Isovaleric acid

Details

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Internal ID 0174833c-6e07-4add-8048-6cfcf8575b0d
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Branched fatty acids > Methyl-branched fatty acids
IUPAC Name 3-methylbutanoic acid
SMILES (Canonical) CC(C)CC(=O)O
SMILES (Isomeric) CC(C)CC(=O)O
InChI InChI=1S/C5H10O2/c1-4(2)3-5(6)7/h4H,3H2,1-2H3,(H,6,7)
InChI Key GWYFCOCPABKNJV-UHFFFAOYSA-N
Popularity 2,916 references in papers

Physical and Chemical Properties

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Molecular Formula C5H10O2
Molecular Weight 102.13 g/mol
Exact Mass 102.068079557 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 1.20
Atomic LogP (AlogP) 1.12
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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3-Methylbutanoic acid
503-74-2
Isopentanoic acid
3-Methylbutyric acid
Delphinic acid
Isopropylacetic acid
Isovalerianic acid
Butanoic acid, 3-methyl-
Isobutylformic acid
Isovalerianic
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Isovaleric acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9910 99.10%
Caco-2 + 0.6577 65.77%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.6618 66.18%
OATP2B1 inhibitior - 0.8643 86.43%
OATP1B1 inhibitior + 0.9519 95.19%
OATP1B3 inhibitior + 0.9427 94.27%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9438 94.38%
P-glycoprotein inhibitior - 0.9835 98.35%
P-glycoprotein substrate - 0.9810 98.10%
CYP3A4 substrate - 0.8084 80.84%
CYP2C9 substrate + 1.0000 100.00%
CYP2D6 substrate - 0.8908 89.08%
CYP3A4 inhibition - 0.9830 98.30%
CYP2C9 inhibition - 0.9679 96.79%
CYP2C19 inhibition - 0.9757 97.57%
CYP2D6 inhibition - 0.9560 95.60%
CYP1A2 inhibition - 0.9161 91.61%
CYP2C8 inhibition - 0.9987 99.87%
CYP inhibitory promiscuity - 0.9910 99.10%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5968 59.68%
Carcinogenicity (trinary) Non-required 0.7478 74.78%
Eye corrosion + 0.9952 99.52%
Eye irritation + 0.9939 99.39%
Skin irritation + 0.8202 82.02%
Skin corrosion + 0.9671 96.71%
Ames mutagenesis - 0.9200 92.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8196 81.96%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.7625 76.25%
skin sensitisation + 0.5794 57.94%
Respiratory toxicity - 0.9222 92.22%
Reproductive toxicity - 0.7098 70.98%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity + 0.4880 48.80%
Acute Oral Toxicity (c) III 0.8102 81.02%
Estrogen receptor binding - 0.9632 96.32%
Androgen receptor binding - 0.8988 89.88%
Thyroid receptor binding - 0.9051 90.51%
Glucocorticoid receptor binding - 0.9373 93.73%
Aromatase binding - 0.9152 91.52%
PPAR gamma - 0.9389 93.89%
Honey bee toxicity - 0.9799 97.99%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity - 0.9000 90.00%
Fish aquatic toxicity - 0.5993 59.93%

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 93.27% 96.09%
CHEMBL2581 P07339 Cathepsin D 93.14% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 83.61% 90.17%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 83.51% 100.00%

Cross-Links

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PubChem 10430
NPASS NPC104195
ChEMBL CHEMBL568737
LOTUS LTS0156600
wikiData Q415536