2-Hydroxy-2-(2-methoxy-2-oxoethyl)butanedioic acid

Details

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Internal ID 5ecb88e2-d29d-4315-b8e9-6ad0f817eb15
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Tricarboxylic acids and derivatives
IUPAC Name 2-hydroxy-2-(2-methoxy-2-oxoethyl)butanedioic acid
SMILES (Canonical) COC(=O)CC(CC(=O)O)(C(=O)O)O
SMILES (Isomeric) COC(=O)CC(CC(=O)O)(C(=O)O)O
InChI InChI=1S/C7H10O7/c1-14-5(10)3-7(13,6(11)12)2-4(8)9/h13H,2-3H2,1H3,(H,8,9)(H,11,12)
InChI Key YUTUUOJFXIMELV-UHFFFAOYSA-N
Popularity 15 references in papers

Physical and Chemical Properties

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Molecular Formula C7H10O7
Molecular Weight 206.15 g/mol
Exact Mass 206.04265265 g/mol
Topological Polar Surface Area (TPSA) 121.00 Ų
XlogP -1.40
Atomic LogP (AlogP) -1.16
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 5

Synonyms

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2-hydroxy-2-(2-methoxy-2-oxoethyl)butanedioic acid
citric acid methyl ester
SCHEMBL454845
CHEMBL4217399
CHEBI:182319
HY-N9540
AKOS040757905
MS-23119
CS-0200245
F82976
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-Hydroxy-2-(2-methoxy-2-oxoethyl)butanedioic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5227 52.27%
Caco-2 - 0.7414 74.14%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.7523 75.23%
OATP2B1 inhibitior - 0.8509 85.09%
OATP1B1 inhibitior + 0.9338 93.38%
OATP1B3 inhibitior + 0.9491 94.91%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9783 97.83%
P-glycoprotein inhibitior - 0.9818 98.18%
P-glycoprotein substrate - 0.9560 95.60%
CYP3A4 substrate - 0.6496 64.96%
CYP2C9 substrate + 0.6108 61.08%
CYP2D6 substrate - 0.8657 86.57%
CYP3A4 inhibition - 0.9523 95.23%
CYP2C9 inhibition - 0.8988 89.88%
CYP2C19 inhibition - 0.9039 90.39%
CYP2D6 inhibition - 0.9350 93.50%
CYP1A2 inhibition - 0.8953 89.53%
CYP2C8 inhibition - 0.9665 96.65%
CYP inhibitory promiscuity - 0.9858 98.58%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7730 77.30%
Carcinogenicity (trinary) Non-required 0.7430 74.30%
Eye corrosion - 0.9172 91.72%
Eye irritation + 0.7513 75.13%
Skin irritation - 0.6476 64.76%
Skin corrosion - 0.8990 89.90%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6195 61.95%
Micronuclear - 0.5300 53.00%
Hepatotoxicity + 0.5784 57.84%
skin sensitisation - 0.8369 83.69%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity - 0.7941 79.41%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity + 0.4559 45.59%
Acute Oral Toxicity (c) III 0.7481 74.81%
Estrogen receptor binding - 0.7836 78.36%
Androgen receptor binding - 0.7317 73.17%
Thyroid receptor binding - 0.7710 77.10%
Glucocorticoid receptor binding - 0.5344 53.44%
Aromatase binding - 0.6572 65.72%
PPAR gamma - 0.7613 76.13%
Honey bee toxicity - 0.9276 92.76%
Biodegradation + 0.8500 85.00%
Crustacea aquatic toxicity - 0.7708 77.08%
Fish aquatic toxicity - 0.7349 73.49%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.64% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.73% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 92.93% 83.82%
CHEMBL2581 P07339 Cathepsin D 88.77% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.15% 99.17%
CHEMBL340 P08684 Cytochrome P450 3A4 82.13% 91.19%
CHEMBL3401 O75469 Pregnane X receptor 81.86% 94.73%

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.
Opuntia ficus-indica

Cross-Links

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PubChem 378532
LOTUS LTS0241095
wikiData Q105364960