6,9-dihydroxy-2-methoxy-9-methyl-7-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-8,10-dihydro-7H-tetracene-5,12-dione

Details

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Internal ID 59be6c65-b9d7-4082-9f2b-eff981970bf0
Taxonomy Phenylpropanoids and polyketides > Anthracyclines
IUPAC Name 6,9-dihydroxy-2-methoxy-9-methyl-7-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-8,10-dihydro-7H-tetracene-5,12-dione
SMILES (Canonical) CC1C(C(C(C(O1)OC2CC(CC3=CC4=C(C(=C23)O)C(=O)C5=C(C4=O)C=C(C=C5)OC)(C)O)O)O)O
SMILES (Isomeric) CC1C(C(C(C(O1)OC2CC(CC3=CC4=C(C(=C23)O)C(=O)C5=C(C4=O)C=C(C=C5)OC)(C)O)O)O)O
InChI InChI=1S/C26H28O10/c1-10-19(27)23(31)24(32)25(35-10)36-16-9-26(2,33)8-11-6-15-18(22(30)17(11)16)21(29)13-5-4-12(34-3)7-14(13)20(15)28/h4-7,10,16,19,23-25,27,30-33H,8-9H2,1-3H3
InChI Key BLESPUUMZLZYHA-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C26H28O10
Molecular Weight 500.50 g/mol
Exact Mass 500.16824709 g/mol
Topological Polar Surface Area (TPSA) 163.00 Ų
XlogP 1.00
Atomic LogP (AlogP) 0.76
H-Bond Acceptor 10
H-Bond Donor 5
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6,9-dihydroxy-2-methoxy-9-methyl-7-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-8,10-dihydro-7H-tetracene-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 + 0.6881 68.81%
Caco-2 - 0.7447 74.47%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.7429 74.29%
Subcellular localzation Mitochondria 0.4876 48.76%
OATP2B1 inhibitior - 0.8547 85.47%
OATP1B1 inhibitior + 0.8796 87.96%
OATP1B3 inhibitior + 0.9603 96.03%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.8417 84.17%
P-glycoprotein inhibitior - 0.5356 53.56%
P-glycoprotein substrate + 0.5354 53.54%
CYP3A4 substrate + 0.6857 68.57%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8418 84.18%
CYP3A4 inhibition - 0.8185 81.85%
CYP2C9 inhibition - 0.9760 97.60%
CYP2C19 inhibition - 0.9552 95.52%
CYP2D6 inhibition - 0.8659 86.59%
CYP1A2 inhibition - 0.5663 56.63%
CYP2C8 inhibition - 0.6780 67.80%
CYP inhibitory promiscuity - 0.9668 96.68%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6098 60.98%
Eye corrosion - 0.9904 99.04%
Eye irritation - 0.9021 90.21%
Skin irritation - 0.7669 76.69%
Skin corrosion - 0.9275 92.75%
Ames mutagenesis + 0.7263 72.63%
Human Ether-a-go-go-Related Gene inhibition + 0.6654 66.54%
Micronuclear + 0.5400 54.00%
Hepatotoxicity - 0.6843 68.43%
skin sensitisation - 0.9005 90.05%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity - 0.6772 67.72%
Acute Oral Toxicity (c) III 0.4259 42.59%
Estrogen receptor binding + 0.7816 78.16%
Androgen receptor binding + 0.6230 62.30%
Thyroid receptor binding + 0.5278 52.78%
Glucocorticoid receptor binding + 0.6892 68.92%
Aromatase binding + 0.6602 66.02%
PPAR gamma + 0.7757 77.57%
Honey bee toxicity - 0.7722 77.22%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9519 95.19%

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 99.87% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 99.65% 91.49%
CHEMBL2581 P07339 Cathepsin D 96.57% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 95.99% 89.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.60% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.56% 95.56%
CHEMBL4208 P20618 Proteasome component C5 94.68% 90.00%
CHEMBL226 P30542 Adenosine A1 receptor 92.83% 95.93%
CHEMBL5608 Q16288 NT-3 growth factor receptor 92.65% 95.89%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.61% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.33% 94.00%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 90.13% 96.21%
CHEMBL241 Q14432 Phosphodiesterase 3A 89.62% 92.94%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.25% 97.09%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 88.45% 99.15%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 88.16% 91.07%
CHEMBL1907 P15144 Aminopeptidase N 87.68% 93.31%
CHEMBL2179 P04062 Beta-glucocerebrosidase 86.64% 85.31%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 85.92% 97.14%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 85.59% 95.89%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.82% 90.71%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 82.37% 100.00%
CHEMBL4940 P07195 L-lactate dehydrogenase B chain 82.02% 95.53%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 81.78% 96.77%
CHEMBL3714130 P46095 G-protein coupled receptor 6 81.55% 97.36%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.50% 99.23%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 80.88% 96.67%

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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Cross-Links

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PubChem 162882114
LOTUS LTS0245199
wikiData Q105300513