methyl (1R,2R,4S)-4-(4-amino-5-hydroxy-6-methyloxan-2-yl)oxy-2-ethyl-2,5,7-trihydroxy-6,11-dioxo-3,4-dihydro-1H-tetracene-1-carboxylate

Details

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Internal ID c9d85521-6f9f-46f3-8c3a-199c42ac9454
Taxonomy Phenylpropanoids and polyketides > Anthracyclines
IUPAC Name methyl (1R,2R,4S)-4-(4-amino-5-hydroxy-6-methyloxan-2-yl)oxy-2-ethyl-2,5,7-trihydroxy-6,11-dioxo-3,4-dihydro-1H-tetracene-1-carboxylate
SMILES (Canonical) CCC1(CC(C2=C(C3=C(C=C2C1C(=O)OC)C(=O)C4=C(C3=O)C(=CC=C4)O)O)OC5CC(C(C(O5)C)O)N)O
SMILES (Isomeric) CC[C@]1(C[C@@H](C2=C(C3=C(C=C2[C@H]1C(=O)OC)C(=O)C4=C(C3=O)C(=CC=C4)O)O)OC5CC(C(C(O5)C)O)N)O
InChI InChI=1S/C28H31NO10/c1-4-28(36)10-17(39-18-9-15(29)23(31)11(2)38-18)20-13(22(28)27(35)37-3)8-14-21(26(20)34)25(33)19-12(24(14)32)6-5-7-16(19)30/h5-8,11,15,17-18,22-23,30-31,34,36H,4,9-10,29H2,1-3H3/t11?,15?,17-,18?,22-,23?,28+/m0/s1
InChI Key MCWLCHNOMBKWNJ-CUNXHAHNSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C28H31NO10
Molecular Weight 541.50 g/mol
Exact Mass 541.19479619 g/mol
Topological Polar Surface Area (TPSA) 186.00 Ų
XlogP 2.10
Atomic LogP (AlogP) 1.56
H-Bond Acceptor 11
H-Bond Donor 5
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of methyl (1R,2R,4S)-4-(4-amino-5-hydroxy-6-methyloxan-2-yl)oxy-2-ethyl-2,5,7-trihydroxy-6,11-dioxo-3,4-dihydro-1H-tetracene-1-carboxylate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7865 78.65%
Caco-2 - 0.8014 80.14%
Blood Brain Barrier - 0.9750 97.50%
Human oral bioavailability - 0.7429 74.29%
Subcellular localzation Nucleus 0.7049 70.49%
OATP2B1 inhibitior - 0.7293 72.93%
OATP1B1 inhibitior + 0.9167 91.67%
OATP1B3 inhibitior + 0.9402 94.02%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.7436 74.36%
P-glycoprotein inhibitior - 0.4841 48.41%
P-glycoprotein substrate + 0.8648 86.48%
CYP3A4 substrate + 0.7000 70.00%
CYP2C9 substrate - 0.8437 84.37%
CYP2D6 substrate - 0.8509 85.09%
CYP3A4 inhibition - 0.8577 85.77%
CYP2C9 inhibition - 0.9139 91.39%
CYP2C19 inhibition - 0.9261 92.61%
CYP2D6 inhibition - 0.9243 92.43%
CYP1A2 inhibition + 0.7486 74.86%
CYP2C8 inhibition - 0.5846 58.46%
CYP inhibitory promiscuity - 0.8922 89.22%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.5916 59.16%
Eye corrosion - 0.9906 99.06%
Eye irritation - 0.9312 93.12%
Skin irritation - 0.8017 80.17%
Skin corrosion - 0.9328 93.28%
Ames mutagenesis + 0.9900 99.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6520 65.20%
Micronuclear + 0.7500 75.00%
Hepatotoxicity - 0.5198 51.98%
skin sensitisation - 0.8844 88.44%
Respiratory toxicity + 0.9889 98.89%
Reproductive toxicity + 0.9889 98.89%
Mitochondrial toxicity + 0.9625 96.25%
Nephrotoxicity - 0.6903 69.03%
Acute Oral Toxicity (c) II 0.6351 63.51%
Estrogen receptor binding + 0.8796 87.96%
Androgen receptor binding + 0.8012 80.12%
Thyroid receptor binding + 0.5651 56.51%
Glucocorticoid receptor binding + 0.8907 89.07%
Aromatase binding + 0.7582 75.82%
PPAR gamma + 0.8301 83.01%
Honey bee toxicity - 0.7506 75.06%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.8851 88.51%

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 99.66% 91.11%
CHEMBL2581 P07339 Cathepsin D 98.36% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.65% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 97.09% 89.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 96.64% 97.09%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 96.47% 96.38%
CHEMBL226 P30542 Adenosine A1 receptor 96.46% 95.93%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.51% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.04% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.41% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.73% 99.23%
CHEMBL5608 Q16288 NT-3 growth factor receptor 89.61% 95.89%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.49% 94.00%
CHEMBL4208 P20618 Proteasome component C5 87.74% 90.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.69% 94.45%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 85.79% 92.88%
CHEMBL340 P08684 Cytochrome P450 3A4 84.91% 91.19%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 84.82% 90.71%
CHEMBL2535 P11166 Glucose transporter 83.86% 98.75%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.19% 99.17%
CHEMBL3830 Q2M2I8 Adaptor-associated kinase 82.87% 83.10%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.97% 100.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.72% 92.94%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.71% 92.62%
CHEMBL3401 O75469 Pregnane X receptor 80.37% 94.73%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 80.37% 99.15%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.12% 91.07%

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 139584274
LOTUS LTS0061029
wikiData Q77309986