2-Isopropylmaleic acid

Details

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Internal ID 37e63c96-1491-442e-a817-601aebbc791f
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Branched fatty acids > Methyl-branched fatty acids
IUPAC Name (Z)-2-propan-2-ylbut-2-enedioic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H10O4/c1-4(2)5(7(10)11)3-6(8)9/h3-4H,1-2H3,(H,8,9)(H,10,11)/b5-3-
InChI Key NJMGRJLQRLFQQX-HYXAFXHYSA-N
Popularity 14 references in papers

Physical and Chemical Properties

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Molecular Formula C7H10O4
Molecular Weight 158.15 g/mol
Exact Mass 158.05790880 g/mol
Topological Polar Surface Area (TPSA) 74.60 Ų
XlogP 0.70
Atomic LogP (AlogP) 0.74
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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beta-isopropylmaleate
2-Isopropylmaleate
(2Z)-2-(propan-2-yl)but-2-enedioic acid
7596-39-6
isopropylmaleate
b-isopropylmaleate
isopropylmaleic acid
SCHEMBL346751
SCHEMBL346752
CHEBI:17275
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-Isopropylmaleic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9452 94.52%
Caco-2 - 0.5548 55.48%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.7880 78.80%
OATP2B1 inhibitior - 0.8596 85.96%
OATP1B1 inhibitior + 0.9426 94.26%
OATP1B3 inhibitior + 0.9500 95.00%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9803 98.03%
P-glycoprotein inhibitior - 0.9696 96.96%
P-glycoprotein substrate - 0.9846 98.46%
CYP3A4 substrate - 0.7571 75.71%
CYP2C9 substrate + 0.7957 79.57%
CYP2D6 substrate - 0.9275 92.75%
CYP3A4 inhibition - 0.9513 95.13%
CYP2C9 inhibition - 0.7810 78.10%
CYP2C19 inhibition - 0.9460 94.60%
CYP2D6 inhibition - 0.9281 92.81%
CYP1A2 inhibition - 0.9661 96.61%
CYP2C8 inhibition - 0.9940 99.40%
CYP inhibitory promiscuity - 0.9601 96.01%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6276 62.76%
Carcinogenicity (trinary) Non-required 0.7415 74.15%
Eye corrosion + 0.6985 69.85%
Eye irritation + 0.9162 91.62%
Skin irritation + 0.6196 61.96%
Skin corrosion + 0.7439 74.39%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8363 83.63%
Micronuclear - 0.8200 82.00%
Hepatotoxicity + 0.6750 67.50%
skin sensitisation + 0.6457 64.57%
Respiratory toxicity - 0.9111 91.11%
Reproductive toxicity - 0.7262 72.62%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.6800 68.00%
Estrogen receptor binding - 0.9306 93.06%
Androgen receptor binding - 0.8931 89.31%
Thyroid receptor binding - 0.8538 85.38%
Glucocorticoid receptor binding - 0.8800 88.00%
Aromatase binding - 0.9259 92.59%
PPAR gamma - 0.8879 88.79%
Honey bee toxicity - 0.9186 91.86%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.9700 97.00%
Fish aquatic toxicity + 0.9403 94.03%

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 82.47% 98.95%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 82.07% 100.00%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 80.05% 96.47%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 5280533
LOTUS LTS0027420
wikiData Q27102295