Oxalic acid-13C2 dihydrate

Details

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Internal ID dc65523e-578d-422f-89cd-96512b9ca8b9
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Dicarboxylic acids and derivatives
IUPAC Name oxalic acid;dihydrate
SMILES (Canonical) C(=O)(C(=O)O)O.O.O
SMILES (Isomeric) [13C](=O)([13C](=O)O)O.O.O
InChI InChI=1S/C2H2O4.2H2O/c3-1(4)2(5)6;;/h(H,3,4)(H,5,6);2*1H2/i1+1,2+1;;
InChI Key GEVPUGOOGXGPIO-BQTCFENJSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C2H6O6
Molecular Weight 128.05 g/mol
Exact Mass 128.02314758 g/mol
Topological Polar Surface Area (TPSA) 76.60 Ų
XlogP 0.00
Atomic LogP (AlogP) -2.49
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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286367-59-7
Oxalic acid(1,2-13c2)
DTXSID50583974
(~13~C_2_)Ethanedioic acid--water (1/2)
Oxalic acid-13C2 dihydrate, 99 atom % 13C
J-017165

2D Structure

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2D Structure of Oxalic acid-13C2 dihydrate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7129 71.29%
Caco-2 - 0.8219 82.19%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.7429 74.29%
Subcellular localzation Mitochondria 0.7734 77.34%
OATP2B1 inhibitior - 0.8673 86.73%
OATP1B1 inhibitior + 0.9776 97.76%
OATP1B3 inhibitior + 0.9605 96.05%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9742 97.42%
P-glycoprotein inhibitior - 0.9839 98.39%
P-glycoprotein substrate - 0.9986 99.86%
CYP3A4 substrate - 0.8491 84.91%
CYP2C9 substrate + 0.6075 60.75%
CYP2D6 substrate - 0.8895 88.95%
CYP3A4 inhibition - 0.9751 97.51%
CYP2C9 inhibition - 0.9267 92.67%
CYP2C19 inhibition - 0.9828 98.28%
CYP2D6 inhibition - 0.9593 95.93%
CYP1A2 inhibition - 0.9621 96.21%
CYP2C8 inhibition - 0.9966 99.66%
CYP inhibitory promiscuity - 0.9962 99.62%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5102 51.02%
Carcinogenicity (trinary) Non-required 0.7539 75.39%
Eye corrosion + 0.5891 58.91%
Eye irritation + 0.9639 96.39%
Skin irritation + 0.5889 58.89%
Skin corrosion - 0.7586 75.86%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8306 83.06%
Micronuclear - 0.7200 72.00%
Hepatotoxicity + 0.7375 73.75%
skin sensitisation - 0.5582 55.82%
Respiratory toxicity - 0.8333 83.33%
Reproductive toxicity - 0.8778 87.78%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity + 0.6586 65.86%
Acute Oral Toxicity (c) IV 0.6275 62.75%
Estrogen receptor binding - 0.9194 91.94%
Androgen receptor binding - 0.9334 93.34%
Thyroid receptor binding - 0.8107 81.07%
Glucocorticoid receptor binding - 0.8647 86.47%
Aromatase binding - 0.8887 88.87%
PPAR gamma - 0.9313 93.13%
Honey bee toxicity - 0.9422 94.22%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.9100 91.00%
Fish aquatic toxicity + 0.6469 64.69%

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
No predicted targets yet!

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.
Capsicum annuum
Cichorium intybus
Cichorium pumilum
Hippophae rhamnoides
Isatis tinctoria
Persicaria tinctoria
Pogostemon cablin
Prunus mume
Punica granatum

Cross-Links

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PubChem 16213469
NPASS NPC150958