5-(6-Amino-2-hydroxy-3-methyl-5,8-dioxonaphthalen-1-yl)-2,4-dimethyl-5-oxopent-3-enoic acid

Details

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Internal ID a4f1efe3-d415-46df-95b0-6d6f479487ed
Taxonomy Benzenoids > Naphthalenes > Naphthoquinones
IUPAC Name 5-(6-amino-2-hydroxy-3-methyl-5,8-dioxonaphthalen-1-yl)-2,4-dimethyl-5-oxopent-3-enoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H17NO6/c1-7(4-9(3)18(24)25)15(21)14-13-10(5-8(2)16(14)22)17(23)11(19)6-12(13)20/h4-6,9,22H,19H2,1-3H3,(H,24,25)
InChI Key VRLJPBYCMKKPQP-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H17NO6
Molecular Weight 343.30 g/mol
Exact Mass 343.10558726 g/mol
Topological Polar Surface Area (TPSA) 135.00 Ų
XlogP 2.10
Atomic LogP (AlogP) 1.77
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-(6-Amino-2-hydroxy-3-methyl-5,8-dioxonaphthalen-1-yl)-2,4-dimethyl-5-oxopent-3-enoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9910 99.10%
Caco-2 - 0.5582 55.82%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.6375 63.75%
OATP2B1 inhibitior - 0.5676 56.76%
OATP1B1 inhibitior + 0.8693 86.93%
OATP1B3 inhibitior + 0.9382 93.82%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.6845 68.45%
P-glycoprotein inhibitior - 0.9001 90.01%
P-glycoprotein substrate - 0.7385 73.85%
CYP3A4 substrate + 0.5282 52.82%
CYP2C9 substrate - 0.5860 58.60%
CYP2D6 substrate - 0.8793 87.93%
CYP3A4 inhibition - 0.7630 76.30%
CYP2C9 inhibition - 0.7414 74.14%
CYP2C19 inhibition - 0.6620 66.20%
CYP2D6 inhibition - 0.7915 79.15%
CYP1A2 inhibition - 0.5483 54.83%
CYP2C8 inhibition - 0.6514 65.14%
CYP inhibitory promiscuity - 0.5862 58.62%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8320 83.20%
Carcinogenicity (trinary) Non-required 0.4250 42.50%
Eye corrosion - 0.9940 99.40%
Eye irritation - 0.6646 66.46%
Skin irritation - 0.8180 81.80%
Skin corrosion - 0.9603 96.03%
Ames mutagenesis + 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7933 79.33%
Micronuclear + 0.7600 76.00%
Hepatotoxicity + 0.5817 58.17%
skin sensitisation - 0.8368 83.68%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.6331 63.31%
Acute Oral Toxicity (c) III 0.6266 62.66%
Estrogen receptor binding + 0.7021 70.21%
Androgen receptor binding + 0.5564 55.64%
Thyroid receptor binding - 0.7589 75.89%
Glucocorticoid receptor binding + 0.6017 60.17%
Aromatase binding - 0.6089 60.89%
PPAR gamma + 0.5599 55.99%
Honey bee toxicity - 0.9104 91.04%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity + 0.9816 98.16%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.18% 95.56%
CHEMBL2581 P07339 Cathepsin D 94.32% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.26% 89.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.15% 91.11%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 91.02% 99.15%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 89.38% 97.21%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 89.23% 90.71%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 85.15% 94.42%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.61% 96.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.18% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.53% 99.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.17% 99.23%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 81.84% 89.62%
CHEMBL3401 O75469 Pregnane X receptor 81.33% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.21% 86.33%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.95% 95.50%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.67% 93.56%

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 163032568
LOTUS LTS0026552
wikiData Q105291840