6-(dihydroxymethylidene)-4,5-dioxopyran-2-carboxylic acid

Details

Top
Internal ID 2d8e0b60-a5ba-4778-9cc2-01870b5a09a3
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives > Dihydropyranones
IUPAC Name 6-(dihydroxymethylidene)-4,5-dioxopyran-2-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H4O7/c8-2-1-3(6(10)11)14-5(4(2)9)7(12)13/h1,12-13H,(H,10,11)
InChI Key SELRUPTWVICDPZ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C7H4O7
Molecular Weight 200.10 g/mol
Exact Mass 199.99570246 g/mol
Topological Polar Surface Area (TPSA) 121.00 Ų
XlogP -0.30
Atomic LogP (AlogP) -0.59
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 6-(dihydroxymethylidene)-4,5-dioxopyran-2-carboxylic acid

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8149 81.49%
Caco-2 - 0.7424 74.24%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Mitochondria 0.7334 73.34%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9479 94.79%
OATP1B3 inhibitior + 0.9664 96.64%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9871 98.71%
P-glycoprotein inhibitior - 0.9667 96.67%
P-glycoprotein substrate - 0.9761 97.61%
CYP3A4 substrate - 0.7495 74.95%
CYP2C9 substrate - 0.8058 80.58%
CYP2D6 substrate - 0.9010 90.10%
CYP3A4 inhibition - 0.9284 92.84%
CYP2C9 inhibition - 0.9171 91.71%
CYP2C19 inhibition - 0.8764 87.64%
CYP2D6 inhibition - 0.9563 95.63%
CYP1A2 inhibition - 0.9678 96.78%
CYP2C8 inhibition - 0.9815 98.15%
CYP inhibitory promiscuity - 0.9575 95.75%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8643 86.43%
Carcinogenicity (trinary) Non-required 0.6175 61.75%
Eye corrosion - 0.9131 91.31%
Eye irritation + 0.9869 98.69%
Skin irritation + 0.6341 63.41%
Skin corrosion - 0.8543 85.43%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.9265 92.65%
Micronuclear + 0.7500 75.00%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation - 0.8028 80.28%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity - 0.5222 52.22%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.6240 62.40%
Acute Oral Toxicity (c) II 0.3084 30.84%
Estrogen receptor binding - 0.6977 69.77%
Androgen receptor binding - 0.7003 70.03%
Thyroid receptor binding - 0.8536 85.36%
Glucocorticoid receptor binding - 0.4834 48.34%
Aromatase binding - 0.8073 80.73%
PPAR gamma - 0.5738 57.38%
Honey bee toxicity - 0.9626 96.26%
Biodegradation + 0.7250 72.50%
Crustacea aquatic toxicity - 0.8400 84.00%
Fish aquatic toxicity + 0.7363 73.63%

Targets

Top

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
CHEMBL2581 P07339 Cathepsin D 87.51% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.58% 91.11%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 84.18% 87.67%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.91% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.39% 99.23%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 80.18% 81.11%

Plants that contains it

Top
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.
Papaver somniferum

Cross-Links

Top
PubChem 5351448
LOTUS LTS0117902
wikiData Q105251269