Griseolutein A

Details

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Internal ID 30b1aff3-545b-4191-91c8-58843b2043ac
Taxonomy Organoheterocyclic compounds > Diazanaphthalenes > Benzodiazines > Quinoxalines > Phenazines and derivatives
IUPAC Name 6-[(2-hydroxyacetyl)oxymethyl]-9-methoxyphenazine-1-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H14N2O6/c1-24-12-6-5-9(8-25-13(21)7-20)14-16(12)19-15-10(17(22)23)3-2-4-11(15)18-14/h2-6,20H,7-8H2,1H3,(H,22,23)
InChI Key LRNVPBRAXOLPTF-UHFFFAOYSA-N
Popularity 8 references in papers

Physical and Chemical Properties

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Molecular Formula C17H14N2O6
Molecular Weight 342.30 g/mol
Exact Mass 342.08518617 g/mol
Topological Polar Surface Area (TPSA) 119.00 Ų
XlogP 1.20
Atomic LogP (AlogP) 1.53
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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573-84-2
BRN 0349472
4-25-00-01289 (Beilstein Handbook Reference)
DTXSID60205918
1-Phenazinecarboxylic acid, 6-(((hydroxyacetyl)oxy)methyl)-9-methoxy-
6-(((Hydroxyacetyl)oxy)methyl)-9-methoxy-1-phenazinecarboxylic acid
1-Phenazinecarboxylic acid, 6-(hydroxymethyl)-9-methoxy-, glycolate (ester)

2D Structure

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2D Structure of Griseolutein A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8253 82.53%
Caco-2 - 0.7214 72.14%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.7234 72.34%
OATP2B1 inhibitior - 0.7172 71.72%
OATP1B1 inhibitior + 0.9491 94.91%
OATP1B3 inhibitior + 0.9417 94.17%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.8898 88.98%
P-glycoprotein inhibitior - 0.8386 83.86%
P-glycoprotein substrate - 0.7114 71.14%
CYP3A4 substrate - 0.5142 51.42%
CYP2C9 substrate - 0.8038 80.38%
CYP2D6 substrate - 0.8911 89.11%
CYP3A4 inhibition - 0.9386 93.86%
CYP2C9 inhibition - 0.7707 77.07%
CYP2C19 inhibition - 0.8216 82.16%
CYP2D6 inhibition - 0.8974 89.74%
CYP1A2 inhibition - 0.6336 63.36%
CYP2C8 inhibition + 0.7959 79.59%
CYP inhibitory promiscuity - 0.7071 70.71%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6110 61.10%
Eye corrosion - 0.9900 99.00%
Eye irritation - 0.8556 85.56%
Skin irritation - 0.8467 84.67%
Skin corrosion - 0.9566 95.66%
Ames mutagenesis - 0.6223 62.23%
Human Ether-a-go-go-Related Gene inhibition - 0.6116 61.16%
Micronuclear + 0.6600 66.00%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation - 0.9170 91.70%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity + 0.6690 66.90%
Acute Oral Toxicity (c) III 0.7522 75.22%
Estrogen receptor binding + 0.8076 80.76%
Androgen receptor binding + 0.7832 78.32%
Thyroid receptor binding - 0.5166 51.66%
Glucocorticoid receptor binding + 0.9194 91.94%
Aromatase binding + 0.8151 81.51%
PPAR gamma + 0.8255 82.55%
Honey bee toxicity - 0.9075 90.75%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.7800 78.00%
Fish aquatic toxicity - 0.7528 75.28%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.66% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 96.21% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.31% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.88% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 92.58% 96.00%
CHEMBL1255126 O15151 Protein Mdm4 90.73% 90.20%
CHEMBL3714130 P46095 G-protein coupled receptor 6 90.61% 97.36%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.17% 99.23%
CHEMBL2581 P07339 Cathepsin D 88.54% 98.95%
CHEMBL2535 P11166 Glucose transporter 88.21% 98.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.77% 94.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 87.07% 95.50%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.66% 99.17%
CHEMBL1811 P34995 Prostanoid EP1 receptor 84.57% 95.71%
CHEMBL2096618 P11274 Bcr/Abl fusion protein 84.23% 85.83%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 82.83% 81.11%
CHEMBL2047 Q96RI1 Bile acid receptor FXR 82.42% 96.10%
CHEMBL3891 P07384 Calpain 1 81.33% 93.04%
CHEMBL3401 O75469 Pregnane X receptor 80.20% 94.73%

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 196985
LOTUS LTS0015792
wikiData Q83079651