Isomalic acid

Details

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Internal ID fcff29cf-f3d3-453b-98f1-ac68679de136
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Dicarboxylic acids and derivatives
IUPAC Name 2-hydroxy-2-methylpropanedioic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C4H6O5/c1-4(9,2(5)6)3(7)8/h9H,1H3,(H,5,6)(H,7,8)
InChI Key LNRVTEQEGXVMEF-UHFFFAOYSA-N
Popularity 19 references in papers

Physical and Chemical Properties

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Molecular Formula C4H6O5
Molecular Weight 134.09 g/mol
Exact Mass 134.02152329 g/mol
Topological Polar Surface Area (TPSA) 94.80 Ų
XlogP -1.00
Atomic LogP (AlogP) -1.09
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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595-48-2
2-Hydroxy-2-methylpropanedioic acid
Isomalic acid
2-Hydroxy-2-methylmalonic acid
2-Methyltartronic acid
Tartronic acid, methyl-
2-Hydroxy-2-methylmalonate
U6K2REG9Q6
Hydroxymethylpropanedioic acid
Propanedioic acid, hydroxymethyl-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Isomalic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.4705 47.05%
Caco-2 - 0.8609 86.09%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.7799 77.99%
OATP2B1 inhibitior - 0.8633 86.33%
OATP1B1 inhibitior + 0.9679 96.79%
OATP1B3 inhibitior + 0.9660 96.60%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9664 96.64%
P-glycoprotein inhibitior - 0.9878 98.78%
P-glycoprotein substrate - 0.9941 99.41%
CYP3A4 substrate - 0.7575 75.75%
CYP2C9 substrate + 0.6165 61.65%
CYP2D6 substrate - 0.8937 89.37%
CYP3A4 inhibition - 0.9195 91.95%
CYP2C9 inhibition - 0.8535 85.35%
CYP2C19 inhibition - 0.9642 96.42%
CYP2D6 inhibition - 0.9553 95.53%
CYP1A2 inhibition - 0.9369 93.69%
CYP2C8 inhibition - 0.9950 99.50%
CYP inhibitory promiscuity - 0.9887 98.87%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.5896 58.96%
Carcinogenicity (trinary) Non-required 0.7488 74.88%
Eye corrosion - 0.9413 94.13%
Eye irritation + 0.8665 86.65%
Skin irritation + 0.4949 49.49%
Skin corrosion - 0.8117 81.17%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8334 83.34%
Micronuclear - 0.6600 66.00%
Hepatotoxicity + 0.7375 73.75%
skin sensitisation - 0.9037 90.37%
Respiratory toxicity - 0.9000 90.00%
Reproductive toxicity - 0.8333 83.33%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity + 0.6058 60.58%
Acute Oral Toxicity (c) III 0.8934 89.34%
Estrogen receptor binding - 0.8649 86.49%
Androgen receptor binding - 0.8604 86.04%
Thyroid receptor binding - 0.7012 70.12%
Glucocorticoid receptor binding - 0.7393 73.93%
Aromatase binding - 0.8719 87.19%
PPAR gamma - 0.7556 75.56%
Honey bee toxicity - 0.9855 98.55%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.8900 89.00%
Fish aquatic toxicity - 0.6100 61.00%

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
CHEMBL2581 P07339 Cathepsin D 82.90% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.29% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.69% 85.14%

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.
Imperata cylindrica

Cross-Links

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PubChem 136386
NPASS NPC163497
LOTUS LTS0088100
wikiData Q83082306