CID 139587060

Details

Top
Internal ID 9171279b-5138-470f-82f2-c6cef6469d8d
Taxonomy Phenylpropanoids and polyketides > Anthracyclines
IUPAC Name (9R)-7-[4-(dimethylamino)-5-hydroxy-6-methyloxan-2-yl]oxy-9-ethyl-4,6,9,10-tetrahydroxy-8,10-dihydro-7H-tetracene-5,12-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C28H33NO9/c1-5-28(36)11-18(38-19-10-16(29(3)4)23(31)12(2)37-19)21-15(27(28)35)9-14-22(26(21)34)25(33)20-13(24(14)32)7-6-8-17(20)30/h6-9,12,16,18-19,23,27,30-31,34-36H,5,10-11H2,1-4H3/t12?,16?,18?,19?,23?,27?,28-/m1/s1
InChI Key IWALHFMBCZSCRZ-URLVKIDWSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C28H33NO9
Molecular Weight 527.60 g/mol
Exact Mass 527.21553163 g/mol
Topological Polar Surface Area (TPSA) 157.00 Ų
XlogP 1.80
Atomic LogP (AlogP) 1.94
H-Bond Acceptor 10
H-Bond Donor 5
Rotatable Bonds 4

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of CID 139587060

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8250 82.50%
Caco-2 - 0.8154 81.54%
Blood Brain Barrier - 0.9500 95.00%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.3702 37.02%
OATP2B1 inhibitior - 0.8581 85.81%
OATP1B1 inhibitior + 0.9141 91.41%
OATP1B3 inhibitior + 0.9491 94.91%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.6650 66.50%
P-glycoprotein inhibitior - 0.4411 44.11%
P-glycoprotein substrate + 0.7978 79.78%
CYP3A4 substrate + 0.7087 70.87%
CYP2C9 substrate - 0.8370 83.70%
CYP2D6 substrate - 0.7744 77.44%
CYP3A4 inhibition - 0.8319 83.19%
CYP2C9 inhibition - 0.8620 86.20%
CYP2C19 inhibition - 0.8720 87.20%
CYP2D6 inhibition - 0.8696 86.96%
CYP1A2 inhibition + 0.5252 52.52%
CYP2C8 inhibition - 0.7041 70.41%
CYP inhibitory promiscuity - 0.9219 92.19%
UGT catelyzed - 0.8000 80.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6005 60.05%
Eye corrosion - 0.9893 98.93%
Eye irritation - 0.9087 90.87%
Skin irritation - 0.8019 80.19%
Skin corrosion - 0.9360 93.60%
Ames mutagenesis + 0.9100 91.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6466 64.66%
Micronuclear + 0.6800 68.00%
Hepatotoxicity + 0.7500 75.00%
skin sensitisation - 0.8996 89.96%
Respiratory toxicity + 0.9111 91.11%
Reproductive toxicity + 0.9556 95.56%
Mitochondrial toxicity + 0.9500 95.00%
Nephrotoxicity - 0.8309 83.09%
Acute Oral Toxicity (c) II 0.4607 46.07%
Estrogen receptor binding + 0.8180 81.80%
Androgen receptor binding + 0.7385 73.85%
Thyroid receptor binding + 0.6221 62.21%
Glucocorticoid receptor binding + 0.7967 79.67%
Aromatase binding + 0.7291 72.91%
PPAR gamma + 0.7978 79.78%
Honey bee toxicity - 0.7759 77.59%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9388 93.88%

Targets

Top

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
CHEMBL2581 P07339 Cathepsin D 99.39% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.69% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 98.47% 89.00%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 97.88% 96.38%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.38% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.87% 95.56%
CHEMBL226 P30542 Adenosine A1 receptor 95.77% 95.93%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.51% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.56% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.19% 99.23%
CHEMBL5608 Q16288 NT-3 growth factor receptor 89.67% 95.89%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 88.71% 96.21%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.38% 94.00%
CHEMBL3004 P33527 Multidrug resistance-associated protein 1 87.35% 96.37%
CHEMBL3401 O75469 Pregnane X receptor 86.69% 94.73%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 86.25% 85.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.75% 100.00%
CHEMBL4208 P20618 Proteasome component C5 84.54% 90.00%
CHEMBL1951 P21397 Monoamine oxidase A 83.50% 91.49%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 83.43% 96.67%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 83.12% 97.50%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 82.91% 93.03%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 82.62% 99.15%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.05% 92.94%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.80% 92.62%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.19% 97.25%

Plants that contains it

Top
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

Top
PubChem 139587060
LOTUS LTS0153876
wikiData Q77520572