Kniphofione A

Details

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Internal ID c03a188a-980c-4b86-bbaf-fcb3b859adfa
Taxonomy Benzenoids > Anthracenes > Anthraquinones
IUPAC Name (4,5-dihydroxy-9,10-dioxoanthracen-2-yl)methyl 4-hydroxybenzoate
SMILES (Canonical) C1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)COC(=O)C4=CC=C(C=C4)O
SMILES (Isomeric) C1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)COC(=O)C4=CC=C(C=C4)O
InChI InChI=1S/C22H14O7/c23-13-6-4-12(5-7-13)22(28)29-10-11-8-15-19(17(25)9-11)21(27)18-14(20(15)26)2-1-3-16(18)24/h1-9,23-25H,10H2
InChI Key JNAZKJLAUIOKDJ-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C22H14O7
Molecular Weight 390.30 g/mol
Exact Mass 390.07395278 g/mol
Topological Polar Surface Area (TPSA) 121.00 Ų
XlogP 3.70
Atomic LogP (AlogP) 2.94
H-Bond Acceptor 7
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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CHEMBL3104873

2D Structure

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2D Structure of Kniphofione A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9656 96.56%
Caco-2 - 0.8075 80.75%
Blood Brain Barrier - 0.8250 82.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.8877 88.77%
OATP2B1 inhibitior + 0.5644 56.44%
OATP1B1 inhibitior + 0.8794 87.94%
OATP1B3 inhibitior + 0.9358 93.58%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.6000 60.00%
P-glycoprotein inhibitior - 0.5654 56.54%
P-glycoprotein substrate - 0.7907 79.07%
CYP3A4 substrate + 0.5411 54.11%
CYP2C9 substrate - 0.8125 81.25%
CYP2D6 substrate - 0.8529 85.29%
CYP3A4 inhibition - 0.8896 88.96%
CYP2C9 inhibition + 0.6898 68.98%
CYP2C19 inhibition - 0.6065 60.65%
CYP2D6 inhibition - 0.8247 82.47%
CYP1A2 inhibition + 0.5351 53.51%
CYP2C8 inhibition + 0.7773 77.73%
CYP inhibitory promiscuity - 0.6449 64.49%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.8214 82.14%
Carcinogenicity (trinary) Non-required 0.5542 55.42%
Eye corrosion - 0.9922 99.22%
Eye irritation + 0.6579 65.79%
Skin irritation - 0.6876 68.76%
Skin corrosion - 0.9826 98.26%
Ames mutagenesis + 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4778 47.78%
Micronuclear + 0.6433 64.33%
Hepatotoxicity + 0.6228 62.28%
skin sensitisation - 0.9040 90.40%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity - 0.6667 66.67%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity + 0.6593 65.93%
Acute Oral Toxicity (c) III 0.5031 50.31%
Estrogen receptor binding + 0.8043 80.43%
Androgen receptor binding + 0.9306 93.06%
Thyroid receptor binding - 0.6139 61.39%
Glucocorticoid receptor binding + 0.7389 73.89%
Aromatase binding - 0.6420 64.20%
PPAR gamma + 0.7644 76.44%
Honey bee toxicity - 0.8810 88.10%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5850 58.50%
Fish aquatic toxicity + 0.9889 98.89%

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
CHEMBL1951 P21397 Monoamine oxidase A 98.18% 91.49%
CHEMBL2581 P07339 Cathepsin D 97.15% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.16% 86.33%
CHEMBL2535 P11166 Glucose transporter 91.57% 98.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.18% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 89.65% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.44% 99.17%
CHEMBL226 P30542 Adenosine A1 receptor 89.37% 95.93%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 88.63% 95.17%
CHEMBL2179 P04062 Beta-glucocerebrosidase 88.04% 85.31%
CHEMBL4208 P20618 Proteasome component C5 87.06% 90.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.47% 91.11%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 86.45% 97.21%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.78% 89.00%
CHEMBL340 P08684 Cytochrome P450 3A4 85.60% 91.19%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.07% 99.23%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.86% 94.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.71% 96.95%
CHEMBL3194 P02766 Transthyretin 84.30% 90.71%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 83.97% 92.67%
CHEMBL3891 P07384 Calpain 1 82.29% 93.04%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 81.51% 100.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.64% 96.09%
CHEMBL2073 P07947 Tyrosine-protein kinase YES 80.64% 83.14%

Plants that contains it

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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.
Kniphofia ensifolia

Cross-Links

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PubChem 73058259
NPASS NPC119767
ChEMBL CHEMBL3104873