYP2C9 substrate - 0.7962 79.62%
CYP2D6 substrate - 0.8440 84.40%
CYP3A4 inhibition - 0.9541 95.41%
CYP2C9 inhibition - 0.6482 64.82%
CYP2C19 inhibition - 0.9317 93.17%
CYP2D6 inhibition - 0.9458 94.58%
CYP1A2 inhibition - 0.7674 76.74%
CYP2C8 inhibition + 0.5737 57.37%
CYP inhibitory promiscuity - 0.8736 87.36%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.5852 58.52%
Eye corrosion - 0.9934 99.34%
Eye irritation - 0.9289 92.89%
Skin irritation - 0.7191 71.91%
Skin corrosion - 0.9343 93.43%
Ames mutagenesis + 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7237 72.37%
Micronuclear + 0.5600 56.00%
Hepatotoxicity + 0.7000 70.00%
skin sensitisation - 0.9141 91.41%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.8000 80.00%
Nephrotoxicity - 0.5878 58.78%
Acute Oral Toxicity (c) I 0.3605 36.05%
Estrogen receptor binding + 0.8411 84.11%
Androgen receptor binding + 0.7018 70.18%
Thyroid receptor binding - 0.5090 50.90%
Glucocorticoid receptor binding + 0.8140 81.40%
Aromatase binding + 0.6316 63.16%
PPAR gamma + 0.7818 78.18%
Honey bee toxicity - 0.8097 80.97%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9709 97.09%

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 99.44% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 99.43% 91.49%
CHEMBL1806 P11388 DNA topoisomerase II alpha 97.87% 89.00%
CHEMBL2581 P07339 Cathepsin D 97.50% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.46% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.95% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 92.24% 99.23%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 91.45% 90.71%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.91% 95.89%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.52% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.87% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.73% 100.00%
CHEMBL3401 O75469 Pregnane X receptor 85.33% 94.73%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 85.06% 96.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.15% 99.15%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 81.99% 93.03%
CHEMBL340 P08684 Cytochrome P450 3A4 81.66% 91.19%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.15% 94.00%
CHEMBL2056 P21728 Dopamine D1 receptor 81.12% 91.00%

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 163108668
LOTUS LTS0000053
wikiData Q104998354