Naphthacemycin A6

Details

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Internal ID 02389c7f-e98f-45e6-bdd3-cff6f0582929
Taxonomy Benzenoids > Naphthacenes > Tetracenequinones
IUPAC Name 7-(3-chloro-4-hydroxy-2-methoxy-6-methylphenyl)-2,4-dihydroxy-9-methoxy-12,12-dimethyltetracene-5,6,11-trione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C29H23ClO8/c1-11-6-18(33)24(30)28(38-5)19(11)14-9-13(37-4)10-15-20(14)26(35)22-23(25(15)34)29(2,3)16-7-12(31)8-17(32)21(16)27(22)36/h6-10,31-33H,1-5H3
InChI Key CFIYQNFHRXLRDH-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C29H23ClO8
Molecular Weight 534.90 g/mol
Exact Mass 534.1081454 g/mol
Topological Polar Surface Area (TPSA) 130.00 Ų
XlogP 6.00
Atomic LogP (AlogP) 5.30
H-Bond Acceptor 8
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Naphthacemycin A6

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9948 99.48%
Caco-2 - 0.5842 58.42%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.8645 86.45%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8364 83.64%
OATP1B3 inhibitior + 0.8580 85.80%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.9783 97.83%
P-glycoprotein inhibitior + 0.6855 68.55%
P-glycoprotein substrate - 0.7908 79.08%
CYP3A4 substrate + 0.6647 66.47%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8433 84.33%
CYP3A4 inhibition - 0.7535 75.35%
CYP2C9 inhibition + 0.7262 72.62%
CYP2C19 inhibition + 0.6069 60.69%
CYP2D6 inhibition - 0.8285 82.85%
CYP1A2 inhibition - 0.5487 54.87%
CYP2C8 inhibition + 0.7347 73.47%
CYP inhibitory promiscuity + 0.8222 82.22%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8020 80.20%
Carcinogenicity (trinary) Danger 0.5152 51.52%
Eye corrosion - 0.9919 99.19%
Eye irritation - 0.7549 75.49%
Skin irritation - 0.7211 72.11%
Skin corrosion - 0.9291 92.91%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3922 39.22%
Micronuclear + 0.5400 54.00%
Hepatotoxicity + 0.5125 51.25%
skin sensitisation - 0.7775 77.75%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity + 0.6560 65.60%
Acute Oral Toxicity (c) III 0.5533 55.33%
Estrogen receptor binding + 0.8915 89.15%
Androgen receptor binding + 0.6711 67.11%
Thyroid receptor binding + 0.6729 67.29%
Glucocorticoid receptor binding + 0.7666 76.66%
Aromatase binding + 0.6653 66.53%
PPAR gamma + 0.8254 82.54%
Honey bee toxicity - 0.8588 85.88%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 1.0000 100.00%

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 98.80% 91.11%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 97.05% 99.15%
CHEMBL1929 P47989 Xanthine dehydrogenase 96.71% 96.12%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.01% 95.56%
CHEMBL4208 P20618 Proteasome component C5 93.92% 90.00%
CHEMBL1951 P21397 Monoamine oxidase A 93.85% 91.49%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.33% 94.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 90.13% 93.99%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.77% 94.45%
CHEMBL2581 P07339 Cathepsin D 89.43% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.34% 86.33%
CHEMBL3180 O00748 Carboxylesterase 2 88.75% 90.00%
CHEMBL3401 O75469 Pregnane X receptor 87.90% 94.73%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 87.23% 91.07%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 86.69% 93.40%
CHEMBL2056 P21728 Dopamine D1 receptor 85.54% 91.00%
CHEMBL1937 Q92769 Histone deacetylase 2 85.10% 94.75%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 84.81% 96.09%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 82.73% 94.42%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 82.70% 92.68%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.27% 96.09%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 82.14% 96.38%
CHEMBL3194 P02766 Transthyretin 81.51% 90.71%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.32% 96.95%
CHEMBL2535 P11166 Glucose transporter 80.65% 98.75%
CHEMBL3492 P49721 Proteasome Macropain subunit 80.30% 90.24%
CHEMBL1907 P15144 Aminopeptidase N 80.22% 93.31%

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 132571610
LOTUS LTS0192383
wikiData Q103817683