9-(Acetyloxymethyl)-2-amino-3-oxophenoxazine-1-carboxylic acid

Details

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Internal ID cfd63639-5120-4ac2-a7ea-72196c59cbfd
Taxonomy Organoheterocyclic compounds > Benzoxazines > Phenoxazines
IUPAC Name 9-(acetyloxymethyl)-2-amino-3-oxophenoxazine-1-carboxylic acid
SMILES (Canonical) CC(=O)OCC1=C2C(=CC=C1)OC3=CC(=O)C(=C(C3=N2)C(=O)O)N
SMILES (Isomeric) CC(=O)OCC1=C2C(=CC=C1)OC3=CC(=O)C(=C(C3=N2)C(=O)O)N
InChI InChI=1S/C16H12N2O6/c1-7(19)23-6-8-3-2-4-10-14(8)18-15-11(24-10)5-9(20)13(17)12(15)16(21)22/h2-5H,6,17H2,1H3,(H,21,22)
InChI Key OOJRQEQZHJFOHW-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C16H12N2O6
Molecular Weight 328.28 g/mol
Exact Mass 328.06953611 g/mol
Topological Polar Surface Area (TPSA) 128.00 Ų
XlogP 1.00
Atomic LogP (AlogP) 1.64
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 9-(Acetyloxymethyl)-2-amino-3-oxophenoxazine-1-carboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8021 80.21%
Caco-2 - 0.8788 87.88%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.3413 34.13%
OATP2B1 inhibitior - 0.7176 71.76%
OATP1B1 inhibitior + 0.9199 91.99%
OATP1B3 inhibitior + 0.9323 93.23%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.5069 50.69%
P-glycoprotein inhibitior - 0.6882 68.82%
P-glycoprotein substrate - 0.6423 64.23%
CYP3A4 substrate + 0.5381 53.81%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8893 88.93%
CYP3A4 inhibition - 0.6135 61.35%
CYP2C9 inhibition - 0.6718 67.18%
CYP2C19 inhibition - 0.5351 53.51%
CYP2D6 inhibition - 0.8042 80.42%
CYP1A2 inhibition + 0.6367 63.67%
CYP2C8 inhibition + 0.5669 56.69%
CYP inhibitory promiscuity - 0.5468 54.68%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6225 62.25%
Eye corrosion - 0.9925 99.25%
Eye irritation - 0.9215 92.15%
Skin irritation - 0.8436 84.36%
Skin corrosion - 0.9568 95.68%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6337 63.37%
Micronuclear + 0.9100 91.00%
Hepatotoxicity + 0.7375 73.75%
skin sensitisation - 0.8950 89.50%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity + 0.7644 76.44%
Acute Oral Toxicity (c) III 0.6849 68.49%
Estrogen receptor binding + 0.8037 80.37%
Androgen receptor binding + 0.8158 81.58%
Thyroid receptor binding - 0.5518 55.18%
Glucocorticoid receptor binding + 0.8339 83.39%
Aromatase binding + 0.6949 69.49%
PPAR gamma + 0.8321 83.21%
Honey bee toxicity - 0.9298 92.98%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.7800 78.00%
Fish aquatic toxicity + 0.6698 66.98%

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
CHEMBL1293249 Q13887 Kruppel-like factor 5 97.09% 86.33%
CHEMBL4040 P28482 MAP kinase ERK2 95.47% 83.82%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.22% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.40% 91.11%
CHEMBL2581 P07339 Cathepsin D 91.89% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 91.42% 94.73%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.14% 99.23%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.46% 94.00%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 89.00% 94.42%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.64% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.00% 99.17%
CHEMBL1811 P34995 Prostanoid EP1 receptor 86.48% 95.71%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 85.75% 95.50%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.62% 96.00%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 82.24% 81.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.92% 96.09%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 80.85% 99.15%

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 14160620
LOTUS LTS0156092
wikiData Q105195408