Meconic acid

Details

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Internal ID a5265b52-6693-4297-9aa7-ae7615ed36fa
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives
IUPAC Name 3-hydroxy-4-oxopyran-2,6-dicarboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H4O7/c8-2-1-3(6(10)11)14-5(4(2)9)7(12)13/h1,9H,(H,10,11)(H,12,13)
InChI Key ZEGRKMXCOCRTCS-UHFFFAOYSA-N
Popularity 131 references in papers

Physical and Chemical Properties

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Molecular Formula C7H4O7
Molecular Weight 200.10 g/mol
Exact Mass 199.99570246 g/mol
Topological Polar Surface Area (TPSA) 121.00 Ų
XlogP 0.00
Atomic LogP (AlogP) -0.26
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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497-59-6
Poppy acid
3-Hydroxy-4-oxopyran-2,6-dicarboxylic acid
3-HYDROXY-4-OXO-4H-PYRAN-2,6-DICARBOXYLIC ACID
NSC-805
DTXSID2060096
V502I79516
RefChem:156212
DTXCID3040722
207-848-2
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Meconic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6419 64.19%
Caco-2 - 0.7875 78.75%
Blood Brain Barrier - 0.8250 82.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.6301 63.01%
OATP2B1 inhibitior - 0.8619 86.19%
OATP1B1 inhibitior + 0.9134 91.34%
OATP1B3 inhibitior + 0.8775 87.75%
MATE1 inhibitior - 0.6000 60.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9832 98.32%
P-glycoprotein inhibitior - 0.9598 95.98%
P-glycoprotein substrate - 0.9729 97.29%
CYP3A4 substrate - 0.7393 73.93%
CYP2C9 substrate - 0.6163 61.63%
CYP2D6 substrate - 0.9086 90.86%
CYP3A4 inhibition - 0.8617 86.17%
CYP2C9 inhibition - 0.8297 82.97%
CYP2C19 inhibition - 0.9355 93.55%
CYP2D6 inhibition - 0.9712 97.12%
CYP1A2 inhibition - 0.9667 96.67%
CYP2C8 inhibition - 0.9539 95.39%
CYP inhibitory promiscuity - 0.9350 93.50%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.8066 80.66%
Eye corrosion - 0.9136 91.36%
Eye irritation + 0.9888 98.88%
Skin irritation + 0.6974 69.74%
Skin corrosion - 0.8679 86.79%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.9066 90.66%
Micronuclear + 0.8700 87.00%
Hepatotoxicity + 0.6750 67.50%
skin sensitisation - 0.6133 61.33%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity - 0.7025 70.25%
Acute Oral Toxicity (c) II 0.4568 45.68%
Estrogen receptor binding - 0.7645 76.45%
Androgen receptor binding - 0.6764 67.64%
Thyroid receptor binding - 0.8212 82.12%
Glucocorticoid receptor binding + 0.7030 70.30%
Aromatase binding - 0.7357 73.57%
PPAR gamma - 0.5433 54.33%
Honey bee toxicity - 0.9533 95.33%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.7600 76.00%
Fish aquatic toxicity + 0.7536 75.36%

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 96.61% 91.11%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 89.94% 89.34%
CHEMBL2581 P07339 Cathepsin D 89.50% 98.95%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 88.81% 83.57%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 87.06% 94.42%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 85.65% 90.71%
CHEMBL3194 P02766 Transthyretin 84.44% 90.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.01% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.83% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.87% 89.00%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 81.07% 93.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 80.87% 99.15%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 80.17% 81.11%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Aloe microstigma
Chrozophora plicata
Papaver somniferum

Cross-Links

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PubChem 10347
NPASS NPC135537
ChEMBL CHEMBL109516
LOTUS LTS0075943
wikiData Q421116