Naphthacemycin A4

Details

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Internal ID 774ad4d3-caae-4a0f-aa8d-b63afcb59a73
Taxonomy Benzenoids > Naphthacenes > Tetracenequinones
IUPAC Name 10-chloro-2,4-dihydroxy-7-(4-hydroxy-2-methoxy-6-methylphenyl)-9-methoxy-12,12-dimethyltetracene-5,6,11-trione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C29H23ClO8/c1-11-6-12(31)9-17(37-4)19(11)14-10-18(38-5)25(30)22-20(14)26(34)23-24(28(22)36)29(2,3)15-7-13(32)8-16(33)21(15)27(23)35/h6-10,31-33H,1-5H3
InChI Key SIHMTOJVROFUNY-UHFFFAOYSA-N
Popularity 3 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 A4

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 + 0.5682 56.82%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.8645 86.45%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8610 86.10%
OATP1B3 inhibitior + 0.8580 85.80%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.9027 90.27%
P-glycoprotein inhibitior + 0.6871 68.71%
P-glycoprotein substrate - 0.7579 75.79%
CYP3A4 substrate + 0.6602 66.02%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8446 84.46%
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 + 0.7547 75.47%
CYP inhibitory promiscuity + 0.8222 82.22%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8020 80.20%
Carcinogenicity (trinary) Danger 0.5152 51.52%
Eye corrosion - 0.9919 99.19%
Eye irritation - 0.7251 72.51%
Skin irritation - 0.7211 72.11%
Skin corrosion - 0.9291 92.91%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6885 68.85%
Micronuclear + 0.5400 54.00%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation - 0.7775 77.75%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity + 0.7697 76.97%
Acute Oral Toxicity (c) III 0.5533 55.33%
Estrogen receptor binding + 0.8824 88.24%
Androgen receptor binding + 0.6474 64.74%
Thyroid receptor binding + 0.6601 66.01%
Glucocorticoid receptor binding + 0.7563 75.63%
Aromatase binding + 0.6623 66.23%
PPAR gamma + 0.7971 79.71%
Honey bee toxicity - 0.8008 80.08%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.6100 61.00%
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 98.53% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.74% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 93.07% 94.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.83% 86.33%
CHEMBL3194 P02766 Transthyretin 91.14% 90.71%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.70% 94.00%
CHEMBL4208 P20618 Proteasome component C5 89.89% 90.00%
CHEMBL1929 P47989 Xanthine dehydrogenase 89.67% 96.12%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 88.50% 96.38%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 88.07% 94.42%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 87.12% 99.15%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.59% 96.95%
CHEMBL2581 P07339 Cathepsin D 85.82% 98.95%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 85.74% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 85.22% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.88% 94.45%
CHEMBL241 Q14432 Phosphodiesterase 3A 82.58% 92.94%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 82.34% 93.03%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 82.33% 96.21%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 82.11% 91.07%
CHEMBL3492 P49721 Proteasome Macropain subunit 81.77% 90.24%
CHEMBL2535 P11166 Glucose transporter 81.59% 98.75%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.97% 96.09%
CHEMBL1951 P21397 Monoamine oxidase A 80.61% 91.49%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.44% 96.00%

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 25206202
LOTUS LTS0028646
wikiData Q104197326