6"-cyano-6"-deoxy-TAN-1120

Details

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Internal ID ec4e9d59-68c0-43b3-bb52-48962ae43ac8
Taxonomy Phenylpropanoids and polyketides > Anthracyclines
IUPAC Name (6aS,8R,10S,10aS)-8-[[(1S,3S)-3-acetyl-3,5,12-trihydroxy-10-methoxy-6,11-dioxo-2,4-dihydro-1H-tetracen-1-yl]oxy]-2-(2-hydroxypropyl)-4,10-dimethyl-4,5,6,6a,7,8,10,10a-octahydropyrano[3,4-d][1,3,6]dioxazocine-5-carbonitrile
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C35H40N2O12/c1-14(38)9-24-46-15(2)21(13-36)37-20-10-25(47-16(3)34(20)49-24)48-23-12-35(44,17(4)39)11-19-27(23)33(43)29-28(31(19)41)30(40)18-7-6-8-22(45-5)26(18)32(29)42/h6-8,14-16,20-21,23-25,34,37-38,41,43-44H,9-12H2,1-5H3/t14?,15?,16-,20-,21?,23-,24?,25-,34+,35-/m0/s1
InChI Key XMDNHTUCEGYMFQ-UWWRACIZSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C35H40N2O12
Molecular Weight 680.70 g/mol
Exact Mass 680.25812472 g/mol
Topological Polar Surface Area (TPSA) 214.00 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.09
H-Bond Acceptor 14
H-Bond Donor 5
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6"-cyano-6"-deoxy-TAN-1120

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8572 85.72%
Caco-2 - 0.8603 86.03%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability - 0.8286 82.86%
Subcellular localzation Nucleus 0.4640 46.40%
OATP2B1 inhibitior - 0.5803 58.03%
OATP1B1 inhibitior + 0.8615 86.15%
OATP1B3 inhibitior + 0.9134 91.34%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8818 88.18%
BSEP inhibitior + 0.8814 88.14%
P-glycoprotein inhibitior + 0.7306 73.06%
P-glycoprotein substrate + 0.8865 88.65%
CYP3A4 substrate + 0.7205 72.05%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7937 79.37%
CYP3A4 inhibition - 0.9585 95.85%
CYP2C9 inhibition - 0.9127 91.27%
CYP2C19 inhibition - 0.9171 91.71%
CYP2D6 inhibition - 0.8780 87.80%
CYP1A2 inhibition - 0.6423 64.23%
CYP2C8 inhibition + 0.4560 45.60%
CYP inhibitory promiscuity - 0.8849 88.49%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5787 57.87%
Eye corrosion - 0.9898 98.98%
Eye irritation - 0.9263 92.63%
Skin irritation - 0.7936 79.36%
Skin corrosion - 0.9369 93.69%
Ames mutagenesis + 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5133 51.33%
Micronuclear + 0.6900 69.00%
Hepatotoxicity - 0.6750 67.50%
skin sensitisation - 0.8852 88.52%
Respiratory toxicity + 0.9000 90.00%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity + 0.5951 59.51%
Acute Oral Toxicity (c) III 0.4092 40.92%
Estrogen receptor binding + 0.8586 85.86%
Androgen receptor binding + 0.8272 82.72%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.8325 83.25%
Aromatase binding + 0.7800 78.00%
PPAR gamma + 0.8038 80.38%
Honey bee toxicity - 0.5925 59.25%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.8519 85.19%

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 99.64% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.88% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 98.28% 89.00%
CHEMBL2581 P07339 Cathepsin D 97.87% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.29% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 95.10% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.50% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.19% 85.14%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 94.03% 96.38%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.49% 94.45%
CHEMBL2535 P11166 Glucose transporter 93.20% 98.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 92.36% 99.23%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.53% 97.25%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 90.07% 92.88%
CHEMBL5608 Q16288 NT-3 growth factor receptor 89.97% 95.89%
CHEMBL3830 Q2M2I8 Adaptor-associated kinase 89.35% 83.10%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.39% 94.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 87.03% 95.50%
CHEMBL226 P30542 Adenosine A1 receptor 86.92% 95.93%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 86.12% 97.14%
CHEMBL340 P08684 Cytochrome P450 3A4 85.92% 91.19%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 85.44% 98.75%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.25% 96.00%
CHEMBL1744525 P43490 Nicotinamide phosphoribosyltransferase 84.13% 96.25%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.93% 99.17%
CHEMBL284 P27487 Dipeptidyl peptidase IV 83.58% 95.69%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.82% 100.00%
CHEMBL213 P08588 Beta-1 adrenergic receptor 81.62% 95.56%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.09% 96.95%

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 132543976
LOTUS LTS0158813
wikiData Q105330667