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

Details

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Internal ID 451ac8d4-2003-4473-b729-bfca6a647678
Taxonomy Phenylpropanoids and polyketides > Anthracyclines
IUPAC Name (7S,9R)-4,6,9-trihydroxy-7-(4-hydroxy-3,5-dimethoxy-6-methyloxan-2-yl)oxy-2-methoxy-9-methyl-8,10-dihydro-7H-tetracene-5,12-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C28H32O11/c1-11-25(36-4)24(33)26(37-5)27(38-11)39-17-10-28(2,34)9-12-6-14-20(22(31)18(12)17)23(32)19-15(21(14)30)7-13(35-3)8-16(19)29/h6-8,11,17,24-27,29,31,33-34H,9-10H2,1-5H3/t11?,17-,24?,25?,26?,27?,28+/m0/s1
InChI Key RPBBLWPRKUUHJZ-JKXJIWQBSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C28H32O11
Molecular Weight 544.50 g/mol
Exact Mass 544.19446183 g/mol
Topological Polar Surface Area (TPSA) 161.00 Ų
XlogP 1.80
Atomic LogP (AlogP) 1.77
H-Bond Acceptor 11
H-Bond Donor 4
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (7S,9R)-4,6,9-trihydroxy-7-(4-hydroxy-3,5-dimethoxy-6-methyloxan-2-yl)oxy-2-methoxy-9-methyl-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 + 0.8952 89.52%
Caco-2 - 0.7426 74.26%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.7857 78.57%
Subcellular localzation Mitochondria 0.6271 62.71%
OATP2B1 inhibitior - 0.8628 86.28%
OATP1B1 inhibitior + 0.8638 86.38%
OATP1B3 inhibitior + 0.9460 94.60%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.8633 86.33%
P-glycoprotein inhibitior + 0.6642 66.42%
P-glycoprotein substrate + 0.5233 52.33%
CYP3A4 substrate + 0.6911 69.11%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8394 83.94%
CYP3A4 inhibition - 0.8737 87.37%
CYP2C9 inhibition - 0.9569 95.69%
CYP2C19 inhibition - 0.9421 94.21%
CYP2D6 inhibition - 0.8673 86.73%
CYP1A2 inhibition + 0.5532 55.32%
CYP2C8 inhibition - 0.6114 61.14%
CYP inhibitory promiscuity - 0.9513 95.13%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5770 57.70%
Eye corrosion - 0.9911 99.11%
Eye irritation - 0.8892 88.92%
Skin irritation - 0.7772 77.72%
Skin corrosion - 0.9435 94.35%
Ames mutagenesis + 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5483 54.83%
Micronuclear + 0.5500 55.00%
Hepatotoxicity - 0.5823 58.23%
skin sensitisation - 0.9174 91.74%
Respiratory toxicity + 0.8222 82.22%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity + 0.4817 48.17%
Acute Oral Toxicity (c) I 0.4028 40.28%
Estrogen receptor binding + 0.7581 75.81%
Androgen receptor binding + 0.6426 64.26%
Thyroid receptor binding + 0.5354 53.54%
Glucocorticoid receptor binding + 0.7470 74.70%
Aromatase binding + 0.7162 71.62%
PPAR gamma + 0.7765 77.65%
Honey bee toxicity - 0.7485 74.85%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9554 95.54%

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 99.77% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.69% 96.09%
CHEMBL1951 P21397 Monoamine oxidase A 96.59% 91.49%
CHEMBL1806 P11388 DNA topoisomerase II alpha 95.86% 89.00%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 95.81% 96.21%
CHEMBL241 Q14432 Phosphodiesterase 3A 95.68% 92.94%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.58% 85.14%
CHEMBL2581 P07339 Cathepsin D 94.34% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.24% 95.56%
CHEMBL4208 P20618 Proteasome component C5 94.20% 90.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 92.95% 91.07%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 92.73% 96.38%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.69% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 92.37% 99.15%
CHEMBL226 P30542 Adenosine A1 receptor 92.17% 95.93%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 92.14% 99.23%
CHEMBL4940 P07195 L-lactate dehydrogenase B chain 89.93% 95.53%
CHEMBL5608 Q16288 NT-3 growth factor receptor 89.29% 95.89%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 87.82% 95.89%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.60% 86.33%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 87.56% 97.14%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.17% 97.09%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 85.71% 96.77%
CHEMBL3714130 P46095 G-protein coupled receptor 6 83.97% 97.36%
CHEMBL2056 P21728 Dopamine D1 receptor 81.35% 91.00%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 80.94% 82.67%
CHEMBL2179 P04062 Beta-glucocerebrosidase 80.91% 85.31%
CHEMBL340 P08684 Cytochrome P450 3A4 80.69% 91.19%

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.
There are no matching plants.

Cross-Links

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PubChem 139587668
LOTUS LTS0014721
wikiData Q77571496