2-Aminomuconic semialdehyde

Details

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Internal ID 37798148-5bef-4711-8727-e45b12826546
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Alpha amino acids
IUPAC Name (2E,4Z)-2-amino-6-oxohexa-2,4-dienoic acid
SMILES (Canonical) C(=CC=O)C=C(C(=O)O)N
SMILES (Isomeric) C(=C\C=O)\C=C(/C(=O)O)\N
InChI InChI=1S/C6H7NO3/c7-5(6(9)10)3-1-2-4-8/h1-4H,7H2,(H,9,10)/b2-1-,5-3+
InChI Key QCGTZPZKJPTAEP-REDYYMJGSA-N
Popularity 16 references in papers

Physical and Chemical Properties

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Molecular Formula C6H7NO3
Molecular Weight 141.12 g/mol
Exact Mass 141.042593085 g/mol
Topological Polar Surface Area (TPSA) 80.40 Ų
XlogP -0.30
Atomic LogP (AlogP) -0.33
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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2-aminomuconate semialdehyde
2-Aminomuconate 6-semialdehyde
2-aminomuconic acid semialdehyde
(2E,4Z)-2-amino-6-oxohexa-2,4-dienoic acid
2-aminomuconic 6-semialdehyde
2-amino-6-oxo-2,4-hexadienoic acid
245128-91-0
SCHEMBL13176449
CHEBI:15745
CHEBI:77634
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2-Aminomuconic semialdehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9777 97.77%
Caco-2 + 0.8192 81.92%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Lysosomes 0.4450 44.50%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9494 94.94%
OATP1B3 inhibitior + 0.9553 95.53%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9493 94.93%
P-glycoprotein inhibitior - 0.9936 99.36%
P-glycoprotein substrate - 0.9743 97.43%
CYP3A4 substrate - 0.7295 72.95%
CYP2C9 substrate - 0.7968 79.68%
CYP2D6 substrate - 0.8565 85.65%
CYP3A4 inhibition - 0.9105 91.05%
CYP2C9 inhibition - 0.8913 89.13%
CYP2C19 inhibition - 0.9391 93.91%
CYP2D6 inhibition - 0.9261 92.61%
CYP1A2 inhibition - 0.9246 92.46%
CYP2C8 inhibition - 0.9687 96.87%
CYP inhibitory promiscuity - 0.9855 98.55%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5008 50.08%
Carcinogenicity (trinary) Non-required 0.5961 59.61%
Eye corrosion - 0.9592 95.92%
Eye irritation + 0.9936 99.36%
Skin irritation - 0.6615 66.15%
Skin corrosion - 0.8920 89.20%
Ames mutagenesis + 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.9501 95.01%
Micronuclear + 0.6600 66.00%
Hepatotoxicity + 0.7413 74.13%
skin sensitisation - 0.8559 85.59%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity - 0.5667 56.67%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.5014 50.14%
Estrogen receptor binding - 0.9667 96.67%
Androgen receptor binding - 0.7973 79.73%
Thyroid receptor binding - 0.8229 82.29%
Glucocorticoid receptor binding - 0.8363 83.63%
Aromatase binding - 0.8999 89.99%
PPAR gamma - 0.7163 71.63%
Honey bee toxicity - 0.9403 94.03%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity - 0.8200 82.00%
Fish aquatic toxicity - 0.4860 48.60%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.90% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.06% 96.09%
CHEMBL4246 P42680 Tyrosine-protein kinase TEC 80.82% 82.05%

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 5280625
LOTUS LTS0143450
wikiData Q2823203