Bezerramycin A

Details

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Internal ID 5ad7b90d-f107-4307-8eea-e010aebb6e81
Taxonomy Organoheterocyclic compounds > Benzoxazines > Phenoxazines
IUPAC Name 2-amino-8-(hydroxymethyl)-3-oxophenoxazine-1-carboxamide
SMILES (Canonical) C1=CC2=C(C=C1CO)N=C3C(=CC(=O)C(=C3C(=O)N)N)O2
SMILES (Isomeric) C1=CC2=C(C=C1CO)N=C3C(=CC(=O)C(=C3C(=O)N)N)O2
InChI InChI=1S/C14H11N3O4/c15-12-8(19)4-10-13(11(12)14(16)20)17-7-3-6(5-18)1-2-9(7)21-10/h1-4,18H,5,15H2,(H2,16,20)
InChI Key HNZCCGYVANEENU-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H11N3O4
Molecular Weight 285.25 g/mol
Exact Mass 285.07495584 g/mol
Topological Polar Surface Area (TPSA) 128.00 Ų
XlogP -0.20
Atomic LogP (AlogP) 0.47
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Bezerramycin A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8350 83.50%
Caco-2 - 0.9132 91.32%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Nucleus 0.3994 39.94%
OATP2B1 inhibitior - 0.5761 57.61%
OATP1B1 inhibitior + 0.8997 89.97%
OATP1B3 inhibitior + 0.9405 94.05%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.6065 60.65%
P-glycoprotein inhibitior - 0.8341 83.41%
P-glycoprotein substrate - 0.7195 71.95%
CYP3A4 substrate - 0.5544 55.44%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8599 85.99%
CYP3A4 inhibition - 0.7253 72.53%
CYP2C9 inhibition - 0.6038 60.38%
CYP2C19 inhibition - 0.7519 75.19%
CYP2D6 inhibition - 0.9048 90.48%
CYP1A2 inhibition + 0.6017 60.17%
CYP2C8 inhibition + 0.4734 47.34%
CYP inhibitory promiscuity - 0.7281 72.81%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.6961 69.61%
Eye corrosion - 0.9928 99.28%
Eye irritation - 0.9600 96.00%
Skin irritation - 0.8452 84.52%
Skin corrosion - 0.9631 96.31%
Ames mutagenesis + 0.5509 55.09%
Human Ether-a-go-go-Related Gene inhibition - 0.5846 58.46%
Micronuclear + 0.9300 93.00%
Hepatotoxicity + 0.5657 56.57%
skin sensitisation - 0.8944 89.44%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity - 0.7153 71.53%
Acute Oral Toxicity (c) III 0.6382 63.82%
Estrogen receptor binding + 0.7491 74.91%
Androgen receptor binding + 0.8883 88.83%
Thyroid receptor binding - 0.5540 55.40%
Glucocorticoid receptor binding + 0.9211 92.11%
Aromatase binding + 0.7818 78.18%
PPAR gamma + 0.9191 91.91%
Honey bee toxicity - 0.9058 90.58%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity - 0.8366 83.66%

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
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.17% 94.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.30% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.74% 86.33%
CHEMBL2581 P07339 Cathepsin D 87.35% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.70% 99.17%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 84.55% 93.65%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 84.35% 95.50%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.44% 90.71%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 82.55% 94.42%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 82.35% 81.11%
CHEMBL4040 P28482 MAP kinase ERK2 80.52% 83.82%

Cross-Links

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PubChem 46183338
NPASS NPC236346
LOTUS LTS0128934
wikiData Q75056968