3-Methylglutaric acid

Details

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Internal ID 30ff0416-5808-4ed8-9ab6-7a2a7f4b2142
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Branched fatty acids > Methyl-branched fatty acids
IUPAC Name 3-methylpentanedioic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H10O4/c1-4(2-5(7)8)3-6(9)10/h4H,2-3H2,1H3,(H,7,8)(H,9,10)
InChI Key XJMMNTGIMDZPMU-UHFFFAOYSA-N
Popularity 272 references in papers

Physical and Chemical Properties

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Molecular Formula C6H10O4
Molecular Weight 146.14 g/mol
Exact Mass 146.05790880 g/mol
Topological Polar Surface Area (TPSA) 74.60 Ų
XlogP 0.10
Atomic LogP (AlogP) 0.57
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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626-51-7
3-Methylpentanedioic acid
Pentanedioic acid, 3-methyl-
beta-Methylglutaric acid
3Q0P190C7B
NSC-14870
CHEBI:68566
DTXSID50211649
RefChem:94904
DTXCID30134140
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 3-Methylglutaric acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7530 75.30%
Caco-2 + 0.5660 56.60%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.7693 76.93%
OATP2B1 inhibitior - 0.8500 85.00%
OATP1B1 inhibitior + 0.9650 96.50%
OATP1B3 inhibitior + 0.9642 96.42%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9797 97.97%
P-glycoprotein inhibitior - 0.9855 98.55%
P-glycoprotein substrate - 0.9877 98.77%
CYP3A4 substrate - 0.7959 79.59%
CYP2C9 substrate + 1.0000 100.00%
CYP2D6 substrate - 0.8908 89.08%
CYP3A4 inhibition - 0.9647 96.47%
CYP2C9 inhibition - 0.9668 96.68%
CYP2C19 inhibition - 0.9752 97.52%
CYP2D6 inhibition - 0.9598 95.98%
CYP1A2 inhibition - 0.9214 92.14%
CYP2C8 inhibition - 0.9986 99.86%
CYP inhibitory promiscuity - 0.9927 99.27%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5852 58.52%
Carcinogenicity (trinary) Non-required 0.7624 76.24%
Eye corrosion + 0.9566 95.66%
Eye irritation + 0.9837 98.37%
Skin irritation - 0.5500 55.00%
Skin corrosion + 0.9670 96.70%
Ames mutagenesis - 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7743 77.43%
Micronuclear - 0.7800 78.00%
Hepatotoxicity + 0.7000 70.00%
skin sensitisation - 0.8808 88.08%
Respiratory toxicity - 0.8889 88.89%
Reproductive toxicity - 0.7335 73.35%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity + 0.4733 47.33%
Acute Oral Toxicity (c) III 0.8700 87.00%
Estrogen receptor binding - 0.9702 97.02%
Androgen receptor binding - 0.8416 84.16%
Thyroid receptor binding - 0.9205 92.05%
Glucocorticoid receptor binding - 0.8549 85.49%
Aromatase binding - 0.8597 85.97%
PPAR gamma - 0.9591 95.91%
Honey bee toxicity - 0.9820 98.20%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity - 0.9300 93.00%
Fish aquatic toxicity + 0.6412 64.12%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.57% 96.09%
CHEMBL2581 P07339 Cathepsin D 92.90% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 84.66% 90.17%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 83.91% 100.00%

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.
There are no matching plants.

Cross-Links

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PubChem 12284
LOTUS LTS0044467
wikiData Q27137013