Butyric Acid

Details

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Internal ID 2a2ff2ce-0d88-4e0a-9127-d32cb8a7e3d8
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Straight chain fatty acids
IUPAC Name butanoic acid
SMILES (Canonical) CCCC(=O)O
SMILES (Isomeric) CCCC(=O)O
InChI InChI=1S/C4H8O2/c1-2-3-4(5)6/h2-3H2,1H3,(H,5,6)
InChI Key FERIUCNNQQJTOY-UHFFFAOYSA-N
Popularity 19,817 references in papers

Physical and Chemical Properties

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Molecular Formula C4H8O2
Molecular Weight 88.11 g/mol
Exact Mass 88.052429494 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 0.80
Atomic LogP (AlogP) 0.87
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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butanoic acid
107-92-6
n-Butyric acid
n-Butanoic acid
propylformic acid
ethylacetic acid
1-propanecarboxylic acid
butyrate
Butanic acid
1-Butyric acid
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Butyric Acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9937 99.37%
Caco-2 + 0.8296 82.96%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.4990 49.90%
OATP2B1 inhibitior - 0.8522 85.22%
OATP1B1 inhibitior + 0.9231 92.31%
OATP1B3 inhibitior + 0.8864 88.64%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9359 93.59%
P-glycoprotein inhibitior - 0.9851 98.51%
P-glycoprotein substrate - 0.9841 98.41%
CYP3A4 substrate - 0.8066 80.66%
CYP2C9 substrate + 0.6720 67.20%
CYP2D6 substrate - 0.8901 89.01%
CYP3A4 inhibition - 0.9720 97.20%
CYP2C9 inhibition - 0.9345 93.45%
CYP2C19 inhibition - 0.9613 96.13%
CYP2D6 inhibition - 0.9519 95.19%
CYP1A2 inhibition + 0.5106 51.06%
CYP2C8 inhibition - 0.9911 99.11%
CYP inhibitory promiscuity - 0.9849 98.49%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5735 57.35%
Carcinogenicity (trinary) Non-required 0.6417 64.17%
Eye corrosion + 0.9861 98.61%
Eye irritation + 0.9948 99.48%
Skin irritation + 0.8974 89.74%
Skin corrosion + 0.9933 99.33%
Ames mutagenesis - 0.9500 95.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8185 81.85%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.6647 66.47%
skin sensitisation + 0.5236 52.36%
Respiratory toxicity - 0.7667 76.67%
Reproductive toxicity - 0.8556 85.56%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity - 0.6907 69.07%
Acute Oral Toxicity (c) III 0.8028 80.28%
Estrogen receptor binding - 0.9529 95.29%
Androgen receptor binding - 0.9612 96.12%
Thyroid receptor binding - 0.9306 93.06%
Glucocorticoid receptor binding - 0.9367 93.67%
Aromatase binding - 0.9218 92.18%
PPAR gamma - 0.9189 91.89%
Honey bee toxicity - 0.9949 99.49%
Biodegradation + 1.0000 100.00%
Crustacea aquatic toxicity - 0.8532 85.32%
Fish aquatic toxicity - 0.6831 68.31%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL325 Q13547 Histone deacetylase 1 16000 nM
IC50
PMID: 21874153
CHEMBL1937 Q92769 Histone deacetylase 2 12000 nM
IC50
PMID: 21874153
CHEMBL1829 O15379 Histone deacetylase 3 9000 nM
IC50
PMID: 21874153
CHEMBL3192 Q9BY41 Histone deacetylase 8 15000 nM
IC50
PMID: 21874153

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.17% 96.09%
CHEMBL2581 P07339 Cathepsin D 91.59% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 90.79% 90.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.06% 99.17%

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.
Acacia adunca
Adiantum philippense
Aethusa cynapium
Ajania fastigiata
Aldama incana
Angelica acutiloba
Angelica decursiva
Angelica gigas
Angelica sinensis
Annona cornifolia
Artemisia pedemontana subsp. assoana
Artemisia xerophytica
Astragalus sempervirens
Calostephane divaricata
Capsicum annuum var. glabriusculum
Caragana aurantiaca
Chaenomeles sinensis
Coffea arabica
Conioselinum anthriscoides
Dumortiera hirsuta
Echeveria secunda
Elettaria cardamomum
Eucalyptus melliodora
Eupatorium lindleyanum
Euphorbia tithymaloides
Glycyrrhiza glabra
Gnetum latifolium
Goniothalamus malayanus
Hedysarum inundatum
Humulus lupulus
Hypericum laricifolium
Ipomoea digitata
Kitagawia praeruptora
Lepisorus ussuriensis
Levisticum officinale
Ligusticum officinale
Lysimachia mauritiana
Mangifera indica
Marrubium anisodon
Naucleopsis ternstroemiiflora
Nelumbo nucifera
Ocotea pittieri
Pastinaca sativa
Pelargonium graveolens
Peltostigma guatemalense
Peristeria elata
Polygala senega
Premna odorata
Prunus domestica
Pueraria montana var. lobata
Pycnandra acuminata
Rauvolfia vomitoria
Rhodanthe chlorocephala subsp. rosea
Rhododendron sichotense
Rumex maritimus
Salvia dorisiana
Salvia syriaca
Scutellaria amoena
Smilax china
Solanum laxum
Spondias mombin
Swertia franchetiana
Vaccinium oxycoccos
Vitis vinifera
Wikstroemia retusa
Zanthoxylum tetraspermum

Cross-Links

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PubChem 264
NPASS NPC149209
ChEMBL CHEMBL14227
LOTUS LTS0175510
wikiData Q193213