4-amino-2,5-dioxo-7-oxabicyclo[4.1.0]hept-3-ene-3-carboxamide

Details

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Internal ID af55a27f-7816-4b22-a235-93def9850aa3
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Cyclic ketones > Cyclohexenones
IUPAC Name 4-amino-2,5-dioxo-7-oxabicyclo[4.1.0]hept-3-ene-3-carboxamide
SMILES (Canonical) C12C(O1)C(=O)C(=C(C2=O)C(=O)N)N
SMILES (Isomeric) C12C(O1)C(=O)C(=C(C2=O)C(=O)N)N
InChI InChI=1S/C7H6N2O4/c8-2-1(7(9)12)3(10)5-6(13-5)4(2)11/h5-6H,8H2,(H2,9,12)
InChI Key MURWZWJFURVRNT-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C7H6N2O4
Molecular Weight 182.13 g/mol
Exact Mass 182.03275668 g/mol
Topological Polar Surface Area (TPSA) 116.00 Ų
XlogP -0.70
Atomic LogP (AlogP) -2.40
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-amino-2,5-dioxo-7-oxabicyclo[4.1.0]hept-3-ene-3-carboxamide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8778 87.78%
Caco-2 - 0.8787 87.87%
Blood Brain Barrier + 0.5371 53.71%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.3714 37.14%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9579 95.79%
OATP1B3 inhibitior + 0.9474 94.74%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9366 93.66%
P-glycoprotein inhibitior - 0.9401 94.01%
P-glycoprotein substrate - 0.9692 96.92%
CYP3A4 substrate - 0.7000 70.00%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8458 84.58%
CYP3A4 inhibition - 0.8547 85.47%
CYP2C9 inhibition - 0.8128 81.28%
CYP2C19 inhibition - 0.7162 71.62%
CYP2D6 inhibition - 0.9063 90.63%
CYP1A2 inhibition - 0.6726 67.26%
CYP2C8 inhibition - 0.9871 98.71%
CYP inhibitory promiscuity - 0.8016 80.16%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8743 87.43%
Carcinogenicity (trinary) Non-required 0.5764 57.64%
Eye corrosion - 0.9793 97.93%
Eye irritation + 0.7159 71.59%
Skin irritation - 0.7509 75.09%
Skin corrosion - 0.9382 93.82%
Ames mutagenesis - 0.6837 68.37%
Human Ether-a-go-go-Related Gene inhibition - 0.7062 70.62%
Micronuclear + 0.9000 90.00%
Hepatotoxicity + 0.7283 72.83%
skin sensitisation - 0.8521 85.21%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity + 0.6811 68.11%
Acute Oral Toxicity (c) III 0.4956 49.56%
Estrogen receptor binding - 0.5703 57.03%
Androgen receptor binding + 0.5485 54.85%
Thyroid receptor binding - 0.6204 62.04%
Glucocorticoid receptor binding - 0.6692 66.92%
Aromatase binding - 0.8340 83.40%
PPAR gamma - 0.5194 51.94%
Honey bee toxicity - 0.9516 95.16%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.7400 74.00%
Fish aquatic toxicity - 0.5760 57.60%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.68% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.26% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.88% 96.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.70% 99.23%

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 3029622
LOTUS LTS0270875
wikiData Q105172690