Xanthommatin(1-)

Details

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Internal ID 7d5ee342-3a4f-484b-a0fd-32fa11137f17
Taxonomy Organoheterocyclic compounds > Benzoxazines > Phenoxazines
IUPAC Name 11-(3-azaniumyl-3-carboxylatopropanoyl)-1,5-dioxo-4H-pyrido[3,2-a]phenoxazine-3-carboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H13N3O8/c21-8(19(27)28)4-10(24)7-2-1-3-13-16(7)23-18-14(31-13)6-12(26)17-15(18)11(25)5-9(22-17)20(29)30/h1-3,5-6,8H,4,21H2,(H,22,25)(H,27,28)(H,29,30)/p-1
InChI Key QLAHWTNCEYYDRR-UHFFFAOYSA-M
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H12N3O8-
Molecular Weight 422.30 g/mol
Exact Mass 422.06243935 g/mol
Topological Polar Surface Area (TPSA) 193.00 Ų
XlogP -1.40
Atomic LogP (AlogP) -2.57
H-Bond Acceptor 9
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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xanthommatin anion
CHEBI:57808
Q27124961
11-(3-azaniumyl-3-carboxylatopropanoyl)-1-hydroxy-5-oxo-5H-pyrido[3,2-a]phenoxazine-3-carboxylate

2D Structure

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2D Structure of Xanthommatin(1-)

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9175 91.75%
Caco-2 - 0.9393 93.93%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.4711 47.11%
OATP2B1 inhibitior - 0.5735 57.35%
OATP1B1 inhibitior + 0.9063 90.63%
OATP1B3 inhibitior + 0.9495 94.95%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8317 83.17%
BSEP inhibitior + 0.6962 69.62%
P-glycoprotein inhibitior - 0.6639 66.39%
P-glycoprotein substrate - 0.5642 56.42%
CYP3A4 substrate + 0.5769 57.69%
CYP2C9 substrate + 0.6105 61.05%
CYP2D6 substrate - 0.8491 84.91%
CYP3A4 inhibition - 0.8948 89.48%
CYP2C9 inhibition - 0.8003 80.03%
CYP2C19 inhibition - 0.8400 84.00%
CYP2D6 inhibition - 0.8421 84.21%
CYP1A2 inhibition - 0.5584 55.84%
CYP2C8 inhibition + 0.5588 55.88%
CYP inhibitory promiscuity - 0.7573 75.73%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.5906 59.06%
Eye corrosion - 0.9905 99.05%
Eye irritation - 0.9854 98.54%
Skin irritation - 0.8328 83.28%
Skin corrosion - 0.9615 96.15%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8184 81.84%
Micronuclear + 0.8600 86.00%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation - 0.9130 91.30%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.6038 60.38%
Acute Oral Toxicity (c) III 0.6773 67.73%
Estrogen receptor binding + 0.6800 68.00%
Androgen receptor binding + 0.8029 80.29%
Thyroid receptor binding + 0.5143 51.43%
Glucocorticoid receptor binding + 0.8152 81.52%
Aromatase binding - 0.5235 52.35%
PPAR gamma + 0.7783 77.83%
Honey bee toxicity - 0.8262 82.62%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity - 0.7205 72.05%

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
CHEMBL4040 P28482 MAP kinase ERK2 96.65% 83.82%
CHEMBL2581 P07339 Cathepsin D 95.34% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.99% 94.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.16% 91.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.92% 99.23%
CHEMBL3401 O75469 Pregnane X receptor 89.90% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.48% 86.33%
CHEMBL2535 P11166 Glucose transporter 89.11% 98.75%
CHEMBL1255126 O15151 Protein Mdm4 88.87% 90.20%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.87% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.64% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.16% 99.15%
CHEMBL1907598 P05106 Integrin alpha-V/beta-3 83.69% 95.71%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.22% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.10% 99.17%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.91% 90.71%
CHEMBL1811 P34995 Prostanoid EP1 receptor 80.96% 95.71%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 80.75% 81.11%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 80.74% 96.21%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.66% 85.14%
CHEMBL255 P29275 Adenosine A2b receptor 80.47% 98.59%
CHEMBL213 P08588 Beta-1 adrenergic receptor 80.32% 95.56%

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.
Phytolacca americana

Cross-Links

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PubChem 46931092
NPASS NPC11869